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. 2021 Jun 9;157(7):874–876. doi: 10.1001/jamadermatol.2021.1850

Table 2. Population-Based Barriers to Health Care Access Among Young Adult Survivors of Melanoma by Annual PSE Status in the Prior Yeara.

Self-reported response No. (%)
All PSE statusb
Yes No
Total 128 75 46
Presence of barriers
None 96 (75) 64 (85) 29 (63)
≥1 30 (23) 11 (15) 17 (40)
Types of barriers experienced in prior year
Financial or health insurance 19 (15) 4 (5) 14 (30)
It costs too much 15 (12) 3 (4) 11 (24)
I had no health insurance 12 (9) 1 (1) 10 (22)
My insurance company didn’t approve a test or visit 7 (5) 2 (3) 5 (11)
Anticipated limits and financial burden 1 (1) 0 1 (2)
Health system/organizational 9 (7) 3 (4) 6 (13)
I didn’t have a doctor that I could call 5 (4) 2 (3) 3 (7)
I didn’t know where to go 5 (4) 1 (1) 4 (9)
I didn’t have a doctor that spoke my language 0 NA NA
I don’t have a doctor that understands my background and values 1 (1) 0 1 (2)
I didn’t know how to make an appointment 0 NA NA
Work/life 14 (11) 8 (11) 6 (13)
I was too busy 11 (9) 7 (9) 4 (9)
I didn’t have childcare 3 (2) 2 (3) 1 (2)
I couldn’t leave work/school 7 (5) 4 (5) 3 (7)
Psychosocial/other 7 (6) 2 (3) 4 (9)
I don’t trust doctors or think they can help me at this time 2 (2) 0 2 (4)
I didn’t want to be reminded about my cancer experience 2 (2) 1 (1) 1 (2)
I was worried that a problem would be discovered 3 (2) 2 (3) 2 (1)
Anxiety 1 (1) 1 (1) 0
None of the above 2 (2) 0 1 (2)

Abbreviations: NA, not applicable; PSE, physician-based skin examinations.

a

Participants were diagnosed with stage 1 or higher melanoma at 24 years or younger in 1996 to 2004 in Los Angeles County and were 18 to 39 years old and 5 or more years postdiagnosis at time of survey in 2015.

b

Seven participants were missing information on either PSE or barriers.