Evidence map›Paper›PMID 41578211›Full record

ArticleBMC infectious diseases2026

Bacteriological profile of early versus late-onset neonatal sepsis at tertiary care hospital in Nepal.

Rabita Karanjit, Sangita Sharma, Shyam Kumar Mishra, Hari Prasad Kattel, Sagun Suwal, Sujata Baidya, Sunita Makaju, Sajal Twanabasu

Abstract read
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Article in BMC infectious diseases, 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Rabita KaranjitDepartment of Laboratory Medicine, Dhading Hospital, Dhadingbesi, Nepal.
Sangita SharmaDepartment of Microbiology, Maharajgunj Medical Campus, Tribhuvan University Teaching Hospital, Institute of Medicine, Maharajgunj, Kathmandu, Nepal. drsangita_sharma@iom.edu.np.ORCID http://orcid.org/0009-0006-5660-7209
Shyam Kumar MishraDepartment of Microbiology, Maharajgunj Medical Campus, Tribhuvan University Teaching Hospital, Institute of Medicine, Maharajgunj, Kathmandu, Nepal.ORCID http://orcid.org/0000-0002-3888-7319
Hari Prasad KattelDepartment of Microbiology, Maharajgunj Medical Campus, Tribhuvan University Teaching Hospital, Institute of Medicine, Maharajgunj, Kathmandu, Nepal.ORCID http://orcid.org/0009-0009-5829-7840
Sagun SuwalDepartment of Laboratory Medicine, Tribhuvan University Teaching Hospital, Institute of Medicine, Maharajgunj, Kathmandu, Nepal.ORCID http://orcid.org/0009-0007-0810-8760
Sujata BaidyaDepartment of Laboratory Medicine, Tribhuvan University Teaching Hospital, Institute of Medicine, Maharajgunj, Kathmandu, Nepal.ORCID http://orcid.org/0000-0003-3180-7459
Sunita MakajuDepartment of Laboratory Medicine, Patan Academy of Health Sciences, Patan, Nepal.
Sajal TwanabasuDhading Hospital, Dhadingbesi, Nepal.ORCID http://orcid.org/0000-0002-2629-6095

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeonatal sepsis is one of the most common causes of neonatal mortality in developing countries like Nepal, ranking third after premature birth and birth asphyxia. This study intended to study the microbial etiology and antimicrobial susceptibility pattern of neonatal sepsis and its association with different birth conditions and C-reactive protein (CRP).

methodsBlood samples were collected aseptically from 120 neonates suspected of sepsis, admitted to the Neonatal Intensive Care Unit (NICU) and Neonate wards of Tribhuvan University Teaching Hospital, Kathmandu, Nepal, and processed according to the protocol of the American Society for Microbiology (ASM). For antimicrobial susceptibility testing, the standard disc diffusion technique of the Kirby-Bauer method recommended by the Clinical and Laboratory Standards Institute (CLSI) 2019 was followed. Along with blood culture, a C-reactive protein (CRP) test was also carried out from each blood sample.

resultsOut of 120 blood cultures, 36 (30.0%) yielded microbial growth, 20 (55.5%) in the early-onset neonatal sepsis, and 16 (44.5%) in the late-onset neonatal sepsis. Among 36 blood culture-positive neonatal sepsis, 25 (69.5%) were born through normal delivery, 11 (30.5%) via Cesarean section (C-section); 23 (63.9%) were pre-term delivered neonates, 13 (36.1%) were termed delivered neonates; 23 (63.9%) were low birth weight neonates and 13 (36.1%) were normal birth weight. Among 36 isolates, 15 (41.7%) were gram-positive and 21 (58.3%) were gram-negative organisms. A higher percentage of Coagulase-negative Staphylococcus (n = 5, 35.0%) was isolated in EONS, whereas Citrobacter freundii (n = 5, 31.2%) was isolated in a higher percentage in LONS. Coagulase-negative Staphylococcus (n = 11, 30.6%) were isolated in higher percentages followed by Citrobacter freundii (n = 8, 22.2%), Klebsiella pneumoniae (n = 6, 16.7%), Acinetobacter baumanii complex (n = 5, 13.9%), Staphylococcus aureus (n = 4, 11.1%), Acinetobacter lwoffii (n = 1, 2.8%), and Pseudomonas aeruginosa (n = 1, 2.8%). Seventeen organisms (47.2%) showed multi-drug resistance of which one was an extended-spectrum beta-lactamase (ESBL) producer. A total of 40 blood samples (33.3%) tested positive for CRP, of which 35 had positive blood culture results. Based on blood culture results, CRP’s sensitivity, specificity, and accuracy in this study were 97.2%, 94.0%, and 95.0% respectively which help to rule out the true infection and potential contamination of Coagulase-negative Staphylococcus in neonatal sepsis.

conclusionGram-positive bacteria stood out as the major causative agent of neonatal sepsis. MDR and ESBL were also prevalent in neonatal sepsis.

trial registrationNot applicable.

Indexed as

BacteriaNeonatal SepsisAnti-Bacterial AgentsC-Reactive ProteinFemaleHumansInfant, NewbornIntensive Care Units, NeonatalMaleMicrobial Sensitivity TestsNepalTertiary Care CentersAnti-Bacterial AgentsC-Reactive ProteinCesarean sectionC-reactive proteinGram-negative organismsGram-positive organismsMultidrug resistanceNeonatal sepsisNormal delivery

Identifiers

PMID41578211
PMCPMC12910986

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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.