尼日利亚贝宁市镰状细胞病受试者的健康相关生活质量

B. Nwogoh, C. Ofovwe, C. Omoti
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引用次数: 4

摘要

背景:镰状细胞病(SCD)是一种发病率和死亡率较高的慢性疾病。血红蛋白病是全球最普遍的遗传病,据估计,尼日利亚2-3%的人患有SCD。这种疾病可能对镰状细胞病患者的生活质量产生不利影响。本研究旨在评估生活在尼日利亚贝宁市的SCD受试者与正常对照者的健康相关生活质量(HRQoL)。方法:采用医学结局研究36项调查工具评估SCD受试者的HRQoL。结果与正常非scd人群进行比较。使用Statistical Package for Social Sciences version 16(芝加哥,SPSS Inc.)对数据进行分析。P值设为0.05。结果:61名SCD受试者和61名正常人(对照组)参与了研究。SCD组和对照组的平均年龄分别为26.7±9.0岁和23.70±3.1岁。SCD患者中有59例(96.7%)为血红蛋白(Hb) SS, 2例(3.3%)为Hb SC。与对照组相比,SCD患者的身体功能、身体健康限制、一般健康状况和疼痛评分显著降低(P分别为0.000、0.000、0.000和0.002)。两组在社交功能和因情绪问题造成的限制方面差异无统计学意义,而活力(能量/疲劳)得分和情绪幸福感得分以SCD组高,但差异无统计学意义(P分别为0.066和0.127)。男性性别、就业、就诊、家庭支持对SCD受试者的HRQoL有正向影响。结论:SCD患者的身体和一般健康功能明显受损。我们地区的临床医生需要审查当前的管理趋势,包括世界最佳实践,如羟基脲的普遍使用和干细胞移植,以改变当前的趋势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Health-related quality of life in sickle cell disease subjects in Benin City, Nigeria
Background: Sickle cell disease (SCD) is a chronic disease associated with increased morbidity and mortality. Hemoglobinopathies are the most prevalent genetic disease globally, and SCD is estimated to affect 2–3% of Nigerians. The disease may adversely impact on the quality of life of sickle cell patients. This study aims to evaluate the health-related quality of life (HRQoL) of SCD subjects compared to normal controls living in Benin City, Nigeria. Methodology: The HRQoL of SCD subjects was evaluated using the Medical Outcome Study 36-item survey tool. The outcome was compared with those of a normal non-SCD population. Data were analyzed with Statistical Package for Social Sciences version 16 (Chicago, SPSS Inc.). P value was set at 0.05.Results: Sixty-one SCD subjects and 61 normal respondents (controls) participated in the study. The mean ages of the SCD group and controls were 26.7 ± 9.0 years and 23.70 ± 3.1 years, respectively. Fifty-nine (96.7%) of the SCD respondents were hemoglobin (Hb) SS and 2 (3.3%) were Hb SC. The physical function, limitations due to physical health, general health, and pain scores were significantly lower in the SCD population compared to the controls (P = 0.000, 0.000, 0.000, and 0.002, respectively. The social function and limitation due to the emotional problem do not differ significantly between both groups while the vitality (energy/fatigue) score and emotional well-being were higher in the SCD group, but they were not statistically significant (P = 0.066 and 0.127, respectively). Male gender, employment, clinic attendance, and family support impacted positively on the HRQoL of SCD subjects. Conclusion: The physical and general health functions of SCD subjects are significantly impaired by the disease. There is a need for clinicians in our region to review current management trends to include world best practices such as the universal use of hydroxyurea and stem cell transplantation to change the prevailing trend.
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