Gastroenterology
Volume 116, Issue 3 , Pages 735-760, March 1999

AGA technical review on anorectal testing techniques

This Technical Review has been endorsed in principle by the American Association for the Study of Liver Disease, the American College of Gastroenterology, and the American Society for Gastrointestinal Endoscopy

Article Outline

Abstract 

This literature review and the recommendations therein were prepared for the American Gastroenterological Association Clinical Practice and Practice Economics Committee. Following external review, the paper was approved by the committee on May 17, 1998.

GASTROENTEROLOGY 1999;116:735-760

 

Anorectal symptoms and disorders are some of the most common and distressing experienced in all ages of the population. Fecal incontinence is reported in 3%–8% of the population.1, 2, 3 Symptoms compatible with constipation are found in 3%–20% of the population; the prevalence increases to 20%–25% in the elderly.1, 3, 4, 5 Anorectal pain compatible with the levator ani syndrome and proctalgia fugax occur in 5%–8% of the population.3, 6 Therefore, a multitude of tests have arisen over the years for assessment of the sensory-motor aspects of the anorectal region. This review evaluates the pertinent literature and the information at hand to provide some direction for the use of the various techniques in patients with these conditions. An attempt has been made to identify the capability of different tests to assess aspects of the defecation and continence mechanisms and the sensory mechanisms involved with symptom production. The review does not describe the technical details of each test (“how to”) or the clinical diagnostic and therapeutic paradigms for their use in different disorders (“when to”). The information is primarily derived from and directed to the adult population, although some mention is made of the pediatric age group as well.

Anorectal symptoms often are not isolated phenomena but can be associated with more generalized systemic or organic diseases (e.g., diabetes with neuropathy, collagen vascular disorders, neural or muscular diseases), and with functional disorders, particularly the irritable bowel syndrome.1, 2, 3, 4, 5, 7

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The literature 

Upon review of the literature on the value of anorectal tests, few large-scale studies are found (1) that have attempted to validate anorectal tests against other techniques, and (2) that include properly controlled treatment trials with placebo components, adequate control populations, and careful outcome assessment. Therefore, most attention has been directed to studies that use sample sizes larger than 25, use objective physiological assessments for comparison, and, in treatment trials, include adequate assessments before and after treatment. The articles were gleaned from a MEDLINE search for the 10 years preceding June 1996 and from the bibliography of recent reviews.

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Definitions 

The symptom complexes related to the anorectal area, particularly definition of terms such as fecal incontinence and constipation, allow for considerable debate. Terms such as dyschezia and tenesmus, although defined by consensus,8 are better ignored because of the many meanings attached to them and the overlap in meaning between the two terms and other definitions of constipation and irritable bowel syndrome. Therefore, in this review, broad definitions are used without limitation as to the presence of organic disease or structural abnormality on one hand or a functional basis for the symptoms on the other. A functional disorder has been defined as “a variable combination of chronic or recurrent gastrointestinal symptoms not explained by biochemical or chemical abnormalities.”9 However, when specific disease entities, structural abnormalities, or functional syndromes have an impact on the use of the techniques, these conditions are incorporated into the discussion.

Fecal incontinence 

The first part of the definition proposed by the Rome criteria on the basis of symptoms9, 10 can provide a broad basis for inclusion in the category of fecal incontinence: continuous or recurrent uncontrolled passage of fecal material (>10 mL) for at least 1 month in an individual older than 3 years of age. The American Psychiatric Association sets the age at older than 4 years.11

Constipation 

Constipation may be conventionally defined by three parameters: symptoms, measurements of defecation, and physiological measurements.8 Based on symptoms alone, functional constipation according to the Rome criteria10 can be defined as the presence of two or more of the following symptoms for at least 3 months: (1) straining at defecation at least one fourth of the time, (2) lumpy and/or hard stools at least one fourth of the time, (3) sensation of incomplete evacuation at least one fourth of the time, and (4) two or fewer bowel movements per week. In this review, constipation is considered to fall under two broad categories: slow colonic transit and anorectal dysfunction leading to impaired evacuation. This review does not deal with tests for the slow transit type of constipation, but concentrates on testing that identifies the role played by the anorectal area. Therefore, terms such as outlet obstruction, anismus, pelvic floor dyssynergia, and paradoxical contraction of pelvic musculature are included under the definition of constipation.

Levator ani syndrome 

The levator ani syndrome (puborectalis syndrome, chronic proctalgia, pyriformis syndrome, and pelvic tension myalgia) has been defined by consensus in the Rome criteria9 as (1) chronic or recurrent anorectal pain or aching for at least 3 months, (2) episodes that last 20 minutes or longer, and (3) exclusion of other likely organic causes of rectal pain.

Proctalgia fugax 

This syndrome is defined by the Rome criteria9 as (1) recurrent episodes of midline pain localized to the anus or lower rectum for at least 3 months, (2) episodes lasting from seconds to minutes, (3) absence of anorectal pain between episodes, and (4) lack of evidence for anorectal disease.

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Anatomic and physiological considerations 

The mechanisms and structures involved in the process of defecation and in the maintenance of continence are multiple and complex (Figure 1).

Overall control involves both voluntary and involuntary components. Colonic and anorectal function are integrated and interrelated. The anal sphincter has both smooth muscle and striated muscle components. Other striated muscles of the pelvic floor, including the puborectalis and levator muscles, perform important functions. Both sensory and motor innervation occur through several nerves including the lumbar colonic nerves, the pudendal nerves, and pelvic nerves with connections to the spinal cord levels from at least L2 to S4. Simple reflexes such as relaxation of the anal sphincter with distention of the rectum, as well as more complicated function such as reservoir function of the rectum, can vary considerably in health and disease. Psychobehavioral factors have an impact on function of the anorectum to the full defecation process. Therefore, it is unreasonable to expect that any single test, or even a battery of tests, can fully characterize each anorectal sensory and motor disorder responsible for the different symptoms and syndromes in this area, whether these be of structural or organic disease origin or functional in nature. However, using a constellation of investigations it is often possible to characterize precisely the nature of a disorder, leading to specific therapies with well-documented outcomes. More detailed descriptions of the anatomy and innervation and of the mechanisms of defecation and continence can be found in recent articles.12, 13

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Techniques 

History 

A complete detailed history is essential to direction of diagnostic and therapeutic approaches to the patient with anorectal symptoms and disorders. Diaries and questionnaires are useful adjuncts in this regard.

Diaries 

Symptom diaries are useful for three purposes: (1) diagnostic evaluation, (2) monitoring of compliance with treatment, and (3) measurement of efficacy of treatment. The diary is a simple, inexpensive way to obtain “objective,” prospective information on stool frequency and consistency, on the nature and frequency of incontinence, and on the occurrence of other symptoms such as pain. Diaries cannot predict colonic transit, rectal emptying, or the cause of impaired defecation.14 Although not completely specific or sensitive for slow transit, they do give some guides; patients with documented infrequent bowel movements are likely to have slow transit.15, 16 Symptom diaries should be considered and described to the patient as aids to memory. Therefore, they must be simple and short. Symptom diaries are discussed at greater length, and a sample is provided, in an earlier review.17

In disorders such as fecal incontinence, it is important to identify the circumstances in which symptoms occur as a means of identifying the most effective strategies for treatment.18, 19 For example, documentation that fecal incontinence is less likely the day after a large bowel movement and more likely when several days have passed without a sizable bowel movement is helpful in suggesting the diagnosis of overflow incontinence.

Symptom diaries are often used in clinical trials to measure outcome20, 21 and are similarly useful in treating individual patients. Symptom diaries are believed to be more objective than patient recall at a scheduled office visit because recall is strongly influenced by poor memory of events and by the relative prominence of the most recent and most severe events.22 A daily record of whether instructions were followed will help to identify problems with treatment adherence that can be addressed with the patient, as well as indicating when a treatment is not working.

Conclusion 

Symptom diaries are recommended for (1) diagnostic evaluation, (2) monitoring of adherence to treatment recommendations, and (3) measurement of efficacy of treatment in patients with constipation and fecal incontinence.

Questionnaires 

Symptom questionnaires, filled out by the patient before the first evaluation, can significantly speed up the interview by identifying areas that can be skipped and by giving the patient a chance to look up and record information on medications and prior illnesses. More importantly, questionnaires help clinicians avoid overlooking significant symptoms that may not be part of the reason the patient is in the clinic but should nevertheless be identified and evaluated in the context of the presenting complaint.

A variety of gastrointestinal symptom questionnaires are available, although most are oriented toward the detection of functional disorders such as the irritable bowel syndrome.23, 24, 25 The most thoroughly validated and extensively used questionnaire is the Mayo Clinic Bowel Symptom Questionnaire developed by Talley et al.26 The Mayo questionnaire has been adapted for use in an elderly population.27 Thompson and Heaton4 developed a structured interview for lower bowel symptoms. The questionnaire developed by Drossman,28 based on the Rome multinational working team reports, is used to identify patients with any of a number of functional gastrointestinal disorders. Drossman et al.29 subsequently developed a short Functional Bowel Disease Severity Index for grading the severity of symptoms in patients with chronic abdominal pain, the irritable bowel syndrome, or other functional bowel disorders. However, this index does not address anorectal disorders.

Conclusion 

At present, there is no symptom questionnaire that satisfactorily addresses anorectal disorders.

Physical examination 

A complete physical examination will identify certain structural disorders (e.g., prolapse, perineal disease) and local and systemic disease processes that may affect anorectal function and dysfunction. In addition, some assessment of perineal innervation can be obtained through observation of perianal sensation and reflex contraction of the external anal sphincter to perianal stimulation and to a cough.

There is limited information on the relationship between specific physical examination maneuvers and objective tests of anorectal function. However, some studies address the agreement between anal canal pressure measurements and digital examination. In a study of 66 patients, Hallan et al.30 found that digital examination by an experienced surgeon correlated (r = 0.56; P < 0.001) with anal canal resting pressure, and digital examination correlated (r = 0.72; P < 0.001) with maximum squeeze pressure, although in individual patients the digital assessment was often inaccurate. Similar observations were made by Felt-Bersma et al.31 in a study of 280 patients. In a study of 64 patients, Eckardt and Kanzler32 found agreement between digital examination results and resting anal canal pressure of 0.41 (contingency coefficient) and the agreement between digital examination results and squeeze pressure of 0.52. These correlations with objective measurements are too low to support the use of digital examination alone in the diagnostic assessment of sphincter function. Hallan et al.30 found the agreement between independent digital examination results to be comparable to the agreement between results of different manometric examinations. This finding suggests that day-to-day variations in anal canal pressures account for some of the differences between independent digital examination results. Physical examination may also provide some qualitative assessment of the levator ani and puborectalis muscle contractions and tenderness. Digital examination will identify fecal impaction in most patients but will miss 30% of fecal impactions in the elderly because a large amount of feces in the upper rectum and in sigmoid colon seen on radiographs may not extend into the distal rectum in reach of the examining finger.33

Measurement of pelvic floor descent can be done objectively. Henry et al.34 developed a mechanical device that can be used externally to quantitatively locate the perineal surface of the anal canal relative to the ischial tuberosities. With the patient in the left lateral position, measurements are made at rest and with straining. However, simple observation of the level of the perineum relative to the ischial tuberosities is adequate. The perineum should not descend beyond the outlet of the bony pelvis on straining effort.

Conclusion 

In experienced hands, assessment of the anal sphincter by digital examination provides limited qualitative assessment of sphincter resting and squeeze pressures.

Endoscopy 

Rigid or flexible examination of the large bowel is an essential part of the examination of every new patient with anorectal symptoms. They may provide information about disease such as a benign or malignant obstructing lesion and mucosal inflammation. Although not as precise as lateral radiography, these examinations may suggest the presence of a megarectum or megacolon.

Conclusion 

Endoscopy is necessary to exclude organic disease in patients with fecal incontinence, constipation, or proctalgia.

Imaging techniques 

Barium enema 

Barium enema is useful primarily for colonic assessment. In patients with a history or examination results suggestive of megarectum or megacolon, there is interest in the rectal and sigmoid dimensions. In these patients, some investigators believe that the optimal investigation is a water-soluble contrast study without bowel preparation.35 Of particular interest are the precise rectal dimensions and the proximal extent of large bowel dilation. Megarectum can be defined as a transverse diameter of the rectum at the pelvic brim larger than 6.5 cm.36 Barium radiographs will show the characteristic denervated bowel segment with proximal dilatation of the colon in Hirschsprung's disease,37 but they do not reliably distinguish between so-called short-segment Hirschsprung's disease and idiopathic constipation.38

Conclusion 

Barium enema is not usually necessary for assessment of the anorectal area in patients with fecal incontinence or constipation, except to help exclude intraluminal mucosal disease or to assess bowel dilation.

Evacuation proctography (defecography) 

Evacuation proctography (defecography) involves imaging the rectum with contrast material and observation of the process, rate, and completeness of rectal evacuation using fluoroscopic techniques.39, 40, 41, 42, 43, 44 A variety of contrast materials have been used, including esophageal contrast barium and barium mixed with oatmeal or other viscous materials. It is not a study of normal defecation, is not performed in response to a desire to defecate, and lacks the normal electromuscular events associated with defecation. Some patients' embarrassment at the nature and the setting of the test may inhibit normal emptying of the contrast material.

Defecography has been criticized on a number of grounds. First, there is poor agreement between independent observers in the measurement of the anorectal angle, a parameter thought to be critical to the interpretation of defecography results.45, 46 It is uncertain whether the central axis of the rectum,41, 44 the entire posterior wall of the rectum,47 or the most distal portion of the posterior wall39, 40, 43, 44, 48 should be used. Second, some of the findings often reported on this examination, especially rectocele, descent of the pelvic floor, and internal intussusception, are seen in a large proportion of asymptomatic individuals,43, 44, 48, 49 and the presence of these entities does not correlate with impaired rectal emptying.49 Third, normal values of rectal emptying vary widely.50, 51 Fourth, rectal evacuation does not correlate with symptoms (infrequent defecation vs. impaired defecation), colonic transit, or anal manometry results.49, 50 Finally, several investigators have argued that defecography adds little data to the results of anorectal manometry52, 53 and/or does not differentiate patients with impaired defecation from those with fecal incontinence or normal controls.54 However, there are some potential uses of this technique.

There is some merit to the objective demonstration of a large rectocele in patients who complain of incomplete evacuation, particularly those who are helped by rectal or vaginal digitation during defecation. However, rectoceles smaller than 2 cm in diameter are normal in women.44 Even large rectoceles are not always associated with symptoms, and correlation between the presence of such a finding, symptoms, and improvement with surgical treatment is not always good.55

Internal rectal intussusception has been implicated as a cause of symptoms and of solitary rectal ulcer. However, its correction correlates poorly with symptomatic benefit, and mucosal prolapse and rectal intussusception have been reported in normal subjects.44, 56

Defecography can be used to determine external rectal prolapse.57, 58, 59, 60, 61, 62 However, it should be possible to demonstrate external prolapse on the commode without radiology.

