Background: Clostridium difficile infection (CDI) is characterized by a relevant intestinal neutrophil infiltrate. So far, role of fecal calprotectin in CDI, has been investigated only in few studies, mainly focused on diagnosis of the disease. Aim: By a longitudinal design, we assess fecal calprotectin concentrations (FCCs) in subjects with CDI, evaluating the correlation between fecal marker and response to therapy. Methods: Clinical (diarrhea scoring) and laboratory (FCCs and leucocytes count) evaluation was performed in 56 subjects with CDI at time of diagnosis (T0) and after a week from starting of therapy (T1). Clinical response to therapy at T1was related with both T0and T1FCC values. FCCs were also related to all-cause 30-day mortality, recurrence and death, both of them within 90 days. Results: FCCs at T1were significantly increased in subjects with persistence of diarrhea in respect to the other ones (285.5â±â270 µg/g vs 150.7â±â147 µg/g, respectively; pâ
Gallo, A., Vallone, C. V., Sabatelli, L., Ventura, G., Covino, M., Cammarota, G., Gasbarrini, A., Landolfi, R., Montalto, M., Fecal calprotectin in management of Clostridium difficile infection: a longitudinal study, <<SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY>>, 2017; (N/A): 1-6. [doi:10.1080/00365521.2017.1392598] [http://hdl.handle.net/10807/112856]
Fecal calprotectin in management of Clostridium difficile infection: a longitudinal study
Gallo, Antonella;Vallone, Carla Vincenza;Ventura, Giulio;Covino, Marcello;Cammarota, Giovanni;Gasbarrini, Antonio;Landolfi, Raffaele;Montalto, Massimo
2017
Abstract
Background: Clostridium difficile infection (CDI) is characterized by a relevant intestinal neutrophil infiltrate. So far, role of fecal calprotectin in CDI, has been investigated only in few studies, mainly focused on diagnosis of the disease. Aim: By a longitudinal design, we assess fecal calprotectin concentrations (FCCs) in subjects with CDI, evaluating the correlation between fecal marker and response to therapy. Methods: Clinical (diarrhea scoring) and laboratory (FCCs and leucocytes count) evaluation was performed in 56 subjects with CDI at time of diagnosis (T0) and after a week from starting of therapy (T1). Clinical response to therapy at T1was related with both T0and T1FCC values. FCCs were also related to all-cause 30-day mortality, recurrence and death, both of them within 90 days. Results: FCCs at T1were significantly increased in subjects with persistence of diarrhea in respect to the other ones (285.5â±â270 µg/g vs 150.7â±â147 µg/g, respectively; pâI documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.