Bedside Snapshot
- Use It For
- Cardiac arrest, any rhythm (adult and pediatric); neonatal resuscitation with heart rate <60/min; shock and atropine-refractory bradycardia (infusion); refractory anaphylaxis; push-dose bridge
- Adult Dose
- Arrest: 1 mg (10 mL) IV/IO every 3–5 min (no max)
- Septic shock: 0.05–2 mcg/kg/min IV infusion to MAP
- Bradycardia: 2–10 mcg/min IV infusion
- Pediatric Dose
- Arrest or bradycardia: 0.01 mg/kg (0.1 mL/kg) IV/IO every 3–5 min (max 1 mg/dose). Newborn: 0.01–0.03 mg/kg (0.1–0.3 mL/kg) IV/IO while HR <60/min
- Onset / Duration
- IV/IO: <5 min / BP effect gone within 20 min; infusion steady state in 10–15 min
- Do Not Give / Hold If
- No absolute contraindication in arrest. Never a 1 mg IV push with a pulse. Reduce or hold for new VT or ectopy, ischemic ECG change or MAP above goal
- Watch For
- Tachyarrhythmias and VF (ECG); myocardial ischemia (ST change, chest pain); severe hypertension or pulmonary edema; distal, gut or renal ischemia; extravasation (blanching at the site)
- Reversal / Rescue
- No antidote: stop; effect fades within minutes. Extravasation: phentolamine 5–10 mg in 10–15 mL 0.9% NaCl infiltrated into the site (within 12 hr)
- Must Remember
- Three strengths, each tenfold apart: 1 mg/mL (IM), 0.1 mg/mL (arrest: 1 mg = 10 mL), 10 mcg/mL (push-dose: 10–20 mcg = 1–2 mL). Name mg/mL and dose on every syringe
Indications
Emergency & Prehospital
- Cardiac arrest, any rhythm (adult and pediatric): asystole and PEA as soon as feasible; VF or pulseless VT after initial defibrillation attempts fail
- Neonatal resuscitation: heart rate still <60/min after 60 seconds of chest compressions with effective ventilation
- Symptomatic bradycardia unresponsive to atropine: infusion as a bridge to transcutaneous pacing
- Refractory anaphylaxis: low-dose IV infusion when symptoms persist after 2 doses of IM epinephrine 1 mg/mL and fluids
- Transient severe hypotension: push-dose boluses as a bridge to an infusion (off-label)
ED / ICU / Transport
- Septic shock in adults: the FDA-labeled use for this concentration, as a diluted infusion. In the Surviving Sepsis Campaign (SSC) 2026 it ranks third, behind norepinephrine and vasopressin. With cardiac dysfunction it moves up to first-line.
- Pediatric septic shock: epinephrine or norepinephrine, chosen by bedside assessment (see Pediatric Shock). SSC 2026 makes no recommendation for either.
- Cardiogenic shock and post-ROSC hypotension: inotrope-vasopressor when output and pressure are both low. AHA 2025 Part 11 finds insufficient evidence for a specific vasopressor after arrest (2b, B-NR)
Dosing & Administration
The doses here are the AHA, AAP and NASEMSO values. Push-dose and the refractory anaphylaxis infusion have no single house dose. Follow protocol and medical direction.
