Caffeine to prevent intermittent hypoxaemia in late preterm infants: randomised controlled dosage trial. Issue 2 (29th August 2022)
- Record Type:
- Journal Article
- Title:
- Caffeine to prevent intermittent hypoxaemia in late preterm infants: randomised controlled dosage trial. Issue 2 (29th August 2022)
- Main Title:
- Caffeine to prevent intermittent hypoxaemia in late preterm infants: randomised controlled dosage trial
- Authors:
- Oliphant, Elizabeth Anne
McKinlay, Christopher JD
McNamara, David
Cavadino, Alana
Alsweiler, Jane M - Abstract:
- Abstract : Objective: To establish the most effective and best tolerated dose of caffeine citrate for the prevention of intermittent hypoxaemia (IH) in late preterm infants. Design: Phase IIB, double-blind, five-arm, parallel, randomised controlled trial. Setting: Neonatal units and postnatal wards of two tertiary maternity hospitals in New Zealand. Participants: Late preterm infants born at 34 +0 –36 +6 weeks' gestation, recruited within 72 hours of birth. Intervention: Infants were randomly assigned to receive a loading dose (10, 20, 30 or 40 mg/kg) followed by 5, 10, 15 or 20 mg/kg/day equivolume enteral caffeine citrate or placebo daily until term corrected age. Primary outcome: IH (events/hour with oxygen saturation concentration ≥10% below baseline for ≤2 min), 2 weeks postrandomisation. Results: 132 infants with mean (SD) birth weight 2561 (481) g and gestational age 35.7 (0.8) weeks were randomised (24–28 per group). Caffeine reduced the rate of IH at 2 weeks postrandomisation (geometric mean (GM): 4.6, 4.6, 2.0, 3.8 and 1.7 events/hour for placebo, 5, 10, 15 and 20 mg/kg/day, respectively), with differences statistically significant for 10 mg/kg/day (GM ratio (95% CI] 0.39 (0.20 to 0.76]; p=0.006) and 20 mg/kg/day (GM ratio (95% CI] 0.33 (0.17 to 0.68]; p=0.003) compared with placebo. The 20 mg/kg/day dose increased mean (SD) pulse oximetry oxygen saturation (SpO2 ) (97.2 (1.0) vs placebo 96.0 (0.8); p<0.001), and reduced median (IQR) percentage of time SpO2 <90%Abstract : Objective: To establish the most effective and best tolerated dose of caffeine citrate for the prevention of intermittent hypoxaemia (IH) in late preterm infants. Design: Phase IIB, double-blind, five-arm, parallel, randomised controlled trial. Setting: Neonatal units and postnatal wards of two tertiary maternity hospitals in New Zealand. Participants: Late preterm infants born at 34 +0 –36 +6 weeks' gestation, recruited within 72 hours of birth. Intervention: Infants were randomly assigned to receive a loading dose (10, 20, 30 or 40 mg/kg) followed by 5, 10, 15 or 20 mg/kg/day equivolume enteral caffeine citrate or placebo daily until term corrected age. Primary outcome: IH (events/hour with oxygen saturation concentration ≥10% below baseline for ≤2 min), 2 weeks postrandomisation. Results: 132 infants with mean (SD) birth weight 2561 (481) g and gestational age 35.7 (0.8) weeks were randomised (24–28 per group). Caffeine reduced the rate of IH at 2 weeks postrandomisation (geometric mean (GM): 4.6, 4.6, 2.0, 3.8 and 1.7 events/hour for placebo, 5, 10, 15 and 20 mg/kg/day, respectively), with differences statistically significant for 10 mg/kg/day (GM ratio (95% CI] 0.39 (0.20 to 0.76]; p=0.006) and 20 mg/kg/day (GM ratio (95% CI] 0.33 (0.17 to 0.68]; p=0.003) compared with placebo. The 20 mg/kg/day dose increased mean (SD) pulse oximetry oxygen saturation (SpO2 ) (97.2 (1.0) vs placebo 96.0 (0.8); p<0.001), and reduced median (IQR) percentage of time SpO2 <90% (0.5 (0.2–0.8) vs 1.1 (0.6–2.4); p<0.001) at 2 weeks, without significant adverse effects on growth velocity or sleeping. Conclusion: Caffeine reduces IH in late preterm infants at 2 weeks of age, with 20 mg/kg/day being the most effective dose. Trial registration number: ACTRN12618001745235. Abstract : In late preterms (132 infants, 34-36 weeks), a randomized controlled trial (placebo, versus different caffeine citrate doses), caffeine reduces intermittent hypoxia events at 2 weeks of age, with 20 mg.kg-1.day-1 being the most effective dose. … (more)
- Is Part Of:
- Archives of disease in childhood. Volume 108:Issue 2(2023)
- Journal:
- Archives of disease in childhood
- Issue:
- Volume 108:Issue 2(2023)
- Issue Display:
- Volume 108, Issue 2 (2023)
- Year:
- 2023
- Volume:
- 108
- Issue:
- 2
- Issue Sort Value:
- 2023-0108-0002-0000
- Page Start:
- 106
- Page End:
- 113
- Publication Date:
- 2022-08-29
- Subjects:
- neonatology -- respiratory medicine -- therapeutics
Infants -- Diseases -- Periodicals
Newborn infants -- Diseases -- Periodicals
Fetus -- Diseases -- Periodicals
618.920105 - Journal URLs:
- http://fn.bmjjournals.com ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/archdischild-2022-324010 ↗
- Languages:
- English
- ISSNs:
- 1359-2998
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 26153.xml