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      快速康復外科理念下全膝關節(jié)置換術圍術期鎮(zhèn)痛進展*

      2016-01-28 17:09:46曲音音綜述審校
      中國微創(chuàng)外科雜志 2016年2期
      關鍵詞:圍術硬膜外膝關節(jié)

      曲音音 綜述 徐 懋 審校

      (北京大學第三醫(yī)院麻醉科,北京 100083)

      ·文獻綜述·

      快速康復外科理念下全膝關節(jié)置換術圍術期鎮(zhèn)痛進展*

      曲音音 綜述 徐 懋**審校

      (北京大學第三醫(yī)院麻醉科,北京 100083)

      全膝關節(jié)置換術圍術期鎮(zhèn)痛向多模式鎮(zhèn)痛轉變。作為快速康復外科(fast track surgery,F(xiàn)TS)中極其重要的一部分,圍術期鎮(zhèn)痛是影響患者快速康復很重要的一環(huán)。本文綜述FTS理念下全膝關節(jié)置換術前、術中、術后各種鎮(zhèn)痛方案的優(yōu)缺點及最新進展。

      全膝關節(jié)置換術; 圍術期鎮(zhèn)痛; 快速康復外科

      Kehlet[1]1997年首次提出快速康復外科(fast track surgery,F(xiàn)TS)理念,涵蓋術前宣教、營養(yǎng)狀況最佳化、標準化鎮(zhèn)痛麻醉配方等眾多圍術期處理措施的綜合優(yōu)化,最終達到降低應激反應、減少并發(fā)癥和早期恢復的目的[2~4]。全膝關節(jié)置換術(total knee arthroplasty,TKA)是治療嚴重膝關節(jié)疾病的主要方法,通過手術可以解除膝關節(jié)疼痛,重建膝關節(jié)功能。但TKA術后15%~20%的患者對鎮(zhèn)痛不滿意[5],患者因疼痛不能進行功能鍛煉,延遲出院,且易出現(xiàn)深靜脈血栓、肺栓塞、感染、術后關節(jié)強直等并發(fā)癥。疼痛程度嚴重制約FTS方案的實施,影響關節(jié)活動度、開始功能鍛煉時間和平均住院日等重要評價指標[6]。因此,TKA圍術期鎮(zhèn)痛是FTS理念下亟待改善的重要課題。本文對目前FTS理念下TKA術前、術中、術后各種鎮(zhèn)痛方案的優(yōu)缺點進行綜述,旨在為TKA圍術期鎮(zhèn)痛方案的選擇和完善提供參考。

      1 術前預防性鎮(zhèn)痛

      FTS強調基礎藥物的應用,術前應用非甾體抗炎藥(NSAIDs)如氟比洛芬酯[7]和選擇性環(huán)氧化酶2(COX-2)抑制劑如帕瑞昔布,能抑制前列腺素合成,減輕炎癥反應,減輕外周敏化和中樞敏化導致疼痛,有效緩解術后疼痛。Straube等[8]的meta分析納入22項隨機對照研究共2246例,與安慰劑組相比,有15個研究結果顯示術前應用COX-2抑制劑組術后疼痛評分顯著降低,患者滿意度提高并且鎮(zhèn)痛藥用量顯著減少。姜天樂等[9]研究顯示,與連續(xù)股神經阻滯組比較,帕瑞昔布鈉聯(lián)合連續(xù)股神經阻滯組TKA術后24 h膝關節(jié)后部靜息VAS評分明顯降低(均值4.0分 vs. 5.5分), 被動活動時膝關節(jié)前部(均值3.0分 vs. 4.0分)及后部(均值6.0分 vs. 8.0分)VAS評分均明顯降低。

