Even experienced providers say prescribing has become too complex and time consuming with Medicare Part D plans, which differ in formularies and prior authorization processes.
Published Online: May 13, 2013
Lenny Lok Shun Chan, PharmD; and Gina Ko, PharmD
Providers’ knowledge of and satisfaction with Medicare Part D (MPD) remained poor 6 years after the initial implementation in 2006. In the San Francisco Department of Public Health, despite providers’ extensive prescribing experience and efforts to prescribe generic over brand medications, identifying a patient’s MPD plan, conforming to the formulary, and completing prior authorization requests remain time consuming and challenging to many providers. We advocate for the federal government to take an active role in simplifying, standardizing, and unifying enrollment and formulary information available to providers by creating a provider portal. New regulations should also require MPD companies to conspicuously post formulary information online for easy access. Educational seminars and online tools are available to help providers understand and navigate MPD.
Am J Manag Care. 2013;19(5):e197-e204
Medicare Part D plans increases providers’ workload substantially due to the various formularies and prior authorization processes.
Providers are in need of education on Medicare Part D to bridge the knowledge gap.
The federal government should take an active role in simplifying, standardizing, and unifying enrollment and formulary information by creating a provider portal. Regulations are needed to ensure easy access to formulary information and to simplify the prior authorization process.
Information technology should be introduced to help providers cope with Medicare Part D.
The Medicare Modernization Act was passed in 2003 with the intention to improve prescription drug access for Medicare beneficiaries. Since its implementation in 2006, enrollment in Medicare Part D (MPD) plans continues to increase, having reached 28 million in 2011.1,2 Although more research is needed to study the effects of MPD on health outcomes, research has shown that cost-related medication nonadherence has decreased after MPD implementation.3-5 The Affordable Care Act, passed in 2010, further expands prescription drug coverage by gradually eliminating the coverage gap by year 2020. Although prescription drug access has improved for patients, providers face an increased challenge when prescribing for patients with stand-alone MPD plans. In 2011, 33 stand-alone prescription drug plans were offered in California.2 Each plan had a different drug formulary and prior authorization (PA) process, which made determining drug coverage and preparing PA requests time consuming. Falling into the coverage gap also increases patients’ out-ofpocket cost, which can decrease adherence.6 These challenges can be especially daunting to providers in the public health setting, where human resources and information technology are lacking.
The purpose of this study was to assess providers’ knowledge of MPD in the San Francisco Department of Public Health and the impact of MPD plans on their practice. The community-based and hospital-based clinics had 206,010 and 156,207 visits from July 2010 to June 2011, respectively, 18.7% and 17.4% of which were covered by Medicare. The top 5 diagnoses were hypertension, type 2 diabetes, hyperlipidemia, depression, and obesity. Our experience in these clinics suggested that MPD was complicated and providers’ understanding of MPD was lacking, which led to difficulties in prescribing. Most studies in the past were conducted to assess the impact of MPD on beneficiaries rather than providers.7-9 The results of this survey can serve as a basis for devising strategies to overcome barriers when prescribing for MPD beneficiaries.
We surveyed providers practicing in the San Francisco Department of Public Health who were authorized to prescribe. The medical staff office provided a current list of 1283 providers and their e-mail addresses. These providers worked in San Francisco General Hospital (acute care hospital and trauma center, on-campus primary care, and specialty clinics), 11 community primary care clinics (located in different neighborhoods), and community behavioral health services (psychiatric services located in different neighborhoods). Some providers worked in both the inpatient and outpatient settings. San Francisco General Hospital serves as a training facility for University of California–San Francisco, but providers in training programs are not included in the medical staff. From that list, we excluded 516 providers who worked in departments where they were unlikely to prescribe outpatient prescriptions for MPD beneficiaries. Since the provider list did not distinguish between inpatient and outpatient providers, and we could not infer the number of interactions a provider might have had with MPD, 2 additional screening questions were used to exclude providers who worked exclusively in the inpatient setting and providers who had not prescribed for MPD patients in the past 3 months. The Figure illustrates how the final list of providers was obtained.
