Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, California.
Library, University of Arkansas for Medical Sciences, Little Rock.
JAMA Netw Open. 2022 Jun 1;5(6):e2214885. doi: 10.1001/jamanetworkopen.2022.14885.
Maternal depression is frequently reported in the postpartum period, with an estimated prevalence of approximately 15% during the first postpartum year. Despite the high prevalence of postpartum depression, there is no consensus regarding which patient-reported outcome measure (PROM) should be used to screen for this complex, multidimensional construct.
To evaluate psychometric measurement properties of existing PROMs of maternal postpartum depression using the Consensus-Based Standards for the Selection of Health Measurement Instruments (COSMIN) guideline and identify the best available patient-reported screening measure.
This systematic review followed the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) reporting guideline. PubMed, CINAHL, Embase, and Web of Science were searched on July 1, 2019, for validated PROMs of postpartum depression, and an additional search including a hand search of references from eligible studies was conducted in June 2021. Included studies evaluated 1 or more psychometric measurement properties of the identified PROMs. A risk-of-bias assessment was performed to evaluate methods of each included study. Psychometric measurement properties of each PROM were rated according to COSMIN criteria. A modified Grading of Recommendations Assessment, Development, and Evaluation approach was used to assess the level of evidence supporting each rating, and a recommendation class (A, recommended for use; B, further research required; or C, not recommended) was given based on the overall quality of each included PROM.
Among 10 264 postpartum recovery studies, 27 PROMs were identified. Ten PROMs (37.0%) met the inclusion criteria and were used in 43 studies (0.4%) involving 22 095 postpartum women. At least 1 psychometric measurement property was assessed for each of the 10 validated PROMs identified. Content validity was sufficient in all PROMs. The Edinburgh Postnatal Depression Scale (EPDS) demonstrated adequate content validity and a moderate level of evidence for sufficient internal consistency (with sufficient structural validity), resulting in a recommendation of class A. The other 9 PROMs evaluated received a recommendation of class B.
The findings of this systematic review suggest that the EPDS is the best available patient-reported screening measure of maternal postpartum depression. Future studies should focus on evaluating the cross-cultural validity, reliability, and measurement error of the EPDS to improve understanding of its psychometric properties and utility.
产后期间经常报告产妇抑郁,估计产后第一年的患病率约为 15%。尽管产后抑郁症的患病率很高,但对于应该使用哪种患者报告的结果测量(PROM)来筛查这种复杂的多维结构,尚无共识。
使用共识基础的健康测量仪器选择标准(COSMIN)指南评估现有的产妇产后抑郁症 PROM 的心理测量学特性,并确定最佳的可用患者报告的筛查措施。
本系统评价遵循系统评价和荟萃分析的首选报告项目(PRISMA)报告指南。2019 年 7 月 1 日,在 PubMed、CINAHL、Embase 和 Web of Science 上搜索了经过验证的产后抑郁症 PROM,并在 2021 年 6 月进行了包括从合格研究中手动搜索参考文献的额外搜索。纳入的研究评估了所确定的 PROM 中的 1 种或多种心理测量学特性。对每个纳入研究的方法进行了风险偏倚评估。根据 COSMIN 标准对每个 PROM 的心理测量学特性进行了评分。使用修改后的推荐评估、制定和评估方法对支持每个评分的证据水平进行了评估,并根据每个纳入的 PROM 的整体质量给出了推荐类别(A,建议使用;B,需要进一步研究;或 C,不建议)。
在 10 264 项产后恢复研究中,确定了 27 种 PROM。10 种 PROM(37.0%)符合纳入标准,并在 43 项涉及 22 095 名产后妇女的研究中使用。在所确定的 10 种经过验证的 PROM 中,每种 PROM 都评估了至少 1 种心理测量学特性。所有 PROM 的内容效度都足够。爱丁堡产后抑郁量表(EPDS)在内容效度方面表现良好,具有足够的内部一致性(结构效度适度),证据水平适中,因此建议使用 A 级。其他 9 种 PROM 的评估结果建议使用 B 级。
本系统评价的结果表明,EPDS 是目前可用于筛查产妇产后抑郁症的最佳患者报告的筛查措施。未来的研究应侧重于评估 EPDS 的跨文化有效性、可靠性和测量误差,以提高对其心理测量特性和实用性的理解。