Assessment of Patient-Reported Outcome Measures for Maternal Postpartum Depression Using the Consensus-Based Standards for the Selection of Health Measurement Instruments Guideline

Author:

Sultan Pervez1,Ando Kazuo1,Elkhateb Rania2,George Ronald B.3,Lim Grace4,Carvalho Brendan1,Chitneni Ahish5,Kawai Ray6,Tulipan Tanya7,Blake Lindsay8,Coker Jessica9,O’Carroll James1

Affiliation:

1. Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, California

2. Department of Anesthesiology, University of Arkansas for Medical Sciences, Little Rock

3. Department of Anesthesiology, University of California, San Francisco

4. Department of Anesthesiology, University of Pittsburgh, Pittsburgh, Pennsylvania

5. Physical Medicine and Rehabilitation, NewYork–Presbyterian–Columbia and Cornell, New York, New York

6. University of California, Davis

7. Department of Psychiatry, Dalhousie University, Halifax, Nova Scotia, Canada

8. Library, University of Arkansas for Medical Sciences, Little Rock

9. Department of Psychiatry, University of Arkansas for Medical Sciences, Little Rock

Abstract

ImportanceMaternal 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.ObjectiveTo 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.Evidence ReviewThis 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.FindingsAmong 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.Conclusions and RelevanceThe 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.

Publisher

American Medical Association (AMA)

Subject

General Medicine

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