Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:

Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_1185_Библиотеки_им_академика_М_И_Перельмана

.pdf
Скачиваний:
0
Добавлен:
15.09.2026
Размер:
17 Мб
Скачать
☆
110 D.G. Kim and W.D. Wong
Other causes of anatomic anal sphincter defects include anorectal trauma or surgery and congenital anomalies. Blunt or penetrating trauma to the perineum may involve the sphincter mechanism. Management often includes fecal diversion, and debridement of the associated perineal soft tis­sues. After the perineal wound has healed, EAUS may be used to assess anal sphincter anatomy to determine if sphinc­ter reconstruction is necessary before colostomy closure.
Patients undergoing anorectal surgery may experience tran­sient minor incontinence in the early postoperative period, which usually resolves spontaneously. Patients who have per­sistent symptoms of incontinence may warrant evaluation. EAUS provides an objective means to evaluate the anal sphinc­ter mechanism in patients with postoperative fecal incontinence after anorectal surgery such as hemorrhoidectomy, fistulotomy, lateral internal sphincterotomy, or sphincteroplasty.
The surgical correction of congenital anorectal anomalies is based on reconstituting the anatomy of the anorectum. The goal of posterior sagittal anorectoplasty (PSARP) is to place
FIGURE 7-14. This image depicts a complete anterior sphincter dis­ruption in a female patient. The hypoechoic internal anal sphincter can be seen completely disrupted in its anterior location (A arrows). Similarly, the hyperechoic external anal sphincter is completely dis­rupted anteriorly (B arrows).
sphincter defect. An examining digit used to measure the perineal body distance in the mid anal canal can accentuate an anterior sphincter defect, helping to identify a sphincter injury (Figure 7-15).
59
the bowel within the striated muscle complex of the levator ani and external anal sphincter.
60
EAUS has been used to accurately confirm the position of the neo-anus within the anal sphincter complex comparing favorably with MRI. EAUS in fact provided greater detail of the anal muscles than MRI and had better correlation with direct perineal muscle stimulation.
61
Adult patients who present with severe fecal incontinence after previous surgical repair of a congenital anorectal malformation can undergo successful PSARP. Usually, the existing anus is anterior to the sphincteric muscle complex.
62
An EAUS can be performed to help define the
relationship of the anus to the sphincteric mechanism.
The identification of localized sphincter defects is impor­tant in the evaluation of the incontinent patient, because these defects may be amenable to surgical repair. EAUS can clearly and objectively image the anal sphincter mechanism and has replaced needle electromyography as the procedure of choice for anal sphincter mapping. EAUS is better tolerated and less painful than needle electromyography sphincter mapping. Anorectal manometry and pudendal nerve terminal motor latency testing are complementary but do not definitively correlate with a surgically correctable defect.
46,52,54,63,64
EAUS remains the definitive test that can identify a surgi­cally correctable defect in a symptomatic patient with fecal incontinence.
61
62
FIGURE 7-15. This image demonstrates the measurement of the ante­rior perineal body in this patient with an anterior sphincter disrup­tion. The curvilinear hyperechoic structure (A) is the examiner’s finger in the vagina. This technique can often accentuate the defect (B) seen in the internal anal sphincter and the external anal sphinc­ter, and documents the decreased thickness of the anterior sphincter and perineal body.
Evaluation of Perianal Sepsis and Fistula-in-Ano
Typically, the diagnosis of a perianal or perirectal abscess is quite apparent on physical examination and only requires proper identification and prompt drainage. Occasionally, an abscess is strongly suspected on clinical grounds but is not readily identified on physical examination. In these situations, an EAUS may be useful in the evaluation of perianal or perirectal abscesses. EAUS can be helpful to localize an obscure abscess to plan the appropriate surgical intervention.
7. Endoluminal Ultrasound 111
Often, clinical examination of perianal or perirectal abscesses is quite painful and examination under anesthesia is required. Because the ultrasound equipment is portable, the EAUS examination can be performed in the operating room while the patient is anesthetized. Abscesses appear as hypoe­choic areas often surrounded by a hyperechoic border. In patients with perianal Crohn’s disease, EAUS may be useful in distinguishing discrete abscesses that require surgical drainage from inflammation that requires medical treatment. The use of EAUS has also been evaluated in patients with ileoanal pouch anastomosis and can be helpful in demonstrat­ing pouch pathology including inflammation, abscesses, and fistulas.
65
The natural history of a drained perianal/rectal abscess is either complete resolution or fistula formation. The majority of fistulas that occur are simple intersphincteric fistulas that are easily identified and treated by simple unroofing. However, occasionally fistula tracts develop that are extensive and highly complex. These complex fistulas present a diag­nostic challenge to even the most experienced colon and rec­tal surgeon. Use of EAUS can be helpful in identification of fistulous communications in patients with complex and recur­rent fistula-in-ano.
66–68
Fistula tracts are generally hypoechoic
defects that can be followed to identify direction and extent.
FIGURE 7-16. This image depicts a fistula-in-ano that has been enhanced by the introduction of hydrogen peroxide. The hypere­choic features posteriorly represent the hydrogen peroxide within the fistula tract (short arrows). There is an obvious hypoechoic defect in the internal anal sphincter in the midline posteriorly (A), represent­ing the internal fistula opening. The hypoechoic horseshoe tract can be seen extending toward the patient’s left.
The anatomic details of the fistula tract can be delineated in relation to the anal sphincter. The EAUS examination should include the anal canal and distal rectum to search for the pres­ence of high blind tracts. Hydrogen peroxide has been used to enhance the imaging of complex fistula.
69–72
Hydrogen perox­ide causes a release of oxygen, accentuating the fistula and appears as a brightly hyperechoic image on the ultrasound image. The technique increases the identification of the inter­nal opening to greater than 90%.
