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SCIENTIFIC LITERATURE · MED

Değişim İçin Hareket Bölüm II: Parkinson hastalığı olan kişiler için EPDA Tüzüğünün etkisini değerlendiren bir Avrupa araştırması.

Move for Change Part II: a European survey evaluating the impact of the EPDA Charter for people with Parkinson's disease.

Makine çevirisi · Editoryal inceleme bekliyor

Eur J Neurol · 2012-10-03

DOI: 10.1111/j.1468-1331.2012.03876.xPMID: 23034057

Open accessResearch Support, Non-U.S. Gov't; research-article; Journal ArticleKaynağa git ↗

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Aşağıdaki metin kaynak makalenin lisansı doğrulanmış orijinal özetidir. cc by

Background and purposeThe Move for Change campaign is a three-part series of pan-European surveys designed by the European Parkinson's Disease Association (EPDA) to assess the impact that the EPDA Charter for People with Parkinson's disease (PD) has had since its launch in 1997. Here, we report results from the second survey, focusing on the third right of the Charter; that is, 'all patients have the right to have access to support services'. Although the level of evidence for different support services varies, it is important to ensure that patients can access services with clinically proven benefits.MethodsThis survey comprised nine questions administered online via the EPDA and PD organization Web sites. Accessibility of support services was defined as 'services/medication/multidisciplinary healthcare professionals, etc. being available and on hand to patients when required'.ResultsNeurologists and general practitioners (GPs) received highest accessibility results (90.0 and 87.0% of respondents, respectively), with moderate results for physiotherapists (68.0%) and PD organizations (72.0%) and lower results for PD specialist nurses (26.0%), occupational therapists (23.0%), and counselors (27.0%). Support provided by neurologists and PD specialists was considered to be 'very helpful' by 59.0 and 55.7%, respectively, whilst only 31.8% of respondents gave such favorable ratings to GPs. Funding of services was variable across Europe.ConclusionsThese data demonstrate the challenges faced by PD patients in accessing the adequate care and support required throughout the course of their disease. These findings can assist healthcare professionals and policymakers in improving access to support services for patients and their families across Europe.

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