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分析 2014-2017 年在西南悉尼公立医院的有和无糖尿病患者的住院死亡率。

Analysis of in-hospital mortality among people with and without diabetes in South Western Sydney public hospitals (2014-2017).

机构信息

Translational Health Research Institute (THRI), School of Medicine, Western Sydney University, Campbelltown, NSW, 2560, Australia.

School of Health Sciences, Western Sydney University, Campbelltown, NSW, 2560, Australia.

出版信息

BMC Public Health. 2021 Nov 3;21(1):1991. doi: 10.1186/s12889-021-12120-w.

Abstract

BACKGROUND

Diabetes is a major public health problem affecting about 1.4 million Australians, especially in South Western Sydney, a hotspot of diabetes with higher than average rates for hospitalisations. The current understanding of the international burden of diabetes and related complications is poor and data on hospital outcomes and/or what common factors influence mortality rate in people with and without diabetes in Australia using a representative sample is lacking. This study determined in-hospital mortality rate and the factors associated among people with and without diabetes.

METHODS

Retrospective data for 554,421 adult inpatients was extracted from the population-based New South Wales (NSW) Admitted Patient Data over 3 financial years (from 1 July 2014-30 June 2015 to 1 July 2016-30 June 2017). The in-hospital mortality per 1000 admitted persons, standardised mortality ratios (SMR) were calculated. Binary logistic regression was performed, adjusting for potential covariates and co-morbidities for people with and without diabetes over three years.

RESULTS

Over three years, 8.7% (48,038 people) of admissions involved people with diabetes. This increased from 8.4% in 2014-15 to 8.9% in 2016-17 (p = 0.007). Across all age groups, in-hospital mortality rate was significantly greater in people with diabetes (20.6, 95% Confidence intervals CI 19.3-21.9 per 1000 persons) than those without diabetes (11.8, 95%CI 11.5-12.1) and more in men than women (23.1, 95%CI 21.2-25.0 vs 17.9, 95%CI 16.2-19.8) with diabetes. The SMR for those with and without diabetes were 3.13 (95%CI 1.78-4.48) and 1.79 (95%CI 0.77-2.82), respectively. There were similarities in the factors associated with in hospital mortality in both groups including: older age (> 54 years), male sex, marital status (divorced/widowed), length of stay in hospital (staying longer than 4 days), receiving intensive care in admission and being admitted due to primary respiratory and cardiovascular diagnoses. The odds of death in admission was increased in polymorbid patients without diabetes (28.68, 95%CI 23.49-35.02) but not in those with diabetes.

CONCLUSIONS

In-patients with diabetes continue to have higher mortality rates than those without diabetes and the Australian population. Overall, similar factors influenced mortality rate in people with and without diabetes, but significantly more people with diabetes had two or more co-morbidities, suggesting that hospital mortality may be driven by those with pre-existing health/comorbidities. Urgent measures in primary care to prevent admissions among people with multiple co-morbidities are needed.

摘要

背景

糖尿病是一个影响着约 140 万澳大利亚人的主要公共卫生问题,特别是在糖尿病高发的澳大利亚西南部,其住院率高于平均水平。目前,国际上对糖尿病的负担以及相关并发症的了解甚少,也缺乏有关澳大利亚使用代表性样本的住院结果和/或影响有糖尿病和无糖尿病患者死亡率的常见因素的数据。本研究旨在确定有糖尿病和无糖尿病患者的住院死亡率以及相关因素。

方法

从人口基础新南威尔士州(NSW)住院病人数据中提取了 3 个财政年度(2014 年 7 月 1 日至 2015 年 6 月 30 日至 2016 年 7 月 1 日至 2017 年 6 月 30 日)内 554421 名成年住院患者的回顾性数据。每 1000 名入院患者的院内死亡率为 48038 人,计算标准化死亡率比(SMR)。对有和无糖尿病的患者进行了 3 年的潜在混杂因素和合并症的二元逻辑回归分析。

结果

3 年来,有 8.7%(48038 人)的住院患者患有糖尿病。这一比例从 2014-15 年的 8.4%上升到 2016-17 年的 8.9%(p=0.007)。在所有年龄组中,有糖尿病的患者的院内死亡率明显高于无糖尿病的患者(每 1000 人中有 20.6 人,95%置信区间 CI 19.3-21.9),且男性高于女性(23.1,95%CI 21.2-25.0 vs 17.9,95%CI 16.2-19.8)。有和无糖尿病的 SMR 分别为 3.13(95%CI 1.78-4.48)和 1.79(95%CI 0.77-2.82)。两组患者的院内死亡率相关因素相似,包括:年龄较大(>54 岁)、男性、婚姻状况(离婚/丧偶)、住院时间(住院超过 4 天)、入院时接受重症监护和因原发性呼吸和心血管诊断而入院。无糖尿病的多合并症患者入院死亡的几率增加(28.68,95%CI 23.49-35.02),但有糖尿病的患者没有。

结论

有糖尿病的住院患者的死亡率继续高于无糖尿病和澳大利亚人口的死亡率。总体而言,有和无糖尿病的患者死亡率的影响因素相似,但有更多糖尿病患者有两种或更多合并症,这表明医院死亡率可能是由已有健康状况/合并症驱动的。需要在初级保健中采取紧急措施,防止有多种合并症的人群住院。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c2c/8567571/627a307dc2de/12889_2021_12120_Fig1_HTML.jpg

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