Septic Shock Clinical Trial
Official title:
Hemodynamic and Inflammatory Effects of Abrupt Versus Tapered Corticosteroid Discontinuation in Septic Shock
The proposed study will evaluate the potential benefit of a tapered course of hydrocortisone compared to abrupt cessation in patients initiated on hydrocortisone for septic shock. The study will include adult patients in the medical intensive care unit (MICU) who meet criteria for corticosteroid therapy for septic shock according to the current MICU protocol.All patients will receive 7 days of hydrocortisone (50mg/Q6hrs) as part of the routine management of septic shock, before being randomly assigned to receive hydrocortisone taper versus no taper. The primary study endpoint is the incidence of hypotension within 7 days after randomization. Secondary endpoints will include incidence of adrenal insufficiency, and changes in the inflammatory status (assessed by cytokine measurements) before, during, and after corticosteroid discontinuation. The cytokines to be measured include IL-1, IL-6, IL-9, IL-10, and TNF. Since there has not been a randomized clinical trial to investigate the potential benefit of weaning septic patients off low-dose hydrocortisone as opposed to stopping abruptly, this study has potential to change clinical practice by leading to a consistent approach of corticosteroid discontinuation and to a better understanding of their impact on the inflammatory modulation in septic shock.
Current therapy for septic shock includes antimicrobials, fluid resuscitation,
catecholamines, and measures to improve tissue oxygen delivery. The use of corticosteroids as
an adjunctive treatment in septic shock has been an area of intensive research over the past
decade. A handful of studies suggest that patients in septic shock benefit from low-dose
glucocorticoids.Low-dose corticosteroids may improve hemodynamics, decrease vasopressor
requirements, and reduce 28-day mortality in patients with vasopressor-refractory septic
shock. A meta-analysis from 2004 also suggested that the use of low-dose corticosteroids does
not significantly increase the risk of superimposed infections, gastrointestinal bleeding, or
hyperglycemia.
The exact mechanism for this beneficial effect has not been completely established, although
direct vascular effects and anti-inflammatory effects of corticosteroids have been proposed.
While there is ongoing debate over which subpopulations of patients derive benefit from
corticosteroids, there is as much controversy regarding the appropriate duration of therapy.
The current Surviving Sepsis Campaign suggests that intravenous IV hydrocortisone
200-300mg/day should be given to adult septic shock patients after it has been confirmed that
their blood pressure is poorly responsive to fluid resuscitation and vasopressor therapy. The
duration of therapy is not specified. There is also no clear evidence to suggest that
patients benefit from tapering steroids as opposed to stopping them abruptly; both strategies
have been employed. Annane showed both a mortality benefit and shorter duration of
vasopressor therapy with an abrupt end to a 7-day course of hydrocortisone and
fludrocortisone in patients with septic shock compared to placebo; while others showed a
similar benefit with a taper.Keh demonstrated reversal of both hemodynamic and immunologic
effects after a three-day treatment of "low-dose" hydrocortisone, suggesting that some of the
beneficial effects of steroids disappear in less than 24 hours. Interestingly, 30% of
patients had to restart vasopressor therapy after discontinuation of corticosteroids in one
of the Keh's study arms.
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