Available Forms
- Prefilled syringe (EMS and code cart): 0.1 mg/mL (1:10,000), 10 mL (1 mg). 1 mg = 10 mL, 0.01 mg = 0.1 mL. Contains sodium metabisulfite
- Premixed infusion bags: in 0.9% NaCl, e.g. 4 mg/250 mL (16 mcg/mL) or 16 mg/250 mL (64 mcg/mL)
- Concentrate vial: 1 mg/mL (1:1,000), for IM use or compounding; never push undiluted IV
- Push-dose syringe: 10 mcg/mL (100 mcg in 10 mL), prefilled where stocked
Adult Dosing
| Indication | Dose & Route | Repeat / Max | Notes |
|---|---|---|---|
| Cardiac arrest (all rhythms) | 1 mg IV/IO every 3–5 min (10 mL of 0.1 mg/mL) | Until ROSC or termination; no fixed max | High-alert Nonshockable: as soon as feasible (AHA 2025 Part 9, 2a, B-NR). Shockable: after initial defibrillation attempts fail (2a, B-NR). IV first (Class 1, A); IO if IV fails or is not feasible (2a, A). High-dose epinephrine not recommended (3: No Benefit, B-R) |
| Septic shock (weight-based infusion) | 0.05–2 mcg/kg/min IV infusion, titrated to MAP | Titrate every 10–15 min by 0.05–0.2 mcg/kg/min; label range up to 2 mcg/kg/min | High-alert SSC 2026: third-line after norepinephrine plus vasopressin; first-line option with cardiac dysfunction |
| Cardiogenic or post-ROSC shock | Weight-based IV infusion as for septic shock, titrated to MAP ≥65 mmHg and perfusion | No fixed max: titrate to effect | High-alert Cardiogenic-shock data suggest a less favorable safety profile than norepinephrine |
| Bradycardia unresponsive to atropine | 2–10 mcg/min IV infusion | Titrate to heart rate and perfusion; bridge to pacing | High-alert After atropine; treat reversible causes; prepare pacing (AHA 2025 Part 9, 2b, C-LD) |
| Refractory anaphylaxis | Start about 0.1 mcg/kg/min IV infusion (10 mcg/mL at 0.5 mL/kg/hr); 1 mL/kg/hr if hypotensive or hypoxic | Titrate to lowest effective rate; no fixed max | High-alert Repeat IM every 5 min until the infusion runs. Experienced clinicians only: 50 mcg IV bolus (0.5 mL of 0.1 mg/mL) while the infusion is set up |
| Push-dose for transient hypotension (off-label) | 10–20 mcg IV (1–2 mL of 10 mcg/mL) | Every 2–5 min to target; start an infusion if repeats are needed | High-alert Bridge only, under protocol. Never push from the undiluted 0.1 mg/mL syringe (except the specialist anaphylaxis bolus above) |
Dosing weight: Arrest dosing is a fixed 1 mg. For mcg/kg/min infusions, pick one convention per patient (usually actual body weight) and say which one at handoff.
Pediatric Dosing
| Indication | Dose (per kg) & Route | Max Single / Max Total | Notes |
|---|---|---|---|
| Cardiac arrest | 0.01 mg/kg (0.1 mL/kg of 0.1 mg/mL) IV/IO every 3–5 min | Max 1 mg/dose; no total max | High-alert Nonshockable: first dose as early as possible (AHA/AAP 2025 Part 8, 2a, C-LD). Shockable: after 2 defibrillation attempts, or sooner only if rapid defibrillation is not possible (2b, C-LD) |
| Bradycardia with poor perfusion | 0.01 mg/kg (0.1 mL/kg) IV/IO every 3–5 min | Max 1 mg/dose | High-alert Heart rate <60/min with poor perfusion despite oxygenation and ventilation; start CPR (Part 8, Class 1) |
| Fluid-refractory or cardiogenic shock | 0.05–0.3 mcg/kg/min IV/IO infusion | Titrate to perfusion and age-based BP; no fixed max | High-alert Differs from the FDA label, which does not establish pediatric septic-shock use. Specialist use; range from NASEMSO Shock (p. 109). |
| Refractory anaphylaxis | 0.5 mcg/kg/min IV/IO infusion after repeated IM doses and 60 mL/kg fluid (NASEMSO v3.0 lists this for all ages; not a pediatric-specific dose) | Titrate to lowest effective rate; no fixed max | High-alert IV boluses in children: specialist use only; no evidence-based dose. RCUK 2021 gives 0.5–1 mL/kg/hr of 10 mcg/mL (0.5 mL/kg/hr is about 0.1 mcg/kg/min; 1 mL/kg/hr about 0.17) in children and adults; follow local protocol and medical direction |
| Push-dose, bradycardia with poor perfusion (off-label outside arrest) | 1 mcg/kg (0.1 mL/kg of 10 mcg/mL) IV/IO push, diluted | Max 10 mcg (1 mL) per dose; every 3–5 min to MAP >65 mmHg | High-alert NASEMSO v3.0 Bradycardia (p. 36). Never use the adult 10–20 mcg push-dose in a child. Protocol use only |
The arrest and bradycardia rows come from AHA/AAP 2025 PALS: 0.01 mg/kg of 0.1 mg/mL, maximum 1 mg, every 3–5 min. Use length-based tape or weight-based dosing checks. A pediatric arrest dose never exceeds the adult 1 mg.
