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早期内镜坏死组织清除术或逐步内镜治疗感染性坏死性胰腺炎(DESTIN):一项单盲、多中心、随机试验

Upfront endoscopic necrosectomy or step-up endoscopic approach for infected necrotising pancreatitis (DESTIN): a single-blinded, multicentre, randomised trial.

作者信息

Bang Ji Young, Lakhtakia Sundeep, Thakkar Shyam, Buxbaum James L, Waxman Irving, Sutton Bryce, Memon Sana F, Singh Shailendra, Basha Jahangeer, Singh Ajay, Navaneethan Udayakumar, Hawes Robert H, Wilcox Charles M, Varadarajulu Shyam

机构信息

Digestive Health Institute, Orlando Health, Orlando, FL, USA.

Asian Institute of Gastroenterology Hospitals, Hyderabad, India.

出版信息

Lancet Gastroenterol Hepatol. 2024 Jan;9(1):22-33. doi: 10.1016/S2468-1253(23)00331-X. Epub 2023 Nov 18.

DOI:10.1016/S2468-1253(23)00331-X
PMID:37980922
Abstract

BACKGROUND

Although the preferred management approach for patients with infected necrotising pancreatitis is endoscopic transluminal stenting followed by endoscopic necrosectomy as step-up treatment if there is no clinical improvement, the optimal timing of necrosectomy is unclear. Therefore, we aimed to compare outcomes between performing upfront necrosectomy at the index intervention versus as a step-up measure in patients with infected necrotising pancreatitis.

METHODS

This single-blinded, multicentre, randomised trial (DESTIN) was done at six tertiary care hospitals (five hospitals in the USA and one hospital in India). We enrolled patients (aged ≥18 years) with confirmed or suspected infected necrotising pancreatitis with a necrosis extent of at least 33% who were amenable to endoscopic ultrasound-guided drainage. By use of computer-generated permuted block randomisation (block size four), eligible patients were randomly assigned (1:1) to receive either upfront endoscopic necrosectomy or endoscopic step-up treatment. Endoscopists were not masked to treatment allocation, but participants, research coordinators, and the statistician were. Lumen-apposing metal stents (20 mm diameter; 10 mm saddle length) were used for drainage in both groups. In the upfront group, direct necrosectomy was performed immediately after stenting in the same treatment session. In the step-up group, direct necrosectomy or additional drainage was done at a subsequent treatment session if there was no clinical improvement (resolution of any criteria of systemic inflammatory response syndrome or sepsis or one or more organ failure and at least a 25% percentage decrease in necrotic collection size) 72 h after stenting. The primary outcome was the number of reinterventions per patient to achieve treatment success from index intervention to 6 months' follow-up, which was defined as symptom relief in conjunction with disease resolution on CT. Reinterventions included any endoscopic or radiological procedures performed for necrosectomy or additional drainage after the index intervention, excluding the follow-up procedure at 4 weeks for stent removal. All endpoints and safety were analysed by intention-to-treat. This study is registered with ClinicalTrials.gov, NCT05043415 and NCT04113499, and recruitment and follow-up have been completed.

FINDINGS

Between Nov 27, 2019, and Oct 26, 2022, 183 patients were assessed for eligibility and 70 patients (24 [34%] women and 46 [66%] men) were randomly assigned to receive upfront necrosectomy (n=37) or step-up treatment (n=33) and included in the intention-to-treat population. At the time of index intervention, seven (10%) of 70 patients had organ failure and 64 (91%) patients had walled-off necrosis. The median number of reinterventions was significantly lower for upfront necrosectomy (1 [IQR 0 to 1] than for the step-up approach (2 [1 to 4], difference -1 [95% CI -2 to 0]; p=0·0027). Mortality did not differ between groups (zero patients in the upfront necrosectomy group vs two [6%] in the step-up group, difference -6·1 percentage points [95% CI -16·5 to 4·5]; p=0·22), nor did overall disease-related adverse events (12 [32%] patients in the upfront necrosectomy group vs 16 [48%] patients in the step-up group, difference -16·1 percentage points [-37·4 to 7·0]; p=0·17), nor procedure-related adverse events (four [11%] patients in the upfront necrosectomy group vs eight [24%] patients in the step-up group, difference -13·4 percentage points [-30·8 to 5·0]; p=0·14).

