From: Socializing the evidence for diabetes control to develop “mindlines”: a qualitative pilot study
Barrier | Details |
---|---|
Patient factors | Patient does not follow through with referral (have to make their own appointments) |
Patients are reluctant to change medications | |
Non-compliant patients who “should not be on our metric list” | |
Patient’s agenda is different than the quality agenda | |
Patients do not trust people on the phone (issue with telephonic care coordination support) | |
Patient desire for one-stop shopping – they are not going to come back to the office multiple times | |
Our patients are sicker, more disadvantaged, etc | |
Lack of transportation | |
Context Factors | Patient load |
Care coordinators are not on site any longer | |
Lack of reliable information transfer between institutions | |
Practice staff too lean (especially nursing) | |
Lack of access to medication samples | |
Difficulty being an outlying clinic (“away from mothership,” “outcast”) | |
Short visit times/crowded agendas | |
Lack of RN (Registered Nurse) time for insulin teaching | |
Quality agenda overrides other patient-centered care | |
Resources | Inability to refer poorly controlled patients to endocrinology |
Lack of nutrition referrals | |
Community resources insufficient | |
Cost | Medication costs, lack of coverage for non-insulin options |
Clinicians do not always know costs |