      盡管NSAIDs可以應用于TKA鎮(zhèn)痛,但仍應注意相關風險。非選擇性NSAIDs藥物有可能損傷胃腸黏膜,影響血小板、腎功能和增加圍術期出血量,選擇性COX-2抑制劑相關不良反應較少,但是有心腦血管風險的顧慮。Utvag等[10]研究顯示無論非選擇性還是選擇性COX-2抑制劑,臨床常規(guī)劑量并不影響骨折的愈合。但Wang等[11]對1993~2012年骨折不愈合發(fā)生率與NSAIDs、COX-2抑制劑處方量的分析提示,藥物處方量增加與骨折不愈合發(fā)病率呈正比。因此,對于高?;颊呷砸斏魇褂肗SAIDs和COX-2抑制劑。我們認為術前預防性鎮(zhèn)痛聯(lián)合宣教可增加患者的配合度和認知度,有助于圍術期疼痛管理及患者早期康復。

      2 術中綜合處理

      2.1 改善手術技巧

      Liu等[12]Meta分析顯示,股內側肌下入路不損傷股四頭肌和伸膝裝置,與內側髕旁入路和經股內側肌入路相比,可減少不必要的手術組織創(chuàng)傷,術后1周關節(jié)活動度明顯改善;經股內側肌入路能夠降低VAS評分,增加關節(jié)活動度。另外,盡量減少止血帶的使用時間和降低止血帶壓力也有利于患者早期恢復。Dennis等[13]研究顯示,與TKA全程使用止血帶相比,不用或只在置入假體時使用止血帶組患者術后股四頭肌肌力明顯改善,疼痛減輕,更有利于早期鍛煉和功能恢復,而術后早期活動正是FTS理念強調的重要內容。因此,術中應注意手術入路選擇,盡量減少止血帶的使用時間。

      2.2 關節(jié)周圍注射或囊內藥物應用(“雞尾酒”療法)

      “雞尾酒”療法發(fā)揮不同鎮(zhèn)痛藥物的協(xié)同作用和多環(huán)節(jié)作用,提高鎮(zhèn)痛特異性,減少單種藥物的劑量和副作用,可有效緩解術后疼痛[14]。常用藥物包括鹽酸羅哌卡因、鹽酸嗎啡、酮洛酸和腎上腺素等。聯(lián)合股神經阻滯,關節(jié)周圍局麻藥注射與坐骨神經阻滯相比,術后疼痛評分、患者滿意度、鎮(zhèn)痛藥用量、康復時間和住院日等指標均無顯著差異[15,16]。關節(jié)周圍組織注射局麻藥的發(fā)展也對外周神經阻滯提出挑戰(zhàn),在疼痛評分、康復進度和住院時間等FTS重點關注指標上,多項研究表明即使單獨應用關節(jié)周圍局麻藥注射,效果類似于單次股神經阻滯[17]、連續(xù)硬膜外阻滯[18]和股神經阻滯聯(lián)合硬膜外自控鎮(zhèn)痛[19]。Fan等[20]Meta分析結果顯示,注射局麻藥組在術后疼痛數(shù)字評分(numerical rating scale, NRS)、嗎啡用量、關節(jié)活動度及住院時間等指標與外周神經阻滯組相近。與外周神經阻滯相比,局部藥物注射操作簡單,可在術中由手術醫(yī)師完成,不需要另行操作,此外,對股四頭肌肌力影響小,有利于早期功能鍛煉,有助于早期恢復,在FTS理念下更有優(yōu)勢[21, 22]。關節(jié)周圍局麻藥注射鎮(zhèn)痛的不足是受藥物時效影響,不能達到長時間鎮(zhèn)痛,留置導管可延長鎮(zhèn)痛時間,但有增加切口感染發(fā)生率的可能[23]。Moghtadaei等[24]比較單次股神經阻滯與關節(jié)周圍局麻藥注射,結果顯示局麻藥注射組術后6 h內嗎啡使用量明顯降低(中位數(shù)10 mg vs. 12.5 mg),VAS評分也降低(中位數(shù)3分 vs. 4分),患者滿意度更高,但12 h VAS評分相對更高(中位數(shù)6分 vs. 5分)??梢?,關節(jié)周圍或囊內局麻藥注射效果較可靠,與傳統(tǒng)鎮(zhèn)痛方案相比優(yōu)勢明顯,但既往薈萃分析中所納入研究異質性較高,鎮(zhèn)痛方案和評價指標不完全一致,且注射藥物配方較多樣,包含多種藥物的“雞尾酒”目前尚無統(tǒng)一配方,還有待進一步深入研究。

