Resumption of anticoagulant therapy after anticoagulant-related gastrointestinal bleeding: A systematic review and meta-analysis

被引:45
|
作者
Little, D. [1 ]
Chai-Adisaksopha, C. [1 ]
Hillis, C. [2 ]
Witt, D. M. [3 ]
Monreal, M. [4 ]
Crowther, M. A. [1 ]
Siegal, D. M. [1 ]
机构
[1] McMaster Univ, Dept Med, 1280 Main St W, Hamilton, ON L8S 4L8, Canada
[2] McMaster Univ, Dept Oncol, 1280 Main St W, Hamilton, ON L8S 4L8, Canada
[3] Univ Utah, Dept Pharmacotherapy, 201 Presidents Circle, Salt Lake City, UT 84112 USA
[4] Hosp Badalona Germans Trias & Pujol, Dept Internal Med, Carretera Canyet S-N, Barcelona 08916, Spain
关键词
Anticoagulants; Gastrointestinal hemorrhage; Hemorrhage; Thromboembolism; Thrombosis; ATRIAL-FIBRILLATION; VENOUS THROMBOEMBOLISM; ANTITHROMBOTIC THERAPY; WARFARIN; STROKE; RISK; INTERRUPTION; MANAGEMENT; MORTALITY; EVENTS;
D O I
10.1016/j.thromres.2019.01.020
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Oral anticoagulation (OAC) is permanently discontinued in up to 50% of patients following a gastrointestinal (GI) bleed. A previous meta-analysis showed a reduced risk of thromboembolism and death, and a non-statistically significant increased risk of re-bleeding associated with resumption. We conducted an updated meta-analysis to determine the risks of recurrent GI bleeding, thromboembolism, and death in patients who resumed OAC compared to those who did not. Materials and methods: We searched EMBASE, MEDLINE, and the Cochrane Central Register of Controlled Trials for new references from January 2014 to September 2017. Randomized controlled trials and observational studies involving adults with OAC-related GI bleeding were included. Risk of bias was assessed using the Cochrane Collaboration's ROBINS-I tool. Pooled relative risk (RR) ratios were calculated using a random-effects model. Results: We identified 12 observational studies involving 3098 patients. There was an increased risk of recurrent GI bleeding (RR 1.91, 95% CI 1.47-2.48, I-2=0%, 11 studies), and a reduced risk of thromboembolism (RR 0.30, 95% CI 0.13-0.68, I-2=59.8%, 9 studies) and death (RR 0.51, 95% CI 0.38-0.70, I-2=71.8%, 8 studies) in patients who resumed OAC compared to those who did not. Eleven studies were judged to be at serious risk of bias due to confounding. Conclusions: Resuming OAC after OAC-related GI bleeding appears to be associated with an increase in recurrent GI bleeding, but a reduction in thromboembolism and death. Further prospective data are needed to identify patients for whom the net clinical benefit favours OAC resumption and the optimal timing of resumption.
引用
收藏
页码:102 / 109
页数:8
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