Multisystem organ dysfunction can follow several acute injury mechanisms, including trauma, sepsis, and shock and is the leading cause of death in critically ill patients. 1 Even after the initial cause of organ injury has been addressed, many organs remote from the initial injury remain "on strike" for days or even weeks, often despite little evidence of direct injury. There are no specific treatments to prevent or reverse this organ dysfunction, so supportive care is the cornerstone of treatment in the intensive care unit (ICU).Long-term treatment with sodium-glucose cotransporter 2 (SGLT-2) inhibitors decrease cardiovascular death, heart failure-related hospitalizations, and progression of chronic kidney disease (CKD) regardless of the presence of diabetes or baseline renal function. 2,3 Data from large randomized trials also suggest that long-term SGLT-2 inhibition may reduce the incidence of acute organ dysfunction, raising the possibility of benefit in critically ill patients. 2,3 For example, in patients with CKD and significant albuminuria, dapagliflozin decreased the risk of acute decline in kidney function in a prespecified post hoc analysis of the Dapagliflozin and Prevention of Adverse Outcomes in Chronic Kidney Disease (DAPA-CKD) trial. 4 Several meta-analyses report a decrease in acute kidney injury in patients with diabetes treated with SGLT-2 inhibitors compared with other oral medications for diabetes or placebo. 5,6 Typically, the benefits of SGLT-2 inhibitor therapy accrue after prolonged exposure. The potential mechanisms leading to organ protection are incompletely understood. In chronic SGLT-2 inhibitor treatment for patients with diabetes, the reduction in intraglomerular hypertension and hyperfiltration through the inhibition of the tubuloglomerular feedback is key. 7 This mechanism may be protective in patients with sepsis with disrupted intrarenal hemodynamics, and critically ill patients may benefit from decreasing hyperfiltration because this may additionally decrease renal hypoxia through reduced tubular epithelial oxygen consumption. At a cellular level, SGLT-2-independent effects including a reduction in local inflammation and inhibition of mediators of maladaptive repair and fibrosis have been described. 8,9 Finally, SGLT-2 inhibition can initiate signaling through known protective pathways, including reduced oxidative stress, and the activation of mitochondrial autophagy and biogenesis. [10][11][12] Whether short-term therapy would yield benefit is unclear, but among patients with COVID-19 who were at risk of cardiometabolic disease, a short-term course of dapaglifozin (median days, 5.5) was well tolerated compared with pla-