69,72
An example of a fistula­in-ano with hydrogen peroxide enhancement is demonstrated in Figure 7-16. When evaluating an anal fistula with ERUS, it is important to use both the balloon-covered transducer to evaluate the perirectal region to assess for any supralevator extension as well as the plastic cap for evaluation of the anus and surrounding anatomy.
evaluation and histologic confirmation by tissue biopsy. Anal canal malignancies evaluated by EAUS include leiomyosar­comas, malignant melanomas, anal canal adenocarcinomas, and squamous cell carcinomas. Squamous cell or epidermoid carcinoma of the anal canal are the most common anal canal malignancy. EAUS can be used in the initial evaluation to stage the lesion as well as in follow-up for patients with squa-
73–76
mous cell carcinoma of the anal canal.
Because squamous cell carcinomas of the anus are primarily treated nonopera­tively with combined chemoradiation therapy, it is desirable to have an accurate method of staging to assess response to multimodality therapy. EAUS accurately stages the initial tumor and can be used in follow-up to detect residual tumors as well as early recurrences after treatment. Surgical treat­ment in the form of abdominoperineal resection is reserved as
Anal Canal Neoplasms
Endoanal ultrasonography images the normal anal canal and associated pathologies quite well. EAUS can have an impor­tant role in the evaluation of benign and malignant anal canal neoplasms. The normal anatomic structures are clearly defined and any changes in the normal anatomy and their rela­tionships with specific anatomic structures are clearly defined. Benign neoplasms such lipomas and leiomyomas can be demonstrated along with their relationship to adjacent anal canal structures. Lesions within the anal canal appear as hypoechoic areas. Tissue diagnosis may be obtained with ultrasound-directed needle biopsies when desired.
Anal canal malignancies are an uncommon cancer in the
gastrointestinal tract. Diagnosis requires appropriate clinical
salvage surgery for those patients who fail standard chemora­diation therapy.
Although clinical (digital) examination is important in the assessment of squamous cell carcinoma of the anus, EAUS is more precise in accurately measuring the actual size and cir­cumferential involvement of the lesion. EAUS staging (uTNM) of anal cancers corresponds to the TNM [UICC (International Union Against Cancer)] staging (Table 7-3). Tumor staging for anal cancer depends primarily on the max­imal tumor diameter, which is accurately measured by EAUS. Additionally, the depth of invasion of the lesion can be meas­ured in relationship to the sphincter mechanism. The extent of sphincter involvement can be determined and other staging systems stage these lesions based on depth of invasion.
76,77
One such staging system is depicted in Table 7-4.77The eval-
4
112 D.G. Kim and W.D. Wong
ABLE 7-3. Ultrasound staging classification (uTNM) for anal canal
T cancer
Primary tumor (T) Tx Primary tumor cannot be assessed T0 No evidence of primary tumor Tis Carcinoma in situ T1 Tumor 2 cm or less in greatest dimension T2 Tumor more than 2 cm but no more than 5 cm in greatest dimension T3 Tumor more than 5 cm in greatest dimension T4 Tumor of any size that invades an adjacent organ(s), e.g., vagina,
urethra, bladder (involvement of the sphincter muscle(s) alone is not
classified as T4) Regional lymph nodes (N) Nx Regional lymph nodes cannot be assessed N0 No regional lymph node metastasis N1 Metastasis in perirectal lymph node(s) N2 Metastasis in unilateral internal iliac and/or inguinal lymph node(s) N3 Metastasis in perirectal and inguinal lymph nodes and/or bilateral
internal iliac and/or inguinal lymph nodes Distant metastasis Mx Distant metastasis cannot be assessed M0 No distant metastasis M1 Distant metastasis
TABLE 7-4. Ultrasound staging classification by depth of invasion (uTNM) for anal canal cancer
uT1 Tumor confined to the submucosa uT2a Tumor invades only the internal anal sphincter uT2b Tumor penetrates into the external anal sphincter uT3 Tumor invades through the sphincter complex and into the
perianal tissues
uT4 Tumor invades adjacent structures
FIGURE 7-17. This three-dimensional ultrasound image demonstrates an anteriorly based rectal cancer that extends full-thickness through the rectal wall (uT3). However, a clear hyperechoic plane can be seen between the prostate gland and the rectal tumor, as depicted by the arrows.
improved the understanding of three-dimensional imaging
and facilitated interpretation of the findings. In another small uation of squamous cell carcinomas of the anus should include an evaluation of the rectum with ERUS to determine the presence of metastatic lymph nodes within the mesorec­tum. The mesorectum as well as the anal canal can also be evaluated in follow-up after treatment. Any suspicious areas detected during follow-up may be biopsied if necessary.
study of 33 patients comparing conventional ERUS to 3D-
ERUS, Kim et al.
79
reported no statistically significant differ­ences in the two modalities in determining depth of invasion or lymph node status. However, it is of interest to note that the accuracy of 3D-ERUS was 90.9% for T2 lesions and 84.8% for T3 lesions compared with 84.8% and 75.8% for conven­tional ultrasound. The accuracy of 3D-ERUS for predicting
Three-dimensional Ultrasound
Three-dimensional ultrasound allows for multiplanar imaging of both the rectum and the anal canal. This new technology is currently being evaluated to compare its efficacy relative to conventional two-dimensional ultrasound as well as to other modalities such as MRI. Three-dimensional ultrasound can be used to assess anal fistulous tracts, to evaluate anal sphincter injury, as well as to stage both rectal and anal tumors. An example of a three-dimensional ERUS image (3D-ERUS) of a rectal cancer is shown in Figure 7-17.
Hunerbein et al. ultrasound with 3D-ERUS and endorectal MRI and reported an accuracy for depth of wall invasion by rectal cancer of 84%, 88%, and 91%, respectively. Because of the small sam­ple size, these differences were not statistically significant. However, they believed that the additional scan planes
78
compared standard two-dimensional
lymph node status was 84.8% compared with 66.7% for con­ventional ERUS. They concluded that although there was no statistical advantage, three-dimensional imaging made the visualization of focal lesions and lymph nodes easier.
