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Sepsis and septic shock

Updated Oct 15, 2026Adults · ED management11 sources · 7 checked in PubMed1 figureSurviving Sepsis Campaign 2026

Bottom line

  • Sepsis is a medical emergency. Start treatment and resuscitation immediately. No single test rules sepsis in or out.1,2
  • Antibiotics within 1 hour for possible, probable or definite septic shock, and for probable or definite sepsis without shock. For possible sepsis without shock, investigate quickly and give antibiotics within 3 hours if the concern persists.1,2
  • Antibiotic delay costs lives; fluid speed less clearly so. In 49,331 New York patients, each hour to antibiotics raised the odds of in-hospital death (OR 1.04 per hour). Time to complete the fluid bolus did not.3
  • Give at least 30 mL/kg of crystalloid within 3 hours for hypoperfusion or septic shock. Prefer balanced crystalloids over saline.1,2
  • Target a MAP of 65, or 60–65 if 65 or older. Norepinephrine is first-line. Start it through a peripheral IV rather than waiting for a central line.1,2

Recognize

  • Screen with NEWS, NEWS2, MEWS or SIRS, not qSOFA. This is a strong recommendation (moderate certainty).1,2
  • Diagnosis is clinical. Don't rule sepsis in or out on one biomarker or test.1,2
  • Measure lactate (conditional, low certainty). Serial lactate can guide resuscitation, with capillary refill time as an adjunct.1,2
  • Get blood cultures as soon as possible, ideally before antibiotics (strong, low certainty).1,2

First hour

  1. Decide how likely infection is, and whether there is shock. That decision sets the antibiotic clock (table below).1,2
  2. Draw blood cultures and lactate, without delaying antibiotics.1,2
  3. Give antibiotics within 1 hour for shock or probable sepsis.1,2
  4. Start crystalloid: at least 30 mL/kg within 3 hours for hypoperfusion or shock. Base the dosing weight on BMI.1,2
  5. If hypotension persists after the first bolus, start norepinephrine, peripherally if needed. In unstable shock, vasopressors can run alongside fluids.1,2
  6. Look for a source that needs control, and aim to control it within 6 hours.1,2
PresentationAntimicrobialsStrength
Possible, probable or definite septic shockImmediately, ideally within 1 hourStrong, very low certainty
Probable or definite sepsis, no shockImmediately, ideally within 1 hourStrong, very low certainty
Possible sepsis, no shockRapid, time-limited workup. Give within 3 hours if concern persistsConditional, very low certainty
Low likelihood of infection, no shockDefer and monitor closelyConditional, very low certainty

From the 2026 Surviving Sepsis Campaign adult guidelines.1,2 Use clinical evaluation, not procalcitonin, to decide whether to start antibiotics.2

FIG 1The sepsis clock. Target windows from recognition, drawn for this page from the 2026 guideline. Solid bars are the target for that presentation. The lighter bar is the outer limit for possible sepsis without shock.1,2

Fluids

  • Crystalloids first (strong, moderate certainty). Prefer balanced crystalloids over 0.9% saline (conditional, moderate). Saline is suggested instead in traumatic brain injury.1,2
  • Crystalloid alone over adding albumin (conditional, moderate). Albumin may suit very large volumes or cirrhosis; avoid it in traumatic brain injury.1,2
  • No starches (strong, high certainty) and no gelatin (conditional).1,2
  • Beyond the first 30 mL/kg, use dynamic measures such as a passive leg raise or fluid challenge over static ones.1,2

What the trials show

  • CLOVERS (n = 1,563, sepsis-induced hypotension after initial fluid): a restrictive, vasopressor-early strategy used about 2.1 L less fluid in 24 hours. Mortality by day 90 was 14.0% vs 14.9%, not significantly different.4,10
  • SMART (n = 15,802 critically ill adults): balanced crystalloids lowered the composite of death, new dialysis or persistent kidney dysfunction (14.3% vs 15.4%).5

Vasopressors

StepRecommendationStrength
TargetMAP 65 mm Hg (practical range about ±5)Strong, moderate
Age ≥ 65MAP 60–65 mm HgConditional, low
First lineNorepinephrineStrong
AccessStart peripherally rather than waiting for a central lineConditional, very low
Rising norepinephrine doseAdd vasopressinConditional, moderate
MAP still low on bothAdd epinephrineConditional, very low
Cardiac dysfunctionNorepinephrine or epinephrine first; add an inotrope for persistent hypoperfusionConditional, very low
AvoidDopamine, terlipressin, beta-blockers in septic shockStrong to conditional

