Abstract
Since ancient times, the transmission of information of medical discoveries has always followed a similar process, although its speed has markedly increased in the past few years and means of communication have improved. On the other hand, the amount of information that becomes available to physicians and patients increases exponentially year after year, and this information comes from a variety of sources, some quite new and unregulated, such as Internet sites. To help physicians cope with this huge amount of information, tools have been developed, such as medical reviews and updates in medical journals or other types of documents (eg, CD-ROMs such as the UpToDate Clinical Reference Library [UpToDate Inc, USA]), Internet sites and distribution materials. Therapeutic guidelines are now part of our environment, the most recent ones being ‘evidence based’. Reference databases (eg, MEDLINE), specific sites and electronic mail systems (eg, Amedeo) perform regular reviews of the literature that are readily accessible on the Internet (this is not to forget continuing medical education [CME] initiatives, symposia and other meetings). For patients, apart from the traditional and most appreciated sources of information (eg, physicians, pharmacists and other caregivers), information is increasingly available in the media and particularly on the Internet. Unfortunately, the quality of information is not always good, often conflicting or associated with commercial interests, and may sometimes antagonize valuable educational initiatives. It is often difficult for the patient (and even for caregivers) to have an idea of the validity of the sources involved. Furthermore, despite these new modes of communication, there is still a significant ‘care gap’ between what is considered to be optimal care and what is currently available; this is considered to explain a large part of the persisting human and socioeconomic burden generated by many chronic diseases (1). Morbidity associated with many respiratory or other types of diseases, while often preventable, is indeed still high, and many deficiencies in respiratory care unfortunately persist. This may be related to a lack of resources or socioeconomic factors, but is often related to insufficient knowledge or to difficulties in integrating current understanding of the diseases to current care. For example, research done in Canada and the United States has shown that patients with asthma do not know the criteria used to evaluate asthma control, or that such control is still far from optimal (2). Furthermore, studies – including some done in Canada – have revealed that physicians’ practices are not always in keeping with current guidelines (3). There is a need to help the public and physicians to acquire and integrate into care relevant and useful information to improve disease management, and to promote preventive measures (4,5). Societies, such as the Canadian Thoracic Society (CTS), have an important role in this regard, and initiatives such as consensus guidelines (and their implementation programs), collaboration on CME activities, symposia, publications and other means of communication (eg, Web sites) should be supported and tailored to current needs (Table 1). New ways to communicate should be developed, and new strategies to help medical practice and patient self-management should be tested. Ideally, messages to caregivers, patients and the public should be uniform to avoid confusion. In Canada, groups such as national or provincial disease-specific networks or associations can play an important role in providing a common
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