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非药物干预措施降低产后疲劳有效性的系统评价方案

Effectiveness of non-pharmacological interventions for reducing postpartum fatigue: a systematic review protocol.

机构信息

School of Nursing, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.

Department of Obstetrics, Zhejiang University School of Medicine Women's Hospital, Hangzhou, Zhejiang, China.

出版信息

BMJ Open. 2021 Oct 25;11(10):e051136. doi: 10.1136/bmjopen-2021-051136.

Abstract

INTRODUCTION

Postpartum fatigue is a common symptom among new mothers after their pregnancy. It has a considerable negative impact on women's functional and mental status as well as the development of babies. Identifying effective interventions to prevent or reduce postpartum fatigue is meaningful to improve the quality of life and avoid adverse outcomes of this vulnerable population. This systematic review aims to synthesise non-pharmacological evidence and evaluate the effectiveness of interventions for reducing postpartum fatigue among puerperas.

METHODS AND ANALYSIS

This review will be conducted in accordance with the Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols. We will systematically search the Cochrane Library, PubMed, Embase, Web of Science, PsycINFO, CINAHL and ProQuest databases to identify clinical trials implementing non-pharmacological interventions conducted during 0-78 weeks postpartum for fatigue reduction. An additional search of OpenGrey will be conducted to identify grey literature. The search will be performed on 30 March 2021 without restrictions on time and language. Two independent reviewers will be responsible for study selection, data extraction and study quality assessment. The Cochrane risk-of-bias tool will be adopted to evaluate the risk biases of the included randomised controlled trials, and the Risk of Bias in Non-randomised Studies of Interventions will be applied to evaluate non-randomised controlled trials. Any disagreements will be referred to a third reviewer to reach a consensus. Findings will be qualitatively synthesised, and a meta-analysis will be conducted for the statistical combination if outcome data are sufficient and available.

ETHICS AND DISSEMINATION

This systematic review will not involve the collection of primary data and will be based on published data. Therefore, ethics approval is not required. The final findings will be disseminated through peer-reviewed journals and academic conferences.

PROSPERO REGISTRATION NUMBER

CRD42021234869.

摘要

简介

产后疲劳是产妇产后常见的症状。它对女性的功能和精神状态以及婴儿的发育都有相当大的负面影响。确定预防或减轻产后疲劳的有效干预措施,对于提高生活质量和避免这一弱势群体的不良后果具有重要意义。本系统评价旨在综合非药物干预措施的证据,并评估其对减少产妇产后疲劳的效果。

方法与分析

本综述将按照系统评价和荟萃分析报告标准进行。我们将系统地检索 Cochrane 图书馆、PubMed、Embase、Web of Science、PsycINFO、CINAHL 和 ProQuest 数据库,以确定在产后 0-78 周期间实施非药物干预措施以减轻疲劳的临床试验。还将对 OpenGrey 进行额外的检索,以确定灰色文献。检索将于 2021 年 3 月 30 日进行,不限制时间和语言。两名独立的审查员将负责研究选择、数据提取和研究质量评估。将采用 Cochrane 偏倚风险工具评估纳入的随机对照试验的偏倚风险,并采用干预措施非随机对照研究的偏倚风险评估非随机对照试验。任何分歧都将提交给第三位评审员以达成共识。如果结果数据足够且可用,将进行定性综合,并进行荟萃分析进行统计组合。

伦理与传播

本系统评价不会涉及原始数据的收集,而是基于已发表的数据。因此,不需要伦理批准。最终结果将通过同行评议的期刊和学术会议进行传播。

PROSPERO 注册号:CRD42021234869。

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