Three-dimensional EAUS has also been applied to benign anal disorders such as anal sphincter injury and anal fistula assessment. Several comparative studies have been reported evaluating its efficacy and comparing 3D-EAUS with MRI. West et al.
80
reported that 3D-EAUS and endoanal MRI were
comparable for detecting external sphincter defects. Gold
81
et al.
determined that 3D-EAUS revealed a direct relation­ship between the length of a sphincter tear and its radial extent. In addition, they demonstrated marked gender differences in anal sphincter configuration using three-dimensional ultra­sound imaging. In the evaluation of anal fistula tracts, West
82
et al.
reported equivalency between 3D-EAUS and endoanal
MRI for the evaluation of anal fistula tracts. In a recent study
7. Endoluminal Ultrasound 113
by Buchanan et al.,833D-EAUS was found to be very accurate in the assessment of both the internal opening and the primary tract of an anal fistula. They reported an accuracy of 90% in identifying the internal opening and an accuracy of 81% in delineating the primary tract. Three-dimensional EAUS was less accurate (68%) in identifying secondary tracts or exten­sions. In their study, the use of hydrogen peroxide did not increase the accuracy but in some instances it did make the tract and internal opening more conspicuous.
Summary
Endoluminal ultrasound has been shown to be extremely use­ful in the evaluation and management of many benign and malignant anorectal conditions. ERUS has become the best imaging technique to accurately stage rectal cancers and anal canal tumors preoperatively. Moreover, ERUS can have a role in the follow-up evaluation of these patients. EAUS is the diagnostic test of choice in the evaluation of fecal inconti­nence and is used routinely. The EAUS has also been used to help define complex anal fistulas to facilitate their manage­ment. The accuracy of diagnosis is operator dependent and improves with experience. Endoluminal ultrasound has made a major contribution to the understanding and management of many anorectal conditions. Three-dimensional ultrasound may prove to be advantageous, but requires further study.
References
1. Wild JJ, Reid JM. Diagnostic use of ultrasound. Br J Phys Med 1956;19(11):248–257.
2. Dragsted J, Gammelgaard J. Endoluminal ultrasonic scanning in the evaluation of rectal cancer: a preliminary report of 13 cases. Gastrointest Radiol 1983;8(4):367–369.
3. Hildebrandt U, Feifel G. Preoperative staging of rectal cancer by intrarectal ultrasound. Dis Colon Rectum 1985;28(1):42–46.
4. Greene FL, et al., ed. AJCC Cancer Staging Manual. 6th ed. New York: Springer; 2002.
5. Beynon J, et al. The endosonic appearances of normal colon and rectum. Dis Colon Rectum 1986;29(12):810–813.
6. Deen KI, Madoff RD, Wong WD. Preoperative staging of rectal neoplasms with endorectal ultrasonography. Semin Colon Rectal Surg 1995;6:78–85.
7. Garcia-Aguilar J, et al. Accuracy of endorectal ultrasonography in preoperative staging of rectal tumors. Dis Colon Rectum 2002;45(1):10–15.
8. Pikarsky A, et al. The use of rectal ultrasound for the correct diagnosis and treatment of rectal villous tumors. Am J Surg 2000;179(4):261–265.
9. Worrell S, et al. Endorectal ultrasound detection of focal carci­noma within rectal adenomas. Am J Surg 2004;187(5):625–629.
10. Kim DG, Madoff RD. Transanal treatment of rectal cancer: abla­tive methods and open resection. Semin Surg Oncol 1998;15(2):101–113.
11. Beynon J, et al. Preoperative assessment of mesorectal lymph node involvement in rectal cancer. Br J Surg 1989;76(3): 276–279.
12. Rifkin MD, Ehrlich SM, Marks G. Staging of rectal carcinoma: prospective comparison of endorectal US and CT. Radiology 1989;170(2):319–322.
13. Orrom WJ, et al. Endorectal ultrasound in the preoperative stag­ing of rectal tumors. A learning experience. Dis Colon Rectum 1990;33(8):654–659.
14. Milsom JW, Graffner H. Intrarectal ultrasonography in rectal cancer staging and in the evaluation of pelvic disease. Clinical uses of intrarectal ultrasound. Ann Surg 1990;212(5):602–606.
15. Pappalardo G, et al. The value of endoluminal ultrasonography and computed tomography in the staging of rectal cancer: a pre­liminary study. J Surg Oncol 1990;43(4):219–222.
16. Thaler W, et al. Preoperative staging of rectal cancer by endolu­minal ultrasound vs. magnetic resonance imaging. Preliminary results of a prospective, comparative study. Dis Colon Rectum 1994;37(12):1189–1193.
17. Tio TL, Tytgat GN. Endoscopic ultrasonography in analysing peri-intestinal lymph node abnormality. Preliminary results of studies in vitro and in vivo. Scand J Gastroenterol Suppl 1986;123:158–163.
18. Hildebrandt U, et al. Endosonography of pararectal lymph nodes. In vitro and in vivo evaluation. Dis Colon Rectum 1990; 33(10):863–868.
19. Herrera-Ornelas L, et al. Metastases in small lymph nodes from colon cancer. Arch Surg 1987;122(11):1253–1256.
20. Katsura Y, et al. Endorectal ultrasonography for the assessment of wall invasion and lymph node metastasis in rectal cancer. Dis Colon Rectum 1992;35(4):362–368.
21. Akasu T, et al. Limitations and pitfalls of transrectal ultrasonog­raphy for staging of rectal cancer. Dis Colon Rectum 1997;40(10 suppl):S10–15.
22. Sunouchi K, et al. Small spot sign of rectal carcinoma by endorectal ultrasonography: histologic relation and clinical impact on postoperative recurrence. Dis Colon Rectum 1998; 41(5):649–653.
23. Sunouchi K, et al. Limitation of endorectal ultrasonography: what does a low lesion more than 5 mm in size correspond to his­tologically? Dis Colon Rectum 1998;41(6):761–764.
