Department of Medicine, Harvard Medical School, Boston, Massachusetts.
Department of Health Policy and Management, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
JAMA Cardiol. 2019 Mar 1;4(3):265-271. doi: 10.1001/jamacardio.2019.0007.
One-third of Medicare beneficiaries are enrolled in Medicare Advantage (MA), Medicare's private plan option. Medicare Advantage incentivizes performance on evidence-based care, but limited information exists using reliable clinical data to determine whether this translates into better quality for patients with coronary artery disease (CAD) enrolled in MA compared with those enrolled in traditional fee-for-service (FFS) Medicare.
To determine differences in evidence-based secondary prevention treatments and intermediate outcomes among patients with CAD enrolled in MA vs FFS Medicare.
DESIGN, SETTING, AND PARTICIPANTS: In this observational, retrospective, cohort study, deidentified data from patients 18 years or older diagnosed as having CAD between January 1, 2013, and May 1, 2014, at cardiology practices participating in the Practice Innovation and Clinical Excellence (PINNACLE) registry were studied, including 35 563 patients enrolled in MA and 172 732 enrolled in FFS Medicare. Data were analyzed from March to July 2018.
Medicare Advantage enrollment.
Medication prescription patterns among eligible patients and intermediate outcomes, including blood pressure and low-density lipoprotein cholesterol.
Of the 35 563 patients with CAD enrolled in MA, 20 193 (56.8%) were male, and the mean (SD) age was 76.7 (7.6) years; of the 172 732 patients with CAD enrolled in FFS Medicare, 100 025 (57.9%) were male, and the mean (SD) age was 77.5 (8.0) years. Patients enrolled in MA were younger, less likely to be white, and more likely to be female and to have heart failure, diabetes, and chronic kidney disease compared with those enrolled in FFS Medicare. Compared with FFS Medicare beneficiaries, MA beneficiaries were more likely to receive secondary prevention treatments, including β-blockers (80.6% vs 78.8%; P < .001), angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers (70.7% vs 65.1%; P < .001), and statins (68.4% vs 64.5%; P < .001). Patients enrolled in MA were also more likely to receive all 3 medications when eligible (48.9% vs 40.4%; P < .001). After adjustment, MA beneficiaries had higher odds of receiving guideline-recommended therapy compared with FFS Medicare beneficiaries for β-blockers (odds ratio, 1.10; 95% CI, 1.04-1.17; P = .002), angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers (odds ratio, 1.13; 95% CI, 1.08-1.19; P < .001), and all 3 medications (odds ratio, 1.23; 95% CI, 1.001-1.50; P = .047). There were no significant differences in intermediate outcomes between those enrolled in MA and FFS Medicare, including systolic and diastolic blood pressure and low-density lipoprotein cholesterol levels.
Among patients with CAD in the PINNACLE registry, MA beneficiaries had more comorbidities than FFS Medicare beneficiaries and were more likely to receive secondary prevention treatments. However, this did not translate into differences in intermediate outcomes. These findings suggest that MA plans may drive improvements in process-based quality measures for Medicare beneficiaries, although this may have a limited effect on improving patient outcomes over FFS Medicare.
三分之一的医疗保险受益人参加了医疗保险优势计划(MA),这是医疗保险的私人计划选择。医疗保险优势计划激励基于证据的护理绩效,但利用可靠的临床数据来确定这是否转化为冠状动脉疾病(CAD)患者的质量改善,这些患者参加 MA 与参加传统按服务收费(FFS)医疗保险的患者相比,相关信息有限。
确定 MA 与 FFS 医疗保险中 CAD 患者的循证二级预防治疗和中间结果的差异。
设计、地点和参与者:在这项观察性、回顾性队列研究中,研究了 2013 年 1 月 1 日至 2014 年 5 月 1 日期间在参与实践创新和临床卓越(PINNACLE)登记处的心脏病学实践中被诊断为 CAD 的 18 岁或以上患者的匿名数据,包括 35563 名参加 MA 的患者和 172732 名参加 FFS 医疗保险的患者。数据分析于 2018 年 3 月至 7 月进行。
医疗保险优势计划的参与。
合格患者的药物处方模式和中间结果,包括血压和低密度脂蛋白胆固醇。
在 35563 名参加 MA 的 CAD 患者中,20193 名(56.8%)为男性,平均(SD)年龄为 76.7(7.6)岁;在 172732 名参加 FFS 医疗保险的 CAD 患者中,100025 名(57.9%)为男性,平均(SD)年龄为 77.5(8.0)岁。与参加 FFS 医疗保险的患者相比,参加 MA 的患者更年轻,不太可能是白人,更可能是女性,更可能患有心力衰竭、糖尿病和慢性肾脏病。与 FFS 医疗保险的受益人相比,MA 受益人的二级预防治疗更有可能,包括β受体阻滞剂(80.6%比 78.8%;P <.001)、血管紧张素转换酶抑制剂或血管紧张素 II 受体阻滞剂(70.7%比 65.1%;P <.001)和他汀类药物(68.4%比 64.5%;P <.001)。有资格时,参加 MA 的患者也更有可能同时接受所有 3 种药物(48.9%比 40.4%;P <.001)。调整后,与 FFS 医疗保险的受益人相比,MA 受益人的β受体阻滞剂(比值比,1.10;95%置信区间,1.04-1.17;P =.002)、血管紧张素转换酶抑制剂或血管紧张素 II 受体阻滞剂(比值比,1.13;95%置信区间,1.08-1.19;P <.001)和所有 3 种药物(比值比,1.23;95%置信区间,1.001-1.50;P =.047)接受指南推荐的治疗的可能性更高。在中间结果方面,参加 MA 和 FFS 医疗保险的患者之间没有显著差异,包括收缩压和舒张压以及低密度脂蛋白胆固醇水平。
在 PINNACLE 登记处的 CAD 患者中,MA 受益人的合并症比 FFS 医疗保险的受益人更多,更有可能接受二级预防治疗。然而,这并没有转化为中间结果的差异。这些发现表明,MA 计划可能会提高医疗保险受益人的基于流程的质量指标,但这可能对改善患者的结果比对 FFS 医疗保险的影响有限。