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Le manque d'interopérabilité dans les sytèmes et les services comme les dossiers médicaux électroniques et les prescriptions en ligne, a été indentifié comme un obstacle majeur au déploiement d'un système de santé en ligne au sein de l'UE. La Commission a lancé une consultation publique sur la question en vue d'adopter des lignes directrices plus tard dans l'année 2007.
The Commission's notion of eHealth interoperability is two-fold. In addition to the technical definition of the term that relates to connecting systems and exchanging information, it also seeks to recognise the concept of connecting people, data, and diverse health systems, while taking into account the relevant social, political, regulatory, business, industry and organisational factors.
The EU's e-Health action plan (2004) defines the block's priorities on the field until 2010. One of them is the development of interoperable healthcare systems across the Union.
In June 2006, the Commission's ICT for Health Unit adopted a new strategy
to promote the transformation of the European healthcare landscape, in line with the Commission's new policy framework i2010. The Unit is currently in the process of drafting guidelines for good practice on eHealth interoperability.
The Commission adopted on 16 July 2007 its Draft Recommendation on eHealth Interoperability
and submitted it to informal public consultation
. The final Recommendation is expected to be adopted later in 2007 and is set to contribute to the achievement of "a European health information space" by the end of the year 2015.
The draft outlines a set of recommended guidelines for good practice on eHealth interoperability and proposes a number of actions addressed to member states, industries and associations that work in the eHealth field. According to the Commission, the Recommendation has relevance also for the European Economic Area (EEA) countries.
The draft proposes actions:
According to the Commission, the ultimate goal of the Recommendation is "to contribute to enabling the provision of a means for authorised healthcare professionals to gain managed access to essential health information about patients [such as the appropriate parts of a patient's electronic health record, patient summary and emergency data], subject to the patient's consent, and with full regard for data protection and security requirements" across Europe.