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1.
Environ Manage ; 72(5): 945-958, 2023 11.
Artigo em Inglês | MEDLINE | ID: mdl-37507631

RESUMO

Riparian buffers along streams can intercept eroding soils, contaminants, and nutrients, improving stream habitats and increasing the health of aquatic communities. Instream and riparian habitats and fish and benthic invertebrate communities were surveyed in a Minnesota stream draining an agricultural watershed before and after implementation of a state-mandated buffer law passed in 2014 and aimed at protecting water quality. Intensive habitat assessments, electrofishing, and benthic invertebrate sampling were used at the same 13 sites in 2005 and 2018. Average buffer width nearly doubled between surveys, and instream abundance of fine sediments and embeddedness of coarse substrates by fine sediments both declined significantly within 1 to 3 years of buffer establishment. Stream sites also were significantly deeper with faster current velocities, and sites had increased riffle habitat and increased instream vegetative cover for fish after buffer mandates. However, fish and invertebrate biotic integrity scores, and other biotic community metrics, did not display significant improvements after buffer establishment. Stream habitats appear to improve quickly when intact and continuous riparian buffers insulate streams from surrounding agricultural activities, but improvements in biotic communities likely will require more time to adapt to changed habitat conditions.


Assuntos
Ecossistema , Rios , Animais , Invertebrados , Agricultura , Solo , Peixes , Monitoramento Ambiental
2.
JAMA Health Forum ; 3(7): e221771, 2022 07.
Artigo em Inglês | MEDLINE | ID: mdl-35977217

RESUMO

Importance: There is limited evaluation of the performance of Medicaid managed care (MMC) private plans in covering substance use disorder (SUD) treatment. Objective: To compare the performance of MMC plans across 19 indicators of access, quality, and outcomes of SUD treatment. Design Setting and Participants: This cross-sectional study used administrative claims and mandatory assignment to plans of up to 159 016 adult Medicaid recipients residing in 1 of the 5 counties (boroughs) of New York, New York, from January 2009 to December 2017 to identify differences in SUD treatment access, patterns, and outcomes among different types of MMC plans. Data from the latest years were received from the New York State Department of Health in October 2019, and analysis began soon thereafter. Approximately 17% did not make an active choice of plan, and a subset of these (approximately 4%) can be regarded as randomly assigned. Exposures: Plan assignment. Main Outcomes and Measures: Percentage of the enrollees achieving performance measures across 19 indicators of access, process, and outcomes of SUD treatment. Results: Medicaid claims data from 159 016 adults (mean [SD] age, 35.9 [12.7] years; 74 261 women [46.7%]; 8746 [5.5%] Asian, 73 783 [46.4%] Black, and 40 549 [25.5%] White individuals) who were auto assigned to an MMC plan were analyzed. Consistent with national patterns, all plans achieved less than 50% (range, 0%-62.1%) on most performance measures. Across all plans, there were low levels of treatment engagement for alcohol (range, 0%-0.4%) and tobacco treatment (range, 0.8%-7.2%), except for engagement for opioid disorder treatment (range, 41.5%-61.4%). For access measures, 4 of the 9 plans performed significantly higher than the mean on recognition of an SUD diagnosis, any service use for the first time, and tobacco use screening. Of the process measures, total monthly expenditures on SUD treatment was the only measure for which plans differed significantly from the mean. Outcome measures differed little across plans. Conclusions and Relevance: The results of this cross-sectional study suggest the need for progress in engaging patients in SUD treatment and improvement in the low performance of SUD care and limited variation in MMC plans in New York, New York. Improvement in the overall performance of SUD treatment in Medicaid potentially depends on general program improvements, not moving recipients among plans.