INTERPRETATION

In stabilised patients with infected necrotising pancreatitis and fully encapsulated collections, an approach incorporating upfront necrosectomy at the index intervention rather than as a step-up measure could safely reduce the number of reinterventions required to achieve treatment success.

FUNDING

None.

摘要

背景

尽管对于感染性坏死性胰腺炎患者,首选的治疗方法是内镜腔内支架置入术,若临床症状无改善则采用内镜坏死组织清除术作为逐步升级的治疗,但坏死组织清除术的最佳时机尚不清楚。因此,我们旨在比较在初次干预时直接进行坏死组织清除术与在感染性坏死性胰腺炎患者中作为逐步升级措施进行坏死组织清除术的疗效。

方法

这项单盲、多中心、随机试验(DESTIN)在六家三级医疗机构(美国的五家医院和印度的一家医院)进行。我们纳入了年龄≥18岁、确诊或疑似感染性坏死性胰腺炎且坏死范围至少达33%、适合内镜超声引导下引流的患者。通过计算机生成的置换区组随机化(区组大小为4),符合条件的患者被随机分配(1:1)接受直接内镜坏死组织清除术或内镜逐步升级治疗。内镜医师不了解治疗分配情况,但参与者、研究协调员和统计学家了解。两组均使用管腔贴附金属支架(直径20mm;鞍长10mm)进行引流。在直接手术组中,支架置入后在同一治疗环节立即进行直接坏死组织清除术。在逐步升级组中,如果在支架置入72小时后没有临床改善(全身炎症反应综合征或脓毒症的任何标准得到缓解或一个或多个器官功能衰竭且坏死灶大小至少减少25%),则在后续治疗环节进行直接坏死组织清除术或额外引流。主要结局是从初次干预到6个月随访期间每位患者为实现治疗成功所需的再次干预次数,治疗成功定义为症状缓解且CT显示疾病消退相结合。再次干预包括初次干预后为进行坏死组织清除术或额外引流而进行的任何内镜或放射学操作,但不包括4周时取出支架的随访操作。所有终点和安全性均采用意向性分析。本研究已在ClinicalTrials.gov注册,注册号为NCT05043415和NCT04113499,招募和随访工作已完成。

研究结果

2019年11月27日至2022年10月26日期间,183例患者接受了资格评估,70例患者(24例[34%]女性和46例[66%]男性)被随机分配接受直接坏死组织清除术(n = 37)或逐步升级治疗(n = 33),并纳入意向性分析人群。在初次干预时,70例患者中有7例(10%)出现器官功能衰竭,64例(91%)患者出现包裹性坏死。直接坏死组织清除术组的再次干预中位数(1[IQR 0至1])显著低于逐步升级治疗组(2[1至4]),差异为−1(95%CI−2至0);p = 0.0027)。两组间死亡率无差异(直接坏死组织清除术组为0例患者,逐步升级治疗组为2例[6%]患者,差异为−6.1个百分点[95%CI−16.5至4.5];p = 0.22),总体疾病相关不良事件也无差异(直接坏死组织清除术组为12例[32%]患者,逐步升级治疗组为16例[48%]患者,差异为−16.1个百分点[−37.4至7.0];p = 0.17),手术相关不良事件也无差异(直接坏死组织清除术组为4例[11%]患者,逐步升级治疗组为8例[24%]患者,差异为−13.4个百分点[−30.8至5.0];p = 0.14)。

解读

对于病情稳定的感染性坏死性胰腺炎患者且有完全包裹性坏死灶,在初次干预时采用直接坏死组织清除术而非逐步升级措施的方法可以安全地减少实现治疗成功所需的再次干预次数。

资金来源

无。

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