結(jié)腸鏡檢查——適應(yīng)癥、禁忌癥以及腸道準(zhǔn)備
David E. Beck 著
林富林 譯
傅傳剛 審
摘要:結(jié)腸鏡檢查在1970年被引入臨床應(yīng)用,最初是用作鋇灌腸檢查的診斷輔助。隨著經(jīng)驗(yàn)的積累和技術(shù)的進(jìn)步,結(jié)腸鏡檢查逐漸成為結(jié)直腸外科的主要組成部分和檢查結(jié)腸疾病的最終手段。本章主要闡述與結(jié)腸鏡檢查相關(guān)的適應(yīng)證、禁忌證、腸道準(zhǔn)備、鎮(zhèn)靜及抗生素應(yīng)用、操作技術(shù)、并發(fā)癥等方面的內(nèi)容。
關(guān)鍵詞:結(jié)腸鏡檢查,適應(yīng)證,禁忌證,腸道準(zhǔn)備,鎮(zhèn)靜,抗生素,操作技術(shù),并發(fā)癥
01
概述
結(jié)腸鏡檢查在1970年被引入臨床應(yīng)用,最初是用作鋇灌腸檢查的診斷輔助。通過結(jié)腸鏡檢查可以觀察并利用活組織檢查證實(shí)大腸病變及黏膜異常,但在早期,內(nèi)鏡醫(yī)生操作的盲腸到達(dá)率僅為 30%~50%。1969年紐約 Hiromi Shinya 醫(yī)生進(jìn)行了第一例結(jié)腸鏡息肉切除術(shù)[1]。隨著經(jīng)驗(yàn)的積累和技術(shù)的進(jìn)步,結(jié)腸鏡檢查逐漸成為結(jié)直腸外科的主要組成部分和檢查結(jié)腸疾病的最終手段。現(xiàn)在的結(jié)腸鏡利用高清視頻系統(tǒng)來提供高質(zhì)量的圖像。
結(jié)腸鏡檢查如果操作得當(dāng),其過程是可以忍受的 , 并發(fā)癥發(fā)生率低且盲腸到達(dá)率超過 95%[2-5]。通過結(jié)腸鏡檢查可以對結(jié)直腸黏膜或病變進(jìn)行活檢,可以切除幾乎所有帶蒂息肉,可以逐塊、多次或采用先進(jìn)的技術(shù)(例如內(nèi)鏡下黏膜下剝離術(shù))切除大部分大的無蒂息肉 [6, 7]。
幾項(xiàng)大樣本結(jié)腸鏡檢查的研究顯示,其中簡單的操作占約25%,有一定挑戰(zhàn)的操作占50%,困難或無法完成的操作占25%[8, 9]。造成結(jié)腸鏡檢查困難的最常見原因是檢查時(shí)腸鏡在一段長的或活動(dòng)的結(jié)腸內(nèi)反復(fù)成袢或弓狀隆起。相對男性(中位數(shù)145cm)而言,女性的結(jié)腸長度(中位數(shù)155cm)更長(P <0.005),其主要的差別在于橫結(jié)腸[9]。許多患者的結(jié)腸具有多個(gè)活動(dòng)的部分 [10]。
▲ 圖 4-1
電子結(jié)腸鏡(160cm )
一位勝任的結(jié)腸鏡檢查醫(yī)生必須經(jīng)過廣泛的訓(xùn)練且要有實(shí)際的操作經(jīng)驗(yàn)。數(shù)據(jù)表明,結(jié)腸鏡檢查的學(xué)習(xí)曲線需150~200例 [11, 12] ,盡管單純看數(shù)據(jù)仍有局限性的(如果技術(shù)較拙劣,即使進(jìn)行了數(shù)百例操作也無法成為一位勝任的結(jié)腸鏡檢查醫(yī)生)。
02
適應(yīng)癥
結(jié)腸鏡檢查的主要適應(yīng)證為結(jié)直腸疾病的診斷、結(jié)直腸息肉的治療、慢性潰瘍性結(jié)腸炎及克羅恩病的隨訪、大腸癌患者術(shù)前術(shù)后的檢查、平均風(fēng)險(xiǎn)及高風(fēng)險(xiǎn)人群的大腸癌篩查等 [13]。對于應(yīng)用新斯的明治療失敗或有使用禁忌的急性假性結(jié)腸梗阻患者,用結(jié)腸鏡檢查進(jìn)行減壓也是一種選擇 [14- 18]。
03
禁忌癥
結(jié)腸鏡檢查的禁忌證相對較少。腸道準(zhǔn)備不良的患者應(yīng)該重新預(yù)約檢查并重新進(jìn)行腸道準(zhǔn)備。檢查過程中如遇腸管有無法拉直的固定成角,則不應(yīng)繼續(xù)進(jìn)行。對于急性炎癥性腸病或急性憩室炎的患者,行遠(yuǎn)端大腸的診斷性檢查是有益的,但近端結(jié)腸是否適合檢查則因人而異。小腸梗阻及伴有肛門狹窄或嚴(yán)重疼痛的患者應(yīng)避免行結(jié)腸鏡檢查。對于大腸梗阻的患者,診斷性結(jié)腸鏡檢查或鏡下放置結(jié)腸支架是有益的 [19, 20]。另外,身體虛弱或全身狀況不穩(wěn)定,無法行腸道準(zhǔn)備的患者,或近期發(fā)生過心肌梗死的患者,不適合行結(jié)腸鏡檢查?;颊呶茨苄薪Y(jié)腸鏡檢查最常見的原因是檢查費(fèi)用問題及無法獲得經(jīng)驗(yàn)豐富的內(nèi)鏡醫(yī)生資源。
04
腸道準(zhǔn)備
