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Mental health and quality of life outcomes in family members of patients with chronic critical illness admitted to the intensive care units of two Brazilian hospitals serving the extremes of the socioeconomic spectrum

机译:患有慢性批判性疾病患者的家庭成员的心理健康和生活质量,录取了两家巴西医院的重症监护单位,服务于社会经济频谱极端的巴西医院

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Chronic critical illness (CCI) is a relevant clinical, social and financial health issue. The aim of this study was to compare the mental outcomes (symptoms of anxiety and depression) and quality of life outcomes of the family members of patients with CCI from different socioeconomic backgrounds who were admitted to one of the intensive care units (ICUs) in two Brazilian hospitals, one private and one public. It is a prospective study involving a public hospital that serves a low-income population and a tertiary private hospital that serves a high-income population. Family members of patients with CCI answered the Hospital Anxiety and Depression Scale (HADS) and The World Health Organization Quality of Life–WHOQOL-bref questionnaires. They responded to the European Quality of life Five Dimension three Level (EuroQol-5D-3L) and the Activities of Daily Living (ADL) questionnaires on behalf of the patients at three time points: during the ICU stay, 30 and 90 days after the patient was discharged. We used logistic regression models to evaluate the main predictors of a binary outcome regarding symptoms of anxiety and depression. We enrolled 186 patients with CCI. Many patients from public hospitals who were independent became dependent for their ADLs at 90 days (41.7% versus 14.3%, p = 0.03). At 30 days, family members from public hospital had worse impact on all domains of WHOQOL-bref compared with families from private hospital. At 90-days, the difference persists in the physical domain, worse for families from public hospital (p = 0.006). The symptoms of depression at 30-days (p = 0.008) and at 90-days (p = 0.013) were worse in the public hospital. CCIs affected quality of life and the emotional condition of family members, especially in families with fewer resources when the patients became more dependent. Family members with higher education were more likely to experience depression, while depression was associated with cohabiting with the patient in low-income families.
机译:慢性危重疾病(CC​​I)是一个相关的临床,社会和金融卫生问题。本研究的目的是将CCI患者的焦虑和抑郁症状的症状和抑郁症状的质量结果与两种重症监护单位(ICU)的不同社会经济背景从不同的社会经济背景中进行了患者。巴西医院,一个私人和一个公众。它是一项涉及公立医院的前瞻性研究,该医院供应低收入人口和高收入人口的高等私人医院。 CCI患者的家庭成员回答了医院焦虑和抑郁规模(曾经)和世界卫生组织的世界卫生组织质量 - WHOQOL-BREF问卷。他们回应了欧洲生活质量五维三级(Euroqol-5d-3L)和日常生活(ADL)问卷的活动,在三个时间点代表患者:在ICU停留期间,30和90天后病人被排出。我们使用了物流回归模型来评估关于焦虑和抑郁症状的二元结果的主要预测因子。我们注册了186名CCI患者。许多来自独立的公立医院的患者在90天内依赖于他们的ADL(41.7%对14.3%,P = 0.03)。 30天,与私立医院的家庭相比,公立医院的家庭成员对WHOQOL-BREF的所有领域的影响更大。在90天,差异在物理领域持续存在,对于公立医院的家庭更糟糕(P = 0.006)。公立医院在30天(P = 0.008)和90天(P = 0.013)的抑郁症症状更差。 CCIS影响了生活质量和家庭成员的情感状况,特别是当患者变得更加依赖时的资源较少的家庭。具有高等教育的家庭成员更有可能体验抑郁症,而抑郁症与低收入家庭的患者同志与患者联系起来。

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