Study: People with psoriasis and psoriatic arthritis spend thousands on health care
Giving up on treatment and prohibitive costs remain the primary reasons for not seeking care
Nearly a quarter of people with psoriasis seek care for their disease from a primary care physician, and insurance status affects how psoriasis and psoriatic arthritis patients seek care, according to data from the National Psoriasis Foundation (NPF). Respondents cited giving up on treatment and prohibitive costs as the primary reasons for not seeking care.
A team of psoriasis researchers led by Dr. April Armstrong of the University of California, Davis, analyzed eight years of NPF data to determine the access-to-care issues and out-of-pocket costs facing people with psoriatic diseases.
Of the more than 5,600 people with psoriasis and psoriatic arthritis analyzed, 92 percent of patients had seen at least one physician in two years. Among those seeking care, 22 percent saw a primary care doctor.
When asked for reasons why they did not see a specialist—dermatologist or rheumatologist—to treat their disease, most patients said they had either given up on treatment (28 percent), it was too expensive (21 percent) or it was too much of a hassle (11 percent).
Although roughly 91 percent of psoriasis and psoriatic arthritis patients were covered by insurance, the majority spent greater than $2,500 per year in out-of-pocket costs for their disease.
Other findings reveal that patients with access to insurance and those with severe psoriasis were significantly more likely to see a specialist to treat their disease. Compared to males, women are 1.5 times more likely to seek care.
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January 14, 2013
About the National Psoriasis Foundation
Over the last 50 years, the National Psoriasis Foundation (NPF) has become the world’s leading nonprofit patient advocacy organization fighting for individuals with psoriasis and psoriatic arthritis. NPF leads this fight by driving efforts for a cure and improving the lives of the more than 8 million Americans affected by this chronic disease. To date, NPF has funded more than $15 million in research grants and fellowships, and to commemorate 50 years, NPF plans to raise an additional $2 million for early scientific career research programs in 2017 alone. Each year, NPF strives to support, educate and advocate on behalf of more individuals living with or caring for someone with the disease than ever before. As part of that effort, NPF established the Patient Navigation Center to offer personalized assistance to everyone with psoriasis or psoriatic arthritis. Join our community today and help drive discovery and create community for all living with psoriatic disease.