Neurodevelopmental outcomes at 2 years in children who received sildenafil therapy in utero: The STRIDER randomised controlled trial

Author:

Sharp Andrew12ORCID,Cornforth Christine13,Jackson Richard3,Harrold Jane3,Turner Mark A.12,Kenny Louise C.1,Baker Philip N.4,Johnstone Edward D.5,Khalil Asma67ORCID,von Dadelszen Peter8ORCID,Papageorghiou Aris T.67,Alfirevic Zarko12,Vollmer Brigitte91011,

Affiliation:

1. Department of Women's and Children's Health University of Liverpool Liverpool UK

2. Liverpool Women's Hospital NHS Foundation Trust Liverpool UK

3. Liverpool Clinical Trials Unit University of Liverpool Liverpool UK

4. College of Life Sciences University of Leicester Leicester UK

5. Faculty of Medicine Biology and Health, Maternal and Fetal Health Research Centre, School of Medical Sciences University of Manchester Manchester UK

6. Fetal Medicine Unit, St George's Hospital University of London London UK

7. Vascular Biology Research Centre, Molecular and Clinical Sciences Research Institute St George's University of London London UK

8. Department of Women's and Children's Health, School of Life Course and Population Sciences King's College London London UK

9. Clinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine University of Southampton Southampton UK

10. Paediatric Neurology, Southampton Children's Hospital University Hospitals Southampton NHS Foundation Trust Southampton UK

11. Department of Women's and Children's Health Karolinska Institutet Stockholm Sweden

Abstract

AbstractObjectiveSevere early‐onset fetal growth restriction (FGR) causes stillbirth, neonatal death and neurodevelopmental impairment. Poor maternal spiral artery remodelling maintains vasoactive responsiveness but is susceptible to treatment with sildenafil, a phosphodiesterase type 5 (PDE5) inhibitor, which may improve perinatal outcomes.DesignSuperiority, double‐blind randomised controlled trial.SettingA total of 20 UK fetal medicine units.PopulationPregnancies affected by FGR, defined as an abdominal circumference below the tenth centile with absent end‐diastolic flow in the umbilical artery between 22+0 and 29+6 weeks of gestation.MethodsTreatment with sildenafil (25 mg three times/day) or placebo until delivery or 32 weeks of gestation.Main outcome measuresAll infants alive at hospital discharge were assessed for cardiovascular function and cognitive, speech/language and neuromotor impairment at 2 years of age. The primary outcome was survival without cerebral palsy or neurosensory impairment, or a Bayley‐III composite score of >85.ResultsIn total, 135 women were randomised between November 2014 and July 2016 (70 to sildenafil and 65 to placebo). We previously published that there was no improvement in time to delivery or perinatal outcomes with sildenafil. In all, 75 babies (55.5%) were discharged alive, with 61 infants eligible for follow‐up (32 sildenafil and 29 placebo). One infant died (placebo), three mothers declined and ten mothers were uncontactable. There was no difference in neurodevelopment or blood pressure following treatment with sildenafil. Infants who received sildenafil had a larger head circumference at 2 years of age (median difference 49.2 cm, IQR 46.4–50.3, vs 47.2 cm, 95% CI 44.7–48.9 cm).ConclusionsSildenafil therapy did not prolong pregnancy or improve perinatal outcomes and did not improve infant neurodevelopment in FGR survivors. Therefore, sildenafil should not be prescribed for this condition.

Publisher

Wiley

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