Comparison of clinical outcomes over time of inpatients with healthcare-associated or community-acquired coronavirus disease 2019 (COVID-19): A multicenter, prospective cohort study.

Grant, Rebecca L; Sauser, Julien; Atkinson, Andrew; D'Incau, Stéphanie; Buetti, Niccolò; Zanella, Marie-Céline; Harbarth, Stephan; Marschall, Jonas; Catho, Gaud (2024). Comparison of clinical outcomes over time of inpatients with healthcare-associated or community-acquired coronavirus disease 2019 (COVID-19): A multicenter, prospective cohort study. Infection control and hospital epidemiology, 45(1), pp. 75-81. Cambridge University Press 10.1017/ice.2023.143

[img]
Preview
Text
comparison-of-clinical-outcomes-over-time-of-inpatients-with-healthcare-associated-or-community-acquired-coronavirus-disease-2019-covid-19-a-multicenter-prospective-cohort-study.pdf - Published Version
Available under License Creative Commons: Attribution (CC-BY).

Download (393kB) | Preview

OBJECTIVE

To compare clinical outcomes over time of inpatients with healthcare-associated coronavirus disease 2019 (HA-COVID-19) versus community-acquired COVID-19 (CA-COVID-19).

DESIGN

We conducted a multicenter, prospective observational cohort study of inpatients with COVID-19.

SETTING

The study was conducted across 16 acute-care hospitals in Switzerland.

PARTICIPANTS AND METHODS

We compared HA-COVID-19 cases, defined as patients with a positive severe acute respiratory coronavirus virus 2 (SARS-CoV-2) test > 5 days after hospital admission, with hospitalized CA-COVID-19 cases, defined as those who tested positive within 5 days of admission. The composite primary outcome was patient transfer to an intensive care unit (ICU) or an intermediate care unit (IMCU) and/or all-cause in-hospital mortality. We used cause-specific Cox regression and Fine-Gray regression to model the time to the composite clinical outcome, adjusting for confounders and accounting for the competing event of discharge from hospital. We compared our results to those from a conventional approach using an adjusted logistic regression model where time-varying effects and competitive risk were ignored.

RESULTS

Between February 19, 2020, and December 31, 2020, we included 1,337 HA-COVID-19 cases and 9,068 CA-COVID-19 cases. HA-COVID-19 patients were significantly older: median, 80 (interquartile range [IQR], 71-87) versus median 70 (IQR, 57-80) (P < .001). A greater proportion of HA-COVID-19 patients had a Charlson comorbidity index ≥ 5 (79% vs 55%; P < .001) than did CA-COVID-19 patients. In time-varying analyses, between day 0 and 8, HA-COVID-19 cases had a decreased risk of death or ICU or IMCU transfer compared to CA-COVID-19 cases (cause-specific hazard ratio [csHR], 0.43; 95% confidence interval [CI], 0.33-0.56). In contrast, from day 8 to 30, HA-COVID-19 cases had an increased risk of death or ICU or IMCU transfer (csHR, 1.49; 95% CI, 1.20-1.85), with no significant effect on the rate of discharge (csHR, 0.83; 95% CI, 0.61-1.14). In the conventional logistic regression model, HA-COVID-19 was protective against transfer to an ICU or IMCU and/or all-cause in-hospital mortality (adjusted odds ratio [aOR], 0.79, 95% CI, 0.67-0.93).

CONCLUSIONS

The risk of adverse clinical outcomes for HA-COVID-19 cases increased substantially over time in hospital and exceeded that for CA-COVID-19. Using approaches that do not account for time-varying effects or competing events may not fully capture the true risk of HA-COVID-19 compared to CA-COVID-19.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Department of Haematology, Oncology, Infectious Diseases, Laboratory Medicine and Hospital Pharmacy (DOLS) > Clinic of Infectiology

UniBE Contributor:

Atkinson, Andrew David, D'Incau, Stéphanie Maria, Marschall, Jonas

Subjects:

600 Technology > 610 Medicine & health

ISSN:

0899-823X

Publisher:

Cambridge University Press

Language:

English

Submitter:

Pubmed Import

Date Deposited:

03 Aug 2023 09:31

Last Modified:

11 Jan 2024 00:12

Publisher DOI:

10.1017/ice.2023.143

PubMed ID:

37529850

BORIS DOI:

10.48350/185184

URI:

https://boris.unibe.ch/id/eprint/185184

Actions (login required)

Edit item Edit item
Provide Feedback