Defecography combined with filling of the small bowel with barium from above may be useful in demonstrating an enterocele,41 and as such may be a useful adjunctive test in the evaluation of patients with impaired defecation and proctalgia.

In theory, quantification of rectal evacuation could be helpful in patients with constipation, especially those with pelvic floor dysfunction or dyssynergia.39, 40, 41, 42, 63 For example, some patients with constipation have poor rectal emptying on proctography.49, 64 However, in one recent study, no differences were observed in patterns of rectal emptying of barium contrast among four study groups: patients with infrequent defecation and normal colonic transit, patients with infrequent defecation with proximal slowing of colonic transit, patients with defecatory difficulty only, and control subjects.49 Furthermore, in younger patients with constipation, information about evacuation has not been proven to alter treatment or to predict the outcome of treatments such as colectomy.65 Therefore, although defecography may disclose significant differences between constipated patients and controls, the degree of overlap renders these studies of limited importance in management decisions. However, if the results of defecography (e.g., inappropriate contraction of the puborectalis muscle) corroborate the results of other studies of anorectal function, they may serve to reinforce the validity of such testing (see discussions of neuromuscular function, anorectal monitoring, constipation, and tests for specific diagnosis or management [constipation/impaired defecation, biofeedback] in this review).

An alternative to proctography involves quantitative measurement of the rate and completeness of rectal evacuation.66 One hundred milliliters of barium paste is inserted into the rectum, and the patient is asked to evacuate as rapidly and completely as possible. The maximum emptying rate, time to achieve maximum emptying, and proportion of barium evacuated are measured using a weight transducer. Normal subjects evacuate quickly and completely. Patients with severe constipation demonstrate a variable evacuation disturbance. Results obtained using this technique have been shown to correlate well with the percentage change in area on evacuation proctography.67 Similar semiquantitative observations about rectal emptying can be made by using a paste containing a radioisotope that can be placed into the rectum and the amount evacuated accurately quantified.47, 50, 68 A low-radiation isotope such as 99mTc exposes the patient to a lower radiation dose than proctography. Two studies have found that rectal emptying of 200 mL of an isotope-labeled artificial stool varies widely among normal controls, ranging from 28% to 98% in 26 control subjects.50, 51 Either total evacuation volumes of 18 constipated subjects were similar to those of controls (mean, 64%; range, 34%–91%), although mean evacuation rates (percent per second) were significantly slower in the constipated patients,51 or evacuation was less in constipated patients than in controls; however, there was a wide overlap between the two groups.50, 69 Measurement of rectal emptying by these two techniques does not give anatomic information about rectal and anal configuration and the changes during emptying.

Another technique, balloon proctography, was introduced before defecography with the intention of outlining the rectum during rectal evacuation.70 A balloon filled with radiolabeled water (scintigraphic balloon topography) has also been used to measure the anorectal angle.71 These techniques depend on the balloon contour's conforming to the rectum. Balloon proctography has been superceded by evacuation proctography, with direct contrast instillation into the rectum.

Conclusion 

(1) Evacuation proctography is not of established value in patients with fecal incontinence. (2) Proctography is of potential value in patients with constipation in whom the following problems are suspected as the cause of impaired defecation: inappropriate contraction of the puborectalis muscle, enterocele (e.g., after hysterectomy), and anterior rectocele (e.g., history of manipulation of the rectal wall per vagina). Otherwise, there is no support for the routine use of this technique.

Anal ultrasonography 

The ability to image the sphincter muscles accurately using anal endosonography has radically altered understanding of the pathogenesis of fecal incontinence as well as its investigation and management.72, 73 Abnormalities of structural integrity involving either muscle can be clearly identified. The procedure is rapid and without radiation exposure, but interpretation is very dependent on the operator. However, anal canal ultrasonography has a high degree of sensitivity and specificity, approaching 100% in the hands of experienced investigators, in identification of anatomic defects in both the external and internal anal sphincters as well as more subtle abnormalities of internal sphincter smooth muscle texture and composition.74, 75, 76, 77, 78 In vitro and in vivo dissection studies have shown close correlation between the endosonographic image and anatomic structures.79, 80

The endosonographic probe rotates through 360° inside a hard plastic cone of 15-mm diameter and provides an image of the internal and external anal sphincters. A plastic cone over the rotating endoprobe provides a superior image to that obtained with a probe covered by a water-filled balloon, as is used in rectal endosonography. Two main probe frequencies have been used. Both 7-MHz and 10-MHz probes provide good resolution of the anal sphincter muscles, but the resolution is slightly superior with the latter. The internal sphincter is seen as a dark homogeneous ring (Figure 2).

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  • Fig. 2. 

    Normal anal ultrasound scan showing the anal sphincter muscles in cross section through the mid anal canal. The darker homogenous ring is the IAS smooth muscle (I). The white heterogeneous ring surrounding this is the EAS (arrows; E). The top of the figure is anterior.

Anal endosonography also allows delineation of the external anal sphincter, although the interpretation of these images is much more subjective than interpretation of those of the internal anal sphincter. There is more anatomic variation of the external sphincter, especially anteriorly. This is clinically important if obstetric damage is not to be overdiagnosed. In women, vaginal as well as anal placement of the probe may be used.81

Using endosonography and manometry, it is at times possible to link different symptoms of incontinence with different muscle pathologies. Passive fecal incontinence, the loss of stool without the patient's awareness, is related to dysfunction of the internal anal sphincter, whereas urge incontinence, the loss of stool because of an inability to suppress defecation, is related to external anal sphincter dysfunction.82

Anal endosonography has been used in assessment of internal anal sphincter defects, such as those that occur after anal stretching,83 anal sexual abuse,84 and lateral sphincterotomy.85 Degeneration of the internal sphincter, as in progressive systemic sclerosis, is also visible.86 Although the internal sphincter is not surgically repairable on its own, the delineation of pathology does allow increased understanding of the disease process and suggests treatment with either a supportive medical approach or newer surgical techniques designed to increase resting tone.

Ultrasonography has been compared to mapping of the external anal sphincter with needle electromyography and has been found to be slightly more accurate77 and better tolerated.74, 87 Ultrasonography is also more accurate than anorectal manometry,77 including vectormanometry. Therefore, anal endosonography has decreased the need for some other investigations, such as electromyography, to identify external anal sphincter defects75 and to provide the potential for more definitive therapy, such as surgical correction of the defect. Use of anal endosonography in patients with obstetrical injury is a prime example (Figure 3).

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  • Fig. 3. 

    Anal ultrasound scan of a woman with anterior obstetric sphincter damage. The top of the figure is anterior. There is disruption of both the IAS (small arrows) and EAS (large arrows) muscles.

In one study, 35% of primiparae who delivered vaginally developed a sphincter defect involving one or both muscles.88 Only 4% of multipara developed new defects. These women can present soon after delivery or up to many years later. Symptoms can date back to the delivery or develop later in life. In women with fecal incontinence in whom the only apparent risk factor is obstetric damage, 90% have endosonographic evidence of structural abnormality of one or both sphincter muscles.89, 90, 91 In a recent series, 55 consecutive women with obstetric-related incontinence for solid or liquid stool had external sphincter damage accurately characterized using endosonography and physiological tests and were treated by anterior overlap sphincter repair.92 Eighty percent of patients became either fully continent or incontinent for gas only; only 2 patients remained incontinent for solid stool. Symptomatic improvement correlated closely with the ability to endosonographically identify overlapping muscle postoperatively. Another study of 28 patients with obstetric injury reported similar results.93

Anal endosonography has also been useful in women who have had third-degree tears and experienced continued symptoms, despite a primary sphincter repair. There is a high incidence of persisting structural damage in these women.94, 95 In one study of 34 women who sustained third-degree tears, half of the women with repaired third-degree tears still had symptoms of anal incontinence or urgency. Sonographic sphincter defects were identified in 85% of those with third-degree tears compared with 33% of control subjects who had not sustained tears.95

Therefore, accurate delineation of structural damage using endosonography allows for correct selection of patients for surgical repair and for postoperative assessment of patients. The relationship between the nature, location, and extent of the structural damage and symptoms requires further testing.

Conclusion 

Anal ultrasonography is presently the simplest, most reliable, least invasive test for definition of anatomic defects in the external and internal anal sphincters.

Magnetic resonance imaging and computed tomographic scanning 

Computed tomographic scanning has little place in the evaluation of anal disease because of its poor resolution of this small area and because of the radiation exposure. However, magnetic resonance imaging (MRI) may have a role. Although anorectal structures can be visualized using standard MRI techniques, the use of an endoanal coil significantly enhances the resolution and allows precise identification of sphincter muscle structural abnormalities.96 Further studies of the value of MRI are needed.

Conclusion 

At present, MRI and computed axial tomographic scanning have no defined role in the evaluation of constipation and fecal incontinence.

Colon transit studies 

Transit studies are discussed only in the context of anorectal disorders. Transit studies enable a distinction between patients with slow and normal colonic transit times. Despite differences in diet and other factors that might affect colonic transit, studies of normal subjects on diets containing 20–30 g fiber/day indicate a consistent upper range of normal.14, 97, 98, 99 Although transit times differ between men and women, these differences appear to be inconsequential for clinical purposes.100 In addition, there are no important differences between the two phases of the menstrual cycle,100 and colonic transit is similar in young and elderly populations.101

The main benefit of transit studies lies in the ability to objectively confirm patients' subjective complaints of constipation and/or decreased bowel frequency. Patients who complain predominantly of infrequent defecation but who repeatedly have normal colonic transit may consciously or unconsciously misrepresent or misperceive bowel habits.14, 102 Therefore, the finding of normal colonic transit on two consecutive studies provides some reassurance that colonic function is appropriate and ends the diagnostic evaluation of patients who complain of infrequent defecation.103

In addition to confirmation of slow transit, transit studies can be used for identification of the colonic region(s) in which slow transit occurs. Markers and radioisotopes have been used for this purpose.97, 98, 99, 104, 105, 106, 107, 108, 109, 110 The region of delay defined by radiopaque markers is close to the regions defined using radioisotope.105

The value of studies documenting regional delays in transit is controversial. In patients in whom study results indicate pelvic floor dysfunction, rectosigmoid transit often is significantly delayed111; however, delayed transit through the rectosigmoid or left colon cannot determine pathophysiology, that is, the cause of the delayed transit. Additional studies of anorectal function may help distinguish pelvic floor dysfunction from other causes of delay in the distal colon such as willful deferral of defecation112 and help select patients for biofeedback treatment (see discussions of tests for specific diagnosis or management).

Conclusion 

Colon transit studies are useful for (1) objective confirmation of patients' subjective complaint of constipation and/or decreased bowel frequency, (2) confirmation of slow transit, and (3) documentation of regional delays in transit.

Neuromuscular function 

Anorectal manometry 

The anal canal is defined as the region in which resting pressures are at least 5 mm Hg higher than rectal pressure. Although age does not relate significantly to length, men have longer anal canals than women,113, 114, 115, 116, 117 albeit with considerable overlap (Table 1).

Table 1. Normal values of length of anal canal
Women (cm)nMen (cm)nStudy
4.0 ± 1.0a184.0 ± 1.0a18Loening-Baucke and Anuras113
3.1 (2.0–4.2)b203.6 (2.4–4.4)b20Rasmussen114
2.2 (2.2–3.8)a352.8 (2.1–3.7)a23cPedersen and Christiansen115
3.7 ± 0.2104.0 ± 0.6b12McHugh and Diamant117
aNot significantly different. bSignificantly different. cExpressed as median (range).

NOTE. Values expressed as mean ± SEM or mean (range).

In the proximal anal canal, anterior quadrant pressures are lower than those in the other three quadrants at rest and with maximal squeeze; distally, posterior quadrant pressures are reduced.116 In the mid anal canal, radial pressures are generally equal in all quadrants.

Satisfactory measurements of anal canal pressures and anal sphincter responses can be obtained with open-tipped or side-opening water-perfused catheters, direct online solid-state microtransducers, or air- or water-filled balloons of various sizes and configurations. Large balloon probes are sufficient for assessment of sphincter responses to rectal distention and other stimuli, but they are not able to measure resting pressures of the anal canal. Knowledge of normal values for each technique is required, especially for age and sex differences. Normal anal canal pressures vary according to sex, age, and techniques used (Tables 2 and 3). In general, pressures are higher in men and younger persons, but there is a considerable overlap in values. Studies to date have not included large numbers of subjects in each age group.

Table 2. Representative normal values of maximal resting anal canal pressures determined manometrically
WomennMennStudy
Station pull-through58 ± 32266 ± 615Read et al.119
54 ± 512Not studied Caruana et al.120
50 ± 1318a63 ± 1218Loening-Baucke and Anuras121
49 ± 31249 ± 37Orkin et al.122
Slow pull-through46 (range, 40–58)3560 (range, 51–98)23Pedersen and Christiansen115
Rapid pull-through100 ± 2210aNot studied Loening-Baucke and Anuras113
106 ± 1810aNot studied Loening-Baucke and Anuras113
102 ± 1935b100 ± 2127bMcHugh and Diamant123
76 ± 2440c97 ± 2031cMcHugh and Diamant123
53 ± 2217d72 ± 233dMcHugh and Diamant123
aSignificant difference between sexes but not between age groups. bAges 20–39 years. cAges 40–69 years. dAges ≥70 years.

NOTE. Values expressed as mm Hg (mean ± SEM) unless indicated.

Table 3. Representative normal values of maximal squeeze anal canal pressures determined manometrically
WomennMennStudy
Station pull-through135 ± 1522218 ± 1815Read et al.119
90 ± 912Not studied Caruana et al.120
159 ± 4518a238 ± 3818Loening-Baucke and Anuras113
Slow pull-through103 (range, 78–190)35163 (range, 76–234)23Pedersen and Christiansen115
Rapid pull-through179 ± 5510aNot studied Loening-Baucke and Anuras113
159 ± 3510Not studied Loening-Baucke and Anuras113
171 ± 4035b240 ± 6527bMcHugh and Diamant123
132 ± 16940c203 ± 4530cMcHugh and Diamant123
116 ± 4017d219 ± 323dMcHugh and Diamant123
aSignificant difference between sexes but not between age groups. bAges 20–39 years. cAges 40–69 years. dAges ≥70 years.

NOTE. Values expressed as mm Hg (mean ± SEM) unless otherwise indicated.

