National and international guidelines for neonatal caffeine use: Are they evidenced-based?

Semin Fetal Neonatal Med. 2020 Dec;25(6):101177. doi: 10.1016/j.siny.2020.101177. Epub 2020 Nov 4.

Abstract

The Caffeine for Apnea of Prematurity (CAP) trial showed that caffeine was safe when used with standard dosing and provided both pulmonary and neurological benefits to preterm infants. Since its publication almost 15 years ago, the use of caffeine in extremely premature infants in Newborn Intensive Care Units worldwide has increased, with almost all receiving the drug during their hospital stay. Subsequent observational studies suggested that administration of caffeine before 3 days of age may have greater benefits, leading many neonatologists to start caffeine prophylactically in all very low birth weight infants. Several publicly available national and international guidelines on caffeine advocate prophylactic use, and some recommend higher doses than those used in the CAP trial. This article will review the evidence basis for neonatal caffeine therapy in light of these guidelines.

Keywords: Apnea; Bronchopulmonary dysplasia; Caffeine; Clinical trial; Drug safety; Neurodevelopment; Prematurity.

Publication types

  • Review

MeSH terms

  • Apnea / drug therapy*
  • Caffeine / therapeutic use*
  • Central Nervous System Stimulants / therapeutic use*
  • Citrates / therapeutic use*
  • Evidence-Based Medicine
  • Humans
  • Infant
  • Infant, Extremely Premature
  • Infant, Newborn
  • Infant, Premature, Diseases / drug therapy*
  • Infant, Very Low Birth Weight*
  • Intensive Care Units, Neonatal
  • Observational Studies as Topic

Substances

  • Central Nervous System Stimulants
  • Citrates
  • Caffeine
  • caffeine citrate