Evidence map›Paper›PMID 42227749›Full record

Observational studyClinical infectious diseases : an official publication of the Infectious Diseases Society of America2026

Mortality and Length of Stay Associated With Community-Acquired Escherichia coli and Staphylococcus aureus Bloodstream Infections: An Observational Study in 9 Low- and Middle-Income Countries.

Jill Hopkins, Olga Tosas-Auguet, Naomi Waithira, Chris Painter, Clare L Ling, Tamalee Roberts, Thyl Miliya, Noah Obeng-Nkrumah, Japheth A Opintan, Emmanuel P Abbeyquaye and 37 more

Abstract readObservational Study
In one paragraph

Observational study in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2026. 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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

47 authors.

Jill HopkinsCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.ORCID 0000-0003-1989-8618
Olga Tosas-AuguetAntimicrobial Resistance Department, World Health Organization, Geneva, Switzerland.
Naomi WaithiraCentre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Chris PainterCentre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-7970-039X
Clare L LingCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.ORCID 0000-0002-5188-0349
Tamalee RobertsCentre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-8599-737X
Thyl MiliyaCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.
Noah Obeng-NkrumahDepartment of Microbiology, School of Biomedical and Allied Health Sciences, University of Ghana, Accra, Ghana.ORCID 0000-0002-1797-822X
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, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Yulia Rosa SaharmanDepartment of Microbiology, Faculty of Medicine Universitas Indonesia, Dr. Cipto Mangunkusumo National Hospital, Jakarta, Indonesia.
Robert SintoDepartment of Internal Medicine, Pelni Hospital, Jakarta, Indonesia.
Mulya Rahma 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 AkechHealth Services Unit, KEMRI Wellcome Trust Research Programme, Kilifi, Kenya.
Elizabeth A AshleyCentre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-7620-4822
Anousone DouangnouvongLao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Microbiology Laboratory, Mahosot Hospital, Vientiane, Lao PDR.
Khamla ChoumlivongSetthathirath Hospital, Vientiane, Lao PDR.
Nicholas A FeaseyMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Blantyre, Malawi.ORCID 0000-0003-4041-1405
Diana KululangaMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Blantyre, Malawi.ORCID 0009-0007-9869-4280
Samantha LissauerMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Blantyre, Malawi.
Abhilasha KarkeyOxford University Clinical Research Unit Nepal, Lalitpur, Nepal.ORCID 0000-0002-5179-650X
Narayan KunwarOxford University Clinical Research Unit Nepal, Lalitpur, Nepal.ORCID 0000-0002-9927-8808
Justice Enosetale ErakhaiwuDepartment of Medical Microbiology and Parasitology, College of Medicine, University of Ibadan, Ibadan, Nigeria.
Iruka N OkekeDepartment of Pharmaceutical Microbiology, Faculty of Pharmacy and Department of Medical Microbiology and Parasitology, College of Medicine, University of Ibadan, Ibadan, Nigeria.ORCID 0000-0002-1694-7587
Ini AdebiyiDepartment of Medical Microbiology and Parasitology, University College Hospital, Ibadan, Nigeria.
Olukemi A AdekanmbiDepartment of Medicine, College of Medicine, University of Ibadan, University College Hospital, Ibadan, Nigeria.ORCID 0000-0002-0290-9563
Abiodun B OduolaDepartment of Medical Microbiology and Parasitology, University College Hospital, Ibadan, Nigeria.ORCID 0009-0006-1583-2039
Babatunde O OgunbosiDepartment of Paediatrics, University College Hospital, Ibadan, Nigeria.
Kehinde A OjifinniDepartment of Emergency Medicine, University College Hospital, Ibadan, Nigeria.ORCID 0000-0002-2252-867X
Olukemi O TongoDepartment of Paediatrics, College of Medicine, University of Ibadan, Ibadan, Nigeria.
Ifeoma A UdePaediatric Infectious Diseases Unit, University College Hospital, Ibadan, Nigeria.
Aaron O AboderinCollege of Health Sciences, Obafemi Awolowo University, Ile-Ife, Nigeria.ORCID 0000-0002-4280-2218
Olusegun AdekanleCollege of Health Sciences, Obafemi Awolowo University, Ile-Ife, Nigeria.
Adeyemi T AdeyemoCollege of Health Sciences, Obafemi Awolowo University, Ile-Ife, Nigeria.ORCID 0000-0003-3544-2530
Sylvester S EdwardCollege of Health Sciences, Obafemi Awolowo University, Ile-Ife, Nigeria.
Ugowe OsagieDepartment of Paediatrics, Obafemi Awolowo University Teaching Hospitals Complex, Ile-Ife, Nigeria.ORCID 0000-0002-8931-0085
Hoa Thi NguyenOxford University Clinical Research Unit Hanoi, Hanoi, Vietnam.
Thach Ngoc PhamInstitute for Training and Research in Tropical Diseases, National Hospital of Tropical Diseases, Hanoi, Vietnam.
Giang Van TranInstitute for Training and Research in Tropical Diseases, National Hospital of Tropical Diseases, Hanoi, Vietnam.
Hương Thị Lan HoàngHue Central Hospital, Hue, Vietnam.
Tùng Hữu TrịnhChildren's Hospital 2, Ho Chi Minh City, Vietnam.
H Rogier van DoornCentre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-9807-1821
Paul TurnerCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.ORCID 0000-0002-1013-7815
Sue J LeeCentre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
ACORN Investigators

