Force by the American College of Critical Care Medicine.Crit Care Med. 2008 Jun;36(6):1937-49.
OBJECTIVE: To develop consensus statements for the diagnosis and management of
corticosteroid insufficiency in critically ill adult patients. PARTICIPANTS: A
multidisciplinary, multispecialty task force of experts in critical care medicine
was convened from the membership of the Society of Critical Care Medicine and the
European Society of Intensive Care Medicine. In addition, international experts
in endocrinology were invited to participate. DESIGN/METHODS: The task force
members reviewed published literature and provided expert opinion from which the
consensus was derived. The consensus statements were developed using a modified
Delphi methodology. The strength of each recommendation was quantified using the
Modified GRADE system, which classifies recommendations as strong (grade 1) or
weak (grade 2) and the quality of evidence as high (grade A), moderate (grade B),
or low (grade C) based on factors that include the study design, the consistency
of the results, and the directness of the evidence. RESULTS: The task force
coined the term critical illness-related corticosteroid insufficiency to describe
the dysfunction of the hypothalamic-pituitary-adrenal axis that occurs during
critical illness. Critical illness-related corticosteroid insufficiency is caused
by adrenal insufficiency together with tissue corticosteroid resistance and is
characterized by an exaggerated and protracted proinflammatory response. Critical
illness-related corticosteroid insufficiency should be suspected in hypotensive
patients who have responded poorly to fluids and vasopressor agents, particularly
in the setting of sepsis. At this time, the diagnosis of tissue corticosteroid
resistance remains problematic. Adrenal insufficiency in critically ill patients
is best made by a delta total serum cortisol of < 9 microg/dL after
adrenocorticotrophic hormone (250 microg) administration or a random total
cortisol of < 10 microg/dL. The benefit of treatment with glucocorticoids at this
time seems to be limited to patients with vasopressor-dependent septic shock and
patients with early severe acute respiratory distress syndrome (PaO2/FiO2 of <
200 and within 14 days of onset). The adrenocorticotrophic hormone stimulation
test should not be used to identify those patients with septic shock or acute
respiratory distress syndrome who should receive glucocorticoids. Hydrocortisone
in a dose of 200 mg/day in four divided doses or as a continuous infusion in a
dose of 240 mg/day (10 mg/hr) for > or = 7 days is recommended for septic shock.
Methylprednisolone in a dose of 1 mg x kg(-1) x day(-1) for > or = 14 days is
Recommended in patients with severe early acute respiratory distress syndrome.
Glucocorticoids should be weaned and not stopped abruptly. Reinstitution of
Treatment should be considered with recurrence of signs of sepsis, hypotension,
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