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Patients with systemic lupus erythematosus are more likely than those in the general population to skip doses, take less medicine and delay filling prescriptions due to cost, according to data published in Arthritis Care & Research.
“Poor outcomes such as increased flares, emergency department visits, hospitalizations, and renal disease have been noted in association with non-adherence in SLE, making it essential to improve understanding of factors that compromise adherence,” Deeba Minhas, MD, of the University of Michigan, and colleagues wrote. “Several studies have documented non-adherence in SLE, and a review by Costedoat-Chalumeau found the most common cause of nonadherence was fear of side effects. However, cost-related aspects of non-adherence have not been a central focus in the existing studies.”
To examine the factors associated with access and cost-related nonadherence among patients with SLE compared with the general population, Minhas and colleagues conducted structured interviews with participants from the Michigan Lupus Epidemiology & Surveillance (MILES) Cohort. Created in 2014-2015, the MILES Cohort includes patients with SLE and controls from southeastern Michigan. Its precursor was the MILES Surveillance Registry, one of the National U.S. Lupus Registries supported by CDC.
The researchers collected detailed clinical and sociodemographic information, as well as health care access and use data, through structured interviews at the MILES baseline visit. Interviews included questions related to prescription medication access and adherence in the preceding 12 months. Participants were also asked whether they had been unable to obtain necessary prescription medicines in the preceding 12 months and, if so, why. Cost-related prescription nonadherence was defined based on participants reporting of at least one of the following: Skipped doses, taking less medicine or a delay in filling a prescription.
In all, 654 participants, including 462 patients with SLE and 192 controls, completed the baseline visit.
According to the researchers, 12.1% of patients with SLE and 9.4% of control participants reported being unable to access prescribed medications. However, those with SLE were about twice as likely as control participants to report cost-related prescription nonadherence in the preceding 12 months — 21.7% compared with 10.4% (P = .001). Among patients with SLE, 23.8% reported asking their physician for lower-cost alternatives, compared with 15.6% among controls (P = .02). The researchers found disparities associated with income, race and health insurance status, but the main findings persisted after adjusting for these and other variables in multivariable models.
“Our data from this epidemiologic study reveal that SLE patients were more likely than controls from the general population to report cost-related non-adherence to prescriptions,” Minhas and colleagues wrote. “Disparities were found in association with income and health insurance status. Racial disparities were noted in strategies to reduce costs.”
“Overall, fewer than one in four patients asked providers for lower cost medications,” they added. “These findings point to the importance of physicians trying to ascertain adherence and being aware of medication costs to individual patients when planning treatment changes and prescribing medications, which could provide a meaningful avenue for improving medication access and adherence through shared decision-making.”