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1.
Ann Intern Med ; 177(3): 353-362, 2024 Mar.
Article in English | MEDLINE | ID: mdl-38316009

ABSTRACT

BACKGROUND: In addition to the physical disease burden of the COVID-19 pandemic, concern exists over its adverse mental health effects. OBJECTIVE: To characterize trends in psychological distress and outpatient mental health care among U.S. adults from 2018 to 2021 and to describe patterns of in-person, telephone, and video outpatient mental health care. DESIGN: Cross-sectional nationally representative survey of noninstitutionalized adults. SETTING: United States. PARTICIPANTS: Adults included in the Medical Expenditure Panel Survey Household Component, 2018 to 2021 (n = 86 658). MEASUREMENTS: Psychological distress was measured with the Kessler-6 scale (range of 0 to 24, with higher scores indicating more severe distress), with a score of 13 or higher defined as serious psychological distress, 1 to 12 as less serious distress, and 0 as no distress. Outpatient mental health care use was measured via computer-assisted personal interviews. RESULTS: Between 2018 and 2021, the rate of serious psychological distress among adults increased from 3.5% to 4.2%. Although the rate of outpatient mental health care increased from 11.2% to 12.4% overall, the rate decreased from 46.5% to 40.4% among adults with serious psychological distress. When age, sex, and distress were controlled for, a significant increase in outpatient mental health care was observed for young adults (aged 18 to 44 years) but not middle-aged (aged 45 to 64 years) and older (aged >65 years) adults and for employed adults but not unemployed adults. In 2021, 33.4% of mental health outpatients received at least 1 video visit, including a disproportionate percentage of young, college-educated, higher-income, employed, and urban adults. LIMITATION: Information about outpatient mental health service modality (in-person, video, telephone) was first fully available in the 2021 survey. CONCLUSION: These trends and patterns underscore the persistent challenges of connecting older adults, unemployed persons, and seriously distressed adults to outpatient mental health care and the difficulties faced by older, less educated, lower-income, unemployed, and rural patients in accessing outpatient mental health care via video. PRIMARY FUNDING SOURCE: None.


Subject(s)
COVID-19 , Psychological Distress , Young Adult , Humans , United States/epidemiology , Aged , Adolescent , Adult , Outpatients , Mental Health , COVID-19/epidemiology , Cross-Sectional Studies , Pandemics , Stress, Psychological/epidemiology , Stress, Psychological/psychology
2.
J Ment Health Policy Econ ; 26(4): 159-183, 2023 Dec 01.
Article in English | MEDLINE | ID: mdl-38113386

ABSTRACT

BACKGROUND: The COVID-19 pandemic has been widely reported to have increased symptoms of anxiety, depression, and other mental health issues. It may also have significantly disrupted continuity of treatment for existing patients and made access for those newly seeking care more difficult at a time when treatment needs are higher. AIMS OF THE STUDY: This study seeks to examine the impact of the COVID-19 pandemic on mental health status and mental health treatment among adults residing in the U.S. civilian, non-institutionalized population. METHODS: The data are drawn from the 2019-2020 Medical Expenditure Panel Survey (MEPS), a nationally representative household survey of the U.S. civilian non-institutionalized population conducted annually since 1996 and used extensively to study mental health treatment in the U.S. I examine unadjusted and regression-adjusted differences between 2019 and 2020 in perceived mental health status (excellent, very good, good, fair, poor) and in the K6 general psychological distress, the PHQ-2 depression screener, and the VR-12 mental component summary score. Similarly, using the detailed MEPS data on health care encounters and prescription drug fills, I examine differences in mental health use treatment between 2019 and 2020. I focus specifically on changes in continuity of treatment among those already in treatment in January and February, before the pandemic fully struck, as well differences in the initiation of new episodes of treatment after the pandemic began. RESULTS: All four mental health scales included in the MEPS show statistically significant declines in mental health between 2019 and 2020, particularly among younger adults. On balance, the percentage of US adults receiving mental health treatment did not change significantly. Continuity of treatment increased slightly in 2020, with 87.1% of adults in treatment January or February still receiving care in the second quarter, an increase of 2.5 percentage points (p=.025). However, there were significant declines in the initiation of new episodes of treatment, especially in the second quarter of 2020. DISCUSSION: While the continuity of treatment among adults already in care when the COVID pandemic first led to nationwide disruptions is welcome news, the decline in new episodes of mental health treatment among those not previously treated is of great concern. In a time of heightened need, the gap between need and treatment likely grew larger. IMPLICATIONS FOR HEALTH CARE PROVISION AND USE, AND IMPLICATIONS FOR HEALTH POLICIES: Continued long-term monitoring of the mental health needs and treatment gaps will be important, especially as many emergency measures designed to mitigate the effects of the pandemic on access to mental health treatment expire.


