Hydrocortisone versus vasopressin for the management of adult patients with septic shock refractory to norepinephrine: A multicenter retrospective study

Study Objective Significant practice variation exists when selecting between hydrocortisone and vasopressin as second line agents in patients with septic shock in need of escalating doses of norepinephrine. The goal of this study was to assess differences in clinical outcomes between these two agent...

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Veröffentlicht in:Pharmacotherapy 2023-08, Vol.43 (8), p.787-794
Hauptverfasser: Kulesza, Steven, Gignac, Lindsey, Colvin, C. Allis, Boll, Skyler, Giuliano, Christopher, Haan, Bradley, Allen, Bryan, Perez, Mary M., Allen, Monica, Edwin, Stephanie B.
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Sprache:eng
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Zusammenfassung:Study Objective Significant practice variation exists when selecting between hydrocortisone and vasopressin as second line agents in patients with septic shock in need of escalating doses of norepinephrine. The goal of this study was to assess differences in clinical outcomes between these two agents. Design Multicenter, retrospective, observational study. Setting Ten Ascension Health hospitals. Patients Adult patients with presumed septic shock receiving norepinephrine prior to study drug initiation between December 2015 and August 2021. Intervention Vasopressin (0.03–0.04 units/min) or hydrocortisone (200–300 mg/day). Measurements and Main Results A total of 768 patients were included with a median (interquartile range) SOFA score of 10 (8–13), norepinephrine dose of 0.3 mcg/kg/min (0.1–0.5 mcg/kg/min), and lactate of 3.8 mmol/L (2.4–7.0 mmol/L) at initiation of the study drug. A significant difference in 28‐day mortality was noted favoring hydrocortisone as an adjunct to norepinephrine after controlling for potential confounding factors (OR 0.46 [95% CI, 0.32–0.66]); similar results were seen following propensity score matching. Compared to vasopressin, hydrocortisone initiation was also associated with a higher rate of hemodynamic responsiveness (91.9% vs. 68.2%, p 
ISSN:0277-0008
1875-9114
DOI:10.1002/phar.2811