Association of Glucose Concentrations at Hospital Discharge With Readmissions and Mortality: A Nationwide Cohort Study.


Journal

The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362

Informations de publication

Date de publication:
01 09 2019
Historique:
received: 30 11 2018
accepted: 04 04 2019
pubmed: 2 5 2019
medline: 28 5 2020
entrez: 2 5 2019
Statut: ppublish

Résumé

Low blood glucose concentrations during the discharge day may affect 30-day readmission and posthospital discharge mortality rates. To investigate whether patients with diabetes and low glucose values during the last day of hospitalization are at increased risk of readmission or mortality. Minimum point of care glucose values were collected during the last 24 hours of hospitalization. We used adjusted rates of 30-day readmission rate, 30-, 90-, and 180-day mortality rates, and combined 30-day readmission/mortality rate to identify minimum glucose thresholds above which patients can be safely discharged. Nationwide cohort study including 843,978 admissions of patients with diabetes at the Veteran Affairs hospitals 14 years. The rate ratios (RRs) increased progressively for all five outcomes as the minimum glucose concentrations progressively decreased below the 90 to 99 mg/dL category, compared with the 100 to 109 mg/dL category: 30-day readmission RR, 1.01 to 1.45; 30-day readmission/mortality RR, 1.01 to 1.71; 30-day mortality RR, 0.99 to 5.82; 90-day mortality RR, 1.01 to 2.40; 180-day mortality RR, 1.03 to 1.91. Patients with diabetes experienced greater 30-day readmission rates, 30-, 90- and 180-day postdischarge mortality rates, and higher combined 30-day readmission/mortality rates, with glucose levels <92.9 mg/dL, <45.2 mg/dL, 65.8 mg/dL, 67.3 mg/dL, and <87.2 mg/dL, respectively. Patients with diabetes who had hypoglycemia or near-normal glucose values during the last day of hospitalization had higher rates of 30-day readmission and postdischarge mortality.

Identifiants

pubmed: 31042288
pii: 5433626
doi: 10.1210/jc.2018-02575
pmc: PMC6642668
doi:

Substances chimiques

Biomarkers 0
Blood Glucose 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

3679-3691

Subventions

Organisme : NIDDK NIH HHS
ID : P30 DK111024
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG028747
Pays : United States
Organisme : CSRD VA
ID : I01 CX001825
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK072488
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002378
Pays : United States

Informations de copyright

Published by Oxford University Press on behalf of the Endocrine Society 2019.

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Auteurs

Elias K Spanakis (EK)

Division of Endocrinology, Baltimore Veterans Affairs Medical Center, Baltimore, Maryland.
Division of Endocrinology, Diabetes, and Nutrition, University of Maryland School of Medicine, Baltimore, Maryland.

Guillermo E Umpierrez (GE)

Division of Endocrinology, Metabolism, and Lipids, Emory University School of Medicine, Atlanta, Georgia.

Tariq Siddiqui (T)

Division of Endocrinology, Diabetes, and Nutrition, University of Maryland School of Medicine, Baltimore, Maryland.
Division of Nephrology, University of Maryland School of Medicine, Baltimore, Maryland.

Min Zhan (M)

Department of Epidemiology and Public Health, University of Maryland, Baltimore, Maryland.

Soren Snitker (S)

Division of Endocrinology, Diabetes, and Nutrition, University of Maryland School of Medicine, Baltimore, Maryland.
Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland.

Jeffrey C Fink (JC)

Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland.
Division of Nephrology, University of Maryland School of Medicine, Baltimore, Maryland.

John D Sorkin (JD)

Baltimore Veterans Affairs Medical Center Geriatric Research, Education, and Clinical Center, Baltimore, Maryland.

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Classifications MeSH