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Effects of Long-term Aerosol Pentamidine for Pneumocystis carinii Prophylaxis on Pulmonary Function FREE TO VIEW

Charles C. Y. Wei; Leslie Lee Pack; Charles K. Chan
Author and Funding Information

From the Division of Respirology, Department of Medicine, The Toronto Hospital, University of Toronto, and the Central Aerosol Pentamidine Clinic, Toronto, Ontario, Canada

Charles K. Chan, MD, FCCP, The Toronto Hospital, 200 Elizabeth St 10EN-220, Toronto, Ontario, Canada M5G 2C4, email: cchan@torhosp.toronto.on.ca

1998 by the American College of Chest Physicians

Chest. 1998;114(3):742-747. doi:10.1378/chest.114.3.742
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Objective: The purpose of the study was to evaluate the long-term effects of aerosolized pentamidine (AP) on the pulmonary function of HIV-positive individuals receiving AP for Pneumocystis carinii pneumonia (PCP) prophylaxis.

Design: A retrospective analysis of serial pulmonary function tests (PFTs) performed on a cohort of HIV-positive patients who had received AP for >2 years.

Methods: Of the 1,787 HIV-positive patients receiving AP prophylaxis in our database, 380 patients had been receiving AP for at least 24 months. Of these 380 patients, the PFTs at baseline and at 24 months after starting AP therapy were documented in 179. We compared the baseline PFTs of these 179 patients with results obtained 24 months later to evaluate if there was any change in pulmonary function parameters.

Results: Baseline and 24-month PFT parameters (total lung capacity [TLC], FVC, residual volume [RV], FEV1, FEV1/FVC, maximum midexpiratory flow rate at 50% of vital capacity [MEF50], diffusion of carbon monoxide [DLCO]) were all within the normal ranges. However, AP therapy over 24 months was associated with a modest decline in lung volume parameters (TLC, FVC, RV), a slight reduction in flow rates (FEV1, FEV1/FVC, and MEF50), but no change in DLCO. The mean treatment duration was 23.8 months (range, 21 to 27 months).

Conclusions: Long-term AP therapy is associated with a mild combined restrictive and obstructive pulmonary defect. Since 24-month PFT parameters remained within the normal ranges, this level of decline is of unclear clinical significance. Overall, AP has good pulmonary tolerance when used up to 24 months for PCP prophylaxis in patients with normal baseline pulmonary function.




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