The healthcare community is looking for new ways to improve diagnosis and treatment of Psoriatic Arthritis (PsA), an inflammatory auto-immune disease (the result of an overactive immune system). Subjective symptoms such as joint pain, stiffness, and tenderness can often lead to frustration and missed opportunities for better care. In fact, one study found that mis-alignment between patients and physicians on treatment satisfaction is associated with increased disease activity and worse impact on quality of life. It’s important for patients with PsA to treat their condition early, because if left untreated, it can lead to permanent and irreversible joint damage.
This challenge is looking for a simple and easy to adopt solution to help:
The solution should easily enable the physician to better understand the patient’s end-to-end experience, regardless of how much the patient recalls or measures their daily impact and how much time the physician has with them to evaluate the patient’s status.
Ultimately, the solution will improve measurement of irregular and variable physical and emotional symptoms so both PsA patients and healthcare providers can evaluate the degree of severity and impact on quality of life. This more accurate understanding of patients’ symptoms will ease the development of treatment plans that match the severity and bothersomeness of patients’ symptoms.
 Furst DE et al. Misalignment between physicians and patient satisfaction with psoriatic arthritis disease control. Clin Rheumatol. 2017;36(9):2045-2054.
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