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2022-23 年澳大利亚和新西兰重症监护病房因原发性、加重性或偶发性 SARS-CoV-2 感染而入院的患者结局:ANZICS 数据的回顾性分析。

Outcomes for people admitted to Australian and New Zealand intensive care units with primary, exacerbating, or incidental SARS-CoV-2 infections, 2022-23: a retrospective analysis of ANZICS data.

机构信息

Australia and New Zealand Intensive Care Research Centre, Monash University, Melbourne, VIC.

St Vincent's Hospital, Melbourne, VIC.

出版信息

Med J Aust. 2024 Aug 19;221(4):209-216. doi: 10.5694/mja2.52390. Epub 2024 Jul 17.

Abstract

OBJECTIVES

To compare in-hospital mortality and intensive care unit (ICU) length of stay for people admitted to Australian and New Zealand ICUs during 2022-23 with coronavirus disease 2019 (COVID-19) pneumonitis, incidental or exacerbating severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections, or without SAR-CoV-2 infections.

STUDY DESIGN

Retrospective cohort study; analysis of Australian and New Zealand Intensive Care Society (ANZICS) Adult Patient Database data.

SETTING, PARTICIPANTS: Adults (16 years or older) admitted to participating ICUs in Australia or New Zealand, 1 January 2022 - 30 June 2023.

MAJOR OUTCOME MEASURES

The primary outcome was in-hospital mortality, the secondary outcome ICU length of stay, each by SARS-CoV-2 infection attribution classification: primary COVID-19; exacerbating SARS-CoV-2 infection (SARS-CoV-2 infection was a contributing factor to the primary cause of ICU admission); incidental SARS-CoV-2 infections (SARS-CoV-2 infection detected during ICU admission but did not contribute to admission diagnosis); no SARS-CoV-2 infection.

RESULTS

A total of 207 684 adults were admitted to 195 Australian and New Zealand ICUs during 2022-23; 2674 people (1.3%) had incidental SARS-CoV-2 infections, 4923 (2.4%) exacerbating infections, and 3620 (1.7%) primary COVID-19. Unadjusted in-hospital mortality for people with incidental SARS-CoV-2 infections (288 deaths, 10.8%) was lower than for those with exacerbating infections (928 deaths, 18.8%) or primary COVID-19 (830 deaths, 22.9%), but higher than for patients without SARS-CoV-2 infections (15 486 deaths, 7.9%). After adjusting for illness severity, frailty, geographic region, and type of hospital, mortality was higher for patients with incidental SARS-CoV-2 infections (adjusted odds ratio [aOR], 1.28; 95% confidence interval [CI], 1.10-1.50), exacerbating infections (aOR, 1.35; 95% CI, 1.22-1.48), or primary COVID-19 (aOR, 2.54; 95% CI, 2.30-2.81) than for patients without SARS-CoV-2 infections. After adjusting for diagnosis and illness severity, ICU stays were longer for people with incidental (mean difference, 3.3 hours; 95% CI, 2.4-4.2 hours) or exacerbating infections (0.8 hours; 95% CI, 0.2-1.5 hours) than for those without SARS-CoV-2 infections.

CONCLUSION

Risk-adjusted in-hospital mortality and ICU length of stay are higher for people admitted to intensive care who have concomitant SARS-CoV-2 infections than for people who do not.

摘要

目的

比较 2022-23 年澳大利亚和新西兰重症监护病房(ICU)因 2019 年冠状病毒病(COVID-19)肺炎、继发或加重严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染或无 SARS-CoV-2 感染而入住的患者的住院死亡率和 ICU 住院时间。

研究设计

回顾性队列研究;对澳大利亚和新西兰重症监护学会(ANZICS)成人患者数据库数据进行分析。

地点、参与者:2022 年 1 月 1 日至 2023 年 6 月 30 日期间,在澳大利亚或新西兰参与 ICU 治疗的 16 岁或以上成年人。

主要观察指标

主要结局指标为住院死亡率,次要结局指标为 ICU 住院时间,每个结局指标按 SARS-CoV-2 感染归因分类:原发性 COVID-19;继发 SARS-CoV-2 感染(SARS-CoV-2 感染是 ICU 入院主要原因的促成因素);偶然 SARS-CoV-2 感染(在 ICU 住院期间检测到 SARS-CoV-2 感染,但未促成入院诊断);无 SARS-CoV-2 感染。

结果

在 2022-23 年期间,共有 207684 名成年人入住澳大利亚和新西兰的 195 家 ICU;2674 人(1.3%)有偶然 SARS-CoV-2 感染,4923 人(2.4%)有继发感染,3620 人(1.7%)有原发性 COVID-19。偶然 SARS-CoV-2 感染患者(288 例死亡,10.8%)的未调整住院死亡率低于继发感染患者(928 例死亡,18.8%)或原发性 COVID-19 患者(830 例死亡,22.9%),但高于无 SARS-CoV-2 感染患者(15486 例死亡,7.9%)。在调整疾病严重程度、脆弱性、地理位置和医院类型后,偶然 SARS-CoV-2 感染患者(调整后的优势比[aOR],1.28;95%置信区间[CI],1.10-1.50)、继发感染患者(aOR,1.35;95% CI,1.22-1.48)或原发性 COVID-19 患者(aOR,2.54;95% CI,2.30-2.81)的死亡率均高于无 SARS-CoV-2 感染患者。在调整诊断和疾病严重程度后,偶然感染(平均差异,3.3 小时;95%CI,2.4-4.2 小时)或继发感染(0.8 小时;95%CI,0.2-1.5 小时)患者的 ICU 住院时间长于无 SARS-CoV-2 感染患者。

结论

与未感染 SARS-CoV-2 的患者相比,同时感染 SARS-CoV-2 的重症监护患者的住院死亡率和 ICU 住院时间的风险调整后更高。

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