Prior Authorization

事先授权
  • 文章类型: Letter
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  • 文章类型: Journal Article
    托管护理计划,与各州签订合同,覆盖四分之三的医疗补助参保人,在解决美国的毒品流行方面发挥着至关重要的作用。然而,药物使用障碍的福利因医疗补助管理式护理计划而异,目前尚不清楚国家在调节其活动中扮演什么角色。为了解决这个问题,我们调查了33个州和华盛顿州,D.C.,关于2021年医疗补助管理式护理计划的物质使用障碍治疗覆盖率和利用管理要求。大多数州都要求覆盖常见形式的物质使用障碍治疗,并禁止在管理式护理中每年最高限额和注册费用分摊。不到三分之一的州禁止管理式护理计划对每项治疗服务进行事先授权。对于大多数治疗药物,不到三分之二的州禁止事先授权,药物测试,\"首先失败,“或管理式护理中的社会心理治疗要求。我们的研究结果表明,许多州给予管理式护理计划广泛的自由裁量权,对承保的物质使用障碍治疗施加要求,这可能会影响获得救生护理。
    Managed care plans, which contract with states to cover three-quarters of Medicaid enrollees, play a crucial role in addressing the drug epidemic in the United States. However, substance use disorder benefits vary across Medicaid managed care plans, and it is unclear what role states play in regulating their activities. To address this question, we surveyed thirty-three states and Washington, D.C., regarding their substance use disorder treatment coverage and utilization management requirements for Medicaid managed care plans in 2021. Most states mandated coverage of common forms of substance use disorder treatment and prohibited annual maximums and enrollee cost sharing in managed care. Fewer than one-third of states forbade managed care plans from imposing prior authorization for each treatment service. For most treatment medications, fewer than two-thirds of states prohibited prior authorization, drug testing, \"fail first,\" or psychosocial therapy requirements in managed care. Our findings suggest that many states give managed care plans broad discretion to impose requirements on covered substance use disorder treatments, which may affect access to lifesaving care.
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  • 文章类型: Journal Article
    背景:尽管特应性皮炎(AD)治疗方法取得了进展,许多患者在获得药物治疗方面面临挑战。这项研究旨在确定AD处方的保险承保延迟和拒绝的频率和原因,并描述相关的等待时间和患者在面对承保问题时该怎么做的程度。
    方法:这是一个横截面,在观察性研究中,美国成年AD患者(18岁以上)或美国儿科AD患者(0~17岁)的护理人员完成了一项在线调查(2021年6月3日至7月16日).
    结果:受访者(N=978)主要是患有AD的成年人(81.8%),女性(67.7%),白色(70.2%)。有645次AD处方的保险延误或拒绝,48.1%(470/978)的受访者在过去一年中至少经历过一次延迟/拒绝。大多数延误/拒绝是局部类固醇(39.2%,253/645),使用最多的处方治疗类(83.9%,821/978)。然而,延迟/拒绝率最高的是生物制品,其中43.6%(109/250)的处方面临延迟或拒绝。拒绝主要由阶梯治疗(27.6%)和事先授权的延迟(55.1%)引起。只有56.0%的受访者表示,如果他们面临AD处方保险的问题,他们会知道该怎么做。
    结论:AD患者在获得推荐治疗时经常会遇到保险相关障碍,当这些障碍出现时,许多人不知道如何应对。需要改进及时获得治疗的策略。
    BACKGROUND: Despite advances in atopic dermatitis (AD) treatments, many patients face challenges obtaining medications. This study aimed to determine the frequency and causes of insurance coverage delays and denials for AD prescriptions and characterize the associated wait times and extent to which patients understand what to do when faced with a coverage issue.
    METHODS: This was a cross-sectional, observational study in which adult U.S. residents (aged 18+ years) with AD or caregivers of pediatric U.S. patients with AD (aged 0-17 years) completed an online survey (3 June-16 July 2021).
    RESULTS: Respondents (N = 978) were primarily adults with AD (81.8%), female (67.7%), and white (70.2%). There were 645 insurance delays or denials for AD prescriptions, with 48.1% (470/978) of respondents experiencing at least one delay/denial in the past year. Most delays/denials were for topical steroids (39.2%, 253/645), the most highly used prescription treatment class (83.9%, 821/978). However, the highest rate of delay/denials was for biologics, of which 43.6% (109/250) of all prescriptions faced a delay or denial. Denials were caused primarily by step therapy (27.6%) and delays by prior authorization (55.1%). Only 56.0% of respondents said they would know what to do if they faced an issue with AD prescription coverage.
