Cited by 95Pediatric health and respiratory diseasesRespiratory viral infections researchPharmaceutical studies and practices

Is an antihistamine-decongestant combination effective in temporarily relieving symptoms of the common cold in preschool children?

Clemens, Conrad J., Taylor, James A., Almquist, Jon R., Quinn, Hal C., Mehta, Alka, Naylor, Gordon S.·1997·The Journal of Pediatrics

Abstract

Objective To determine whether an antihistamine-decongestant combination (ADC) is superior to placebo in temporarily relieving symptoms of upper respiratory tract infection (URI) in preschool children. Design Randomized, double-blind, placebo-controlled trial. Setting Four pediatric offices in the Seattle, Wash, area. Participants Children 6 months through 5 years of age with a URI of less than 7 days' duration. Methods Children were randomly assigned to receive an ADC (brompheniramine maleate-phenylpropanolamine hydrochloride) or placebo as needed for URI symptoms. Two hours after each dose of study medication, changes in the child's runny nose, nasal congestion, cough, and sleep status were assessed by means of a standardized questionnaire. Results A total of 175 responses were recorded for 59 patients. There were no statistically significant differences in symptom improvement between the ADC and the placebo group (runny nose, p = 0.48; nasal congestion, p = 0.94; cough, p = 0.66). However, the proportion of children asleep 2 hours after receiving the ADC was significantly higher than the proportion receiving placebo (46.6% vs 26.5%; p = 0.01). Results were unchanged after control for the correlated nature of repeated responses, age, symptom duration, use of acetaminophen, time that the medication was given, and parental desire for medication. Conclusions The ADC was equivalent to placebo in providing temporary relief of URI symptoms in preschool children. However, the ADC…

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Crossref · 10.1016/s0022-3476(97)70211-7

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  • In Clemens 1997, there was no difference between groups in the proportion of responses reporting an improvement in runny nose or nasal congestion (P = 0.54 and P = 0.94, respectively).

    “In Clemens 1997, there was no difference between groups in the proportion of responses reporting an improvement in runny nose or nasal congestion (P = 0.54 and P = 0.94, respectively).”

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References 18 · Cited by 95

Authors
Clemens, C. J., Taylor, J. A., Almquist, J. R., Quinn, H. C., Mehta, A., & Naylor, G. S.
Affiliations
  • University of Washington (US)
  • Moses H Cone Memorial Hospital (US)
Venue
The Journal of Pediatrics
Publisher
Elsevier BV
Published
1997-03
Volume
130
Issue
3
Pages
463-466
ISSN
0022-3476 (ISSN-L)
OpenAlex
W2018077130
Cited by
95
References
18
Citations by year
2025: 2 · 2022: 4 · 2021: 2 · 2020: 1 · 2017: 2 · 2016: 3 · 2015: 6 · 2014: 5 · 2013: 2 · 2012: 6
FWCI
6.26
Type
journal article
Language
en
Open access
closed
Locations
  • The Journal of Pediatrics (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Health Professions › Emergency Medical Services › Pediatric health and respiratory diseases
  • Health Sciences › Medicine › Epidemiology › Respiratory viral infections research
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Pharmaceutical studies and practices
Keywords
common cold, upper respiratory tract infection, preschool children, brompheniramine, phenylpropanolamine, nasal congestion, rhinorrhea, cough, sleep, sedative effects, symptom relief
MeSH terms
Brompheniramine, Child, Preschool, Common Cold, Double-Blind Method, Drug Combinations, Female, Histamine H1 Antagonists, Humans, Infant, Male, Phenylephrine, Phenylpropanolamine, Time Factors, Pseudoephedrine

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