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2.
Am J Manag Care ; 26(1): e14-e20, 2020 01 01.
Artigo em Inglês | MEDLINE | ID: mdl-31951362

RESUMO

OBJECTIVES: To (1) assess whether hospitals in states requiring explicit patient consent ("opt-in") for health information exchange (HIE) are more likely to report regulatory barriers to HIE and (2) analyze whether these policies correlate with hospital volume of HIE. STUDY DESIGN: Cross-sectional analysis of US nonfederal acute care hospitals in 2016. METHODS: We combined legal scholarship surveying HIE-relevant state laws with the American Hospital Association Annual Information Technology Supplement for regulatory barriers and hospital characteristics. Data from CMS reports for hospitals attesting to Meaningful Use stage 2 (MU2; renamed "Promoting Interoperability" in 2018) in 2016 captured hospital HIE volume. We used multivariate logistic regression and linear regression to estimate the association of opt-in state consent policies with reported regulatory barriers and HIE volume, respectively. RESULTS: Hospitals in states with opt-in consent policies were 7.8 percentage points more likely than hospitals in opt-out states to report regulatory barriers to HIE (P = .03). In subgroup analyses, this finding held among hospitals that did not attest to MU2 (7.7 percentage points; P = .02). Among hospitals attesting, we did not find a relationship between opt-in policies and regulatory barriers (8.0 percentage points; P = .13) or evidence of a relationship between opt-in policies and HIE volume (ß = 0.56; P = .76). CONCLUSIONS: Our findings suggest that opt-in consent laws may carry greater administrative burdens compared with opt-out policies. However, less technologically advanced hospitals may bear more of this burden. Furthermore, opt-in policies may not affect HIE volume for hospitals that have already achieved a degree of technological sophistication. Policy makers should carefully consider the incidence of administrative burdens when crafting laws pertaining to HIE.


Assuntos
Troca de Informação em Saúde/legislação & jurisprudência , Interoperabilidade da Informação em Saúde/legislação & jurisprudência , Administração Hospitalar , Consentimento Livre e Esclarecido/legislação & jurisprudência , Uso Significativo/legislação & jurisprudência , American Hospital Association , Estudos Transversais , Regulamentação Governamental , Governo Estadual , Estados Unidos
3.
J Pediatr Orthop ; 39(9): e722-e728, 2019 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-31503236

RESUMO

INTRODUCTION: Electronic medical record (EMR) use among pediatric orthopaedic surgeons has evolved substantially within the past decade. In response to the Patient Protection and Affordable Care Act, large hospitals and tertiary pediatric medical centers rapidly acquired and implemented EMRs with uncertainty as to the potential impact on patient care and operational efficiency of subspecialists. This study reviews the background and regulatory framework for Meaningful Use of EMR and assesses the current landscape of EMR utilization by pediatric orthopaedic surgeons. METHODS: In 2015, the Practice Management Committee distributed a survey regarding EMR use and satisfaction to members of the Pediatric Orthopaedic Society of North America. Survey responses from 324 members were used to analyze levels of satisfaction by EMR platform and practice type and to consider drivers of satisfaction or dissatisfaction of end users. RESULTS: Although there were no differences in overall satisfaction based on vendor or practice type, significant differences were noted for 5 specific parameters of satisfaction, including: usefulness of templates, efficiency of practice workflow, information services support, number of logon events, and speed of the system. A user/vendor map is provided to facilitate networking among providers and groups utilizing common EMR platforms to help bring about rational improvements in EMR functionality for the future. CONCLUSIONS: Substantial effort needs to be made to improve subspecialty-specific EMR documentation, order entry, research tools, and clinical workflows to enhance the processes of care for children with orthopaedic conditions in the era of EMR. LEVEL OF EVIDENCE: Level IV.


