Indocyanine green near-infrared fluorescence bowel perfusion assessment to prevent anastomotic leakage in minimally invasive colorectal surgery (AVOID): a multicentre, randomised, controlled, phase 3 trial.

IF 30.9 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Lancet Gastroenterology & Hepatology Pub Date : 2024-10-01 Epub Date: 2024-08-13 DOI:10.1016/S2468-1253(24)00198-5
Robin A Faber, Ruben P J Meijer, Daphne H M Droogh, Jasmijn J Jongbloed, Okker D Bijlstra, Fran Boersma, Jeffrey P B M Braak, Elma Meershoek-Klein Kranenbarg, Hein Putter, Fabian A Holman, J Sven D Mieog, Peter A Neijenhuis, Esther van Staveren, Johanne G Bloemen, Jacobus W A Burger, Tjeerd S Aukema, Mark A M Brouwers, Andreas W K S Marinelli, Marinke Westerterp, Pascal G Doornebosch, Annelies van der Weijde, Koop Bosscha, Henricus J M Handgraaf, Esther C J Consten, Daan J Sikkenk, Jacobus Burggraaf, Stijn Keereweer, Joost R van der Vorst, Merlijn Hutteman, Koen C M J Peeters, Alexander L Vahrmeijer, Denise E Hilling
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In the FGBA group, surgeons marked anastomosis levels per conventional perfusion assessment and then administered 5 mg of ICG by 2 mL intravenous bolus. They assessed bowel perfusion using NIR fluorescence imaging and adjusted (or kept) transection lines accordingly. Only conventional methods for bowel perfusion assessment were used in the CBA group. The primary outcome was the difference in the rate of clinically relevant anastomotic leakage (ie, requiring active therapeutic intervention but manageable without reoperation [grade B] or requiring reoperation [grade C], per the International Study Group of Rectal Cancer) between the FGBA group and the CBA group within 90 days post-surgery. The primary outcome and safety were assessed in the intention-to-treat population. 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No adverse events related to ICG use were observed. 313 serious adverse events in 229 (25%) patients were at 90-day follow-up (159 serious adverse events in 113 [24%] patients in the FGBA group and 154 serious adverse events in 116 [25%] patients in the CBA group). 18 (2%) people died by 90 days (ten in the FGBA group and eight in the CBA group).</p><p><strong>Interpretation: </strong>ICG NIR fluorescence imaging did not reduce 90-day anastomotic leakage rates in this trial across all types of colorectal surgeries. 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Abstract

Background: Anastomotic leakage is a severe postoperative complication in colorectal surgery and compromised bowel perfusion is considered a major contributing factor. Conventional methods to assess bowel perfusion have a low predictive value for anastomotic leakage. We therefore aimed to evaluate the efficacy of real-time assessment with near-infrared (NIR) fluorescence imaging with indocyanine green (ICG) in the prevention of anastomotic leakage.

Methods: This multicentre, randomised, controlled, phase 3 trial was done in eight hospitals in the Netherlands. We included adults (aged >18 years) who were scheduled for laparoscopic or robotic colorectal surgery (with planned primary anastomosis) for benign and malignant diseases. Preoperatively, patients were randomly assigned (1:1) to fluorescence-guided bowel anastomosis (FGBA) or conventional bowel anastomosis (CBA) by variable block randomisation (block sizes 4, 6, and 8) and stratified by site. The operating surgeon and investigators analysing the data were not masked to group assignment. Patients were unmasked after the surgical procedure or after study end. In the FGBA group, surgeons marked anastomosis levels per conventional perfusion assessment and then administered 5 mg of ICG by 2 mL intravenous bolus. They assessed bowel perfusion using NIR fluorescence imaging and adjusted (or kept) transection lines accordingly. Only conventional methods for bowel perfusion assessment were used in the CBA group. The primary outcome was the difference in the rate of clinically relevant anastomotic leakage (ie, requiring active therapeutic intervention but manageable without reoperation [grade B] or requiring reoperation [grade C], per the International Study Group of Rectal Cancer) between the FGBA group and the CBA group within 90 days post-surgery. The primary outcome and safety were assessed in the intention-to-treat population. This study was registered with ToetsingOnline.nl (NL7502) and ClinicalTrials.gov (NCT04712032) and is complete.

