Evidence map›Paper›PMID 41120197›Full record

ArticleBMJ global health2025

Factors associated with positive blood cultures in children in nine African and Asian countries: the ACORN2 surveillance network.

Cristina Ardura-Garcia, Jill Hopkins, Sue J Lee, Naomi Waithira, Chris Painter, Clare L Ling, Tamalee Roberts, Thyl Miliya, Noah Obeng-Nkrumah, Japheth A Opintan and 33 more

Abstract read
In one paragraph

Article in BMJ global health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

43 authors.

Cristina Ardura-GarciaCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia crisardura@gmail.com.ORCID 0000-0001-7924-518X
Jill HopkinsCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.
Sue J LeeCentre for Tropical Medicine and Global Health, University of Oxford Nuffield Department of Medicine, Oxford, UK.ORCID 0000-0002-8409-4248
Naomi WaithiraCentre for Tropical Medicine and Global Health, University of Oxford Nuffield Department of Medicine, Oxford, UK.ORCID 0000-0002-2267-9347
Chris PainterCentre for Tropical Medicine and Global Health, University of Oxford Nuffield Department of Medicine, Oxford, UK.
Clare L LingCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.
Tamalee RobertsCentre for Tropical Medicine and Global Health, University of Oxford Nuffield Department of Medicine, Oxford, UK.ORCID 0000-0001-8599-737X
Thyl MiliyaCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.
Noah Obeng-NkrumahDepartment of Microbiology, University of Ghana School of Biomedical and Allied Health Sciences, Accra, Ghana.
Japheth A OpintanDepartment of Medical Microbiology, University of Ghana Medical School, Accra, Ghana.
Emmanuel P AbbeyquayePaediatric Division, 37 Military Hospital, Accra, Ghana.
Raph L HamersCentre for Tropical Medicine and Global Health, University of Oxford Nuffield Department of Medicine, Oxford, UK.
Yulia R SaharmanDepartment of Microbiology, Faculty of Medicine Universitas Indonesia, Dr. Cipto Mangunkusumo National Hospital, Jakarta, Indonesia.
Robert SintoPT PELNI Hospital, Jakarta, Jakarta, Indonesia.
Mulya R KaryantiDepartment of Child Health, Faculty of Medicine Universitas Indonesia, Dr. Cipto Mangunkusumo National Hospital, Jakarta, Indonesia.
R Fera IbrahimDepartment of Microbiology, Faculty of Medicine Universitas Indonesia, Dr. Cipto Mangunkusumo National Hospital, Jakarta, Indonesia.
Samuel O AkechKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Anousone DuangnouvongMicrobiology Laboratory, Mahosot Hospital, Lao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Vientiane, Lao People's Democratic Republic.
Khamla ChoumlivongSetthathirath Hospital, Vientiane, Lao People's Democratic Republic.
Nicholas A FeaseyMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Blantyre, Malawi.
Diana KululangaMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Blantyre, Malawi.
Samantha LissauerMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Blantyre, Malawi.
Abhilasha KarkeyOxford University Clinical Research Unit Nepal, Lalitpur, Nepal.
Narayan KunwarOxford University Clinical Research Unit Nepal, Lalitpur, Nepal.
Justice E ErakhaiwuDepartment of Medical Microbiology and Parasitology, University of Ibadan College of Medicine, Ibadan, Nigeria.
Iruka N OkekeDepartment of Pharmaceutical Microbiology, Faculty of Pharmacy / Department of Medical Microbiology and Parasitology, University of Ibadan College of Medicine, Ibadan, Nigeria.ORCID 0000-0002-1694-7587
Ini AdebiyiDepartment of Medical Microbiology and Parasitology, University College Hospital Ibadan, Ibadan, Nigeria.
Abiodun B OduolaDepartment of Medical Microbiology and Parasitology, University College Hospital Ibadan, Ibadan, Nigeria.
Babatunde O OgunbosiUniversity College Hospital Ibadan, Ibadan, Nigeria.
Olukemi O TongoDepartment of Padiatrics, University of Ibadan College of Medicine, Ibadan, Nigeria.
Ifeoma A UdePaediatric Infectious Diseases Unit, University College Hospital Ibadan, Ibadan, Nigeria.
Oladipo AboderinObafemi Awolowo University College of Health Sciences, Ile-Ife, Nigeria.
Adeyemi T AdeyemoObafemi Awolowo University College of Health Sciences, Ile-Ife, Nigeria.
Sylvester S EdwardObafemi Awolowo University College of Health Sciences, Ile-Ife, Nigeria.
Ugowe OsagieObafemi Awolowo University Teaching Hospital Complex, Ile-Ife, Nigeria.
Hoa Nguyen ThiOxford University Clinical Research Unit, Hanoi, Viet Nam.
Pham Ngoc ThachNational Hospital of Tropical Diseases, Hanoi, Viet Nam.
Tran Van GiangNational Hospital of Tropical Diseases, Hanoi, Viet Nam.
Lan Huong Hoang ThiHue Central Hospital, Hue, Viet Nam.
Huu Tung TrinhChildren's Hospital 2, Ho Chi Minh City, Viet Nam.
H Rogier van DoornCentre for Tropical Medicine and Global Health, University of Oxford Nuffield Department of Medicine, Oxford, UK.
Elizabeth A AshleyCentre for Tropical Medicine and Global Health, University of Oxford Nuffield Department of Medicine, Oxford, UK.
Paul TurnerCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.ORCID 0000-0002-1013-7815

