Davies, Hannah G., Kyohere, Mary, Tusubira, Valerie, Amone, Alexander, Wamawobe, Amusa, Komugisha, Cleophas, Musoke, Philippa, Hookham, Lauren, Ravji, Pooja, Etti, Melanie, Nsimire Sendagala, Juliet, Shelley, Dan R., Farley, Caitlin, Voysey, Merryn, Spiller, Owen B. ![]() ![]() |
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Abstract
Background Epidemiological evidence about the etiology and antimicrobial resistance of neonatal infections remains limited in low-resource settings. We aimed to describe the etiology of neonatal infections in a prospective observational cohort study conducted at two hospital sites in Kampala, Uganda. Methods Babies admitted to either unit with risk factors or signs of sepsis, pneumonia, or meningitis had a blood culture, nasopharyngeal swab, and lumbar puncture (if indicated) collected. Basic demographics were collected, and babies were followed up until discharge or death to determine admission outcome. Blood cultures were processed using the BACTEC system and identification confirmed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Cerebrospinal fluid was processed using standard microbiological testing and swabs were processed using the multiplex real-time polymerase chain reaction assay. Antimicrobial susceptibilities of bacterial isolates to World Health Organization–recommended first-line antibiotics (ampicillin or benzylpenicillin and gentamicin) were assessed using e-tests. Results A total of 7323 infants with signs or risk factors for sepsis had blood cultures, 2563 had nasopharyngeal swabs, and 23 had lumbar punctures collected. Eleven percent of blood cultures and 8.6% of swabs were positive. Inpatient mortality was 12.1%, with 27.7% case fatality observed among infants with Gram-negative bloodstream infections. Escherichia coli (14.8%), Acinetobacter spp. (10.3%), and Klebsiella spp. (7.6%), were notable contributors to Gram-negative sepsis, whereas Group B Streptococcus was the predominant Gram-positive pathogen identified (13.5%). Almost 60% of Gram-negative pathogens were ampicillin- and gentamicin-resistant.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Schools > Medicine |
Publisher: | Oxford University Press |
ISSN: | 2328-8957 |
Funders: | Bill & Melinda Gates Foundation |
Date of First Compliant Deposit: | 17 March 2025 |
Date of Acceptance: | 30 January 2025 |
Last Modified: | 18 Mar 2025 10:47 |
URI: | https://orca.cardiff.ac.uk/id/eprint/176923 |
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