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50 L.E. Smith and G.J. Blatchford
Anismus
Anismus is a nonrelaxing puborectalis or levator muscle com­plex, which is seen as a fixed anorectal angle with a puborectalis indentation in the face of straining down or evacuation.
17–19,22
Normally the puborectalis relaxes, and the anorectal angle opens up. The patient with anismus complains of severe straining to evacuate, and sometimes pain. If the act of defecation is timed, patients with anismus take >30 seconds to empty, starting when the anal canal begins to open. Normally evacuation takes 10 seconds after the anal canal starts to open. In addition, the anal canal width is narrow.
Intussusception/Prolapse
FIGURE 4-13. Defecography. A rectocele. R is the rectocele; A is the margin of the distal anus.
Bowel can be seen to indent the upper rectum or, if a space is present in front of the rectum, to herniate down toward the perineum. It is abnormal for bowel to descend below the upper rectum, and it is abnormal for a space to be present of >2 cm between the rectum and vagina. The postevacuation film may show the abnormal movement of bowel into the deep cul-de-sac. It is not necessary for viscera to enter the space to be abnormal. The best way to detect the depth of the pouch of Douglas is to introduce water-soluble contrast into the peritoneal cavity.
20,21
This finding is suspected in only
half of the cases.
The rectum may be seen to prolapse or intussuscept during straining or evacuation (Figure 4-15A–C).
17–19
The intussus­ception or prolapse can be characterized as upper, mid, or lower rectal, and the origin can be described as anterior or posterior. The intussusception usually begins at 6–8 cm above the anus. Generally the upper rectum should remain attached to the sacrum and the retrorectal (presacral) space should not vary. The distal part of the rectum may be in either a vertical or horizontal plane and still be normal. Radiologists have some difficulty deciding whether the enfolding is a full-thickness intussusception or a normal rectal fold. Measurement of the thickness of the enfolding rectal wall will be twice as thick as the rectal wall or a nor­mal fold of the rectum, because it represents two adjacent layers of the wall.
23
Megarectum
This diagnosis is a combination of a large measurement of the diameter of the rectum and incomplete emptying. The meas­urement of the width of the rectum at the level of the distal sacrum >9 cm suggests megarectum.
Incontinence
During the procedure, incontinent patients may not be able to hold the barium in the rectum, and it can be seen to run out of the anal canal before the instruction to defecate is given. Incontinence is often associated with other pathology.
FIGURE 4-14. Defecography. An enterocele. V is the vagina; E is the enterocele descending between the vagina and rectum.
Balloon Expulsion Test
The balloon expulsion test measures the ability of the patient to expel a balloon inflated with 50–60 mL of water. Condoms and Foley catheter balloons have been used for this
24
test.
Patients with outlet obstruction are not able to pass this balloon readily. The problem is that some patients may pass the balloon, but have undetected outlet obstruction. Conversely, patients with outlet obstruction may call upon compensatory mechanisms to pass the balloon.
2
4. Physiologic Testing 51
Indication
If a defect in the sphincter mechanism is suspected, ultra­sound is the diagnostic technique of choice.
25
It is most use­ful in the work-up of incontinence. The obstetric injury is readily seen, and the ability to find the defect approaches 100%.
Equipment
The most often used ultrasound machine displays a 360­degree image made possible by a mechanically rotating trans­ducer on a hand probe. The 10-MHz transducer provides the clearest images. The transducer is covered by a plastic cap.
25,26
Technique
The only preparation is a small enema. Sedation is not neces­sary. The patient is placed in the left decubitus position. The ultrasound system is assembled, and water is introduced to fill the cap covering the transducer. Air bubbles must be removed, because they cause an artifact. A digital examina­tion is performed to find abnormality, but also to define the direction for insertion of the probe. The probe is introduced blindly to the point where the transducer is in the rectum. Images are made in the upper, middle, and distal anus, which is the distal 4–5 cm.
FIGURE 4-15. A–C Defecography. Intussusception of the rectum. R is the rectum; A is the margin of the distal anus. The arrows show the progressive infolding of the rectum.
Anal Ultrasound
Anal ultrasound is used to look for anatomic abnormality of the anal sphincters. See the chapter on Endoluminal Ultrasound, to see images of anal ultrasounds. Ultrasound has replaced EMG as the best means to define an injury.
