Literature DB >> 24922290

The Italian institutional accreditation model for Haemophilia Centres.

Gabriele Calizzani1, Fabio Candura1, Ivana Menichini2, Romano Arcieri3, Giancarlo Castaman4, Alessandro Lamanna5, Maria R Tamburrini6, Antonio Fortino7, Monica Lanzoni8, Samantha Profili1, Simonetta Pupella1, Giancarlo M Liumbruno1, Giuliano Grazzini1.   

Abstract

BACKGROUND: In Italy, basic health needs of patients with inherited bleeding disorders are met by a network of 50 haemophilia centres belonging to the Italian Association of Haemophilia Centres. Further emerging needs, due to the increased life expectancy of this patient group, require a multi-professional clinical management of the disease and provide a challenge to the organisation of centres.In order to achieve harmonised quality standards of haemophilia care across Italian Regions, an institutional accreditation model for haemophilia centres has been developed.
MATERIAL AND METHODS: To develop an accreditation scheme for haemophilia centres, a panel of experts representing medical and patient bodies, the Ministry of Health and Regional Health Authorities has been appointed by the National Blood Centre. Following a public consultation, a technical proposal in the form of recommendations for Regional Health Authorities has been formally submitted to the Ministry of Health and has formed the basis for a proposal of Agreement between the Government and the Regions.
RESULTS: The institutional accreditation model for Haemophilia Centres was approved as an Agreement between the Government and the Regions in March 2013. It identified 23 organisational requirements for haemophilia centres covering different areas and activities. DISCUSSION: The Italian institutional accreditation model aims to achieve harmonised quality standards across Regions and to implement continuous improvement efforts, certified by regional inspection systems. The identified requirements are considered as necessary and appropriate in order to provide haemophilia services as "basic healthcare levels" under the umbrella of the National Health Service. This model provides Regions with a flexible institutional accreditation scheme that can be potentially extended to other rare diseases.

Entities:  

Mesh:

Year:  2014        PMID: 24922290      PMCID: PMC4044797          DOI: 10.2450/2014.0058-14s

Source DB:  PubMed          Journal:  Blood Transfus        ISSN: 1723-2007            Impact factor:   3.443


  18 in total

Review 1.  Present and future challenges in the treatment of haemophilia: the patient's perspective.

Authors:  Romano Arcieri; Angelo C Molinari; Stefania Farace; Giuseppe Mazza; Alberto Garnero; Gabriele Calizzani; Paola Giordano; Emily Oliovecchio; Lorenzo Mantovani; Lamberto Manzoli; Paul Giangrande
Journal:  Blood Transfus       Date:  2013-09       Impact factor: 3.443

Review 2.  Present and future challanges in the treatment of haemophilia: a clinician's perspective.

Authors:  Pier Mannuccio Mannucci; Massimo Franchini
Journal:  Blood Transfus       Date:  2013-09       Impact factor: 3.443

Review 3.  The modern treatment of haemophilia: a narrative review.

Authors:  Massimo Franchini
Journal:  Blood Transfus       Date:  2012-07-04       Impact factor: 3.443

Review 4.  Emerging issues on comprehensive hemophilia care: preventing, identifying, and monitoring age-related comorbidities.

Authors:  Antonio Coppola; Cristina Santoro; Massimo Franchini; Caterina Mannucci; Selene Mogavero; Angelo Claudio Molinari; Piercarla Schinco; Annarita Tagliaferri; Rita Carlotta Santoro
Journal:  Semin Thromb Hemost       Date:  2013-09-08       Impact factor: 4.180

Review 5.  The Italian National Centre for Rare Diseases: where research and public health translate into action.