Subject(s)
COVID-19 , Mental Health , Adult , Humans , Pandemics , Psychotherapy , Data Collection
3.
Cancer ; 127(15): 2752-2761, 2021 08 01.
Article in English | MEDLINE | ID: mdl-33945632

ABSTRACT

BACKGROUND: Although informal caregivers such as family and friends provide people with cancer needed physical care and emotional support, little is known about which individuals have access to such caregivers. The purpose of this article is to provide a nationally representative description of the sociodemographic characteristics of cancer survivors who have or had an informal caregiver in the United States. METHODS: Cross-sectional data were taken from the Experiences With Cancer Survivorship Supplement of the Medical Expenditure Panel Survey in 2011, 2016, and 2017. People were cancer survivors from diagnosis until the end of life. The study population consisted of adult survivors of cancer other than nonmelanoma skin cancer who were treated for cancer less than 3 years before the survey and were living in the community (n = 720). The main outcome measure was whether or not the cancer survivor reported having an informal caregiver. RESULTS: In the United States, 55.2% of cancer survivors reported having an informal caregiver during or after their cancer treatment. The relationship of the caregiver to the survivor varied by sex: males were more likely to have a spouse as their caregiver, and females were more likely to have a child as their caregiver. In multivariate analyses, cancer survivors who were female, were married, were of a race/ethnicity other than White, or were in poor health were more likely to have an informal caregiver. CONCLUSIONS: Future research can examine whether those without informal caregivers might need more formal support as they undergo cancer treatment and transition into cancer survivorship.


Subject(s)
Cancer Survivors , Neoplasms , Adult , Caregivers/psychology , Child , Cross-Sectional Studies , Female , Humans , Male , Neoplasms/therapy , Quality of Life/psychology , Survivors
4.
Am J Public Health ; 111(12): 2157-2166, 2021 12.
Article in English | MEDLINE | ID: mdl-34878880

ABSTRACT

The COVID-19 pandemic caused substantial disruptions in the field operations of all 3 major components of the Medical Expenditure Panel Survey (MEPS). The MEPS is widely used to study how policy changes and major shocks, such as the COVID-19 pandemic, affect insurance coverage, access, and preventive and other health care utilization and how these relate to population health. We describe how the MEPS program successfully responded to these challenges by reengineering field operations, including survey modes, to complete data collection and maintain data release schedules. The impact of the pandemic on response rates varied considerably across the MEPS. Investigations to date show little effect on the quality of data collected. However, lower response rates may reduce the statistical precision of some estimates. We also describe several enhancements made to the MEPS that will allow researchers to better understand the impact of the pandemic on US residents, employers, and the US health care system. (Am J Public Health. 2021;111(12):2157-2166. https://doi.org/10.2105/AJPH.2021.306534).


Subject(s)
COVID-19/epidemiology , Health Expenditures/statistics & numerical data , Surveys and Questionnaires/statistics & numerical data , Electronic Health Records/statistics & numerical data , Health Services/statistics & numerical data , Humans , Insurance Coverage/organization & administration , Insurance Coverage/statistics & numerical data , Pandemics , Patient Acceptance of Health Care/statistics & numerical data , Population Health/statistics & numerical data , Quality of Health Care/statistics & numerical data , SARS-CoV-2 , Telemedicine/statistics & numerical data , United States/epidemiology
7.
J Ment Health Policy Econ ; 23(3): 151-182, 2020 Sep 01.
Article in English | MEDLINE | ID: mdl-33411677

