Validation of parental recall questionnaire to classify preterm delivery subtypes: Spontaneous preterm labour, preterm premature rupture of membranes and clinician‐initiated preterm delivery

Author:

Rich‐Edwards Janet W.12ORCID,Stuart Jennifer J.12,Becene Iris A.1,Largier Louise F.3,Rexrode Kathryn M.1,Cantonwine David E.3,Carpenter Maribel O.4,McElrath Thomas F.3,Gray Kathryn J.3ORCID

Affiliation:

1. Division of Women's Health, Department of Medicine Brigham and Women's Hospital and Harvard Medical School Boston Massachusetts USA

2. Department of Epidemiology, Harvard T. H. Chan School of Public Health Boston Massachusetts USA

3. Division of Maternal‐Fetal Medicine, Department of Obstetrics and Gynecology Brigham and Women's Hospital, Harvard Medical School Boston Massachusetts USA

4. Middlebury College Middlebury Vermont USA

Abstract

AbstractBackgroundPreterm delivery (PTD) includes three main presenting subtypes: spontaneous preterm labour (sPTL), preterm premature rupture of membranes (pPROM) and clinician‐initiated preterm delivery (ciPTD). PTD subtype data are rarely available from birth registries and are onerous to derive from medical records.ObjectivesTo develop and test the validity of a questionnaire to classify PTD subtype based on birthing parent recall of labour and delivery events.MethodsThe questionnaire was sent in 2022 to 581 patients with PTD history documented in the LIFECODES study, a hospital‐based birth cohort in Boston, Massachusetts. Eighty‐two respondents reported 94 PTDs that could be linked to medical records. Data on PTD subtype were extracted from medical records as the reference standard.ResultsMedical records indicated 47 spontaneous (24 sPTL, 23 pPROM) and 47 ciPTD deliveries occurring a median eight years earlier. The sensitivity and specificity of the recall questionnaire were 88% (95% confidence interval: 68, 97%) and 89% (79, 95%) for sPTL; 96% (78, 100%) and 94% (86, 98%) for pPROM; and 83% (69, 92%) and 100% (92, 100%) for ciPTD, respectively. Greater time since pregnancy did not degrade the sensitivity or specificity of the parental recall questionnaire.ConclusionsAlthough derived from a modest sample, the moderate‐to‐high sensitivity and specificity of the parental recall questionnaire to classify sPTL, pPROM and ciPTD demonstrates its potential for large studies of PTD and for correction of misclassification bias. Future studies are required to test the questionnaire in a variety of populations.

Funder

National Institutes of Health

Publisher

Wiley

Subject

Pediatrics, Perinatology and Child Health,Epidemiology

Reference35 articles.

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