Am J Perinatol 2023; 40(16): 1770-1780
DOI: 10.1055/s-0041-1739504
Original Article

Eligibility, Utilization, and Effectiveness of 17-Alpha Hydroxyprogesterone Caproate in a Statewide Population-Based Cohort of Medicaid Enrollees

Xi Wang
1   PolicyLab, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
,
Stephanie M. Garcia
1   PolicyLab, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
,
Katherine S. Kellom
1   PolicyLab, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
,
Rupsa C. Boelig
2   Department of Obstetrics and Gynecology, Department of Pharmacology and Experimental Therapeutics, Division of Maternal Fetal Medicine, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania
,
Meredith Matone
1   PolicyLab, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
3   University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania
› Institutsangaben

Funding This study has been funded by the Pennsylvania Department of Health Bureau of Family Health.
Preview

Abstract

Objective The primary objective was to estimate the initiation and adherence rates of 17 α-hydroxyprogesterone caproate (17OHPC) among eligible mothers in a statewide population-based cohort of Medicaid enrollees. The secondary objectives were to (1) determine the association of maternal sociodemographic and clinical characteristics with 17OHPC utilization and (2) assess the real-world effectiveness of 17OHPC on recurrent preterm birth prevention and admission to neonatal intensive care unit (NICU).

Study Design This is a retrospective cohort study using a linked, longitudinal administrative dataset of birth certificates and medical assistance claims. Medicaid-enrolled mothers in Pennsylvania were included in this study if they had at least one singleton live birth from 2014 to 2016 following at least one spontaneous preterm birth. Maternal Medicaid claims were used to ascertain the use of 17OHPC from various manufacturers, including compounded formulations. Propensity score matching was used to create a covariate balance between 17OHPC treatment and comparison groups.

Results We identified 4,781 Medicaid-covered 17OHPC-eligible pregnancies from 2014 to 2016 in Pennsylvania, 3.4% of all Medicaid-covered singleton live births. The population-based initiation rate was 28.5% among eligible pregnancies. Among initiators, 50% received ≥16 doses as recommended, while 10% received a single dose only. The severity of previous spontaneous preterm birth was the strongest predictor for the initiation and adherence of 17OHPC. In the matched treatment (n = 1,210) and comparison groups (n = 1,210), we found no evidence of 17OHPC effectiveness. The risks of recurrent preterm birth (relative risk [RR] 1.10, 95% confidence interval [CI] 0.97–1.24) and births admitted to NICU (RR 1.00, 95% CI 0.84–1.18) were similar in treated and comparison mothers.

Conclusion The 17OHPC-eligible population represented 3.4% of singleton live births. Less than one-third of eligible mothers initiated treatment. Among initiators, 50% were treatment adherent. We found no difference in the risk of recurrent preterm birth or admission to NICU between treatment and comparison groups.

Key Points

  • About 3.4% of singleton live births were eligible for 17OHPC.

  • About 30% of eligible mothers initiated treatment.

  • We found no association of 17OHPC with recurrent preterm birth.

Supplementary Material



Publikationsverlauf

Eingereicht: 03. Dezember 2020

Angenommen: 04. Oktober 2021

Artikel online veröffentlicht:
16. November 2021

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