24. Solomon MJ, McLeod R.S. Endoluminal transrectal ultrasonog­raphy: accuracy, reliability, and validity. Dis Colon Rectum 1993;36(2):200–205.
25. Glaser F, Schlag P, Herfarth C. Endorectal ultrasonography for the assessment of invasion of rectal tumours and lymph node involvement. Br J Surg 1990;77(8):883–887.
26. Kruskal JB, et al. Pitfalls and sources of error in staging rectal cancer with endorectal US. Radiographics 1997;17(3):609–626.
27. Bernini A, et al. Preoperative adjuvant radiation with chemo­therapy for rectal cancer: its impact on stage of disease and the role of endorectal ultrasound. Ann Surg Oncol 1996;3(2): 131–135.
28. Fleshman JW, et al. Accuracy of transrectal ultrasound in pre­dicting pathologic stage of rectal cancer before and after preop­erative radiation therapy. Dis Colon Rectum 1992;35(9): 823–829.
29. Meade PG, et al. Preoperative chemoradiation downstages locally advanced ultrasound-staged rectal cancer. Am J Surg 1995;170(6):609–612; discussion 612–613.
30. Rau B, et al. Accuracy of endorectal ultrasound after preopera­tive radiochemotherapy in locally advanced rectal cancer. Surg Endosc 1999;13(10):980–984.
114 D.G. Kim and W.D. Wong
31. Williamson PR, et al. Endorectal ultrasound of T3 and T4 rectal cancers after preoperative chemoradiation. Dis Colon Rectum 1996;39(1):45–49.
32. Brown CL, et al. Response to preoperative chemoradiation in stage II and III rectal cancer. Dis Colon Rectum 2003;46(9): 1189–1193.
33. Michelassi F, et al. Local recurrence after curative resection of colorectal adenocarcinoma. Surgery 1990;108(4):787–792; dis­cussion 792–793.
34. Sagar PM, Pemberton JH. Surgical management of locally recur­rent rectal cancer. Br J Surg 1996;83(3):293–304.
35. Beynon J, et al. The detection and evaluation of locally recurrent rectal cancer with rectal endosonography. Dis Colon Rectum 1989;32(6):509–517.
36. de Anda EH, et al. Endorectal ultrasound in the follow-up of rec­tal cancer patients treated by local excision or radical surgery. Dis Colon Rectum 2004;47(6):818–824.
37. Mascagni D, et al. Endoluminal ultrasound for early detection of local recurrence of rectal cancer [see comment]. Br J Surg 1989;76(11):1176–1180.
38. Ramirez JM, et al. Endoluminal ultrasonography in the follow­up of patients with rectal cancer. Br J Surg 1994;81(5):692–694.
39. Rotondano G, et al. Early detection of locally recurrent rectal cancer by endosonography. Br J Radiol 1997;70(834):567–571.
40. Tjandra JJ, et al. Endoluminal ultrasound defines anatomy of the anal canal and pelvic floor. Dis Colon Rectum 1992;35(5): 465–470.
41. Sentovich SM, Wong WD, Blatchford GJ. Accuracy and relia­bility of transanal ultrasound for anterior anal sphincter injury. Dis Colon Rectum 1998;41(8):1000–1004.
42. Rieger N, Tjandra J, Solomon M. Endoanal and endorectal ultra­sound: applications in colorectal surgery. ANZ J Surg 2004; 74(8):671–675.
43. Tjandra JJ, et al. Endoluminal ultrasound is preferable to elec­tromyography in mapping anal sphincteric defects. Dis Colon Rectum 1993;36(7):689–692.
44. Mellgren A, et al. Long-term cost of fecal incontinence second­ary to obstetric injuries. Dis Colon Rectum 1999;42(7):857–865; discussion 865–867.
45. Allen RE, et al. Pelvic floor damage and childbirth: a neuro­physiological study [see comment]. Br J Obstet Gynaecol 1990; 97(9):770–779.
46. Sultan AH, et al. Anal-sphincter disruption during vaginal deliv­ery [comment]. N Engl J Med 1993;329(26):1905–1911.
47. Poen AC, et al. Third-degree obstetric perineal tear: long-term clinical and functional results after primary repair. Br J Surg 1998;85(10):1433–1438.
48. Sorensen M, et al. Sphincter rupture in childbirth. Br J Surg 1993;80(3):392–394.
49. Tetzschner T, et al. Anal and urinary incontinence in women with obstetric anal sphincter rupture [see comment]. Br J Obstet Gynaecol 1996;103(10):1034–1040.
50. Burnett SJ, et al. Unsuspected sphincter damage following child­birth revealed by anal endosonography. Br J Radiol 1991; 64(759):225–227.
51. Varma A, et al. Obstetric anal sphincter injury: prospective eval­uation of incidence [see comment]. Dis Colon Rectum 1999;42(12):1537–1543.
52. Zetterstrom J, et al. Effect of delivery on anal sphincter morphol­ogy and function. Dis Colon Rectum 1999;42(10):1253–1260.
53. Sultan AH, Kamm MA, Hudson CN, Bartram CI. Effect of preg­nancy on anal sphincter morphology and function. Int J Colorectal Dis 1993;8(4):206–209.
54. Willis S, Faridi A, Schelzig S, et al. Childbirth and incontinence: a prospective study on anal sphincter morphology and function before and early after vaginal delivery. Langenbecks Arch Surg 2002;387(2):101–107.
55. Tsang CB, et al. Anal sphincter integrity and function influences outcome in rectovaginal fistula repair. Dis Colon Rectum 1998;41(9):1141–1146.
56. Deen KI, et al. Anal sphincter defects. Correlation between endoanal ultrasound and surgery. Ann Surg 1993;218(2):201–205.
57. Falk PM, et al. Transanal ultrasound and manometry in the evalua­tion of fecal incontinence. Dis Colon Rectum 1994;37(5):468–472.
