Effectiveness of non-pharmacological interventions to prevent anemia in pregnant women: a quantitative systematic review protocol.

IF 1.5 Q3 HEALTH CARE SCIENCES & SERVICES JBI evidence synthesis Pub Date : 2024-06-01 DOI:10.11124/JBIES-23-00081
Qiongai Jin, Mikiko Shimizu, Masato Sugiura, Yumi Akashi, Keisuke Iwase, Hironori Tsuzuki, Noriko Suzuki, Tomoko Tanaka, Yukie Kitamura, Miyae Yamakawa
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Abstract

Objective: This review will identify the effectiveness of non-pharmacological interventions in preventing iron deficiency anemia in pregnant women with a normal course of pregnancy.

Introduction: The global prevalence of anemia among pregnant women is 36.5%, posing risks to women and fetuses. This underscores the need for effective prevention; however, the effectiveness of non-pharmacological approaches in preventing pregnancy anemia remains unclear.

Inclusion criteria: This review will encompass experimental and quasi-experimental studies on the following approaches to prevent anemia during pregnancy: recommendations for dietary supplements, oral iron supplements (over the counter), provision of supplements to promote iron absorption, participation in anemia prevention education, and provision of information. There will be no restrictions on the duration or frequency of intervention, and longitudinal intervention studies will be included. In studies with a control group, the comparator may be usual care or pharmacological interventions; in studies without, it may involve no intervention, temporal comparisons, or baseline periods without non-pharmacological interventions. Evaluation of hemoglobin, hematocrit, and ferritin will be included as primary outcomes. Low birth weight, preterm birth, amount of blood loss at delivery, small for gestational age, and Apgar scores will be included as secondary outcomes.

Methods: A search will be conducted in MEDLINE (Ovid), Embase, CINAHL (EBSCOhost), Scopus, Australian New Zealand Clinical Trials Registry, Cochrane Central Register of Controlled Trials, and ICHUSHI-Web. Researchers will screen studies, extract data, assess the quality of studies, and analyze the data in accordance with the JBI guidance for systematic reviews of effectiveness. The Grading of Recommendations, Assessment, Development and Evaluation approach will be used to assess the certainty of the findings.

Review registration: PROSPERO CRD42022344155.

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预防孕妇贫血的非药物干预措施的有效性:定量系统综述方案。
目的:本综述旨在确定非药物干预措施在预防正常妊娠妇女缺铁性贫血方面的有效性:本综述旨在确定非药物干预措施对预防孕期正常的孕妇缺铁性贫血的有效性:全球孕妇贫血患病率为 36.5%,这对妇女和胎儿都构成了风险。这凸显了有效预防的必要性;然而,非药物疗法在预防妊娠贫血方面的有效性仍不明确:本综述将包括有关以下预防孕期贫血方法的实验和准实验研究:推荐膳食补充剂、口服铁补充剂(非处方药)、提供促进铁吸收的补充剂、参与贫血预防教育和提供信息。对干预的持续时间或频率没有限制,并将纳入纵向干预研究。在有对照组的研究中,比较对象可以是常规护理或药物干预;在没有对照组的研究中,比较对象可以是无干预、时间比较或无非药物干预的基线期。血红蛋白、血细胞比容和铁蛋白的评估将作为主要结果。低出生体重、早产、分娩失血量、胎龄小和阿普加评分将作为次要结果:方法:将对 MEDLINE (Ovid)、Embase、CINAHL (EBSCOhost)、Scopus、澳大利亚-新西兰临床试验注册中心、Cochrane 对照试验中央注册中心和 ICHUSHI-Web 进行检索。研究人员将筛选研究、提取数据、评估研究质量,并根据 JBI 的有效性系统回顾指南分析数据。将使用 GRADE 评估研究结果的确定性:ProCORMBERCO CRD42022344155.
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JBI evidence synthesis
JBI evidence synthesis Nursing-Nursing (all)
CiteScore
4.50
自引率
3.70%
发文量
218
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