Sarcoidosis: patient treatment priorities

Autor: Jeanette Boyd, Jack Richardson, Robert P. Baughman, Johann Hochreiter, Ginger Spitzer, Dominique Valeyre, Rita Barriuso, Chris Knoet, Filippo Martone, Gianluca Ziosi, Bernd Quadder, Kelli Beyer
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Zdroj: ERJ Open Research, Vol 4, Iss 4 (2018)
ERJ Open Research
ISSN: 2312-0541
Popis: Sarcoidosis is a rare disease with the number of patients in the European Union (28 member states), Norway, Iceland and Lichtenstein estimated as ∼102 000 [1, 2]. Some 40% of individuals experience sarcoidosis as a chronic condition, while >60% of individuals find that the disease resolves within 2–5 years [3]. However, it has been shown that patients can still have symptoms that result in a reduced quality of life (QoL) even after clinical signs of disease have disappeared. These symptoms include fatigue, pain, everyday cognitive failure, small fibre neuropathy, exercise limitation and depressive symptoms [4, 5]. Findings from a recent survey of patients and their partners in the Netherlands also showed that sarcoidosis has a significant impact on their lives [6].
Sarcoidosis patient survey reveals QoL and functionality are required as core outcomes in treatment and care, along with more multidisciplinary working by clinicians and the establishment of specialist sarcoidosis centres in every European country http://ow.ly/DTvt30mQnqc
Databáze: OpenAIRE