Diagnostic performance of the QIAstat-Dx gastrointestinal panel compared with conventional methods in pediatric gastroenteritis

ABSTRACT Pediatric gastroenteritis remains a significant public health issue, underscoring the need for better laboratory diagnostic methods. Traditional diagnostic techniques, such as stool culture and ova and parasite (O&P) examination, are limited by long turnaround times and low detection rates. This study assessed the diagnostic capabilities of the QIAstat-Dx Gastrointestinal Panel (QGP), a multiplex PCR test, against conventional stool culture and O&P examination in 4,801 clinical stool samples from pediatric patients at Sidra Medicine. The study involved stool specimens collected from patients aged ≤18 years who were being tested for gastroenteritis using one or more of the following methods: QGP, stool culture, and O&P examination. QGP demonstrated a higher pathogen detection rate (42.3%; 2,033/4,801) than stool culture (12.6%; 255/2,018) and O&P examination (6.3%; 63/986). A total of 2,814 pathogens were identified in the 2,033 QGP-positive samples, with EPEC being the most prevalent pathogen found in 631 samples (13.1%). QGP showed high concordance with conventional methods, with >98% negative percent agreement (NPA) for all targets and 100% positive percent agreement (PPA) for all targets, except Salmonella spp. (84.4% PPA). The lower PPA for Salmonella spp. was attributed to isolates detected only by culture after enrichment with Selenite F broth. QGP had a shorter median turnaround time from sample collection to final results (2.8 h) than stool culture (67.6 h) and O&P examination (38.8 h). QGP is a valuable diagnostic tool due to improved detection rate, ability to detect co-infection, and quicker turnaround time, providing a more efficient and comprehensive approach in pediatric gastroenteritis diagnosis. IMPORTANCE This study highlights the benefits of using multiplex PCR panels, such as the QIAstat-Dx Gastrointestinal Panel (QGP), which provides results for 23 pathogens simultaneously within 80 min. This extensive retrospective study evaluated the performance of QGP in 4,801 stool samples collected in a pediatric tertiary care center in Qatar. The QGP showed superior diagnostic performance compared with traditional methods, including enhanced pathogen detection and faster results, helping clinicians optimize the treatment of children with gastroenteritis.

Institutions

Publication Details

Journal
Microbiology Spectrum
Published
2026-05-19
DOI
https://doi.org/10.1128/spectrum.00055-26
Primary Topic
Viral gastroenteritis research and epidemiology
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Diagnostic performance of the QIAstat-Dx gastrointestinal panel compared with conventional methods in pediatric gastroenteritis

Microbiology Spectrum
Viral gastroenteritis research and epidemiology
article

Diagnostic performance of the QIAstat-Dx gastrointestinal panel compared with conventional methods in pediatric gastroenteritis

article en

Abstract

ABSTRACT Pediatric gastroenteritis remains a significant public health issue, underscoring the need for better laboratory diagnostic methods. Traditional diagnostic techniques, such as stool culture and ova and parasite (O&P) examination, are limited by long turnaround times and low detection rates. This study assessed the diagnostic capabilities of the QIAstat-Dx Gastrointestinal Panel (QGP), a multiplex PCR test, against conventional stool culture and O&P examination in 4,801 clinical stool samples from pediatric patients at Sidra Medicine. The study involved stool specimens collected from patients aged ≤18 years who were being tested for gastroenteritis using one or more of the following methods: QGP, stool culture, and O&P examination. QGP demonstrated a higher pathogen detection rate (42.3%; 2,033/4,801) than stool culture (12.6%; 255/2,018) and O&P examination (6.3%; 63/986). A total of 2,814 pathogens were identified in the 2,033 QGP-positive samples, with EPEC being the most prevalent pathogen found in 631 samples (13.1%). QGP showed high concordance with conventional methods, with >98% negative percent agreement (NPA) for all targets and 100% positive percent agreement (PPA) for all targets, except Salmonella spp. (84.4% PPA). The lower PPA for Salmonella spp. was attributed to isolates detected only by culture after enrichment with Selenite F broth. QGP had a shorter median turnaround time from sample collection to final results (2.8 h) than stool culture (67.6 h) and O&P examination (38.8 h). QGP is a valuable diagnostic tool due to improved detection rate, ability to detect co-infection, and quicker turnaround time, providing a more efficient and comprehensive approach in pediatric gastroenteritis diagnosis. IMPORTANCE This study highlights the benefits of using multiplex PCR panels, such as the QIAstat-Dx Gastrointestinal Panel (QGP), which provides results for 23 pathogens simultaneously within 80 min. This extensive retrospective study evaluated the performance of QGP in 4,801 stool samples collected in a pediatric tertiary care center in Qatar. The QGP showed superior diagnostic performance compared with traditional methods, including enhanced pathogen detection and faster results, helping clinicians optimize the treatment of children with gastroenteritis.

Microbiology Spectrum
Sidra Medical and Research Center (QA), Weill Cornell Medical College in Qatar (QA), Qatar University (QA)
Good health and well-being
Openalex Percentile: Top 5%
Viral gastroenteritis research and epidemiology
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.