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Article
December 1980

Intravenous Aminophylline in Patients With Cystic Fibrosis: Pharmacokinetics and Effect on Pulmonary Function

Author Affiliations

From the Departments of Pediatrics, National Jewish Hospital and Research Center (Drs Larsen, Barron, and Landay) and University of Colorado Medical Center (Drs Cotton and Brooks), Denver; and the School of Pharmacy and Pharmacal Sciences (Dr Gonzalez), Purdue University, West Lafayette, Ind. Dr Brooks is now with the University of Rochester (NY) School of Medicine and Dentistry.

Am J Dis Child. 1980;134(12):1143-1148. doi:10.1001/archpedi.1980.02130240027009
Abstract

• Intravenous aminophylline was administered to ten patients with cystic fibrosis (CF) to determine if the medication would improve pulmonary function and to study theophylline pharmacokinetics. Intravenous normal saline was given on another day as a control. Thoracic gas volume and airway resistance, measured in a volume displacement body plethysmograph, and maximal expiratory flow-volume curves were performed before and after each infusion. No significant improvement was noted in pulmonary function after normal saline infusion. Following aminophylline infusion, significant improvement in thoracic gas volume, residual volume, specific airway conductance, and maximal expiratory flow at 60% of total lung capacity was noted. The pharmacokinetic analysis revealed a mean half-life of 4.7 hours, a total clearance of 91 mL/hr/kg, and a volume of distribution of 574 mL/kg. Intravenous aminophylline can acutely decrease airway obstruction in children with CF.

(Am J Dis Child 134:1143-1148, 1980)

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