scholarly journals Use of Telemedicine for Buprenorphine Inductions in Patients With Commercial Insurance or Medicare Advantage

2022 ◽  
Vol 5 (1) ◽  
pp. e2142531
Author(s):  
Benjamin A. Barsky ◽  
Alisa B. Busch ◽  
Sadiq Y. Patel ◽  
Ateev Mehrotra ◽  
Haiden A. Huskamp
2021 ◽  
Vol 10 (3) ◽  
Author(s):  
Vinay Kini ◽  
Bridget Mosley ◽  
Sridharan Raghavan ◽  
Prateeti Khazanie ◽  
Steven M. Bradley ◽  
...  

Background Quality of care incentives and reimbursements for cardiovascular testing differ between insurance providers. We hypothesized that there are differences in the use of guideline‐concordant testing between Medicaid versus commercial insurance patients <65 years, and between Medicare Advantage versus Medicare fee‐for‐service patients ≥65 years. Methods and Results Using data from the Colorado All‐Payer Claims Database from 2015 to 2018, we identified patients eligible to receive a high‐value test recommended by guidelines: assessment of left ventricular function among patients hospitalized with acute myocardial infarction or incident heart failure, or a low‐value test that provides minimal patient benefit: stress testing prior to low‐risk surgery or routine stress testing within 2 years of percutaneous coronary intervention or coronary artery bypass graft surgery. Among 145 616 eligible patients, 37% had fee‐for‐service Medicare, 18% Medicare Advantage, 22% Medicaid, and 23% commercial insurance. Using multilevel logistic regression models adjusted for patient characteristics, Medicaid patients were less likely to receive high‐value testing for acute myocardial infarction (odds ratio [OR], 0.84 [0.73–0.98]; P =0.03) and heart failure (OR, 0.59 [0.51–0.70]; P <0.01) compared with commercially insured patients. Medicare Advantage patients were more likely to receive high‐value testing for acute myocardial infarction (OR, 1.35 [1.15–1.59]; P <0.01) and less likely to receive low‐value testing after percutaneous coronary intervention/ coronary artery bypass graft (OR, 0.63 [0.55–0.72]; P <0.01) compared with Medicare fee‐for‐service patients. Conclusions Guideline‐concordant testing was less likely to occur among patients with Medicaid compared with commercial insurance, and more likely to occur among patients with Medicare Advantage compared with fee‐for‐service Medicare. Insurance plan features may provide valuable targets to improve guideline‐concordant testing.


Medical Care ◽  
2017 ◽  
Vol 55 (11) ◽  
pp. 931-939 ◽  
Author(s):  
Elizabeth A. Carter ◽  
Pamela E. Morin ◽  
Keith D. Lind

Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 664-664
Author(s):  
Christopher T Su ◽  
Matthew J. Pianko ◽  
Minal Patel ◽  
Christine Veenstra

Abstract Introduction Currently, there are three FDA-approved novel multiple myeloma (MM) oral agents commonly used in clinical practice in the United States: two immunomodulators (lenalidomide [len] and pomalidomide [pom]) and one proteasome inhibitor (ixazomib [ixa]). The financial burden faced by patients with MM on these drugs can be considerable due to increasing long-term survival and extended periods of continuous single agent maintenance or multidrug combination regimens. To better understand the financial burden associated with extended use of these medications, we sought to leverage a real-world, all-claims insurance database to examine the outpatient drug copayments, associated fill patterns, and duration of therapy of these MM oral agents, stratified by insurance type. We hypothesize that copayments associated with oral MM agents will comprise a major portion of the overall drug copayment per patient, and fill patterns and duration of therapy of these medications will vary across patients of different insurance types. Methods We utilized outpatient drug claims derived from the 2014-2018 IBM/Truven MarketScan Commercial, Medicare Advantage, and Medicaid all-claims databases and extracted all outpatient claims from patients who filled at least one prescription (≥28-day duration) for len, pom, or ixa. Annual outpatient medication copayment and number of outpatient scripts were calculated for each patient, both for oral MM agents only and all outpatient prescriptions. Copayments were normalized to the cost per annum. Multivariable linear regression was used to compare outcomes between patients of the three insurance types. Results From 2014-2018, we identified 10,750 patients on len, 2,355 patients on pom, and 794 patients on ixa. These included patients with commercial insurance (53.5%), Medicare Advantage (37.8%), and Medicaid (8.7%). The average adjusted annual copayment per patient of len was $445 for commercial, $480 for Medicare Advantage, and $48 for Medicaid (Table 1). Len copayment comprised of 77-83% of the total outpatient drug copayment per patient. For pom, adjusted copayments were $460 for commercial, $749 for Medicare Advantage, and $128 for Medicaid. Pom copayment comprised 54-90% of the total. For ixa, adjusted copayments were $584 for commercial, $448 for Medicare Advantage and $2 for Medicaid. Ixa copayment comprised 7-48% of the total. Patients with commercial insurance generally filled more scripts for oral MM agents per year (6 len, 4 pom, 5 ixa) compared to those with Medicare Advantage (5 len, 5 pom, 4 ixa) and Medicaid (4 len, 4 pom, 4 ixa) (Table 2). However, patients with commercial insurance filled fewer overall outpatient scripts per year (31-37) compared to Medicare Advantage (35-42) and Medicaid (40-52). Insurance type was associated with the number of scripts filled for len (p&lt;0.0001) and ixa (p=0.01) after adjustment for age, but not pom (p=0.14). Among patients on oral MM therapy for more than one year, insurance type was associated with time on therapy for len (828 days for commercial, 873 days for Medicare Advantage, and 791 days for Medicaid, p=0.0004) (Table 3). However, insurance type was not associated with time on therapy for pom (p=0.83) or ixa (p=0.11). Discussion Our results demonstrate that copayments for oral MM agents comprise the majority of total outpatient drug copayments for patients with MM, suggesting that the out-of-pocket costs of these agents may be a key driver of financial burden. In addition to differences observed in the oral MM drug copayments, insurance type was also associated with the number of scripts filled and time on therapy for patients taking len. Thus, this suggests insurance type is also linked to drug utilization patterns and may indicate a differential financial burden in patients with MM on chronic oral therapy. Reducing the cumulative impact of financial toxicity for patients with MM is an important consideration for prescribers, payors, and health systems to achieve optimal clinical outcomes. Although our current dataset lacks diagnostic and treatment data, further correlative studies incorporating care utilization data, including inpatient admissions and outpatient clinical visits, are in progress. Figure 1 Figure 1. Disclosures Pianko: Karyopharm: Honoraria.