Interpretation
Bartram canal: l) a hyperechoic layer that is the interface of the cone with the tissues; 2) a hypoechoic layer that represents the mucosa; 3) a hyperechoic layer that represents the submu­cosa; 4) a hypoechoic layer that is the internal anal sphincter;
5) a hyperechoic layer that represents the intersphincteric plane and the longitudinal muscle; and 6) a layer of mixed echogenicity representing the external anal sphincter.
loop around the upper anus. In the middle anus, both the inter­nal and external sphincters may be seen. In the distal anus, the subcutaneous portion of the external sphincter is visualized, but the internal sphincter does not extend this far. The thickness of the internal sphincter stands out in the middle of the anus. The normal adult sphincter is 2–3 mm thick. A neonate may have a sphincter of 1 mm, and in the elderly 3–4 mm thick.
Incontinence
A thin muscle suggests primary degeneration of the internal sphincter. After lateral internal sphincterotomy, a distal defect can be seen in the internal sphincter. Obstetric trauma may extend into the transverse perineus muscle, the external sphincter, or completely down through the internal sphincter. The injury blurs out portions of the normal rings of tissue described above.
26,27
describes six ultrasonographic layers in the anal
In the upper anal canal, the puborectalis muscle is seen to
28
52 L.E. Smith and G.J. Blatchford
Magnetic Resonance Imaging
MRI of pelvic floor function is developing rapidly. Dynamic studies have yielded additional information compared with static examinations alone. Identification of the anal and rectal structures is fairly easy on MRI because the perirectal fat shows a high degree of contrast when compared with the musculature. Indications for MRI examination are primarily sepsis, trauma, congenital abnormalities, and tumor.
There is a significant change in T1 and T2 weighted imag­ing associated with infection. This change produces high soft tissue contrast and enables abscess and fistulous tracks to be demonstrated. Sensitivity of MRI using the body coil can be as high as 89% in identifying fistulas, but demonstration of site of internal opening and differentiation of various muscle layers is not always possible. cordance between MRI and surgical findings for the primary tract and secondary tracts of 86% and 93%, respectively.
Muscular anatomy is seen so well that MRI has become useful in the evaluation of anal trauma. When compared with endorectal ultrasound, endoanal coil MRI is superior in identi­fying the outer aspect of the external sphincter muscle. Concordance between MRI and surgical findings has been shown with regard to location of sphincter tears after obstetric
30
trauma.
Studies have shown endoanal MRI to be comparable to endoanal ultrasound for identifying defects and/or thinning of the internal sphincter. MRI, however, may also show thin­ning of the external sphincter and puborectalis, which are not easily seen on endoanal ultrasound. This may represent atro­phy in the pelvic musculature. Atrophy may correlate with a poor result after sphincter repair. Determination of atrophy on endoanal MRI may help in predicting the outcome after sphincteroplasty.
31
Atrophy on MRI has been shown to corre­late with single fiber needle EMG which confirms denervation at the level of the muscle. even in the presence of external anal sphincter atrophy. Prolongation of the PNTML reflects damage to only the large heavily myelinated nerve fibers and does not reflect the nerve function at the muscle level.
Congenital abnormalities of the anus and rectum can be delineated by MRI examination. tify sphincter involvement by rectal tumors. Distance from the distal aspect of the tumor to the levator muscle can be accu­rately assessed before surgical planning. Because of the length of the endorectal coil, visualization of the musculature of the sphincter up to 2 cm above the levator ani only is
34
seen.
Visualization of depth of invasion by tumor can be done by manipulation of contrast with the use of T2 weighted images.
Defecatory problems may also be evaluated by MRI. Dynamic pelvic MRI (or MRI proctography) is now possible since techniques for rapid MRI acquisition have been devel­oped. This allows pelvic floor motion to be visualized in real time during defecation. Generally this does not require addition of contrast although some limitations with motion artifact can
29
In this study, there was con-
32
However, PNTML may be normal
33
MRI can be used to iden-
be seen. It has been suggested that examination in the supine position (MRI) compared with the study in a seated position (balloon proctography) shows minimal and probably clinically insignificant differences in pelvic organ prolapse between these two techniques.
35
MRI is able to demonstrate peritoneoceles, cystoceles, perineal descent, and prolapse during evacuation. Evidence of obstruction defecation may be seen with the anorectal angle becoming more acute with straining, suggesting paradoxical contraction of the puborectalis.
EMG of the Anal Sphincter
EMG is used primarily in evaluating fecal incontinence. EMG is a means of assessing the motor unit. The integrity of the mus­cle may be assessed as well as its nerve supply. The integrity of external anal sphincter innervation after sphincter injury can be demonstrated. Sphincter reinnervation secondary to pelvic neu­ropathy can be demonstrated. EMG may also be used to “map” specific anatomic sphincter defects. This mapping technique has largely been replaced by anal ultrasonography, which is simple, accurate, and painless. Anal EMG may also be used to demonstrate appropriate relaxation and contraction of the anal muscle and can be used in biofeedback therapy.
