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Authors
Vicentini, Costanza
Bussolino, Roberta
Gastaldo, Claudia
Castagnotto, Marta
D’Ancona, Fortunato “Paolo”
Zotti, Carla Maria
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Bert, Fabrizio
Bolla, Cesare
Broda, Roberta
D’Aloia, Francesco
De Gregorio, Francesco
Di Nardo, Francesco
Fenu, Piero
Ferrauto, Gerolamo
Franco, Mauro
Gatti, Scipione
Gremo, Franca
Maiello, Agostino
Morabito, Domenica
Muca, Aida
Palladino, Roberta
Paudice, Alessandro
Pellegrino, Paolo
Plazzotta, Claudio
Porretto, Simone
Ripamonti, Giorgio
Salvatico, Maurizio
Silvaplana, Paola
Silvestre, Carlo
Tangolo, Domenico
Venturino, Valentina
Viroletti, Maria Rita
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Funding
Funding for this research was provided by:
Ministero dell'Università e della Ricerca (Project no. PE00000007, INF-ACT, Project no. PE00000007, INF-ACT)
Ministero della Salute (Sostegno alla Sorveglianza delle infezioni correlate all’assistenza anche a supporto del PNCAR, Sostegno alla Sorveglianza delle infezioni correlate all’assistenza anche a supporto del PNCAR)
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Article History
Received: 16 January 2024
Accepted: 5 April 2024
First Online: 11 April 2024
Declarations
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: The study was approved by the Bioethics Committee of the University of Turin (protocol number 0421518, 29/07/2022).
: The institutional framework of the national PPS was a quality improvement program coordinated by public entities, namely the Italian National Health Institute (ISS), the Italian Centre for Disease Control (CCM) and Ministry of Health, therefore the written consent of patients was not requested. However, patients were provided with an information sheet notifying them of their participation in the PPS. Only anonymized data were collected and sent to the national coordinating center.
: The authors declare no competing interests.