      新型布比卡因(布比卡因脂質體)可實現(xiàn)手術部位單次注射鎮(zhèn)痛效果長達72 h,而且延長術后到第1次輔助應用阿片類藥物時間(14.3 h vs. 1.2 h)[25,26]。布比卡因脂質體注射用懸浮液(EXPAREL)2011年經FDA批準應用于單次局部浸潤,目前國內尚未引進或應用。長效布比卡因(POSIDUR)是布比卡因的緩釋注射劑,目前處于試驗階段,尚未獲得FDA批準。新型布比卡因的應用尚需大量研究指導臨床的應用,但是已經顯示出良好的應用前景。

      3 術后鎮(zhèn)痛

      3.1 硬膜外自控鎮(zhèn)痛

      持續(xù)硬膜外鎮(zhèn)痛效果可靠,廣泛應用于臨床術后鎮(zhèn)痛,但可能引起低血壓、尿潴留等并發(fā)癥[27]。對于TKA而言,可能影響肌力和運動功能,延遲術后康復鍛煉,導致患者延遲出院[18]。Spreng等[28]研究表明,與羅哌卡因局部浸潤鎮(zhèn)痛對比,硬膜外鎮(zhèn)痛組患者恢復運動能力更慢且住院時間更長(均值5.5 d vs.3.5 d)。另外,TKA大多需要抗凝治療,硬膜外鎮(zhèn)痛由于有硬膜外血腫的顧慮,應用也受到影響。鑒于對肌力影響和血腫方面的考量,在FTS理念下,硬膜外自控鎮(zhèn)痛逐漸被其他鎮(zhèn)痛方案替代。

      3.2 靜脈自控鎮(zhèn)痛

      靜脈自控鎮(zhèn)痛操作方便,肌力影響小,在臨床鎮(zhèn)痛管理中應用廣泛,但阿片類藥物的應用,會增加惡心、嘔吐、呼吸抑制等阿片類藥物相關不良反應發(fā)生率,延長患者住院時間并增加費用支出[29]。阿片類藥物不能有效抑制導致疼痛的炎癥反應及痛覺過敏,而且不良反應相對較多,與神經阻滯等其他鎮(zhèn)痛方式相比無明顯優(yōu)勢。Peng等[30]研究顯示,與連續(xù)股神經阻滯相比,靜脈自控鎮(zhèn)痛組術后慢性疼痛發(fā)生率(50.7% vs.37.1%)、補救藥物用量(帕瑞昔布均值31.5 mg vs.22.4 mg)及術后3、9、12個月關節(jié)屈曲角度上均明顯處于劣勢,外周神經阻滯更有助于患者康復,其他研究也有類似的結果[31,32]。因此,靜脈自控鎮(zhèn)痛在TKA圍術期不作為首選鎮(zhèn)痛方案,多作為多模式鎮(zhèn)痛的一種補充手段。

      3.3 連續(xù)股神經阻滯

      股神經阻滯鎮(zhèn)痛效果相對可靠,不引起惡心、嘔吐、瘙癢和鎮(zhèn)靜等并發(fā)癥,與硬膜外鎮(zhèn)痛及靜脈自控鎮(zhèn)痛比可增大屈膝角度, 有利于早期活動。Chan等[33]的Meta分析顯示,與靜脈自控鎮(zhèn)痛比較,股神經阻滯鎮(zhèn)痛顯著減輕術后24 h靜息痛(標準均數(shù)差-0.72)和活動痛(標準均數(shù)差-0.94),惡心嘔吐風險低(相對危險度0.47),膝關節(jié)活動度更大(均數(shù)差6.48°);與硬膜外鎮(zhèn)痛比較,盡管在疼痛評分和膝關節(jié)活動度無明顯差異,但惡心、嘔吐風險低(相對危險度0.63)。近年來,由于超聲和神經刺激器的應用,股神經阻滯在臨床膝關節(jié)鎮(zhèn)痛應用日趨廣泛,神經損傷的發(fā)生率也明顯降低[34]。Chan等[35]報道與單次股神經阻滯相比,連續(xù)股神經阻滯VAS評分更低(均數(shù)差-0.57,P<0.05),阿片類藥物用量更少(術后第1日晨均數(shù)差-18.5 mg;術后第2日晨均數(shù)差-24.4 mg),惡心、嘔吐等阿片相關不良反應更少(優(yōu)勢比0.24)。但連續(xù)股神經阻滯也存在導管脫落[31]、導管相關感染、降低股四頭肌肌力進而影響患者術后活動和增加患者跌倒風險(1.6%~2.7%)等問題[23,36~38],部分患者需要再次手術(0.4%)。另外,由于神經支配區(qū)域限制,對于膝關節(jié)后側坐骨神經支配區(qū)域疼痛需要聯(lián)合阻滯,由此增加操作時間,可能增大對肌力的影響。近年來,隨著局部浸潤技術的發(fā)展,以及FTS理念下追求更快的患者恢復和功能鍛煉,股神經阻滯的地位也受到挑戰(zhàn)。

