Sex-specific prevalence and outcomes of frailty in critically ill patients.

Critical care Female Frailty Mechanical ventilation Mortality Outcomes Renal replacement therapy Sex

Journal

Journal of intensive care
ISSN: 2052-0492
Titre abrégé: J Intensive Care
Pays: England
ID NLM: 101627304

Informations de publication

Date de publication:
2020
Historique:
received: 25 08 2020
accepted: 22 09 2020
entrez: 2 10 2020
pubmed: 3 10 2020
medline: 3 10 2020
Statut: epublish

Résumé

The prevalence of frailty, an important risk factor for short- and long-term outcomes in hospitalized adults, differs by sex. Studies in critically ill adults have also found differences in mortality and organ support rates in males and females. The objective of this study was to determine if these observed differences in mortality and organ support rates can be explained by sex and frailty alone, or if the interaction between sex and frailty is an important risk factor. This is a retrospective multi-centre population-based cohort study of all adult patients (≥ 18 years) admitted to the seventeen intensive care units (ICUs) across Alberta, Canada, between 2016 and 2017. On admission, physicians assigned a Clinical Frailty Scale (CFS) score (1 = very fit, 9 = terminally ill) to all patients. Patients with missing CFS scores or who died within 24 h of ICU admission were excluded. Frailty was defined as CFS ≥ 5. Outcomes included all-cause hospital mortality, ICU mortality, and organ support rates. A propensity score for female sex was generated and 1:1 matching on sex was performed. Multivariable Cox regression or logistic regression, as appropriate, was performed to evaluate the association between sex, frailty, and the sex-frailty interaction term with outcomes. Of 15,238 patients included in the cohort, after propensity score matching 11,816 patients remained (mean [standard deviation] age 57.3 [16.9]). In the matched cohort, females had a higher prevalence of frailty than males (32% vs. 27%, respectively) and higher odds of frailty (odds ratio [95% confidence interval (CI)] 1.29 [1.20-1.40]). Though females were less likely to receive invasive mechanical ventilation (hazard ratio [95% CI] 0.78 [0.71-0.86]), the interaction between sex and frailty (i.e., males and females with and without frailty) was not associated with differences in organ support rates. Receipt of dialysis and vasoactive support, as well as hospital mortality and ICU mortality were associated with frailty but were not associated with female sex or the interaction between sex and frailty. Although frailty and sex were individually associated with mortality and differences in organ support in the ICU, there does not appear to be a significant interaction between sex and frailty with regards to these outcomes.

Sections du résumé

BACKGROUND BACKGROUND
The prevalence of frailty, an important risk factor for short- and long-term outcomes in hospitalized adults, differs by sex. Studies in critically ill adults have also found differences in mortality and organ support rates in males and females. The objective of this study was to determine if these observed differences in mortality and organ support rates can be explained by sex and frailty alone, or if the interaction between sex and frailty is an important risk factor.
METHODS METHODS
This is a retrospective multi-centre population-based cohort study of all adult patients (≥ 18 years) admitted to the seventeen intensive care units (ICUs) across Alberta, Canada, between 2016 and 2017. On admission, physicians assigned a Clinical Frailty Scale (CFS) score (1 = very fit, 9 = terminally ill) to all patients. Patients with missing CFS scores or who died within 24 h of ICU admission were excluded. Frailty was defined as CFS ≥ 5. Outcomes included all-cause hospital mortality, ICU mortality, and organ support rates. A propensity score for female sex was generated and 1:1 matching on sex was performed. Multivariable Cox regression or logistic regression, as appropriate, was performed to evaluate the association between sex, frailty, and the sex-frailty interaction term with outcomes.
RESULTS RESULTS
Of 15,238 patients included in the cohort, after propensity score matching 11,816 patients remained (mean [standard deviation] age 57.3 [16.9]). In the matched cohort, females had a higher prevalence of frailty than males (32% vs. 27%, respectively) and higher odds of frailty (odds ratio [95% confidence interval (CI)] 1.29 [1.20-1.40]). Though females were less likely to receive invasive mechanical ventilation (hazard ratio [95% CI] 0.78 [0.71-0.86]), the interaction between sex and frailty (i.e., males and females with and without frailty) was not associated with differences in organ support rates. Receipt of dialysis and vasoactive support, as well as hospital mortality and ICU mortality were associated with frailty but were not associated with female sex or the interaction between sex and frailty.
CONCLUSIONS CONCLUSIONS
Although frailty and sex were individually associated with mortality and differences in organ support in the ICU, there does not appear to be a significant interaction between sex and frailty with regards to these outcomes.

Identifiants

pubmed: 33005426
doi: 10.1186/s40560-020-00494-9
pii: 494
pmc: PMC7525935
doi:

Types de publication

Journal Article

Langues

eng

Pagination

75

Informations de copyright

© The Author(s) 2020.

Déclaration de conflit d'intérêts

Competing interestsDr. Bagshaw is supported by a Canada Research Chair in Critical Care Nephrology. Dr. Stelfox is supported by CIHR Embedded Clinician Researcher Award.

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Auteurs

Erin Hessey (E)

Department of Critical Care Medicine, Faculty of Medicine and Dentistry and Alberta Health Services-Edmonton Zone, University of Alberta, 8440-112 ST NW, Edmonton, T6G2B7 Canada.

Carmel Montgomery (C)

Department of Critical Care Medicine, Faculty of Medicine and Dentistry and Alberta Health Services-Edmonton Zone, University of Alberta, 8440-112 ST NW, Edmonton, T6G2B7 Canada.

Danny J Zuege (DJ)

Department of Critical Care Medicine, Cumming School of Medicine, University of Calgary and Alberta Health Services-Calgary Zone, Calgary, Canada.
Alberta Critical Care Strategic Clinical Network, Alberta Health Services, Alberta, Canada.

Darryl Rolfson (D)

Division of Geriatric Medicine, Department of Medicine, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Canada.

Henry T Stelfox (HT)

Department of Critical Care Medicine, Cumming School of Medicine, University of Calgary and Alberta Health Services-Calgary Zone, Calgary, Canada.
Alberta Critical Care Strategic Clinical Network, Alberta Health Services, Alberta, Canada.
Department of Community Health Sciences and O'Brien Institute for Public Health, Cumming School of Medicine, University of Calgary, Calgary, Canada.

Kirsten M Fiest (KM)

Department of Critical Care Medicine, Cumming School of Medicine, University of Calgary and Alberta Health Services-Calgary Zone, Calgary, Canada.
Department of Community Health Sciences and O'Brien Institute for Public Health, Cumming School of Medicine, University of Calgary, Calgary, Canada.

Sean M Bagshaw (SM)

Department of Critical Care Medicine, Faculty of Medicine and Dentistry and Alberta Health Services-Edmonton Zone, University of Alberta, 8440-112 ST NW, Edmonton, T6G2B7 Canada.
Alberta Critical Care Strategic Clinical Network, Alberta Health Services, Alberta, Canada.

Classifications MeSH