Evidence map›Paper›PMID 40778290›Full record

ArticleFrontiers in cellular and infection microbiology2025

Comparative performance evaluation of FilmArray RP 2.1 and targeted next-generation sequencing in upper respiratory tract infections.

Wenxiang Jin, Zehan Dai, Pengyuan Zhu, Oliver Ma, Jiahao Li, Ava Kong, Junbin Wu, Feifei Liu, Miaozhi Li, Zixin Du and 6 more

Abstract readComparative StudyEvaluation Study
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Observational
  2. Article
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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

16 authors.

Wenxiang JinDepartment of Laboratory Diagnosis, KingMed Diagnostics, Guangzhou, Guangdong, China.
Zehan DaiResearch and Development Department, Guangzhou KingCreate Biotechnology Co., Ltd, Guangzhou, China.
Pengyuan ZhuResearch and Development Department, Guangzhou KingCreate Biotechnology Co., Ltd, Guangzhou, China.
Oliver MaKingMed Diagnostics, Hong Kong, Hong Kong SAR, China.
Jiahao LiDepartment of Laboratory Diagnosis, KingMed Diagnostics, Guangzhou, Guangdong, China.
Ava KongKingMed Diagnostics, Hong Kong, Hong Kong SAR, China.
Junbin WuDepartment of Laboratory Diagnosis, KingMed Diagnostics, Guangzhou, Guangdong, China.
Feifei LiuDepartment of Laboratory Diagnosis, KingMed Diagnostics, Guangzhou, Guangdong, China.
Miaozhi LiDepartment of Laboratory Diagnosis, KingMed Diagnostics, Guangzhou, Guangdong, China.
Zixin DuDepartment of Laboratory Diagnosis, KingMed Diagnostics, Guangzhou, Guangdong, China.
Dan XueDepartment of Laboratory Diagnosis, KingMed Diagnostics, Guangzhou, Guangdong, China.
Ganqiang YangKingMed Diagnostics, Hong Kong, Hong Kong SAR, China.
Nafen YeDepartment of Laboratory Diagnosis, KingMed Diagnostics, Guangzhou, Guangdong, China.
Chunleung LoKingMed Diagnostics, Hong Kong, Hong Kong SAR, China.
Chaohui HuResearch and Development Department, Guangzhou KingCreate Biotechnology Co., Ltd, Guangzhou, China.
Lei ZhangDepartment of Laboratory Diagnosis, KingMed Diagnostics, Guangzhou, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Upper respiratory tract infections (URTIs) represent a significant global health burden, impacting patient morbidity and quality of life. The implementation of accurate pathogen detection methods is crucial for precise diagnosis and effective clinical management of URTIs. This study evaluates the clinical performance of targeted next-generation sequencing (tNGS) as a diagnostic tool for comprehensive identification of URTI-associated pathogens. Methods: A total of 190 nasopharyngeal swab specimens from patients were enrolled for the study. These specimens underwent pathogen identification using both tNGS and the FilmArray respiratory panel. The results obtained from these two methods were then compared. Results: Overall, tNGS identified 164 positive samples, compared to 91 positives identified by FilmArray. Regarding the shared target species or subtypes, tNGS identified 97 positive samples, whereas the FilmArray respiratory panel detected 88 positives out of 190 specimens. tNGS identified a diverse array of 34 different pathogens, significantly surpassing the 12 pathogens identified by the FilmArray panel. The detection rates for tNGS and FilmArray were 51.05% (97/190) and 46.32% (88/190), respectively. Statistical analysis revealed no significant difference in the detection rates of 10 specific respiratory pathogens (with ≥3 positives). Furthermore, the overall pathogen detection accuracy of tNGS was determined to be 90.16% (95% Conclusions: The tNGS method demonstrates broader pathogen detection capability compared to the FilmArray, achieving a higher positive detection rate in upper respiratory tract infections. It demonstrates high accuracy and sensitivity, offering a viable and rapid diagnostic approach for upper respiratory tract infections.

Indexed as

High-Throughput Nucleotide SequencingMultiplex Polymerase Chain ReactionNasopharyngeal DiseasesRespiratory Tract InfectionsHumansRetrospective StudiesFilmArray RP 2.1 panelmultiplex PCRpathogen identificationtargeted next-generation sequencingupper respiratory tract infections

Identifiers

PMID40778290
PMCPMC12329660

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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.