Calizzani Gabriele, Candura Fabio, Menichini Ivana, Arcieri Romano, Castaman Giancarlo, Lamanna Alessandro, Tamburrini Maria R, Fortino Antonio, Lanzoni Monica, Profili Samantha, Pupella Simonetta, Liumbruno Giancarlo M, Grazzini Giuliano
National Blood Centre, National Institute of Health, Rome, Italy.
Italian Federation of Haemophilia Societies (FedEmo), Rome, Italy Necstep Studio Associato, Modena, Italy.
Blood Transfus. 2014 Apr;12 Suppl 3(Suppl 3):s510-4. doi: 10.2450/2014.0058-14s.
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.
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.
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.
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.
在意大利,遗传性出血性疾病患者的基本医疗需求由隶属于意大利血友病中心协会的50个血友病中心网络来满足。由于该患者群体预期寿命的增加,进一步出现的需求要求对该疾病进行多专业临床管理,并给中心的组织工作带来了挑战。为了在意大利各地区实现血友病护理质量标准的统一,已制定了血友病中心的机构认证模式。
为制定血友病中心认证方案,国家血液中心任命了一个由代表医疗和患者团体、卫生部及地区卫生当局的专家组成的小组。经过公众咨询后,以给地区卫生当局的建议形式提出的一项技术提案已正式提交给卫生部,并成为政府与各地区之间协议提案的基础。
血友病中心的机构认证模式于2013年3月作为政府与各地区之间的协议获得批准。它确定了血友病中心在不同领域和活动方面的23项组织要求。
意大利的机构认证模式旨在实现各地区质量标准的统一,并通过地区检查系统认证来实施持续改进措施。所确定的要求被认为是必要且适当的,以便在国家卫生服务的框架下将血友病服务作为“基本医疗保健水平”来提供。该模式为各地区提供了一个灵活的机构认证方案,有可能扩展到其他罕见疾病。