Assuntos
Medicaid , Transtornos Relacionados ao Uso de Substâncias , Adulto , Estudos Transversais , Feminino , Acessibilidade aos Serviços de Saúde , Humanos , New York/epidemiologia , Transtornos Relacionados ao Uso de Substâncias/epidemiologia , Estados Unidos/epidemiologia
3.
Med Care ; 60(11): 806-812, 2022 11 01.
Artigo em Inglês | MEDLINE | ID: mdl-36038524

RESUMO

OBJECTIVE: The aim was to assess the magnitude of health care disparities in treatment for substance use disorder (SUD) and the role of health plan membership and place of residence in observed disparities in Medicaid Managed Care (MMC) plans in New York City (NYC). DATA SOURCE: Medicaid claims and managed care plan enrollment files for 2015-2017 in NYC. RESEARCH DESIGN: We studied Medicaid enrollees with a SUD diagnosis during their first 6 months of enrollment in a managed care plan in 2015-2017. A series of linear regression models quantified service disparities across race/ethnicity for 5 outcome indicators: treatment engagement, receipt of psychosocial treatment, follow-up after withdrawal, rapid readmission, and treatment continuation. We assessed the degree to which plan membership and place of residence contributed to observed disparities. RESULTS: We found disparities in access to treatment but the magnitude of the disparities in most cases was small. Plan membership and geography of residence explained little of the observed disparities. One exception is geography of residence among Asian Americans, which appears to mediate disparities for 2 of our 5 outcome measures. CONCLUSIONS: Reallocating enrollees among MMC plans in NYC or evolving trends in group place of residence are unlikely to reduce disparities in treatment for SUD. System-wide reforms are needed to mitigate disparities.


Assuntos
Medicaid , Transtornos Relacionados ao Uso de Substâncias , Etnicidade , Geografia , Disparidades em Assistência à Saúde , Humanos , Programas de Assistência Gerenciada , Cidade de Nova Iorque , Transtornos Relacionados ao Uso de Substâncias/terapia , Estados Unidos
4.
Am J Orthod Dentofacial Orthop ; 151(3): 539-558, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28257739

RESUMO

INTRODUCTION: Genetic studies of malocclusion etiology have identified 4 deleterious mutations in genes DUSP6,ARHGAP21, FGF23, and ADAMTS1 in familial Class III cases. Although these variants may have large impacts on Class III phenotypic expression, their low frequency (<1%) makes them unlikely to explain most malocclusions. Thus, much of the genetic variation underlying the dentofacial phenotypic variation associated with malocclusion remains unknown. In this study, we evaluated associations between common genetic variations in craniofacial candidate genes and 3-dimensional dentoalveolar phenotypes in patients with malocclusion. METHODS: Pretreatment dental casts or cone-beam computed tomographic images from 300 healthy subjects were digitized with 48 landmarks. The 3-dimensional coordinate data were submitted to a geometric morphometric approach along with principal component analysis to generate continuous phenotypes including symmetric and asymmetric components of dentoalveolar shape variation, fluctuating asymmetry, and size. The subjects were genotyped for 222 single-nucleotide polymorphisms in 82 genes/loci, and phenotpye-genotype associations were tested via multivariate linear regression. RESULTS: Principal component analysis of symmetric variation identified 4 components that explained 68% of the total variance and depicted anteroposterior, vertical, and transverse dentoalveolar discrepancies. Suggestive associations (P < 0.05) were identified with PITX2, SNAI3, 11q22.2-q22.3, 4p16.1, ISL1, and FGF8. Principal component analysis for asymmetric variations identified 4 components that explained 51% of the total variations and captured left-to-right discrepancies resulting in midline deviations, unilateral crossbites, and ectopic eruptions. Suggestive associations were found with TBX1AJUBA, SNAI3SATB2, TP63, and 1p22.1. Fluctuating asymmetry was associated with BMP3 and LATS1. Associations for SATB2 and BMP3 with asymmetric variations remained significant after the Bonferroni correction (P <0.00022). Suggestive associations were found for centroid size, a proxy for dentoalveolar size variation with 4p16.1 and SNAI1. CONCLUSIONS: Specific genetic pathways associated with 3-dimensional dentoalveolar phenotypic variation in malocclusions were identified.


Assuntos
Má Oclusão/genética , Adolescente , Adulto , Idoso , Pontos de Referência Anatômicos , Criança , Tomografia Computadorizada de Feixe Cônico , Feminino , Fator de Crescimento de Fibroblastos 23 , Estudos de Associação Genética , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade , Fenótipo , Análise de Componente Principal , Reprodutibilidade dos Testes
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