Journal article
Morphine versus clonidine for neonatal abstinence syndrome
Pediatrics (Evanston), Vol.135(2), pp.e383-e391
02/2015
DOI: 10.1542/peds.2014-2377
PMID: 25624389
Abstract
The study goal was to determine whether clonidine treatment of neonatal abstinence syndrome (NAS) would result in a better neurobehavioral performance compared with morphine.
This pilot study prospectively enrolled infants ≥ 35 weeks' gestational age admitted for treatment of NAS. After informed consent was obtained, infants were randomized to receive morphine (0.4 mg/kg per day) or clonidine (5 μg/kg per day) divided into 8 doses. A 25% dose escalation every 24 hours was possible per protocol (maximum of 1 mg/kg per day for morphine and 12 μg/kg per day for clonidine). After control of symptoms, the dose was tapered by 10% every other day. Clinical staff monitored infants by using Finnegan scoring. Masked research staff administered the NICU Network Neurobehavioral Scale (NNNS) at 1 week and at 2 to 4 weeks after initiation of treatment and the Bayley Scales III, and Preschool Language Scale IV, at 1-year adjusted age. Analyses included descriptive statistics, repeated measures analysis of variance, and Wilcoxon tests.
Infants treated with morphine (n = 15) versus clonidine (n = 16) did not differ in birth weight or age at treatment. Treatment duration was significantly longer for morphine (median 39 days) than for clonidine (median 28 days; P = .02). NNNS summary scores improved significantly with clonidine but not with morphine. On subsequent assessment, those receiving clonidine had lower height of arousal and excitability (P < .05). One-year motor, cognitive, and language scores did not differ between groups.
Clonidine may be a favorable alternative to morphine as a single-drug therapy for NAS. A multicenter randomized trial is warranted.
Details
- Title: Subtitle
- Morphine versus clonidine for neonatal abstinence syndrome
- Creators
- Henrietta S Bada - Departments of Pediatrics, College of Medicine, hbada2@uky.eduThitinart Sithisarn - Departments of Pediatrics, College of MedicineJulia Gibson - Department of Pharmacy, Kentucky Children's Hospital, Lexington, Kentucky; andKaren Garlitz - Department of Pharmacy, Kentucky Children's Hospital, Lexington, Kentucky; andRhonda Caldwell - Departments of Pediatrics, College of MedicineGilson Capilouto - Rehabilitation Sciences, College of Health SciencesYinglei Li - Statistics, College of Arts and Sciences andMarkos Leggas - Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KentuckyPatrick Breheny - Department of Biostatistics, College of Public Health, University of Iowa, Iowa City, Iowa
- Resource Type
- Journal article
- Publication Details
- Pediatrics (Evanston), Vol.135(2), pp.e383-e391
- DOI
- 10.1542/peds.2014-2377
- PMID
- 25624389
- NLM abbreviation
- Pediatrics
- ISSN
- 1098-4275
- eISSN
- 1098-4275
- Publisher
- American Academy of Pediatrics; United States
- Language
- English
- Date published
- 02/2015
- Academic Unit
- Biostatistics
- Record Identifier
- 9983997367702771
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