58. Farouk R, Bartolo DC. The use of endoluminal ultrasound in the assessment of patients with faecal incontinence. J R Coll Surg Edinb 1994;39(5):312–318.
59. Zetterstrom JP, et al. Perineal body measurement improves eval­uation of anterior sphincter lesions during endoanal ultrasonog­raphy. Dis Colon Rectum 1998;41(6):705–713.
60. deVries PA, Pena A. Posterior sagittal anorectoplasty. J Pediatr Surg 1982;17(5):638–643.
61. Jones NM, et al. The value of anal endosonography compared with magnetic resonance imaging following the repair of anorec­tal malformations. Pediatr Radiol 2003;33(3):183–185.
62. Simmang CL, et al. Posterior sagittal anorectoplasty in adults: secondary repair for persistent incontinence in patients with anorectal malformations. Dis Colon Rectum 1999;42(8): 1022–1027.
63. Gilliland R, et al. Pudendal neuropathy is predictive of failure following anterior overlapping sphincteroplasty. Dis Colon Rectum 1998;41(12):1516–1522.
64. Donnelly V, et al. Obstetric events leading to anal sphincter dam­age. Obstet Gynecol 1998;92(6):955–961.
65. Solomon MJ, et al. Assessment of peripouch inflammation after ileoanal anastomosis using endoluminal ultrasonography. Dis Colon Rectum 1995;38(2):182–187.
66. Deen KI, et al. Fistulas in ano: endoanal ultrasonographic assess­ment assists decision making for surgery. Gut 1994;35(3): 391–394.
67. Cataldo PA, Senagore A, Luchtefeld MA. Intrarectal ultrasound in the evaluation of perirectal abscesses. Dis Colon Rectum 1993;36(6):554–558.
68. Law PJ, et al. Anal endosonography in the evaluation of perianal sepsis and fistula in ano. Br J Surg 1989;76(7):752–755.
69. Lengyel AJ, Hurst NG, Williams JG. Pre-operative assessment of anal fistulas using endoanal ultrasound. Colorectal Dis 2002;4(6):436–440.
70. Cheong DM, et al. Anal endosonography for recurrent anal fis­tulas: image enhancement with hydrogen peroxide. Dis Colon Rectum 1993;36(12):1158–1160.
71. Poen AC, et al. Hydrogen peroxide-enhanced transanal ultra­sound in the assessment of fistula-in-ano. Dis Colon Rectum 1998;41(9):1147–1152.
72. Navarro-Luna A, et al. Ultrasound study of anal fistulas with hydrogen peroxide enhancement. Dis Colon Rectum 2004; 47(1):108–114.
73. Goldman S, et al. Transanorectal ultrasonography in the staging of anal epidermoid carcinoma. Int J Colorectal Dis 1991;6(3): 152–157.
7. Endoluminal Ultrasound 115
74. Herzog U, Boss M, Spichtin HP. Endoanal ultrasonography in the follow-up of anal carcinoma. Surg Endosc 1994;8(10): 1186–1189.
75. Roseau G, et al. Endoscopic ultrasonography in the staging and follow-up of epidermoid carcinoma of the anal canal. Gastrointest Endosc 1994;40(4):447–450.
76. Giovannini M, et al. Anal carcinoma: prognostic value of endorectal ultrasound (ERUS). Results of a prospective multi­center study. Endoscopy 2001;33(3):231–236.
77. Tarantino D, Bernstein MA. Endoanal ultrasound in the staging and management of squamous-cell carcinoma of the anal canal: potential implications of a new ultrasound staging system. Dis Colon Rectum 2002;45(1):16–22.
78. Hunerbein M, et al. Prospective comparison of endorectal ultra­sound, three-dimensional endorectal ultrasound, and endorectal MRI in the preoperative evaluation of rectal tumors. Preliminary results. Surg Endosc 2000;14(11):1005–1009.
79. Kim JC, et al. Comparative study of three-dimensional and con­ventional endorectal ultrasonography used in rectal cancer stag­ing. Surg Endosc 2002;16(9):1280–1285.
80. West RL, Dwarkasing S, Briel JW, et al. Can three-dimensional endoanal ultrasonography detect external anal sphincter atrophy? A comparison with endoanal magnetic resonance imaging. Int J Colorectal Dis 2005;20(4):328–333.
81. Gold DM, et al. Three-dimensional endoanal sonography in assessing anal canal injury. Br J Surg 1999;86(3):365–370.
82. West RL, et al. Hydrogen peroxide-enhanced three-dimensional endoanal ultrasonography and endoanal magnetic resonance imaging in evaluating perianal fistulas: agreement and patient preference. Eur J Gastroenterol Hepatol 2004;16(12):1319–1324.
83. Buchanan GN, et al. Value of hydrogen peroxide enhancement of three-dimensional endoanal ultrasound in fistula-in-ano. Dis Colon Rectum 2005;48(1):141–147.
84. Romano G, et al. Intrarectal ultrasound and computed tomogra­phy in the pre- and postoperative assessment of patients with rec­tal cancer. Br J Surg 1985;72(suppl):S117–119.
85. Hildebrandt U, et al. Endorectal ultrasound: instrumentation and clinical aspects. Int J Colorectal Dis 1986;1(4):203–207.
86. Holdsworth PJ, et al. Endoluminal ultrasound and computed tomography in the staging of rectal cancer. Br J Surg 1988; 75(10):1019–1022.
87. Beynon J. An evaluation of the role of rectal endosonography in rectal cancer. Ann R Coll Surg Engl 1989;71(2):131–139.
88. Dershaw DD. Endorectal sonography for rectal carcinoma. Bull NY Acad Med 1990;68(3):411–419.
89. Glaser F, et al. Influence of endorectal ultrasound on surgical treatment of rectal cancer. Eur J Surg Oncol 1990;16(4):304–311.