The survey study was approved by the Committee of Human Research at University of California–San Francisco. It was conducted using Survey Monkey, a web-based survey service. Due to the relatively small number of providers in our health system, no personal identifiers were collected except sex and practice characteristics (Table 1). The survey was divided into 2 parts. Part 1 of the survey asked providers to rate their level of agreement (scale of 1-10, where 0 = disagree and 10 = agree) with 16 statements concerning the quality of MPD plans, potential barriers to providing patients with needed medications, and current practice with regard to medication costs (Table 2). Part 2 of the survey tested participants’ understanding of MPD plans via a hypothetical patient scenario (Table 3, Appendix). We also asked survey participants whether they had attended educational seminars on MPD. The online survey was tested for content validity by about 10 providers in paper format in 2 primary care clinics. Providers eligible for the online survey received an initial recruitment e-mail and 2 reminder e-mails. The survey was open for 5 weeks beginning on June 29, 2011. A $5 gift card was offered at the conclusion of the survey as compensation for time and effort.
The response rate was 19% (146 out of the 760 medical providers). A total of 31 providers were excluded after the initial screening questions, 2 did not finish the screening questions, 4 did not give consent to participate, and 3 did not answer any question except the screening questions; therefore, all were excluded. Results were tabulated for the 106 providers who completed at least part of the survey and met study inclusion criteria (Table 2, Table 3).
Table 2 shows the survey questions in Part 1, the number of responses for each statement, and the median and the interquartile range on the agreement scale of 0 to 10. A median score of 4 to 6 showed that providers were neutral about the statement. A score of 7 to 10 conveyed agreement, and a score of 0 to 3 conveyed disagreement. A score closer to the ends of the scale (0 or 10) indicated a stronger agreement or disagreement with the statement. The interquartile range measured the variability of the opinion. A narrow range indicated that opinion was concentrated around the median.
Most providers were unsatisfied with their professional interactions with MPD plans (statement 1, median = 2). They felt that MPD plans did not make needed medications accessible compared with other accepted insurance plans (statement 2, median = 2). Providers also did not feel that they knew how to identify a patient’s MPD plan (statement 3, median = 3), whether a drug was covered (statement 4, median = 1), or how to request nonformulary drugs (statement 5, median = 3).
Providers neither agreed nor disagreed that nonformulary drugs could be obtained when medically justified (statement 6, median = 4). Providers were neutral when asked if they had switched patients to drugs that were less effective or safe because of plan coverage (statement 7, median = 6). They were also neutral when asked whether they often needed to switch patients’ medications because they did not have time to submit PAs (statement 8, median = 6). When a medication was changed because of formulary coverage, the patient usually needed to be contacted (statement 9, median = 8), but additional blood tests (statement 10, median = 2) were often not required. Providers were neutral with regard to the need for additional provider visits because of these medication changes (statement 11, median = 4). Providers were neutral when asked whether retail pharmacists were able to provide plan and formulary information (statement 12, median = 5). Conforming to the formulary and completing PA requests increased workload substantially (statement 13, median = 8). Most providers we surveyed considered generic options before brand medications (statement 14, median = 10), and explained to patients that brand and generic medications were therapeutically equivalent (statement 15, median = 10).
Table 3 shows the concepts tested by the hypothetical case and the number of correct, incorrect, and unanswered or “do not know” responses. Of the 106 providers, 78 (74%) knew that a brand medication would be more costly to the patient. A total of 22 of the 106 providers (21%) understood the concept of open enrollment. Of the 106 providers, 15 (14%) knew that Medicare-Medicaid dually eligible patients would be responsible for much lower copayments than patients who had stand-alone MPD plans. Less than half (49%, 52/106) of providers were able to provide at least 1 reliable formulary resource. Less than half of them (43%, 46/106) could locate information on patient assistance programs for those in the coverage gap or had any practical strategies to lower patient out-of-pocket costs on medications (45%, 48/106). A total of 16 (15%) respondents had attended seminars on MPD.
The response rate was low in this survey study. Providers who worked predominately in the inpatient setting could not be excluded using the list obtained from the medical staff. These providers were unlikely to be interested in our study on MPD. In addition, the low response rate was attributable to the low participation from the specialty clinic providers. Only 11% (18 of 171) of providers from dermatology, neurology, ophthalmology, otolaryngology, and urology participated in the study. In retrospect, the study should have focused on primary care providers instead of all outpatient clinic providers, because primary care providers generally have more interactions with MPD plans in the medical system. A post hoc subgroup analysis was done to examine responses from providers who worked in the community primary care clinics, in which 34% of providers participated in the survey (43/125). Their responses were found to be similar to those from the overall providers (Tables 2 and 3).
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