Cystic echinococcosis (CE), a worldwide zoonosis, is highly endemic in southern and eastern Europe. Its actual prevalence is unknown due to the lack of efficient reporting systems designed to take into account the particular features of the disease. Neglect of CE makes diagnosis and clinical management difficult outside referral centres, with inconsistencies in clinical practice and often unnecessary procedures carried out that have associated risks and costs. The Italian registry of CE (RIEC) is a prospective multicentre registry of CE patients seen from January 2012 in Italian health centres; data are voluntarily submitted to the registry. Its aims are to show the prevalence of CE in Italy, bring the importance of this infection to the attention of health authorities, encourage public health policies towards its control, and stimulate biological, epidemiological and clinical research on CE. From January 2012 to February 2014, a total 346 patients were enrolled in 11 centres, outnumbering national reports of many CE-endemic European countries. We discuss preliminary data and challenges of the RIEC, template for the European registry of CE, which has been implemented within the Seventh Framework Programme project HERACLES (Human cystic Echinococcosis ReseArch in CentraL and Eastern Societies) since September 2014.

The Italian registry of cystic echinococcosis (RIEC): the first prospective registry with a European future

TAMAROZZI, FRANCESCA;MARICONTI, MARA;BRUNETTI, ENRICO
2015-01-01

Abstract

Cystic echinococcosis (CE), a worldwide zoonosis, is highly endemic in southern and eastern Europe. Its actual prevalence is unknown due to the lack of efficient reporting systems designed to take into account the particular features of the disease. Neglect of CE makes diagnosis and clinical management difficult outside referral centres, with inconsistencies in clinical practice and often unnecessary procedures carried out that have associated risks and costs. The Italian registry of CE (RIEC) is a prospective multicentre registry of CE patients seen from January 2012 in Italian health centres; data are voluntarily submitted to the registry. Its aims are to show the prevalence of CE in Italy, bring the importance of this infection to the attention of health authorities, encourage public health policies towards its control, and stimulate biological, epidemiological and clinical research on CE. From January 2012 to February 2014, a total 346 patients were enrolled in 11 centres, outnumbering national reports of many CE-endemic European countries. We discuss preliminary data and challenges of the RIEC, template for the European registry of CE, which has been implemented within the Seventh Framework Programme project HERACLES (Human cystic Echinococcosis ReseArch in CentraL and Eastern Societies) since September 2014.
2015
Clinical Immunology & Infectious Disease
Environmental Medicine & Public Health
Esperti anonimi
Inglese
Internazionale
STAMPA
20
18
1
6
6
Primo articolo sul primo registro dell'echinococcosi cistica che sia mai stato istituito a livello mondiale. I dati, pur preliminari, sono fondamentali per valutare l'enorme discrepanza fra le cifre ufficiali della prevalenza di questa parassitosi negletta, e l'effetiva presenza sul territorio nazionale ed europeo
registry, register, echinococcosis, prevalence, international,cystic echinococcosis, hydatidosis, epidemiology, control, morbidity, Europe
http://www.eurosurveillance.org/images/dynamic/EE/V20N18/art21115.pdf
no
9
info:eu-repo/semantics/article
262
Tamarozzi, Francesca; Rossi, P; Galati, F; Mariconti, Mara; Nicoletti, G. J; Rinaldi, F; Casulli, A; Pozio, E; Brunetti, Enrico
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1108440
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