Concentric Needle EMG
Concentric needle EMG focuses on different motor unit char­acteristics. A concentric needle electrode will record muscle contractions as motor unit potentials (MUPs). A single MUP is caused by depolarization of the muscle from a single motor unit. Three variables are noted within a MUP: amplitude, duration, and shape. Amplitude is dependent on the number of muscle fibers discharging. The larger the number of fibers, the greater is the amplitude of the MUP. Generally only the fibers lying within 1 mm of the electrode (typically less than
20) contribute to the spike of the MUP. Distance may also influence amplitude to some degree. Duration of the MUP is a result of dispersion of the action potentials originating from the different muscle fibers of a motor unit. Duration of MUPs increases with age. Denervation also causes a prolongation of duration and polyphasic potentials. Shape of the MUP results from summation of the single fiber action potentials in the motor unit. Most normal MUPs are bi- or triphasic. Polyphasic potentials (four or more phases) have been reported in up to 25% of normal external anal sphincter mus­cles. Polyphasic potentials of short duration occur in myo­pathic disorders and those with long duration correlate with histologic evidence of regeneration in denervated muscle. Concentric needle EMG can be of particular value in the diag­nosis of specific neurologic problems, including conditions of the cone and cauda equina, sacral roots, pudendal nerve, and for differential diagnosis of the various types of multisystemic atrophy. duration is <6 ms.
36
Normal amplitude of the MUP is <600 μV and
37
4. Physiologic Testing 53
Single Fiber EMG
Single fiber EMG electrodes are used because the area of measurement is so small each fiber generates a single spike. In normal circumstances, only a few muscle fibers from a sin­gle motor unit are within the recording area of a single fiber electrode. In reinnervated muscle, the numbers of fibers belonging to a single motor unit increase, thereby increasing action potentials are recorded at the electrode. The number of spikes can be recorded from separate potentials and fiber den­sity can be calculated. Fiber density is the measurement of the mean number of muscle fibers innervated by one alpha-motor unit. This is usually an average from numerous separate potentials. Technique of single fiber EMG involves placing a sterilized fine needle (single fiber electrode) with a recording surface of 25 μm into the external anal sphincter just outside the anal verge. Readings are taken in both the left and right lateral areas with 20 needle positions or more done for calcu­lation of fiber density. A value >1.7 is considered abnormal. Criteria for pudendal nerve damage in single fiber EMG are the presence of an increased fiber density, increase of MUP duration and amplitude at rest, decrease of the number of MUPs during maximum contraction, and presence of “jitter and blocking” phenomena.
39
amplitude from 8–10 μV, endurance (maintenance of sus­tained contraction) of 30–40 seconds. Normal patients demonstrated no evidence of paradoxical activity.
37
Pudendal Nerve Terminal Motor Latency
The pudendal nerve originates from S2, S3, S4 nerve roots and travels along the lateral pelvic wall down to near the ischial spine where it exits the pelvis to supply the external anal sphincter and the periurethral muscles through its termi­nal perineal branch. Prolongation in the pudendal nerve con­duction indicates injury to the pudendal nerve sheath that results in focal demyelination with resultant slowing of con­duction. Testing is usually done with a St. Mark’s electrode with a stimulating electrode mounted at the fingertip portion and a recording electrode mounted at the finger base portion. The electrode has a constant distance of 50 mm between stim­ulation of the nerve and recording of the external anal sphinc-
38
ter response. Latency between stimulation and response can then be recorded (Figure 4-16). This latency reflects the myelin function of the peripheral nerve. Therefore, a normal PNTML does not exclude partial damage. However, when unilaterally or bilaterally severely prolonged, PNTML has been shown to affect results after sphincter repair.
39,42,43
Surface Electrodes
Surface EMG electrodes are generally used to document anal sphincter activity at rest, strain, and squeeze. Documentation of paradoxical sphincter contraction may improve assessment of patients with defecation disorders. When compared with proctography, both needle EMG and surface EMG have a low positive predictive value, but they have high negative predic­tive values. nosing the presence of nonrelaxing puborectalis. Surface electrodes avoid the pain of needle EMG.