Rogers et al.118 examined the reproducibility of anorectal manometry in 16 patients by having these patients evaluated blindly by two different investigators approximately 20 days apart. The average difference between studies was 10 cm H2O (95% confidence interval [CI], −25 to 4.7 cm H2O) for resting pressure, and 9 cm H2O (CI, −32 to 14 cm H2O) for squeeze pressure. These confidence intervals are relatively large, amounting to 30% of the range for resting pressure and 22% of the range for squeeze pressure. However, the number of subjects studied was small. In a separate study of 14 subjects, Hallan et al.30 found that independent resting pressure measurements correlated (r = 0.77; P < 0.001), as did independent squeeze pressure measurements (r = 0.66; P < 0.01). Another study in 11 subjects showed that individual variation of resting pressures measured on 2 separate days were less than 12%.117

Resting anal canal pressures 

Resting anal canal pressures may be assessed by station pull-through or rapid pull-through techniques.113, 115, 117, 119, 120, 121, 122, 123 Measured pressures tend to be higher with rapid pull-through than with station pull-through techniques (Table 2). Resting pressures reflect the tonic activities of both the internal anal sphincter (IAS) and external anal sphincter (EAS); approximately 75%–85% of this pressure is derived from the IAS. However, if the patient is not completely relaxed, a larger contribution from the EAS (and therefore higher pressures) will be recorded. Resting pressures of the anal canal may be expressed as the average obtained from each transducer or as a range to identify asymmetry of anal canal pressures.116

Squeeze pressures 

Squeeze pressures may be obtained by asking the patient to maximally contract the EAS as the probe is sequentially positioned through the anal canal (station pull-through technique) or to squeeze maximally during the rapid pull-through method (Table 3).113, 115, 117, 119, 120, 121, 123 With the latter method, at least three separate trials are recommended, and maximal pressures from each transducer are averaged. The duration of maximal squeeze should also be obtained (Table 4); methods have varied from a single squeeze to an average of three trials to the minimum pressures that must be sustained during a prolonged squeeze.119, 124

Table 4. Duration of EAS maximum squeeze
Duration (s)anCriteriaStudy
49 ± 116Mean 3 trialsChiarioni124
10 mm Hg ↑ in lower anal canal
122 ± 21375 mm Hg ↑ in lower anal canalRead et al.119
aMean ± SEM.

Reflex anal sphincter responses 

Normally, the IAS is tonically inhibited either in response to rectal distention or during attempted defecation (Figure 4).

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  • Fig. 4. 

    Reflex relaxation of the anal sphincter. The rectal balloon is first rapidly inflated and deflated with 50 mL of air (arrow) using a syringe attached to a three-way stopcock. Reflex relaxation of the IAS is recorded as well as the ability of the patient to sense rectal distention. (Reprinted with permission from Gastroenterology 1974:67;216–220.)

Reflex inhibition may be elicited by distending a rectal balloon with different volumes of air or by asking the subject to expel the manometer (pseudodefecation)113, 120, 124, 125, 126 (Table 5).
Table 5. Thresholds of IAS relaxation
Thresholds (mL)nCharacteristics of distending balloonStudy
14 ± 1165 cm long, 5 cm from anal vergeChiarioni124
20 (10–30)115 cm long, 5 cm from anal vergeWald and Tunuguntla125
22 ± 3 (10–40)125 cm long, 5 cm from anal vergeCaruara et al.120
25 ± 217b5 cm long, 5 cm from anal vergeMerkel et al.126
19 ± 618c2.5 × 3 cm, 5 cm from anal vergeLoening-Baucke and Anuras113
23 ± 1118d2.5 × 3 cm, 5 cm from anal vergeLoening-Baucke and Anuras113
aMean ± SEM and/or (range). bElderly, >age 60 years. cElderly, >age 66 years. dYoung, ages 21–40 years.
Inhibition of IAS tone is influenced by volume and speed of distention and by rectal volume and compliance; that is, if the rectum is enlarged (megarectum), greater volumes of rectal distention are required to elicit the inhibitory reflex. This balloon distention reflex remains intact in patients with extrinsic denervation but disappears with neuropathy and loss of ganglion cells of the myenteric plexus and/or with atrophy and fibrosis of the IAS.86, 127 Determination of the clinical importance of distinguishing between neural and muscle abnormality will require further studies. Although EAS inhibition can be satisfactorily assessed with all types of anorectal manometers, simultaneous electromyography (EMG) recordings ensure that decreased pressures are caused by inhibition of EAS activity.

Prolonged anorectal manometry 

Methods have been reported to monitor anorectal motor events over prolonged periods and even in fully ambulant subjects. These methods have used pressure microtransducers with or without simultaneous EMG recordings of the EAS128, 129, 130 or a multilumen-perfused sleeve device to monitor anal canal pressures.122 These techniques show promise as investigational techniques, but their clinical applicability has not been established.

Vector manometry (vectometry) 

This approach assesses the radial pressure profile along the anal sphincter, and it is likely that up to eight radially oriented recording ports are necessary for adequate resolution.131, 132, 133, 134 The reproducibility of vectormetric studies has not been reported. However, several studies have reported agreement with ultrasound and needle EMG. Tjandra et al.131 studied 26 patients with obstructed defecation and 20 patients with fecal incontinence by means of anorectal manometry, vectometry, and anal canal ultrasonography. Based on history and physical examination, 4 of 20 incontinent patients had disruption of the EAS and IAS. This was confirmed by ultrasound examination in all 4 and by vectometrogram in 3 of 4 patients. The false-positive rate was not reported. Similar findings have been reported recently in abstract form.135

Braun et al.132 studied 23 fecal incontinent female patients, including 11 with sphincter muscle disruption defined by ultrasonography or MRI and 12 with idiopathic fecal incontinence. Those with traumatic sphincter injury showed significantly higher asymmetry indices than patients with idiopathic fecal incontinence or (historical) controls. However, individual values were not given.

Yang and Wexner133 studied 50 consecutive patients with fecal incontinence; 34 (68%) showed abnormal indices of asymmetry. Of 46 patients evaluated by needle EMG, 38 showed evidence of sphincter injury, but in only 5 of the 38 was the defect localized in the same quadrant by vectometry. Of 33 patients tested by ultrasonography, 27 were found to have sphincter defects, but in only 3 was the defect localized to the same quadrant by vectometry. The investigators concluded that vectometry had no apparent value, but they used only four recording ports rather than eight ports at 45° intervals as in some other studies.131, 132, 134

Only one study provides data that allow for the calculation of the sensitivity and specificity of vectometry. Perry et al.134 studied 69 consecutive women with functional anorectal disorders, including 9 with fecal incontinence dating back to a recognized sphincter injury, 40 with fecal incontinence who were not suspected on clinical grounds of having sphincter injuries, and 20 with chronic constipation who were not suspected of having sphincter injuries. Women in the last two groups were subdivided into those who had or had not had at least one episiotomy each. All subjects in the sphincter injury group had a symmetry index of less than 0.6, resulting in a sensitivity of 100%. When 21 healthy controls, 7 constipated women without episiotomy, and 12 incontinent women without episiotomy were compared, the specificity was 90%. Among incontinent women with a history of episiotomy who were not suspected on clinical grounds of having sphincter injuries, 57% were found to have an abnormal symmetry index of less than 0.6. The authors interpret these data as indicating that vectometry is of clinical value in identification of patients with traumatic sphincter injury. However, the sensitivity and specificity of vector manometry are too low to determine which patients should be treated surgically.

Although some of these data can be interpreted as indicating that vectometry is of clinical value in identification of patients with traumatic sphincter injuries, anal canal ultrasonography is the preferred test for identification of such patients.

Fecal incontinence 

Sensitivity and specificity of anal canal pressures for discrimination of fecal incontinent patients from continent patients and controls were investigated by Felt-Bersma et al.136 They studied 350 patients, 178 of whom were fecal incontinent by history, plus 80 controls. Of the anorectal parameters studied, maximum squeeze pressure had the greatest sensitivity and specificity; at a cutoff of less than 60 mm Hg in females, sensitivity was 60% and specificity was 78%. At a cutoff of 120 mm Hg in males, sensitivity was 67% and specificity was 67%. The maximum resting anal canal pressure was less sensitive and specific than maximum squeeze pressure, but it was superior to the maximum tolerable volume or the saline infusion test.

A similarly large study was reported by Sun et al.,137 who compared anorectal physiological test results in 302 fecal incontinent subjects and 65 healthy controls. Taking the mean − 2 SD for controls as the cutoff, they found the sensitivity for maximum squeeze pressure to be 92%, with a specificity of 97%. Basal anal canal pressure using a similar cutoff had a sensitivity of only 32%.

It is not logical to expect anal canal pressure to be perfectly correlated with continence because of the wide range of normal pressures, and other factors may cause fecal incontinence in the absence of decreased anal canal pressures. The relationship between these other factors and anal canal pressures requires future study.

Constipation 

Manometry may be used to obtain selected information concerning anorectal function in patients with chronic constipation. These include the presence of IAS relaxation in response to rectal distention and rectal and EAS pressure changes during efforts to expel the manometer or rectal balloon (pseudodefecation). Anorectal manometry is of potential value in constipated adults who exhibit pelvic floor dyssynergia (Figure 5).

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  • View full-size image.
  • Fig. 5. 

    Pressure changes in rectum and anal canal and EMG recordings from the EAS during pseudodefecation. (A) Normal defecation is characterized by increased rectal (intra-abdominal) pressure, decreased anal pressure, and decreased direct and integrated EMG activity as measured by surface electrodes. (B) In patients with pelvic floor dyssynergia, there is increased anal pressure and EMG activity of the external sphincter during attempted defecation. (Courtesy of Dr. Vera Loening, University of Iowa Hospitals, Iowa City, Iowa). (Reprinted with permission.223)

The absence of IAS relaxation in response to rectal distention strongly suggests Hirschsprung's disease in the appropriate clinical setting138 (Figure 6).

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  • Fig. 6. 

    IAS responses to rectal distention in a patient with Hirschsprung's disease are compared with those of a normal subject using the Schuster-type balloon manometer. The congenital aganglionosis of Hirschsprung's disease invariably affects the IAS. In contrast to normal reflexive relaxation of the IAS after rectal distention (arrows), no such relaxation occurs in the patient with Hirschsprung's disease.

However, in a patient with megarectum, it is necessary to use larger volumes of rectal distention before concluding that relaxation of the IAS is absent. In the absence of IAS relaxation, a confirmatory biopsy should be done because absence of the reflex is not specific for Hirschsprung's disease. The presence of IAS relaxation in response to rectal distention excludes Hirschsprung's disease from consideration. Therefore, manometry is a relatively noninvasive screening technique for this uncommon disorder in children and adults with life-long constipation, especially in the presence of megarectum.

Manometry may be used to assess anorectal patterns during attempted expulsion of a rectal balloon (pseudodefecation). Pressures recorded inside the balloon indicate intra-abdominal pressures generated during expulsion efforts while at the same time, pressure recordings from the anal transducers indicate relaxation or inappropriate contraction of the EAS.42 The latter pattern is suggestive of pelvic floor dyssynergia, also known as anismus or the puborectalis syndrome.139 To assure that increased pressures within the anal canal are derived from the EAS, surface EMG electrodes may be used simultaneously to record increased EMG activity of the sphincter muscle. However, it is uncertain whether a manometric pattern suggestive of dyssynergia alone is a sufficient diagnostic criterion. In one study, when manometry indicated dyssynergia, defecography was in agreement in only 36% of patients, whereas when manometry indicated normal expulsion, defecography was in agreement 88% of the time.49 There was also no relationship between dyssynergia patterns and colonic transit times or patients' complaints of infrequent defecation or defecatory difficulty, reflecting overlap of these clinical syndromes. It is not clear whether this represents limitations of manometry, defecography, or both.

Anorectal manometry is clinically useful in relatively few patients with chronic constipation. The technique has potential value in exclusion of Hirschsprung's disease and in assessment and treatment of constipated adults who exhibit pelvic floor dyssynergia, especially if this is corroborated by anal sphincter EMG and by impaired expulsion of contrast with defecography (see discussion in this review of tests for specific diagnosis or management).

Conclusion 

(1) Anorectal manometry can measure sphincter pressures with reasonable reproducibility, but normal ranges must be established in each laboratory for each technique used. (2) There are no controlled clinical trials validating the usefulness of anorectal manometry in the diagnosis and treatment of constipation. These are needed. (3) Clinical practice and uncontrolled studies suggest the following indications for anorectal manometry: fecal incontinence—to define functional weakness of one or both sphincter muscles, in which anal endosonography is complimentary in demonstrating whether this weakness is caused by anatomic derangement, and to perform and predict responses to biofeedback training; pelvic floor dyssynergia—to support findings of other tests and to perform, monitor outcome, and possibly predict responses to biofeedback training; Hirschsprung's disease; and anatomic defects of the anal sphincters—vectormanometry if no other method (e.g., ultrasonography) is available. (4) The clinical usefulness of prolonged anorectal manometry is not yet established.

Sensory testing: Rectal sensation 
Balloon distention 

This technique is used to detect the threshold (smallest volume of rectal distention) for three common sensations, the first detectable sensation (rectal sensory threshold), the sensation of urgency to defecate, and the sensation of pain (often defined as maximum tolerable volume). The clinical significance of the last two thresholds is less well established than that of the first.

The method used by most investigators to test the threshold for first perception of distention is to physically distend a balloon with a hand-held syringe. This is defined as the rectal sensory threshold.120, 121, 124, 125, 126 The air usually is rapidly injected into the balloon and immediately withdrawn,140, 141 although rapid, continuous infusion has been used by some investigators.142, 143 It is known that the type of inflation (phasic vs. continuous) and the speed of continuous inflation affect the threshold volume required for healthy control subjects to perceive rectal distentions144; in fact, the studies that have used continuous filling of a rectal balloon are among the few that have failed to show a sensory deficit in fecally incontinent patients,142, 143, 145 as opposed to use of phasic and bolus distentions.120, 137, 146, 147 Also, the size and shape of the balloon will affect the threshold volume. As a consequence of both factors, there are differences between laboratories in ranges regarded as normal. Some of this variability can be reduced by using a high-compliance balloon and a continuous-infusion pump or a barostat. It may also be helpful to measure the threshold in terms of balloon pressure or wall tension (which compensate for differences in the physical characteristics of the balloon). Within groups, sensory thresholds vary widely with an upper range of normal of 30 mL for a 5 × 4–cm latex balloon situated 5 cm above the anal verge (Table 6).

Table 6. Representative normal values for thresholds of conscious perception of rectal distention
Rectal Sensation (mL)anTechniqueStudy
12 ± 116Balloon, 5.5 × 4 cmChiarioni124
13 ± 2 (10–30)115 cm from anal vergeWald and Tunuguntla125
13 ± 3 (5–30)12 Caruana et al.120
14 ± 317b Merkel et al.126
17 ± 936 Loening-Baucke and Anuras121
aMean ± SEM (range). bAges 60–79 years; no differences between sex or age groups.
However, the numbers of subjects reported in these studies are small (11–36).120, 121, 124, 125, 126 Thresholds also appear to vary with the distance of the balloon from the anal verge; this distance should be standardized in each laboratory.