    CONCLUSIONS: Patients with AD frequently experience insurance-related barriers to obtaining recommended therapies, and many do not know how to respond when these barriers arise. Strategies to improve timely therapeutic access are needed.
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  • 文章类型: Journal Article
    本观点讨论了新的医疗保险和医疗补助服务中心(CMS)互操作性和事先授权最终规则的规定和潜力。
    This Viewpoint discusses the provisions and potential of the new Centers for Medicare and Medicaid Services (CMS) Interoperability and Prior Authorization Final Rule.
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  • 文章类型: Journal Article
    背景:事先授权(PA)是保险公司批准患者药物或治疗通常需要的管理任务。皮肤科实践经常聘请协调员专注于完成PA,在其他解决方案中。在学术中心提供这种支持的程度,重要的是,皮肤科居民在教育追求上花费了多少时间,这在很大程度上是未知的。作者试图确定PA对皮肤科居民的影响。
    方法:将IRB批准的(#NCR213814)13个问题的调查分发给全国皮肤科居民,以了解PA对临床和学术活动方面的影响。结果:1462名皮肤科居民中的150名,10.3%,回答了调查。70%的回应居民为获得PA做出了贡献。58.7%的人表示他们的计划雇用了PA协调员;但是,其中,63.6%的人仍然依赖居民获得PA。84%的人表示,在接下来的一个月里,他们担心PA的负担会导致患者治疗失败。72.7%的人由于PA而避免开某些药物。64%的人表示PA负担阻碍了他们进行学术活动的能力。80.7%的人表示PA负担导致职业倦怠或士气下降。
    结论:我们的数据突出表明,皮肤科居民受到PA负担的负面影响,导致学习时间减少,研究,最好的照顾他们的病人。皮肤科居民和患者将受益于减轻PA的负担,特别是通过减少皮肤病学PA的改革或法规对居民,或者由学术机构尽可能好地从居民那里免除这些责任。药物Dermatol.2024;23(6):485–488。doi:10.36849/JDD.7617。
    BACKGROUND: Prior authorizations (PAs) are administrative tasks commonly required by insurers to approve medications or therapies for patients. Dermatology practices frequently employ coordinators to focus on completing PAs, among other solutions. The degree to which this support is offered in academic centers and, importantly, how much time dermatology residents spend on PAs over educational pursuits is largely unknown. The authors sought to identify the impact of PAs on dermatology residents.
    METHODS: An IRB-approved (#NCR213814) 13-question survey was distributed nationwide to dermatology residents regarding the impact of PAs on aspects of clinical and scholarly activities.  Results: 150 of 1462 dermatology residents, 10.3%, responded to the survey. 70% of responding residents contribute to obtaining PAs. 58.7% indicated that their program employed a PA coordinator; though, of these, 63.6% still relied on residents for PAs. 84% indicated that for the following month they feared the burden of PAs would lead to a lapse in treatment for patients. 72.7% avoided prescribing certain medications due to PAs. 64% indicated the PA burden impedes their ability to perform scholarly activities. 80.7% indicated the PA burden contributed to burnout or decreased morale.
    CONCLUSIONS: Our data highlight that dermatology residents are negatively impacted by the burden of PAs, resulting in reduced time to study, research, and best care for their patients. Dermatology residents and patients would benefit from reducing the burden of PAs, especially on residents by reforms or regulations that reduce dermatologic PAs, or by academic institutions removing these responsibilities from residents as best as possible. Drugs Dermatol. 2024;23(6):485-488.    doi:10.36849/JDD.7617.
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  • 文章类型: Journal Article
    美国过敏学会事先授权工作组,哮喘和免疫学(AAAAI),大卫·汗的总统倡议,MD,FAAAI,旨在制定AAAAI立场声明,概述改善患者医疗保健的方法,支持倡导事先授权(PA)改革的立法,并通过问卷调查确定PA对其成员的影响。本文介绍了本次调查的结果。开发了电子匿名调查问卷,以评估PA对AAAAI成员及其工作人员和患者的影响和负担。调查已发送给美国AAAAI的随机选择的成员和研究员。AAAAI的信息服务团队和该工作组报告的作者使用描述性统计数据来分析结果。过敏免疫学专家的问卷答复在人口统计上反映了AAAAI成员资格,并表明PA可以显着影响患者的护理交付并增加临床实践的行政负担。在某些情况下导致严重不良事件。关于不同药物类别的PA的差异反应可能反映了医生的患者群体,可以改变处方模式。事先授权是一个严重的医疗保健问题,浪费了财政资源,并且在患者无法获得临床管理所需的药物或医疗服务时不必要地将患者置于危险之中。这项问卷调查研究的结果支持最近的AAAAI关于PA的立场声明中提出的建议。
    The Prior Authorization Task Force of the American Academy of Allergy, Asthma & Immunology (AAAAI), a presidential initiative of David Khan, MD, FAAAI, was established to develop an AAAAI position statement outlining ways to improve health care for our patients, to support legislation that advocates for prior authorization (PA) reform and identify the impact PA has on its membership using a questionnaire survey. This article describes the results of this survey. An electronic anonymous survey questionnaire was developed to assess the impact and burden of PA on AAAAI members and their staff and patients. Surveys were sent to randomly selected members and fellows of the AAAAI in the United States. Descriptive statistics were used to analyze the results by the Information Services team of the AAAAI and the authors of this work group report. The questionnaire responses from allergy immunology specialists demographically reflected the AAAAI membership and indicate that PAs can significantly affect patient care delivery and increase administrative burden to clinical practices, leading to serious adverse events in some circumstances. Differential responses regarding PAs for various medication classes likely reflect the physician\'s patient population, which can shift prescribing patterns. Prior authorization is a serious health care problem that is wasting financial resources and needlessly placing patients in danger when they are unable to access medications or medical services required for clinical management. The results of this questionnaire study support the recommendations made in the recent AAAAI position statement on PA.
