Low versus standard central venous pressure during laparoscopic liver resection: A systematic review, meta-analysis and trial sequential analysis.

IF 1.1 Q4 GASTROENTEROLOGY & HEPATOLOGY Annals of hepato-biliary-pancreatic surgery Pub Date : 2024-05-31 Epub Date: 2024-02-16 DOI:10.14701/ahbps.23-137
Mina Stephanos, Christopher M B Stewart, Ameen Mahmood, Christopher Brown, Shahin Hajibandeh, Shahab Hajibandeh, Thomas Satyadas
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Abstract

To compare the outcomes of low central venous pressure (CVP) to standard CVP during laparoscopic liver resection. The study design was a systematic review following the PRISMA statement standards. The available literature was searched to identify all studies comparing low CVP with standard CVP in patients undergoing laparoscopic liver resection. The outcomes included intraoperative blood loss (primary outcome), need for blood transfusion, mean arterial pressure, operative time, Pringle time, and total complications. Random- effects modelling was applied for analyses. Type I and type II errors were assessed by trial sequential analysis (TSA). A total of 8 studies including 682 patients were included (low CVP group, 342; standard CVP group, 340). Low CVP reduced intraoperative blood loss during laparoscopic liver resection (mean difference [MD], -193.49 mL; 95% confidence interval [CI], -339.86 to -47.12; p = 0.01). However, low CVP did not have any effect on blood transfusion requirement (odds ratio [OR], 0.54; 95% CI, 0.28-1.03; p = 0.06), mean arterial pressure (MD, -1.55 mm Hg; 95% CI, -3.85-0.75; p = 0.19), Pringle time (MD, -0.99 minutes; 95% CI, -5.82-3.84; p = 0.69), operative time (MD, -16.38 minutes; 95% CI, -36.68-3.39; p = 0.11), or total complications (OR, 1.92; 95% CI, 0.97-3.80; p = 0.06). TSA suggested that the meta-analysis for the primary outcome was not subject to type I or II errors. Low CVP may reduce intraoperative blood loss during laparoscopic liver resection (moderate certainty); however, this may not translate into shorter operative time, shorter Pringle time, or less need for blood transfusion. Randomized controlled trials with larger sample sizes will provide more robust evidence.

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腹腔镜肝脏切除术中低中心静脉压与标准中心静脉压的比较:系统综述、荟萃分析和试验序列分析。
比较腹腔镜肝脏切除术中低中心静脉压(CVP)与标准 CVP 的效果。研究设计采用了符合 PRISMA 声明标准的系统性综述。对现有文献进行检索,以确定所有对腹腔镜肝切除术患者进行低中心静脉压与标准中心静脉压比较的研究。结果包括术中失血量(主要结果)、输血需求、平均动脉压、手术时间、普林格尔时间和总并发症。分析采用随机效应模型。通过试验序列分析(TSA)评估了I型和II型误差。共纳入了 8 项研究,包括 682 名患者(低 CVP 组,342 人;标准 CVP 组,340 人)。低 CVP 降低了腹腔镜肝脏切除术的术中失血量(平均差 [MD],-193.49 mL;95% 置信区间 [CI],-339.86 至 -47.12;P = 0.01)。然而,低 CVP 对输血需求(几率比 [OR],0.54;95% CI,0.28-1.03;P = 0.06)、平均动脉压(MD,-1.55 mm Hg;95% CI,-3.85-0.75;P = 0.19)、普林格尔时间(MD,-0.99 分钟;95% CI,-5.82-3.84;P = 0.69)、手术时间(MD,-16.38 分钟;95% CI,-36.68-3.39;P = 0.11)或总并发症(OR,1.92;95% CI,0.97-3.80;P = 0.06)。TSA表明,主要结果的荟萃分析不存在I型或II型错误。低 CVP 可能会减少腹腔镜肝脏切除术中的术中失血(中等确定性);但这可能不会转化为更短的手术时间、更短的 Pringle 时间或更少的输血需求。样本量更大的随机对照试验将提供更可靠的证据。
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