Researchers and clinicians may also measure the threshold for a sustained sensation of urgency to defecate and the threshold for pain.140, 148 The maximum tolerable volume or pain threshold may be reduced in patients who have a noncompliant rectum (e.g., abdominoperineal pull-through, proctitis, rectal ischemia),17 and the pain threshold may also be reduced in patients with functional bowel disorders.17, 149, 150, 151, 152 When testing for these thresholds, most investigators use tonic distentions. The rectal balloon typically is distended in a stepwise fashion by adding 20 mL or another bolus increment of air every minute or every 2 minutes.140 Some investigators have used a continuous slow inflation to define these thresholds.144 Considerations regarding balloon size and shape are important, and some investigators have suggested reporting pressure and/or wall tension in addition to, or as an alternative to, volume thresholds.153 However, the reproducibility and value of reporting pressure or wall tension has not been established.

To overcome patient unreliability and other causes of response bias, three approaches can be used: sham distentions randomly interspersed with true distentions; a forced-choice technique; and tracking or double random staircase technique. With the forced-choice technique, patients are told that the distentions will always occur in one of two intervals, and they are to indicate in which it occurred. The sensory threshold is then defined as the lowest volume at which accuracy is 75%.140 The forced-choice technique is appropriate for defining the threshold for perception of the smallest volume of distention but is not useful for defining thresholds for urgency or pain. The double random staircase techniques are useful in research studies but are too complex and lengthy to be used in clinical settings. These techniques have been described previously.153

Electrical stimulation 

Rectal sensory testing using an electrical stimulus passed across the rectal mucosa can be used to obtain a quantitative guide to distal colon and anorectal innervation and may help distinguish between functional and neurological disorders causing constipation.154 The value of this technique is yet to be established.

Fecal incontinence 

Significant loss of the ability to sense rectal distention (rectal sensory threshold) is a sufficient but not a necessary condition for fecal incontinence. This is best documented for patients with diabetes mellitus125 and multiple sclerosis120 but may also be seen in some other types of patients. The explanation for this association is that contraction of the pelvic floor muscles, which is critical to the preservation of continence when stool enters the rectum, is a learned voluntary response, and the critical cue to know when to contract the sphincter is the perception of rectal distention.155 Some studies suggest that the single most important component of biofeedback training for fecal incontinence is an improved ability to detect rectal distention.156, 157, 158 Rectal sensation is also decreased in children and adults with megarectum, many of whom are incontinent,159 but this sensory impairment may be secondary to the development of megarectum.160, 161

Constipation 

The threshold for urge to defecate may be absent or elevated in patients with chronic constipation,160, 161 but it is not known whether this preceded and was a cause of constipation or whether it represents an accommodation to chronic constipation. The threshold for pain, sometimes measured as the maximum tolerable volume, is elevated in some types of constipation,161 but it is unknown whether this is a contributing cause or a consequence of constipation. Rectal sensory testing with an electrical stimulus may help distinguish between functional and neurological disorders causing constipation.154

Conclusion 

(1) The first detectable sensation (rectal sensory threshold) to rectal balloon distention is of value in the biofeedback training of patients with fecal incontinence; normalization or reduction of the threshold correlates with success, and poor or absent sensation makes a good response unlikely. (2) The maximum tolerable volume, if less than 100 mL, may have value in indicating the presence of visceral hypersensitivity, poor rectal compliance, or rectal irritability, thereby influencing the direction of therapy. (3) There is insufficient information to support use of the sensory thresholds for diagnosis and biofeedback training of patients with constipation. These aspects need to be studied further.

Sensory testing: Anal canal sensation 

The anal canal has a greater variety of afferent nerve endings than the rectum, and they are located in the mucosa rather than in the surrounding mesentery. In addition, the configuration of the nerve plexuses in the rectum serve as specialized sensory receptors, especially in relation to distention. As a result, subjects are able to detect differences in touch, temperature, and pain from the anal canal, whereas they can detect only distention-related sensations of fullness, urgency to defecate, and pain from the rectum.162, 163 There are frequent spontaneous relaxations of the IAS (the so-called sampling reflex) during which the anal canal sensory fields are exposed to the rectal contents, and some investigators believe this sensory information is critical to the preservation of continence. This is supported by clinical research studies showing that many patients with fecal incontinence have a significant impairment in ability to perceive electrical or other types of stimulation of the anal canal.142, 143, 164, 165, 166

Electrical stimulation of the anal canal 

The simplest technique to quantify anal canal sensation is to pass electric current between bipolar electrodes positioned in the anal canal, increasing the voltage or current until sensation is reported. Sensory thresholds measured in this way are reproducible.118, 167 The ease with which anal sensation can be quantified and the fact that there are fewer technical pitfalls (such as balloon size and speed of inflation) to its measurement have led some laboratories to prefer this test to tests that use rectal distention. However, these tests are not interchangeable: the afferent nerve pathways are different, and thresholds measured by the two techniques show a relatively low correlation.147

Conclusion 

At present, assessment of anal canal sensation is not of established value for the diagnosis and treatment of patients with constipation or fecal incontinence, except when it is necessary to distinguish an idiopathic or functional disorder from a primary disorder or from a secondary disorder affecting extrinsic or intrinsic nerves (e.g., diabetes mellitus, amyloidosis).

Sensory evoked potentials 

Cortical evoked potentials can be elicited from electrical168, 169 or mechanical170 stimulation of the esophagus. However, it is more difficult to produce an interpretable cortical evoked potential by electrical or mechanical stimulation of the anus and rectum,171, 172 and when a cortical evoked potential is seen, there is substantial variability both within and between subjects.171, 172 The value of also assessing cortical blood flow with positron emission topography (PET) has not been established.173

Conclusion 

Sensory evoked potentials are not currently established as clinically useful for the investigation of anorectal sensation.

Muscle tone 

Muscle tone refers to the tonic state of contraction of smooth muscle (usually measured at a low distending pressure), whereas compliance refers to the resistance of the muscle to stretching. Compliance is measured as the ratio of pressure to volume over a range of distending pressures. Muscle tone and compliance are related concepts because muscle tone is normally the principal determinant of compliance until the maximum capacity of the viscus is approached. A recent report of a working team153 details the measurement of tone and compliance; the results are therefore not discussed in detail here.

Muscle tone is not static. In response to imposed stretching, there is an immediate active contraction associated with an increase in intraluminal pressure, followed by relaxation to a new stable pressure.174 The stable phase also reflects the effects of tonic contraction of the muscle, as can be shown by administration of a drug such as glucagon to completely abolish muscle tone and observation of a further decrease in intraluminal pressure.175, 176 Muscle tone may vary at different distending volumes. Physiological influences on smooth muscle tone in the rectum and colon include eating,177 sleep,178 and cholinergic drugs.176, 179 Thus, although compliance is measured over a wide range of distending volumes or pressures, muscle tone is usually measured at a low static pressure or low distending volume.

Muscle tone is usually measured with an isotonic or isobaric recording device. The device uses feedback circuitry to keep the pressure in a distending balloon constant by either pumping air into or withdrawing air from the balloon. The measure of muscle tone is the average volume of air in the bag over an extended period, e.g., 15 minutes.153 The measurement interval must be long enough to average out the effects of phasic contractions on the volume measurement. Physical or technical factors known to affect the measurement of muscle tone include the size and shape of the balloon and the elastic properties of the balloon. To minimize measurement error from these sources, it is recommended that the distending balloon be made of thin-walled plastic, which is infinitely compliant, rather than of latex, and that the bag be designed to have a maximum diameter much greater than the maximum diameter of the viscus under investigation. It is further recommended that bags of a standard length be used to facilitate comparisons between subjects and between laboratories.153

Only limited studies have assessed muscle tone in clinical states such as ulcerative colitis,180 constipation,181, 182 the irritable bowel syndrome,183, 184 and incontinence.

Conclusion 

At present, measurement of muscle tone is not of established clinical value. Further studies are needed.

Compliance 

Compliance is measured as the ratio of pressure to volume at several different distending volumes185 or of volume to pressure at several different distending pressures when using a barostat. In the former case, the walls of the latex balloon contribute to the pressures in the balloon in a nonlinear fashion, and it is necessary to subtract this factor by recording pressures when the balloon is distended outside the rectum.120, 121, 125, 126 Technical factors that affect the measurement of compliance include the size and shape of the balloon and the materials from which the balloon is constructed. With this method, normal values vary according to the range of distention volumes; some investigators have measured pressures over a predetermined range of volumes (50–250 mL), whereas others measure pressures up to the maximal tolerable volume, which varies greatly in control subjects (Table 7).

Table 7. Rectal compliance
Rectal compliance (mL/mm Hg)anTechniqueStudy
13 ± 212Balloon, 10 × 4 cmCaruana120
14 ± 355 cm from anal verge;Wald and Tunuguntla125
14 ± 2b170–250 mLMerkel et al.126
9 ± 6b,c36Balloon, 2.5 × 3 cm; 6.5–7 cm from anal vergeLoening-Baucke and Anuras121
aMean ± SEM. bAges 60–79 years; no difference between sex or age groups. c0–173 ± 64 mL = critical volume.
The reproducibility of rectal compliance using water as a distending agent and an infusion pump was quite good in one study, with a mean coefficient of variation of less than 7%.186 There are insufficient studies with the barostat to establish normal values with confidence, considering the various techniques used.

To achieve a single measure of compliance, investigators sometimes report the slope of the curve, fitting all volumes or pressures tested, or they may report the ratio of pressure to volume at one relatively high volume such as the maximum tolerable volume.187 However, for both technical and physiological reasons, the compliance curve is nonlinear; for research purposes it should be expressed as a graph or table showing all volumes tested rather than as a single number reflecting the average slope of the pressure-volume curve.

Alterations in rectal compliance may result in decreased or increased rectal capacity, impair ability to perceive rectal distention, and alter the threshold of reflexive IAS inhibition by rectal distention. Physiological factors that decrease compliance include (in addition to those listed above as influencing muscle tone) inflammation, fibrosis, surgical revision resulting in the replacement of rectum with sigmoid colon or Koch pouch,17 and drugs. Substantial decreases in compliance are associated with an increased frequency of stools, rapid transit of stool through the rectum, and increased risk of fecal incontinence.17 Physiological factors associated with increased compliance include megarectum.

Conclusion 

The compliance of the rectum, as with the maximum tolerated volume, may identify factors contributing to altered bowel habits and incontinence and may thereby influence the direction of therapy.

Wall tension 

It is possible to measure circumferential wall tension using Laplace's law188 if the diameter of the distending balloon is known and if it can be assumed that the distending balloon is cylindrical or spherical. This has a potential advantage over pressure-volume curves in that measurement artifacts associated with the size and shape of the distending balloon are eliminated. The diameter of the distending balloon can be measured accurately by impedance plethysmography,188 and the assumptions required for the estimation of circumferential wall tension appear to be satisfied for tubular organs such as the esophagus, small intestine, and colon. The appropriateness of the assumptions for sacklike organs such as the stomach and rectum has not been demonstrated.

Conclusion 

At present, the measurement of circumferential wall tension is not of established clinical value.

Electromyography 

EMG of the pelvic floor is performed for three purposes: (1) to identify areas of sphincter injury by mapping the sphincter, (2) to determine whether the muscle contracts or relaxes (by the number of motor units firing), and (3) to identify denervation-reinnervation potentials indicative of nerve injury.

EMG of the striated pelvic floor muscles can be performed using a needle electrode, a surface electrode on the perianal skin, or an anal plug. A needle electrode may be either a concentric needle that samples a large number of motor units simultaneously or a single-fiber electrode whose small recording surface samples the electrical activity of one motor unit at a time. Results of single-fiber EMG have been shown to be reproducible between observers.118 However, useful information can be obtained from surface EMG recorded within the anal canal, with less discomfort to the patient and less risk of infection.189, 190 The number of motor units recruited during squeezing correlates highly with anal canal squeeze pressures.191 In assessment of EAS activity, the response recorded from an anal sponge or a concentric needle electrode correlates well with manometric measurements in the anal canal during squeezing. A hard anal plug electrode may provide fewer reproducible results190 because the rigid plug does not conform well to the anatomy of the anal canal, resulting in less reliable contact with the muscle.

EMG has been used in assessment of damage to the innervation of the EAS in patients with fecal incontinence; patients with incontinence have a higher single-fiber density or longer average motor potential duration than age- and sex-matched controls.191, 192, 193, 194 This is thought to reflect neurogenic damage to the innervating pudendal nerves. However, these EMG findings have not been validated against histological evidence of damage. Similarly, polyphasic motor unit potentials recorded from needle EMG electrodes are also interpreted as indicative of pudendal nerve injury (i.e., as evidence of denervation and reinnervation). However, their interpretation requires specialized training and experience. The severity of EMG changes is not correlated with the magnitude of incontinence.195, 196

Needle EMG has a practical clinical role in mapping the presence or absence of striated muscle around the superficial EAS ring. This is useful in assessment of EAS muscle damage that may have occurred as a result of trauma (obstetric, surgical, or other), and in patients who have developmental abnormalities of the anorectum such as congenital imperforate anus. In the latter group, EMG is used to determine if, at previous surgery, the bowel has been pulled through the anal sphincter. Mapping of the sphincter by needle EMG agrees well with anal canal ultrasonography in identifying the area of sphincter injury,74, 191 but when both are compared with surgical or histological evidence of sphincter damage, ultrasonography appears to be more sensitive.77 Moreover, ultrasound examination is less painful and therefore better tolerated than needle EMG,74, 87 is less subject to sampling error (and therefore more accurate), and can visualize the entire length of the anal canal.

Surface electrodes provide qualitative information about muscle behavior and may therefore be used in constipated patients to determine the presence of appropriate sphincter relaxation during defecation or simulated defecation in the laboratory. In one study using EMG techniques, the dyssynergia pattern correlated with inability to expel from the rectum a balloon filled with 50 mL of water in 82% of patients studied.197 Surface EMG may also be used to provide a visual or audible signal during biofeedback pelvic floor retraining.

Ambulatory anal sphincter EMG can also be used to assess sphincter activity, which can be combined with pressure recordings. Such investigations at present are not of established clinical value.128, 198

Smooth muscle EMG has also been proposed for study of the IAS,199, 200, 201, 202 but its clinical value has not been assessed.

Conclusion 

(1) Needle EMG cannot be recommended for evaluation of fecally incontinent patients. In defining EAS trauma, anal endosonography has largely supplanted EMG. (2) Needle EMG is of use in patients with imperforate anus to confirm proper surgical placement of the bowel if ultrasound examination is not possible or not available. (3) Surface EMG appears to have a definite role in the evaluation of sphincter function and in the use of biofeedback training. (4) At present, measurement of the smooth muscle EMG is not of established clinical value.