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  • 文章类型: Journal Article
    美国每年的医疗行政支出约为1万亿美元。一个主要的业务领域是金融交易生态系统,每年有大约2000亿美元的支出。来自其他行业和国家的高效金融交易生态系统表现出两个特点:即时支付保证和整个过程中高度使用自动化。目前的系统在私人付款人和提供者之间,平均每笔索赔的交易成本为12至19美元,每年超过90亿笔索赔;每个索赔平均需要4至6周的时间来处理和支付。对于简单的索赔,私人付款人和提供者的交易成本为7到10美元;对于复杂的索赔,35到40美元。对大约5000个代码的事先授权,私人付款人每次提交的平均费用为40至50美元,提供者每次提交的平均费用为20至30美元。与更有效的金融交易生态系统相一致的干预措施可以减少400亿美元至600亿美元的支出;大约一半是在组织层面(由领先的私人付款人和提供商实施的扩展干预措施),一半是在行业层面(采用集中的自动化索赔交换所,为先前授权的子集标准化医疗政策,并将医生执照标准化为国家提供者目录)。
    US health care administrative spending is approximately $1 trillion annually. A major operational area is the financial transactions ecosystem, which has approximately $200 billion in spending annually. Efficient financial transactions ecosystems from other industries and countries exhibit 2 features: immediate payment assurance and high use of automation throughout the process. The current system has an average transaction cost of $12 to $19 per claim across private payers and providers for more than 9 billion claims per year; each claim on average takes 4 to 6 weeks to process and pay. For simple claims, the transaction cost is $7 to $10 across private payers and providers; for complex claims, $35 to $40. Prior authorization on approximately 5000 codes has an average cost of $40 to $50 per submission for private payers and $20 to $30 for providers. Interventions aligned with a more efficient financial transactions ecosystem could reduce spending by $40 billion to $60 billion; approximately half is at the organizational level (scaling interventions being implemented by leading private payers and providers) and half at the industry level (adopting a centralized automated claims clearinghouse, standardizing medical policies for a subset of prior authorizations, and standardizing physician licensure for a national provider directory).
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  • 文章类型: Journal Article
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  • 文章类型: Journal Article
    背景:获得保险批准是美国医疗保健的必要组成部分,据估计,拒绝这些索赔会导致收入损失3%至5%。
    目的:检查鼻部手术保险否认的趋势。
    方法:对从2021年1月1日至2023年6月30日由3个机构的参与医生治疗的患者的未识别财务数据进行回顾性审查。通过CPT代码查询数据的鼻学和非鼻学程序。累积保险拒绝按程序和保险类型进行计算和分层。注销是与最终拒绝相关的美元金额。
    结果:对102,984个程序和访问的样本显示,各机构的最终拒绝率在2.2%至2.9%之间(p=.72)。最终注销的前三个鼻学程序是:鼻内窥镜检查(16.24%,$111,836.87),鼻清创术或息肉切除术(6.48%,$79,457.51),和鼻内病变的破坏(2.11%,56,932.20美元)。与Medicare或Medicaid相比,每种程序的注销百分比在商业保险付款人中最高。
    结论:鼻学手术的最终否认率介于2%和3%之间。诸如鼻内窥镜检查和鼻清创术之类的常见程序是最高的注销程序。拒绝保险可能会导致明显的收入损失。鼻学实践必须继续了解保险报销对其实践的变化和影响。
    BACKGROUND: Obtaining insurance approval is a necessary component of healthcare in the United States and denials of these claims have been estimated to result in a loss of 3% to 5% of revenue.