Biofeedback training is often done using surface elec­trodes. This may be done for fecal incontinence or for diffi­culties with evacuation, particularly if paradoxical sphincter contraction is present. A plug electrode may be used within the anal canal or surface electrodes may be placed near the anus in a lateral position. Surface electrodes are easy and painless to apply and therefore well tolerated by patients. They come with self-adhesive or can be secured with tape. They should be placed over the subcutaneous part of the external anal sphincter 1 cm from the anal verge in right and left lateral positions. A grounding electrode is then placed on the patient’s buttock. EMG recordings from the external anal sphincter during straining using surface electrodes applied to the skin correlate well with the result from needle electrodes inserted into the muscle. anal plug electrodes correlate well with anal manometry and with wire electrodes during rest, squeezing, and straining. Normal values for surface EMG show short contraction (3-second) amplitude from 8–10 μV, 10-second contraction
40
Therefore, EMG alone is not optimal for diag-
41
Other studies have shown that the
Evaluation of Transit
The time it takes for food to travel through the digestive tract is known as bowel transit time. Gastric emptying, small bowel transit, and colonic transit may be studied. Transit is depend­ent on diet and varies greatly from person to person. For this reason, a dietary history and bowel evacuation history should be obtained in conjunction with any transit testing. Dietary history can be evaluated for fiber, fat, and calorie intake. Patients who believe they eat a high fiber diet may be shown to have a very modest fiber intake. Stool history will further delineate the extent of the patient’s problem. In patients com­plaining of chronic constipation who believed that they had less than or equal to three stools per week for more than 6 months, a 4-week stool diary revealed that only 49% actu­ally met this criteria. The remaining 51% of patients had, on average, six stools per week. history of psychiatric illness was five times more frequent among those whose bowel symptoms correlated poorly with objective evidence of constipation.
Colonic Transit
The rate at which fecal residue moves through the colon is important in determining whether the stool is liquid, semi­formed, or hard. Evaluation of constipation and pelvic prob­lems may require determination of colonic transit times in order to assist in treatment. Transit may be measured by radiopaque markers or radionucleotide techniques.
44
This study also showed that a
54 L.E. Smith and G.J. Blatchford
Pudendal
R
Right P - Recturn Left P - Right P
MNCV Curves
Right Pudendal Right P-Rectum Left P-Rectum
2.0
2.4
0.5
0.1 −88
Stim
10mA 10mA
0.1mV 2ms
FIGURE 4-16. PNTML curves showing a latency of the right nerve of 2.0 msD and the left nerve of 2.4 msD.
Colonic transit is most easily measured by use of a marker test. The patient ingests a capsule containing radiopaque markers, which are then followed through the colon by abdominal radiographs. Markers consist of a capsule contain­ing radiopaque markers, which are commercially available (Sitz-Mark, Konsyl Pharmaceuticals, Fort Worth, TX) or can be individually created by filling gel capsules with small cir­cles cut from radiopaque tubing. In the most simplified colon transit technique, the patient takes one marker tablet which
of markers present in each section is counted on both the 4­and 7-day films. A table can then be made with the values (Table 4-1). Average normal transit is 11.3 hours, 11.3 hours, and 12.4 hours for the right, left, and rectosigmoid colon, respectively. Normal total transit averages 35 hours. Segmental colectomy is not indicated for constipation even in the face of markedly abnormal segmental transit time. Stool weight has been shown to correlate with transit time in con­stipated patients.
44
contains 24 markers on day 0. On day 5, a supine abdominal film is taken to determine the number and position of remain­ing markers. If five or fewer markers are remaining, the patient has normal colonic transit. If more than five markers are present, then the pattern of residual markers is noted. Diffuse scattering throughout the colon would suggest colonic inertia or decreased motility. If the markers are pres­ent in the rectosigmoid region, then the presence of pelvic
Radionuclide Transit
Transit may be measured by radionuclide gamma scinti­graphic techniques. ods correlate well. The major advantage of scintigraphy is that 24–48 hours of scanning is needed compared with 5–7 days for marker test completion.
46
Radiographic and scintigraphic meth-
outlet problems should be considered. Segmental transit may be calculated as described by Metcalf et al. and day 2, the patient takes one marker capsule for a total of three capsules. On day 4, an abdominal film is taken. If there are more than a total of 50 markers remaining, transit time is abnormal and an additional abdominal radiograph is taken on day 7 to determine the location and number of residual mark­ers. The abdominal radiograph is divided into the following sections: right colon, left colon, and rectosigmoid. The number
45
On day 0, day 1,
TABLE 4-1. Results of a colon transit study
Right colon Left colon Rectosigmoid Total
Day-4 film 15 21 16 52 Day-7 film 0 4 14 18 Transit time (h) 15 25 30 70
The theoretical numbers of ingested markers by time and colonic segment. This example shows a right colon transit of 15 h, left colon of 25 h, rectosig­moid of 30 h, and a total colonic transit of 70 h.
4. Physiologic Testing 55
Small Bowel Transit
Small intestinal transit should be evaluated before surgical treatment of constipation because the patient may have a global motility problem. Small bowel transit may be meas­ured by breath hydrogen analysis. Hydrogen breath analysis depends on the presence of bacteria in the large intestine to metabolize lactulose. Up to 25% of the population cannot metabolize the sugar because they lack certain bacterial strains in the colon.
