Stephanos Mina, Stewart Christopher M B, Mahmood Ameen, Brown Christopher, Hajibandeh Shahin, Hajibandeh Shahab, Satyadas Thomas
Department of General Surgery, Weston General Hospital, Weston-Super-Mare, UK.
Department of General Surgery, University Hospital of Wales, Cardiff, UK.
Ann Hepatobiliary Pancreat Surg. 2024 May 31;28(2):115-124. doi: 10.14701/ahbps.23-137. Epub 2024 Feb 16.
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; = 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; = 0.06), mean arterial pressure (MD, -1.55 mm Hg; 95% CI, -3.85-0.75; = 0.19), Pringle time (MD, -0.99 minutes; 95% CI, -5.82-3.84; = 0.69), operative time (MD, -16.38 minutes; 95% CI, -36.68-3.39; = 0.11), or total complications (OR, 1.92; 95% CI, 0.97-3.80; = 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.
比较腹腔镜肝切除术中低中心静脉压(CVP)与标准CVP的效果。研究设计为遵循PRISMA声明标准的系统评价。检索现有文献以确定所有比较接受腹腔镜肝切除术患者的低CVP与标准CVP的研究。结局指标包括术中失血量(主要结局)、输血需求、平均动脉压、手术时间、Pringle阻断时间和总并发症。采用随机效应模型进行分析。通过试验序贯分析(TSA)评估I型和II型错误。共纳入8项研究,包括682例患者(低CVP组342例;标准CVP组340例)。低CVP可减少腹腔镜肝切除术中的术中失血量(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(比值比[OR],0.54;95% CI,0.28 - 1.03;P = 0.06)、平均动脉压(MD,-1.55 mmHg;95% CI,-3.85至0.75;P = 0.19)、Pringle阻断时间(MD,-0.99分钟;95% CI,-5.82至3.84;P = 0.69)、手术时间(MD,-16.38分钟;95% CI,-36.68至3.39;P = 0.11)或总并发症(OR,1.92;95% CI,0.97 - 3.80;P = 0.06)均无影响。TSA提示主要结局的Meta分析不受I型或II型错误影响。低CVP可能减少腹腔镜肝切除术中的术中失血量(中等确定性);然而,这可能不会转化为更短手术时间、更短Pringle阻断时间或更少输血需求。样本量更大的随机对照试验将提供更有力的证据。