      3.4 收肌管阻滯

      收肌管阻滯主要阻滯隱神經,對股四頭肌影響極小[39]。Grevstad等[40]報道收肌管阻滯組患者最大等長隨意收縮肌力增加到基線值的193%,而股神經阻滯組減少到基線值的16%,有顯著性差異。與股神經阻滯相比,行收肌管阻滯的患者術后第1、2天運動距離均顯著延長,且平均住院時間為2.67 d,明顯短于股神經組3.01 d[41]。而連續(xù)收肌管阻滯與連續(xù)股神經阻滯相比,患者的運動功能明顯增強,計時起立行走測試、10 m行走試驗、30 s椅子測試及行走距離等指標均有顯著差異,患者可以更早進行康復鍛煉,加快恢復[42, 43]。但是收肌管阻滯中由于隱神經辨識存在一定難度,要求操作者更富有經驗;同時,藥物在收肌管內擴散也有影響肌力的可能,Chen等[44]報道隱神經阻滯造成股四頭肌運動阻滯的現(xiàn)象。

      3.5 坐骨神經阻滯

      坐骨神經阻滯可有效緩解膝關節(jié)后側牽拉痛和屈膝運動疼痛,通常作為多模式鎮(zhèn)痛的一部分與其他方案聯(lián)合應用,具有外周神經阻滯的優(yōu)點,可避免硬膜外鎮(zhèn)痛相關并發(fā)癥[27,45]。Tanikawa等[15]對比股神經阻滯分別聯(lián)合坐骨神經阻滯和關節(jié)局部藥物浸潤的研究結果顯示,2組術后1~21 d疼痛評分和關節(jié)活動度、到達康復目標的時間(如直腿抬高時間2.5 d vs. 3.0 d,P=0.44)和住院時間(33.0 d vs.37.0 d,P=0.95)均無明顯差異。坐骨神經阻滯和關節(jié)局部藥物浸潤均可作為股神經阻滯的一種補充[16]。作為股神經阻滯/腰叢阻滯的一種補充,持續(xù)輸注相比單次注射VAS評分(靜息及被動運動)更低,并發(fā)癥發(fā)生率也更低,有效運動更多,更有助于患者早期恢復[46]。但坐骨神經阻滯與局部藥物浸潤相比操作復雜,2個部位神經阻滯所需操作時間更長。

      3.6 其他

      口服或肌注鎮(zhèn)痛藥,如塞來昔布、曲馬多、哌替啶等,可作為其他鎮(zhèn)痛方案的補救措施,也可以作為多模式鎮(zhèn)痛的一部分在圍術期應用。但嗎啡等阿片類藥物用量過大存在惡心、嘔吐等風險,不利于患者早期恢復。Zhu等[47]對100例TKA的研究結果顯示,與鹽水對照組相比,術后應用COX-2抑制劑帕瑞昔布可顯著降低術后6、12、24、48、72 h各時間點VAS評分(P<0.01),顯著增加術后24、48、72 h各時間點關節(jié)活動度(P<0.01),并減少24 h嗎啡用量(均值8.40 mg vs. 14.18 mg)。Lin等[48]的薈萃分析顯示,TKA圍術期應用COX-2抑制劑可顯著降低術后VAS評分,改善關節(jié)活動度。另外,芬太尼透皮貼劑[49]、冷凍療法[50]及舒芬太尼舌下含服[51]等其他方案也可用于術后鎮(zhèn)痛。