Assuntos
Atitude do Pessoal de Saúde , Comportamento do Consumidor , Registros Eletrônicos de Saúde/estatística & dados numéricos , Ortopedia/estatística & dados numéricos , Pediatria/estatística & dados numéricos , Registros Eletrônicos de Saúde/legislação & jurisprudência , Registros Eletrônicos de Saúde/normas , Humanos , Uso Significativo/legislação & jurisprudência , Patient Protection and Affordable Care Act , Software/normas , Inquéritos e Questionários , Estados Unidos , Fluxo de Trabalho
5.
Int J Med Inform ; 110: 42-51, 2018 02.
Artigo em Inglês | MEDLINE | ID: mdl-29331254

RESUMO

OBJECTIVES: Using the context of the healthcare sector, this study examines the impact of regulatory change on technology implementation and use. Hospitals are now federally mandated to showcase meaningful use of information technology (IT). We theorize that IT plan scope structured prior to a regulatory change by means of a long-term planning horizon, top management involvement, and steering committee engagement impacts organizations' ability to fulfill meaningful use requirements three to five years later. Furthermore, we contend that this impact is contingent on the specific IT adoption strategy. METHODS: Data from the HIMSS and HITECH Act databases were combined to analyze 688 hospitals. Regression analyses were used to test the hypotheses. RESULTS: The results of this longitudinal study show that frequency of steering committee meetings and length of planning horizon broaden IT plan scope. Broader IT plan scope is positively associated with the ability of organizations to meaningfully use IT. CONCLUSIONS: The link between IT plan scope and meaningful use metric is particularly significant for organizations that adopt a more integrated approach towards IT adoption. Average reimbursement amount differences are provided and discussed between the different IT adoption strategies.


Assuntos
Atenção à Saúde/normas , Registros Eletrônicos de Saúde/legislação & jurisprudência , Hospitais/normas , Tecnologia da Informação/legislação & jurisprudência , Tecnologia da Informação/normas , Uso Significativo/legislação & jurisprudência , Bases de Dados Factuais , Atenção à Saúde/organização & administração , Humanos , Estudos Longitudinais
6.
J Am Med Inform Assoc ; 25(6): 694-701, 2018 06 01.
Artigo em Inglês | MEDLINE | ID: mdl-29370425

RESUMO

Objective: The federal meaningful use (MU) program was aimed at improving adoption and use of electronic health records, but practicing physicians have criticized it. This study was aimed at quantifying the benefits (ie, usefulness) and burdens (ie, workload) of the MU program for practicing family physicians. Materials and Methods: An interdisciplinary national panel of experts (physicians and engineers) identified the work associated with MU criteria during patient encounters. They conducted a national survey to assess each criterion's level of patient benefit and compliance burden. Results: In 2015, 480 US family physicians responded to the survey. Their demographics were comparable to US norms. Eighteen of 31 MU criteria were perceived as useful for more than half of patient encounters, with 13 of those being useful for more than two-thirds. Thirteen criteria were useful for less than half of patient encounters. Four useful criteria were reported as having a high compliance burden. Discussion: There was high variability in physicians' perceived benefits and burdens of MU criteria. MU Stage 1 criteria, which are more related to basic/routine care, were perceived as beneficial by most physicians. Stage 2 criteria, which are more related to complex and population care, were perceived as less beneficial and more burdensome to comply with. Conclusion: MU was discontinued, but the merit-based incentive payment system within the Medicare Access and CHIP Reauthorization Act of 2015 adopted its criteria. For many physicians, MU created a significant practice burden without clear benefits to patient care. This study suggests that policymakers should not assess MU in aggregate, but as individual criteria for open discussion.


Assuntos
Atitude do Pessoal de Saúde , Registros Eletrônicos de Saúde , Uso Significativo , Médicos de Família , Atitude Frente aos Computadores , Registros Eletrônicos de Saúde/legislação & jurisprudência , Registros Eletrônicos de Saúde/normas , Pesquisas sobre Atenção à Saúde , Política de Saúde , Uso Significativo/legislação & jurisprudência , Medicare/legislação & jurisprudência , Reembolso de Incentivo/legislação & jurisprudência , Estados Unidos
9.
J Am Med Inform Assoc ; 24(4): 729-736, 2017 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-28339642

