Summary
Synopsis
Salmeterol is a selective β2-receptor agonisl with long duration of action that permits twice daily administration. It is effective in the prophylaxis of asthma symptoms, including nocturnal and exercise-induced asthma, and it has shown clinical benefits in both adults and children. Because of its slow onset of action, salmeterol is not intended for relief of acute symptoms.
The addition of salmeterol 50μg twice daily to existing asthma therapy has a positive effect on patient quality of life in the short term (up to 3 months), as assessed by the Living With Asthma Questionnaire and Asthma Quality of Life Questionnaire. This improvement in well-being appears to be greater than that associated with salbutamol (albuterol). Furthermore, in patients with asthma symptoms despite inhaled corticosteroid therapy, a reduced dose of corticosteroid plus salmeterol produced a greater improvement in quality of life as assessed by a daily symptom lliaty (hut lint by the Living With Asthma Questionnaire), and was more clinically effective than a higher dose of corticosteroid alone. Evaluation of the effects of salmeterol on quality of life compared witll other standard therapies, and extension of these results into the long term are required to consolidale these conclusions.
Salmeterol 50μg twice daily was associated with an estimated incremental cost of £736 per symptom-free patient in the final week of 7.5 months’ therapy.£648 per patient with improve morning (am) peak expiratoty flow rate (PEFR)and £1013 per patient with improved evenig (pm) PEFR compared with .flIlblllamol (400μg twice daily) in a cost-effectiveness analysis. However, these results should be tested by sensitivity analyses and compared with the incremental costs of other asthma interventions more applicable to recommended clinical practice.
The cost effectiveness of salmeterol relative to other asthma therapies, and the effect of salmeterol of patient quality of life in the long term require further investigation. However, when added to existing asthma therapy, salmeterol improves patient quality of life in the short term (up to 3 months). It may also have some beneficial effects on patient well-being when used to provide a steroid-sparing effect.
General Considerations
Recent studies suggest the prevalence of asthma, as well as hospital isation and mortality rates, may now have stabilised in some countries following an increase over the last several decades.
Economic assessments of intervention strategies for asthma are few. Drug acquisition costs and costs of hospitalisation appear to be the greatest contributors to direct costs of asthma, but indirect costs also contribute significantly to the total costs associated with the disease. Intangible costs are probably the greatest component of total asthma costs. but they are difficult to quantify in a monetary sense. However, they may be assessed in terms of effects on patient quality of life.
There are several specific instruments available to assess quality of life in patients with asthma, with considerable evidence to support their content validity. General instruments assessing quality of life are probably insensitive to clinical change in patients with mild asthma. although a combination of generic and specific instruments may be useful to assess new thempeutic regimens.
Pharmacoeconomic Assessment of Salmeterol
Salmeterol 50μg twice daily added to existing asthma therapy improved quality of life relative to placebo or salbutamol (albuterol) in 5 short term studies (up to 3 months). The positive effects of salmeterol compared with other treatments were observed for global assessments and for individual domains of 2 validated instruments (Living With Asthma Questionnaire and Asthma Quality of Life Questionnaire) for measuring quality of life in asthma. A further short term study evaluated patients with asthma symptoms despite inhaled corticosteroid therapy. A reduced dose of corticosteroid plus salmeterol produced a greater improvement in quality of life as assessed by a daily symptom diary (but not by the Living With Asthma Questionnaire) than a higher dose of corticosteroid alone.
Two briefly reported st udies have assessed the cost effectiveness of salmeterol using direct costs only. The estimated incremental cost of salmeterol 50μg twice daily compared with salbutamol 400μg twice daily was £736 per symptom-free patient in the final week of 7.5 months’ therapy, £648 per patient with improved morning (am) peak expiratory flow rate (PEFR) and £1013 per patient with improved evening (pm) PEFR. These conclusions should be tested by sensitivity analyses and compared with the incremental costs of salmelerol versus other asthma inlerventions more applicable to recommended clinical practice. Salmeterol was also considered to be morc cost effective than salbutamol when priced up to $Can2.06 per day in a Canadian analysis using clinically relevant regimens.
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Various sections of the manuscript reviewed by: M.L. Burr, University of Wales College of Medicine, Temple of Peace and Health, Cardiff, Wales; M.J. Buxton, Health Economics Research Group, Brunei University, Uxbridge, England; P.W. Jones, Division of Physiological Medicine, St George’s Hospital Medical School, London, England; M.E. Hyland, Faculty of Human Sciences, Department of Psychology, University of Plymouth, Plymouth, England; K.-H. Carlsen, Voksentoppen Center of Asthma and Allergy, University of Oslo, National Hospital of Children’s Asthma, Allergy and Chronic Lung Diseases, Oslo, Norway; E. Juniper, McMaster University Medical Centre, Department of Clinical Epidemiology and Biostatistics, Hamilton, Ontario, Canada; C.M. Mellis, Royal Alexandra Hospital for Children, Department of Respiratory Medicine, Camperdown, New South Wales, Australia; D.S. Pearlman, Colorado Asthma and Allergy Clinic, Aurora, Colorado, USA; B.H. Rowe, Northeastern Ontario Family Medicine Residency Program, Health Science Resource Education Centre, Laurentian University, Sudbury, Ontario, Canada; M.P.M.H. Rutten-van Mölken, Department of Health Economics, University of Limburg, Maastricht, The Netherlands; A. Siracusa, Istuto di Medicina del Lavoro, Università di Perugia, Perugia, Italy; C. Trautner, Diabetes Research Unit at Düsseldorf University, Department of Biometrics and Epidemiology, Düsseldorf, Germany; K.B. Weiss, Rush-Presbyterian-St Luke’s Medical Center, Primary Care institute, Center for Health Services Research, Chicago, Illinois, USA; M. Yamakido, Hiroshima University School of Medicine, Hiroshima, Japan.
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Peters, D.H., Faulds, D. Salmeterol. Pharmacoeconomics 7, 562–574 (1995). https://doi.org/10.2165/00019053-199507060-00010
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DOI: https://doi.org/10.2165/00019053-199507060-00010