| Receptor | Action | Agents |
|---|---|---|
| α₁ | Vasoconstriction (↑ SVR) | norepi, phenylephrine, epi (high) |
| β₁ | Inotropy + chronotropy (↑ CO/HR) | dobutamine, epi, dopamine, iso |
| β₂ | Vasodilation / bronchodilation | epi, isoproterenol, dobutamine |
| V₁ | Vasoconstriction (non-adrenergic) | vasopressin |
| PDE3 / AT₁ | Inodilation / vasoconstriction | milrinone / angiotensin II |
| Agent | Receptor | Typical dose | Effect & niche |
|---|---|---|---|
| Norepinephrine | α₁ > β₁ | 0.01–0.5+ mcg/kg/min | ↑SVR, variable CO — first-line in septic shock and reasonable initial support in hypotensive cardiogenic shock |
| Epinephrine | β₁ β₂ > α₁ | 0.01–0.5 mcg/kg/min | ↑CO ↑HR ↑SVR, ↑lactate — IM first for anaphylaxis. More refractory shock in small AMI-CS trial, not a universal mortality comparison |
| Phenylephrine | pure α₁ | 0.5–6 mcg/kg/min | ↑SVR, reflex ↓HR — selected vasodilatory hypotension or LVOT obstruction. May reduce CO |
| Vasopressin | V₁ | 0.03 U/min (fixed) | ↑SVR, catecholamine-sparing — septic-shock add-on. Common fixed dose, but labeled regimens allow titration |
| Dopamine | D / β / α (dose) | 2–20 mcg/kg/min | Arrhythmogenic — generally avoid (SOAP-II), except selected bradycardia |
| Dobutamine | β₁ > β₂ | 2–20 mcg/kg/min | ↑CO, ↓SVR (may ↓BP) — cardiogenic/low-output "cold" HF |
| Milrinone | PDE3 inhib. | 0.125–0.75 mcg/kg/min | Inodilator ↑CO ↓SVR ↓PVR — RV failure/PH, β-blocked. Renal clearance, longer t½ |
| Isoproterenol | β₁ β₂ | 0.5–10 mcg/min | Chronotrope/inodilator — selected bradycardia or acquired, pause-dependent torsades. Avoid congenital long QT |
| Angiotensin II | AT₁ | Start 20 ng/kg/min | Vasodilatory shock. Max 80 ng/kg/min for first 3 h, then 40. Concurrent VTE prophylaxis |
| Agent | MAP | CO | HR | SVR | PCWP | Hemodynamic signature |
|---|---|---|---|---|---|---|
| Norepinephrine | ↑↑ | ↑/↔ | ↔/↓ | ↑↑ | ↔ | CO depends on preload, afterload and ventricular function |
| Epinephrine | ↑↑ | ↑↑ | ↑↑ | ↑ | ↔ | ↑ lactate via β₂ glycolysis (not always hypoperfusion) |
| Phenylephrine | ↑ | ↓/↔ | ↓ | ↑↑ | ↑ | reflex bradycardia, can ↓CO |
| Vasopressin | ↑ | ↓/↔ | ↓/↔ | ↑↑ | variable | May decrease CO. Higher doses increase ischemic risk |
| Dopamine | ↑ | ↑↑ | ↑↑ | ↑* | ↑ | arrhythmogenic. *α emerges at high dose |
| Dobutamine | ↔/↓ | ↑↑ | ↑ | ↓ | ↓ | inodilator — may drop BP → pair a pressor |
| Milrinone | ↓ | ↑↑ | ↔/↑ | ↓↓ | ↓↓ | ↓ PVR too, renal clearance, long t½ (AKI) |
| Isoproterenol | ↓ | ↑↑ | ↑↑↑ | ↓ | ↓ | pure chronotrope/inodilator |
| Angiotensin II | ↑↑ | ↔ | ↔ | ↑↑ | ↔ | AT₁ vasoconstriction, catecholamine-sparing |
Norepinephrine for septic shock.
Add vasopressin, then epinephrine if MAP remains low.
Correct rhythm, filling and cause. Consider dobutamine or milrinone.
If hypotensive, support MAP with norepinephrine. Reassess output and perfusion.
Pressor for vascular pressure plus inotrope for persistent low output.
Escalating requirements warrant repeat echo/hemodynamics and timely support-team review.
Qualitative decision map. Shock can occur without MAP below 65. A pressure response alone does not establish adequate perfusion.
| Shock | Sequence |
|---|---|
| Cardiogenic | Norepinephrine if hypotensive. Add dobutamine/milrinone for persistent low-output hypoperfusion. Consider tMCS if refractory |
| Septic / distributive | Norepinephrine → add vasopressin → epinephrine if MAP remains low. With cardiac dysfunction, SSC 2026 suggests norepinephrine or epinephrine initially. For persistent hypoperfusion after adequate volume/BP, add dobutamine to norepinephrine or use epinephrine alone. |
| RV failure | Norepi/vasopressin for MAP (coronary perfusion) + milrinone/dobutamine, iNO/pulmonary vasodilator. Avoid hypoxia/hypercarbia |
| Anaphylactic | Epinephrine (IM → infusion), fluids, adjuncts |
| Hypovolemic / hemorrhagic | Volume / blood first — pressors only as a bridge |
| Bradycardic | Atropine if appropriate → pacing and/or epi/dopamine. Do not delay pacing for unstable high-grade block |