Evidence map›Paper›PMID 42369922›Full record

ArticlePakistan journal of medical sciences2026

Early targeted next-generation sequencing accelerates clinical recovery in children with community-acquired pneumonia: A retrospective study.

Di Lian, Dong Wang, Chenye Lin, QiuYu Tang

Abstract read
In one paragraph

Article in Pakistan journal of medical sciences, 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

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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

4 authors.

Di LianDi Lian, MMed, College of Clinical Medicine for Obstetrics and Gynecology and Pediatrics, Fujian Medical University, China.
Dong WangDong Wang, MMed, Fujian Children's Hospital, (Fujian Branch of Shanghai Children's Medical Center), Fuzhou, Fujian 350014, China.
Chenye LinChenye Lin, MMed, Fujian Children's Hospital, (Fujian Branch of Shanghai Children's Medical Center), Fuzhou, Fujian 350014, China.
QiuYu TangQiuYu Tang, MMed, College of Clinical Medicine for Obstetrics and Gynecology and Pediatrics, Fujian Medical University, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & Objective: The clinical impact of testing timing for targeted next-generation sequencing (tNGS) in pediatric community-acquired pneumonia (CAP) is poorly understood. We hypothesized that early tNGS implementation accelerates clinical recovery and evaluated its comprehensive value. Methodology: In a retrospective study at Fujian Children's Hospital (2021-2023), 199 hospitalized children with CAP (BALF tested) were analyzed. Patients were grouped by tNGS vs. conventional testing (CT), with the tNGS group stratified into early (≤48h) and late (>48h) testing. We compared diagnostic yield, clinical outcomes, therapeutic adjustments, and costs. Results: tNGS demonstrated significantly higher sensitivity than CT for both bacteria (86.0% vs. 19.0%, P<0.001) and viruses (88.1% vs. 26.2%, P<0.001), and excelled at identifying mixed infections (55.8%). Critically, the early-testing group showed significantly shorter times to cough improvement (median 6.0 vs. 9.0 days, P=0.002) and rale resolution (median 7.0 vs. 8.0 days, P=0.027) compared to the late-testing group. This was associated with more timely therapeutic adjustments (P<0.05). A non-significant trend toward lower costs and shorter hospital stays was also observed. Conclusion: Early tNGS implementation in pediatric CAP not only enhances diagnostic yield but, more importantly, accelerates clinical recovery by facilitating timely, targeted therapeutic interventions. These findings provide strong evidence for integrating early tNGS into clinical workflows, marking a shift from simple pathogen identification to an outcome-driven diagnostic strategy.

Indexed as

ChildrenClinical outcomeCommunity-acquired pneumoniaDiagnostic valueEconomic valueTargeted next-generation sequencing (tNGS)

Identifiers

PMID42369922
PMCPMC13309825

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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.