Findings: Between July 2, 2020, and Feb 21, 2023, 982 patients were enrolled, of whom 490 were assigned to FGBA and 492 were assigned to CBA. After excluding 51 patients, the intention-to-treat population comprised 931 (463 assigned FGBA and 468 assigned CBA). Patients had a median age of 68·0 years (IQR 59·0-75·0) and 485 (52%) were male and 446 (48%) were female. Ethnicity data were not available. The overall 90-day rate of clinically relevant anastomotic leakage was not significantly different between the FGBA group (32 [7%] of 463 patients) and the CBA group (42 [9%] of 468 patients; relative risk 0·77 [95% CI 0·50-1·20]; p=0·24). No adverse events related to ICG use were observed. 313 serious adverse events in 229 (25%) patients were at 90-day follow-up (159 serious adverse events in 113 [24%] patients in the FGBA group and 154 serious adverse events in 116 [25%] patients in the CBA group). 18 (2%) people died by 90 days (ten in the FGBA group and eight in the CBA group).

Interpretation: ICG NIR fluorescence imaging did not reduce 90-day anastomotic leakage rates in this trial across all types of colorectal surgeries. Further research should be done in subgroups, such as rectosigmoid resections, for which evidence suggests ICG NIR might be beneficial.

Funding: Olympus Medical, Diagnostic Green, and Intuitive Foundation.

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吲哚菁绿近红外荧光肠道灌注评估以预防微创结直肠手术中的吻合口漏(AVOID):一项多中心、随机对照的 3 期试验。
背景:吻合口漏是结直肠手术中一种严重的术后并发症,而肠道灌注受损被认为是导致吻合口漏的主要因素。传统的肠道灌注评估方法对吻合口漏的预测价值较低。因此,我们旨在评估吲哚青绿(ICG)近红外(NIR)荧光成像实时评估在预防吻合口漏方面的功效:这项多中心、随机对照的 3 期试验在荷兰的 8 家医院进行。我们纳入了因良性和恶性疾病而计划接受腹腔镜或机器人结直肠手术(计划进行主吻合)的成人(年龄大于 18 岁)。术前,患者通过可变区块随机分配(区块大小为 4、6 和 8)被随机分配(1:1)到荧光引导肠吻合术(FGBA)或传统肠吻合术(CBA),并按部位进行分层。手术医生和分析数据的研究人员不对分组分配进行蒙蔽。患者在手术后或研究结束后才会被揭去面具。在 FGBA 组,外科医生根据常规灌注评估标记吻合口水平,然后通过 2 毫升静脉注射 5 毫克 ICG。他们使用近红外荧光成像技术评估肠道灌注情况,并相应调整(或保留)横切线。CBA组仅使用传统方法评估肠道灌注。主要结果是 FGBA 组和 CBA 组在术后 90 天内发生临床相关吻合口漏(即需要积极治疗干预,但无需再次手术即可控制[B 级]或需要再次手术[C 级],根据国际直肠癌研究小组的标准)的比率差异。主要结果和安全性在意向治疗人群中进行评估。该研究已在ToetsingOnline.nl(NL7502)和ClinicalTrials.gov(NCT04712032)注册,研究结果已完成:2020年7月2日至2023年2月21日期间,982名患者入组,其中490人被分配到FGBA,492人被分配到CBA。排除51名患者后,意向治疗人群为931人(463人分配到FGBA,468人分配到CBA)。患者的中位年龄为68-0岁(IQR为59-0-75-0),男性485人(52%),女性446人(48%)。种族数据不详。FGBA 组(463 例患者中的 32 [7%] 例)和 CBA 组(468 例患者中的 42 [9%] 例;相对风险 0-77 [95% CI 0-50-1-20];P=0-24)的 90 天临床相关吻合口漏总发生率无显著差异。未观察到与使用 ICG 相关的不良事件。229例(25%)患者中的313例严重不良事件发生在90天的随访中(FGBA组113例[24%]患者中发生了159例严重不良事件,CBA组116例[25%]患者中发生了154例严重不良事件)。18人(2%)在90天内死亡(FGBA组10人,CBA组8人):ICG近红外荧光成像并没有降低该试验中所有类型结直肠手术的 90 天吻合口漏率。有证据表明ICG近红外荧光成像可能对直肠乙状结肠切除术等亚组有益,因此应针对这些亚组开展进一步研究:资金来源:奥林巴斯医疗、Diagnostic Green 和 Intuitive Foundation。
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期刊介绍: The Lancet Gastroenterology & Hepatology is an authoritative forum for key opinion leaders across medicine, government, and health systems to influence clinical practice, explore global policy, and inform constructive, positive change worldwide. The Lancet Gastroenterology & Hepatology publishes papers that reflect the rich variety of ongoing clinical research in these fields, especially in the areas of inflammatory bowel diseases, NAFLD and NASH, functional gastrointestinal disorders, digestive cancers, and viral hepatitis.
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