Support for the lower target in older adults: in the 65 trial (n = 2,463, age ≥ 65), permissive hypotension cut vasopressor exposure. Mortality at 90 days was 41.0% vs 43.8%, not significant.8 The guideline's new recommendation is MAP 60–65 for this group.2

Corticosteroids

The guideline suggests IV corticosteroids in septic shock (conditional, low certainty).1,2

  • ADRENAL (n = 3,800, ventilated septic shock): hydrocortisone 200 mg/day did not lower 90-day mortality (27.9% vs 28.8%), but shock resolved faster (median 3 vs 4 days).6
  • APROCCHSS (n = 1,241): hydrocortisone plus fludrocortisone lowered 90-day mortality (43.0% vs 49.1%).7

Antimicrobials and source control

  • Cover multidrug-resistant organisms only if the patient is at high risk for them. Skip routine empiric antifungal and anaerobic coverage unless risk factors are present.1,2
  • Give beta-lactams as a prolonged infusion after a loading dose (strong, moderate certainty).1,2
  • Evaluate quickly for a source needing emergent control (good practice), and control it early, ideally within 6 hours.1,2
  • De-escalate once a pathogen and its susceptibilities are known.1,2

Other ED decisions

  • Oxygen: for hypoxemic respiratory failure, high-flow nasal cannula over conventional oxygen and as first-line over noninvasive ventilation (conditional).1,2
  • Bicarbonate: not for improving hemodynamics in lactic acidemia. Consider it when pH ≤ 7.2 with stage 2–3 acute kidney injury (conditional, very low).1,2
  • Glucose: start insulin at ≥ 180 mg/dL (strong).1,2
  • Not recommended: IV vitamin C, IV immunoglobulin, routine blood purification.1,2
  • Transfusion: restrictive thresholds over liberal (strong).1,2
  • Prehospital: screening en route and, where in-hospital evaluation will take over 60 minutes, antibiotics for septic shock once a structured screening process exists.1,2

Where experts disagree

Dissenting opinion

A group of emergency and critical care physicians published a rebuttal to the 2026 guidelines. They argue the recommendations have drifted toward mandated bundles and metric-driven care, and they urge clinicians to individualize resuscitation rather than follow protocols by rote.9 Most 2026 recommendations rest on low or very low certainty evidence.2

Pitfalls

  • Using qSOFA as the screening tool. The guideline recommends against it as a single screen.1,2
  • Waiting for a central line before starting norepinephrine.1,2
  • Holding antibiotics while cultures are drawn. Cultures should come first only if they don't delay treatment.1,2
  • Pushing fluid past the first 30 mL/kg without checking whether the patient is still fluid-responsive.1,2,4
  • Chasing a MAP above 65 in older adults by default.2,8

How strong is the evidence?

The 2026 update has 129 statements, 46 of them new, and covers evidence through June 2025. Most recommendations are conditional and rest on low or very low certainty evidence.2 The guideline's full text was not openly accessible, so the recommendations here come from the official SCCM summary and are cited to both.1,2 For a podcast discussion of CLOVERS, see REBEL EM.10

On-shift teaching

Questions to ask a learner at the bedside. Tap a question to see the answer. Every answer uses facts cited above.