Neonatal Resuscitation
- When: heart rate <60/min after 60 seconds of compressions with effective ventilation. Fix ventilation first.
- Intravascular (preferred): 0.01–0.03 mg/kg (0.1–0.3 mL/kg of 0.1 mg/mL) via low-lying UVC or IO (AHA 2025 Part 5, Class 1, B-NR), then 3 mL 0.9% NaCl flush.
- Endotracheal (only while access is obtained): 0.05–0.1 mg/kg (0.5–1 mL/kg of 0.1 mg/mL) (Part 5, 2a, C-LD).
- Repeat: every 3–5 min while heart rate stays <60/min (Part 5, 2b, C-LD). Known blood loss without response: 10–20 mL/kg 0.9% NaCl or O-negative blood over 5–10 min.
The full resuscitation sequence is in Neonatal Resuscitation.
Continuous Infusion
| Setting | Example Concentration | Start | Titrate | Usual Range / Max |
|---|---|---|---|---|
| Adult septic or cardiogenic shock | 4 mg/250 mL (16 mcg/mL), example (institution-specific) | 0.05 mcg/kg/min | 0.05–0.2 mcg/kg/min every 10–15 min | Label range up to 2 mcg/kg/min |
| Adult bradycardia (fixed rate) | 4 mg/250 mL (16 mcg/mL), example | 2 mcg/min | To heart rate and BP | 2–10 mcg/min |
| Refractory anaphylaxis (adult) | 1 mg in 100 mL D5W or D5/0.9% NaCl (about 10 mcg/mL), example | 0.5 mL/kg/hr (about 0.1 mcg/kg/min) | Up or down by response; steady state in 5–10 min | 1 mL/kg/hr if severe; no fixed max |
| Anaphylaxis with shock (NASEMSO, all ages) | Smart-pump standard concentration (institution-specific) | 0.5 mcg/kg/min after repeated IM doses and 60 mL/kg fluid | To perfusion and BP | 0.5 mcg/kg/min (NASEMSO v3.0, all ages); RCUK 2021: 0.5–1 mL/kg/hr of 10 mcg/mL in children and adults; no fixed max |
| Pediatric shock | Smart-pump standard concentration (institution-specific) | 0.05 mcg/kg/min | To perfusion and age-based BP | 0.05–0.3 mcg/kg/min |
Push-Dose Epinephrine Preparation (Adults)
- Use a prefilled 10 mcg/mL syringe if your system stocks one.
- Otherwise dilute: a 10 mL syringe with 9 mL 0.9% NaCl plus 1 mL (0.1 mg) from the 0.1 mg/mL syringe: 10 mL of 10 mcg/mL (100 mcg).
- Label at once: "EPINEPHrine 10 mcg/mL, push-dose", with time and initials.
- Give and read back in mcg and mL: 10–20 mcg = 1–2 mL IV; recheck BP before each repeat, and start an infusion if hypotension persists.
Preparation & Administration
- Arrest push: the 0.1 mg/mL syringe undiluted as a rapid IV/IO push, then a saline flush; do not pause compressions.
- Infusion dilution: premixed bag when available. Compounded dilutions use D5W or D5/0.9% NaCl (saline alone is not recommended for this compounded dilution). Discard pink, brown or cloudy solution.
- Line: smart pump on a dedicated line. SSC 2026 (adults) suggests starting vasopressors peripherally rather than delaying for central access, with frequent site checks. Avoid leg veins in older adults and in vascular disease. Move to a central line for prolonged or high-dose infusions.
- Weaning: taper gradually (label example: reduce every 30 min over 12–24 hr). Abrupt stops cause rebound hypotension.
Contraindications & Precautions
Contraindications
- None absolute in cardiac arrest, neonatal resuscitation or life-threatening shock (the FDA label lists none).
- Sulfite allergy (relative): the products contain sodium metabisulfite. That should not stop use in a life-threatening emergency.
Precautions
- Coronary disease or cardiomyopathy: more arrhythmias and ischemia. Use the lowest effective dose.
- Pre-existing tachyarrhythmia: may worsen the rate; consider an alternative vasopressor.
- Aortic dissection or uncontrolled hypertension: avoid or use minimal doses outside cardiac arrest.
