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We studied respiratory patterns and transcutaneous gas pressures in two infants with Arnold-Chiari type II malformation referred to us due to repeated episodes of stridor and cyanosis. During both active and quiet sleep, respiration was irregular and absent or inverse thoracic breathing movements and frequent decreases in oxygen saturation to below 80% were observed. When breathing air with 2% CO2 or when given acetazolamide 10 mg/kg, chest wall movements normalized and oxygenation increased to near normal levels. After three months of treatment with acetazolamide 20 mg/kg/24 h no further episodes of hypoventilation or hypoxemia were observed and further treatment could be discontinued. We conclude that stimulation of respiration by CO2 or by acetazolamide appears to recruit chest wall muscles and promote upper airway patency in Arnold-Chiari malformation. A treatment trial with acetazolamide seems justifiable in these infants when respiratory problems are present.

Original publication

DOI

10.1111/j.1651-2227.1992.tb12311.x

Type

Journal article

Journal

Acta paediatrica (Oslo, Norway : 1992)

Publication Date

08/1992

Volume

81

Pages

609 - 612

Addresses

Department of Pediatrics, Karolinska Hospital, Stockholm, Sweden.

Keywords

Humans, Sleep Apnea Syndromes, Hydrocephalus, Arnold-Chiari Malformation, Meningomyelocele, Carbon Dioxide, Oxygen, Acetazolamide, Respiration, Infant, Female