2017 ◽  
Vol 35 (8_suppl) ◽  
pp. 6-6 ◽  
Author(s):  
Jonas A. De Souza ◽  
Yen Yvonne Duong

6 Background: Pembrolizumab (PEM) and nivolumab (NIV) are FDA-approved immunotherapy agents for specific indications. These drugs are extremely costly to the health care system, payers, and ultimately, patients, and little is known about their utilization for non-FDA labeled indications (off-label). Methods: We reviewed claims for PEM and NIV using the focalPoint database by onPoint oncology, which provides access to clearinghouse data for 168 community oncology practices and 2000+ providers throughout the US. Clearinghouse data is unique as it links claims data with remittance (payer response) data. ICD codes representing malignancies other than head and neck cancer, melanoma, non-small cell lung cancer ,and claims for 3 indications prior to their FDA-approval were considered off-label. Primary insurance for the patients, as well as patients’ financial responsibility and amounts paid by the insurance were evaluated. Results: A total of 1,570 patients received PEM or NIV from January 1st 2015 to September 1st 2016 for a cumulative total of 7,687 distinct claims. Of these patients, 285 (18%) received these agents for off-label indications for a total of 978 distinct claims. The total cost for the insurance for off-label claims was $13.36 million with the following breakdown: $7.74 million for 111 patients with commercial insurance, $125 thousand for 5 patients with Medicaid, $3.85 million for 126 patients with Original Medicare, and $1.90 million for 43 patients with Medicare Advantage. The patient responsibility for the off-label immunotherapy agents, which included the co-insurance and co-pay, totaled to $1.06 million or $3,731 per patient. Patient responsibility for off-label therapy per payer was as follows: $657 per patient for commercial insurance, $0 for Medicaid, $7,436 for Original Medicare, and $1,248 for Medicare Advantage. Conclusions: A substantial number of patients received unsupported off-label immunotherapy treatment. The costs of these therapies to the health care system, payers, and patients warrant increased efforts to regulate their use in off-label settings lacking sufficient scientific evidence or while clinical trials are in progress.


Neurosurgery ◽  
2019 ◽  
Vol 66 (Supplement_1) ◽  
Author(s):  
Panagiotis Kerezoudis ◽  
Mohammed A Alvi ◽  
Anshit Goyal ◽  
Yagiz U Yolcu ◽  
Stephanie Payne ◽  
...  

Abstract INTRODUCTION Lumbar spine surgery has been reported to be associated with extremely high direct and associated costs and has thus been prioritized as a target for several quality improvement interventions. We aimed to identify factors associated with higher 90-d costs following elective posterior lumbar fusion (PLF) for degenerative lumbar spine disease among patients with commercial insurance and those on Medicare Advantage, using an administrative database. METHODS Optum Labs Data Warehouse was queried for patients undergoing PLF for degenerative lumbar spine disease between 2012 and 2015. Patients were stratified by insurance status (commercial or Medicare Advantage) and by the 9 US census regions. The primary outcome was all postoperative 90-d costs. RESULTS A total of 25 556 patients underwent a PLF, of which 67.6% had commercial insurance and 32.4% had Medicare Advantage. Regional 90-d adjusted mean costs per patient varied significantly between the 2o insurance groups, most notably for patients with commercial insurance ($123,950.38 for Mid-Atlantic region to $59,213.52 for patients in East South Central region). Multivariable regression analyses revealed that geographic region where surgery was performed, the number of operated levels, number of readmissions and number of ED visits were significantly associated with higher costs for each procedure. CONCLUSION There is significant regional variation in 90-d postoperative adjusted costs for patients on commercial and Medicare insurance undergoing PLF. These analyses are important to help surgeons develop region-specific interventions to alleviate the cost burden for patients and assist policy makers in designing more effective reimbursement policies for providers and hospitals.


