The Interaction of Vasopressin and Corticosteroids in Septic Shock: A Pilot Randomized Controlled Trial

被引:97
作者
Gordon, Anthony C. [1 ,2 ]
Mason, Alexina J. [3 ]
Perkins, Gavin D. [4 ,5 ]
Stotz, Martin [2 ]
Terblanche, Marius [6 ,7 ]
Ashby, Deborah [3 ]
Brett, Stephen J. [2 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Fac Med, Sect Anaesthet Pain Med & Intens Care, London, England
[2] Imperial Coll Healthcare NHS Trust, Ctr Perioperat Med & Crit Care Res, London, England
[3] Univ London Imperial Coll Sci Technol & Med, Sch Publ Hlth, Fac Med, Imperial Clin Trials Unit, London, England
[4] Univ Warwick, Warwick Clin Trials Unit, Dept Crit Care, Coventry CV4 7AL, W Midlands, England
[5] Heart England NHS Fdn Trust, Birmingham, W Midlands, England
[6] Kings Coll London, Div Asthma Allergy & Lung Biol, London WC2R 2LS, England
[7] Guys & St Thomas NHS Fdn Trust, London, England
关键词
adrenal cortex hormones; drug interactions; intensive care; multiple organ failure; sepsis; vasopressins; ADVANCED VASODILATORY SHOCK; ATRIAL-NATRIURETIC-PEPTIDE; LOW-DOSE VASOPRESSIN; ACUTE KIDNEY INJURY; ARGININE-VASOPRESSIN; ORGAN FAILURE; NOREPINEPHRINE; INFUSION; CORTISOL; MANAGEMENT;
D O I
10.1097/CCM.0000000000000212
中图分类号
R4 [临床医学];
学科分类号
100218 [急诊医学];
摘要
Objectives: Vasopressin and corticosteroids are both commonly used adjunctive therapies in septic shock. Retrospective analyses have suggested that there may be an interaction between these drugs, with higher circulating vasopressin levels and improved outcomes in patients treated with both vasopressin and corticosteroids. We aimed to test for an interaction between vasopressin and corticosteroids in septic shock. Design: Prospective open-label randomized controlled pilot trial. Setting: Four adult ICUs in London teaching hospitals. Patients: Sixty-one adult patients who had septic shock. Interventions: Initial vasopressin IV infusion titrated up to 0.06 U/min and then IV hydrocortisone (50 mg 6 hourly) or placebo. Plasma vasopressin levels were measured at 6-12 and 24-36 hours after hydrocortisone/placebo administration. Measurements and Main Results: Thirty-one patients were allocated to vasopressin + hydrocortisone and 30 patients to vasopressin + placebo. The hydrocortisone group required a shorter duration of vasopressin therapy (3.1 d; 95% CI, 1.1-5.1; shorter in hydrocortisone group) and required a lower total dose of vasopressin (ratio, 0.47; 95% CI, 0.32-0.71) compared with the placebo group. Plasma vasopressin levels were not higher in the hydrocortisone group compared with the placebo group (64 pmol/L difference at 6- to 12-hour time point; 95% CI, -32 to 160 pmol/L). Early vasopressin use was well tolerated with only one serious adverse event possibly related to study drug administration reported. There were no differences in mortality rates (23% 28-day mortality in both groups) or organ failure assessments between the two treatment groups. Conclusions: Hydrocortisone spared vasopressin requirements, reduced duration, and reduced dose, when used together in the treatment of septic shock, but it did not alter plasma vasopressin levels. Further trials are needed to assess the clinical effectiveness of vasopressin as the initial vasopressor therapy with or without corticosteroids.
引用
收藏
页码:1325 / 1333
页数:9
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