Evidence map›Paper›PMID 42062936›Full record

ArticleBMC infectious diseases2026

Diagnostic performance of the Sepsis qPCR MX-30

Fatma Burçin Kurtipek, Ayça Koca Yozgat, Elif Gökçek, Dilek Kaçar, Bedia Dinç, Neşe Yaralı

Abstract readComparative Study
In one paragraph

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

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Fatma Burçin KurtipekAnkara Bilkent City Hospital, Ankara Health Sciences University, Division of Paediatric Hematology and Oncology, Ankara, Turkey. burcindogan86@gmail.com.ORCID http://orcid.org/0000-0001-9382-3927
Ayça Koca YozgatAnkara Bilkent City Hospital, Ankara Health Sciences University, Division of Paediatric Hematology and Oncology, Ankara, Turkey.
Elif GökçekAnkara Bilkent City Hospital, Division of Pediatric, Ankara, Turkey.
Dilek KaçarAnkara Bilkent City Hospital, Ankara Health Sciences University, Division of Paediatric Hematology and Oncology, Ankara, Turkey.
Bedia DinçAnkara Bilkent City Hospital, Division of Medical Microbiology, Ankara, Turkey.
Neşe YaralıAnkara Bilkent City Hospital, Ankara Health Sciences University, Division of Paediatric Hematology and Oncology, Ankara, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFebrile neutropenia (FN) is a frequent and potentially life-threatening complication in patients with hematologic malignancies. Prompt and accurate identification of bloodstream pathogens is essential to optimize antimicrobial therapy and improve outcomes. Although conventional blood culture (BC) remains the diagnostic gold standard, its limitations have led to increased interest in rapid molecular diagnostics such as real-time polymerase chain reaction (RT-qPCR).

objectiveThis study aimed to evaluate the diagnostic performance of the Sepsis qPCR MX-30

methodsA retrospective analysis was conducted on 251 febrile neutropenia episodes in 80 children with hematologic disorders between February 2023 and November 2024. Blood samples for both BC and the Sepsis qPCR MX-30

resultsOf the 251 episodes, the qPCR panel detected pathogens in 54 episodes (21.5%), while BC confirmed infection in 45 episodes (17.9%). Overall accuracy was 68.5% (172/251 episodes with agreement on presence or absence of infection). Among the 10 episodes positive by both methods, pathogen-level concordance (same organism detected) was observed in 7 episodes (70%). The calculated sensitivity, specificity, PPV, and NPV of the qPCR panel were 22.2%, 78.6%, 18.5%, and 82.2%, respectively. Discordant results were frequent: 44 qPCR-positive cases were BC-negative, and 35 BC-positive cases were not detected by qPCR.Notably, the panel enabled early detection of several antimicrobial resistance genes and fungal pathogens not identified by culture.

conclusionThe Sepsis qPCR MX-30 CLINICAL TRIAL: Not applicable.

Indexed as

Blood CultureFebrile NeutropeniaMolecular Diagnostic TechniquesReal-Time Polymerase Chain ReactionSepsisAdolescentChildChild, PreschoolFemaleHumansImmunocompromised HostInfantMalePredictive Value of TestsRetrospective StudiesSensitivity and SpecificityBlood cultureBloodstream infectionFebrile neutropeniaMolecular diagnosticsPediatric hematologyqPCRSepsis

Identifiers

PMID42062936
PMCPMC13289128

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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.