47
A meal of lactulose and beans is ingested and hydrogen breath analysis is undertaken. Fermentation of the meal occurs when the substrate reaches the colon. The fermentation process releases hydrogen gas that is absorbed and excreted by the lungs. Time to a 20-ppm increase in hydrogen in the breath correlates with small bowel transit. Some conditions such as low colonic pH, bacterial overgrowth, or antibiotic administration may interfere with the use of this test for small bowel transit.
Small bowel transit may also be determined by scinti­graphic techniques. These techniques have the advantage of also measuring gastric emptying. Scintigraphy has a tendency toward slightly shorter transit times, but this is probably not clinically significant. Radiation exposure with scintigraphy is highest for the colon and can be reduced by the administration of laxatives after the procedure. Radiation to the ovaries is less than in a plain abdominal X-ray.
References
1. Wexner SD, Jorge JMN. Colorectal physiological tests: use or abuse of technology? Eur J Surg 1994;160:167–174.
2. Lowry AC, Simmang CL, Boulos P, et al. Report of the tripartite consensus conference on definitions for anorectal physiology and rectal cancer, Washington, D.C., May 1, 1999. Dis Colon Rectum 2001;44(7):915–919.
3. Pedersen IK, Christiansen J. A study of the physiological varia­tion in anal manometry. Br J Surg 1989;76:69–71.
4. Loening-Baucke V, Anuras S. Effects of age and sex on anorec­tal manometry. Am J Gastroenterol 1991;80:50–53.
5. Hallan RI, Marzouk DEMM, Waldron DJ, et al. Comparison of digital and manometric assessment of anal sphincter function. Br J Surg 1989;76:973–975.
6. Felt Bersma RJF, Klinkenberg-Knol, Meuwissen SGM. Anorectal function investigations in incontinent and continent patients. Dis Colon Rectum 1990;33:479–486.
7. Duthie HL, Watts JM. Contribution of the external anal sphinc­ter to the pressure zone in the anal canal. Gut 1965;17:64–68.
8. 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.
9. Rattan S, Chakder S. Role of nitric oxide as a mediator of inter­nal anal sphincter relaxation. Am J Physiol 1992;262:G107–112.
10. Perry RE, Blatchford GJ, Christensen MA, et al. Manometric diagnosis of anal sphincter injuries. Am J Surg 1990;159: 112–117.
11. Tjandra JJ, Sharma BRK, McKirdy HC, et al. Anorectal physio­logical testing in defecatory disorders: a prospective study. Aust N Z J Surg 1994;64:322–326.
12. Bouchoucha M, Faye A, Arsac M, Rocaries F. Anal sphincter response to distension. Int J Colorectal Dis 2001;16:119–125.
13. Tobon F, Reid NCRW, Talbert JL, et al. Nonsurgical test for the diagnosis of Hirschsprung’s disease. N Engl J Med 1968;278: 188–194.
14. Preston DM, Lennard-Jones JE. Anismus in chronic constipa­tion. Dig Dis Sci 1985;30:413–418.
15. Bremmer S. Peritoneocele: a radiological study with defaeco­peritoneography. Acta Radiol Suppl 1998;413:1–33.
16. Maglinte DD, Kelvin FM, Hale DS. Dynamic cystoproctogra­phy: a unifying diagnostic approach to pelvic floor and anorectal dysfunction. AJR Am J Roentgenol 1999;169:759–767.
17. Jorge JMN, Habr-Gama A, Wexner S. Clinical applications and techniques of cinedefecography. Am J Surg 2001;182:93–101.
18. Wiersma T, Mulder CJJ, Reeders WAJ. Dynamic rectal exami­nation: its significant clinical value. Endoscopy 1997;29: 462–471.
19. Jones HJS, Blake H, Swift RI. A prospective audit of the useful­ness of evacuating proctography. Ann R Coll Surg Engl 1998;80:40–45.
20. Halligan S, Bartram C, Hall C, et al. Enterocele revealed by simultaneous evacuation proctography and peritoneography: does “defecation block” exist? AJR Am J Roentgenol 1996;167: 461–466.
21. Sentovich SM, Rivela LJ, Thorson AG, et al. Simultaneous dynamic proctography and peritoneography for pelvic floor dis­orders. Dis Colon Rectum 1995;38:912–915.
22. Halligan S, Malouf A, Bartram C, et al. Predictive value of impaired evacuation at proctography in diagnosing anismus. AJR Am J Roentgenol 2001;177:633–637.
