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成人镰状细胞病慢性疼痛多维度的文献综述。

A review of the literature on the multiple dimensions of chronic pain in adults with sickle cell disease.

机构信息

Department of Physiological Nursing, University of California at San Francisco, San Francisco, California 94143-0610, USA.

出版信息

J Pain Symptom Manage. 2010 Sep;40(3):416-35. doi: 10.1016/j.jpainsymman.2009.12.027. Epub 2010 Jul 24.

DOI:10.1016/j.jpainsymman.2009.12.027
PMID:20656451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2989986/
Abstract

Sickle cell disease (SCD) is a major health care and societal problem that affects millions of people worldwide. In Nigeria, 45,000 to 90,000 babies are born each year with SCD. In the United States, SCD is the most common genetic disorder, affecting more than 80,000 people, the majority of whom are African American. Sickle cell pain is the hallmark feature of SCD. Most of the research on pain from SCD has focused on children with acute pain associated with sickle cell crisis. Consequently, very little is known about the occurrence and characteristics of chronic pain, especially in adults with SCD. Individuals with SCD who experience chronic pain are often underserved, and their pain is undertreated. This undertreatment may result in millions of dollars per year spent on emergency room visits, hospitalizations, and lost work productivity. The primary purpose of this literature review was to summarize the findings from studies that evaluated the characteristics of chronic pain in adults with SCD. Each of the studies included in this review was evaluated to determine if it provided data on the following multidimensional characteristics of chronic pain: occurrence, number of pain episodes, duration, pattern, quality, location, intensity, aggravating factors, relieving factors, and impact of pain on function. A secondary purpose was to identify gaps in knowledge and directions for future research on the multiple dimensions of chronic pain in adults with SCD.

摘要

镰状细胞病(SCD)是一个全球性的重大医疗和社会问题,影响着全球数百万人。在尼日利亚,每年有 45000 至 90000 名婴儿患有 SCD。在美国,SCD 是最常见的遗传疾病,影响着超过 80000 人,其中大多数是非洲裔美国人。镰状细胞疼痛是 SCD 的主要特征。大多数关于 SCD 疼痛的研究都集中在与镰状细胞危象相关的急性疼痛的儿童身上。因此,对于慢性疼痛的发生和特征,尤其是在患有 SCD 的成年人中,知之甚少。患有慢性疼痛的 SCD 患者往往得不到充分的治疗,他们的疼痛也未得到充分的治疗。这种治疗不足可能导致每年花费数百万美元用于急诊室就诊、住院和失去工作生产力。本文献综述的主要目的是总结评估成人 SCD 慢性疼痛特征的研究结果。本综述中包含的每项研究都进行了评估,以确定其是否提供了有关慢性疼痛以下多维特征的数据:发生、疼痛发作次数、持续时间、模式、质量、位置、强度、加重因素、缓解因素以及疼痛对功能的影响。次要目的是确定成人 SCD 慢性疼痛多维度研究的知识空白和未来研究方向。

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本文引用的文献

1
Daily assessment of pain in adults with sickle cell disease.镰状细胞病成人患者疼痛的每日评估
Ann Intern Med. 2008 Jan 15;148(2):94-101. doi: 10.7326/0003-4819-148-2-200801150-00004.
2
The prevention of pain from sickle cell disease by trandolapril.群多普利预防镰状细胞病疼痛
J Natl Med Assoc. 2007 Mar;99(3):276-8.
3
Pain management in sickle cell disease.镰状细胞病的疼痛管理
Chronic Illn. 2006 Mar;2(1):39-50. doi: 10.1177/17423953060020011101.
4
Hydroxyurea and sickle cell anemia: effect on quality of life.羟基脲与镰状细胞贫血:对生活质量的影响
Health Qual Life Outcomes. 2006 Aug 31;4:59. doi: 10.1186/1477-7525-4-59.
5
Pain management for sickle cell disease.镰状细胞病的疼痛管理
Cochrane Database Syst Rev. 2006 Apr 19(2):CD003350. doi: 10.1002/14651858.CD003350.pub2.
6
Gender differences in pain and healthcare utilization for adult sickle cell patients: The PiSCES Project.成年镰状细胞病患者疼痛及医疗服务利用方面的性别差异:PiSCES项目
J Womens Health (Larchmt). 2006 Mar;15(2):146-54. doi: 10.1089/jwh.2006.15.146.
7
Moderate chronic pain, weight and dietary intake in African-American adult patients with sickle cell disease.患有镰状细胞病的非裔美国成年患者的中度慢性疼痛、体重及饮食摄入量
J Natl Med Assoc. 2005 Dec;97(12):1622-9.
8
Pain and stress in sickle cell disease: an analysis of daily pain records.镰状细胞病中的疼痛与应激:每日疼痛记录分析
Int J Behav Med. 1998;5(3):185-203. doi: 10.1207/s15327558ijbm0503_1.
9
Health related quality of life in sickle cell patients: the PiSCES project.镰状细胞病患者的健康相关生活质量:PiSCES项目
Health Qual Life Outcomes. 2005 Aug 29;3:50. doi: 10.1186/1477-7525-3-50.
10
Religiosity/spirituality and pain in patients with sickle cell disease.镰状细胞病患者的宗教信仰/精神性与疼痛
J Nerv Ment Dis. 2005 Apr;193(4):250-7. doi: 10.1097/01.nmd.0000158375.73779.50.