Running Out of Options: Managing Refractory Septic Shock
Dr Samir S. Awad presents a patient case and holds panel discussion on vasopressor escalation strategy at our symposium at SCCM 2026.
VIDEOS & RESOURCES
Dr Samir S. Awad presents a patient case and holds panel discussion on vasopressor escalation strategy at our symposium at SCCM 2026.
Dr Richard G. Wunderink presents a patient case and holds panel discussion on guiding treatment by perfusion markers at our symposium at SCCM 2026.
Dr Rawn Salenger reviews patient and operative characteristics associated with vasoplegia in cardiac surgeries.
Dr Rawn Salenger explains the ramifications of patients falling below a MAP of 65 mmHg post CPB.
Dr Rawn Salenger talks about his experience with using GIAPREZA post CPB.
Dr David W. Boldt presents a patient case and holds panel discussion on addressing ANG II deficiency after cardiac surgeries at our symposium at SCCM 2026.
Associate Professor of Surgery
Chief of Surgery and Medical Director Surgical Intensive Care Unit
Professor of Medicine, Pulmonary and Critical Care
Chief, Division of Trauma and Adult Multi-Specialty Anesthesiology
Ordering Sheet
DownloadDOSING & Administration GUIDE
DownloadPerioperative Vasoplegia Protocol
DownloadACUTE KIDNEY INJURY SUBGROUP ANALYSIS
DownloadRAAS PATHWAY BROCHURE
DownloadSeptic Shock Brochure
DownloadVasoplegia Brochure
DownloadWastage & warranty information sheet
Download0.5mg/mL vial quick guide
DownloadANG=angiotensin; CPB=cardiopulmonary bypass; MAP=mean arterial pressure; MOA=mechanism of action; RAAS=renin-angiotensin-aldosterone system; SCCM=Society of Critical Care Medicine.
GIAPREZA® (angiotensin II) increases blood pressure in adults with septic or other distributive shock.
The safety of GIAPREZA was evaluated in 321 adults with septic or other distributive shock in a randomized, double-blind, placebo-controlled study, ATHOS-3. There was a higher incidence of arterial and venous thrombotic and thromboembolic events in patients who received GIAPREZA compared to placebo-treated patients in the ATHOS-3 study (13% vs. 5%). The major imbalance was in deep venous thromboses. Use concurrent venous thromboembolism (VTE) prophylaxis.
The most common adverse reactions reported in greater than 10% of GIAPREZA-treated patients were thromboembolic events. Adverse reactions occurring in ≥4% of patients treated with GIAPREZA and ≥1.5% more often than placebo-treated patients in the ATHOS-3 study were thromboembolic events (including deep vein thrombosis), thrombocytopenia, tachycardia, fungal infection, delirium, acidosis, hyperglycemia, and peripheral ischemia.
Angiotensin converting enzyme (ACE) inhibitors may increase response to GIAPREZA. Angiotensin II receptor blockers (ARBs) may reduce response to GIAPREZA.
You are encouraged to report negative side effects of prescription drugs to the FDA. To report SUSPECTED ADVERSE REACTIONS, please contact:
Before administering, please see the Full Prescribing Information for GIAPREZA.