23. Pomerri F, Zuliani M, Mazza C, et al. Defecographic measure­ments of rectal intussusception and prolapse in patients and in asymptomatic subjects. AJR Am J Roentgenol 2001;176:641–645.
24. Rao SS, Hatfield R, Soffer E. Manometric tests of anorectal function in healthy adults. Am J Gastroenterol 1999;94:773–783.
25. Sentovich SM, Blatchford GJ, Rivela LJ, et al. Diagnosing anal sphincter injury with transanal ultrasound and manometry. Dis Colon Rectum 1997;40:1430–1434.
26. Bartram CI, Burnett SJD. Atlas of Anal Endosonography. Oxford: Butterworth-Heinemann; 1991.
27. Bartram C. Radiologic evaluation of anorectal disorders. Gastroenterol Clin North Am 2001;30:55–75.
28. Sultan AH, Kamm MA, Talbot IC, et al. Anal endosonography for identifying external sphincter defects confirmed histologi­cally. Br J Surg 1994;81(3):463–465.
29. Barker PG, Lunniss PJ, Armstrong P, et al. Magnetic resonance imaging of fistula-in-ano: technique, interpretation and accuracy. Clin Radiol 1994;49:7–13.
30. Fletcher JG, Busse RF, Reiderer SJ, et al. Magnetic resonance imaging of anatomic and dynamic defects of the pelvic floor in defecatory disorders. Am J Gastroenterol 2003;98:399–411.
31. Briel JW, Stoker J, Rociu E, et al. External anal sphincter atro­phy on endoanal magnetic resonance imaging adversely affects continence after sphincteroplasty. Br J Surg 1999;86:1322–1327.
32. William AB, Bartram CI, Modhwadia D, et al. Endocoil mag­netic resonance imaging quantification of external anal sphincter atrophy. Br J Surg 2001;88:853–859.
33. Sato T, Konishi F, Kanazawa K. Variations in motor evoked potential latencies in the anal sphincter system with sacral mag­netic stimulation. Dis Colon Rectum 2000;43:966–970.
56 L.E. Smith and G.J. Blatchford
34. deSouza NM, Hall AS, Puni R, et al. High resolution magnetic resonance imaging of the anal sphincter using a dedicated endoanal coil. Dis Colon Rectum 1996;39:926–934.
35. Fletcher JG, Busse RF, Riederer SJ, et al. Magnetic resonance imaging of anatomic and dynamic defects of the pelvic floor in defecatory disorders. Am J Gastroenterol 2003;98:399–411.
36. Del Rey AP, Entrena BF. Reference values of motor unit poten­tials (MUPs) of the external anal sphincter muscle. Clin Neurophysiol 2002;113:1832–1839.
37. Ferrara A, Lujan JH, Cebrian J, et al. Clinical, manometric, and EMG characteristics of patients with fecal incontinence. Tech Coloproctol 2001;5:13–18.
38. Osterberg A, Graf W, Eeg-Olofsson KE, et al. Results of neuro­physiologic evaluation in fecal incontinence. Dis Colon Rectum 2000;43(9):1256–1261.
39. Jacobs PPM, Scheuer M, Kuijpers JHC, et al. Obstetric fecal incontinence: role of pelvic floor denervation and results of delayed sphincter repair. Dis Colon Rectum 1990;33(6):494–497.
40. Yeh CY, Pikarsky A, Wexner SD, et al. Electromyographic find­ings of paradoxical puborectalis contraction correlate poorly with cinedefecography. Tech Coloproctol 2003;7:77–81.
41. Lopez A, Nilsson BY, Mellgren A, et al. Electromyography of the external anal sphincter: comparison between needle and sur­face electrodes. Dis Colon Rectum 1999;42:482–485.
42. Laurberg S, Swash M, Henry MM. Delayed external sphincter repair for obstetric tear. Br J Surg 1998;75:786–788.
43. Wexner SD, Marchetti F, Jagelmen DG. The role of sphinctero­plasty for fecal incontinence reevaluated: a prospective physio­logic and functional review. Dis Colon Rectum 1991;34:22–30.
44. Ashraf W, Park F, Lof J, et al. An examination of the reliability of reported stool frequency in the diagnosis of idiopathic consti­pation. Am J Gastroenterol 1996;91:26–32.
45. Metcalf AM, Phillips SF, Zinsmeister AR, et al. Simplified assessment of segmental colonic transit. Gastroenterology 1987; 92:40–47.
46. Charles F, Camilleri M, Phillips SF, Thomforde GM, Forstrom LA. Scintigraphy of the whole gut: clinical evaluation of transit disorders. Mayo Clin Proc 1995;70(2):113–118.
47. Caride VJ, Prokop EK, Troncale FJ, et al. Scintigraphic determination of small intestinal transit time: comparison with the hydrogen breath technique. Gastroenterology 1984;86: 714–720.
