4.5 Article

Long-term effects of almitrine bismesylate in COPD patients with chronic hypoxaemia

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RESPIRATORY MEDICINE
卷 97, 期 6, 页码 599-605

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W B SAUNDERS CO LTD
DOI: 10.1053/rmed.2003.1486

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almitrine bismesylate; COPD; chronic hypoxaemia

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Background: Almitrine bismesylate (AB) is a peripheral chemoreceptor agonist which is believed to improve oxygenation of COPD patients with chronic hypoxaemia, probably by improving the ventilation perfusion mismatch. We studied the long-term effects of AB in COPD patients with chronic hypoxaemia. Methods: Design Prospective, randomised, double-blind, placebo-controlled trial. Setting: Eight hundred bed teaching hospital with a catchment population of 350 000 inhabitants. Patient recruitment: COPD outpatients consulting between September 95 and September 99. Inclusion criteria: (I)- COPD ( FEV1<50%), (2) PaO(2)less than or equal to65 mmHg. (3) Stable arterial blood gases (ABG), spirometry (S) and clinical state. Exclusion criteria: Asthma, restrictive disease, sleep apnoea syndrome, advanced renal or hepatic disease, peripheral neuropathy, use of respiratory stimulants or psychotrophic drugs. Treatment: ABI mg/kg/day (weight <75 kg = 50 mg/day; weight greater than or equal to 75 kg = 100 mg/day) in an intermittent schedule with resting periods of 1 month after the third, 6th and 9th months during I year. Instrumentation: Stabilisation period: S, ABG. Run-in period: S, ABG, 6-min walking test (WT), nocturnal pulse oximetry (NP) and quality of life evaluation (CRQ). Third, 6th and 9th months: S, ABG. End of the study: S, ABG,WT NP, CRQ. Statistics: ANOVA for repeated measurements. Results: Two hundred and eighty-nine patients were evaluated and 81 were included in the study. Sixty-six were followed for 6 months,53 for 9 months and 42 for 1 year. All and placebo groups did not present significant differences in ABG and S in the 6th,9th and 12th months. Evolution in WT NP and CRQ were similar in the two groups, No relevant side-effects were detected: only two patients stopped treatment (one placebo and one AB). Conclusion: In an intermittent schedule, although well tolerated, at doses of 1 mg/kg/day, AB was not effective in long-term treatment of chronic hypoxemia in COPD patients. (C) 2003 Elsevier Sclence Ltd. All rights reserved.

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