Nerve latency measurements 

Injuries to the pudendal nerve innervating the EAS and resulting in a weak sphincter place patients at risk for fecal incontinence. A normally innervated sphincter muscle may also produce inadequate squeeze pressures if there is an anatomic separation of the muscle as may occur during childbirth. In deciding on treatment, it is important to be able to distinguish between muscle weakness due to pudendal nerve injury and muscle weakness due to muscle injury.

A stimulating and recording electrode has been developed to measure the conduction of the pudendal nerves,203 the pudendal nerve terminal motor latency (PNTML). This technique is operator dependent and requires accurate placement of the examining finger as close as possible to the pudendal nerve as it courses around the pelvic rim, thereby obtaining the shortest latency possible. The latency measured reflects the function of the fastest conducting nerve fibers.

In an early paper, Kiff and Swash203 reported that PNTMLs were prolonged in patients with idiopathic fecal incontinence compared with healthy controls, and measurement of these latencies has become standard in some laboratories. However, recent studies fail to show that this test has adequate specificity and sensitivity. Wexner et al.204 found that approximately half of patients with prolonged PNTML had normal anal canal squeeze pressures and that PNTML was prolonged in 27% of patients with chronic constipation and 42% of patients with proctalgia. Many patients with prolonged pudendal latencies have subsequently been shown by anal endosonography to have structural sphincter damage, and this finding appears to be more important in determining functional impairment and symptom development.73 Other studies191, 205 have similarly failed to find an association between delays in PNTML and decreased anal canal squeeze pressures. Cheong et al.191 suggest that this lack of agreement between PNTML and squeeze pressures may occur for technical reasons: (1) PNTML increases with age independently of continence status, and this was not controlled in most studies; and (2) PNTML measures only the fastest conducting fibers in the pudendal nerve, with the result that a damaged nerve may nevertheless show a normal conduction time as long as some fast-conducting fibers remain. Although early small studies suggested that patients with prolonged pudendal nerve latencies fared less well with anterior EAS repair,206 a study involving 55 patients that also used anal endosonography found that pudendal nerve function was not predictive of surgical results.92 Pudendal nerve testing is also not predictive of the results of postanal repair for “neurogenic” incontinence.207

Although interesting from a research point of view, the clinical usefulness of this test is controversial. The test lacks sensitivity and specificity for detection of EAS muscle weakness caused by pudendal nerve damage.

Conclusion 

The PNTML cannot be recommended for evaluation of patients with fecal incontinence.

Other functional tests 
Balloon expulsion 

Balloon expulsion from the rectum is a test of motor function and coordination. Normal subjects can expel a balloon containing 50, 100, or 150 mL of water from the rectum. Patients with constipation, including those with slow or normal intestinal transit, and those with megarectum, are often unable to expel such a balloon even though their intrarectal pressure increases during straining to a degree similar to that in control subjects.208, 209 This evacuation abnormality may relate to a lack of sphincter relaxation or to mechanical obstruction.

The test has not proven to be specific or sensitive enough to direct decisions for particular medical or surgical techniques. However, it may help predict outcome after colectomy for constipation65 and help identify those patients with pelvic dyssynergia.69 Its value for predicting the effectiveness of biofeedback training in those patients with pelvic floor dyssynergia is not yet known.

Conclusion 

At present, the balloon expulsion test is of no proven clinical value on its own, but it may be used to support the symptom of inability to defecate. However, it is a simple test, and failure to expel the balloon when there is an adequate increase in intra-abdominal pressure should be an indication for further testing.

Saline infusion 

Infusion of saline into the rectum is a test designed to stress the anal sphincter.119 The patient is seated on a commode, and saline is infused into the rectum via a tube; 1500 mL is infused at a constant rate of 60 mL/min by a pump. The time (and volume) of first leak, as well as the total volume leaked, can be assessed. Patients with weak IAS or EAS can retain a lesser volume of infused fluid. However, the test is not specific or sensitive enough to select patients for specific therapies.

A similar technique has been used with substances that have stool-like consistency, such as porridge, to test continence mechanisms before closure of a stoma.210 However, no prospective studies have established the predictive value of such tests.

Conclusion 

At present, the saline infusion test is not of established clinical value.

Rectal motor response to distention or fluid infusion 

The threshold volume of distention or fluid for induction of a motor response has been used to assess irritability of the rectum in conditions such as the irritable bowel syndrome and inflammatory bowel disease.151, 152, 211, 212 The clinical value of this assessment is unknown, although the response may relate to the maximal tolerable volume.

Conclusion 

At present, the rectal motor response to distention or fluid infusion is not of established clinical value.

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Tests for specific diagnosis or management 

Fecal incontinence 

Continence depends on multiple physiological mechanisms. Therefore, it should not be expected that any one test will be positive in all patients with fecal incontinence. There is no standard protocol for anorectal physiological assessment. As noted earlier in this review, the following procedures and tests are of value or possible value in the diagnosis and management of fecal incontinence.

Procedures of value 

Procedures of value include (1) symptom diaries (for diagnostic evaluation and for monitoring of adherence to and efficacy of treatment); (2) digital examination (a simple qualitative assessment of resting and squeeze pressures); (3) anal ultrasound examination (simple, reliable, relatively noninvasive assessment of structural damage to anal sphincter, especially the IAS); (4) anorectal manometry (to define functional sphincter weakness and to perform and predict response to biofeedback training); (5) rectal and anal sensory testing (for rectal response to biofeedback training, as an indication of rectal irritability or poor compliance, and for identification of patients with afferent nerve injury as a contributing cause of incontinence); and (6) rectal compliance (more direct assessment of poor compliance and rectal irritability).

Procedures of possible value 

Procedures of possible value include (1) surface EMG (for the evaluation of sphincter function and for performance of biofeedback training) and (2) evacuation proctography (when rectal prolapse is suspected).

Habit training 

In approximately 96% of children with fecal incontinence, the symptom is caused by constipation with a large mass of stool in the rectum and overflow around this mass.213, 214 The treatment of choice for overflow incontinence is a form of behavior modification for constipation that is often called habit training.215, 216, 217, 218, 219 However, recent studies220, 221, 222 suggest that 30%–50% of children with overflow incontinence have pelvic floor dyssynergia as the cause of constipation. The significance of this finding is not yet established, but it suggests that biofeedback training may be more effective than habit training or laxatives in these children.

Conclusions 

(1) Neither the diagnosis of overflow incontinence nor treatment with habit training requires anorectal testing. (2) Biofeedback training requires assessment in patients with overflow incontinence.

Biofeedback training 

Neurogenic fecal incontinence associated with weakness of the EAS and/or decreased ability to perceive rectal distention because of nerve injury can be treated with biofeedback training designed to teach the patient (1) how to recognize small volumes of rectal distention and (2) how to contract the EAS while simultaneously keeping intra-abdominal pressure low.223, 224 To accomplish these goals, a measure of sphincter contraction, which can be based on anal canal pressures or pelvic floor EMG, and a measure of abdominal wall contraction, which can be based on pressures in a rectal balloon or a skin-surface measure of abdominus rectus EMG, must be displayed to the patient, and it is necessary to be able to distend the rectum with graded volumes of air in a balloon.

Conclusion 

(1) Fecal incontinence associated with structurally intact sphincter rings (i.e., weakness of the EAS or decreased ability to perceive rectal distension because of nerve injury) can be treated with biofeedback training. (2) Biofeedback training and objective monitoring of its outcome require the use of anorectal study techniques, including a measure of sphincter contraction (e.g., anal canal pressures or pelvic floor EMG), a measure of abdominal wall contraction (e.g., pressures in a rectal balloon), and distention of the rectum with graded volumes of air in a balloon.

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Constipation/impaired defecation 

Constipation falls under two broad categories with regard to pathophysiological mechanisms: slow colonic transit and anorectal dysfunction. The two may coexist. In terms of the anorectal area, terms such as outlet obstruction, anismus, pelvic floor dyssynergia, and paradoxical contraction of pelvic musculature are included under the definition of constipation. As noted earlier in this review, the following anorectal procedures and tests are of value or possible value in the diagnosis and management of constipation, including impaired defecation.

Procedures of value 

Procedures of value include (1) symptom diaries (for diagnostic evaluation and for monitoring of adherence to and efficacy of treatment); (2) colon transit studies (to confirm complaint of constipation and/or decreased stool frequency and to assess slow transit and regional delay); (3) anorectal manometry (to exclude Hirschsprung's disease and to support findings of other tests of pelvic floor dysfunction; in the use of biofeedback training; and for vectormanometry if ultrasonography is unavailable); and (4) surface EMG (for evaluation of sphincter function and for performance of biofeedback training).

Procedures of possible value 

Procedures of possible value include (1) evacuation proctography (to support the symptom of inability to defecate); (2) balloon expulsion (to support the symptom of inability to defecate); and (3) rectal sensory testing (to help distinguish between functional and neurological disorders causing constipation).

Biofeedback 

It was hypothesized that anorectal dysfunction in patients with associated pelvic floor dyssynergia might be amenable to biofeedback techniques.225 The use of EMG biofeedback techniques has now been reported in seven studies of constipated adult patients in which a total of 92 adults have been evaluated with an overall improvement rate of 84% (Table 8).

Table 8. Biofeedback studies using anal sphincter EMG in obstructed defecation
Diagnosis confirmed by
No. of patientsManometryDefecographyEMG% ImprovedStudy
10++70Bleijenberg and Kuijpers234
15+++87Kawimbe et al.235
9+++78Dahl et al.236
18+++89Wexner et al.237
9+++100Fleshman et al.238
20++85Koutsomanis et al.239
11++73Bleijenberg and Kuipers226
To perform these studies, anorectal testing techniques are required. Pelvic floor dyssynergic should be corroborated by at least two different tests from among the following: manometry, defecography, and sphincter EMG, and sphincter EMG or manometric techniques are used for biofeedback sessions. One study compared sphincter EMG biofeedback with a balloon pullout method of biofeedback and found that EMG biofeedback produced superior results.226 Comparable trials using anal sphincter manometry are required. Another study (5 patients completed and assessed) using relaxation-based therapy alone reported symptom improvement.227

Conclusion 

(1) The diagnosis of impaired defecation requires confirmation by at least two different tests. (2) EMG biofeedback training is of value in the management of pelvic floor dyssynergia.

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Proctalgia and other sensory syndromes 

Levator ani syndrome 

The levator ani syndrome is defined as a chronic or intermittent dull, aching pain or discomfort in the rectum that is worse when sitting than when standing.9, 228 The symptoms may also include a chronic sensation of rectal fullness and urge to defecate. Physical examination should include traction on the pelvic floor muscles, which will often elicit the patient's characteristic dull pain (not a sensation of burning, which is indicative of other processes such as fissure or thrombosed hemorrhoids). This physical examination finding is not required for the diagnosis but increases confidence in the diagnosis.228 The levator ani syndrome is frequently seen in association with pelvic floor dyssynergia.229 The physiological mechanism for the symptoms of levator ani syndrome is not firmly established, but the syndrome has been attributed to chronic tension in the striated pelvic floor muscles.228

Diagnosis of the levator ani syndrome is based on clinical symptoms and physical examination; anorectal manometry is not required, although it may be helpful in confirming the association of the symptoms with elevated pelvic floor or anal canal muscle tension.

No treatment has been established as efficacious for the levator ani syndrome. Treatments are usually directed at relaxing the pelvic floor muscles and include (1) biofeedback, (2) electrogalvanic stimulation of the pelvic floor, (3) administration of drugs such as cyclobenzaprine and diazepam that relax striated muscle, (4) application of heat, (5) massage of the tense levator muscles, (6) surgical myectomy, and (7) botulinum toxin injection.228

Conclusion 

(1) Anorectal testing is not required for diagnosis of the levator ani syndrome. (2) No treatment for the levator ani syndrome is of proven efficacy, but most treatments used clinically are directed at relaxing striated pelvic floor muscle tension. (3) Biofeedback training for the syndrome requires a biofeedback signal (e.g., averaged EMG from the pelvic floor muscles recorded from a sponge or anal plug electrode229).

Proctalgia fugax 

Proctalgia fugax involves sharp, fleeting pains from the anal canal or rectum.9, 228 In most patients, the symptoms are infrequent (less than six times per year in half of patients), and few patients consult physicians. In most patients, the physiological basis for these symptoms is unknown, and the diagnosis is based solely on symptom criteria and exclusion of other diseases. A more recent study indicates that paroxyms of contraction of the anal canal may be involved.230 In a small group of patients with severe proctalgia, there may be a myopathy of the IAS.231

Conclusion 

Anorectal physiological measurement plays no role in the diagnosis or treatment of proctalgia fugax unless a specific sphincter myopathy is suspected.

Irritable bowel syndrome 

The irritable bowel syndrome has been defined on the basis of symptoms according to the Rome criteria.232 Multiple experiments dating from the original observations of Ritchie233 show that patients with the irritable bowel syndrome report pain at a lower volume of rectal distention than do healthy controls.149 These data have been interpreted as showing that patients with the irritable bowel syndrome have visceral hyperalgesia,149, 183 although it is known that perceptual response bias also contributes to the reports of increased pain sensitivity in these patients.153

It has been suggested that the threshold for pain or discomfort from distention of the rectum may be used as a diagnostic marker for IBS.149, 183 However, it is premature to recommend this for clinical evaluation of patients because (1) the mechanism for altered sensitivity has not been established (including the possible contribution of perceptual response bias), and (2) there is as yet no consensus on the best method to test sensory thresholds in the gastrointestinal tract.153 Further research is needed.

Conclusion 

At present, sensory testing is not of established value for clinical evaluation and treatment of patients with the irritable bowel syndrome.

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Acknowledgements 

The Clinical Practice and Practice Economics Committee acknowledges the following individuals, whose critiques of this review paper provided valuable guidance to the authors: Jeffrey L. Barnett, M.D., William L. Hasler, M.D., and Michael Camilleri, M.D.