ABSTRACT

BACKGROUND: The Affordable Care Act (ACA) gives states the option of expanding Medicaid coverage to low-income individuals; however, not all states have chosen to expand Medicaid. The ACA Medicaid expansions are particularly important for Americans with mental health conditions because they are substantially more likely than other Americans to have low incomes. AIMS OF THE STUDY: We examine the impact of Medicaid expansion on adults who were newly eligible for Medicaid using the 2008-2017 Medical Expenditure Panel Survey (MEPS). METHODS: We use the AHRQ PUBSIM model to identify low-income adults aged 19-64 who were either newly Medicaid eligible if they lived in an expansion state or would have been eligible had their state opted to expand its Medicaid program. We estimate linear probability models within a difference-in-difference framework. An additional interaction term allows us to test for differences among those with serious psychological distress (SPD) or probable depression (PD). Outcomes of interest are insurance coverage by type, behavioral health treatment by service (specifically, any behavioral health treatment, any specialty treatment, any psychotropic medication, any ambulatory treatment outside of an emergency department, and any emergency department treatment), quantities of behavioral health treatment services, and out of pocket spending on healthcare. RESULTS: Our adjusted difference-in-differences estimates indicate Medicaid expansion increased any insurance coverage by 14.2 percentage points and increased Medicaid coverage by 21.2 percentage points. Insurance coverage for individuals with SPD/PD in expansion states increased by an additional 12.9 percentage points. Medicaid expansion did not have an effect on behavioral health treatment for the newly eligible population as a whole or for the subset with SPD/PD. DISCUSSION: Consistent with previous Medicaid expansions, we find that the ACA Medicaid expansions substantially increased insurance rates for the newly Medicaid-eligible population, regardless of mental health status but the overall effect on insurance coverage was stronger among those with SPD/PD. The lack of an effect on treatment use suggests that providing insurance coverage alone may be insufficient to guarantee that people with mental illness will receive the treatment they need. Limitations include that our difference-in-difference estimator may not account for time-varying factors that change contemporaneously with the expansions. Our estimates may also be affected by other provisions of the ACA that went into effect at the same time as the Medicaid expansions. IMPLICATIONS FOR HEALTH CARE PROVISION AND USE AND IMPLICATIONS FOR HEALTH POLICIES: Although the ACA has resulted in increased coverage for low-income individuals, more outreach efforts may be needed to encourage individuals with mental illness to get the treatment they need.


Subject(s)
Health Services Accessibility/statistics & numerical data , Insurance Coverage/statistics & numerical data , Medicaid , Mental Disorders/therapy , Mental Health Services/statistics & numerical data , Patient Protection and Affordable Care Act/statistics & numerical data , Adult , Humans , Insurance, Health , Mental Disorders/economics , Middle Aged , United States , Young Adult
8.
Health Econ ; 28(9): 1151-1158, 2019 09.
Article in English | MEDLINE | ID: mdl-31264323

ABSTRACT

Many older Americans have poor access to dental care, resulting in a high prevalence of oral health problems. Because traditional Medicare does not include dental care benefits, only older Americans who are employed, have post-retirement dental benefits or spousal coverage, or enroll in certain Medicare Advantage plans are able to obtain dental care coverage. We seek to determine the extent to which poor access to dental insurance and high out-of-pocket costs affect dental service use by the elderly. Using the 2007-2015 Medical Expenditure Panel Survey and supplemental data on dental care prices, we estimate a demand system for preventive dental services and basic and major restorative services. Selection into dental and medical insurance is addressed using a correlated random effects panel data specification. Consistent with prior studies of the nonelderly population, dental service use was not sensitive to out-of-pocket prices. However, private dental insurance increased preventive service use by 25%, and dental coverage through Medicaid increased basic and major service use by 23% and 36%, respectively. The use of services was more responsive to dental insurance for women than men. These estimates suggest that a Medicare dental benefit could significantly increase dental service use by older Americans.


