Oral Prednisone for Acute Vascular Shock
Oral prednisone is NOT indicated for acute vascular shock—intravenous hydrocortisone (200–300 mg/day) is the evidence-based corticosteroid for vasopressor-unresponsive septic shock, and oral formulations have no role in the acute resuscitation phase. 1
Why IV Hydrocortisone, Not Oral Prednisone?
Route and Formulation Requirements
Intravenous administration is mandatory in acute shock states because oral absorption is unreliable in patients with hypoperfusion, ileus, altered mental status, or inability to take medications by mouth. 1
Hydrocortisone 200–300 mg/day IV (typically 50 mg every 6 hours or continuous infusion) is the specifically recommended corticosteroid for septic shock, not prednisone. 1, 2
The 2013 Surviving Sepsis Campaign guidelines explicitly recommend intravenous hydrocortisone at 200 mg/day for patients with vasopressor-unresponsive septic shock, with no mention of oral alternatives during the acute phase. 1
Clinical Indication Criteria
Corticosteroids should only be used when:
The patient has septic shock (not just vascular shock from other causes). 1
Adequate fluid resuscitation has been completed and the patient remains hypotensive. 1
Vasopressor therapy is required and the patient remains hemodynamically unstable despite moderate-to-high dose vasopressors (typically norepinephrine). 1
The shock has persisted for more than 60 minutes despite appropriate resuscitation. 1
Evidence Base for IV Hydrocortisone
The French consensus conference (2006) established that hydrocortisone 200–300 mg/day for at least 5 days followed by tapering is the standard approach in septic shock unresponsive to vasopressors. 1
The CORTICUS trial and subsequent meta-analyses demonstrated that low-dose corticosteroids (hydrocortisone) significantly reduce time on vasopressors and may improve shock reversal, though mortality benefit remains controversial. 1, 3, 4
A 2009 meta-analysis of 1,876 patients showed corticosteroid therapy resulted in significant shock reversal at 7 days (RR 1.41,95% CI 1.22–1.64) without increasing superinfection risk. 4
Specific Dosing and Administration
For adult septic shock:
Hydrocortisone 50 mg IV bolus every 6 hours (total 200 mg/day) OR continuous infusion of 200 mg over 24 hours. 1, 2
Continue for at least 5–7 days at full dose, then taper gradually rather than abrupt cessation. 1, 5
Fludrocortisone 50 μg once daily enterally may be added to hydrocortisone in vasopressor-unresponsive shock, based on the APROCCHSS trial. 5
For pediatric septic shock:
- Hydrocortisone 1 mg/kg every 6 hours is the recommended dose. 1
Common Pitfalls and Caveats
When NOT to Use Corticosteroids
Do NOT use corticosteroids if hemodynamic stability is achieved with fluids and vasopressors alone—the 2024 AASLD guidelines and 2013 Surviving Sepsis Campaign both recommend against routine use in this scenario. 1, 5
Avoid high-dose corticosteroids (methylprednisolone ≥30 mg/kg/day or equivalent)—these provide no benefit and may increase mortality. 2
Do NOT use ACTH stimulation testing to decide who receives corticosteroids, as it does not reliably identify patients who will benefit. 1, 5
Transition to Oral Therapy
Oral prednisone may be considered only after:
Conversion ratio: Hydrocortisone 20 mg = Prednisone 5 mg (4:1 ratio). 6
If transitioning from hydrocortisone 200 mg/day IV to oral prednisone, the equivalent would be approximately 50 mg prednisone daily, then taper. 6
First-Line Vasopressor Therapy
Norepinephrine remains the first-line vasopressor for all shock states, including septic shock—corticosteroids are adjunctive, not primary therapy. 1, 7, 8
Vasopressin or angiotensin II may be added as second-line agents for norepinephrine-sparing effects in refractory shock. 1
Monitoring and Safety
Monitor for hyperglycemia, superinfection risk, and electrolyte disturbances during corticosteroid therapy, though the 2009 meta-analysis found no significant increase in superinfection rates (RR 1.11,95% CI 0.86–1.42). 4
Invasive arterial monitoring should be in place for all patients requiring vasopressors and corticosteroids. 1
Target mean arterial pressure ≥65 mmHg with ongoing assessment of end-organ perfusion (urine output, lactate, mental status). 1