90. Jochem RJ, et al. Endorectal ultrasonographic staging of rectal carcinoma. Mayo Clin Proc 1990;65(12):1571–1577.
91. Herzog U, et al. How accurate is endorectal ultrasound in the preoperative staging of rectal cancer? Dis Colon Rectum 1993;36(2):127–134.
92. Sentovich SM, et al. Transrectal ultrasound of rectal tumors. Am J Surg 1993;166(6):638–641; discussion 641–642.
93. Adams DR, et al. Use of preoperative ultrasound staging for treat­ment of rectal cancer. Dis Colon Rectum 1999;42(2):159–166.
94. Marusch F, et al. Routine use of transrectal ultrasound in rectal carcinoma: results of a prospective multicenter study. Endoscopy 2002;34(5):385–390.
95. Manger T, Stroh C. Accuracy of endorectal ultrasonography in the preoperative staging of rectal cancer. Tech Coloproctol 2004;8(suppl 1):14–15.
8
Preoperative Management—Risk Assessment, Medical Evaluation, and Bowel Preparation
Conor P. Delaney and John M. MacKeigan
Preparation of the patient for surgery is a vital component of optimizing recovery after surgery, and must be individually tailored to the medical status of the patient. undergo colorectal surgery may present in normal health, such as in a young patient undergoing hemorrhoid surgery, or may present in extreme ill health, such as the octogenarian with multiple medical conditions, who has developed perfo­rated diverticulitis. Preoperative assessment and medical intervention are important components of care, and may account for the difference in perioperative mortality noted after abdominal and colorectal surgery between the United States and some European countries.
Since the initial studies by Tyson and Spaulding in the 1950s, preparation of the bowel before surgery has been con­sidered an essential component of care. More recently, this has become a contentious issue, and metaanalyses have sug­gested that bowel preparation provides no benefit, and may actually increase the incidence of some complications.
This chapter addresses the issues of medical evaluation and bowel preparation before surgery. These are considered on the background of reviewing some of the more important scoring systems for risk assessment before surgery, which permit comparison among different surgeons, institutions, and care pathways.
2
1
Patients who
Perioperative Risk Assessment Scoring Systems
The risk related to surgery is a function of many factors. Patient-related factors include the underlying disease processes and the patient’s physical ability to tolerate the physiologic stress related to the surgical procedure. Increasing amounts of data now show that risk is also affected by the volume of a procedure performed at the medical insti­tution, but perhaps most importantly by the experience, train­ing, and volume of surgery performed by the individual surgeon.
Scoring systems assess the patients’ risk for morbidity and mortality as a result of anesthesia and surgery. These systems generally use data acquired during pre-hospital and in-hospital care, and some supplement this with components measuring operative severity. Some classification systems are designed to allow comparison of results between institutions and sur­geons, whereas others are designed to distinguish patients who subsequently will have postoperative adverse events from those who will not. tors on overall morbidity and mortality is currently unknown but an ideal risk scoring system would incorporate all of these factors allowing accurate evaluation of surgical risk to the patient.
Thus, a primary aim of a scoring system is the evaluation of therapeutic benefit, i.e., the ratio of the relative harm and the relative benefit that are likely to follow a specific opera­tion for a specific illness, whether in a specific patient, insti­tution, or health system. Parameters that are useful in this evaluation include the natural history of the disease process, and the urgency of a specific procedure. Age may have an influence on operative risk, as many elderly patients require concurrent management of multiple organ degenerative dis­ease. Elderly patients often tolerate operations well but com­plications poorly, hence prediction of the potential morbidity of an operation is particularly important in this group of patients. Scoring systems also provide a useful means of com­paring outcomes from different institutions and patient groups by correcting for different comorbidities. Various scoring sys­tems have been developed in an effort to quantify the risk of a patient from disease or intervention, and systems can be classified as preoperative or physiologic (Table 8-1).
Some scores are useful in predicting outcomes in specific conditions, such as Ranson’s for pancreatitis, Child for liver failure, and the Burns index, but they are not of use for the general assessment of patients with other disorders. Some studies have tried to predict risk in a less specific manner, and have suggested that a surgeon’s gut feeling upon completion of a major procedure may be a good indicator of subsequent outcome.
5
3,4
The influence of each of these fac-
116
8. Preoperative Management—Risk Assessment, Medical Evaluation, and Bowel Preparation 117
TABLE 8-1. Perioperative scoring systems (references in text)
Physiologic scores Preoperative scores APACHE (I and II) ASA grading
E-PASS Goldman cardiac risk index ISS/TRISS Hospital prognostic index POSSUM Prognostic nutritional index P-POSSUM Pulmonary complication risk SAPS Sepsis score Sickness score Therapeutic intervention score
Risk Assessment for Complications from Specific Organ Systems
Some scoring systems define patient characteristics that are associated with increased morbidity and mortality because of involvement of a particular organ system. Scoring systems that have been described to predict the risk of death include those for respiratory, disease.
11,12
Cardiac Risk
Goldman Cardiac Risk
The Goldman risk model is probably the best-accepted model for pure determination of cardiac risk for surgery. Point scores are assigned to each of nine clinical factors and patients are divided into four risk classes based on the total point score (Table 8-2). This is an important score because it reminds cli­nicians of the major cardiac risk factors in noncardiac surgery. Although the system is easy to use and utilizes relative weighting of risk factors, it was designed in the 1970s, and has not been updated for modern practice in anesthesia, med­icine, or surgery. Cardiac risk for patients undergoing noncar­diac surgery has also been evaluated by other studies.
