Sepsis (peds)
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This page is for adult patients. For pediatric patients, see: Sepsis.
Background
- Defined as a dysregulated host response to infection that leads to life-threatening organ dysfunction[1]
- Tachycardia is typically most predominant, hypotension is a late and ominous sign
Clinical Features
Shock: Warm vs Cold Shock
Warm Shock | Cold Shock | |
---|---|---|
Peripheries | Warm, Flushed | Mottled, Cold, Clammy |
Cap Refill | <2 sec | >2 sec |
Pulse | Bounding | Weak, Thready |
BP | Compensated | Hypotension |
HR | Tachy | Tachy or Brady |
Pulse Pressure | Widen | Narrow |
Neonatal Sepsis
- Early onset
- First few days of life
- Fulminant, associated with maternal or perinatal risk factors
- Septic shock and neutropenia are more common
- Late onset
- Occurs after 1 week of age
- Gradual
- Meningitis more likely
- Consider if feeding disturbance, rash, lethargy, irritability, seizure, apnea, tachypnea, grunting, vomiting, poor PO, gastric distention, diarrhea
Differential Diagnosis
Sick Neonate
THE MISFITS [2]
- Trauma
- Heart
- Congenital heart disease
- Hypovolemia
- Endocrine
- Metabolic
- Sodium
- Calcium
- Glucose
- Inborn errors of metabolism
- Seizure
- Formula / feeding problems
- Intestinal Disasters
- Toxin
- Sepsis
Pediatric fever
- Upper respiratory infection (URI)
- UTI
- Sepsis
- Meningitis
- Febrile seizure
- Juvenile rheumatoid arthritis
- Pneumonia
- Acute otitis media
- Whooping cough
- Unclear source
- Kawasaki disease
- Neonatal HSV
- Specific virus
Evaluation
Work-Up
- CBC, CMP
- Coags, D-dimer, fibrinogen
- Lactate, CRP
- Blood glucose
- Urinalysis/urine culture
- CXR
- Blood cultures
- Consider LP for CSF
Diagnosis
- Initial screening and decision to send studies is based on provider judgement
- Use the Phoenix Sepsis Score to calculate sepsis criteria, including septic shock.[3][4]
- Not indicated for adults, preterm (<37 weeks), or peri-birth hospitalizations
Management
Initial Resuscitation Focus
- Treat hypoxemia with supplemental oxygen (goal SpO2 92-98%)[5]
- Obtain intravenous/intraosseous access
- Rapidly transition to IO access, if difficulties with starting IV
- Collect diagnostic tests (including blood culture, lactate, ionized calcium; see workup above)
- Treat hypoglycemia, if present
- Early empiric broad-spectrum antibiotics (see below)
- Administer bolus intravenous fluid therapy administration (see below), if shock is present
- Start vasoactive agents, if shock persists
- Airway
- Consider CPAP (may buy time for fluid resuscitation prior intubation)
- Consider intubation, especially in fluid refractory shock
- Consider use of ketamine for sedation (less hypotension)
- Be prepared for cardiovascular collapse
- Consider corticosteroids[6]
- Continue to reassess (see below)
Empiric Broad-Spectrum Antibiotics
If in shock, administer as soon as possible. If not, it is reasonable to perform expedited diagnostics before administration.[7]
Neonatal
- Ampicillin 50mg/kg q8h + gentamicin 2.5mg/kg q24h + acyclovir
- If gram-negative strongly suspected replace gentamicin with cefotaxime or ceftazadine
- Have better CNS penetration
- If gram-negative strongly suspected replace gentamicin with cefotaxime or ceftazadine
Peds
Treatment will differ by local protocols
- Extended-spectrum penicillin (e.g. piperacillin-tazobactam) ± aminoglycoside ± vancomycin
OR
- 3rd or 4th generation cephalosporin ± aminoglycoside ± vancomycin
OR
Fluid Resuscitation
- For shock, 20 mL/kg boluses of isotonic crystalloid fluid titrated to clinical markers of cardiac output[8]
- Frequently ≥40 mL/kg in the first hour of resuscitation
- In low-resource settings (e.g., low income countries), fluid bolus therapy should be avoided unless the child exhibits hypotension[9]
Vasopressors
- Indicated for children that have:
- Myocardial dysfunction
- Shock in the setting of fluid overload
- Continue to have abnormal perfusion after 40-60 mL/kg of fluid resuscitation
- 1st line: epinephrine or norepinephrine (i.e., not dopamine)[10][11][12]
- 2nd and 3rd line: consider epinephrine, norepinephrine, dobutamine, milrinone, vasopressin, angiotensin II[13]
Corticosteroids
- Intravenous hydrocortisone recommended only for children with fluid-refractory, catecholamine-resistant shock.[14]
- There are no data on the addition of fludrocortisone to enhance the mineralocorticoid effect in pediatric septic shock.[15]
Reevaluation
- Patients should be continuously reassessed for signs of:
- Ongoing or worsening shock
- Iatrogenic fluid overload (e.g., pulmonary rales, hepatomegaly, peripheral edema, and echocardiographic findings that may suggest fluid overload)
- Golden Hour Goals
- Cap refill <2 sec
- Normal BP
- Normal pulses, similar central and peripheral
- Warm extremities
- UOP >1 mL/kg/hr
- Normal mental status
Disposition
- Admit
See Also
External Links
References
- ↑ Weiss SL, Fitzgerald JC. Pediatric Sepsis Diagnosis, Management, and Sub-phenotypes. Pediatrics (2024) 153 (1): e2023062967. https://doi.org/10.1542/peds.2023-062967
- ↑ Brousseau T, Sharieff GQ. Newborn emergencies: the first 30 days of life. Pediatr Clin North Am. 2006 Feb;53(1):69-84, vi.
