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孕期皮下注射肝素的给药方法。

Methods for administering subcutaneous heparin during pregnancy.

作者信息

Sasaki Hatoko, Yonemoto Naohiro, Hanada Nobutsugu, Mori Rintaro

机构信息

Department of Health Policy, National Center for Child Health and Development, Tokyo, Japan.

出版信息

Cochrane Database Syst Rev. 2013 Mar 28;2013(3):CD009136. doi: 10.1002/14651858.CD009136.pub2.

Abstract

BACKGROUND

Pregnant women with a history of venous thromboembolism (VTE), antithrombin deficiency, or other risk factors for VTE, need heparin (unfractionated heparin (UFH) or low-molecular weight heparin (LMWH)) prophylaxis, mainly through administering subcutaneously. Several methods of administering heparin (UFH or LMWH) subcutaneously have been introduced to prevent adverse pregnant outcomes. The effectiveness and safety of different methods administering subcutaneous heparin (UFH or LMWH) during pregnancy have not been systematically evaluated.

OBJECTIVES

To compare the effectiveness and safety of different methods of administering subcutaneous heparin (UFH or LMWH) to pregnant women.

SEARCH METHODS

We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (31 January 2013) and reference lists of retrieved studies.

SELECTION CRITERIA

All randomised controlled trials (individual and cluster) comparing the effectiveness and safety of different methods of administering subcutaneous heparin (UFH or LMWH) during pregnancy. Studies reported only as abstracts were eligible for inclusion and would have been placed in studies awaiting assessment, pending the full publication of their results. Quasi-randomised studies and cross-over trials were not eligible for inclusion..Methods of administering subcutaneous heparin include intermittent injections versus indwelling catheters or programmable (auto) external infusion pumps, or any other devices to facilitate the subcutaneous administration of heparin (UFH or LMWH) during pregnancy.

DATA COLLECTION AND ANALYSIS

If eligible trials had been identified, trial quality would have been assessed and data extracted, unblinded by review authors independently.

MAIN RESULTS

No trials met the inclusion criteria for the review.

AUTHORS' CONCLUSIONS: There is no evidence from randomised controlled trials to evaluate the effectiveness and safety of different methods of administering subcutaneous heparin (UFH or LMWH) to pregnant women.

摘要

背景

有静脉血栓栓塞(VTE)病史、抗凝血酶缺乏或其他VTE危险因素的孕妇,需要使用肝素(普通肝素(UFH)或低分子肝素(LMWH))进行预防,主要通过皮下注射给药。已经引入了几种皮下注射肝素(UFH或LMWH)的方法来预防不良妊娠结局。孕期不同皮下注射肝素(UFH或LMWH)方法的有效性和安全性尚未得到系统评估。

目的

比较不同皮下注射肝素(UFH或LMWH)方法对孕妇的有效性和安全性。

检索方法

我们检索了Cochrane妊娠与分娩组试验注册库(2013年1月31日)以及检索到的研究的参考文献列表。

选择标准

所有比较孕期不同皮下注射肝素(UFH或LMWH)方法的有效性和安全性的随机对照试验(个体和整群)。仅以摘要形式报道的研究符合纳入标准,在其结果全文发表之前,将被纳入等待评估的研究中。半随机研究和交叉试验不符合纳入标准。皮下注射肝素的方法包括间歇注射与留置导管或可编程(自动)外部输液泵,或任何其他便于孕期皮下注射肝素(UFH或LMWH)的装置。

数据收集与分析

如果确定了符合条件的试验,将由综述作者独立评估试验质量并提取数据,不设盲。

主要结果

没有试验符合该综述的纳入标准。

作者结论

随机对照试验中没有证据可用于评估不同皮下注射肝素(UFH或LMWH)方法对孕妇的有效性和安全性。

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