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The effects of vasopressin on acute kidney injury...
Journal article

The effects of vasopressin on acute kidney injury in septic shock

Abstract

ObjectiveTo compare the effects of vasopressin versus norepinephrine infusion on the outcome of kidney injury in septic shock.Design and settingPost-hoc analysis of the multi-center double-blind randomized controlled trial of vasopressin versus norepinephrine in adult patients who had septic shock (VASST).Patients and interventionSeven hundred seventy-eight patients were randomized to receive a blinded infusion of either low-dose vasopressin (0.01–0.03 U/min) or norepinephrine infusion (5–15 μg/min) in addition to open-label vasopressors and were included in the outcome analysis. All vasopressors were titrated and weaned to maintain a target blood pressure.Measurement and resultsRIFLE criteria for acute kidney injury were used to compare the effects of vasopressin versus norepinephrine. In view of multiple simultaneous comparisons, a p value of 0.01 was considered statistically significant. Kidney injury was present in 464 patients (59.6%) at study entry. In patients in the RIFLE “Risk” category (n = 106), vasopressin as compared with norepinephrine was associated with a trend to a lower rate of progression to renal “Failure” or “Loss” categories (20.8 vs. 39.6%, respectively, p = 0.03), and a lower rate of use of renal replacement therapy (17.0 vs. 37.7%, p = 0.02). Mortality rates in the “Risk” category patients treated with vasopressin compared to norepinephrine were 30.8 versus 54.7%, p = 0.01, but this did not reach significance in a multiple logistic regression analysis (OR = 0.33, 99% CI 0.10–1.09, p = 0.02). The interaction of treatment group and RIFLE category was significant in predicting mortality.ConclusionsVasopressin may reduce progression to renal failure and mortality in patients at risk of kidney injury who have septic shock.

Authors

Gordon AC; Russell JA; Walley KR; Singer J; Ayers D; Storms MM; Holmes CL; Hébert PC; Cooper DJ; Mehta S

Journal

Intensive Care Medicine, Vol. 36, No. 1, pp. 83–91

Publisher

Springer Nature

Publication Date

January 1, 2010

DOI

10.1007/s00134-009-1687-x

ISSN

0342-4642

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