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Prevalence and risk factors for milk allergy overdiagnosis in the BEEP trial cohort.
Allen, Hilary I; Wing, Olivia; Milkova, Dara; Jackson, Emilia; Li, Karen; Bradshaw, Lucy E; Wyatt, Laura; Haines, Rachel; Santer, Miriam; Murphy, Andrew W; Brown, Sara J; Kelleher, Maeve; Perkin, Michael R; Jay, Nicola; Smith, Timothy D H; Moriarty, Frank; Montgomery, Alan A; Williams, Hywel C; Boyle, Robert J.
Afiliação
  • Allen HI; National Heart and Lung Institute, Imperial College London, London, UK.
  • Wing O; National Heart and Lung Institute, Imperial College London, London, UK.
  • Milkova D; National Heart and Lung Institute, Imperial College London, London, UK.
  • Jackson E; Centre of Evidence Based Dermatology, Lifespan and Population Health, University of Nottingham, Nottingham, UK.
  • Li K; National Heart and Lung Institute, Imperial College London, London, UK.
  • Bradshaw LE; Nottingham Clinical Trials Unit, School of Medicine, University of Nottingham, Nottingham, UK.
  • Wyatt L; Nottingham Clinical Trials Unit, School of Medicine, University of Nottingham, Nottingham, UK.
  • Haines R; Nottingham Clinical Trials Unit, School of Medicine, University of Nottingham, Nottingham, UK.
  • Santer M; Primary Care Research Centre, University of Southampton, Southampton, UK.
  • Murphy AW; Department of General Practice & HRB Clinical Trial Network Primary Care Ireland, University of Galway, Galway, Ireland.
  • Brown SJ; Centre for Genomic and Experimental Medicine, University of Edinburgh, Edinburgh, UK.
  • Kelleher M; Children's Health Ireland, Crumlin Children's Hospital, Dublin, Ireland.
  • Perkin MR; Population Health Research Institute, St George's University of London, London, UK.
  • Jay N; Sheffield Children's NHS Foundation Trust, Sheffield, UK.
  • Smith TDH; NIHR Clinical Research Network North West Coast Primary Care Team, Liverpool, UK.
  • Moriarty F; School of Pharmacy and Biomolecular Sciences, RCSI University of Medicine and Health Sciences, Dublin, Ireland.
  • Montgomery AA; Nottingham Clinical Trials Unit, School of Medicine, University of Nottingham, Nottingham, UK.
  • Williams HC; Centre of Evidence Based Dermatology, Lifespan and Population Health, University of Nottingham, Nottingham, UK.
  • Boyle RJ; National Heart and Lung Institute, Imperial College London, London, UK.
Allergy ; 2024 Jun 20.
Article em En | MEDLINE | ID: mdl-38899450
ABSTRACT

BACKGROUND:

Cow's milk allergy (CMA) overdiagnosis in young children appears to be increasing and has not been well characterised. We used a clinical trial population to characterise CMA overdiagnosis and identify individual-level and primary care practice-level risk factors.

METHODS:

We analysed data from 1394 children born in England in 2014-2016 (BEEP trial, ISRCTN21528841). Participants underwent formal CMA diagnosis at ≤2 years. CMA overdiagnosis was defined in three separate ways parent-reported milk reaction; primary care record of milk hypersensitivity symptoms; and primary care record of low-allergy formula prescription.

RESULTS:

CMA was formally diagnosed in 19 (1.4%) participants. CMA overdiagnosis was common 16.1% had parent-reported cow's milk hypersensitivity, 11.3% primary care recorded milk hypersensitivity and 8.7% had low-allergy formula prescription. Symptoms attributed to cow's milk hypersensitivity in participants without CMA were commonly gastrointestinal and reported from a median age of 49 days. Low-allergy formula prescriptions in participants without CMA lasted a median of 10 months (interquartile range 1, 16); the estimated volume consumed was a median of 272 litres (26, 448). Risk factors for CMA overdiagnosis were high practice-based low-allergy formula prescribing in the previous year and maternal report of antibiotic prescription during pregnancy. Exclusive formula feeding from birth was associated with increased low-allergy formula prescription. There was no evidence that practice prescribing of paediatric adrenaline auto-injectors or anti-reflux medications, or maternal features such as anxiety, age, parity and socioeconomic status were associated with CMA overdiagnosis.

CONCLUSION:

CMA overdiagnosis is common in early infancy. Risk factors include high primary care practice-based low-allergy formula prescribing and maternal report of antibiotic prescription during pregnancy.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article