scholarly journals Cancer history, insurance coverage, and cost-related medication nonadherence in Medicare beneficiaries, 2013-2018

2021 ◽  
Vol 27 (12) ◽  
pp. 1750-1756
Author(s):  
Meng Li ◽  
Mark Bounthavong
2019 ◽  
Vol 111 (8) ◽  
pp. 795-802 ◽  
Author(s):  
Sarah Knerr ◽  
Erin J A Bowles ◽  
Kathleen A Leppig ◽  
Diana S M Buist ◽  
Hongyuan Gao ◽  
...  

Abstract Background Genetic testing to determine BRCA status has been available for over two decades, but there are few population-based studies of test diffusion. We report 10-year trends in BRCAtesting in an integrated health-care system with long-standing access to genetic services. Methods A cohort of women aged 18 years and older was created to ascertain BRCA testing (n = 295 087). Annual testing rates between 2005 and 2015 were calculated in all women with and without incident (ie, newly diagnosed) breast and ovarian cancers and in clinically eligible subgroups by family cancer history, personal cancer history, and age at diagnosis. Secular trends were assessed using Poisson regression. Women tested early (2005–2008), midway (2009–2012), and late (2013–2015) in the study period were compared in cross-sectional analyses. Results Between 2005 and 2015, annual testing rates increased from 0.6/1000 person-years (pys) (95% confidence interval [CI] = 0.4 to 0.7/1000 pys) to 0.8/1000 pys (95% CI = 0.6 to 1.0/1000 pys) in women without incident breast or ovarian cancers. Rates decreased from 71.5/1000 pys (95% CI = 42.4 to 120.8/1000 pys) to 44.4/1000 pys (95% CI = 35.5 to 55.6/1000 pys) in women with incident diagnoses, despite improvements in provision of timely BRCA testing during this time frame. We found no evidence of secular trends in clinically eligible subgroups including women with family history indicating increased hereditary cancer risk, but no personal cancer history. At the end of the study period, 97.0% (95% CI = 96.6% to 97.3%) of these women remained untested. Conclusion Many eligible women did not receive BRCA testing despite having insurance coverage and access to specialty genetic services, underscoring challenges to primary and secondary hereditary cancer prevention.


Circulation ◽  
2018 ◽  
Vol 137 (suppl_1) ◽  
Author(s):  
Gabriel Tajeu ◽  
Shia T Kent ◽  
Lei Huang ◽  
Daichi Shimbo ◽  
Marie Krousel-Wood ◽  
...  

Introduction: Nonadherence to antihypertensive medication is common and associated with cardiovascular disease events. A previous study reported improvements in antihypertensive medication adherence among adults ≥65 years of age. It is unclear if this trend has also occurred among younger adults. Methods: Changes in antihypertensive medication nonadherence were calculated among commercially-insured US adults <65 years of age initiating treatment from 2007 to 2014 using MarketScan claims data. We required beneficiaries have ≥2 diagnoses for hypertension (ICD-9, 401.xx) and insurance coverage for 365 days prior to and following antihypertensive medication initiation. Initiation was defined by a pharmacy claim for antihypertensive medication with no claims for medication within the previous 365 days. During the 365 days after initiation, nonadherence was defined as having a proportion of days covered <80%. Results: The percentage of patients who were nonadherent to their antihypertensive medication was 55.6% in 2007 and 54.1% in 2014 (p-trend<0.001) ( Table ). After multivariable adjustment, the relative risk (RR) of nonadherence in 2014 compared with 2007 was 0.98 (95% CI 0.96-0.99). Risk for nonadherence was lower at older age (RR 0.73, 95% CI 0.71-0.74 comparing adults 55-64 to <25 years of age). Nonadherence was more common among adults that were female versus male (RR 1.05; 95% CI 1.05-1.06), initiated treatment with a loop diuretic (RR 1.26; 95% CI 1.24-1.28), had diabetes (RR 1.11; 95% CI 1.10-1.12), or experienced a serious fall injury after medication initiation (RR 1.10; 95% CI 1.06-1.15), and less common among adults initiating treatment with an angiotensin receptor blocker (RR 0.96; 95% CI 0.95-0.96), multiclass regimen (RR 0.89; 95% CI 0.88-0.90), receiving 90-day fills (RR 0.73; 95% CI 0.73-0.74), or medications by mail (RR 0.92; 95% CI 0.91-0.93). Conclusion: Among adults <65 years of age, nonadherence to antihypertensive medication did not meaningfully decrease between 2007 and 2014.


2015 ◽  
Vol 33 (4) ◽  
pp. 312-318 ◽  
Author(s):  
Joan L. Warren ◽  
Eboneé N. Butler ◽  
Jennifer Stevens ◽  
Christopher S. Lathan ◽  
Anne-Michelle Noone ◽  
...  

Purpose Medicare beneficiaries with cancer bear a greater portion of their health care costs, because cancer treatment costs have increased. Beneficiaries have supplemental insurance to reduce out-of-pocket costs; those without supplemental insurance may face barriers to care. This study examines the association between type of supplemental insurance coverage and receipt of chemotherapy among Medicare patients with cancer who, per National Comprehensive Cancer Network treatment guidelines, should generally receive chemotherapy. Patients and Methods This retrospective, observational study included 1,200 Medicare patients diagnosed with incident cancer of the breast (stage IIB to III), colon (stage III), rectum (stage II to III), lung (stage II to IV), or ovary (stage II to IV) from 2000 to 2005. Using the National Cancer Institute Patterns of Care Studies and linked SEER-Medicare data, we determined each Medicare patient's supplemental insurance status (private insurance, dual eligible [ie, Medicare with Medicaid], or no supplemental insurance), consultation with an oncologist, and receipt of chemotherapy. Using adjusted logistic regression, we evaluated the association of type of supplemental insurance with oncologist consultation and receipt of chemotherapy. Results Dual-eligible patients were significantly less likely to receive chemotherapy than were Medicare patients with private insurance. Patients with Medicare only who saw an oncologist had comparable rates of chemotherapy compared with Medicare patients with private insurance. Conclusion Dual-eligible Medicare beneficiaries received recommended cancer chemotherapy less frequently than other Medicare beneficiaries. With the increasing number of Medicaid patients under the Affordable Care Act, there will be a need for patient navigators and sufficient physician reimbursement so that low-income patients with cancer will have access to oncologists and needed treatment.


2020 ◽  
Vol 68 (12) ◽  
pp. 2872-2880
Author(s):  
Shirley M. Bluethmann ◽  
Eileen Flores ◽  
Grace Campbell ◽  
Heidi D. Klepin

1998 ◽  
Vol 26 (4) ◽  
pp. 267-289 ◽  
Author(s):  
Diane E. Hoffmann

The problem of inadequate pain management for both terminally ill patients and patients with chronic pain has recently been documented by a number of authors and studies. A 1997 report by the Institute of Medicine (IOM), for example, states that “a significant proportion of dying patients and patients with advanced disease experience serious pain, despite the availability of effective pharmacological and other options for relieving most pain.” There are particularly impressive data that pain associated with cancer is not adequately treated.The problem has been attributed to (1) inadequate education of physicians on approaches to pain management and an often misguided belief that prolonged therapy with certain pain medication will lead to addiction; (2) legal obstacles, such as physicians’ fear of criminal prosecution and other disciplinary actions by state licensing boards for overprescribing narcotics; and (3) inadequate insurance coverage as a result of narrow eligibility criteria for hospice care for Medicare beneficiaries, and inadequate reimbursement more generally for pain management and palliative care.


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