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundBlood culture (BC) in children has relatively low diagnostic yield and high contamination rates, limiting cost-effectiveness. We aimed to determine readily available baseline characteristics to identify hospitalised children with a likelihood of higher diagnostic yield in low- and middle-income countries.

methodsWe used data from ACORN2, a prospective clinical surveillance network including 19 hospitals across Africa and Asia. We included participants <18 years, hospitalised for a suspected infection, prescribed parenteral antibiotics and with a BC sample. Sociodemographic and clinical data were recorded for each infection episode and linked to routine microbiology data. We described true pathogen (non-contaminant) BC positivity proportion and performed mixed-effects logistic regression, with study site and patient as the random effect, to identify factors associated with BC positivity.

resultsOf the 26 407 paediatric infection episodes, 17 815 (67%) had a BC sample and 15 384 were included in the analysis. BC results were: true pathogens in 689 (4.5%), contaminants in 1399 (9%) and uncertain pathogens in 143 (0.9%). In the multivariable model, factors associated with a positive BC were age (29 days-12-month-olds OR 1.33, 95% CI 1.06 to 1.66 and 5-18 year-olds OR 1.62, 95% CI 1.30 to 2.01 vs 1-4 year-olds), number of clinical severity signs (OR 1.29, 95% CI 1.18 to 1.40 per one sign) and hospital acquired infection (OR 3.05, 95% CI 2.30 to 4.06 vs community-acquired). Suspected diagnosis of sepsis (OR 2.09, 95% CI 1.67 to 2.61), gastrointestinal/abdominal (OR 2.36, 95% CI 1.78 to 3.13), skin and soft tissue or bone (OR 3.64, 95% CI 2.57 to 5.14) and genitourinary infection (OR 2.22, 95% CI 1.39 to 3.56) were more likely to have a positive BC, compared with respiratory infections.

conclusionWe confirmed the low BC yield among hospitalised children. We identified groups for which diagnostic stewardship efforts to increase BC uptake should be prioritised and others in which it could be limited in times of financial or logistic constraints.

Indexed as

Blood CultureAdolescentAfricaAsiaChildChild, PreschoolFemaleHumansInfantInfant, NewbornMaleProspective StudiesRisk FactorsAfrica South of the SaharaBlood disordersGlobal HealthOther diagnostic or toolPaediatrics

Identifiers

PMID41120197
PMCPMC12542579

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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.