      4 多模式鎮(zhèn)痛

      多模式鎮(zhèn)痛指應用2種或2種以上不同作用機制的鎮(zhèn)痛藥或方法,前述鎮(zhèn)痛方法或藥物可以進行互補性聯(lián)合應用改善鎮(zhèn)痛效果,減少單藥用量,避免單藥過量所致不良反應,是FTS著重強調的圍術期鎮(zhèn)痛模式,大量研究證實多模式鎮(zhèn)痛的優(yōu)勢。Sarridou等[52]研究顯示帕瑞昔布聯(lián)合股神經阻滯相比單獨股神經阻滯術后VAS評分更低(術后4、12、24 h,P<0.01),嗎啡用量更少(P=0.054),有利于患者早期康復。Perlas等[53]研究顯示與單獨應用連續(xù)股神經阻滯相比,局部浸潤和局部浸潤聯(lián)合收肌管阻滯可明顯改善術后第1天可行走距離(中位數(shù)20 m vs.30 m vs.0 m,P<0.0001),疼痛評分低且阿片類藥物應用更少;聯(lián)合應用相對單獨局部浸潤,患者出院后直接返家而非進入康復中心的比例更高(88.2% vs.73.2%,P=0.018)。多模式鎮(zhèn)痛聯(lián)用可以改善圍術期鎮(zhèn)痛效果,降低不良反應,已經得到臨床廣泛認可,但是具體聯(lián)合藥物和方法仍有一定爭議,不同地區(qū)和中心的方案不盡相同,新的方法和藥物的出現(xiàn)也提供了更多的選擇和更好的效果。

      5 小結

      TKA圍術期鎮(zhèn)痛是FTS理念下的重要組成部分,直接關系到患者能否早期進行康復鍛煉,快速恢復和及早出院。目前,FTS理念下多模式鎮(zhèn)痛已成基本共識,多模式鎮(zhèn)痛是從術前、術中到術后的一系列嚴格方案,但各中心的方案不盡相同,麻醉方式、靜脈鎮(zhèn)痛藥物、外周神經阻滯和局部浸潤麻醉配方不同,至今也尚未有統(tǒng)一的最佳方案。關節(jié)周圍注射是近年研究的熱點,在多模式疼痛控制方案中顯示出優(yōu)勢。關于局部浸潤所采用的最佳藥物配方、藥物注射部位,如何與其他方案聯(lián)用,尚需進一步研究。新的局麻藥的應用可能有助于改善圍術期的鎮(zhèn)痛效果,減少相關不良反應,但尚需大量研究證實。

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      (修回日期:2015-12-01)

      (責任編輯:李賀瓊)

      Progress of Perioperative Analgesia of Total Knee Arthroplasty in Fast Track Surgery Protocol

      QuYinyin,XuMao.

      DepartmentofAnesthesiology,PekingUniversityThirdHospital,Beijing100083,China

      Correspondingauthor:XuMao,E-mail:anae@163.com

      【Summary】 In total knee arthroplasty, perioperative analgesia is transforming into multimodal analgesia. As a significantly important part of fast track surgery (FTS) protocol, perioperative analgesia does affect the recovery of patients. We reviewed the advantages and disadvantages of perioperative (pre-operative, intra-operative and post-operative) analgesia in FTS protocols in total knee arthroplasty, including the latest progress of the field.

      Total knee arthroplasty; Perioperative analgesia; Fast track surgery

      北京大學第三醫(yī)院臨床重點項目青年項目(項目編號:BYSY2014019)

      A

      1009-6604(2016)02-0172-05

      10.3969/j.issn.1009-6604.2016.02.021

      2015-08-27)

      **通訊作者,E-mail:anae@163.com

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