4.2 Article

Development and validation across trimester of the Prenatal Eating Behaviors Screening tool

期刊

ARCHIVES OF WOMENS MENTAL HEALTH
卷 25, 期 4, 页码 705-716

出版社

SPRINGER WIEN
DOI: 10.1007/s00737-022-01230-y

关键词

Pregnancy; Psychometrics; Mental health; Feeding and eating disorders; Pregnancy trimesters; Reproducibility of results; Anorexia nervosa; Bulimia nervosa; Binge eating disorder

资金

  1. Ophelia Fund/Rhode Island Foundation
  2. National Institute of General Medical Sciences of the National Institutes of Health [5U54GM104942-05]

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This study developed a rapid screening tool for eating disorders in pregnant women and found that the tool with 12 questions can reliably and sensitively detect eating disorders across pregnancy trimesters.
Rapid screening tools are useful for identifying at-risk patients and referring them for further assessment and treatment, but none exist that consider the unique medical needs of pregnant women with eating disorders (EDs). There is a need for a rapid, sensitive, and specific screening tool that can be used to identify a potential ED in pregnancy. We started with a set of 25 questions, developed from our qualitative work along with other ED screening tools, and tested on a development (n = 190) and validation sample (n = 167). Statistical analysis included factor analysis and logistic regressions with ROC curves. Development and validation samples were combined for trimester analysis (n = 357). Refining the tool to 12 items demonstrated strong internal reliability (development alpha = 0.95, validation alpha = 0.91). With correlated errors, questions demonstrated acceptable CFA fit (development: GFI: 0.91, RMSEA: 0.10, NNFI: 0.95; validation: GFI: 0.85, RMSEA: 0.14, NNFI: 0.86). Similar fits were seen by trimester: first trimester n = 127, GFI: 0.89, RMSEA: 0.12, NNFI: 0.94; second trimester n = 150, GFI: 0.83, RMSEA: 0.14, NNFI: 0.88; third trimester n = 80, GFI: 0.99, NNFI: 0.99. Validation against current ED diagnosis demonstrated acceptable sensitivity and specificity using a cutoff of 39 (development sensitivity = 80.7%, specificity = 79.7%, OR = 16.42, 95% CI: 7.51, 35.88; validation sensitivity = 69.2%, specificity = 86.5%, OR: 17.43, 95% CI: 6.46, 47.01). Findings suggest the PEBS tool can reliably and sensitively detect EDs across pregnancy trimesters with 12 questions. A further implication of this work is to reduce health and mental health treatment disparities through this standard and rapid screening measure to ensure early identification and treatment.

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