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Economic evaluation of high-technology home treatment for cystic fibrosis: preliminary results
Introduction The natural history of cystic fibrosis (CF) is characterised by repeated infective respiratory exacerbations leading to continued decline in lung function. Patients generally undergo treatment for exacerbations with 14-day courses of intravenous antibiotics administered either in hospital or at home. As home treatment is well established but there are no robust evaluations of cost-effectiveness, the aim of this study was to compare the economic impact of home and hospital treatment. Methods Patients from an adult CF unit participated in this retrospective one-year study. The Local Research Ethics Committee was informed of the study and approval was deemed not necessary. Lung function (forced expiratory volume in one second, FEV1) was chosen as the clinical outcome measure and data were collected from the patients' clinical records. Fixed, variable, and patients' own resource data were collected from patients' clinical records, through observation, and questionnaire use. Antibiotic costs only are reported here. Preliminary results
Discussion The preliminary results indicate a greater improvement in FEV1 after one course of treatment for patients treated in hospital compared with those treated at home. However, a number of factors affecting outcome must be taken into account including severity of illness. The effect of these factors will be examined using regression techniques. Outcome after one year will also be assessed. The economic evaluation will compare cost-effectiveness of home and hospital treatment with i.v. antibiotics for both one course and one year of treatment. Presented at the HSRPP Conference 2002, Leeds
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