Renin Kinetics Are Superior to Lactate Kinetics for Predicting In-Hospital Mortality in Hypotensive Critically Ill Patients.


Journal

Critical care medicine
ISSN: 1530-0293
Titre abrégé: Crit Care Med
Pays: United States
ID NLM: 0355501

Informations de publication

Date de publication:
01 01 2022
Historique:
pubmed: 25 6 2021
medline: 17 2 2022
entrez: 24 6 2021
Statut: ppublish

Résumé

Whole blood lactate concentration is widely used in shock states to assess perfusion. We aimed to determine if the change in plasma renin concentration over time would be superior to the change in lactate concentration for predicting in-hospital mortality in hypotensive patients on vasopressors. Prospective, observational cohort study. Tertiary academic ICU. Adult patients on vasopressors for greater than 6 hours to maintain a mean arterial pressure greater than or equal to 65 mm Hg during January 2020. Plasma renin concentrations were measured at enrollment and at 24, 48, and 72 hours. Whole blood lactate measurements were performed according to normal standard of care. Logistic regression was performed to evaluate whether the change in renin or lactate concentration could predict in-hospital mortality. Generalized estimating equations were used to analyze the association between renin and lactate concentration and in-hospital mortality. The area under the receiver operating characteristics curve was performed to measure the discriminative ability of initial and peak renin and lactate concentration to predict mortality. The association between renin and lactate concentration above the upper limit of normal at each timepoint with in-hospital mortality was also examined. The study included 197 renin and 148 lactate samples obtained from 53 patients. The slope of the natural log (ln) of renin concentration was independently associated with mortality (adjusted odds ratio, 10.35; 95% CI, 1.40-76.34; p = 0.022), but the slope of ln-lactate concentration was not (adjusted odds ratio, 4.78; 95% CI, 0.03-772.64; p = 0.55). The generalized estimating equation models found that both ln-renin (adjusted odds ratio, 1.18; 95% CI, 1.02-1.37; p = 0.025) and ln-lactate (adjusted odds ratio, 2.38; 95% CI, 1.05-5.37; p = 0.037) were associated with mortality. Area under the receiver operating characteristics curve analysis demonstrated that initial renin could predict in-hospital mortality with fair discrimination (area under the receiver operating characteristics curve, 0.682; 95% CI, 0.503-0.836; p = 0.05), but initial lactate could not (area under the receiver operating characteristics curve, 0.615; 95% CI, 0.413-0.803; p = 0.27). Peak renin (area under the receiver operating characteristics curve, 0.728; 95% CI, 0.547-0.888; p = 0.01) and peak lactate (area under the receiver operating characteristics curve, 0.746; 95% CI, 0.584-0.876; p = 0.01) demonstrated moderate discrimination. There was no significant difference in discriminative ability between initial or peak renin and lactate concentration. At each study time point, a higher proportion of renin values exceeded the threshold of normal (40 pg/mL) in nonsurvivors than in survivors, but this association was not significant for lactate. Although there was no significant difference in the performance of renin and lactate when examining the absolute values of each laboratory, a positive rate of change in renin concentration, but not lactate concentration, over 72 hours was associated with in-hospital mortality. For each one-unit increase in the slope of ln-renin, the odds of mortality increased 10-fold. Renin levels greater than 40 pg/mL, but not lactate levels greater than 2 mmol/L, were associated with in-hospital mortality. These findings suggest that plasma renin kinetics may be superior to lactate kinetics in predicting mortality of hypotensive, critically ill patients.

Identifiants

pubmed: 34166293
doi: 10.1097/CCM.0000000000005143
pii: 00003246-202201000-00004
doi:

Substances chimiques

Lactic Acid 33X04XA5AT
Renin EC 3.4.23.15

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

50-60

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 by the Society of Critical Care Medicine and Wolters Kluwer Health, Inc. All Rights Reserved.

Déclaration de conflit d'intérêts

Dr. McCurdy was formally on the Speaker’s Bureau for La Jolla Pharmaceutical Company. Dr. Devarajan is funded by a grant from the National Institutes of Health (P50DK096418). He is a coinventor on patents submitted for the use of neutrophil gelatinase-associated lipocalin as a biomarker of kidney injury. Dr. Chow has served on the Speaker’s Bureau for La Jolla Pharmaceutical Company. Drs. Jeyaraju, McCurdy, and Chow are coinventors on a patent submitted for the detection of biomarkers in patients with circulatory shock. The remaining authors have disclosed that they do not have any potential conflicts of interest.

Références

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Auteurs

Maniraj Jeyaraju (M)

University of Maryland School of Medicine, Baltimore, MD.

Michael T McCurdy (MT)

Division of Pulmonary and Critical Care Medicine, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD.

Andrea R Levine (AR)

Division of Pulmonary and Critical Care Medicine, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD.

Prasad Devarajan (P)

Division of Nephrology and Hypertension, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.

Michael A Mazzeffi (MA)

Department of Anesthesiology and Critical Care Medicine, George Washington University School of Medicine and Health Sciences, Washington, DC.

Kristin E Mullins (KE)

Department of Pathology, University of Maryland School of Medicine, Baltimore, MD.

Michaella Reif (M)

Department of Medicine, University of Wisconsin-Madison, Madison, WI.

David N Yim (DN)

University of Maryland School of Medicine, Baltimore, MD.

Christopher Parrino (C)

University of Maryland School of Medicine, Baltimore, MD.

Allison S Lankford (AS)

Department of Obstetrics and Gynecology, University of Maryland School of Medicine, Baltimore, MD.
R. Adams Cowley Shock Trauma Center, Surgical Critical Care, Baltimore, MD.

Jonathan H Chow (JH)

Department of Anesthesiology and Critical Care Medicine, George Washington University School of Medicine and Health Sciences, Washington, DC.

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