安全且精確的結(jié)腸鏡檢查需要清潔的腸道準(zhǔn)備。最初的結(jié)腸清潔劑是由鋇灌腸準(zhǔn)備制劑改良而來,經(jīng)過多年的演變,目前有多種方法可選擇。這些方法之間的多項(xiàng)對照研究得出了不同的結(jié)果,患者按照指導(dǎo)完成腸道準(zhǔn)備比選擇何種準(zhǔn)備方法更為重要。所有的腸道準(zhǔn)備方法都會采用某種形式的飲食限制,腸道準(zhǔn)備制劑主要分為等滲性制劑、高滲性制劑和刺激性制劑等 [21]。
一
等滲性制劑
包括聚乙二醇( polyethylene glycol,PEG)在內(nèi)的等滲性制劑是一類滲透性平衡、高容量、不可吸收且非發(fā)酵的電解質(zhì)溶液(表 4- 1)。這類溶液在20世紀(jì)80年代開始應(yīng)用,清腸時(shí)較少發(fā)生水、電解質(zhì)交換,通過大容量灌洗的機(jī)械效應(yīng)達(dá)到排空腸道的目的 [22, 23]。由于采用硫酸鈉制劑,缺少主動(dòng)吸收過程中對抗電化學(xué)梯度所必需的陰離子——氯離子,小腸對鈉的吸收大大減少 [24]。成人常規(guī)的總劑量為4L,每10min口服240ml,直至排泄物清潔為止,也可以將制劑通過鼻胃管以20~30ml/min的速度注入;也有人提倡分次服用,即檢查前一天晚上服用一半劑量,檢查當(dāng)天早上再服用剩余劑量 [25, 26]。低容量PEG制劑聯(lián)合刺激性瀉藥或者維生素C一起使用;一種方法是每10min口服240ml制劑直至排泄物清潔或者服完總量2L的制劑為止,其中第一次排便后口服10mg比沙可啶片;另一種方法是在2L PEG溶液中加入維生素C,同樣以每10min240ml劑量服用 [27, 28]。在后一種方法中,建議患者再服用至少1L液體,總劑量達(dá)到3L。一種用作治療便秘、不含電解質(zhì)的PEG-3350制劑(MiraLAX, Schering Plough Healthcare Products, Summit,NJ)(表4- 1), 曾被用作清腸劑 [29] ;不過這類不含電解質(zhì)的PEG制劑并沒有被批準(zhǔn)用來進(jìn)行腸道準(zhǔn)備,且其用于腸道準(zhǔn)備所需的劑量和安全性尚未得到充分界定。
▲ 表 4-1
二
高滲性制劑
高滲性制劑通過將水分吸入腸腔來刺激腸蠕動(dòng)和排空。這類制劑服用劑量較少,但是由于其高滲性質(zhì),會引起體液變化和短暫的電解質(zhì)紊亂。
一種由匹克硫酸鈉、枸櫞酸鎂和無水枸櫞酸組成的低容量刺激性、滲透性瀉藥(PM/C)(Prepopik,Ferring Pharmaceuticals, Parsippany ,NJ )可配制成總量300ml的清腸溶液和1920ml清流質(zhì),分兩次服用。PM/C制劑可以在結(jié)腸鏡 檢查前一天服用(間隔6h),也可以分次服用 [30]。磷酸鈉制劑是一類為了增加患者依從性而采取的低容量、更可口的清腸劑,口服磷酸鈉制劑分為溶液( Phosphosoda and Fleet Phos-phosoda EZ Prep, Fleet Pharmaceuticals, Lynchburg, VA)和片劑(Visicol, InKine Pharmaceutical Co.,Inc., Blue Bell, PA; Osmoprep, Salix Pharmaceuticals)兩種劑型。與口服腸道灌洗液相比,磷酸鹽制劑具有同等的清腸效果和更好的耐受性 [31, 32]。
磷酸鈉制劑通過其高滲性質(zhì)將水吸入腸腔來發(fā)揮清腸作用,可能會導(dǎo)致水、電解質(zhì)紊亂。健康受試者服用磷酸鈉制劑后曾出現(xiàn)高磷血癥、低鈣血癥、甲狀旁腺素升高及尿環(huán)磷酸腺苷升高等情況,上述發(fā)現(xiàn)引起了對磷酸鈉制劑在心臟、腎臟和肝臟疾病患者中使用安全性的關(guān)注 [33] ,同時(shí)也發(fā)現(xiàn)有患者用藥后出現(xiàn)急性磷酸鹽腎病的現(xiàn)象[34] 。這些證據(jù)促使美國食品藥品監(jiān)督管理局(food and drug administration,F(xiàn)DA )發(fā)布了關(guān)于使用磷酸鹽產(chǎn)品處方的警示,包括黑框警告,并限制非處方購買磷酸鹽進(jìn)行腸道準(zhǔn)備??诜姿徕c溶液制劑已退出市場;片劑目前仍然可用,方法上需分次服用(Osmoprep, Salix Pharmaceuticals)并充分水化。磷酸鈉制劑似乎是一種有吸引力的能替代腸道灌洗的清腸方式,但由于有發(fā)生水、代謝及電解質(zhì)紊亂的風(fēng)險(xiǎn),兒童、老年、疑似腸梗 阻、其他腸道結(jié)構(gòu)異常、腸道動(dòng)力障礙、活動(dòng)性 結(jié)腸炎、腎功能不全、肝功能不全、心力衰竭以及因?yàn)殡娊赓|(zhì)異?;蝮w液變化而有并發(fā)癥風(fēng)險(xiǎn)的患者不應(yīng)使用 [35, 36]。建議在服用時(shí)充分水化以降低發(fā)生急性磷酸鹽腎病的風(fēng)險(xiǎn); Pelham等發(fā)現(xiàn)健康年輕男性給予多達(dá)4.4L水化后,即便沒有脫水的跡象,也發(fā)生高磷血癥 [36]。
