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1.
Drug Alcohol Depend ; 221: 108652, 2021 04 01.
Artigo em Inglês | MEDLINE | ID: mdl-33667785

RESUMO

BACKGROUND: Since the introduction of the National Medical Cannabis Programme in The Netherlands, many other countries in Europe have made medical cannabis (MC) and cannabis-based medicines (CBMs) available. However, each of them has implemented a unique legal framework and reimbursement strategy for these products. Therefore, it is vital to study healthcare professionals' knowledge level (HCP) and HCPs in-training regarding both medical uses and indications and understand their safety concerns and potential barriers for MC use in clinical practice. METHODS: A comprehensive, systematic literature review was performed using PubMed/MEDLINE, EMBASE, and Google Scholar databases, as well as PsychINFO. Grey literature was also included. Due to the high diversity in the questionnaires used in the studies, a narrative synthesis was performed. RESULTS: From 6995 studies retrieved, ten studies, all of them being quantitative survey-based studies, were included in the review. In most studies, the majority of participants were in favor of MC and CBMs use for medical reasons. Other common findings were: the necessity to provide additional training regarding medical applications of cannabinoids, lack of awareness about the legal status of and regulations regarding MC among both certified physicians, as well as prospective doctors and students of other medicals sciences (e.g., nursing, pharmacy). CONCLUSIONS: For most European countries, we could not identify any studies evaluating HCPs' knowledge and attitudes towards medicinal cannabis. Therefore, similar investigations are highly encouraged. Available evidence demonstrates a need to provide medical training to the HCPs in Europe regarding medical applications of cannabinoids.


Assuntos
Canabinoides/uso terapêutico , Prescrições de Medicamentos , Conhecimentos, Atitudes e Prática em Saúde , Pessoal de Saúde/tendências , Maconha Medicinal/uso terapêutico , Analgésicos/uso terapêutico , Cannabis , Europa (Continente)/epidemiologia , Alucinógenos/uso terapêutico , Pessoal de Saúde/legislação & jurisprudência , Humanos , Narração , Estudos Prospectivos
2.
Acupunct Med ; 39(4): 327-333, 2021 08.
Artigo em Inglês | MEDLINE | ID: mdl-32783507

RESUMO

INTRODUCTION: The National Academy of Medicine recommends, and Joint Commission requires, offering non-pharmacologic approaches to pain management, including acupuncture, to reduce opioid overuse in the United States. This study describes 2019 state training requirements to evaluate how they represent opportunities and barriers to increasing access to acupuncture. METHODS: We searched publicly available databases to identify Acupuncture Practice Acts and additional statutes and regulations pertaining to acupuncture training requirements on state licensure board websites. We then extracted state-specific acupuncture training requirements for individuals with and without a healthcare-related professional license. RESULTS: Thirty-three states allow physicians to provide acupuncture without requiring any additional training requirements, 11 states and the District of Columbia (DC) require 200-300 training hours, and three require physicians to obtain a separate acupuncture license. Three states have no regulatory agency ruling. Forty states require non-healthcare professionals to complete an accredited program of more than 1900 h and pass an examination. Twenty-three states have an Acupuncture Detoxification Specialist designation allowing individuals without a clinical professional license to provide auricular acupuncture for substance use disorder treatment after a 70-h training course. DISCUSSION: State-level training requirements are intended to increase safe and effective care, but variations represent a potential barrier to increasing the number of acupuncture providers in the United States. Allowing non-physician medical professionals to complete reduced training requirements for specific indications could be a model to increase access to acupuncture. The influence of training requirements on acupuncture access and opioid overuse needs examination.


Assuntos
Acupuntura/educação , Pessoal de Saúde/educação , Ensino/normas , Acupuntura/legislação & jurisprudência , Pessoal de Saúde/legislação & jurisprudência , Pessoal de Saúde/normas , Humanos , Licenciamento , Ensino/legislação & jurisprudência , Ensino/estatística & dados numéricos , Fatores de Tempo , Estados Unidos
3.
Med Law Rev ; 28(3): 526-548, 2020 Aug 01.
Artigo em Inglês | MEDLINE | ID: mdl-32462185

RESUMO

This article explores the merits of employing a restorative justice approach in cases of gross negligence manslaughter involving healthcare professionals, in line with the recent policy turn towards developing a just culture in addressing episodes of healthcare malpractice within the National Health Service in England. It is argued that redress for victims and rehabilitation of offenders should operate as key values, underpinning the adoption of a restorative justice approach in such cases. It would also be vital that a structured pathway was designed that established suitable protocols and safeguards for both victims and offenders taking account of problematic issues such as the informality of the process, power asymmetries between parties, and the context in which the offence took place. Taking all such matters into account, we propose that consideration be given to establishing a pilot involving the use of restorative justice in cases of gross negligence manslaughter involving healthcare professionals, which would be subject to judicial and stakeholder oversight to ensure transparency and accountability, which in turn could inform future policy options.