- MAO inhibitors or tricyclic antidepressants: severe, prolonged hypertension; start low.
- Hypothermic cardiac arrest: AHA 2025 Part 10 (2b, C-EO) says it may be reasonable to defer epinephrine until core temperature reaches ≥30 °C (86 °F), in adults and children.
- Obstetrics and labor: inhibits contractions. Outside resuscitation, the label says to avoid it in the second stage of labor, and when maternal BP is above 130/80 mmHg.
- Occlusive vascular disease: avoid leg veins (limb ischemia).
Hold / Reassess If
- MAP above target on two readings: wean the infusion; do not stop abruptly.
- New ventricular ectopy, VT, ischemic ST changes or chest pain: reduce or stop and reassess.
- Tachycardia, tremor or pallor with normal or raised BP during an anaphylaxis infusion: excess epinephrine; reduce the rate.
- Swelling, blanching or coolness at the site: stop that line, restart elsewhere, treat extravasation.
Adverse Effects & Toxicity
Common
- Palpitations, tachycardia, anxiety, tremor, headache
- Pallor, sweating, cool extremities; nausea and vomiting
- Hyperglycemia, hypokalemia and rising lactate
Serious / Life-Threatening
- Arrhythmias (including fatal VF): reduce or stop; correct K⁺, Mg²⁺ and hypoxia; ACLS.
- Myocardial ischemia or infarction: lowest effective dose; 12-lead ECG; consider an alternative vasopressor.
- Severe hypertension, cerebral hemorrhage: stop; short-acting vasodilator or α-blocker if needed; neuro assessment.
- Pulmonary edema: stop or reduce; oxygen and ventilatory support.
- Peripheral, digital or mesenteric ischemia; renal vasoconstriction: cold, mottled or dusky digits, abdominal pain, falling urine output. Infusions into ankle veins can end in gangrene. Use the lowest effective dose and reassess volume and output.
- Extravasation necrosis: blanching, cold, hard, pale skin along the vein. Stop, restart elsewhere; phentolamine 5–10 mg in 10–15 mL 0.9% NaCl infiltrated through the area as soon as possible (within 12 hr).
Overdose & Toxicity Management
- Signs: extreme hypertension, pulmonary edema, ventricular ectopy progressing to VT or VF, myocardial ischemia, lactic acidosis, renal failure.
- Immediate: stop the drug. Epinephrine is inactivated within minutes, so care is supportive. There is no specific antidote.
- Treat: phentolamine for pulmonary edema or hypertension; β-blocker (e.g. propranolol) for arrhythmias; another vasopressor if hypotension follows.
Monitoring
| Parameter | When / How Often | Target / Act If |
|---|---|---|
| Clinical: rhythm (arrest) | Every 2-min rhythm check | Record dose times; after ROSC watch for tachyarrhythmia and hypertension |
| Clinical: ECG and blood pressure | Continuous ECG; BP every 2–5 min while titrating and before every push-dose | New VT, frequent ectopy or ST change: reduce or stop. Septic shock: MAP 65 mmHg (60–65 if ≥65 yr). Post-ROSC: MAP ≥65 mmHg |
| Clinical: perfusion | Hourly: mental status, capillary refill, skin, urine output | Urine <0.5 mL/kg/hr or dusky digits at goal MAP: suspect distal or gut ischemia; reassess output, volume and dose |
| Clinical: neonatal heart rate | Continuous ECG during compressions and after each dose | Still <60/min: repeat every 3–5 min, recheck ventilation |
| Laboratory: lactate, glucose, potassium | Baseline, and with ectopy or on prolonged infusion | Rising lactate with good perfusion may be a drug effect; hyperglycemia: treat per protocol; low K⁺: replace |
| Infusion safety: site | At least hourly and after every move | Blanching or swelling: stop, restart elsewhere, phentolamine |
Interactions & Compatibility
Clinically Significant Interactions
| Drug / Class | Effect | What To Do |
|---|---|---|
| β-blockers (e.g. propranolol) | Unopposed α effect: severe hypertension and reflex bradycardia; poor response in anaphylaxis | Titrate cautiously. In anaphylaxis refractory to epinephrine and fluids on a β-blocker, consider glucagon (off-label: RCUK 2021 adult 1 mg IV; AHA 2025 Part 10, 2b, C-EO: 1–5 mg IV in adults, 20–30 mcg/kg IV up to 1 mg in children) |
| MAO inhibitors, tricyclic antidepressants | Severe, prolonged hypertension | Start low; arterial line if possible |
| Halogenated anesthetics, digoxin, quinidine, thyroid hormone, antihistamines | Increased arrhythmia risk | Continuous ECG; treat arrhythmias promptly |
| α-blockers, phenothiazines, vasodilators, ergot alkaloids, antihypertensives, diuretics | Blunted pressor effect | Expect higher dose needs; reassess the cause |
| Diuretics, corticosteroids, theophylline | Additive hypokalemia | Monitor and replace K⁺ |
| Other vasopressors and inotropes, oxytocin, clonidine, doxapram, COMT inhibitors (e.g. entacapone) | Potentiated pressor effect | Titrate one drug at a time; track total vasopressor dose |
IV Compatibility
- Diluents: D5W or D5/0.9% NaCl for compounded infusions (label). Commercial premixes in 0.9% NaCl come as separately approved products.
