Psychometric analysis of the adult sickle cell quality of life measurement information system (ACSQ-Me) in a UK population

Author:

Cooper Owen,McBain Hayley,Tangayi Sekayi,Telfer Paul,Tsitsikas Dimitris,Yardumian Anne,Mulligan Kathleen

Publisher

Springer Science and Business Media LLC

Subject

Public Health, Environmental and Occupational Health,General Medicine

Reference41 articles.

1. Streetly A, Latinovic R, Henthorn J. Positive screening and carrier results for the England-wide universal newborn sickle cell screening programme by ethnicity and area for 2005–07. J Clin Pathol. 2010;63:626–9.

2. National Institute for Health and Clinical Excellence clinical guideline 143: Sickle cell acute painful episode: Management of an Acute Painful Sickle Cell Episode in hospital. 2012.

3. Lucas SB, Mason DG, Mason M, Weyman D on behalf of NCEPOD: A sickle crisis?: A report of the National Confidential Enquiry into Patient Outcome and death. NCEPOD; 2008.

4. Anie KA, Steptoe A, Bevan DH. Sickle cell disease: pain, coping and quality of life in a study of adults in the UK. Br J Health Psychol. 2002;7:331–44.

5. Panepinto JA. Health-related quality of life in patients with hemoglobinopathies. Hematology American Society of Hematology Educ Program Book. 2012;2012:284–9.

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