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References 

  1. Talley NJ, O'Keefe EA, Zinsmeister AR, Melton LJ. Prevalence of gastrointestinal symptoms in the elderly: a population-based study. Gastroenterology. 1992;102:895–901
  2. Drossman DA, Sandler RS, Bromm M, McKee DC. Urgency and fecal soiling in people with bowel dysfunction. Dig Dis Sci. 1986;31:1221–1225
  3. Drossman DA, Li Z, Andruzzi E, Temple RD, Talley NJ, Thompson WG, et al. U.S. householder survey of functional gastrointestinal disorders. Prevalence, sociodemography, and health impact. Dig Dis Sci. 1993;38:1569–1580
  4. Thompson WG, Heaton KW. Functional bowel disorders in apparently healthy people. Gastroenterology. 1980;79:283–288
  5. Drossman DA, Sandler RS, McKee DC, Lovitz AJ. Bowel patterns among subjects not seeking health care. Use of a questionnaire to identify a population with bowel dysfunction. Gastroenterology. 1982;83:529–534
  6. Thompson WG. Proctalgia fugax. J R Coll Phys Lond. 1980;14:247–248
  7. Probert CS, Emmett PM, Cripps HA, Heaton KW. Evidence for the ambiguity of the term constipation: the role of irritable bowel syndrome. Gut. 1994;35:1455–1458
  8. The functional gastrointestinal disorders: diagnosis, pathophysiology and treatment. New York: Little, Brown; 1994;
  9. Drossman DA, Funch-Jensen P, Janssens J, Talley NJ, Thompson WG, Whitehead WE. Identification of sub-groups of functional gastrointestinal disorders. Gastroenterol Int. 1990;3:159–172
  10. Thompson WG, Creed F, Drossman DA, Heaton KW, Mazzacca G. Functional bowel disease and functional abdominal pain. Gastroenterol Int. 1992;5:75–91
  11. Diagnostic and statistical manual of mental disorders (DSM-IV). 4th ed. Washington, DC: American Psychiatric Association; 1994;
  12. Grotz RL, Pemberton JH. Mechanisms of continence and defecation. In:  Kuijepers HC editors. Colorectal physiology. Fecal incontinence. Boca Raton, FL: CRC; 1994;p. 26–34
  13. Sagar PM, Pemberton JH. Anorectal and pelvic floor function. Relevance to continence, incontinence, and constipation. Gastroenterol Clin North Am. 1996;25:163–182
  14. Wald A, Hinds JP, Caruana BJ. Psychological and physiological characteristics of patients with severe idiopathic constipation. [see comments] Gastroenterology. 1989;97:932–937
  15. Moreno-Osset E, Ballester J, Minguez M, Tomas-Ridocci M, Mora F, Benages A. Chronic idiopathic constipation: the importance of transit time studies. Ital J Gastroenterol. 1991;23:20–24
  16. Heaton KW, Radvan J, Cripps H, Mountford RA, Braddon FE, Hughes AO. Defecation frequency and timing, and stool form in the general population: a prospective study. Gut. 1992;33:818–824
  17. Whitehead WE, Schuster MM. Gastrointestinal disorders: behavioral and physiological basis for treatment. Orlando, FL: Academic; 1985;
  18. Ciminero AR, Nelson RO, Lipinski DP. Self-monitoring procedures. In:  Ciminero AR,  Calhoun KS,  Adams HE editor. Handbook of behavioral assessment. New York: Wiley; 1977;p. 195–232
  19. Georges JM, Heitkemper MM. Dietary fiber and distressing gastrointestinal symptoms in midlife women. Nurs Res. 1994;43:357–361
  20. Whitehead WE, Parker L, Bosmajian L, Morrill-Corbin E, Mid-daugh S, Garwood M, et al. Treatment of fecal incontinence in children with spina bifida: comparison of biofeedback and behavior modification. Arch Phys Med Rehabil. 1986;67:218–224
  21. Richards RD, Valenzuela GA, Davenport KG, Fisher KLK, McCallum RW. Objective and subjective results of a randomized, double-blind, placebo-controlled trial using cisapride to treat gastroparesis. Dig Dis Sci. 1993;38:811–816
  22. Orr WC, Mellow MH, Yates C, Johnson P. What is constipation? Behavioral, physiological, and radiographic measurements. (abstr) Gastroenterology. 1995;104:A562
  23. Whitehead WE, Crowel MD, Bosmajian L, Zonderman A, Costa PTJ, Benjamin C, et al. Existence of irritable bowel syndrome supported by factor analysis of symptons in two community samples. Gastroenterology. 1990;98:336–340
  24. Manning AP, Thompson WG, Heaton KW, Morris AF. Towards positive diagnosis of the irritable bowel. Br Med J. 1978;2:653–654
  25. Kruis W, Thieme CH, Weinzierl M, Schussler P, Holl J, Paulus W. A diagnostic score for the irritable bowel syndrome. Its value in the exclusion of organic disease. Gastroenterology. 1984;87:1–7
  26. Talley NJ, Phillips SF, Melton LJI, Wiltgen C, Zinsmeister AR. A Patient questionnaire to identify bowel disease. Ann Intern Med. 1989;111:671–674
  27. O'Keefe EA, Talley NJ, Tangalos EG, Zinsmeister AR. A bowel symptom questionnaire for the elderly. J Gerontol Med Sci. 1992;47:M116–M121
  28. Drossman DA. A questionnaire for functional bowel disorders. Ann Intern Med. 1989;111:627–629
  29. Drossman DA, Li Z, Toner BB, Diamant NE, Creed FH, Thompson D, et al. Functional bowel disorders: a multicenter comparison of health status and development of an illness severity index. Dig Dis Sci. 1995;40:986–995
  30. Hallan RI, Marzouk DEMM, Waldron DJ, Womack NR, Williams NS. Comparison of digital and manometric assessment of anal sphincter function. Br J Surg. 1989;76:973–975
  31. Felt-Bersma RJF, Klinkenberg-Knol EC, Meuwissen SGM. Investigation of anorectal function. Br J Surg. 1988;75:53–55
  32. Eckardt VF, Kanzler G. How reliable is digital examination for the evaluation of anal sphincter tone?. Int J Colorectal Dis. 1993;8:95–97
  33. Smith RG, Lewis S. The relationship between digital rectal examination and abdominal radiographs in elderly patients. Age Ageing. 1990;19:142–143
  34. Henry MM, Parks AG, Swash M. The pelvic floor musculature in the descending perineum syndrome. Br J Surg. 1982;69:470–472
  35. Bartram CI. The barium enema and evacuation proctography. In:  Kamm MA,  Lennard-Jones JE editor. Constipation. PA: Wrightson Biomedical; 1994;p. 137–143
  36. Barnes PR, Lennard-Jones JE. Balloon expulsion from the rectum in constipation of dif ferent types. Gut. 1985;26:1049–1052
  37. Anuras S, Hade JE, Soffer E, Lu CC, Loening-Baucke V, Soper RT, et al. Natural history of adult Hirschsprung's disease. J Clin Gastroenterol. 1984;6:205–210
  38. Patriquin H, Martelli H, Devroede G. Barium enema in chronic constipation: is it meaningful?. Gastroenterology. 1978;75:619–622
  39. Mahieu P, Pringot J, Bodart P. Defecography: II. Contribution to the diagnosis of defecation disorders. Gastrointest Radiol. 1984;9:253–261
  40. Mahieu P, Pringot J, Bodart P, Defecography: I. Description of a new procedure and results in normal patients. Gastrointest Radiol. 1984;9:247–251
  41. Ekberg O, Nylander G, Fork F. Defecography. Radiology. 1985;155:45–48
  42. Loening-Baucke V, Cruikshank BM. Abnormal defecation dynamics in chronically constipated children with encopresis. J Pediatr. 1986;108:562–566
  43. Bartram CI, Turnbull GK, Lennard-Jones JE. Evacuation proctography: an investigation of rectal expulsion in 20 subjects without defecatory disturbance. Gastrointest Radiol. 1988;13:72–80
  44. Shorvon PJ, McHugh S, Diamant NE, Somers S, Stevenson GW. Defecography in normal volunteers: results and implications. Gut. 1989;30:1737–1749
  45. Penninckx F, Debruyne C, Lestar B, Kerremans R. Observer variation in the radiological measurement of the anorectal angle. Int J Colorectal Dis. 1990;5:94–97
  46. Ferrante SL, Perr y RE, Schreiman JS, Cheng S, Frick MP. The reproducibility of measuring the anorectal angle in defecography. Dis Colon Rectum. 1991;34:51–55
  47. Papachrysostomou M, Stevenson AJM, Ferrington C, Merrick MV, Smith AN. Evaluation of isotope proctography in constipated subjects. Int J Colorectal Dis. 1993;8:18–23
  48. Turnbull GK, Bartram CI, Lennard-Jones JE. Radiologic studies of rectal evacuation in adults with idiopathic constipation. Dis Colon Rectum. 1988;31:190–197
  49. Wald A, Caruana BJ, Freimanis MG, Bauman DH, Hinds JP. Contributions of evacuation proctography and anorectal manometry to evaluation of adults with constipation and defecatory difficulty. Dig Dis Sci. 1990;35:481–487
  50. Wald A, Jafri F, Rehder J, Holeva K. Scintigraphic studies of rectal emptying in patients with constipation and defecatory dif ficulty. Dig Dis Sci. 1993;38:353–358
  51. Hutchinson R, Mostafa AB, Grant EA. Scintigraphic defecography: quantitative and dynamic assessment of anorectal function. Dis Colon Rectum. 1993;36:1132–1138
  52. Rex DK, Lappas JC. Combined anorectal manometry and defecography in 50 consecutive adults with fecal incontinence. Dis Colon Rectum. 1992;35:1040–1045
  53. Berkelmans I, Heresbach D, Leroi A, Touchais J, Martin P, Weber J, et al. Perineal descent at defecography in women with straining at stool: a lack of specificity or predictive value for future anal incontinence?. Eur J Gastroenterol Hepatol. 1995;7:75–79
  54. Hiltunen K, Kolehmainen H, Matikainen M. Does defecography help in diagnosis and clinical decision-making in defecation disorders?. Abdom Imaging. 1994;19:355–358
  55. Siproudhis L, Ropert A, Lucas J, Raoul JL, Heresbach D, Bretagne JF, et al. Defecatory disorders, anorectal and pelvic floor dysfunction: a polygamy?. Int J Colorectal Dis. 1992;7:102–107
  56. Freimanis MG, Wald A, Caruana B, Bauman DH. Evacuation proctolography in normal volunteers. Invest Radiol. 1991;26:581–585
  57. Broden B, Snellman B. Procidentia of the rectum studied with cineradiography: a contribution to the discussion of causative mechanism. Dis Colon Rectum. 1968;11:330–347
  58. Bacon HE. Anus, rectum, sigmoid colon: diagnosis and treatment. Prolapse and procidentia. In: New York: Lippincott; 1941;p. 400–441
  59. Fry IK, Griffiths JD, Smart PJG. Some observations on the movement of the pelvic floor and rectum with special reference to rectal prolapse. Br J Surg. 1966;53:784–787
  60. Goei R, Baeten C, Arends JW. Solitary rectal ulcer syndrome: findings at barium enema study and defecography. Radiology. 1988;168:303–306
  61. Kuijpers JH, DeMorree H. Toward a selection of the most appropriate procedure in the treatment of complete rectal prolapse. Dis Colon Rectum. 1988;31:355–357
  62. Kuijpers HC, Strijk SP. Diagnosis of disturbances of continence and defecation. Dis Colon Rectum. 1984;27:658–662
  63. Whitehead WE, Chaussade S, Corazziari E, Kumar D. Report of an international workshop on management of constipation. Gastroenterol Int. 1991;4:99–113
  64. Turnbull GK, Lennard-Jones JE, Bartram CI. Failure of rectal expulsion as a cause of constipation: why fiber and laxatives sometimes fail. Lancet. 1986;1:767–769
  65. van der Sijp JRM, Kamm MA, Lennard-Jones JE. Age of onset and rectal emptying: predicting outcome of colectomy for severe idiopathic constipation. Int J Colorectal Dis. 1992;7:35–37
  66. Kamm MA, Bartram CI, Lennard-Jones JE. Rectodynamics—quantifying rectal evacuation. Int J Colorectal Dis. 1989;4:161–163
  67. Halligan S, McGee S, Bartram CI. Quantification of evacuation proctography. Dis Colon Rectum. 1994;37:1151–1154
  68. O'Connell PR, Kelly KA, Brown ML. Scintigraphic assessment of neorectal motor function. J Nucl Med. 1986;27:460–464
  69. Pezim ME, Pemberton JH, Levin KE, Litchy WJ, Phillips SF. Parameters of anorectal and colonic motility in health and in severe constipation. Dis Colon Rectum. 1993;36:484–491
  70. Preston DM, Lennard-Jones JE, Thomas BM. The balloon proctogram. Br J Surg. 1984;71:29–32
  71. Barkel DC, Pemberton JH, Pezim ME, Phillips SF, Kelly KA, Brown ML. Scintigraphic assessment of the anorectal angle in health and after ileal pouch-anal anastomosis. Ann Surg. 1988;208:42–49
  72. Law PJ, Kamm MA, Bartram CI. Anal endosonography in the investigation of faecal incontinence. Br J Surg. 1991;78:312–314
  73. Kamm MA. Obstetric damage and faecal incontinence. Lancet. 1994;344:730–733
  74. Law PJ, Kamm MA, Bartram CI. A comparison between electromyography and anal endosonography in mapping external anal sphincter defects. Dis Colon Rectum. 1990;33:370–373
  75. Burnett SJD, Speakman CTM, Kamm MA, Bartram CI. Confirmation of endosonographic detection of external anal sphincter defects by simultaneous electromyographic mapping. Br J Surg. 1991;78:448–450
  76. Felt-Bersma RJF, Cuesta MA, Koorevaar M, Strijers RLM, Meuwissen SGM, Dercksen EJ, et al. Anal endosonography: relationship with anal manometry and neurophysiologic tests. Dis Colon Rectum. 1992;35:944–949
  77. Sultan AH, Kamm MA, Talbot IC, Nicholls RJ, Bartram CI. Anal endosonography for identifying external sphincter defects confirmed histologically. Br J Surg. 1994;81:463–465
  78. Felt-Bersma RJF, vanBaren R, Koorevaar M, Strijers RLM, Cuesta MA. Unsuspected sphincter defects shown by anal endosonography after anorectal surgery. A prospective study. Dis Colon Rectum. 1995;38:249–253
  79. Sultan AH, Nicholls RJ, Kamm MA, Hudson CN, Beynon J, Bartram CI. Anal endosonography and correlation with in vitro and in vivo anatomy. Br J Surg. 1993;80:508–511
  80. Sultan AH, Kamm MA, Hudson CN, Nicholls JR, Bartram CI. Endosonography of the anal sphincters: normal anatomy and comparison with manometry. Clin Radiol. 1994;49:368–374
