We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com.
Despite guidelines recommending early and aggressive therapy in rheumatoid arthritis, disease-modifying antirheumatic drug adoption for older patients remains low, according to data published in ACR Open Rheumatology.
“These medications have really changed the landscape of rheumatology, allowing low disease activity and remission to be achieved in people with rheumatoid arthritis, and now there needs to be a shifting consideration of how we can better target their use among older adults,” Jiha Lee, MD, MHS, the lead author of the paper and a rheumatologist at the University of Michigan, in Ann Arbor, said in a press release. “The prescription rates for these disease-modifying drugs have improved over the past few decades, but there is more work to be done to ensure older adults are on optimized treatment.”
Lee and colleagues compared DMARD use among older patients who attended RA-related ambulatory visits from rheumatologists and primary care physicians. They analyzed National Ambulatory Medical Care Survey data from 2005 through 2016, including information on all rheumatology and primary care visits for patients aged older than 65 who had RA recorded as one of their top diagnoses related to the visit.
The authors categorized DMARD use either “any DMARD,” “any conventional synthetic DMARD (csDMARD)” or “any biologic DMARD (bDMARD)” use.
Five csDMARDS, including methotrexate, leflunomide, azathioprine, hydroxychloroquine and sulfasalazine, and nine bDMARDS, including adalimumab (Humira, AbbVie), etanercept (Enbrel, Amgen), certolizumab (Cimzia, UCB), golimumab (Simponi, Janssen), infliximab (Remicade, Janssen), abatacept (Orencia, Bristol Myers Squibb), anakinra (Kineret, SOBI), tofacitinib (Xeljanz, Pfizer) and tocilizumab (Actemra, Genentech), were identified based only on the first eight listed drugs to be consistent across all years, the authors wrote.
Finally, the researchers recorded independent variables including demographic characteristics, diagnosis, reasons for visits, medication and provider specialties.
In all, Lee and colleagues included 7,873,246 visits in their analysis. Of those, 74% were with rheumatologists.
According to the researchers, DMARD use of any kind was recorded at 56% of rheumatology visits and 30% of primary care visits. Among visits where any kind of DMARD use was recorded, 20% of rheumatology visits recorded two or more, while only 6% of primary care visits recorded two or more. Over the study period, there was no statistically significant difference in conventional synthetic DMARD use. Biologic DMARD use was “likely to incrementally increase” at rheumatology visits, compared with primary care visits (P = .003), the researchers wrote.
“The world population is aging, and rheumatologists must be prepared to care for older adults with rheumatic diseases while addressing additional diseases and medications they may have,” Lee said in the release. “We can work more closely with primary care providers and learn from our colleagues in geriatrics and adopt age-friendly approaches to improve prescribing practices for older adults with rheumatoid arthritis.”