低分子肝素与阿司匹林治疗妊娠期血栓形成及对凝血功能影响的meta分析。

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Discovery medicine Pub Date : 2023-04-01 DOI:10.24976/Discov.Med.202335175.11
Meng Yin, Xiaosong Qin
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引用次数: 0

摘要

背景:目前临床还没有对低分子肝素(LMWH)治疗妊娠期血栓形成的疗效和安全性进行综合评价。本研究旨在系统评价低分子肝素对患者的治疗效果及对凝血功能的影响,为妊娠期血栓形成的临床治疗及预后评价提供参考。方法:采用PubMed、Web of Science、Embase数据库以及中国国家知识基础设施数据库和万方数据库进行数据检索。对低分子肝素治疗妊娠期血栓形成的疗效进行了比较研究。采用Stata 16.0软件(Stata, College Station, TX, USA)进行meta分析。结果:共检索相关文献487篇,最终纳入14项研究。低分子肝素联合低剂量阿司匹林组患者的活产率显著高于阿司匹林或低分子肝素治疗组(or(优势比)= 4.54,95% CI(可信区间):2.76,7.45)。低分子肝素联合低剂量阿司匹林组不良反应发生率低于阿司匹林或低分子肝素治疗组(or = 0.40, 95% CI: 0.29, 0.56)。治疗后,低分子肝素联合低剂量阿司匹林组患者的d -二聚体(SMD(标准化平均差异)= -1.50,95% CI: -2.19, 0.80)和血小板计数(PLT;SMD = -0.13, 95% CI: -0.35, 0.09)高于阿司匹林或低分子肝素治疗组。然而,活化的部分凝血活素时间(APTT;SMD = 0.16, 95% CI: -0.10, 0.42),凝血酶时间(TT;SMD = 0.60, 95% CI: -0.14, 1.34),血浆凝血酶原时间(PT;SMD = 0.42, 95% CI: -0.71, 1.56)和纤维蛋白值(FIB;低分子肝素联合低剂量阿司匹林组的SMD = -0.92, 95% CI: -2.12, 0.28)显著高于阿司匹林或低分子肝素治疗组。结论:低分子肝素联合小剂量阿司匹林可有效纠正孕妇凝血功能,改善血栓形成前状态,提高活产率,具有较高的临床价值。
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Meta-Analysis of the Efficacy of Low Molecular Weight Heparin and Aspirin in the Treatment of Thrombosis During Pregnancy and Effects on Coagulation Function.

Background: At present, there is no comprehensive evaluation of the efficacy and safety of low molecular weight heparin (LMWH) for the treatment of thrombophilia during pregnancy in clinical practice. This study aimed to systematically evaluate the efficacy of LMWH in the treatment of patients and its effects on coagulation function, thereby providing a reference for the clinical treatment and prognosis evaluation of thrombophilia during pregnancy.

Methods: Database PubMed, Web of Science and Embase as well as China National Knowledge Infrastructure and Wanfang Database were applied for the search of data. A comparative study on the efficacy of LMWH in the treatment of gestational thrombophilia was enrolled. Stata 16.0 software (Stata, College Station, TX, USA) was utilized to conduct the meta-analysis.

Results: A total of 487 relevant articles were retrieved and 14 studies were finally included. Patients in the LMWH combined with the low-dose aspirin group had a significantly higher live birth rate than those in the aspirin or LMWH treat group (OR (odds ratio) = 4.54, 95% CI (confidence interval): 2.76, 7.45). The adverse effects rate was lower in the LMWH combined with the low-dose aspirin group than in the aspirin or LMWH treatment group (OR = 0.40, 95% CI: 0.29, 0.56). After treatment, patients in the LMWH combined with the low-dose aspirin group had significantly lower D-dimer (SMD (standardized mean differences) = -1.50, 95% CI: -2.19, 0.80) and platelet count (PLT; SMD = -0.13, 95% CI: -0.35, 0.09) than those in the aspirin or LMWH treatment group. However, activated partial thromboplastin time (APTT; SMD = 0.16, 95% CI: -0.10, 0.42), thrombin time (TT; SMD = 0.60, 95% CI: -0.14, 1.34), plasma prothrombin time (PT; SMD = 0.42, 95% CI: -0.71, 1.56), and fibrin values (FIB; SMD = -0.92, 95% CI: -2.12, 0.28) were significantly higher in the LMWH combined with low-dose aspirin group than those in the aspirin or LMWH treatment group.

Conclusions: LMWH heparin combined with low-dose aspirin can effectively correct coagulation function in pregnant women, improve prothrombotic state and increase the live birth rate, which has high clinical value.

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来源期刊
Discovery medicine
Discovery medicine MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
5.40
自引率
0.00%
发文量
80
审稿时长
6-12 weeks
期刊介绍: Discovery Medicine publishes novel, provocative ideas and research findings that challenge conventional notions about disease mechanisms, diagnosis, treatment, or any of the life sciences subjects. It publishes cutting-edge, reliable, and authoritative information in all branches of life sciences but primarily in the following areas: Novel therapies and diagnostics (approved or experimental); innovative ideas, research technologies, and translational research that will give rise to the next generation of new drugs and therapies; breakthrough understanding of mechanism of disease, biology, and physiology; and commercialization of biomedical discoveries pertaining to the development of new drugs, therapies, medical devices, and research technology.
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