Subject(s)
Dental Care for Aged/economics , Health Services Accessibility/economics , Health Services Needs and Demand/economics , Aged , Female , Humans , Insurance, Dental/economics , Male , Medicaid/economics , Medicare/economics , Medicare Part C/economics , Models, Economic , United States
9.
J Gen Intern Med ; 33(8): 1317-1323, 2018 08.
Article in English | MEDLINE | ID: mdl-29855861

ABSTRACT

BACKGROUND: US Preventive Services Task Force (USPSTF) released new recommendations on statin use for atherosclerotic cardiovascular disease (ASCVD) prevention. The Affordable Care Act (ACA) mandates USPSTF recommendations with an "A" or "B" grade receive insurance coverage without copayment. We assessed the potential impact of these recommendations. OBJECTIVE: To assess the US population meeting criteria for statin use and factors associated with use, and calculate associated costs. DESIGN AND MEASURES: We estimated 10-year ASCVD event risk scores from National Health and Nutrition Examination Survey data using Pooled Cohort Equations from the American College of Cardiology/American Heart Association and applied them to Medical Expenditure Panel Survey data. We estimated the population meeting USPSTF criteria and calculated the number of statin prescription fills and out-of-pocket and total costs. We assessed associations between statin use and sociodemographic and health characteristics and national trends in use from 1996 to 2014. PARTICIPANTS: A nationally representative sample of people aged ≥ 40 years, representing 150 million people living in the USA. KEY RESULTS: Of 26.8 million adults recommended for statins, only 41.8% were taking them. Female sex, Hispanic ethnicity, uninsured status, or living in the South was associated with lower odds of using statins. Under ACA, people with private insurance would avoid out-of-pocket cost of $9 for each generic prescription, resulting in savings of approximately $44 in annual costs. ACA's mandate for insurance coverage would result in a $193 million shift in out-of-pocket cost for statins from patients to private insurers. CONCLUSIONS: New USPSTF recommendations may result in decreased out-of-pocket costs and expanded access to statins. Previous research has shown that eliminating copayments increased adherence and decreased rates of ASCVD events without increasing overall healthcare costs. Future research will determine whether the USPSTF's recommendations will result in similar findings.


Subject(s)
Atherosclerosis/prevention & control , Guideline Adherence , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Adult , Aged , Aged, 80 and over , Atherosclerosis/epidemiology , Female , Health Surveys , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/economics , Male , Middle Aged , Primary Prevention/economics , Primary Prevention/methods , Risk Factors , United States/epidemiology
10.
Health Econ ; 23(1): 14-32, 2014 Jan.
Article in English | MEDLINE | ID: mdl-23349123

ABSTRACT

Chronic tooth decay is the most common chronic condition in the United States among children ages 5-17 and also affects a large percentage of adults. Oral health conditions are preventable, but less than half of the US population uses dental services annually. We seek to examine the extent to which limited dental coverage and high out-of-pocket costs reduce dental service use by the nonelderly privately insured and uninsured. Using data from the 2001-2006 Medical Expenditure Panel Survey and an American Dental Association survey of dental procedure prices, we jointly estimate the probability of using preventive and both basic and major restorative services through a correlated random effects specification that controls for endogeneity. We found that dental coverage increased the probability of preventive care use by 19% and the use of restorative services 11% to 16%. Both conditional and unconditional on dental coverage, the use of dental services was not sensitive to out-of-pocket costs. We conclude that dental coverage is an important determinant of preventive dental service use, but other nonprice factors related to consumer preferences, especially education, are equal if not stronger determinants.


