Literature DB >> 19670995

Pain management and quality of life in sickle cell disease.

Jo Howard1, Veronica J Thomas, Heather M Rawle.   

Abstract

Sickle cell disease (SCD) is the most common inherited disease worldwide and is responsible for a massive health burden. Its main clinical feature is severe pain that is unpredictable and recurrent, and this, in addition to the other acute and chronic features of SCD, may have a huge impact on the quality of life of both the patient and their families and carers. We consider medical and psychological methods of pain management in SCD, drawing on recently published UK Standards of Care, and also consider the effect of SCD on quality of life.

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Year:  2009        PMID: 19670995     DOI: 10.1586/erp.09.32

Source DB:  PubMed          Journal:  Expert Rev Pharmacoecon Outcomes Res        ISSN: 1473-7167            Impact factor:   2.217


  3 in total

1.  Spirituality, Self-Efficacy, and Quality of Life among Adults with Sickle Cell Disease.

Authors:  Maxine Adegbola
Journal:  South Online J Nurs Res       Date:  2011-04

2.  Behavioral impact of sickle cell disease in young children with repeated hospitalization.

Authors:  Mohamed H Bakri; Eman A Ismail; Ghada O Elsedfy; Mostafa A Amr; Ahmed Ibrahim
Journal:  Saudi J Anaesth       Date:  2014-10

3.  Pain measurement as part of primary healthcare of adult patients with sickle cell disease.

Authors:  Andreza Aparecida Felix Signorelli; Sonia Beatriz Felix Ribeiro; Helio Moraes-Souza; Lucas Felix de Oliveira; João Batista Ribeiro; Sheron Hellen da Silva; Daniel Fachinelli Felix de Oliveira; Matheus Fernando Felix Ribeiro
Journal:  Rev Bras Hematol Hemoter       Date:  2013
  3 in total

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