    OBJECTIVE: Examine the trends in insurance denials for rhinological procedures.
    METHODS: A retrospective review of deidentified financial data of patients who were treated by participating physicians across 3 institutions from January 1, 2021, to June 30, 2023. The data was queried for rhinological and non-rhinological procedures via CPT codes. Cumulative insurance denials were calculated and stratified by procedure and insurance type. Write-offs were dollar amounts associated with final denials.
    RESULTS: A sample of 102,984 procedures and visits revealed a final denial rate between 2.2% and 2.9% across institutions (p = .72). The top three rhinological procedures for final write-offs were: nasal endoscopy (16.24%, $111,836.87), nasal debridement or polypectomy (6.48%, $79,457.51), and destruction of intranasal lesion (2.11%, $56,932.20). The write-off percentage for each procedure was highest among commercial insurance payers as opposed to Medicare or Medicaid.
    CONCLUSIONS: Final denial rates of rhinology procedures ranged between 2% and 3%. Common procedures such as nasal endoscopy and nasal debridement are among the highest written-off procedures. Insurance denials can lead to notable revenue loss. Rhinology practices must continue to remain knowledgeable of the changes and effects of insurance reimbursement on their practice.
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  • 文章类型: Journal Article
    背景:由于增加的行政负担和不必要的治疗延误,事先授权(PA)过程经常受到医生的批评。PA政策对全髋关节置换术(THA)和全膝关节置换术(TKA)的影响尚未得到很好的描述。这项研究的目的是分析PA在4个州的大批量骨科实践中的使用。
    方法:我们前瞻性地收集了2020年至2023年在我们机构进行的28,725个主要THA和TKA的数据。收集的数据包括患者人口统计学,付款人批准或拒绝,批准或拒绝的时间,最初否认的次数,对等(P2P)或附录的数量,以及否认的理由。
    结果:七千五百二十八例(56.4%)接受THA的患者和8,283例(54%)接受TKA的患者需要PA,平均批准时间为26.3±34.6和33.7±41.5天,分别。在7,528名(4.6%)THA患者中的608名和8,283名(8.9%)TKA患者中的737名要求补遗。在总共312名(4.1%)最初否认的THA患者中,要求50名(0.7%)患者进行P2P,PA程序后,只有27人(0.4%)得到维持。在总共509名(6.1%)TKA患者中,要求55名(0.7%)患者进行P2P,PA程序后,只有26人(0.3%)得到维持。THA组的平均拒绝时间为64.7±83.5,拒绝的最常见原因是临床记录不佳(25.9%)和缺乏覆盖率(25.9%)。TKA组的平均拒绝时间为63.4±103.9天,付款人未指定最常见的拒绝原因(46.1%)。
    结论:使用PA批准选择性THA和TKA导致手术等待时间增加,外科医生和医护人员的行政负担很高。
    BACKGROUND: The prior authorization (PA) process is often criticized by physicians due to increased administrative burden and unnecessary delays in treatment. The effects of PA policies on total hip arthroplasty (THA) and total knee arthroplasty (TKA) have not been well described. The purpose of this study was to analyze the use of PA in a high-volume orthopaedic practice across 4 states.
    METHODS: We prospectively collected data on 28,725 primary THAs and TKAs performed at our institution between 2020 and 2023. Data collected included patient demographics, payer approval or denial, time to approval or denial, the number of initial denials, the number of peer-to-peer (P2P) or addenda, and the reasons for denial.
    RESULTS: Seven thousand five hundred twenty eight (56.4%) patients undergoing THA and 8,283 (54%) patients undergoing TKA required PA, with a mean time to approval of 26.3 ± 34.6 and 33.7 ± 41.5 days, respectively. Addenda were requested in 608 of 7,528 (4.6%) THA patients and 737 of 8,283 (8.9%) TKA patients. From a total of 312 (4.1%) THA patients who had an initial denial, a P2P was requested for 50 (0.7%) patients, and only 27 (0.4%) were upheld after the PA process. From a total of 509 (6.1%) TKA patients who had an initial denial, a P2P was requested for 55 (0.7%) patients, and only 26 (0.3%) were upheld after the PA process. The mean time to denial in the THA group was 64.7 ± 83.5, and the most common reasons for denial were poor clinical documentation (25.9%) and lack of coverage (25.9%). The mean time to denial in the TKA group was 63.4 ± 103.9 days, and the most common reason for denial was not specified by the payer (46.1%).
    CONCLUSIONS: The use of PA to approve elective THA and TKA led to increased surgical waiting times and a high administrative burden for surgeons and healthcare staff.
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