硫酸鈉制劑( SUPREP, Braintree Laboratories,Braintree,MA )通常用水稀釋后分為兩劑服用 [37], 多項(xiàng)對照研究表明其能產(chǎn)生同樣的清潔效果,但患者不適感較小。FDA最近批準(zhǔn)了一種改良的口服硫酸鹽電解質(zhì)灌洗溶液(SuClear,Braintree Laboratories, Inc, Braintree,MA) [30]。
三
刺激性制劑
番瀉葉是一種蒽環(huán)類衍生物,經(jīng)由結(jié)腸細(xì)菌分解,其有效成分蒽醌及其糖苷可促進(jìn)結(jié)腸蠕動(dòng),服用后約6h出現(xiàn)腸道反應(yīng)。配合流質(zhì)飲食時(shí),番瀉葉曾被用作主要的清腸劑,尤其是在兒童中使用 [38]。
四
輔助藥物
比沙可啶是一種二苯甲烷衍生物,在小腸中吸收較差,被內(nèi)源性酯酶水解 [39]。其活性代謝物可刺激結(jié)腸蠕動(dòng),服用后6~10h起效。有報(bào)道缺血性腸炎的發(fā)生與使用比沙可啶有相關(guān)性 [40]。
甲氧氯普胺是一種多巴胺受體拮抗劑,能使組織對乙酰膽堿敏感,從而促進(jìn)胃收縮和小腸蠕動(dòng),其半衰期為5~6h。另外多種飲食方案、水化電解質(zhì)溶液、灌腸劑及去泡劑等也可作為腸道準(zhǔn)備的輔助藥物。
重要的是醫(yī)師要充分認(rèn)識到在腸道準(zhǔn)備過程中哪些基礎(chǔ)疾病會使患者面臨并發(fā)癥的風(fēng)險(xiǎn)。因?yàn)楝F(xiàn)有的腸道清潔劑都有一定風(fēng)險(xiǎn),所以應(yīng)由醫(yī)師來決定哪些患者不宜進(jìn)行腸道準(zhǔn)備。
參考文獻(xiàn)
[1] Shinya H. Colonoscopy: Diagnosis and Treatment of Colonic Diseases. New York, NY: Igaku-Shoin; 1982
[2] Jentschura D, Raute M, Winter J, Henkel T, Kraus M, Manegold BC. Complica- tions in endoscopy of the lower gastrointestinal tract. Therapy and progno- sis. Surg Endosc. 1994; 8(6):672–676
[3] Nivatvongs S. Colonic perforations during colonoscopy. Perspect Colon Rec- tal Surg. 1988; 1(2):107–112
[4] Nivatvongs S. How to teach colonoscopy. Clin Colon Rectal Surg. 2001; 14:387–392
[5] Waye JD, Bashko? E. Total colonoscopy: is it always possible? Gastrointest Endosc. 1991; 37(2):152–154
[6] Nivatvongs S, Snover DC, Fang DT. Piecemeal snare excision of large sessile co- lon and rectal polyps: is it adequate? Gastrointest Endosc. 1984; 30(1):18–20
[7] Shinya H, Wol? WI. Morphology, anatomic distribution and cancer potential of colonic polyps. Ann Surg. 1979; 190(6):679–683
[8] Hull T, Church JM. Colonoscopy–how di?cult, how painful? Surg Endosc. 1994; 8(7):784–787
[9] Saunders BP, Fukumoto M, Halligan S, et al. Why is colonoscopy more di?- cult in women? Gastrointest Endosc. 1996; 43(2, Pt 1):124–126
[10] Saunders BP, Phillips RK, Williams CB. Intraoperative measurement of colon- ic anatomy and attachments with relevance to colonoscopy. Br J Surg. 1995; 82(11):1491–1493