TABLE 8-2. Goldman cardiac risk index
Cardiac risk event Points Myocardial infarction within 6 mo 10
Age >70 y 5 S3 gallop or jugular venous distension 11 Important aortic valve stenosis 3 Rhythm other than sinus, or sinus rhythm and atrial premature
contractions on last preoperative electrocardiogram 7
More than five premature ventricular contractions per
minute anytime before surgery 7 Poor general medical status 3 Intraperitoneal, intrathoracic, or aortic operation 3 Emergency operation 4
Class Points complication risk (%) risk (%) I 0–5 0.7 0.2
II 6–12 5 2 III1 3–25 11 2 IV ≥26 22 56
6
gastrointestinal,
13
Life-threatening Cardiac death
7–10
and cardiovascular
11,12
Respiratory Risk
Pulmonary Complication Risk
Findings on respiratory examination, chest X-ray, Goldman’s cardiac risk index, and the Charlson comorbidity index have been used for predicting respiratory complications.
6
Risk Assessment for Postoperative Morbidity and Mortality
American Society of Anesthesiologists Classification
The American Society of Anesthesiologists (ASA) classifica­tion system (Table 8-3) thesiologists to preexisting diseases. Because of the ease of use, and the fact that no tests are required, it has also been used to estimate operative risk. lates with perioperative mortality and morbidity correlates significantly with perioperative variables such as intraoperative blood loss, duration of postoperative ventila­tion, and duration of intensive care unit (ICU) stay. severity of operative procedure, higher ASA class, symptoms of respiratory disease, and malignancy predicted postopera­tive morbidity in one study.
Disadvantages to using the ASA score are that the score awarded depends on the subjective clinical judgment of the attending anesthesiologist, and that the small numbers of groups available means there can be little meaningful com­parison between different surgeons or institutions.
Prognostic Nutritional Index
The prognostic nutritional index (PNI) was devised21to pre­dict complication risk based on mortality, and correlates with postoperative sepsis and death. The PNI uses four factors, namely, serum albumin level, serum transferrin level, triceps skinfold thickness, and cutaneous delayed-type hypersensitiv­ity. Serum albumin level, serum transferrin level, and delayed hypersensitivity were the only accurate predictors of postop­erative morbidity and mortality. In addition to predicting post­operative morbidity and mortality, PNI can be used for predicting patients who might need nutritional support in the perioperative period. The authors concluded that periopera­tive nutritional support might reduce operative morbidity and mortality in malnourished patients, although this has not been routinely agreed with in the literature.
TABLE 8-3. ASA classification scheme
I Normal healthy patient II Mild systemic disease III Severe, noncapacitating systemic disease IV Incapacitating systemic disease, threatening life V Moribund, not expected to survive 24 h E Emergency
14
was initially developed to alert anes-
15,16
ASA class directly corre-
20
17–19
and also
19
The
118 C.P. Delaney and J.M. MacKeigan
APACHE (Acute Physiology and Chronic Health Evaluation) Scoring Systems
APACHE was initially described in 198122and subsequently replaced in 1985 designed primarily for patients in the ICU but has been used for the assessment of patients with severe trauma, abdominal sepsis, postoperative enterocutaneous fistulas, acute pancre­atitis, and to predict postoperative outcome. advantage is that it is not independent of the effects of treatment, thus scoring for emergency patients being admitted to the ICU is best performed before surgical intervention. Other disadvantages are that it is relatively complex and does not take into consideration the nutritional status of the patient or cardiology findings that add to operative risk. APACHE scores also do not take into account the extent of surgery. The APACHE III has been proposed more recently, but it is also very complex for routine use. tems have also been developed from the APACHE system. These include SAPS (simplified acute physiology score), which uses 14 of the 34 variables, and SAPS II, which also takes into consideration the urgency of the procedure and any associated chronic medical illness.
23
by APACHE II. This score was initially
24
The main dis-
26
Several simpler scoring sys-
POSSUM
The POSSUM (Physiological and Operative Severity Score for enUmeration of Mortality and morbidity) was developed by multivariate discriminant analysis prospective data, primarily to permit surgical audit for assess­ment of quality of care. It has been suggested that it works independent of geographical factors, and several publications have now come from the United States suggesting that it may also have a role in this health care system.
POSSUM calculates expected death and expected morbidity rates based on 12 physiologic variables and six operative vari­ables each of which are scored 1, 2, 4, or 8 (Table 8-4). The major advantage is that it predicts both morbidity and mortal­ity and has successfully been used for a comparative audit of performance among surgical units, hospitals, and countries. Disadvantages include that it does not take into account differ­ences among surgeons, anesthetists, and operating time, all of which may influence outcome. This is because POSSUM was
TABLE 8-4. Parameters for calculation of the POSSUM score
Physiologic parameters Operative parameters Age (y) Operative severity
Cardiac signs/chest X-ray Multiple procedures Respiratory signs/chest X-ray Total blood loss (mL) Pulse rate Peritoneal soiling Systolic blood pressure (mm Hg) Presence of malignancy Glasgow coma score Mode of surgery Hemoglobin (g/dL) White cell count (×10 Urea concentration (mmol/L)
+
and K+levels (mmol/L)
Na Electrocardiogram
12
/l)
28
of retrospective and
2,29
developed as a scoring system for audit, so other factors may need to be considered when using POSSUM for risk assess­ment of patients for surgery. POSSUM also does not use pri­mary diagnosis as a factor for scoring. Nevertheless, comparison of APACHE II with POSSUM showed that POS­SUM is superior in predicting mortality in patients admitted to a high-dependency unit after general surgery.
30
Portsmouth Modification of POSSUM (P-POSSUM)
One concern with POSSUM has been that it may overpredict
25
mortality and morbidity rates by up to six times with a mini­mum mortality of 1.1%. P-POSSUM was therefore developed using a different mathematical formula to counter these disad­vantages,
31
with the minimum mortality score in P-POSSUM reduced to 0.2%. Whereas some studies found that both scor­ing systems overpredicted mortality rates for vascular surgery patients, dictor of mortality and morbidity than POSSUM for vascu-
27
lar,
32,33
others found that P-POSSUM was a better pre-
34
gastrointestinal,35and laparoscopic colorectal surgery.
Other Scoring Systems
Various other scoring systems have also been developed pri­marily for assessment of critically ill patients in the ICU and for trauma and sepsis, and these are listed in Table 8-1.
