Tiotropium for stable chronic obstructive pulmonary disease: a meta-analysis
- 1Irving Assistant Professor of Medicine and Epidemiology, Columbia University Medical Centre, New York, NY, USA
- 2Associate Professor of Medicine, McGill University Health Centre, Montreal, Quebec, Canada
- 3Associate Professor of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA
- 4Senior Lecturer in Respiratory Medicine and Clinical Pharmacology, School of Health Sciences, Massey University, Auckland, New Zealand
- Correspondence to:
Dr R G Barr
Division of General Medicine, PH-9 East Room 105, Columbia University Medical Centre, 630 West 168th Street, New York, NY 10032, USA;
- Received 29 March 2006
- Accepted 16 June 2006
- Published Online First 14 July 2006
Background: A systematic review was undertaken to evaluate the efficacy of tiotropium, a long acting anticholinergic drug, on clinical events, symptom scales, pulmonary function, and adverse events in stable chronic obstructive pulmonary disease (COPD).
Methods: A systematic search was made of the Cochrane trials database, MEDLINE, EMBASE, CINAHL, and a hand search of 20 respiratory journals. Missing data were obtained from authors and the manufacturer. Randomised controlled trials of ⩾12 weeks’ duration comparing tiotropium with placebo, ipratropium bromide, or long acting β2 agonists (LABA) were reviewed. Studies were pooled to yield odds ratios (OR) or weighted mean differences with 95% confidence intervals (CI).
Results: Nine trials (8002 patients) met the inclusion criteria. Tiotropium reduced the odds of a COPD exacerbation (OR 0.73; 95% CI 0.66 to 0.81) and related hospitalisation (OR 0.68; 95% CI 0.54 to 0.84) but not pulmonary (OR 0.50; 95% CI 0.19 to 1.29) or all-cause (OR 0.96; 95% CI 0.63 to 1.47) mortality compared with placebo and ipratropium. Reductions in exacerbations and hospitalisations compared with LABA were not statistically significant. Similar patterns were evident for quality of life and symptom scales. Tiotropium yielded greater increases in forced expiratory volume in 1 second (FEV1) and forced vital capacity (FVC) from baseline to 6–12 months than did placebo, ipratropium, and LABA. Decline in FEV1 over 1 year was 30 ml (95% CI 7 to 53) slower with tiotropium than with placebo and ipratropium (data were not available for LABA). Reports of dry mouth and urinary tract infections were increased with tiotropium.
Conclusions: Tiotropium reduced COPD exacerbations and related hospitalisations, improved quality of life and symptoms, and may have slowed the decline in FEV1. Long term trials are warranted to evaluate the effects of tiotropium on decline in FEV1 and to clarify its role compared with LABA.
- COPD, chronic obstructive pulmonary disease
- FEV1, forced expiratory volume in 1 second
- FVC, forced vital capacity
- LABA, long acting β2 agonist
- SGRQ, St George’s Respiratory Questionnaire
- TDI, Transitional Dyspnoea Index
Published Online First 14 July 2006
Funding: Robert Wood Johnson Generalist Physician Faculty Scholar Award and National Institutes of Health (USA) HL075476, HL077612, HL063841.
Competing interests: Dr Barr: none. Dr Bourbeau has received honoraria for CME, membership on advisory boards and financial support from government agencies, contract and investigator initiated research studies for a number of companies including Altana, Astra Zeneca, Bayer, Boehringer-Ingelheim, GlaxoSmithKline, Novartis and Pfizer. Dr Camargo has received investigator initiated grants and consulting/lecture honoraria from AstraZeneca, Boehringer-Ingelheim, GlaxoSmithKline, and Novartis. Dr Ram: none.