Q1Which screening tools does the 2026 guideline recommend, and which one does it recommend against as a single screen?
NEWS, NEWS2, MEWS or SIRS over qSOFA (strong recommendation, moderate certainty).1,2
Q2In the New York sepsis mandate data, which mattered more: time to antibiotics or time to finish the fluid bolus?
Antibiotics. Each hour of delay raised the odds of in-hospital death (OR 1.04 per hour). Time to complete the fluid bolus was not associated with mortality.3
Q3A patient with possible sepsis is not in shock. How fast do antibiotics need to go in?
Do a rapid, time-limited workup, then give antibiotics within 3 hours if the concern persists. With shock, or with probable or definite sepsis, the target is within 1 hour.1,2
Q4What did CLOVERS show about restrictive versus liberal fluids?
The restrictive, vasopressor-early arm used about 2.1 L less fluid in 24 hours. Mortality by day 90 was 14.0% vs 14.9%, not significantly different.4
Q5What MAP should you target in a 78-year-old with septic shock?
60–65 mm Hg, a new conditional recommendation for patients 65 and older.2 In the 65 trial, permissive hypotension cut vasopressor exposure without a significant mortality difference (41.0% vs 43.8%).8
Q6Two large steroid trials disagreed. What did each find?
ADRENAL: hydrocortisone 200 mg/day did not lower 90-day mortality but shortened shock (median 3 vs 4 days).6 APROCCHSS: hydrocortisone plus fludrocortisone lowered 90-day mortality (43.0% vs 49.1%).7 The guideline suggests steroids in septic shock (conditional).2

References

  1. 1
    Prescott HC, Antonelli M, Alhazzani W, et al. Surviving Sepsis Campaign: International Guidelines for Management of Sepsis and Septic Shock 2026. Crit Care Med. 2026;54(4):725–812.GuidelinePMID 41869847DOIPubMed record; full text not openly accessible
  2. 2
    Society of Critical Care Medicine. Surviving Sepsis Campaign: International Guidelines for Management of Sepsis and Septic Shock 2026 (recommendation summary).Summarysccm.orgPage read
  3. 3
    Seymour CW, Gesten F, Prescott HC, et al. Time to treatment and mortality during mandated emergency care for sepsis. N Engl J Med. 2017;376(23):2235–2244.CohortPMID 28528569PMCPubMed
  4. 4
    NHLBI PETAL Clinical Trials Network; Shapiro NI, Douglas IS, et al. Early restrictive or liberal fluid management for sepsis-induced hypotension (CLOVERS). N Engl J Med. 2023;388(6):499–510.RCTPMID 36688507PMCPubMed
  5. 5
    Semler MW, Self WH, Wanderer JP, et al. Balanced crystalloids versus saline in critically ill adults (SMART). N Engl J Med. 2018;378(9):829–839.RCTPMID 29485925PMCPubMed
  6. 6
    Venkatesh B, Finfer S, Cohen J, et al. Adjunctive glucocorticoid therapy in patients with septic shock (ADRENAL). N Engl J Med. 2018;378(9):797–808.RCTPMID 29347874PubMed
  7. 7
    Annane D, Renault A, Brun-Buisson C, et al. Hydrocortisone plus fludrocortisone for adults with septic shock (APROCCHSS). N Engl J Med. 2018;378(9):809–818.RCTPMID 29490185PubMed
  8. 8
    Lamontagne F, Richards-Belle A, Thomas K, et al. Effect of reduced exposure to vasopressors on 90-day mortality in older critically ill patients with vasodilatory hypotension (65 trial). JAMA. 2020;323(10):938–949.RCTPMID 32049269PMCPubMed
  9. 9
    Spiegel R, Haycock K, Miller A, et al. The 2026 Surviving Sepsis Campaign Guidelines: the dissenting opinion. Am J Emerg Med. 2026;110:411–415.CommentaryPMID 42767105PubMed
  10. 10
    REBEL EM. REBEL Cast Ep116: The CLOVERS trial: restrictive vs liberal fluids in sepsis-induced hypotension.FOAMrebelem.comLink checked
  11. 11
    Emergency Medicine Cases. Sepsis. Further reading; not used for any claim above.FOAMemergencymedicinecases.comLink checked
How this page was made
  • Written from scratch. No source text was copied; facts are restated and cited.
  • The 2026 guideline's full text could not be retrieved, so recommendations and their strength come from the Society of Critical Care Medicine's official summary page. Each is cited to both the guideline and that summary.
  • Trial results were checked against their PubMed abstracts.
  • Figure 1 was drawn for this page from the guideline's time targets. No openly licensed sepsis images suitable for the bedside were found.
  • Not for clinical use until physician review.
Not for clinical use

AI-generated draft. Not reviewed by a physician. This page is for education only and may contain errors, including in doses. Do not use it to diagnose, treat or make decisions about any patient. Rely on your own clinical judgment, your institution's protocols and current drug labeling. Reading this page does not create a physician-patient relationship. Full terms