ReviewFolia microbiologica2026
The role of rapid molecular diagnostics in managing bloodstream infections: a microbiological insight.
Review in Folia microbiologica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
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.
Who cites it
1 citing paper in PubMed.
- Duplex Recombinase Polymerase Amplification-Lateral Flow Assay for Rapid Visual Detection of Critical Antibiotic Resistance Genes in Escherichia coli and Klebsiella pneumoniae From Positive Blood Cultures.Journal of clinical laboratory analysis · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Bloodstream infections (BSIs) represent a significant clinical challenge due to their high morbidity and mortality rates, compounded by the increasing prevalence of antimicrobial resistance (AMR). Even though they are regarded as the gold standard, traditional diagnostic techniques like blood cultures frequently have low sensitivity and delayed findings. Rapid molecular diagnostics (RMDs) have completely changed how BSIs are identified and treated. By using cutting-edge methods like next-generation sequencing (NGS), loop-mediated isothermal amplification (LAMP), polymerase chain reaction (PCR), and microarray-based approaches, RMDs allow for the quick, precise, and thorough identification of pathogens and resistance markers straight from blood samples. By drastically cutting down on diagnostic delays, these technologies enable early targeted therapy start, better clinical results, and less need on broad-spectrum antibiotics, which are the primary cause of AMR. Additionally, advancements like NGS improve diagnostic accuracy by offering profound insights into pathogen genomes, virulence factors, and resistance mechanisms. Barriers including high prices, integration difficulties, and the requirement for specialized knowledge prevent them from being widely adopted, despite their transformational potential. Nevertheless, these issues are being addressed by continuous developments in automation and point-of-care (POC) systems, which should make RMDs more affordable and widely available. In order to improve therapeutic accuracy, reduce AMR, and advance infection control techniques, this research emphasizes the crucial role that RMDs play in the management of BSI. In order to improve customized medicine strategies, future initiatives include streamlining diagnostic processes and combining molecular diagnostics with clinical decision support technologies.
Indexed as
Identifiers
41108514What OpenQuestion holds
Registered trials
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.