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Emollients for preventing atopic eczema: Cost-effectiveness analysis of the BEEP trial.
Sach, Tracey H; Lartey, Stella T; Davies, Charlotte; Chalmers, Joanne R; Haines, Rachel H; Bradshaw, Lucy E; Montgomery, Alan A; Thomas, Kim S; Brown, Sara J; Ridd, Matthew J; Lawton, Sandra; Cork, Mike J; Flohr, Carsten; Mitchell, Eleanor; Swinden, Richard; Wyatt, Laura; Tarr, Stella; Davies-Jones, Susan; Jay, Nicola; Kelleher, Maeve M; Perkin, Michael R; Boyle, Robert J; Williams, Hywel C.
Afiliación
  • Sach TH; Health Economics Group, Norwich Medical School, University of East Anglia, Norwich, UK.
  • Lartey ST; Health Economics Group, Norwich Medical School, University of East Anglia, Norwich, UK.
  • Davies C; Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, UK.
  • Chalmers JR; Centre of Evidence Based Dermatology, School of Medicine, University of Nottingham, Nottingham, UK.
  • Haines RH; Nottingham Clinical Trials Unit, University of Nottingham, Nottingham, UK.
  • Bradshaw LE; Nottingham Clinical Trials Unit, University of Nottingham, Nottingham, UK.
  • Montgomery AA; Nottingham Clinical Trials Unit, University of Nottingham, Nottingham, UK.
  • Thomas KS; Centre of Evidence Based Dermatology, School of Medicine, University of Nottingham, Nottingham, UK.
  • Brown SJ; Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.
  • Ridd MJ; Population Health Sciences, University of Bristol, Bristol, UK.
  • Lawton S; Rotherham NHS Foundation Trust, Rotherham, UK.
  • Cork MJ; Sheffield Dermatology Research, Department of Infection and Immunity, University of Sheffield, Sheffield, UK.
  • Flohr C; Unit for Population-Based Dermatology Research, St John's Institute of Dermatology, Guy's & St Thomas' NHS Foundation Trust and King's College London, London, UK.
  • Mitchell E; Nottingham Clinical Trials Unit, University of Nottingham, Nottingham, UK.
  • Swinden R; Nottingham Clinical Trials Unit, University of Nottingham, Nottingham, UK.
  • Wyatt L; Nottingham Clinical Trials Unit, University of Nottingham, Nottingham, UK.
  • Tarr S; Nottingham Clinical Trials Unit, University of Nottingham, Nottingham, UK.
  • Davies-Jones S; Centre of Evidence Based Dermatology, School of Medicine, University of Nottingham, Nottingham, UK.
  • Jay N; Sheffield Children's Hospital, Sheffield, UK.
  • Kelleher MM; National Heart and Lung Institute, Imperial College London, London, UK.
  • Perkin MR; Population Health Research Institute, St. George's University of London, London, UK.
  • Boyle RJ; National Heart and Lung Institute, Imperial College London, London, UK.
  • Williams HC; Centre of Evidence Based Dermatology, School of Medicine, University of Nottingham, Nottingham, UK.
Clin Exp Allergy ; 53(10): 1011-1019, 2023 10.
Article en En | MEDLINE | ID: mdl-37574761
BACKGROUND: Recent discoveries have led to the suggestion that enhancing skin barrier from birth might prevent eczema and food allergy. OBJECTIVE: To determine the cost-effectiveness of daily all-over-body application of emollient during the first year of life for preventing atopic eczema in high-risk children at 2 years from a health service perspective. We also considered a 5-year time horizon as a sensitivity analysis. METHODS: A within-trial economic evaluation using data on health resource use and quality of life captured as part of the BEEP trial alongside the trial data. Parents/carers of 1394 infants born to families at high risk of atopic disease were randomised 1:1 to the emollient group, which were advised to apply emollient (Doublebase Gel or Diprobase Cream) to their child at least once daily to the whole body during the first year of life or usual care. Both groups received advice on general skin care. The main economic outcomes were incremental cost-effectiveness ratio (ICER), defined as incremental cost per percentage decrease in risk of eczema in the primary cost-effectiveness analysis. Secondary analysis, undertaken as a cost-utility analysis, reports incremental cost per Quality-Adjusted Life Year (QALY) where child utility was elicited using the proxy CHU-9D at 2 years. RESULTS: At 2 years, the adjusted incremental cost was £87.45 (95% CI -54.31, 229.27) per participant, whilst the adjusted proportion without eczema was 0.0164 (95% CI -0.0329, 0.0656). The ICER was £5337 per percentage decrease in risk of eczema. Adjusted incremental QALYs were very slightly improved in the emollient group, 0.0010 (95% CI -0.0069, 0.0089). At 5 years, adjusted incremental costs were lower for the emollient group, -£106.89 (95% CI -354.66, 140.88) and the proportion without eczema was -0.0329 (95% CI -0.0659, 0.0002). The 5-year ICER was £3201 per percentage decrease in risk of eczema. However, when inpatient costs due to wheezing were excluded, incremental costs were lower and incremental effects greater in the usual care group. CONCLUSIONS: In line with effectiveness endpoints, advice given in the BEEP trial to apply daily emollient during infancy for eczema prevention in high-risk children does not appear cost-effective.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dermatitis Atópica / Eccema Tipo de estudio: Clinical_trials / Health_economic_evaluation Aspecto: Patient_preference Límite: Humans / Infant Idioma: En Revista: Clin Exp Allergy Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2023 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dermatitis Atópica / Eccema Tipo de estudio: Clinical_trials / Health_economic_evaluation Aspecto: Patient_preference Límite: Humans / Infant Idioma: En Revista: Clin Exp Allergy Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2023 Tipo del documento: Article Pais de publicación: Reino Unido