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Updated: Feb 10, 2026

A Neonatal Imaging Model of Gram-Negative Bacterial Sepsis
Published on: August 12, 2020
Reviewing the WHO guidelines for antibiotic use for sepsis in neonates and children
Aline Fuchs1, Julia Bielicki1,2, Shrey Mathur2
1a Paediatric Pharmacology and Pharmacometrics , University Children's Hospital Basel , Basel , Switzerland.
Insights
Updated guidelines for treating neonatal sepsis in low- and middle-income countries (LMIC) confirm current World Health Organization (WHO) recommendations. Evidence supports existing antibiotic therapies for suspected sepsis in neonates and young infants.
Area of Science:
- Pediatrics
- Infectious Diseases
- Antimicrobial Resistance
Background:
- Previous guidelines (2005, 2015) recommended specific antibiotic regimens for suspected sepsis in low- and middle-income countries (LMIC).
- Increasing antimicrobial resistance necessitates an updated review of empirical sepsis therapy in neonates and children.
- Consideration of susceptibility patterns, cost, and adverse events is crucial for effective treatment.
Purpose of the Study:
- To review and update recommendations for empirical antibiotic therapy for suspected sepsis in neonates and children in LMIC.
- To evaluate current treatment guidelines in light of rising antimicrobial resistance.
- To identify gaps in research, particularly for hospital-acquired sepsis.
Main Methods:
- Systematic literature review of published evidence.
- Analysis of international guidelines on sepsis treatment.
- Identification of studies comparing antibiotic treatments in LMIC settings.
Main Results:
- Five studies evaluated simplified antibiotic treatments for infants in LMIC not requiring inpatient care.
- Current World Health Organization (WHO) guidelines for hospital-based and outpatient sepsis treatment are supported by available evidence.
- Limited evidence exists for second-line therapies like cephalosporins in high-resistance areas.
Conclusions:
- Existing WHO guidelines for gentamicin and penicillin (hospital) or gentamicin and amoxicillin (outpatient) remain appropriate.
- No strong evidence mandates changes to current empirical sepsis treatment protocols.
- Further research is critically needed for hospital-acquired sepsis in neonates and children, given rising resistance rates.
Abstract:
Background Guidelines from 2005 for treating suspected sepsis in low- and middle-income countries (LMIC) recommended hospitalisation and prophylactic intramuscular (IM) or intravenous (IV) ampicillin and gentamicin. In 2015, recommendations when referral to hospital is not possible suggest the administration of IM gentamicin and oral amoxicillin. In an era of increasing antimicrobial resistance, an updated review of the appropriate empirical therapy for treating sepsis (taking into account susceptibility patterns, cost and risk of adverse events) in neonates and children is necessary. Methods Systematic literature review and international guidelines were used to identify published evidence regarding the treatment of (suspected) sepsis. Results Five adequately designed and powered studies comparing antibiotic treatments in a low-risk community in neonates and young infants in LMIC were identified. These addressed potential simplifications of the current WHO treatment of reference, for infants for whom admission to inpatient care was not possible. Research is lacking regarding the treatment of suspected sepsis in neonates and children with hospital-acquired sepsis, despite rising antimicrobial resistance rates worldwide. Conclusions Current WHO guidelines supporting the use of gentamicin and penicillin for hospital-based patients or gentamicin (IM) and amoxicillin (oral) when referral to a hospital is not possible are in accordance with currently available evidence and other international guidelines, and there is no strong evidence to change this. The benefit of a cephalosporin alone or in combination as a second-line therapy in regions with known high rates of non-susceptibility is not well established. Further research into hospital-acquired sepsis in neonates and children is required.
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