Assuntos
Criminosos/legislação & jurisprudência , Pessoal de Saúde/legislação & jurisprudência , Homicídio , Imperícia , Vítimas de Crime/legislação & jurisprudência , Inglaterra , Programas Nacionais de Saúde , Justiça Social/normas
4.
Complement Ther Med ; 37: 6-12, 2018 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-29609938

RESUMO

OBJECTIVES: This study aims to provide an empirical examination of how complementary medicine practice in Australia is actually regulated under the current national registration model. METHODS: Data was obtained from Australian Health Practitioner Regulation Agency (AHPRA) Annual Reports for the years 2011/12-2014/15 and supplemented by the Chinese Medical Registration Board of Victoria (CMRBV) Annual Reports in 2011/12 for Chinese Medicine complaints. The data analysed includes complaint statistics, stage of closure of complaints and the outcome of complaints concerning Chinese medicine, chiropractic and osteopathy under the National Law. RESULTS: During 2014-2015 the number of complaints per 100 registrants for was highest for the medical board (4.4), while much lower for the chiropractic (1.5), osteopath (0.7) and Chinese medicine (0.5) boards. For conventional boards, 58% of complaints were closed at the assessment stage, while 57%, 29% and 16% of complaints to the osteopath, Chinese medicine and chiropractic boards respectively were closed at the assessment stage. The decision to suspend or cancel registration of health professionals was 17% from the Chinese medicine board, 14% from the Osteopathy Board, 1.5% from the chiropractor board and 0.6% from the medical board. CONCLUSION: It appears that complementary medicine practitioner regulation works at least as well as conventional regulation, and at most complementary medicine boards take a stricter interpretation of misconduct though more research would need to be undertaken to state this definitively. Our findings indicate that the public are using the statutory complaint mechanisms available to them with respect to the three CM groups.


Assuntos
Acreditação/legislação & jurisprudência , Terapias Complementares/legislação & jurisprudência , Pessoal de Saúde/legislação & jurisprudência , Austrália , Terapias Complementares/organização & administração , Pessoal de Saúde/organização & administração , Humanos
5.
J Integr Med ; 16(1): 1-5, 2018 01.
Artigo em Inglês | MEDLINE | ID: mdl-29397086

RESUMO

In recent decades, acupuncture has been used more widely and extensively in the United States (U.S.). However, there have been no national surveys or analyses reported in academic journals on the number of practicing or licensed acupuncturists. This study was conducted to identify the approximate number of licensed acupuncturists active in 2015. The Board of Acupuncture or Board of Medicine in each state or U.S. territory was contacted to collect data. Online license information searching was also performed in order to get accurate numbers of licensed acupuncturists for those states in which a board was unable to be contacted. The study found that the number of licensed acupuncturists in 2015 in the U.S. was 34,481. Of this, more than 50% were licensed in three states alone: California (32.39%), New York (11.89%) and Florida (7.06%). The number of licensed acupuncturists increased 23.30% and 52.09%, compared to the year 2009 (n = 27,965) and 2004 (n = 22,671), respectively; increasing about 1,266 per year. There were 62 and 10 accredited acupuncture institutions providing master and doctoral degrees, respectively. The West Coast comprised 51.39% of degree granting programs, while the East Coast comprised 29.17%; together the coastal states housed more than 80% of all programs, with the remainder sprinkled across the southern (9.72%), northern (8.33%), and the middle/central states (1.39%). Forty-four states and the District of Columbia regulated acupuncture practice by law at the time of data collection. Acupuncture continues to be a quickly growing profession in the U.S.