[11] Ward ST, Mohammed MA, Walt R, Valori R, Ismail T, Dunckley P. An analysis of the learning curve to achieve competency at colonoscopy using the JETS database. Gut. 2014; 63(11):1746–1754
[12] Sedlack RE. Training to competency in colonoscopy: assessing and defining competency standards. Gastrointest Endosc. 2011; 74(2):355–366.e1-2
[13] Nivatvongs S. Diagnosis. In: Gordon PH, Nivatvongs S, eds. Principles and Practice of Surgery for the Colon, Rectum, and Anus. 3rd ed. New York, NY:Informa; 2007:65–98
[14] Nivatvongs S, Vermeulen FD, Fang DT. Colonoscopic decompression of acute pseudo-obstruction of the colon. Ann Surg. 1982; 196(5):598–600
[15] Dorudi S, Berry AR, Kettlewell MGW. Acute colonic pseudo-obstruction. Br J Surg. 1992; 79(2):99–103
[16] Jetmore AB, Timmcke AE, Gathright JB, Jr, Hicks TC, Ray JE, Baker JW. Ogil- vie’s syndrome: colonoscopic decompression and analysis of predisposing factors. Dis Colon Rectum. 1992; 35(12):1135–1142
[17] Sgambati SA, Armstrong DN, Ballantyne GH. Management of acute colonic pseudo-obstruction. (Ogilvie’s syndrome). Perspect Colon Rectal Surg. 1994; 7:77–96
[18] Ponec RJ, Saunders MD, Kimmey MB. Neostigmine for the treatment of acute colonic pseudo-obstruction. N Engl J Med. 1999; 341(3):137–141
[19] Beck DE. Endoscopic colonic stents and dilatation. Clin Colon Rectal Surg. 2010; 23(1):37–41
[20] Sagar J. Colorectal stents for the management of malignant colonic obstruc- tions. Cochrane Database Syst Rev. 2011(11):CD007378
[21] Mamula P, Adler DG, Conway JD, et al. ASGE Technology Committee. Colono- scopy preparation. Gastrointest Endosc. 2009; 69(7):1201–1209
[22] Ernsto? JJ, Howard DA, Marshall JB, Jumshyd A, McCullough AJ. A random- ized blinded clinical trial of a rapid colonic lavage solution (Golytely) com- pared with standard preparation for colonoscopy and barium enema. Gas- troenterology. 1983; 84(6):1512–1516
[23] Shawki S, Wexner SD. Oral colorectal cleansing preparations in adults.Drugs. 2008; 68(4):417–437
[24] Wexner SD, Beck DE, Baron TH, et al. A consensus document on bowel pre- paration before colonoscopy: prepared by a task force from the American Society of Colon and Rectal Surgeons (ASCRS), the American Society of Gas- trointestinal Endoscopy (ASGE), and the Society of American Gastrointesti- nal and Endoscopic Surgeons (SAGES). Surg Endosc. 2006; 20:147–160