RESUMO

OBJECTIVE: Nationwide initiatives have promoted greater adoption of health information technology as a means to reduce adverse drug events (ADEs). Hospital adoption of electronic health records with Meaningful Use (MU) capabilities expected to improve medication safety has grown rapidly. However, evidence that MU capabilities are associated with declines in in-hospital ADEs is lacking. METHODS: Data came from the 2010-2013 Medicare Patient Safety Monitoring System and the 2008-2013 Healthcare Information and Management Systems Society (HIMSS) Analytics Database. Two-level random intercept logistic regression was used to estimate the association of MU capabilities and occurrence of ADEs, adjusting for patient characteristics, hospital characteristics, and year of observation. RESULTS: Rates of in-hospital ADEs declined by 19% from 2010 to 2013. Adoption of MU capabilities was associated with 11% lower odds of an ADE (95% confidence interval [CI], 0.84-0.96). Interoperability capability was associated with 19% lower odds of an ADE (95% CI, 0.67- 0.98). Adoption of MU capabilities explained 22% of the observed reduction in ADEs, or 67,000 fewer ADEs averted by MU. DISCUSSION: Concurrent with the rapid uptake of MU and interoperability, occurrence of in-hospital ADEs declined significantly from 2010 to 2013. MU capabilities and interoperability were associated with lower occurrence of ADEs, but the effects did not vary by experience with MU. About one-fifth of the decline in ADEs from 2010 to 2013 was attributable to MU capabilities. CONCLUSION: Findings support the contention that adoption of MU capabilities and interoperability spurred by the Health Information Technology for Economic and Clinical Health Act contributed in part to the recent decline in ADEs.


Assuntos
Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos/epidemiologia , Registros Eletrônicos de Saúde/estatística & dados numéricos , Interoperabilidade da Informação em Saúde , Hospitais/estatística & dados numéricos , Uso Significativo , Erros de Medicação/tendências , Adulto , Idoso , Registros Eletrônicos de Saúde/legislação & jurisprudência , Feminino , Humanos , Masculino , Uso Significativo/legislação & jurisprudência , Informática Médica/legislação & jurisprudência , Medicare , Erros de Medicação/prevenção & controle , Pessoa de Meia-Idade , Estados Unidos/epidemiologia
10.
J Med Pract Manage ; 31(6): 332-5, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27443051

RESUMO

In October 2015, the Centers for Medicare & Medicaid Services released its final rule on the new guidelines for alterations to the long-standing EHR Incentive Program. These Modified Stage 2 and upcoming Stage 3 Meaningful Use Rules were developed in response to provider and organizational feedback during the last few years. This article provides a comprehensive overview for the new rules as they relate to Medicare and Medicaid Eligible Providers. Reporting deadlines for previous calendar year compliance and the basic criteria for automatic provider hardship exemptions to avoid reimbursement penalties also are discussed.


Assuntos
Uso Significativo , Medicaid , Medicare , Planos de Incentivos Médicos , Humanos , Uso Significativo/economia , Uso Significativo/legislação & jurisprudência , Uso Significativo/normas , Estados Unidos
18.
Med Econ ; 92(16): 38-40, 42, 2015 Aug 25.
Artigo em Inglês | MEDLINE | ID: mdl-26540785
20.
Fed Regist ; 80(200): 62601-759, 2015 Oct 16.
Artigo em Inglês | MEDLINE | ID: mdl-26477063

RESUMO

This final rule finalizes a new edition of certification criteria (the 2015 Edition health IT certification criteria or "2015 Edition'') and a new 2015 Edition Base Electronic Health Record (EHR) definition, while also modifying the ONC Health IT Certification Program to make it open and accessible to more types of health IT and health IT that supports various care and practice settings. The 2015 Edition establishes the capabilities and specifies the related standards and implementation specifications that Certified Electronic Health Record Technology (CEHRT) would need to include to, at a minimum, support the achievement of meaningful use by eligible professionals (EPs), eligible hospitals, and critical access hospitals (CAHs) under the Medicare and Medicaid EHR Incentive Programs (EHR Incentive Programs) when such edition is required for use under these programs.


Assuntos
Certificação/legislação & jurisprudência , Registros Eletrônicos de Saúde/legislação & jurisprudência , Troca de Informação em Saúde/legislação & jurisprudência , Troca de Informação em Saúde/normas , Informática Médica/legislação & jurisprudência , American Recovery and Reinvestment Act , Codificação Clínica/legislação & jurisprudência , Codificação Clínica/normas , Segurança Computacional/legislação & jurisprudência , Segurança Computacional/normas , Análise Custo-Benefício , Registros Eletrônicos de Saúde/normas , Humanos , Uso Significativo/legislação & jurisprudência , Uso Significativo/normas , Medicaid/legislação & jurisprudência , Medicaid/normas , Informática Médica/normas , Medicare/legislação & jurisprudência , Medicare/normas , Privacidade/legislação & jurisprudência , Estados Unidos
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