  81. Poen AC, Felt-Bersma RJF, Koorevaar M, Cuesta MA, Meuwissen SGM. Vaginal endosonography in the diagnosis of anorectal disease. (abstr) Gastroenterology. 1996;109:A737
  82. Engel AF, Kamm MA, Bartram CI, Nicholls RJ. Relationship of symptoms in faecal incontinence to spcific sphincter abnormalities. Int J Colorectal Dis. 1995;10:152–155
  83. Speakman CT, Burnett SJ, Kamm M, Bartram CI. Sphincter injury after anal dilatation demonstrated by anal endosonography. Br J Surg. 1991;78:1429–1430
  84. Engel AF, Kamm MA, Bartram CI. Unwanted anal penetration as a physical cause of faecal incontinence. Eur J Gastroenterol Hepatol. 1995;7:65–67
  85. Sultan AH, Kamm MA, Nicholls RJ, Bartram CI. Prospective study of the extent of internal anal sphincter division during lateral sphincterotomy. Dis Colon Rectum. 1994;37:1031–1033
  86. Engel AF, Kamm MA, Talbot IC. Progressive systemic sclerosis of the internal anal sphincter leading to passive faecal incontinence. Gut. 1991;35:857–859
  87. Tjandra JJ, Milsom JW, Schroeder T, Fazio VW. Endoluminal ultrasound is preferable to electromyography in mapping anal sphincteric defects. Dis Colon Rectum. 1993;36:689–692
  88. Sultan AH, Kamm MA, Hudson CN, Thomas JM, Bartram CI. Anal-sphincter disruption during vaginal delivery. N Engl J Med. 1993;329:1905–1911
  89. Burnett SJD, Spence-Jones C, Speakman CTM, Kamm MA, Hudson CN, Bartram CI. Unsuspected sphincter damage following childbirth revealed by anal endosonography. Br J Surg. 1991;64:225–227
  90. Deen KI, Kumar D, Williams JG, Ollif f J, Keighley MRB. The prevalence of anal sphincter defects in faecal incontinence: a prospective endosonic study. Gut. 1993;34:685–688
  91. Nielsen MB, Hauge C, Pedersen JF, Christiansen J. Endosonographic evaluation of patients with anal incontinence: findings and influence on surgical management. AJR. 1993;160:771–775
  92. Engel AF, Kamm MA, Sultan AH, Bartram CI, Nicholls RJ. Anterior anal sphincter repair in patients with obstetric trauma. Br J Surg. 1994;81:1231–1234
  93. Fleshman JW, Dreznik Z, Fry RD, Kodner IJ. Anal sphincter repair for obstetric injury: manometric evaluation of functional results. Dis Colon Rectum. 1991;34:1061–1067
  94. Sorensen M, Tetzschner T, Rasmussen OO, Christiansen J. Sphincter rupture in childbirth. Br J Surg. 1993;80:392–394
  95. Sultan AH, Kamm MA, Bartram CI, Hudson CN. Third degree obstetric anal sphincter tears: risk factors and outcome of primary repair. Br Med J. 1994;308:887–891
  96. deSouza NM, Kmiot WA, Puni R, Hall AS, Burl M, Bartram CI, et al. High resolution magnetic resonance imaging of the anal sphincter using an internal coil. Gut. 1995;37:284–287
  97. Chaussade S, Roche H, Khyari A, Couturier D, Guerre J. Measure de temps de transit colique (TTC): description et validation d'une nouvelle technique. Gastroenterol Clin Biol. 1986;10:385–389
  98. Metcalf AM, Phillips SF, Zinsmeister AR, MacCarty RL, Beart RW, Wolf f BG. Simplified assessment of segmental colonic transit. Gastroenterology. 1987;92:40–47
  99. Evans RC, Kamm MA, Hinton JM, Lennard-Jones JE. The normal range and a simple diagram for recording whole gut transit time. Int J Colorectal Dis. 1992;7:15–17
  100. Hinds JP, Stoney B, Wald A. Does gender or the menstrual cycle affect colonic transit?. Am J Gastroenterol. 1989;84:123–126
  101. Merkel IS, Locher J, Towers A, Ohleger K, Burgio K, Wald A. Physiological and psychological evaluation of chronic functional constipation in the elderly. (abstr) Am J Gastroenterol. 1992;87:1327
  102. Grotz RL, Pemberton JH, Talley NJ, Rath DM, Zinsmeister AR. Discriminant value of psychological distress, symptom profiles, and segmental colonic dysfunction in outpatients with severe idiopathic constipation. Gut. 1994;35:798–802
  103. Pemberton JH, Rath DM, Ilstrup DM. Evaluation and surgical treatment of severe chronic constipation. Ann Surg. 1991;214:403–413
  104. Hinton JM, Lennard-Jones JE, Young AC. A new method for studying gut transit times using radioopaque markers. Gut. 1969;10:842–847
  105. van der Sijp JRM, Kamm MA, Nightingale JMD, Britton KE, Granowska M, Akkermans LMA, et al. Radioisotope determination of regional colonic transit in severe constipation. Gut. 1993;34:402–408
  106. Stivland T, Camilleri M, Vassallo M, Proano M, Rath D, Brown M, et al. Scintigraphic measurement of regional gut transit in idiopathic constipation. Gastroenterology. 1991;101:107–115
  107. van der Sijp JRM, Kamm MA, Nightingale JMD, Walker E, Granowska M, Britton K, et al. Disturbed gastric and small bowel transit in severe idiopathic constipation. Dig Dis Sci. 1993;38:837–844
  108. Arhan P, Devroede G, Jehannin B, Lanza M, Faverdin C, Dornic C, et al. Segmental colonic transit time. Dis Colon Rectum. 1981;24:625–629
  109. Bassotti G, Gaburri M, Imbimbo BP, Rossi L, Farroni F, Pelli MA, et al. Colonic mass movements in idiopathic chronic constipation. Gut. 1988;29:1173–1179
  110. Bassotti G, Chiarioni G, Imbimbo BP, Betti C, Bonfante F, Vantini I, et al. Impaired colonic motor response to cholinergic stimulation in patients with severe chronic idiopathic (slow transit type) constipation. Dig Dis Sci. 1993;38:1040–1045
  111. Martelli H, Devroede G, Arhan P, Duguay C. Mechanisms of idiopathic constipation: outlet obstruction. Gastroenterology. 1978;75:623–631
  112. Klauser AG, Voderhoizer WA, Heinrich CA. Behavioral modification of colonic function: can constipation be learned?. Dig Dis Sci. 1990;35:1271–1275
  113. Loening-Baucke V, Anuras S. Anorectal manometry in healthy elderly subjects. Am Geriatr Soc. 1984;32:636–639
  114. Rasmussen H. Dynamic anal manometry: physiological variations and pathophysiological findings in fecal incontinence. Gastroenterology. 1992;103:103–113
  115. Pedersen IK, Christiansen J. A study of the physiological variation in anal manometry. Br J Surg. 1989;76:69–71
  116. Taylor BM, Beart RW, Phillips SF. Longitudinal and radial variations of pressure in the human anal sphincter. Gastroenterology. 1984;86:693–697
  117. McHugh SM, Diamant NE. Anal canal pressure profile: a reappraisal as determined by rapid pullthrough technique. Gut. 1987;28:1234–1241
  118. Rogers J, Laurberg S, Misiewicz JJ, Henry MM, Swash M. Anorectal physiology validated: a repeatability study of the motor and sensory tests of anorectal function. Br J Surg. 1989;76:607–609
  119. Read NW, Harford WV, Schmulen AC, Read MG, Santa Ana C, Fordtran JS. A clinical study of patients with fecal incontinence and diarrhea. Gastroenterology. 1979;76:747–756
  120. Caruana BJ, Wald A, Hinds JP, Eidelman BH. Anorectal sensory and motor function in neurogenic fecal incontinence. Comparison between multiple sclerosis and diabetes mellitus. Gastroenterology. 1991;100:465–470
  121. Loening-Baucke V, Anuras S. Effects of age and sex on anorectal manometry. Am J Gastroenterol. 1985;80:50–53
  122. Orkin BA, Hanson RB, Kelly KA, Phillips SF, Dent J. Human anal motility while fasting, after feeding, and during sleep. Gastroenterology. 1991;100:1016–1023
  123. McHugh SM, Diamant NE. Effect of age, gender, and parity on anal canal pressures. Contribution of impaired anal sphincter function to fecal incontinence. Dig Dis Sci. 1987;32:726–736
  124. Chiarioni G. Liquid stool incontinence with severe urgency: anorectal function and effective biofeedback treatment. Gut. 1993;34:1576–1580
  125. Wald A, Tunuguntla AK. Anorectal sensorimotor dysfunction in fecal incontinence and diabetes mellitus. Modification with biofeedback therapy. N Engl J Med. 1984;310:1282–1287
  126. Merkel IS, Locher J, Burgio K, Towers A, Wald A. Physiologic and psychologic characteristics of an elderly population with chronic constipation. Am J Gastroenterol. 1993;88:1854–1859
  127. Chiou AW-H, Lin J, Wang F. Anorectal abnormalities in prospective systemic sclerosis. Dis Colon Rectum. 1989;32:417–421
  128. Kumar D, Waldron D, Williams NS, Browning C, Hutton MRE, Wingate DL. Prolonged anorectal manometry and external anal sphincter electromyography in ambulant human subjects. Dig Dis Sci. 1990;35:641–648
  129. Ferrara A, Pemberton JH, Grotz RL, Hanson RB. Prolonged ambulatory recording of anorectal motility in patients with slow-transit constipation. Am J Surg. 1994;167:73–79
  130. Ferrara A, Pemberton JH, Levin KE, Hanson RB. Relationship between anal canal tone and rectal motor activity. Dis Colon Rectum. 1993;36:337–342
  131. Tjandra JJ, Sharma BRK, McKirdy HC, Lowndes RH, Mansel RE. Anorectal physiological testing in defecatory disorders: a prospective study. Aust N Z J Surg. 1994;64:322–326
  132. Braun JC, Treutner KH, Dreuw B, Klimaszewski M, Schumpelick V. Vectormanometry for dif ferentail diagnosis of fecal incontinence. Dis Colon Rectum. 1994;37:989–996
  133. Yang Y, Wexner SD. Anal pressure vectography is of no apparent benefit for sphincter evaluation. Int J Colorectal Dis. 1994;9:92–95
  134. Perr y RE, Blatchford GJ, Christensen MA, Thorson AG, Attwood SEA. Manometric diagnosis of anal sphincter injuries. Am J Surg. 1990;159:112–117
  135. Eberi T, Zeller C, Barnert J, Wienbeck M. Anal pressure vectography and transanal ultrasonography: which method is best in anal sphincter assessment. (abstr)? Gastroenterology. 1996;110:A659
  136. Felt-Bersma RJF, Klinkenberg-Knol EC, Meuwissen SGM. Anorectal function investigations in incontinent and continent patients. Dis Colon Rectum. 1990;33:479–486
  137. Sun WM, Donnelly TC, Read NW. Utility of a combined test of anorectal manometry, electromyography, and sensation in determining the mechanism of ‘idiopathic’ faecal incontinence. Gut. 1992;33:807–813
  138. Tobon F, Reid NCRW, Talbert JL, Schuster MM. Nonsurgical test for the diagnosis of Hirschsprung's disease. N Engl J Med. 1968;278:188–194
  139. Preston DM, Lennard-Jones JE. Anismus in chronic constipation. Dig Dis Sci. 1985;30:413–418
  140. Whitehead WE, Schuster MM. Anorectal physiology and pathophysiology. Am J Gastroenterol. 1987;82:487–497
  141. Corazziari E. Anorectal manometry: a round-table discussion. Gastroenterol Int. 1989;2:115–117
  142. Aitchison M, Fisher BM, Carter K, McKee R, MacCuish AC, Finlay IG. Impaired anal sensation and early diabetic faecal incontinence. Diabetic Med. 1991;8:960–963
  143. Ferguson GH, Redford J, Barrett JA, Kif f ES. The appreciation of rectal distention in fecal incontinence. Dis Colon Rectum. 1989;32:964–967
  144. Sun WM, Read NW, Prior A, Daly J, Chea SK, Grundy D. Sensory and motor responses to rectal distension vary according to rate and pattern of balloon inflation. Gastroenterology. 1990;99:1008–1015
  145. Rogers J, Henry MM, Misiewicz JJ. Combined sensory and motor deficit in primary neuropathic faecal incontinence. Gut. 1988;29:5–9
  146. Allen ML, Orr WC, Robinson MG. Anorectal functioning in fecal incontinence. Dig Dis Sci. 1988;33:36–40
  147. Bielefeldt K, Enck P, Erckenbrecht JF. Sensory and motor function in the maintenance of anal continence. Dis Colon Rectum. 1990;33:674–678
  148. Wald A. Colonic and anorectal motility testing in clinical practice. [see comments] Am J Gastroenterol. 1994;89:2109–2115
  149. Mayer EA, Gebhart GF. Basic and clinical aspects of visceral hyperalgesia. Gastroenterology. 1994;107:271–293
  150. Prior A, Maxton DG, Whorwell PJ. Anorectal manometry in irritable bowel syndrome: differences between diarrhoea and constipation predominant subjects. Gut. 1990;31:458–462
  151. Whitehead WE, Engel BT, Schuster MM. Irritable bowel syndrome. Physiological and psychological dif ferences between diarrhea-predominant and constipation-predominant patients. Dig Dis Sci. 1980;25:404–413
  152. Whitehead WE, Holtkotter B, Enck P, Hoelzl R, Holmes KD, Anthony J, et al. Tolerance for rectosigmoid distention in irritable bowel syndrome. Gastroenterology. 1990;98:1187–1192
  153. Whitehead WE, Delvaux MD, The Working Team . Standardization of barostat procedures for testing smooth muscle tone and sensory thresholds in the gastrointestinal tract. Dig Dis Sci. 1997;42:223–241
  154. Kamm MA, Lennard-Jones JE. Rectal mucosal electrosensory testing. Evidence for a sensory neuropathy in severe constipation. Dis Colon Rectum. 1990;33:419–423
  155. Whitehead WE, Orr WC, Engel BT, Schuster MM. External anal sphincter response to rectal distension: Learned response or reflex. Psychophysiology. 1982;19:57–62
  156. Latimer PR, Campbell D, Kasperski J. A components analysis of biofeedback in the treatment of fecal incontinence. Biofeedback Self Regul. 1995;9:311–324
  157. Wald A. Biofeedback for neurogenic fecal incontinence: rectal sensation is a determinant of outcome. J Pediatr Gastroenterol Nutr. 1983;2:302–306
  158. Miner PB, Donnelly TC, Read NW. Investigation of mode of action of biofeedback in treatment of fecal incontinence. Dig Dis Sci. 1990;35:1291–1298
  159. Meunier P, Marechal JM, Jaubert de Beaujeu M. Rectoanal pressures and rectal sensitivity studies in chronic childhood constipation. Gastroenterology. 1979;77:330–336