Subject(s)
Dental Health Services/economics , Dental Prophylaxis/economics , Health Services Needs and Demand/economics , Insurance, Dental/economics , Adolescent , Adult , Child , Child, Preschool , Chronic Disease , Dental Care for Children/economics , Dental Care for Children/statistics & numerical data , Dental Caries/epidemiology , Dental Health Services/statistics & numerical data , Dental Health Services/trends , Dental Prophylaxis/statistics & numerical data , Financing, Personal/economics , Financing, Personal/trends , Health Services Needs and Demand/trends , Humans , Infant , Insurance, Dental/standards , Insurance, Dental/trends , Medicaid/economics , Medicaid/statistics & numerical data , Middle Aged , United States/epidemiology , Young Adult
11.
J Ambul Care Manage ; 47(2): 64-83, 2024.
Article in English | MEDLINE | ID: mdl-38345888

ABSTRACT

The COVID-19 pandemic produced an unprecedented shock to the U.S. health care system. Prior literature documenting 2020 changes has been limited to certain types of care or subsets of patients. We use the nationally representative Medical Expenditure Panel Survey to summarize changes in all types of health care from 2018 through 2020. Outpatient visits, emergency department visits, and inpatient admissions each fell about 35% in April 2020. Dental visits fell over 80%. Ophthalmology visits declined 71% and mammograms 82%. Psychiatric visits rose slightly (1.6%). By the end of 2020, specialist physician visits recovered, though primary care and dental visits remained 12% lower than 2019.


Subject(s)
Emergency Service, Hospital , Pandemics , Humans , United States , Delivery of Health Care , Hospitalization , Emergency Room Visits
12.
JAMA Psychiatry ; 81(6): 606-610, 2024 Jun 01.
Article in English | MEDLINE | ID: mdl-38477899

ABSTRACT

Importance: Despite a federal declaration of a national child and adolescent mental health crisis in 2021, little is known about recent national trends in mental health impairment and outpatient mental health treatment of US children and adolescents. Objective: To characterize trends in mental health impairment and outpatient mental health care among US children and adolescents from 2019 to 2021 across demographic groups and levels of impairment. Design, Setting, and Participants: Survey study with a repeated cross-sectional analysis of mental health impairment and outpatient mental health care use among youth (ages 6-17 years) within the 2019 and 2021 Medical Expenditure Panel Surveys, nationally representative surveys of US households. Race and ethnicity were parent reported separately from 15 racial categories and 8 ethnic categories that were aggregated into Black, non-Hispanic; Hispanic; Other, non-Hispanic; and White, non-Hispanic. Exposure: Time period from 2019 to 2021. Main Outcomes and Measures: Age- and sex-adjusted differences between 2019 and 2021 in mental health impairment measured with the Columbia Impairment Scale (a score ≥16 indicates severe; 1-15, less severe; and 0, no impairment) and age-, sex-, and Columbia Impairment Scale strata-adjusted differences in the use of any outpatient mental health care in 2019 and 2021. Results: The analysis involved 8331 participants, including 4031 girls and 4300 boys; among them, 1248 were Black and 3385 were White. The overall mean (SE) age was 11.6 (3.4) years. The percentage of children and adolescents with severe mental health impairment was 9.7% in 2019 and 9.4% in 2021 (adjusted difference, -0.3%; 95% CI, -1.9% to 1.2%). Between 2019 and 2021, there was also no significant difference in the percentage of children and adolescents with less severe impairment and no impairment. The overall annual percentages of children with any outpatient mental health care showed little change: 11.9% in 2019 and 13.0% in 2021 (adjusted difference, 1.3%; 95% CI, -0.4% to 3.0%); however, this masked widening differences by race. Outpatient mental health care decreased for Black youth from 9.2% in 2019 to 4.0% in 2021 (adjusted difference, -4.3%; 95% CI, -7.3% to -1.4%) and increased for White youth from 15.1% to 18.4% (adjusted difference, 3.0%; 95% CI, 0.0% to 6.0%). Conclusions and Relevance: Between 2019 and 2021, there was little change in the overall percentage of US children and adolescents with severe mental health impairment. During this period, however, there was a significant increase in the gap separating outpatient mental health care of Black and White youth.


