Evidence map›Paper›PMID 41648042›Full record

ArticleThe Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale2026

Assessing Nanopore Targeted Sequencing for the Diagnosis of Pulmonary Infections: A Comparative Multidisease Approach.

Ying Zhao, Guannan Ma, Tianxiao Ma, Yongshuai Miao, Heya Na, Yuhui Liu, Xiaohua Li

Abstract read
In one paragraph

Article in The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Assessing Nanopore Targeted Sequencing for the Diagnosis of Pulmonary Infections: A Comparative Multidisease Approach.The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Ying ZhaoAffiliated Chifeng Clinical Medical College of Inner Mongolia Medical University, Chifeng, China.ORCID https://orcid.org/0009-0005-5088-542X
Guannan MaMedical Research Center, Zhejiang Key Laboratory of Digital Technology in Medical Diagnostics, Hangzhou, China.ORCID https://orcid.org/0000-0002-4108-5296
Tianxiao MaAffiliated Chifeng Clinical Medical College of Inner Mongolia Medical University, Chifeng, China.ORCID https://orcid.org/0009-0008-2481-3264
Yongshuai MiaoAffiliated Chifeng Clinical Medical College of Inner Mongolia Medical University, Chifeng, China.ORCID https://orcid.org/0009-0009-6200-2857
Heya NaAffiliated Chifeng Clinical Medical College of Inner Mongolia Medical University, Chifeng, China.ORCID https://orcid.org/0009-0009-8337-1096
Yuhui LiuAffiliated Chifeng Clinical Medical College of Inner Mongolia Medical University, Chifeng, China.ORCID https://orcid.org/0009-0003-0534-8612
Xiaohua LiAffiliated Chifeng Clinical Medical College of Inner Mongolia Medical University, Chifeng, China.ORCID https://orcid.org/0009-0009-7561-3534

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary infections remain a significant global health burden, particularly in immunocompromised individuals and patients with chronic respiratory or systemic diseases. Conventional microbiological tests (CMTs), though widely used, often have limited sensitivity and delayed results, especially in polymicrobial or atypical infections. This study evaluated the diagnostic performance of nanopore targeted sequencing (NTS) in 284 patients with suspected lower respiratory tract infections at Chifeng Municipal Hospital, using CMTs and clinical diagnosis as references. NTS demonstrated markedly higher sensitivity (91.85%) compared to CMTs (74.81%), with substantial improvements in detecting fungal (81.7%) and mixed infections (99.65%). A total of 259 pathogens were detected. Among them, bacteria were the most frequently identified pathogens (69.5%), followed by fungi (15.44%) and viruses (14.28%). Pathogen distribution varied by clinical subgroup, such as community-acquired pneumonia and chronic obstructive pulmonary disease, reflecting infection heterogeneity. Patients with hypertension (HBP) showed a higher incidence of fungal and mixed infections than non-HBP patients. NTS was particularly effective in detecting opportunistic pathogens in the HBP group, suggesting an association between cardiovascular comorbidity and altered pathogen susceptibility.

Indexed as

chronic obstructive pulmonary disease (COPD)conventional microbiological tests (CMTs)hypertension (HBP)nanopore targeted sequencing (NTS)pathogen detectionpulmonary infection

Identifiers

PMID41648042
PMCPMC12868382

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Registered trials

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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.