- Incompatible: sodium bicarbonate and other alkaline solutions, plus oxidizing agents. Blood or plasma goes through its own line.
- Dedicated line or lumen for infusions. Verify against an institutional compatibility resource.
Special Populations
- Pediatrics: Arrest and bradycardia doses are weight-based and capped at 1 mg. The label does not establish septic-shock use in children. See Pediatric Cardiac Arrest.
- Neonates: Give only after effective ventilation and 60 seconds of compressions. The intravascular route is preferred.
- Pregnancy: Human data are limited, and they show no established risk of birth defects or miscarriage. Don't hold back life-sustaining treatment. Epinephrine is part of maternal ACLS. It can cut uterine blood flow and slow labor.
- Lactation: No data exist. Infant exposure is expected to be very low: poor oral bioavailability and a short half-life.
- Older Adults: Start infusions at the low end of the range and avoid leg veins. Older patients carry a higher risk of ischemia, arrhythmia and hypertensive stroke.
- Renal Impairment: No specific adjustment is established. Epinephrine constricts renal vessels and can cut urine output. Titrate to effect.
- Hepatic Impairment: No specific adjustment is established. Titrate to effect.
- Obesity / Dosing Weight: The adult arrest dose stays a fixed 1 mg. For infusions, pick one dosing weight per patient.
Field & Transport Considerations
- Scope: cardiac-arrest doses: AEMT and above. The NHTSA model allows AEMT epinephrine during cardiac arrest. Push-dose epinephrine and infusions: Paramedic, RN and critical-care transport (CCT) only, under medical direction. Whoever mixes a push-dose syringe labels it right away and checks 10 mcg/mL with a second clinician where the agency requires it. Scope varies by state and agency protocol.
- Storage & Stability: 20–25 °C (68–77 °F), protected from light; do not refrigerate or freeze. Discard pink, brown or cloudy solution.
- Carried Concentration: 1 mg/mL (IM) and 0.1 mg/mL (IV syringe) sit side by side in drug boxes. Say the mg/mL out loud, store them apart and make a separately labeled push-dose syringe.
- Infusions in Transport: pump with drug library on a dedicated line, bag volume for the trip plus delays, site check at every reassessment; verify concentration and dosing units at handoff.
- Handoff Essentials: number and times of arrest doses and time of ROSC; push-dose total in mcg; infusion concentration, current rate (mcg/min or mcg/kg/min and dosing weight), last titration and response; any extravasation.
Clinical Pearls
Pharmacology
Nonselective α- and β-agonist. The α₁ effect is constriction. It raises diastolic and coronary perfusion pressure during CPR and SVR in shock. The β₁ effect raises contractility and heart rate, at the cost of oxygen demand and arrhythmia risk. IV/IO onset is under 5 min. The effect is gone within 20 min. Effective plasma half-life is under 5 min. MAO and COMT break it down, and it leaves no active metabolites. For the full pharmacology and a wider vasopressor comparison, see the Vasopressor and Inotrope Guide.
