Evidence map›Paper›PMID 41627835›Full record

SynthesisJAMA pediatrics2026

Clinical Signs Associated With Mortality and Sepsis in Young Infants: A Systematic Review and Meta-Analysis.

Sophie Driker, Sitarah Mathias, Alastair Fung, Suci Ardini Widyaningsih, Naomi Schmeck, Jana Adnan, Yumin Kim, Anum S Hussaini, Tessa Kehoe, Krysten North and 6 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in JAMA pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Sophie DrikerDepartment of Pediatrics, Division of Newborn Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Sitarah MathiasDepartment of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Alastair FungDivision of Paediatric Medicine, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Suci Ardini WidyaningsihDepartment of Pediatrics, Division of Newborn Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Naomi SchmeckDepartment of Pediatrics, Division of Newborn Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Jana AdnanVayu Global Health Foundation, Medford, Massachusetts.
Yumin KimGlobal Alliance for Infant and Maternal Health Research, Department of Pediatrics, Warren Alpert Medical School, Brown University, Providence, Rhode Island.
Anum S HussainiDepartment of Pediatrics, Division of Newborn Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Tessa KehoeDepartment of Pediatrics, Division of Newborn Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Krysten NorthDepartment of Pediatrics, Division of Newborn Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Amber HoeyBryn Mawr College, Bryn Mawr, Pennsylvania.
Yasir ShafiqCentre for Global Child Health, The Hospital for Sick Children, Toronto, Ontario, Canada.
Carrie G WadeCountway Library, Harvard Medical School, Boston, Massachusetts.
Rishi P MedirattaDepartment of Pediatrics, Division of Pediatric Hospital Medicine, Stanford University School of Medicine, Stanford, California.
Chris A ReesDivision of Pediatric Emergency Medicine, Emory University School of Medicine, Atlanta, Georgia.
Anne Cc LeeDepartment of Pediatrics, Division of Newborn Medicine, Brigham and Women's Hospital, Boston, Massachusetts.

Funding

Advancing Approaches to Identify Young Children at Risk for Post-Discharge MortalityK23HL173694 · NHLBI · EMORY UNIVERSITY · PI Christopher A. Rees · 2024 to 2026
$585k
Nourishing Growing Brains: Maternal Micronutrient Supplementation during Lactation, Human Milk B-Complex Vitamins, and Infant NeurodevelopmentK23HD118179 · NICHD · BRIGHAM AND WOMEN'S HOSPITAL · PI Krysten North · 2025 to 2026
$335k
NHLBI NIH HHS K23 HL173694NICHD NIH HHS K23 HD118179
6 · The paper itself

Abstract

Importance: Early and accurate identification of clinical warning signs in young infants may help avert sepsis morbidity and mortality in resource-limited settings. Objective: To systematically review evidence on the association and accuracy of clinical signs to diagnose sepsis or predict mortality in young infants aged 0 to 59 days to inform management in settings with limited laboratory diagnostics. Data Sources: MEDLINE, Embase, CINAHL, Global Index Medicus, and Cochrane CENTRAL Register were searched from inception through May 2023, with updated searches on September 5, 2024. An umbrella search of systematic reviews was conducted in January 2024. Study Selection: Included studies reported data on 24 infant clinical signs informed by current World Health Organization (WHO) Integrated Management of Childhood Illness (IMCI) and hospital-based algorithms for the care of sick young infants reporting odds ratios (OR), risk ratios, or sensitivity and specificity. Data Extraction and Synthesis: Data were extracted independently by 2 reviewers. Quality assessment used the Newcastle-Ottawa, Quality Assessment of Diagnostic Accuracy Studies 2 (QUADAS-2), and Quality Assessment of Prognostic Accuracy Studies (QUAPAS) scales. OR data were pooled using random-effects models. Data analysis was performed from July to September 2025. Main Outcomes and Measures: OR of all-cause mortality, culture-confirmed sepsis, or clinical sepsis (with access to laboratory investigations). Results: Of 7641 studies, 52 studies with 140 885 participants were included. A total of 16 clinical signs were significantly associated with mortality, 11 with culture-confirmed sepsis, and 13 with clinical sepsis. For mortality, the 5 strongest associations were weak, abnormal, or absent cry (OR, 20.48; 95% CI, 6.59-63.67); not able to feed at all (OR, 18.32; 95% CI, 6.00-55.97); not feeding well (OR, 13.39; 95% CI, 6.97-25.72); drowsiness or unconsciousness (OR, 12.46; 95% CI, 6.06-25.62); and prolonged capillary refill (OR, 12.06; 95% CI, 2.77-52.53). The top 5 signs associated with culture-confirmed sepsis were not feeding well (OR, 4.52; 95% CI, 1.10-18.59); prolonged capillary refill (OR, 3.59; 95% CI, 2.05-6.28); lethargy (OR, 3.44; 95% CI, 1.89-6.26); drowsiness or unconsciousness (OR, 3.07; 95% CI, 2.01-4.68); and feeding intolerance (OR, 2.95; 95% CI, 1.67-5.21). Conclusions and Relevance: All current WHO IMCI clinical signs were significantly associated with mortality or culture-confirmed sepsis. Several signs not in IMCI were identified that may improve identification of life-threatening illness in young infants in resource-limited settings where clinical sign algorithms are the primary diagnostic tool.

Indexed as

SepsisHumansInfantInfant, Newborn

Identifiers

PMID41627835
PMCPMC12865698

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.