虚弱指数在预测长期住院的血管性认知障碍患者肺炎复发和死亡方面的有效性。

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引用次数: 0

摘要

研究目的目的:预测使用虚弱指数(FI)预测50岁以上血管性认知障碍(VCI)患者长期住院期间肺炎复发和死亡的有效性:这项回顾性队列研究在中国西部的一家教学医院进行,研究对象包括接受长期住院治疗的年龄≥50岁的血管性认知障碍患者。相关数据来自电子病历系统。FI基于31个参数,以临界值(0.2)作为稳健性(FI结果)来定义组别:共纳入了 252 名年龄≥50 岁的长期住院脑梗死患者,其中男性 115 名(45.6%)。97名患者(38.5%)被定义为FRAIL。住院患者的中位住院时间为 37 个月。总体而言,215 名患者在住院期间患上了肺炎,平均在入院后 14.5 个月发病,151 人(59.9%)肺炎复发,155 人(61.5%)死亡。其中,143 例死于住院期间,12 例死于出院后。在复发性肺炎的发生率方面,FRAIL 和长期住院的健壮型 VCI 患者没有明显差异(FRAIL vs. robust:66.0 % vs. 56.1 %,P = 0.121),而 FRAIL 患者的死亡率高于健壮型患者(FRAIL vs. robust:71.1 % vs. 55.5 %,P = 0.013)。在进一步进行 Cox 回归分析并调整单变量分析中发现的重要混杂因素(包括年龄、性别、吸烟史和日常生活活动(ADL)评分)后,FRAIL 患者的死亡风险高于健康患者(HR = 1.595,95 % CI:1.149-2.213)。此外,在模型 2 的基础上,将单变量分析中无统计学意义但可能对结果产生影响的混杂变量(包括婚姻状况、教育程度、饮酒史、合并症和康复治疗)纳入模型 3 进行进一步校正。结果依然未变,即与体格健壮的患者相比,FRAIL 患者的死亡风险更高(HR = 1.771,95 % CI:1.228-2.554):结论:FI定义的虚弱可有效预测50岁或以上长期住院的VCI患者的死亡风险,但不能预测复发性肺炎的风险。
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Effectiveness of the frailty index in predicting recurrent pneumonia and death in long-term hospitalized patients with vascular cognitive impairment

Objective

The aim was to predict the effectiveness of using frailty, defined by the frailty index (FI), for predicting recurrent pneumonia and death in patients over 50 years and older with vascular cognitive impairment (VCI) during long-term hospitalization.

Measurements

This retrospective cohort study was conducted at a teaching hospital in western China and included VCI patients aged ≥50 years undergoing long-term hospitalization. The relevant data were collected from the electronic medical record system. The FI was based on 31 parameters and groups were defined using a cutoff value (0.2) as robust (FI < 0.2) and FRAIL (≥0.2). The definition of recurrent pneumonia was a minimum of two episodes within a year, with the symptoms, signs, and imaging results of pneumonia disappearing completely between episodes, and a minimum interval between episodes of seven days. Death was recorded by the hospital as the result of cardiac and respiratory arrest and survival was defined as the interval between hospital admission and confirmed death. Logistic regression models were used to assess the association between FI and recurrent pneumonia, while associations between FI and death were assessed by Cox proportional hazards models.

Results

A total of 252 long-term hospitalized VCI patients ≥50 years old were enrolled, of whom 115 were male (45.6 %). Ninety-seven patients (38.5 %) were defined as FRAIL. The median length of stay for hospitalized patients was 37 months. Overall, 215 patients developed pneumonia during hospitalization, which occurred an average of 14.5 months after admission, while 151 (59.9 %) had recurrent pneumonia, and 155 (61.5 %) died. Of these, 143 died in the hospital and 12 died after discharge. No significant differences were seen in the incidence of recurrent pneumonia between FRAIL and robust long-term hospitalized VCI patients (FRAIL vs. robust: 66.0 % vs. 56.1 %, P = 0.121) while FRAIL patients had a higher mortality rate than robust patients (FRAIL vs. robust: 71.1 % vs. 55.5 %, P = 0.013). After further Cox regression analysis and adjustment for possible confounders found to be significant in the univariate analysis (including age, sex, smoking history, and activities of daily living (ADL) score), FRAIL patients had a higher risk of death than healthy patients (HR = 1.595, 95 % CI: 1.149–2.213). In addition, based on Model 2, confounding variables that were not statistically significant in the univariate analysis but may have had an impact on the results (including marital status, educational level, drinking history, comorbidity and rehabilitation treatment) were incorporated into Model 3 for further correction. The result remained unchanged, namely, that compared with robust patients, FRAIL patients had a higher risk of death (HR = 1.771, 95 % CI: 1.228–2.554).

Conclusions and implications

Frailty defined by the FI was effective for predicting the risk of mortality but not that of recurrent pneumonia in long-term hospitalized VCI patients aged 50 or older.

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来源期刊
Experimental gerontology
Experimental gerontology Ageing, Biochemistry, Geriatrics and Gerontology
CiteScore
6.70
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0.00%
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审稿时长
66 days
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