- ↑ Schlapbach LJ, et al. International Consensus Criteria for Pediatric Sepsis and Septic Shock. JAMA. 2024 Feb 27;331(8):665-674. doi: 10.1001/jama.2024.0179.
- ↑ Sanchez-Pinto LN, et al. Development and Validation of the Phoenix Criteria for Pediatric Sepsis and Septic Shock. JAMA. 2024 Feb 27;331(8):675-686. doi: 10.1001/jama.2024.0196.
- ↑ Weiss SL, Fitzgerald JC. Pediatric Sepsis Diagnosis, Management, and Sub-phenotypes. Pediatrics (2024) 153 (1): e2023062967. https://doi.org/10.1542/peds.2023-062967
- ↑ Weiss SL, Fitzgerald JC. Pediatric Sepsis Diagnosis, Management, and Sub-phenotypes. Pediatrics (2024) 153 (1): e2023062967. https://doi.org/10.1542/peds.2023-062967
- ↑ Weiss SL, Fitzgerald JC. Pediatric Sepsis Diagnosis, Management, and Sub-phenotypes. Pediatrics (2024) 153 (1): e2023062967. https://doi.org/10.1542/peds.2023-062967
- ↑ Weiss SL, Fitzgerald JC. Pediatric Sepsis Diagnosis, Management, and Sub-phenotypes. Pediatrics (2024) 153 (1): e2023062967. https://doi.org/10.1542/peds.2023-062967
- ↑ Weiss SL, Fitzgerald JC. Pediatric Sepsis Diagnosis, Management, and Sub-phenotypes. Pediatrics (2024) 153 (1): e2023062967. https://doi.org/10.1542/peds.2023-062967
- ↑ Marik PE. Dopamine increases mortality in pediatric septic shock. Journal of Pediatrics. January 2016, Volume 168, Pages 253–256.
- ↑ Ventura AM, Shieh HH, Bousso A, Goes PF, Fernandes IC, de Souza DC, et al. Double-Blind Prospective Randomized Controlled Trial of Dopamine Versus Epinephrineas First-Line Vasoactive Drugs in Pediatric Septic Shock. Crit Care Med 2015;43:2292-302.
- ↑ Weiss SL, Fitzgerald JC. Pediatric Sepsis Diagnosis, Management, and Sub-phenotypes. Pediatrics (2024) 153 (1): e2023062967. https://doi.org/10.1542/peds.2023-062967
- ↑ Weiss SL, Fitzgerald JC. Pediatric Sepsis Diagnosis, Management, and Sub-phenotypes. Pediatrics (2024) 153 (1): e2023062967. https://doi.org/10.1542/peds.2023-062967
- ↑ Weiss SL, Fitzgerald JC. Pediatric Sepsis Diagnosis, Management, and Sub-phenotypes. Pediatrics (2024) 153 (1): e2023062967. https://doi.org/10.1542/peds.2023-062967
- ↑ Weiss SL, Fitzgerald JC. Pediatric Sepsis Diagnosis, Management, and Sub-phenotypes. Pediatrics (2024) 153 (1): e2023062967. https://doi.org/10.1542/peds.2023-062967