Effect of Theophylline on Lung Function Tests, Sleep Quality, and Nighttime SaO2in Children with Cystic Fibrosis
- 1 December 1991
- journal article
- clinical trial
- Published by American Thoracic Society in American Review of Respiratory Disease
- Vol. 144 (6) , 1245-1249
- https://doi.org/10.1164/ajrccm/144.6.1245
Abstract
The effect of theophylline (T) was studied in 12 children with cystic fibrosis (CF) (seven males and five females) aged 7 to 17 yr (mean, 11.8 +/- 2.8). T or placebo (P) was taken for 10 days in a double-blind, crossover controlled trial. During Nights 9 and 10 of each study period, the subjects slept in a sleep laboratory, where complete polysomnographs were recorded. Patients were subdivided according to T blood levels above or below 10 micrograms/ml: five children had a mean serum T of 11.7 +/- 1.6 micrograms/ml (Group 1), and seven patients had serum T levels of 6.7 +/- 1.5 micrograms/ml (Group 2). There was no difference in pulmonary function between the two periods, but Group 2 had significantly better baseline lung function (p less than 0.01). During sleep while on T, Group 1 had a higher mean SaO2 (93.1 +/- 0.3% T versus 90.7 +/- 0.3% P; p less than 0.0001), less time with a decrease greater than 5% in SaO2 from baseline (43.7 +/- 7.9 min T versus 85.8 +/- 7.9 min P; p less than 0.01), and a lower heart rate (HR), (77.9 +/- 5.1 bpm T versus 86.1 +/- 4.2 bpm P; p less than 0.01). Group 2 did not show differences in these parameters. T significantly disrupted sleep as measured by sleep efficiency and total wake time independently of serum level (p less than 0.01). There was no significant effect of T on the incidence of apnea, hypopnea, or body movements during sleep.(ABSTRACT TRUNCATED AT 250 WORDS)Keywords
This publication has 7 references indexed in Scilit:
- Nocturnal home oxygen in the treatment of hypoxemic cystic fibrosis patientsThe Journal of Pediatrics, 1989
- Ventilation And Oxygenation Changes During Sleep In Cystic FibrosisChest, 1983
- Intravenous Aminophylline in Patients With Cystic FibrosisAmerican Journal of Diseases of Children, 1980
- Hemoglobin DesaturationAmerican Journal of Diseases of Children, 1980
- Mechanism of Hemoglobin Desaturation During Rapid-Eye-Movement Sleep in Normal Subjects and in Patients with Cystic Fibrosis1,2American Review of Respiratory Disease, 1980
- Bronchial Lability in Children Suffering from Some Diseases of the BronchiRespiration, 1975
- The variable effect of a bronchodilating agent on pulmonary function in cystic fibrosisThe Journal of Pediatrics, 1973