Thiamine for Renal Protection in Septic Shock (TRPSS): A Randomized, Placebo-controlled, Clinical Trial.

Ari Moskowitz, Katherine M Berg, Anne V Grossestreuer, Lakshman Balaji, Xiaowen Liu, Michael N Cocchi, Maureen Chase, Michelle Ng Gong, Jonathan Gong, Samir M Parikh, Long Ngo, Noa Berlin, Michael W Donnino

Journal: American journal of respiratory and critical care medicine 2023;208(5):570-578

PMID: 37364280

Abstract

Kidney injury is common and associated with worse outcomes in patients with septic shock. Mitochondrial resuscitation with thiamine (vitamin B1) may attenuate septic kidney injury. To assess whether thiamine supplementation attenuates kidney injury in septic shock. The TRPSS (Thiamine for Renal Protection in Septic Shock) trial was a multicenter, randomized, placebo-controlled trial of thiamine versus placebo in septic shock. The primary outcome was change in serum creatinine between enrollment and 72 hours after enrollment. Eighty-eight patients were enrolled (42 patients received the intervention, and 46 received placebo). There was no significant between-groups difference in creatinine at 72 hours (mean difference, -0.57 mg/dl; 95% confidence interval, -1.18, 0.04;  = 0.07). There was no difference in receipt of kidney replacement therapy (14.3% vs. 21.7%,  = 0.34), acute kidney injury (as defined by stage 3 of the Kidney Disease: Improving Global Outcomes acute kidney injury scale; 54.7% vs. 73.9%,  = 0.07), or mortality (35.7% vs. 54.3%,  = 0.14) between the thiamine and placebo groups. Patients who received thiamine had more ICU-free days (median [interquartile range]: 22.5 [0.0-25.0] vs. 0.0 [0.0-23.0],  < 0.01). In the thiamine-deficient cohort (27.4% of patients), there was no difference in rates of kidney failure (57.1% thiamine vs. 81.5% placebo) or in-hospital mortality (28.6% vs. 68.8%) between groups. In the TRPSS trial, there was no statistically significant difference in the primary outcome of change in creatinine over time. Patients who received thiamine had more ICU-free days, but there was no difference in other secondary outcomes. Clinical trial registered with www.clinicaltrials.gov (NCT03550794).

Address: Division of Critical Care Medicine, Montefiore Medical Center, The Bronx, New York.; Bronx Center for Critical Care Outcomes and Resuscitation Research, The Bronx, New York.; Center for Resuscitation Science.; Division of Pulmonary, Critical Care, and Sleep Medicine.; Department of Emergency Medicine, and.; Department of Emergency Medicine, Long Island Jewish Medical Center, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, New Hyde Park, New York; and.; Division of Nephrology, University of Texas Southwestern Medical Center, Dallas, Texas.; Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
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