Authors:  Domenica Taruscio; Linda Agresta; Annalisa Amato; Giuseppe Bernardo; Luana Bernardo; Francesca Braguti; Pietro Carbone; Claudio Carta; Marina Ceccarini; Federica Censi; Simona Coppola; Patrizia Crialese; Marta De Santis; Stefano Diemoz; Carlo Donati; Sabina Gainotti; Gianluca Ferrari; Giovanna Floridia; Claudio Frank; Rosa Giuseppa Frazzica; Amalia E Gentile; Orietta Granata; Yllka Kodra; Manuela Latrofa; Paola Laricchiuta; Armando Magrelli; Cristina Morciano; Agata Polizzi; Stefania Razeto; Marco Salvatore; Antonella Sanseverino; Daniele Savini; Paola Torreri; Fabrizio Tosto; Flavia Villani; Giorgio Vincenti; Luciano Vittozzi
Journal:  Blood Transfus       Date:  2014-04       Impact factor: 3.443

6.  A study of variations in the reported haemophilia B prevalence around the world.

Authors:  J S Stonebraker; P H B Bolton-Maggs; J Michael Soucie; I Walker; M Brooker
Journal:  Haemophilia       Date:  2011-06-07       Impact factor: 4.287

7.  Hemophilia care in Italy.

Authors:  P M Mannucci; Z M Ruggeri
Journal:  Thromb Haemost       Date:  1976-06-30       Impact factor: 5.249

8.  A study of variations in the reported haemophilia A prevalence around the world.

Authors:  J S Stonebraker; P H B Bolton-Maggs; J Michael Soucie; I Walker; M Brooker
Journal:  Haemophilia       Date:  2009-10-21       Impact factor: 4.287

9.  Models for institutional and professional accreditation of haemophilia centres in Italy.

Authors:  G Calizzani; S Vaglio; R Arcieri; I Menichini; A Tagliaferri; S Antoncecchi; M T Carloni; A Breda; E Santagostino; A Ghirardini; M R Tamburrini; M Morfini; P M Mannucci; G Grazzini
Journal:  Haemophilia       Date:  2013-04-05       Impact factor: 4.287

Review 10.  Past, present and future of hemophilia: a narrative review.

Authors:  Massimo Franchini; Pier Mannuccio Mannucci
Journal:  Orphanet J Rare Dis       Date:  2012-05-02       Impact factor: 4.123

View more
  4 in total

1.  Haemophilia Centre Certification Systems: optional or optimal choice for healthcare systems?

Authors:  Gabriele Calizzani; Michael Makris; Pier Mannuccio Mannucci; Domenica Taruscio; Giuliano Grazzini; Fabrizio Oleari
Journal:  Blood Transfus       Date:  2014-04       Impact factor: 3.443

Review 2.  Uncovered needs in the management of inherited bleeding disorders in Italy.

Authors:  Romano Arcieri; Angelo C Molinari; Stefania Farace; Giuseppe Mazza; Alberto Garnero; Gabriele Calizzani; Paola Giordano; Emily Oliovecchio; Lorenzo Mantovani; Lamberto Manzoli; Paul Giangrande
Journal:  Blood Transfus       Date:  2014-04       Impact factor: 3.443

3.  Definition of an organisational model for the prevention and reduction of health and social impacts of inherited bleeding disorders.

Authors:  Gabriele Calizzani; Ivana Menichini; Fabio Candura; Monica Lanzoni; Samantha Profili; Maria Rita Tamburrini; Antonio Fortino; Stefania Vaglio; Giuseppe Marano; Giuseppina Facco; Emily Oliovecchio; Massimo Franchini; Antonio Coppola; Romano Arcieri; Cinzia Bon; Mario Saia; Sabina Nuti; Massimo Morfini; Giancarlo M Liumbruno; Giovanni Di Minno; Giuliano Grazzini
Journal:  Blood Transfus       Date:  2014-04       Impact factor: 3.443

4.  Comparing regional models of congenital bleeding disorders: preliminary steps in the Italian context.

Authors:  Sabina Nuti; Chiara Seghieri; Francesco Niccolai; Federica Vasta; Giuliano Grazzini
Journal:  BMC Res Notes       Date:  2017-06-26
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.