5
Diagnostic Evaluations—Endoscopy: Rigid, Flexible Complications
Santhat Nivatvongs and Kenneth A. Forde
The large intestine from cecum to anus can be effectively and accurately examined as part of a complete physical examina­tion. An ultimate diagnosis of large bowel diseases can only be made by direct observation of the abnormalities and, if indicated, a biopsy. Different equipment is designed and used for different purposes.
Anoscopy
Anoscopy is the examination of the anal canal. The lower part of the rectal mucosa, upper anal mucosa, anoderm, dentate line, internal and external hemorrhoids can be seen through this examination.
There are basically two types of anoscopes: beveled type such as the Buie or Hirschman scope (Figure 5-1) and the lighted Welch-Allen scope (Figure 5-2) that uses the same light source as the rigid proctosigmoidoscope. Another type is the side-opening Vernon-David scope with Hirschman handle (Figure 5-3). The Hinkel-James anoscope (Figure 5-4) is much longer than the Vernon-David scope and is suitable for patients with deep buttock cheeks.
Indications
Any anal and perianal diseases or conditions require a full examination of the anal canal. These include anal fissures, anal fistulas, anal Crohn’s disease, anal tumors, hemorrhoids, anal condyloma, bright red rectal bleeding, and pruritus ani.
Anoscopy is frequently used in conjunction with colonoscopy, flexible sigmoidoscopy, and rigid proctosigmoi­doscopy as part of the examination.
Contraindications
Patients who have severe anal pain such as an acute anal fis­sure or a perianal or intersphincteric abscess may not tolerate the examination. In general, if a patient can tolerate a digital examination, anoscopy can usually be done. A 2% lidocaine
jelly should be used in patients with anal pain. Anal stricture or severe anal stenosis is another contraindication.
Preparation
No preparation is required.
Positioning
A prone jackknife position gives the best exposure. An alter­native is a left lateral recumbent position.
Technique
The Vernon-David, which is a side-opening endoscope, gives the best examination. Inspection of the anal area should always precede any other examination and, for this, good lighting is essential. The cheeks of the buttock are gently spread to gain exposure. Skin tags, excoriation, and change in color or thick­ness of the anal verge and perianal skin can be detected quickly. A scarred, patulous, or irregularly shaped anus may give clues to the cause of anal incontinence. Particularly in multiparous women, the anal verge may be pushed down quite far during straining—a feature of the descending perineum syndrome. When the anal verge is pricked with a needle, the external sphincter visibly contracts because of the anal reflex. It is useful for testing the sensibility of the anal canal, which may be absent in areas of previous scar or defect, or in patients with an underlying neuropathy.
The next step is to do a digital examination. The index fin­ger should be well lubricated with a lubricant jelly, and the finger pressed on the anal aperture to “warn” the patient. Then the finger should be gradually inserted and swept all around the anal canal to detect any mass or induration. In men, the prostate should be felt. In women, the posterior vaginal wall should be pushed anteriorly to detect any evi­dence of a rectocele. Anal tone, whether tight or loose, can be easily estimated. A stricture or narrowing from scarring or a defect in the internal or external sphincters from a previous
57
58 S. Nivatvongs and K.A. Forde
FIGURE 5-1. Buie anoscope.
operation can be felt. A fibrous cord or induration in the anal area and the anal canal may indicate a fistulous tract. The external sphincter, puborectalis, and levator ani muscles can also be appreciated by digital examination. When the pub­orectalis is pulled in the posterior quadrant, the anus will gape but will close immediately when the traction is released. Persistence of the gaping indicates an abnormal reflex path­way in the thoracolumbar region frequently seen in para­plegic patients. The finger should press gently on these muscles for signs of tenderness. When the person with good anal function is asked to contract the muscles, the examiner not only feels the squeeze of the muscle on the examining finger but also feels the finger pulled forward by the pub­orectalis muscle.
Insertion of the anoscope should always be done with the obturator in place. The obturator is removed during exami­nation and reinserted to rotate the instrument to another area. However, if the beveled type of endoscope is used, the
FIGURE 5-3. Vernon-David with Hirschman handle anoscope.
endoscope can be rotated all around without having to reinsert the obturator. If an inverted (jackknife) position is used, the examination table need not be tipped down more than 10–15 degrees. If a left lateral position is used, an assistant needs to pull up the right cheek of the buttock for exposure. During examination, the patient is asked to strain with the anoscope sliding out to detect any prolapse of the rectal mucosa and the anal cushion. Excoriation, meta­plastic changes, and friable mucosa indicate a prolapsed hemorrhoid.
