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chloral hydrate and Cystic Fibrosis

chloral hydrate has been researched along with Cystic Fibrosis in 2 studies

Cystic Fibrosis: An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.

Research Excerpts

ExcerptRelevanceReference
" The commonly used dose range exceeds the maximum recommended dose; however, the effects of this dosage regimen during pulmonary function testing have not been studied."1.27Effect of chloral hydrate on arterial oxygen saturation in wheezy infants. ( Mallol, J; Sly, PD, 1988)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Koucký, V1
Skalická, V1
Pohunek, P1
Mallol, J1
Sly, PD1

Other Studies

2 other studies available for chloral hydrate and Cystic Fibrosis

ArticleYear
Nitrogen multiple breath washout test for infants with cystic fibrosis.
    The European respiratory journal, 2018, Volume: 52, Issue:2

    Topics: Breath Tests; Chloral Hydrate; Cystic Fibrosis; Female; Humans; Infant; Male; Nitrogen; Pulmonary Ga

2018
Effect of chloral hydrate on arterial oxygen saturation in wheezy infants.
    Pediatric pulmonology, 1988, Volume: 5, Issue:2

    Topics: Bronchiolitis, Viral; Chloral Hydrate; Cystic Fibrosis; Humans; Infant; Oxygen; Respiratory Function

1988