  160. De Medici A, Badiali D, Corazziari E, Bausano G, Anzini F. Rectal sensitivity in chronic constipation. Dig Dis Sci. 1989;34:747–753
  161. Read NW, Abouzekry L, Read MG, Howell P, Ottewell D, Donnelly TC. Anorectal function in elderly patients with fecal impaction. Gastroenterology. 1985;89:959–966
  162. Miller R, Bartolo DCC, Roe A, Cervero F, McC Mortensen NJ. Anal sensation and the continence mechanism. Dis Colon Rectum. 1988;31:433–438
  163. Rogers J. Testing for and the role of anal rectal sensation. Bailliers Clin Gastorenterol. 1992;6:179–191
  164. Roe AM, Bartolo DCC, McC Mortensen NJ. New method for assessment of anal sensation in various anorectal disorders. Br J Surg. 1986;73:310–312
  165. Miller R, Bartolo DCC, Cervero F, McC Mortensen NJ. Anorectal temperature sensation: a comparison of normal and incontinent patients. Br J Surg. 1987;74:511–515
  166. Barrett JA, Brocklehurst JC, Kif f ES, Ferguson G, Faragher EB. Anal function in geriatric patients with faecal incontinence. Gut. 1989;30:1244–1251
  167. Ho YH, Goh HS. Unilateral anal electrosensation. Modified technique to improve quantification of anal sensory loss. Dis Colon Rectum. 1995;38:239–244
  168. Castell DO, Wood JD, Frieling T, Wright FS, Vieth RF. Cerebral electrical potentials evoked by balloon distention of the human esophagus. Gastroenterology. 1990;98:662–666
  169. Frieling T, Enck P, Wienbeck M. Cerebral responses evoked by electrical stimulation of the esophagus in normal subjects. Gastroenterology. 1989;97:475–478
  170. Aziz Q, Furlong PL, Barlow J, Hobson A, Alani S, Bancewicz J, et al. Topographic mapping of cortical potentials evoked by distension of the human proximal and distal oesophagus. Electroenceph Clin Neurophysiol. 1995;96:219–228
  171. Speakman CTM, Kamm MA, Swash M. Rectal sensory evoked potentials: an assessment of their clinical value. Int J Colorectal Dis. 1993;8:23–28
  172. Loening-Baucke V, Read NW, Yamada T. Further evaluation of the afferent nervous pathways from the rectum. Am J Physiol. 1992;262:G927–G933
  173. Rothstein RD, Stecker M, Reivich M, Alavi A, Ding X, Jaggi J, et al. Use of positron emission tomography and evoked potentials in the detection of cortical afferents from the gastrointestinal tract. Am J Gastroenterol. 1996;91:2372–2376
  174. Akervall S, Fasth S, Nordgren S, Oresland T, Hulten L. Rectal reservoir and sensory function studied by graded isobaric distension in normal man. Gut. 1989;30:496–502
  175. Steadman CJ, Phillips SF, Camilleri M, Haddad AC, Hanson RB. Variation of muscle tone in the human colon. Gastroenterology. 1991;101:373–381
  176. Bradette M, Delvaux M, Staumont G, Fioramonti J, Bueno L, Frexinos J. Evaluation of colonic sensory thresholds in IBS patients using a barostat. Definition of optimal conditions and comparison with healthy subjects. Dig Dis Sci. 1994;39:449–457
  177. Bell AM, Pemberton JH, Hanson RB, Zinsmeister AR. Variations in muscle tone of the human rectum: recordings with an electromechanical barostat. Am J Physiol. 1991;260:G17–G25
  178. Vassallo MJ, Camilleri M, Phillips SF, Steadman CJ, Talley NJ, Hanson RB, et al. Colonic tone and motility in patients with irritable bowel syndrome. [see comments] Mayo Clin Proc. 1992;67:725–731
  179. Steadman CJ, Phillips SF, Camilleri M, Talley NJ, Haddad A, Hanson R. Control of muscle tone in the human colon. Gut. 1992;33:541–546
  180. Farthing MJG. Irritable bowel, irritable body, or irritable brain?. BMJ. 1995;310:171–175
  181. Grotz RL, Pemberton JH, Levin KE, Bell AM, Hanson RB. Rectal wall contractility in healthy subjects and in patients with chronic severe constipation. Ann Surg. 1993;218:761–768
  182. O'Brien MD, Camilleri M, von der Ohe MR, Phillips SF, Pemberton JH, Prather CM, et al. Motility and tone of the left colon in constipation: a role in clinical practice?. Am J Gastroenterol. 1996;91:2532–2538
  183. Mertz H, Naliboff B, Munakata J, Niazi N, Mayer EA. Altered rectal perception is a biological marker of patients with irritable bowel syndrome. Gastroenterology. 1995;109:40–52
  184. Naliboff BD, Munakata J, Fullerton S, Gracely RH, Kodner A, Harraf F, et al. Evidence for two distinct perceptual alterations in irritable bowel syndrome. Gut. 1997;41:505–512
  185. Madoff RD, Orrom WJ, Rothenberger DA, Goldberg SM. Rectal compliance: a critical reappraisal. Int J Colorectal Dis. 1990;5:37–40
  186. Varma JS, Smith AN. Reproducibility of the proctometrogram. Gut. 1986;27:288–292
  187. Meunier PD. Tube digestif et pancreas. Anorectal manometry. A collective international experience. Gastroenterol Clin Biol. 1991;15:697–702
  188. Orvar KB, Gregersen H, Christensen J. Biomechanical characteristics of the human esophagus. Dig Dis Sci. 1993;38:197–205
  189. Pinho M, Hosie K, Bielecki K, Keighley MR. Assessment of noninvasive intra-anal electromyography to evaluate sphincter function. Dis Colon Rectum. 1991;34:69–71
  190. Sorensen M, Tetzschner T, Rasmussen OO, Christiansen J. Relation between electromyography and anal manometry of the external anal sphincter. Gut. 1991;32:1031–1034
  191. Cheong DMO, Vaccaro CA, Salanga VD, Waxner SD, Phillips RC, Hanson MR. Electrodiagnostic evaluation of fecal incontinence. Muscle Nerve. 1995;18:612–619
  192. Bartolo DCC, Jarratt JA, Read MG, Donnelly TC, Read NW. The role of partial denervation of the puborectalis in idiopathic faecal incontinence. Br J Surg. 1983;70:664–667
  193. Rogers J, Levy DM, Henry MM, Misiewicz JJ. Pelvic floor neuropathy: a comparative study of diabetes mellitus and idiopathic faecal incontinence. Gut. 1988;29:756–761
  194. Womack NR, Morrison JF, Williams NS. The role of pelvic floor denervation in the aetiology of idiopathic faecal incontinence. Br J Surg. 1986;73:404–407
  195. Felt-Bersma RJF, Strijers RLM, Janssen JJWM, Visser SL, Meuwissen SGM. The external anal sphincter. Relationship between anal manometry and anal electromyography and its clinical relevance. Dis Colon Rectum. 1989;32:112–116
  196. Infantino A, Melega E, Negrin P, Masin A, Carnio S, Lise M. Striated anal sphincter electromyography in idiopathic fecal incontinence. Dis Colon Rectum. 1995;38:27–31
  197. Jones PN, Lubowski DZ, Swash M, Henry MM. Is paradoxical contraction of puborectalis muscle of functional importance?. Dis Colon Rectum. 1987;30:667–670
  198. Farouk R, Duthie GS, Pryde A, Bartolo DCC. Abnormal transient internal sphincter relaxation in idiopathic prurit ani: physiological evidence from ambulatory monitoring. Br J Surg. 1994;81:603–606
  199. Lubowski DZ, Nicholls RJ, Burleigh DE, Swash M. Internal anal sphincter in neurogenic fecal incontinence. Gastroenterology. 1988;95:997–1002
  200. Monges H, Salducci J, Naudy B, Ranieri F, Gonella J, Bouvier M. The electrical activity of the internal anal sphincter: a comparative study in man and cats. In:  Christensen J editors. Gastrointestinal motility. New York: Raven; 1980;p. 495–501
  201. Ustach TJ, Tobon F, Hambrecht T, Bass DD, Schuster MM. Electrophysiological aspects of human sphincter function. J Clin Invest. 1970;49:41–48
  202. Wankling WJ, Brown BH, Collins CD, Duthie HL. Basal electrical activity in the anal canal in man. Gut. 1968;9:457–460
  203. Kiff ES, Swash M. Slowed conduction in the pudendal nerves in idiopathic (neurogenic) faecal incontinence. Br J Surg. 1984;71:614–616
  204. Wexner SD, Marchetti F, Salanga VD, Corredor C, Jagelman DG. Neurophysiologic assessment of the anal sphincters. Dis Colon Rectum. 1991;34:606–612
  205. Vernava AMI, Longo WE, Daniel GL. Pudendal neuropathy and the importance of EMG evaluation of fecal incontinence. Dis Colon Rectum. 1993;36:23–27
  206. Laurberg S, Swash M, Henry MM. Delayed external sphincter repair for obstetric tear. Br J Surg. 1988;75:786–788
  207. Setti Carraro P, Kamm MA, Nicholls RJ. Long-term results of postanal repair for neurogenic faecal incontinence. Br J Surg. 1994;81:140–144
  208. Barnes PRH, Lennard-Jones JE. Balloon expulsion from the rectum in constipation of dif ferent types. Gut. 1985;26:1049–1052
  209. Read NW, Timms JM, Barfield LJ, Donnelly TC, Bannister JJ. Impairment of defecation in young women with severe constipation. Gastroenterology. 1986;90:53–60
  210. Pemberton JH. Scintigraphic assessment of the anorectal angle and evacuation. Endosc Rev. 1990;3
  211. Rao SSC, Read NW, Davison PA, Bannister JJ, Holdsworth CD. Anorectal sensitivity and responses to rectal distension in patients with ulcerative colitis. Gastroenterology. 1987;93:1270–1275
  212. Rao SS, Read NW, Stobart JA, Haynes WG, Benjamin S, Holdsworth CD. Anorectal contractility under basal conditions and during rectal infusion of saline in ulcerative colitis. Gut. 1988;29:769–777
  213. Levine MD. Children with encopresis: a descriptive analysis. Pediatrics. 1975;56:412–416
  214. Lowery SP, Srour JW, Whitehead WE, Schuster MM. Habit training as treatment of encopresis secondary to chronic constipation. J Pediatr Gastroenterol Nutr. 1985;4:397–401
  215. Young GC. The treatment of childhood encopresis by conditioned gastroileal reflex training. Behav Res Ther. 1973;11:499–503
  216. Wright L. Outcome of a standardized program for treating psychogenic encopresis. Prof Psychol. 1975;6:453–456
  217. Levine MD, Bakow H. Children with encopresis: a study of treatment outcome. Pediatrics. 1976;58:845–852
  218. Christophersen ER, Rainey SK. Management of encopresis through a pediatric outpatient clinic. J Pediatr Psychol. 1976;4:38–41
  219. Schuster MM. Constipation. Curr Ther. 1976;349–353
  220. Wald A, Chandra R, Gabel S, Chiponis D. Evaluation of biofeedback in childhood encopresis. J Pediat Gastroenterol Nutr. 1987;6:554–558
  221. Loening-Baucke V. Modulation of abnormal defecation dynamics by biofeedback treatment in chronically constipated children with encopresis. J Pediatr. 1990;116:214–222
  222. Cox DJ, Sutphen J, Borowitz S, Dickens MN, Singles J. Simple electromyographic biofeedback treatment for chronic pediatric constipation/encopresis: preliminary report. Biofeedback Self Regul. 1994;19:41–50
  223. Whitehead WE, Thompson WG. Motility as a therapeutic modality. In:  Schuster MM editors. Atlas of gastrointestinal motility in health and disease. Baltimore, MD: Williams & Wilkins; 1994;p. 300–316
  224. Enck P, Daublin G, Lubke HJ, Strohmeyer G. Long-term efficacy of biofeedback training for fecal incontinence. Dis Colon Rectum. 1994;37:997–1001
  225. Enck P. Biofeedback training in disordered defecation: a critical review. Dig Dis Sci. 1993;38:1953–1960
  226. Bleijenberg G, Kuijpers HC. Biofeedback treatment of constipation: a comparison of two methods. Am J Gastroenterol. 1994;89:1021–1026
  227. Turnbull GK, Ritvo PG. Anal sphincter biofeedback relaxation treatment for women with intractable constipation symptoms. Dis Colon Rectum. 1992;35:530–536
  228. Whitehead WE. Functional disorders of the anus and rectum. In:  Drossman DA,  Richter JE,  Talley NJ,  Thompson WG,  Corazziari E,  Whitehead WE editor. The functional gastrointestinal disorders. Boston: Brown; 1994;p. 217–263
  229. Grimaud J, Bouvier M, Naudy B, Guien C, Salducci J. Manometric and radiologic investigations and biofeedback treatment of chronic idiopathic anal pain. Dis Colon Rectum. 1991;34:690–695
  230. Rao SSC, Hatfield RA. Paroxysmal anal hyperkinesis: a characteristic feature of proctalgia fugax. Gut. 1996;39:609–612
  231. Kamm MA, Hoyle CHV, Burleigh D, Law PJ, Swash M, Martin JE, et al. Hereditary internal anal sphincter myopathy causing proctalgia fugax and constipation. A newly identified condition. Gastroenterology. 1991;100:805–810
  232. Thompson WG, Dotevall G, Heaton KW, Kruis W. Irritable bowel syndrome: guidelines for the diagnosis. Gastroenterol Int. 1989;2:92–95
  233. Ritchie J. Pain from distension of the pelvic colon by inflating a balloon in the irritable colon syndrome. Gut. 1973;14:125–132
  234. Bleijenberg G, Kuijpers JHC. Treatment of the spastic pelvic floor syndrome with biofeedback. Dis Colon Rectum. 1987;30:108–111
  235. Kawimbe BM, Papachrysostomou M, Binnie NR, Clare N, Smith AN. Outlet obstruction constipation (anismus) managed by biofeedback. Gut. 1991;32:1175–1179
  236. Dahl JA, Lindquist BL, Tysk C, Leissner P, Philipson L, Jarnerot G. Behavioral medicine treatment in chronic constipation with paradoxical anal sphincter contraction. Dis Colon Rectum. 1991;34:769–776
  237. Wexner SD, Cheape JD, Jorge JMN, Heymen S, Jagelman DG. Prospective assessment of biofeedback for the treatment of paradoxical puborectalis contraction. Dis Colon Rectum. 1992;35:145–150
  238. Fleshman JW, Dreznik Z, Meyer K, Fry RD, Carney R, Kodner IJ. Outpatient protocol for biofeedback therapy of pelvic floor outlet obstruction. Dis Colon Rectum. 1992;35:1–7
  239. Koutsomanis D, Lennard-Jones JE, Kamm MA. Prospective study of biofeedback treatment for patients with slow and normal transit constipation. Eur J Gastroenterol Hepatol. 1994;6:131–137

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Gastroenterology
Volume 116, Issue 3 , Pages 735-760, March 1999