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人类免疫缺陷病毒感染患者的生活质量:社会支持、应对方式和绝望感的影响

Quality of life in patients with human immunodeficiency virus infection: impact of social support, coping style and hopelessness.

作者信息

Swindells S, Mohr J, Justis J C, Berman S, Squier C, Wagener M M, Singh N

机构信息

University of Nebraska Medical Center, Omaha, USA.

出版信息

Int J STD AIDS. 1999 Jun;10(6):383-91.

Abstract

We aimed to determine whether the quality of life (QOL) in the patients infected with human immunodeficiency virus (HIV) infection was influenced by satisfaction with social support, coping style and hopelessness. One hundred and thirty-eight HIV-infected patients were prospectively studied in this multicentre, longitudinal study. The QOL was assessed by Medical Outcome Study Health Survey SF-36, social support by Sarason Social Support Questionnaire, hopelessness by Beck Hopelessness Scale, and coping by Billing and Moos Inventory of coping with illness. The QOL did not correlate with age, sex, race, HIV risk factor, education or marital status. Employment (P = 0.0001), higher income (P = 0.03), satisfaction with social support (P = 0.04), regardless of the source of that support, and problem-focused coping (P = 0.03) were associated with a significantly better QOL, while, emotion-focused coping (r = -0.19, P = 0.04), avoidant coping (r = 0.40, P = 0.0001), hopelessness (r = -0.64, P = 0.0001) and AIDS (P = 0.09) were predictors of poorer QOL. Physical functioning correlated positively with employment (P = 0.0001), and inversely with AIDS (P = 0.0002), hopelessness (P = 0.03), avoidant coping (P = 0.03), and age (P = 0.10). At 6 months follow up, QOL score had changed in 20% of the patients; older age (P = 0.01), and lesser satisfaction with social support (P = 0.15) were associated with a decline in QOL, while adherence with antiretroviral therapy (P = 0.006) was associated with an increase in QOL score. Seven of 138 patients died during follow up; these patients had significantly lower QOL at baseline than all other patients (P = 0.003). Interventions to alleviate hopelessness, maladaptive coping, and enhancement of satisfaction with social support may improve overall QOL in HIV-infected patients. Older patients with HIV were less satisfied with their social support, were more likely to utilize unhealthy coping styles, and experienced a greater decline in QOL over time.

摘要

我们旨在确定感染人类免疫缺陷病毒(HIV)的患者的生活质量(QOL)是否受到社会支持满意度、应对方式和绝望感的影响。在这项多中心纵向研究中,对138例HIV感染患者进行了前瞻性研究。生活质量通过医学结局研究健康调查简表SF - 36进行评估,社会支持通过萨拉森社会支持问卷进行评估,绝望感通过贝克绝望量表进行评估,应对方式通过比林和莫斯应对疾病量表进行评估。生活质量与年龄、性别、种族、HIV风险因素、教育程度或婚姻状况无关。就业情况(P = 0.0001)、较高收入(P = 0.03)、对社会支持的满意度(P = 0.04,无论支持来源如何)以及以问题为导向的应对方式(P = 0.03)与显著更好的生活质量相关,而以情绪为导向的应对方式(r = -0.19,P = 0.04)、回避应对方式(r = 0.40,P = 0.0001)、绝望感(r = -0.64,P = 0.0001)和艾滋病(P = 0.09)是生活质量较差的预测因素。身体功能与就业情况呈正相关(P = 0.0001),与艾滋病(P = 0.0002)、绝望感(P = 0.03)、回避应对方式(P = 0.03)和年龄(P = 0.10)呈负相关。在6个月的随访中,20%的患者生活质量得分发生了变化;年龄较大(P = 0.01)以及对社会支持的满意度较低(P = 0.15)与生活质量下降相关,而坚持抗逆转录病毒治疗(P = 0.006)与生活质量得分增加相关。138例患者中有7例在随访期间死亡;这些患者在基线时的生活质量显著低于所有其他患者(P = 0.003)。减轻绝望感、不良应对方式以及提高社会支持满意度的干预措施可能会改善HIV感染患者的总体生活质量。感染HIV的老年患者对其社会支持的满意度较低,更有可能采用不健康的应对方式,并且随着时间的推移生活质量下降幅度更大。

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