Real-world characterization of blood glucose control and insulin use in the intensive care unit.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
01 07 2020
Historique:
received: 21 01 2020
accepted: 09 06 2020
entrez: 3 7 2020
pubmed: 3 7 2020
medline: 15 12 2020
Statut: epublish

Résumé

The heterogeneity of critical illness complicates both clinical trial design and real-world management. This complexity has resulted in conflicting evidence and opinion regarding the optimal management in many intensive care scenarios. Understanding this heterogeneity is essential to tailoring management to individual patients. Hyperglycaemia is one such complication in the intensive care unit (ICU), accompanied by decades of conflicting evidence around management strategies. We hypothesized that analysis of highly-detailed electronic medical record (EMR) data would demonstrate that patients vary widely in their glycaemic response to critical illness and response to insulin therapy. Due to this variability, we believed that hyper- and hypoglycaemia would remain common in ICU care despite standardised approaches to management. We utilized the Medical Information Mart for Intensive Care III v1.4 (MIMIC) database. We identified 19,694 admissions between 2008 and 2012 with available glucose results and insulin administration data. We demonstrate that hyper- and hypoglycaemia are common at the time of admission and remain so 1 week into an ICU admission. Insulin treatment strategies vary significantly, irrespective of blood glucose level or diabetic status. We reveal a tremendous opportunity for EMR data to guide tailored management. Through this work, we have made available a highly-detailed data source for future investigation.

Identifiants

pubmed: 32612144
doi: 10.1038/s41598-020-67864-z
pii: 10.1038/s41598-020-67864-z
pmc: PMC7329880
doi:

Substances chimiques

Biomarkers 0
Blood Glucose 0
Glycated Hemoglobin A 0
Hypoglycemic Agents 0
Insulin 0
hemoglobin A1c protein, human 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

10718

Subventions

Organisme : NIDCR NIH HHS
ID : R01 DE017205
Pays : United States
Organisme : NIBIB NIH HHS
ID : R01 EB017205
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY017205
Pays : United States

Références

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Auteurs

Lawrence Baker (L)

RAND Corporation, Santa Monica, CA, USA.

Jason H Maley (JH)

Division of Pulmonary, Critical Care, and Sleep Medicine, Beth Israel Deaconess Medical Center, 330 Brookline Ave., Boston, MA, 02215, USA. jmaley@bidmc.harvard.edu.
Center for Healthcare Delivery Science, Beth Israel Deaconess Medical Center, Boston, MA, USA. jmaley@bidmc.harvard.edu.
Harvard Medical School, Boston, MA, USA. jmaley@bidmc.harvard.edu.

Aldo Arévalo (A)

MIT Laboratory for Computational Physiology Harvard-MIT Division of Health Sciences and Technology, Cambridge, MA, USA.
IDMEC, Instituto Superior Técnico, University of Lisbon, Lisbon, Portugal.

Francis DeMichele (F)

Landmark Health, Huntington Beach, CA, USA.

Roselyn Mateo-Collado (R)

Division of Endocrinology and Metabolism, Rush University Medical Center, Chicago, IL, USA.

Stan Finkelstein (S)

Harvard Medical School, Boston, MA, USA.

Leo Anthony Celi (LA)

Division of Pulmonary, Critical Care, and Sleep Medicine, Beth Israel Deaconess Medical Center, 330 Brookline Ave., Boston, MA, 02215, USA.
Harvard Medical School, Boston, MA, USA.
MIT Laboratory for Computational Physiology Harvard-MIT Division of Health Sciences and Technology, Cambridge, MA, USA.

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