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Day-90 survival in critically-ill patients with COVID-19 and hydroxychloroquine: a propensity analysis.
Cour, Martin; Amaz, Camille; Bohé, Julien; Rimmelé, Thomas; Ovize, Michel; Argaud, Laurent.
  • Cour M; Medical Intensive Care Department, Hospices Civils de Lyon, Edouard Herriot Hospital, Lyon, France.
  • Amaz C; Hospices Civils de Lyon, Investigation Clinical Center of Lyon, Lyon, France.
  • Bohé J; Medical Intensive Care Department, Hospices Civils de Lyon, Lyon-Sud Hospital, Lyon, France.
  • Rimmelé T; Anesthesia and Critical Care Department, Hospices Civils de Lyon, Edouard Herriot Hospital, Lyon, France.
  • Ovize M; Hospices Civils de Lyon, Investigation Clinical Center of Lyon, Lyon, France.
  • Argaud L; Medical Intensive Care Department, Hospices Civils de Lyon, Edouard Herriot Hospital, Lyon, France.
Ann Transl Med ; 9(7): 524, 2021 Apr.
Article in English | MEDLINE | ID: covidwho-1229549
ABSTRACT

BACKGROUND:

There are limited data on the effect of hydroxychloroquine on medium term outcomes in patients with coronavirus disease 2019 (COVID-19) requiring intensive care. We aimed to evaluate the effects of hydroxychloroquine on day 90 mortality in this specific population.

METHODS:

This retrospective, multicenter, propensity matched cohort analysis, used data of adult patients with laboratory confirmed COVID-19 admitted to 3 university affiliated intensive care units between March 7, 2020, to April 7, 2020 in Lyon, France. Patients received either hydroxychloroquine (loading dose of 400 mg twice daily at day 1 followed by 200 mg twice daily from day 2 to day 10) or standard of care without hydroxychloroquine. We compared all-cause mortality at day-90 after ICU admission between propensity score matched groups receiving hydroxychloroquine or standard of care.

RESULTS:

A total of 157 patients were included with a day-28 and day-90 mortality rate of 23.6% and 32.5%, respectively. The median (interquartile) age was 67 years (56-76 years), 105 (66.9%) were men, 65 (41.4%) fulfilled criteria for acute respiratory distress syndrome, and 64 (41%) received hydroxychloroquine (HCQ) for 10 days (4-10 days). In the propensity score matched cohort (59 patients in each group), day-90 mortality was 35.6% for patients who received HCQ and 23.7% for patients who did not (P=0.23). Kaplan Meier survival analysis showed no statistically significant association between HCQ therapy and mortality (P=0.20 by log-rank test).

CONCLUSIONS:

In this study, off-label use of HCQ in critically ill patients with COVID-19 was not associated with any significant change in medium-term prognosis, confirming results of studies in less severe patients.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Language: English Journal: Ann Transl Med Year: 2021 Document Type: Article Affiliation country: Atm-20-7811

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Language: English Journal: Ann Transl Med Year: 2021 Document Type: Article Affiliation country: Atm-20-7811