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Fecal specimens from hospitalized patients (n = 230) suspected of having CDI were tested by both assays.
In this study, a panel of 22 fecal specimens was used to assess the reactivity of the system.
Twenty two fecal specimens from acute gastroenteritis were used in this study with approval of the FDA RIHSC.
The laboratory diagnosis of Clostridium difficile-associated disease (CDAD) is based on culture and toxin detection in fecal specimens.
Fecal specimens were evaluated with Lugol's stain and trichrome staining [35].
A series of 700 fecal specimens were prospectively collected to investigate the prevalence of M. smithii and M. stadtmanae.
Serum and fecal specimens were collected weekly after inoculation.
Fecal specimens were processed according to the WHO protocol (4 ).
SaV was detected in 19 (4%) of 477 fecal specimens.
Fecal specimens were also assayed for HEV RNA.
No pathogens were detected in fecal specimens from 292 children.
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