A biopsy via an anoscope is not advisable because of its poor exposure. If indicated, a biopsy via a rigid proctosig­moidoscope or a flexible sigmoidoscope is more appropriate.
Complications
Anal tear, especially at the posterior midline, can occur in patients with anal stenosis.
FIGURE 5-2. Lighted Welch-Allen anoscope.
FIGURE 5-4. Hinkel-James anoscope.
5. Diagnostic Evaluations—Endoscopy: Rigid, Flexible Complications 59
Rigid Proctosigmoidoscope
Three sizes of rigid proctosigmoidoscope are available (Figure 5-5). A 19 mm × 25 cm scope is the standard size for a general examination and for polypectomy or electrocoagulation. A 15 mm × 25 cm endoscope is an ideal size for general examination. It is much better tolerated by the patient, caus­ing less spasm of the rectum and, thus, minimal air insuffla­tion, yet enables as adequate an examination as the standard-size endoscope. An 11 mm × 25 cm endoscope should be available for examining the patient who has anal or rectal stricture, such as Crohn’s disease. Some physicians and surgeons prefer a disposable standard-size rigid proctosig­moidoscope for routine examination.
Indications
Rigid proctosigmoidoscopy has largely been replaced by flex­ible sigmoidoscopy. However, rigid proctosigmoidoscopy is still useful in examination of the anorectum. One of its advan­tages is that any blood clots or stool can easily be washed out. In fact, in a patient who has massive gastrointestinal bleeding, a rigid proctosigmoidoscopy is the first line of examination to rule out the source of bleeding in the anorectum.
A rigid proctosigmoidoscopy is used when an abnormality of the anal canal and rectum is suspected such as nonspecific proctitis, radiation proctitis, anorectal ulcer, anorectal neo­plasm, infectious proctitis, and anorectal Crohn’s disease. Rigid proctosigmoidoscopy is also useful to identify the pre­cise site and size of rectal neoplasm.
Contraindications
Patients with severe anal pain from an acute fissure, thrombosed external hemorrhoids, and perianal abscess may not allow an examination. The examination should be postponed to some other date. Anal stricture that will not allow the passage of the smallest size rigid proctosigmoidoscope is a contraindication to its use.
F
IGURE 5-5. Rigid proctosigmoidoscope. Top, 19 mm × 25 cm;
middle, 15 mm × 25 cm; bottom, 11 mm × 25 cm.
Patients with acute abdomen of any cause, rectal and sig­moid anastomosis less than 2 weeks postoperatively should not have a rigid proctosigmoidoscopy.
Preparation
Two phosphate enemas should be given within 2 hours of the examination. This is not necessary in a patient who has diar­rhea or active bleeding. Sedation is unnecessary.
Positioning
A prone jackknife is the position of choice. However, a left lateral position also gives an adequate examination and should be used in conditions such as pregnancy, severe hyper­tension, retinal detachment or postoperative eye surgery, and some apprehensive patients.
Technique
Although a standard proctosigmoidoscope is 25 cm in length, the average distance that the scope can be passed is 20 cm. In men, the scope can be passed to 21–25 cm half of the time, and in women, it can be passed that distance one-third of the
1
time.
Rigid proctosigmoidoscopy is suitable only to examine the rectum and, in some patients, the distal sigmoid colon. The pain experienced from proctosigmoidoscopy is from stretching the mesentery of the rectosigmoid colon when the scope is pushed against the rectal wall, and from the air insuf­flation. When properly performed, rigid proctosigmoidoscopy should produce no pain or only mild discomfort. Most patients are fearful of the examination because of past bad experience with the procedure or from what they have heard. A few words of reassurance will be helpful.
With the obturator in place and held steady with the right thumb, the well-lubricated rigid proctosigmoidoscope is gen­tly inserted into the anal canal, aiming toward the umbilicus for a distance of about 4–5 cm. Then the endoscope is angled toward the sacrum and advanced another 4–5 cm into the rec­tum. The obturator is removed and the bowel lumen is nego­tiated under direct vision. Air insufflation is limited to the amount necessary to open the lumen. When an angle is encountered, the endoscope is withdrawn 3–4 cm and then readvanced. This may be repeated several times to straighten the angulation. If further advancement is unsuccessful, the procedure is terminated at this point. Careful examination is done as the instrument is withdrawn. It is usually necessary to insufflate a small amount of air for good visualization of the lumen. The instrument should be rotated on withdrawal to ensure examination of the entire circumference. The mucosal folds in the rectum (valves of Houston) can be flattened with the tip of the endoscope to see the area behind them.
The length of insertion should be measured from the anal verge without stretching the bowel wall. Some physicians measure it in relation to the dentate line. The appearance of the