Risk Assessment for Colorectal Disease
Preoperative pulmonary and nutritional problems have been significant contributing factors in patients who died from sep­sis after colon resection in the elderly. Others have suggested that age, congestive heart failure, hepatic, renal or pulmonary impairment, and extent of involvement by malignancy and postoperative complications were associated with greater mortality after colon surgery. Subsequently, it has been reported that age influenced mortality but not 5-year sur-
46
vival. ety of preoperative risk factors on operative outcomes and
2
Ondrula et al.47assessed the predictive value of a vari-
defined a colon index that assessed patients’ operative risk. More recently, POSSUM was found to allow a realistic com­parison of performance of different units performing colorec­tal resection and also permit comparison of outcome after colorectal resection among different surgeons.
48,49
has also been reported in patients undergoing laparoscopic colectomy
29
but even the P-POSSUM overpredicted mortality and morbidity. Further modifications may be required to pro­vide a validated tool for comparisons between laparoscopic and open approaches to colorectal resection.
Preoperative Medical Evaluation
Once a patient has a diagnosis requiring colorectal surgery, most surgeons intuitively categorize them into those needing minimal assessment, or extensive medical evaluation and
36
37–45
POSSUM
8. Preoperative Management—Risk Assessment, Medical Evaluation, and Bowel Preparation 119
treatment before surgery. Young patients having minor sur­gery will require no assessment. Young patients having more significant surgery may require minor evaluation, whereas older patients having minor surgery may require a similar level of evaluation. Older patients, and those with more exten­sive comorbidities will require assessment and possible treat­ment before surgery. Few definite guidelines exist as to who requires any exact pattern of assessment, and the benefits of individual tests are described below.
At the Cleveland Clinic, a questionnaire called Health Quest is given to patients who complete this on-line. Based on their answers, a score of 1–5 is generated indicating a level of complexity of medical history that can help stratify patients for level of preoperative assessment.
50
This process is also associated with a reduction in preoperative surgical delay, and increased patient satisfaction.
Evaluation is performed with a combination of history, physical examination, and selected investigations. In a large prospective clinical-epidemiologic study, Arvidsson and col-
3
leagues
found that a standardized assessment before surgery, by a combination of questionnaires, interview, physical exam­ination, and laboratory screening identified a high proportion of patients who were likely to have an adverse event in the postoperative period.
Preanesthesia Interview
Of the techniques available that are used in preoperative eval­uation of patients, namely, history, physical examination, and investigations, history taking is the most efficient and prof-
3,51
itable. including history of anesthesia and surgery helps identify many potential problems that can occur perioperatively. Questionnaires have previously been found to be efficient and reliable for anesthesia preadmission assessment. operative questionnaire is suitable for patients undergoing daycare surgery, because most of these patients are at low risk.
History taking should include information on the condition for which the procedure is being performed, history of surgical procedures (local procedures that may complicate surgery such as reoperative pelvic surgery, as well as general procedures that may complicate recovery such as prior splenectomy), and prior outcomes with intubation and anesthesia. Special consideration should be given to cardiopulmonary function, allergy, renal and hepatic function, bleeding tendency, and medication use. History of chronic medical conditions of the cardiorespiratory system and medications including dosage is important. In chil­dren, history should be focused on other specific factors such as birth history and history of recent infections, especially pneu­monia and upper respiratory tract infections. Aspirin and other nonsteroidal anti-inflammatory drugs are best discontinued 1 week before surgery. Other questions should pertain to immu­nization, smoking, and alcohol and drug use. Cessation of smoking 8 or more weeks before surgery helps optimize the mucociliary apparatus of the patient before surgery. Review of
A thorough review of previous medical records
52
Thus, a pre-
functional status of the patient, activities of daily living (ADL), and social support are also important, although this primarily relates to longer term recovery, hospital stay, and likely dis­charge status from hospital, rather than direct perioperative morbidity and mortality.
History taking for cardiac assessment has been reasonably
well standardized, and very well reviewed recently by
53
Mukherjee and Eagle.
The primary factors to be considered are whether the patient has recent myocardial infarction, decompensated heart failure, unstable angina, symptomatic arrhythmias, or symptomatic valvular heart disease. In gen­eral, noninvasive testing is most effective in intermediate-risk patients, whereas invasive evaluation should be considered in those with multiple risk factors and ischemia on preoperative testing, because perioperative beta-blockade may be inade­quate.
Formal anesthetic evaluation is also needed for many patients. Similar to the selective levels of medical work-up, not all patients will need to be seen by an anesthesiologist preoperatively. Young, healthy patients with normal anatomy, and no adverse findings in history or examination, may not need any evaluation. Patients having more major surgery should probably all meet the anesthesia service before sur­gery, for assessment as well as instruction about what will happen around the time of surgery. This may be expediently performed by nurse practitioners. Some patients with com­plex anesthetic histories or with major perioperative risk fac­tors may require formal anesthetic assessment by a staff anesthesiologist. Usually, such guidelines are institution­specific, but it is recommended that the surgeon and anesthe­siologist have a similar plan for assessment, so that unexpected surprises are avoided on the day of surgery.
Physical Examination
A review of preoperative evaluation54noted that history and physical examination focusing on risk factors for cardiac, pul­monary, and infectious complications and determination of a patient’s functional capacity are important for preoperative evaluation of patients. General indicators of fitness of a patient for surgery include activities of daily living compe­tence (ADL) and general mobility. Specific evaluation for subtle signs of cardiopulmonary dysfunction is important, because these have been shown to correlate strongly with major perioperative complications.
13
Preoperative Tests
Preoperative tests serve to complement the history and phys­ical examination in assessing the suitability of the patient for surgery. They have been used to assess levels of known dis­ease, detect unsuspected but modifiable conditions that may be treated to reduce risk before surgery, or detect unsuspected conditions that may not be possible to treat, and therefore simply be baseline results before surgery.