Enrollment of Extremely Low Birth Weight Infants in a Clinical Research Study May Not Be Representative

Author:

Rich Wade1,Finer Neil N.1,Gantz Marie G.2,Newman Nancy S.3,Hensman Angelita M.4,Hale Ellen C.5,Auten Kathy J.6,Schibler Kurt7,Faix Roger G.8,Laptook Abbot R.5,Yoder Bradley A.8,Das Abhik2,Shankaran Seetha9,

Affiliation:

1. University of California at San Diego, San Diego, California;

2. Statistics and Epidemiology Unit, RTI International, Rockville, Maryland;

3. Department of Pediatrics, Rainbow Babies & Children’s Hospital, Case Western Reserve University, Cleveland, Ohio;

4. Department of Pediatrics, Women & Infants Hospital, Brown University, Providence, Rhode Island;

5. Department of Pediatrics, Emory University School of Medicine, and Children’s Healthcare of Atlanta, Atlanta, Georgia;

6. Department of Pediatrics, Duke University, Durham, North Carolina;

7. Department of Pediatrics, Cincinnati Children’s Hospital Medical Center and University of Cincinnati, Cincinnati, Ohio;

8. Department of Pediatrics, Division of Neonatology, University of Utah School of Medicine, Salt Lake City, Utah; and

9. Department of Pediatrics, Wayne State University, Detroit, Michigan

Abstract

BACKGROUND AND OBJECTIVE: The Surfactant Positive Airway Pressure and Pulse Oximetry Randomized Trial (SUPPORT) antenatal consent study demonstrated that mothers of infants enrolled in the SUPPORT trial had significantly different demographics and exposure to antenatal steroids compared with mothers of eligible, but not enrolled infants. The objective of this analysis was to compare the outcomes of bronchopulmonary dysplasia, severe retinopathy of prematurity, severe intraventricular hemorrhage or periventricular leukomalacia (IVH/PVL), death, and death/severe IVH/PVL for infants enrolled in SUPPORT in comparison with eligible, but not enrolled infants. METHODS: Perinatal characteristics and neonatal outcomes were compared for enrolled and eligible but not enrolled infants in bivariate analyses. Models were created to test the effect of enrollment in SUPPORT on outcomes, controlling for perinatal characteristics. RESULTS: There were 1316 infants enrolled in SUPPORT; 3053 infants were eligible, but not enrolled. In unadjusted analyses, enrolled infants had significantly lower rates of death before discharge, severe IVH/PVL, death/severe IVH/PVL (all < 0.001), and bronchopulmonary dysplasia (P = .003) in comparison with eligible, but not enrolled infants. The rate of severe retinopathy of prematurity was not significantly different. After adjustment for perinatal factors, enrollment in the trial was not a significant predictor of any of the tested clinical outcomes. CONCLUSIONS: The results of this analysis demonstrate significant outcome differences between enrolled and eligible but not enrolled infants in a trial using antenatal consent, which were likely due to enrollment bias resulting from the antenatal consent process. Additional research and regulatory review need to be conducted to ensure that large moderate-risk trials that require antenatal consent can be conducted in such a way as to ensure the generalizability of results.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

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