Names & Classification
- Generic Name
- Epinephrine (as epinephrine hydrochloride); adrenaline (international)
- Brand Names
- Adrenalin (vials and premixed bags); generic 0.1 mg/mL prefilled syringes and premixed bags
- Controlled Substance
- Not controlled
- ISMP High-Alert
- Yes: ISMP high-alert medication (adrenergic agonists, IV)
- Look-Alike / Sound-Alike
- EPINEPHrine / ePHEDrine (ISMP list); practical mix-up with norepinephrine and between the 1 mg/mL and 0.1 mg/mL strengths
- Error-Prone Abbreviations to Avoid
- Ratio strengths alone (1:1,000, 1:10,000) and "epi" on orders: write the drug name, mg/mL and the dose in mg or mcg
References
- International Medication Systems, Ltd. (2024). Epinephrine injection USP 1 mg/10 mL (0.1 mg/mL), for intravenous use: prescribing information. DailyMed, U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f2b5f15b-8541-466a-a27a-ee57bc4aac67
- Wigginton, J. G., Agarwal, S., Bartos, J. A., Coute, R. A., et al. (2025). Part 9: Adult advanced life support: 2025 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation, 152(16 Suppl 2), S538–S577. https://doi.org/10.1161/CIR.0000000000001376
- Cao, D., Arens, A. M., Chow, S. L., Easter, S. R., et al. (2025). Part 10: Adult and pediatric special circumstances of resuscitation: 2025 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation, 152(16 Suppl 2), S578–S672. https://doi.org/10.1161/CIR.0000000000001380
- Lasa, J. J., Dhillon, G. S., Duff, J. P., Hayes, J., et al. (2025). Part 8: Pediatric advanced life support: 2025 American Heart Association and American Academy of Pediatrics Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation, 152(16 Suppl 2), S479–S537. https://doi.org/10.1161/CIR.0000000000001368
- Lee, H. C., Strand, M. L., Finan, E., Illuzzi, J., et al. (2025). Part 5: Neonatal resuscitation: 2025 American Heart Association and American Academy of Pediatrics Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation, 152(16 Suppl 2), S385–S423. https://doi.org/10.1161/CIR.0000000000001367
- Hirsch, K. G., Amorim, E., Coppler, P. J., Drennan, I. R., et al. (2025). Part 11: Post–cardiac arrest care: 2025 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation, 152(suppl 2), S673–S718. https://doi.org/10.1161/CIR.0000000000001375
- Prescott, H. C., Antonelli, M., Alhazzani, W., Møller, M. H., et al. (2026). Surviving Sepsis Campaign: International guidelines for management of sepsis and septic shock 2026. Critical Care Medicine. https://doi.org/10.1097/CCM.0000000000007075
- Resuscitation Council UK. (2021). Emergency treatment of anaphylaxis: Guidelines for healthcare providers (including refractory anaphylaxis). https://www.resus.org.uk/library/additional-guidance/guidance-anaphylaxis/emergency-treatment
- Sucena Rodrigues, B., Caldeira, D., Dantas, J., & Faria, R. (2025). Push-dose pressors outside the operating room: Systematic review and meta-analysis of observational studies. Journal of Emergency Medicine, 79, 260–279. https://doi.org/10.1016/j.jemermed.2025.04.021
- National Highway Traffic Safety Administration. (2021). National EMS Scope of Practice Model, 2019, including Change Notices 1.0 and 2.0 (DOT HS 813 151), Section V and footnote 5. https://mn.gov/oems/assets/National_EMS_Scope_of_Practice_Model_2021_%20%28002%29_tcm1221-744908.pdf
- National Association of State EMS Officials. (2022). National Model EMS Clinical Guidelines, Version 3.0, Shock (pp. 108–110). Copy hosted by Iowa HHS. https://hhs.iowa.gov/media/198/download
- Weiss, S., Peters, M. J., Oczkowski, S. J., et al. (2026). Surviving Sepsis Campaign international guidelines for the management of sepsis and septic shock in children 2026. Pediatric Critical Care Medicine, published March 23, 2026. DOI: https://doi.org/10.1097/PCC.0000000000003927. Verified text: SCCM guideline page ("insufficient evidence to issue a recommendation on the preferred use of epinephrine or norepinephrine").
Medical Disclaimer
- For Educational Purposes Only: This content is intended for educational reference and should not be used for clinical decision-making.
- Not a Substitute for Professional Judgment: Always consult your local protocols, institutional guidelines, and supervising physicians.
- Verify Before Acting: Users are responsible for verifying information through authoritative sources before any clinical application.