Ceftazidime/avibactam and ceftolozane/tazobactam for severe paediatric infections: A systematic review, meta-analysis, and evidence map

ElsevierVolume 67, Issue 2, February 2026, 107710International Journal of Antimicrobial AgentsAuthor links open overlay panelPaula Pimenta-de-Souza a, Alice Ramos-Silva a, Valcieny Sandes a, Patrícia Portella a, Thaís Gouvêa a, Fernando Fernandez-Llimos b, Elisangela Costa Lima aShow moreHIGHLIGHTS•

First systematic review on ceftazidime/avibactam and ceftolozane/tazobactam in children.

High clinical and microbiological cure rates (>80%) across study designs.

Mortality absent in RCTs but reached 8% in observational studies.

Adverse events were rare, but higher in neonates, especially preterms.

Major evidence gaps remain for pneumonia, bacteraemia, and resistant infections.

AbstractBackground

The growing prevalence of multidrug-resistant Gram-negative bacilli poses major challenges to the management of severe paediatric infections. Ceftazidime/avibactam (CZA) and ceftolozane/tazobactam (C/T) are newer β-lactam/β-lactamase inhibitor combinations with established efficacy in adults.

Objective

To synthesize current evidence on the efficacy, effectiveness, and safety of CZA and C/T in hospitalized children with severe infections.

Methods

We conducted a systematic review, meta-analysis, and evidence map (PROSPERO CRD420251025715). Searches were performed in PubMed, Scopus, CENTRAL, Epistemonikos, LILACS, SciELO, and Web of Science. Eligible designs included randomized controlled trials (RCTs), cohort studies, case series, and case reports evaluating CZA or C/T for complicated intra-abdominal infections, complicated urinary tract infections (cUTI), pneumonia, or bacteraemia in patients aged 0–18 y. The primary outcome was 30-d mortality; secondary outcomes were clinical and microbiological cure and adverse events.

Results

Nineteen studies (4 RCTs, 9 case series, 6 case reports) involving 472 patients were included. Sixteen studies evaluated CZA and three evaluated C/T. All RCTs were phase II, industry-sponsored, and excluded critically ill children and carbapenem-resistant infections. According to the updated RoB 2 assessment, two trials had overall low risk of bias, and two presented some concerns, mainly related to missing outcome data. No deaths occurred in RCTs, whereas observational studies reported 8% mortality. Clinical and microbiological cure exceeded 80% across study designs. Adverse events were generally infrequent; neonatal events clustered in case series, but evidence was insufficient for statistical comparison across age groups. Certainty of evidence ranged from moderate (cUTI with susceptible pathogens) to very low (pneumonia and resistant infections).

Conclusions

CZA and C/T appear promising for paediatric cUTI and complicated intra-abdominal infections, but the evidence base remains narrow and largely dependent on small, industry-funded trials. Independent RCTs including critically ill children and resistant infections are urgently needed.

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Ceftazidime-avibactam

Ceftolozane-tazobactam

Paediatric severe infections

Multidrug-resistant Gram-negative bacteria

Systematic review and meta-analysis

Antimicrobial stewardship

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© 2026 The Author(s). Published by Elsevier Ltd.

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