Septic Shock Clinical Trial
Official title:
Evaluation of the Role of Hydrocortisone Either Alone or Combined With Fludrocortisone in the Outcome of Septic Shock in Adults
During Infection, oflfending microbes interact with the host immune system producing a
downstream inflammatory cascade involving cytokines and other mediators, which in turn
triggers a systemic response. The resultant effects linclude vasodilation, increased vascular
permeability, myocardial depression, and impairment of the coagulation cascade, resulting in
global imbalance of systemic oxygen supply and demand. During the late stage of sepsis,
immunosuppression predominates, leading to multi-organ dysfunction and further clinical
deterioration .
Sepsis is defined as life-threatening organ dysfunction caused by a dysregulated host
response to infection with two or three on Quick Sepsis-related organ failure assessment
score (qSOFA). Septic shock is defined as the presence of sepsis and refractory hypotension
to fluid management. Vasopressors are needed to maintain systolic blood pressure more than
90mmHg or mean blood pressure more than 65 mmHg .
Experimental and Clinical evidence suggests that sepsis is associated with dysregulated
response of Hypothalamic-pituitary-adrenal axis that may involve any of the steps from
cortisol production to cortisol use by cells .
Glucocorticoid therapy for the treatment of septic shock remains controversial, with
conflicting evidence regarding a mortality benefit. It has been used in patients with septic
shock who remained hypotensive after fluid and vasopressor resuscitation.
Fludrocortisone is a corticosteroid and acts as a powerful mineralocorticoid along with some
additional but comparatively very weak glucocorticoid activity. Relative to cortisol, it is
to 10 times the glucocorticoid potency but 250 to 800 times the mineralocorticoid potency .
Fludrocortisone is added to hydrocortisone to provide additional mineralocorticoid potency.
The rationale for adding mineralocorticoid treatment is that an experimental sepsis study
showed marked nuclear factor NF-κB mediated down regulation of vascular mineralocorticoid
receptors .
Corticosteroids attenuate inflammation in various organs an effect partly related to
inhibition of nuclear factor NF-κB. Improve cardiovascular function by restoring effective
blood volume through increased mineralocorticoid activity and by increasing systemic vascular
resistance through vascular α-Adrenergic responsiveness and reduces inflammation-mediated
vasodilation .
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