[25] R?sch T, Classen M. Fractional cleansing of the large bowel with “Golytely” for colonoscopic preparation: a controlled trial. Endoscopy. 1987; 19 (5):198–200
[26] Aoun E, Abdul-Baki H, Azar C, et al. A randomized single-blind trial of split- dose PEG-electrolyte solution without dietary restriction compared with whole dose PEG-electrolyte solution with dietary restriction for colonoscopy preparation. Gastrointest Endosc. 2005; 62(2):213–218
[27] Ell C, Fischbach W, Bronisch HJ, et al. Randomized trial of low-volume PEG solution versus standard PEG + electrolytes for bowel cleansing before colo- noscopy. Am J Gastroenterol. 2008; 103(4):883–893
[28] Bitoun A, Ponchon T, Barthet M, Co?n B, Dugué C, Halphen M, Norcol Group. Results of a prospective randomised multicentre controlled trial comparing a new 2-L ascorbic acid plus polyethylene glycol and electrolyte solution vs. sodium phosphate solution in patients undergoing elective colonoscopy. Ali- ment Pharmacol Ther. 2006; 24(11–12):1631–1642
[29] Pashankar DS, Uc A, Bishop WP. Polyethylene glycol 3350 without electro- lytes: a new safe, e?ective, and palatable bowel preparation for colonoscopy in children. J Pediatr. 2004; 144(3):358–362
[30] Landreneau SW, Di Palma JA. Colon cleansing for colonoscopy 2013: current status. Curr Gastroenterol Rep. 2013; 15(8):341–347
[31] Belsey J, Epstein O, Heresbach D. Systematic review: oral bowel preparation for colonoscopy. Aliment Pharmacol Ther. 2007; 25(4):373–384
[32] Johanson JF, Popp JW, Jr, Cohen LB, et al. A randomized, multicenter study comparing the safety and e?cacy of sodium phosphate tablets with 2 L poly- ethylene glycol solution plus bisacodyl tablets for colon cleansing. Am J Gas- troenterol. 2007; 102(10):2238–2246
[33] DiPalma JA, Buckley SE, Warner BA, Culpepper RM. Biochemical e?ects of oral sodium phosphate. Dig Dis Sci. 1996; 41(4):749–753
