Literature DB >> 30051971

Antenatal exposure to nonsteroidal anti-inflammatory drugs and risk of neonatal hypertension.

Mounira Habli1,2, Corey C Clifford3,4, Tammy M Brady5, Zahidee Rodriguez6, Michaela Eschenbacher7, Malcolm Wu8, Emily DeFranco9,10, James Gresh8, Beena D Kamath-Rayne9,11.   

Abstract

Nonsteroidal anti-inflammatory drugs (NSAIDs) are used as tocolytics, which are medications that suppress uterine contractions for preterm birth prevention. Their effect on cerebral/systemic vascular beds poses the question of whether antenatal NSAID exposure is associated with neonatal hypertension. We performed a retrospective case-control study in a tertiary neonatal intensive care unit, including 40 hypertension cases (hospitalized neonates ≥ 35 weeks with systolic BP > 100 mm Hg on three consecutive days) compared to 134 controls matched by gestational age at delivery, plurality, and delivery date. Cases and controls were compared by antenatal NSAID exposure, other common tocolytics, and maternal/neonatal characteristics and complications. Multivariable logistic regression was used to estimate the odds of hypertension among those with prenatal exposure to NSAIDs versus those without exposure. Newborns with hypertension had a lower gestational age at delivery and increased incidence of neonatal complications, including respiratory distress syndrome, bronchopulmonary dysplasia, surfactant administration, longer duration of ventilation, and history of umbilical artery catheterization. Days of indomethacin exposure were positively associated with greater odds of neonatal hypertension (OR 1.17 [1.00 to 1.38], P = 0.055), even after adjustment for other factors associated with neonatal hypertension. Newborns with hypertension were less likely to have been exposed to calcium channel blockers as a tocolytic. The results of our study suggest an association between prenatal exposure to nonsteroidal anti-inflammatory drugs and neonatal hypertension. Furthermore, our data suggest that prenatal calcium channel blocker exposure may protect against the development of neonatal hypertension. Future multicenter studies are needed to understand the risks of tocolytics and subsequent consequences in preterm infants. ©2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  NSAIDs; neonatal hypertension; prematurity; tocolytic

Mesh:

Substances:

Year:  2018        PMID: 30051971      PMCID: PMC6135701          DOI: 10.1111/jch.13354

Source DB:  PubMed          Journal:  J Clin Hypertens (Greenwich)        ISSN: 1524-6175            Impact factor:   3.738


  31 in total

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4.  Childhood risk factors for high adult blood pressure: the Muscatine Study.

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Journal:  Pediatrics       Date:  1989-10       Impact factor: 7.124

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Authors:  Anish Pillai; Deepak Sharma; Pratichi Kadam
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Journal:  Curr Med Chem       Date:  2016       Impact factor: 4.530

7.  Resistant hypertension: diagnosis, evaluation, and treatment: a scientific statement from the American Heart Association Professional Education Committee of the Council for High Blood Pressure Research.

Authors:  David A Calhoun; Daniel Jones; Stephen Textor; David C Goff; Timothy P Murphy; Robert D Toto; Anthony White; William C Cushman; William White; Domenic Sica; Keith Ferdinand; Thomas D Giles; Bonita Falkner; Robert M Carey
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Review 8.  Common Substances That May Contribute to Resistant Hypertension, and Recommendations for Limiting Their Clinical Effects.

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10.  Characteristics of systemic hypertension in preterm children.

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Journal:  J Clin Hypertens (Greenwich)       Date:  2015-03-16       Impact factor: 3.738

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1.  Neonatal hypertension: concerns within and beyond the neonatal intensive care unit.

Authors:  Kathleen Altemose; Janis M Dionne
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2.  Antenatal exposure to nonsteroidal anti-inflammatory drugs and risk of neonatal hypertension.

Authors:  Mounira Habli; Corey C Clifford; Tammy M Brady; Zahidee Rodriguez; Michaela Eschenbacher; Malcolm Wu; Emily DeFranco; James Gresh; Beena D Kamath-Rayne
Journal:  J Clin Hypertens (Greenwich)       Date:  2018-07-27       Impact factor: 3.738

Review 3.  Landscape of Preterm Birth Therapeutics and a Path Forward.

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