Subject(s)
Ambulatory Care , Mental Disorders , Mental Health Services , Humans , Adolescent , Child , Male , Female , United States , Mental Disorders/therapy , Mental Disorders/epidemiology , Mental Disorders/ethnology , Ambulatory Care/statistics & numerical data , Mental Health Services/statistics & numerical data , Cross-Sectional Studies , Ethnicity/statistics & numerical data
13.
Psychiatr Serv ; 74(7): 674-683, 2023 Jul 01.
Article in English | MEDLINE | ID: mdl-36597696

ABSTRACT

OBJECTIVE: The authors aimed to compare national rates and patterns of use of outpatient mental health care among Hispanic, non-Hispanic Black, and non-Hispanic White individuals. METHODS: Data from the 2018-2019 Medical Expenditure Panel Survey, a nationally representative survey of U.S. households, were analyzed, focusing on use of any outpatient mental health care service by non-Hispanic White (N=29,126), non-Hispanic Black (N=7,965), and Hispanic (N=12,640) individuals ages ≥4 years (N=49,731). Among individuals using any mental health care, analyses focused on those using psychotropic medications, psychotherapy, or both and on receipt of minimally adequate mental health care. RESULTS: The annual rate per 100 persons of any outpatient mental health service use was more than twice as high for White (25.3) individuals as for Black (12.2) or Hispanic (11.4) individuals. Among those receiving outpatient mental health care, Black (69.9%) and Hispanic (68.4%) patients were significantly less likely than White (83.4%) patients to receive psychotropic medications, but Black (47.7%) and Hispanic (42.6%) patients were significantly more likely than White (33.3%) patients to receive psychotherapy. Among those treated for depression, anxiety, attention-deficit hyperactivity disorder, or disruptive behavior disorders, no significant differences were found in the proportions of White, Black, or Hispanic patients who received minimally adequate treatment. CONCLUSIONS: Large racial-ethnic gaps in any mental health service use and smaller differences in patterns of treatment suggest that achieving racial-ethnic equity in outpatient mental health care delivery will require dedicated efforts to promote greater mental health service access for Black and Hispanic persons in need.


Subject(s)
Healthcare Disparities , Mental Health , Humans , Ethnicity , Healthcare Disparities/ethnology , Healthcare Disparities/statistics & numerical data , Hispanic or Latino , Outpatients , Psychotropic Drugs/therapeutic use , Racial Groups , United States , Mental Health Services , Black or African American , White
14.
Health Serv Res ; 57 Suppl 2: 183-194, 2022 12.
Article in English | MEDLINE | ID: mdl-35811358

ABSTRACT

OBJECTIVE: To estimate the effects of Affordable Care Act (ACA) Medicaid expansion on insurance and health services use for adults with disabilities who were newly eligible for Medicaid. DATA SOURCES: 2008-2018 Medical Expenditure Panel Survey data. STUDY DESIGN: We used the Agency for Healthcare Research and Quality (AHRQ) PUBSIM model to identify adults aged 26-64 years with disabilities who were newly Medicaid-eligible in expansion states or would have been eligible in non-expansion states had those states opted to expand. Outcomes included insurance coverage; access to care; receipt of primary care, outpatient specialty physician services, and preventive services; and out-of-pocket health care spending. To estimate the effects of Medicaid expansion, we used two-way fixed effects models and a triple differences framework to compare pre-post changes in each outcome in expansion and non-expansion states for adults with and without disabilities. EXTRACTION METHODS: We simulated Medicaid eligibility with the AHRQ PUBSIM model, which uses state-specific Medicaid rules and MEPS data on family relationships, state of residence, and income. PRINCIPAL FINDINGS: Among adults with disabilities who were newly eligible for Medicaid, Medicaid expansion was associated with significant increases in full-year Medicaid coverage (35.9 percentage points [pp], p < 0.001), receipt of primary care (15.5 pp, p < 0.01), and receipt of flu shots (19.2 pp, p < 0.01), and a significant decrease in out-of-pocket spending (-$457, p < 0.01). There were larger improvements for adults with disabilities compared to those without disabilities in full-year Medicaid coverage (11.0 pp, p < 0.01) and receipt of flu shots (18.0 pp, p < 0.05). CONCLUSIONS: Medicaid expansion was associated with improvements in full-year insurance coverage, receipt of primary and preventive care, and out-of-pocket spending for adults with disabilities who were newly eligible for Medicaid. For insurance coverage, preventive care, and some primary care measures, there were differentially larger improvements for adults with disabilities than for those without disabilities.


