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镰状细胞病的疼痛管理与生活质量

Pain management and quality of life in sickle cell disease.

作者信息

Howard Jo, Thomas Veronica J, Rawle Heather M

机构信息

Department of Haematology, St Thomas' Hospital, Guy's and St Thomas' NHS Foundation Trust, Westminster Bridge Road, London SE1 7EH, UK.

出版信息

Expert Rev Pharmacoecon Outcomes Res. 2009 Aug;9(4):347-52. doi: 10.1586/erp.09.32.

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.

摘要

镰状细胞病(SCD)是全球最常见的遗传性疾病,造成了巨大的健康负担。其主要临床特征是严重疼痛,这种疼痛不可预测且反复发作,除此之外,SCD的其他急慢性特征可能会对患者及其家人和护理人员的生活质量产生巨大影响。我们借鉴最近发布的英国护理标准,探讨SCD疼痛管理的医学和心理方法,同时也考虑SCD对生活质量的影响。

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