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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.
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页码:102 / 109
页数:8
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