Subject(s)
Disabled Persons , Medicaid , Adult , United States , Humans , Patient Protection and Affordable Care Act , Insurance, Health , Health Services Accessibility , Insurance Coverage , Health Services
15.
Inquiry ; 48(3): 242-59, 2011.
Article in English | MEDLINE | ID: mdl-22235548

ABSTRACT

This paper assesses the quality of the Medical Expenditure Panel Survey (MEPS) drug data and the impact that misreporting prescription drug data has on descriptive and behavioral analyses. It does this by matching MEPS participants with Medicare Part D coverage during the period 2006-2007 to their Part D claims data. In the validation sample, the number of drug fills and total expenditures are reasonably accurate compared with claims. Household respondents tended to underreport the number of different drugs taken, but tended to overreport the number of fills of each drug. Behavioral analyses of the determinants of medication use and expenditures were largely unaffected because underreporting cut across most sociodemographic groups.


Subject(s)
Data Collection/methods , Health Services Research/methods , Medicare Part D/statistics & numerical data , Prescription Drugs/economics , Prescription Fees/statistics & numerical data , Aged , Aged, 80 and over , Drug Utilization , Female , Humans , Male , Middle Aged , Reproducibility of Results , Socioeconomic Factors , United States
16.
Med Care Res Rev ; 78(4): 392-403, 2021 08.
Article in English | MEDLINE | ID: mdl-32028834

ABSTRACT

A long line of studies document substantial and persistent racial and ethnic disparities in the use of mental health services. Many recent studies follow the Institute of Medicine's definition of disparities, adjusting only for differences in health and mental health status across groups. However, controlling for mental health may mask important changes in the magnitudes of disparities at different levels of mental health need. We extend the previous literature by explicitly estimating how differences in treatment use across groups change at different levels of psychological distress. We used detailed data on sociodemographic characteristics, health insurance coverage, treatment, and the K6 psychological distress scale from the 2010 to 2015 Medical Expenditure Panel Survey to estimate nonlinear models of ambulatory and prescription drug mental health treatment. We find that in contrast to physical health treatment, Black-White and Hispanic-White disparities in any mental health treatment use widen with higher levels of psychological distress.


Subject(s)
Black or African American , Mental Health , Ethnicity , Health Services Accessibility , Healthcare Disparities , Hispanic or Latino , Humans , United States , White People
17.
Acad Pediatr ; 21(3): 488-496, 2021 04.
Article in English | MEDLINE | ID: mdl-32650049

ABSTRACT

OBJECTIVE: To measure pediatric preventive counseling at patient-centered medical homes (PCMHs) compared with practices that reported undertaking some or no quality-related activities. METHODS: We analyzed 4814 children and adolescents ages 0 to 17 who visited their usual sources of care in the nationally representative Medical Expenditure Panel Survey Medical Organizations Survey (MEPS-MOS), a household survey combined with a survey of household members' usual sources of care. We identified PCMHs using lists from certifying or accrediting organizations. For other practices in the MEPS-MOS, 2 quality-related activities were 1) reports to physicians about their clinical quality of care, and 2) electronic health record system reminders to physicians. Regressions controlled for practice, child, and family characteristics. RESULTS: Compared with other practices, PCMHs were generally associated with greater likelihood of receiving preventive counseling. Estimates varied with the quality-related activities of the comparison practices. Counseling against smoking in the home was 10.4 to 18.7 percentage points (both P < .01) more likely for PCMHs. More associations were statistically significant for PCMHs compared with practices that undertook 1 of 2 quality-related activities examined. Among children ages 2 to 5, compared with practices undertaking both quality-related activities, those with PCMHs were more likely to receive counseling on 3 of 5 topics. Among adolescents, compared with practices undertaking both quality-related activities, those with PCMHs were more likely to receive counseling on smoking, exercise, and eating healthy. CONCLUSIONS: PCMHs were associated with substantially greater receipt of pediatric preventive counseling. Evaluations of PCMHs need to account for the quality-related activities of comparison practices.