[34] Markowitz GS, Stokes MB, Radhakrishnan J, D’Agati VD. Acute phosphate nephropathy following oral sodium phosphate bowel purgative: an underre- cognized cause of chronic renal failure. J Am Soc Nephrol. 2005; 16 (11):3389–3396
[35] Wexner SD, Beck DE, Baron TH, et al. American Society of Colon and Rectal Surgeons, American Society for Gastrointestinal Endoscopy, Society of Amer- ican Gastrointestinal and Endoscopic Surgeons. A consensus document on bowel preparation before colonoscopy: prepared by a task force from the American Society of Colon and Rectal Surgeons (ASCRS), the American Soci- ety for Gastrointestinal Endoscopy (ASGE), and the Society of American Gas- trointestinal and Endoscopic Surgeons (SAGES). Gastrointest Endosc. 2006; 63(7):894–909
[36] Pelham R, Dobre A, van Diest K, Cleveland MVB. Oral sodium phosphate bowel preparations: how much hydration is enough? Gastrointest Endosc. 2007; 65(5):AB314
[37] Patel V, Nicar M, Emmett M, et al. Intestinal and renal e?ects of low-volume phosphate and sulfate cathartic solutions designed for cleansing the colon: pathophysiological studies in five normal subjects. Am J Gastroenterol. 2009; 104(4):953–965
[38] Trautwein AL, Vinitski LA, Peck SN. Bowel preparation before colonoscopy in the pediatric patient: a randomized study. Gastroenterol Nurs. 1996; 19 (4):137–139
[39] Manabe N, Cremonini F, Camilleri M, Sandborn WJ, Burton DD. E?ects of bi- sacodyl on ascending colon emptying and overall colonic transit in healthy volunteers. Aliment Pharmacol Ther. 2009; 30(9):930–936
[40] Baudet JS, Castro V, Redondo I. Recurrent ischemic colitis induced by colono- scopy bowel lavage. Am J Gastroenterol. 2010; 105(3):700–701
閱讀原文
相關(guān)知識
腸鏡禁忌癥
直腸鏡檢查禁忌
腸鏡檢查,你真的準(zhǔn)備好了嗎? ——談?wù)勀c鏡檢查前的準(zhǔn)備
直腸內(nèi)鏡檢查的禁忌
電子腸鏡檢查禁忌證
腸鏡檢查的不良反應(yīng)和并發(fā)癥
腸鏡檢查前,如何進(jìn)行高質(zhì)量的腸道準(zhǔn)備?
腸道準(zhǔn)備 腸鏡檢查前的“必做功課”
結(jié)腸鏡檢查腸道清潔優(yōu)化指南
腸鏡檢查健康教育.pptx
網(wǎng)址: 結(jié)腸鏡檢查——適應(yīng)癥、禁忌癥以及腸道準(zhǔn)備 http://www.u1s5d6.cn/newsview1238396.html
推薦資訊
- 1發(fā)朋友圈對老公徹底失望的心情 12775
- 2BMI體重指數(shù)計(jì)算公式是什么 11235
- 3補(bǔ)腎吃什么 補(bǔ)腎最佳食物推薦 11199
- 4性生活姿勢有哪些 盤點(diǎn)夫妻性 10428
- 5BMI正常值范圍一般是多少? 10137
- 6在線基礎(chǔ)代謝率(BMR)計(jì)算 9652
- 7一邊做飯一邊躁狂怎么辦 9138
- 8從出汗看健康 出汗透露你的健 9063
- 9早上怎么喝水最健康? 8613
- 10五大原因危害女性健康 如何保 7828