2021 ◽  
Vol 4 (9) ◽  
pp. e2127349
Author(s):  
Alexander Everhart ◽  
Katrina Harper ◽  
Molly Moore Jeffery ◽  
Zachary Levin ◽  
Nancy E. Morden ◽  
...  

2019 ◽  
Vol 33 (09) ◽  
pp. 919-926
Author(s):  
Hunter Starring ◽  
William H. Waddell ◽  
William Steward ◽  
Stuart Schexnayder ◽  
Jack McKay ◽  
...  

AbstractAs more commercial insurance companies adopt a bundled reimbursement model, similar to the Comprehensive Care for Joint Replacement (CJR) algorithm for Medicare beneficiaries, accurate risk adjustment of patient-reported outcomes (PROs) is critical to ensure success. With this movement toward bundled reimbursement, it is unknown if a formula adjusting for similar risks in the Medicare population could be applied to PROs in commercially insured and Medicare Advantage populations undergoing total knee arthroplasty (TKA). This study was performed to compare PROs after TKA in these insurance groups after adjusting for proposed risks. Demographics and clinical data were abstracted from medical records of 302 patients who underwent TKA performed by a single surgeon at a university-based orthopaedic practice during 2013 to 2017. Differences in PROs between commercially insured, Medicare Advantage, and Medicare patients during the 6 months following surgery were evaluated while controlling for demographics, clinical data, and baseline PRO scores. Medicare and Medicare Advantage patients were older (p < 0.001) and had more comorbidities (p = 0.001) than commercial patients. During the first 3 months following TKA, patients in all three groups experienced similar rates of recovery. At 6 months after surgery, outcomes began to diverge by insurance group. Medicare patients reported significantly less ability to perform activities of daily living (78.6 vs. 63.2; p = 0.001), worse physical function (39.6 vs. 44.9; p = 0.003), and more pain interference (57.9 vs. 52.4; p = 0.018) at day 180 than commercially insured patients. There were no statistically significant differences between Medicare Advantage patients and either commercially insured or Medicare patients. Therefore, commercial insurance companies that intend to apply a risk-adjusted equation similar to the CJR algorithm to commercial populations should be cautioned since the postoperative outcomes in this investigation differed after adjusting for the same risk factors that have been proposed for inclusion in the CJR algorithm. Nonetheless, further studies should be performed to ensure that companies participating in bundled reimbursement models have a positive influence on comprehensive health care for patients and providers. This is a level III, retrospective prognostic study


Neurosurgery ◽  
2019 ◽  
Vol 66 (Supplement_1) ◽  
Author(s):  
Panagiotis Kerezoudis ◽  
Mohammed A Alvi ◽  
Anshit Goyal ◽  
Yagiz U Yolcu ◽  
Stephanie Payne ◽  
...  

Abstract INTRODUCTION Anterior Cervical Discectomy and Fusion (ACDF) has been shown to be associated with high direct and associated costs. We aimed to identify factors associated with higher 90-day costs following elective ACDF for degenerative cervical spine disease among patients with commercial insurance and those on Medicare Advantage, using an administrative database. METHODS Optum Labs Data Warehouse (OLDH) was queried for patients undergoing an anterior cervical decompression and fusion (ACDF) for degenerative cervical spine disease. between 2012 and 2015. Geographic variations were evaluated as per U.S. Census Division. Patients were stratified by insurance status (commercial or Medicare advantage) and by the 9 US census regions. The primary outcome was all postoperative 90-d costs. RESULTS A total of 29 380 patients underwent an ACDF of which 86.7% patients had commercial insurance while 13.3% had Medicare Advantage. Regional 90-d adjusted mean costs per patient varied significantly between the 2 insurance groups, most notably for patients with commercial insurance undergoing ACDF ($70,765.17 for Mid-Atlantic to $29,364.02 for East South Central). Multivariable regression analyses revealed that the geographic region where procedure was performed, number of operated levels, number of readmissions and number of ED visits were significantly associated with higher costs. CONCLUSION There is significant regional variation in 90-d postoperative adjusted costs for patients on commercial and Medicare insurance undergoing elective ACDF. These analyses are important to help surgeons develop region-specific interventions to alleviate the cost burden for patients and assist policymakers in designing better risk-adjusted reimbursement policies for providers and hospitals.


2021 ◽  
Vol 4 (2) ◽  
pp. e2035792
Author(s):  
Rozalina G. McCoy ◽  
Holly K. Van Houten ◽  
Yihong Deng ◽  
Pinar Karaca Mandic ◽  
Joseph S. Ross ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document