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Association of Blood Glucose Variability with Sepsis-Related Disseminated Intravascular Coagulation Morbidity and Mortality.
Liu, Dan; Fan, YiWen; Zhuang, YuGang; Peng, Hu; Gao, ChengJin; Chen, YanQing.
Afiliación
  • Liu D; Emergency Department, Shanghai Tenth People's Hospital, Affiliated with Tongji University School of Medicine, Shanghai, People's Republic of China.
  • Fan Y; Department of Pathology and Medical Biology, Groningen Research Institute for Asthma and COPD (GRIAC), University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
  • Zhuang Y; Emergency Department, Shanghai Tenth People's Hospital, Affiliated with Tongji University School of Medicine, Shanghai, People's Republic of China.
  • Peng H; Emergency Department, Shanghai Tenth People's Hospital, Affiliated with Tongji University School of Medicine, Shanghai, People's Republic of China.
  • Gao C; Emergency Department, Xinhua Hospital, affiliated with the Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China.
  • Chen Y; Emergency Department, Shanghai Tenth People's Hospital, Affiliated with Tongji University School of Medicine, Shanghai, People's Republic of China.
J Inflamm Res ; 15: 6505-6516, 2022.
Article en En | MEDLINE | ID: mdl-36474519
ABSTRACT

Purpose:

Sepsis-related disseminated intravascular coagulation (DIC) is closely associated with poor prognosis and high mortality. Higher blood glucose (BG) variability indicates an increased risk of mortality in sepsis; however, its relationship with sepsis-related DIC has not been investigated. This study aimed to determine the association between glucose variability and sepsis-related DIC. Patients and

Methods:

Patients with sepsis admitted to the intensive care unit were enrolled between October 2017 and January 2021. Baseline data and BG records from the first 72 h were collected. We calculated the glucose liability index (GLI), largest amplitude of glucose excursion, BG standard deviation, and coefficient of variation on days 1 and 3. The relationship between GLI and morbidity of sepsis-related DIC was explored using a competing risk model. In subgroup analysis, we divided patients with and without diabetes into three groups according to the BG range.

Results:

Of the 238 patients enrolled, 28.2% developed DIC during hospitalization (n=67). GLI on day 3 was found to have the closest relationship with DIC incidence as it has the largest area under the ROC curve and the highest associated odds ratio of death per unit change (GLI3-day AUC=0.891 OR=1.84), also independently increased the occurrence of DIC after adjusting for the competing risk of death (sub-distribution hazard ratios=1.866, p<0.01). In subgroup analysis, patients with diabetes had worse outcomes under hypoglycemia than under hyperglycemia. Patients without diabetes having stable BG had the best outcomes.

Conclusion:

Our study suggested that a higher GLI in patients with sepsis at 72 h was independently associated with an increased risk of sepsis-related DIC, which was not associated with pre-existing diabetes.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Inflamm Res Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Inflamm Res Año: 2022 Tipo del documento: Article