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Peer-reviewedCC BYBMC pediatrics

Time-critical sepsis interventions and clinical outcomes among children in a tertiary Tanzanian emergency department.

4 more authors
6 affiliations
  1. 1Department of Pediatrics, University of California San Francisco, Box 0110, 550 16 St, Floor 4, San Francisco, CA, 94143, USA. [email protected].
  2. 2Muhimbili National Hospital, Dar Es Salaam, Tanzania.
  3. 3Muhimbili University of Health and Allied Sciences, Dar Es Salaam, Tanzania.
  4. 4Department of Epidemiology & Biostatistics, University of California San Francisco, San Francisco, CA, USA.
  5. 5University of California San Francisco, Institute for Global Health Sciences, San Francisco, CA, USA.
  6. 6Department of Pediatrics, University of California San Francisco, Box 0110, 550 16 St, Floor 4, San Francisco, CA, 94143, USA.

Abstract

Background

Pediatric sepsis remains a leading cause of mortality in resource-limited settings. We evaluated the delivery of time-critical sepsis interventions and their association with in-hospital mortality among children in Tanzania.Methods

We conducted a secondary analysis of a prospective cohort of children (28 days to 14 years) presenting with sepsis to the Emergency Medicine Department at Muhimbili National Hospital, Dar es Salaam, Tanzania (July 2022 to November 2024). Sepsis was defined as fever and at least one World Health Organization warning sign. Local pediatric sepsis guidelines recommend antibiotics and intravenous fluids (IVF) for all patients with sepsis, regardless of the source. Primary exposures were receipt and timing of antibiotics and IVF. The primary outcome was in-hospital mortality. Multivariable logistic regression adjusted for age, nutritional status, referral status, and illness severity.Results

Among 755 children, 61.2% (n = 462) received antibiotics, and 55.6% (n = 420) received IVF. Median time to intervention was 2.4 h (IQR 1.6-3.7). 35.5% (n = 268) received both interventions, and only 3.7% (n = 28) received them within one hour. In-hospital mortality was 19.6% (n = 148), with a median time to death of 4.1 days (IQR 1.6-9.5). In a multivariable analysis, time to initiation of both antibiotics and IVF was not significantly associated with in-hospital mortality (adjusted OR 1.29; 95% CI 0.83-2.0; p = 0.264). When modeled continuously, a longer time to IVF administration was associated with increased mortality risk (HR 1.05 per hour delay; 95% CI 1.01-1.10).Conclusions

Receipt of time-critical sepsis interventions (antibiotics and IVF) was delayed and inconsistent, with no observed association with decreased mortality, although residual confounding may remain. This both highlights gaps in early evidence-based care delivery and suggests additional, system-related influences on pediatric sepsis outcomes. Our findings underscore the need for context-specific strategies to strengthen pediatric sepsis management in resource-limited settings.

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BibTeX
@article{sorensen2026timecritical,
  title = {{Time-critical sepsis interventions and clinical outcomes among children in a tertiary Tanzanian emergency department.}},
  author = {Abigail M Sorensen and Raya Y Mussa and Erasto M Sunzula and Victoria M Mlele and Scott P Oltman and Cecilia L Msemwa and Lushona K Mathias and Kathleen S Sun and Jazmin M Baez-Maidana and Juma A Mfinanga and Victoria T Chu and Anneka M Hooft and Namala P Mkopi and Joel P Manyahi and Teresa B Kortz and Hendry R Sawe},
  journal = {BMC pediatrics},
  year = {2026},
  month = jul,
  doi = {10.1186/s12887-026-07369-2},
  url = {https://europepmc.org/article/MED/42907788},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Time-critical sepsis interventions and clinical outcomes among children in a tertiary Tanzanian emergency department.
AU  - Abigail M Sorensen
AU  - Raya Y Mussa
AU  - Erasto M Sunzula
AU  - Victoria M Mlele
AU  - Scott P Oltman
AU  - Cecilia L Msemwa
AU  - Lushona K Mathias
AU  - Kathleen S Sun
AU  - Jazmin M Baez-Maidana
AU  - Juma A Mfinanga
AU  - Victoria T Chu
AU  - Anneka M Hooft
AU  - Namala P Mkopi
AU  - Joel P Manyahi
AU  - Teresa B Kortz
AU  - Hendry R Sawe
PY  - 2026
DA  - 2026/07/01
JO  - BMC pediatrics
DO  - 10.1186/s12887-026-07369-2
UR  - https://europepmc.org/article/MED/42907788
AB  - Background  Pediatric sepsis remains a leading cause of mortality in resource-limited settings. We evaluated the delivery of time-critical sepsis interventions and their association with in-hospital mortality among children in Tanzania.Methods  We conducted a secondary analysis of a prospective cohort of children (28 days to 14 years) presenting with sepsis to the Emergency Medicine Department at Muhimbili National Hospital, Dar es Salaam, Tanzania (July 2022 to November 2024). Sepsis was defined as fever and at least one World Health Organization warning sign. Local pediatric sepsis guidelines recommend antibiotics and intravenous fluids (IVF) for all patients with sepsis, regardless of the source. Primary exposures were receipt and timing of antibiotics and IVF. The primary outcome was in-hospital mortality. Multivariable logistic regression adjusted for age, nutritional status, referral status, and illness severity.Results  Among 755 children, 61.2% (n = 462) received antibiotics, and 55.6% (n = 420) received IVF. Median time to intervention was 2.4 h (IQR 1.6-3.7). 35.5% (n = 268) received both interventions, and only 3.7% (n = 28) received them within one hour. In-hospital mortality was 19.6% (n = 148), with a median time to death of 4.1 days (IQR 1.6-9.5). In a multivariable analysis, time to initiation of both antibiotics and IVF was not significantly associated with in-hospital mortality (adjusted OR 1.29; 95% CI 0.83-2.0; p = 0.264). When modeled continuously, a longer time to IVF administration was associated with increased mortality risk (HR 1.05 per hour delay; 95% CI 1.01-1.10).Conclusions  Receipt of time-critical sepsis interventions (antibiotics and IVF) was delayed and inconsistent, with no observed association with decreased mortality, although residual confounding may remain. This both highlights gaps in early evidence-based care delivery and suggests additional, system-related influences on pediatric sepsis outcomes. Our findings underscore the need for context-specific strategies to strengthen pediatric sepsis management in resource-limited settings.
SN  - 1471-2431
ER  -