Subject(s)
Patient-Centered Care , Physicians , Adolescent , Child , Child, Preschool , Counseling , Exercise , Humans , Infant , Infant, Newborn , Surveys and Questionnaires
18.
Psychiatr Serv ; 72(1): 16-22, 2021 01 01.
Article in English | MEDLINE | ID: mdl-33076792

ABSTRACT

OBJECTIVE: Rapid increases in the prevalence of autism spectrum disorder (ASD) and increased access to intensive behavioral interventions have likely increased health care spending. This study estimated recent changes in spending among privately insured children with and without current ASD. METHODS: A repeated cross-sections analysis of 2011-2017 claims data from large-employer-sponsored health plans assessed changes in annual expenditures by service type for children ages 3-7 enrolled for ≥1 year and with two or more claims with ASD billing codes within a calendar year and for all other children. RESULTS: Mean spending per child with a current-year ASD diagnosis increased by 51% in 2017 U.S. dollars, from roughly $13,000 in 2011 to $20,000 in 2017. Among children who did not meet the current-year ASD case definition, per-child spending increased by 8%. Spending on children with ASD accounted for 41% of spending growth for children ages 3-7 during 2011-2017. Outpatient behavioral intervention-related spending per child with ASD increased by 376%, from $1,746 in 2011 to $8,317 in 2017; spending on all other services increased by 2%. Their share of behavioral intervention-related spending increased from 13.2% in 2011 to 41.7% in 2017. In 2011, 2.5% of children with current-year ASD diagnoses incurred ≥$20,000 in outpatient behavioral intervention-related spending, which increased to 14.4% in 2017. CONCLUSIONS: During 2011-2017, spending increased six times as much for privately insured children ages 3-7 with current-year ASD as for children without ASD, largely from increased behavioral intervention-related spending. One in seven children received at least $20,000 in services in 2017.


Subject(s)
Autism Spectrum Disorder , Autism Spectrum Disorder/therapy , Behavior Therapy , Child , Child, Preschool , Family , Health Expenditures , Humans , Prevalence , United States
19.
J Autism Dev Disord ; 51(8): 2950-2958, 2021 Aug.
Article in English | MEDLINE | ID: mdl-33113106

ABSTRACT

Published healthcare cost estimates for children with autism spectrum disorder (ASD) vary widely. One possible contributor is different methods of case ascertainment. In this study, ASD case status was determined using two sources of parent reports among 45,944 children ages 3-17 years in the Medical Expenditure Panel Survey (MEPS) linked to the National Health Interview Survey (NHIS) Sample Child Core questionnaire. In a two-part regression model, the incremental annual per-child cost of ASD relative to no ASD diagnosis was $3930 (2018 US dollars) using ASD case status from the NHIS Child Core and $5621 using current-year ASD case status from MEPS. Both estimates are lower than some published estimates but still represent substantial costs to the US healthcare system.


Subject(s)
Autism Spectrum Disorder/economics , Health Care Costs , Adolescent , Autism Spectrum Disorder/diagnosis , Autism Spectrum Disorder/therapy , Child , Child, Preschool , Female , Health Expenditures , Humans , Male , United States
20.
Health Econ ; 19(3): 297-315, 2010 Mar.
Article in English | MEDLINE | ID: mdl-19350688

ABSTRACT

Consumers' price responsiveness is central to US health-care reform proposals, but the best available estimates are now more than 25 years old. We estimate health-care demands by calculating expected end-of-year prices and incorporating them into a zero-inflated ordered probit model applied to several overlapping panels of data from 1996 to 2003. Results from our correlated random effects specification indicate that the price responsiveness of ambulatory mental health treatment has decreased substantially and is now slightly lower than physical health treatment. This suggests that concerns over moral hazard alone do not warrant less generous coverage for mental health. However, prescription drug demand is more price elastic.


Subject(s)
Health Services Needs and Demand , Mental Health Services , Ambulatory Care/economics , Direct Service Costs , Drug Costs , Health Expenditures , Health Services/economics , Health Services/supply & distribution , Health Services Needs and Demand/economics , Humans , Mental Health Services/economics , Mental Health Services/supply & distribution , Models, Econometric , Prescription Drugs/economics , United States
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