Impact of Medicare Part D opioid safety policies on disabled beneficiaries before and during the COVID-19 pandemic
Medicare D 部分阿片类药物安全政策在 COVID-19 大流行之前和期间对残疾受益人的影响
基本信息
- 批准号:10345593
- 负责人:
- 金额:$ 70.11万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-08-15 至 2026-06-30
- 项目状态:未结题
- 来源:
- 关键词:Accident and Emergency departmentAdverse eventAgeAmericanAuthorization documentationBuprenorphineCOVID-19COVID-19 pandemicCaringClinicalConsultConsultationsCoupledDataDisabled PersonsDoseDrug Utilization ReviewEmergency SituationEnsureEnvironmentEvaluationFederal GovernmentHealthcareHospitalizationImprove AccessInpatientsIntellectual functioning disabilityInterventionMedicalMedicareMedicare claimMental disordersMorphineMusculoskeletal DiseasesOpioidPatientsPharmaceutical PreparationsPharmacistsPlayPoliciesPopulationQuasi-experimentRegulationRuralRural CommunitySafetySignal TransductionSystemTimeUnited States Centers for Medicare and Medicaid Servicesbasebeneficiarycare coordinationchronic paincohortdisabilityethnic minorityfight againstflexibilityhigh riskhigh risk populationimplicit biasinterestmedically underservedmilligramminority patientmortalityopioid epidemicopioid taperingopioid therapyopioid use disorderoverdose deathpandemic diseasepost interventionprescription opioidracial and ethnicresponserural patientstelehealth
项目摘要
PROJECT SUMMARY/ABSTRACT
Representing ~3% of the U.S. population, non-elderly disabled Medicare beneficiaries (henceforth “disabled
beneficiaries”) account for ~25% of overdose deaths and hospitalizations related to prescription opioids.
Among disabled beneficiaries, opioid-related harms are concentrated in the 20-25% who are prescribed long-
term opioid therapy, primarily for chronic pain. We will first examine effects of a recent, important policy
intervention – Medicare Part D opioid safety edits – on an understudied, high-risk cohort of disabled
beneficiaries who are prescribed long-term, high-dose opioid therapy (Aim 1). Effective January 1, 2019,
Medicare Part D plans are required to incorporate a set of enhanced safety edits into their drug utilization
review systems. The most salient is a “care coordination edit” alerting pharmacists when daily doses of opioid
prescriptions exceed 90 morphine milligram equivalence. The new Medicare Part D opioid safety policy is
intended to identify overprescribing through pharmacist-prescriber consultation without directly restricting
patient access (intended beneficial effect). It may also encourage the initiation of buprenorphine for opioid use
disorder treatment in lieu of high-dose opioid regimes (beneficial spillover effect). However, the possible
misinterpretation of the 90-MME threshold as a “hard stop”, coupled with administrative burdens, may prompt
rapid dose reduction and abrupt discontinuation (unintended detrimental effect). Furthermore, overrepresented
among disabled beneficiaries, racial/ethnic minority patients and rural patients may be less likely to benefit
from the Medicare Part D opioid safety policy and more susceptible to unintended harms (Aim 2). The
Medicare Part D opioid safety policy is now playing out against a backdrop of the COVID-19 pandemic. To
minimize potential disruptions to health care, the federal government has made temporary changes to the
Medicare telehealth and opioid regulations, which may facilitate the beneficial effects of the Medicare Part D
opioid safety policy and alleviate the detrimental policy effects (Aim 3). We will use 2017-22 Medicare claims
data and a quasi-experimental design. We will assess appropriate opioid tapering (intended beneficial effect),
inappropriate opioid tapering (unintended detrimental effect), buprenorphine initiation (beneficial spillover
effect), and opioid-related adverse events in emergency department and inpatient settings (downstream
effect). We aim to: 1. Examine effects of the first-year, pre-pandemic implementation of the Medicare Part D
opioid safety policy on disabled beneficiaries who are prescribed long-term, high-dose opioid therapy; 2.
