ArticleEuropean journal of pediatrics2005
Pharmacodynamics of chloral hydrate in former preterm infants.
Article in European journal of pediatrics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 51 citations in OpenAlex.
- Midazolam oral solution for neonatal MRI: study protocol of a randomised controlled trial.BMJ open · 2026Article
- A solution based on melatonin, tryptophan, and vitamin B6 (Melamil Tripto©) for sedation in newborns during brain MRI.Italian journal of pediatrics · 2019Article
- Short-term effects of single-dose chloral hydrate on neonatal auditory perception: An auditory event-related potential study.PloS one · 2019Article
- [Preclinical safety evaluation of chloral hydrate after topical application using the example of psoriatic itch].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2017Article
- Efficacy and safety of chloral hydrate sedation in infants for pulmonary function tests.Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo · 2016Article
- MRI evaluation and safety in the developing brain.Seminars in perinatology · 2015Review
- Clinical practice: analgesia in neonates.European journal of pediatrics · 2009Review
- Drugs of choice for sedation and analgesia in the neonatal ICU.Clinics in perinatology · 2009Article
- Pharmacological therapy for analgesia and sedation in the newborn.Archives of disease in childhood. Fetal and neonatal edition · 2006Review
- Article
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
unlabelledThe aim of this study was to document the pharmacodynamics of chloral hydrate in former preterm infants at term post-conception age. The degree of sedation (COMFORT), feeding behaviour and cardiorespiratory events (bradycardic events, apnoeas) before and after administration of chloral hydrate (oral, 30 mg/kg) were prospectively evaluated in former preterm infants during procedural sedation. Characteristics at birth, during neonatal stay and at inclusion were collected. Paired Wilcoxon and McNemar tests were used to study the impact of chloral hydrate. Characteristics of infants who displayed severe bradycardic events were compared to infants in whom no bradycardic events were recorded (Mann Whitney U, Fischer's exact). A significant increase in sedation (decrease COMFORT scale) was observed up to 12 h after administration. There was a minor but significant decrease in oral intake (161 to 156 ml/kg/day, P < 0.01). A significant increase in the number of bradycardic events (<80/min: 38 to 82 events, of which < 70/min: 30 to 79 of which < 60/min: 15 to 45; at least P < 0.01) and in the duration of the most severe bradycardic event (8-12.5 s) was observed. Therefore, further inclusion was stopped when 26 neonates were included. Infants who displayed severe bradycardic (< 60/min) events ( n = 13) after administration of chloral hydrate had a lower gestational age at birth without difference in post-conception age at inclusion.
conclusionChloral hydrate was associated with an increase in unintended side-effects in former preterm infants, likely reflecting population specific pharmacodynamics and kinetics of chloral hydrate.
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