2013
DOI: 10.1017/s0950268813002367
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The increasing application of multiplex nucleic acid detection tests to the diagnosis of syndromic infections

Abstract: On 14 January 2013, the US Food and Drug Administration (FDA) announced permission for a multiplex nucleic acid test, the xTAG® Gastrointestinal Pathogen Panel (GPP) (Luminex Corporation, USA), which simultaneously detects 11 common viral, bacterial and parasitic causes of infectious gastroenteritis, to be marketed in the USA. This announcement reflects the current move towards the development and commercialization of detection technologies based on nucleic acid amplification techniques for diagnosis of syndro… Show more

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Cited by 69 publications
(53 citation statements)
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“…Specimens collected for culture-independent testing may, in some cases, be incompatible with culture because of the collection methods or media that are used for collection. And, a strict reliance on culture-independent diagnostics would limit our ability to detect new causes of diarrheal disease ( 26,(48)(49)(50)(51). Th e future may hold a therapies, and avoidance of antibiotics for viral pathogens or more specifi c anti-microbials for parasitic protozoan etiologies.…”
Section: Diagnosismentioning
confidence: 99%
“…Specimens collected for culture-independent testing may, in some cases, be incompatible with culture because of the collection methods or media that are used for collection. And, a strict reliance on culture-independent diagnostics would limit our ability to detect new causes of diarrheal disease ( 26,(48)(49)(50)(51). Th e future may hold a therapies, and avoidance of antibiotics for viral pathogens or more specifi c anti-microbials for parasitic protozoan etiologies.…”
Section: Diagnosismentioning
confidence: 99%
“…It is anticipated that multiplex testing will increase diagnostic positivity, identify co-infections, faster turnaround time and may reduce the use of antibiotics. There are multiplex RT-PCR based laboratory developed test (LDT) and commercial assays (mostly not FDA approved yet) available for gastrointestinal pathogen testing 25, 39 . As more multiplex testing becomes available, the value of using such a test will be assessed and recognized.…”
Section: Detection and Identification Of Gi Pathogens In A Multiplex mentioning
confidence: 99%
“…Recent studies have demonstrated the test sensitivity range to be between 90 and 100%, depending on the pathogen present, and specificity range between 91 and 99% [27], [28]. The main advantages of this test are the high sample throughput that can be achieved; the number of different analytes detected by the test; and also the ability to determine co-infection in patients [29], [30], [31]. However, a disadvantage of the test is it is not an integrated platform.…”
Section: End Point Pcr – Array Technologiesmentioning
confidence: 99%