Compare racial/ethnic and rural-urban differences in policy effects; 3. Extend Aims 1 and 2 to the pandemic
and post-pandemic eras to elucidate the interaction of the Medicare Part D opioid safety policy with flexibilities
provided during the COVID-19 emergency and beyond. Our findings will enable policymakers to develop
clinically and culturally nuanced policies and practices tailored to the disabled population, the racial/ethnic
minority patients and rural patients, and the evolving pandemic/post-pandemic environment.
项目总结/文摘
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Hefei Wen其他文献
Hefei Wen的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Hefei Wen', 18)}}的其他基金
Impact of Medicare Part D opioid safety policies on disabled beneficiaries before and during the COVID-19 pandemic
Medicare D 部分阿片类药物安全政策在 COVID-19 大流行之前和期间对残疾受益人的影响
- 批准号:
10681207 - 财政年份:2022
- 资助金额:
$ 70.11万 - 项目类别:
相似海外基金
Planar culture of gastrointestinal stem cells for screening pharmaceuticals for adverse event risk
胃肠道干细胞平面培养用于筛选药物不良事件风险
- 批准号:
10707830 - 财政年份:2023
- 资助金额:
$ 70.11万 - 项目类别:
Hospital characteristics and Adverse event Rate Measurements (HARM) Evaluated over 21 years.
医院特征和不良事件发生率测量 (HARM) 经过 21 年的评估。
- 批准号:
479728 - 财政年份:2023
- 资助金额:
$ 70.11万 - 项目类别:
Operating Grants
Analysis of ECOG-ACRIN adverse event data to optimize strategies for the longitudinal assessment of tolerability in the context of evolving cancer treatment paradigms (EVOLV)
分析 ECOG-ACRIN 不良事件数据,以优化在不断发展的癌症治疗范式 (EVOLV) 背景下纵向耐受性评估的策略
- 批准号:
10884567 - 财政年份:2023
- 资助金额:
$ 70.11万 - 项目类别:
AE2Vec: Medical concept embedding and time-series analysis for automated adverse event detection
AE2Vec:用于自动不良事件检测的医学概念嵌入和时间序列分析
- 批准号:
10751964 - 财政年份:2023
- 资助金额:
$ 70.11万 - 项目类别:
Understanding the real-world adverse event risks of novel biosimilar drugs
了解新型生物仿制药的现实不良事件风险
- 批准号:
486321 - 财政年份:2022
- 资助金额:
$ 70.11万 - 项目类别:
Studentship Programs
Pediatric Adverse Event Risk Reduction for High Risk Medications in Children and Adolescents: Improving Pediatric Patient Safety in Dental Practices
降低儿童和青少年高风险药物的儿科不良事件风险:提高牙科诊所中儿科患者的安全
- 批准号:
10676786 - 财政年份:2022
- 资助金额:
$ 70.11万 - 项目类别:
Pediatric Adverse Event Risk Reduction for High Risk Medications in Children and Adolescents: Improving Pediatric Patient Safety in Dental Practices
降低儿童和青少年高风险药物的儿科不良事件风险:提高牙科诊所中儿科患者的安全
- 批准号:
10440970 - 财政年份:2022
- 资助金额:
$ 70.11万 - 项目类别:
Improving Adverse Event Reporting on Cooperative Oncology Group Trials
改进肿瘤学合作组试验的不良事件报告
- 批准号:
10642998 - 财政年份:2022
- 资助金额:
$ 70.11万 - 项目类别:
Planar culture of gastrointestinal stem cells for screening pharmaceuticals for adverse event risk
胃肠道干细胞平面培养用于筛选药物不良事件风险
- 批准号:
10482465 - 财政年份:2022
- 资助金额:
$ 70.11万 - 项目类别:
Expanding and Scaling Two-way Texting to Reduce Unnecessary Follow-Up and Improve Adverse Event Identification Among Voluntary Medical Male Circumcision Clients in the Republic of South Africa
扩大和扩大双向短信,以减少南非共和国自愿医疗男性包皮环切术客户中不必要的后续行动并改善不良事件识别
- 批准号:
10191053 - 财政年份:2020
- 资助金额:
$ 70.11万 - 项目类别:














{{item.name}}会员




