Department of Medical Science and Public Health, University of Cagliari, Cagliari, Italy.
Department of Anesthesia, Resuscitation and Pain Therapy, University of Cagliari, Cagliari, Italy.
Lung. 2023 Apr;201(2):135-147. doi: 10.1007/s00408-023-00599-6. Epub 2023 Feb 4.
International COVID-19 guidelines recommend thromboprophylaxis for non-critically ill inpatients to prevent thrombotic complications. It is still debated whether full-dose thromboprophylaxis reduces all-cause mortality. The main aim of this updated systematic review and meta-analysis is to evaluate the effect of full-dose heparin-based thromboprophylaxis on survival in hospitalized non-critically ill COVID-19 patients.
A systematic review was performed across Pubmed/Medline, EMBASE, Cochrane Central Register of clinical trials, Clinicaltrials.gov, and medRxiv.org from inception to November 2022. We conducted a meta-analysis of randomized clinical trials (RCTs) comparing full-dose heparin-based anticoagulation to prophylactic or intermediate dose anticoagulation or standard treatment in hospitalized non-critically ill COVID-19 patients. The risk of bias was assessed using the Cochrane risk-of-bias tool for randomized trials and Grading of Recommendations Assessment, Development and Evaluation was applied. The primary outcome was all-cause mortality at the longest follow-up available.
We identified 6 multicenter RCTs involving 3297 patients from 13 countries across 4 continents. The rate of all-cause mortality was 6.2% (103/1662) in the full-dose group vs 7.7% (126/1635) in the prophylactic or intermediate dose group (Risk Ratio [RR] = 0.76; 95% confidence interval [CI] = 0.59-0.98; P = 0.037). The probabilities of any mortality difference and of NNT ≤ 100 were estimated at 98.2% and 84.5%, respectively. The risk of bias was low for all included RCTs and the strength of the evidence was "moderate."
Our meta-analysis of high-quality multicenter RCTs suggests that full-dose anticoagulation with heparin or low molecular weight heparin reduces all-cause mortality in hospitalized non-critically ill COVID-19 patients.
PROSPERO, review no. CRD42022348993.
国际 COVID-19 指南建议对非危重症住院患者进行血栓预防,以预防血栓并发症。全剂量血栓预防是否降低全因死亡率仍存在争议。本更新的系统评价和荟萃分析的主要目的是评估全剂量肝素为基础的血栓预防对住院非危重症 COVID-19 患者生存的影响。
从成立到 2022 年 11 月,通过 Pubmed/Medline、EMBASE、Cochrane 临床试验中央注册库、Clinicaltrials.gov 和 medRxiv.org 进行了系统评价。我们对比较全剂量肝素抗凝与预防性或中等剂量抗凝或标准治疗在住院非危重症 COVID-19 患者中的随机临床试验 (RCT) 进行了荟萃分析。使用 Cochrane 随机试验偏倚风险工具评估偏倚风险,并应用推荐评估、制定与评价分级。主要结局是最长随访时间的全因死亡率。
我们确定了来自四大洲 13 个国家的 6 项多中心 RCT,涉及 3297 名患者。全剂量组的全因死亡率为 6.2%(103/1662),预防性或中等剂量组为 7.7%(126/1635)(风险比[RR] = 0.76;95%置信区间[CI] = 0.59-0.98;P = 0.037)。任何死亡率差异的概率和 NNT ≤ 100 的概率分别估计为 98.2%和 84.5%。所有纳入的 RCT 偏倚风险均较低,证据强度为“中等”。
我们对高质量多中心 RCT 的荟萃分析表明,肝素或低分子量肝素的全剂量抗凝可降低住院非危重症 COVID-19 患者的全因死亡率。
PROSPERO,审查编号 CRD42022348993。