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundAntimicrobial resistance disproportionally affects low- and middle-income countries. We calculated the burden of resistant and susceptible Escherichia coli and Staphylococcus aureus bloodstream infections (BSIs) in ACORN2, a prospective clinical surveillance study in adults and children.

methodsPatients with culture-confirmed community-acquired susceptible and resistant E. coli (third-generation cephalosporin susceptible [3GC-S] and resistant [3GC-R]) and S. aureus (methicillin-resistant [MRSA] and methicillin-susceptible [MSSA]) BSIs were compared against blood culture-negative patients (controls). Cause-specific hazard ratios (HRs) were calculated for competing events of in-hospital mortality and discharge alive. Length of hospital stay (LOS) was calculated.

resultsFrom 22 802 blood cultures taken, there were 329 E. coli (177 [53.8%] 3GC-R) and 363 S. aureus (132 [36.4%] MRSA) BSIs. In-hospital mortality was 8.4% for controls, 20.1% for E. coli (20.3% 3GC-R; 19.7% 3GC-S), and 13.1% for S. aureus (12.2% MRSA; 13.7% MSSA). 3GC-S but not 3GC-R E. coli BSI cases had higher adjusted hazard of death than controls (HRs, 1.73 [95% confidence interval {CI}, 1.20-2.49] and 1.38 [95% CI, .99-1.94]); risk of dying was the same for 3GC-S compared with 3GC-R infections (P = .882). Neither MSSA nor MRSA BSI patients were more likely to die than controls (HRs, 1.33 [95% CI, .91-1.93] and 1.00 [95% CI, .61-1.66]) nor MSSA versus MRSA (P = .891). The hazard of discharge alive for both resistant and susceptible S. aureus and E. coli decreased significantly when compared with controls. LOS was 2 (95% CI, 0-3) days and 1 (95% CI, -1 to 3) day longer for resistant compared with susceptible infections, for E. coli and S. aureus.

conclusionsAntimicrobial-resistant infections were not associated with increased mortality in ACORN2. Drug-resistant BSI had longer LOS compared with susceptible infections, but CIs encompassed 0 days.

Indexed as

BacteremiaCommunity-Acquired InfectionsEscherichia coli InfectionsLength of StayStaphylococcal InfectionsAdolescentAdultAgedAged, 80 and overAnti-Bacterial AgentsChildChild, PreschoolDeveloping CountriesDrug Resistance, BacterialEscherichia coliFemaleAnti-Bacterial Agentsantimicrobial resistanceattributable mortalitybloodstream infectionLMICsurveillance

Identifiers

PMID42227749
PMCPMC13537153

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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.