Assuntos
Acupuntura/educação , Pessoal de Saúde/legislação & jurisprudência , Licenciamento/legislação & jurisprudência , Escolas para Profissionais de Saúde , Acupuntura/legislação & jurisprudência , Acupuntura/organização & administração , Pessoal de Saúde/educação , Humanos , Escolas para Profissionais de Saúde/legislação & jurisprudência , Estados Unidos , Recursos Humanos
6.
J Altern Complement Med ; 24(4): 307-313, 2018 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-29359948

RESUMO

The World Health Organization (WHO) has called for the increased statutory regulation of traditional and complementary medicine practitioners and practices, currently implemented in about half of nations surveyed. According to recent WHO data, however, the absence of policy guidelines in this area represents a significant barrier to implementation of such professional regulations. This commentary reviews several key challenges that distinguish the statutory regulation of traditional medicine practitioners and practices from biomedical professional regulation, providing a foundation for the development of policy making parameters in this area. Foremost in this regard are the ongoing impacts of the European colonial encounter, which reinforce biomedicine's disproportionate political dominance across the globe despite traditional medicine's ongoing widespread use (particularly in the global South). In this light, the authors discuss the conceptual and historical underpinnings of contemporary professional regulatory structures, the tensions between institutional and informal traditional medicine training pathways, and the policy challenges presented by the prospect of standardizing internally diverse indigenous healing approaches. Epistemic and evidentiary tensions, as well as the policy complexities surrounding the intersection of cultural and clinical considerations, present additional challenges to regulators. Conceptualizing professional regulation as an intellectual property claim under the law, the authors further consider what it means to protect traditional knowledge and prevent misappropriation in this context. Overall, the authors propose that innovative professional regulatory approaches are needed in this area to address safety, quality of care, and accessibility as key public interest concerns, while prioritizing the redress of historical inequities, protection of diverse indigenous knowledges, and delivery of care to underserved populations.


Assuntos
Terapias Complementares , Pessoal de Saúde , Medicina Tradicional/normas , Guias de Prática Clínica como Assunto , Terapias Complementares/legislação & jurisprudência , Terapias Complementares/normas , Pessoal de Saúde/legislação & jurisprudência , Pessoal de Saúde/normas , Humanos , Organização Mundial da Saúde
7.
BMC Complement Altern Med ; 18(1): 11, 2018 Jan 10.
Artigo em Inglês | MEDLINE | ID: mdl-29321023

RESUMO

BACKGROUND: Many European citizens are seeking complementary and alternative medicine (CAM). These treatments are regulated very differently in the EU/EFTA countries. This may demonstrate differences in how risk associated with the use of CAM is perceived. Since most CAM treatments are practiced fairly similarly across Europe, differing risk understandings may influence patient safety for European CAM users. The overall aim of this article is thus to contribute to an overview and awareness of possible differing risk understandings in the field of CAM at a policymaking/structural level in Europe. METHODS: The study is a re-analysis of data collected in the CAMbrella EU FP7 document and interview study on the regulation of CAM in 39 European countries. The 12 CAM modalities included in the CAMbrella study were ranked with regard to assumed risk potential depending on the number of countries limiting its practice to regulated professions. The 39 countries were ranked according to how many of the included CAM modalities they limit to be practiced by regulated professions. RESULTS: Twelve of 39 countries generally understand the included CAM treatments to represent "high risk", 20 countries "low risk", while the remaining 7 countries understand CAM treatments as carrying "very little or no risk". The CAM modalities seen as carrying a risk high enough to warrant professional regulation in the highest number of countries are chiropractic, acupuncture, massage, homeopathy and osteopathy. The countries understanding most of the CAM modalities in the study as potentially high-risk treatments are with two exceptions (Portugal and Belgium) all concentrated in the southeastern region of Europe. CONCLUSION: The variation in regulation of CAM may represent a substantial lack of common risk understandings between health policymakers in Europe. We think the discrepancies in regulation are to a considerable degree also based on factors unrelated to patient risk. We argue that it is important for patient safety that policy makers across Europe address this confusing situation. This could be done by applying the WHO patient safety definitions and EU's policy to facilitate access to "safe and high-quality healthcare", and regulate CAM accordingly.


Assuntos
Terapias Complementares , Pessoal de Saúde , Segurança do Paciente , Terapias Complementares/legislação & jurisprudência , Terapias Complementares/organização & administração , Terapias Complementares/normas , Europa (Continente) , Pessoal de Saúde/legislação & jurisprudência , Pessoal de Saúde/normas , Pessoal de Saúde/estatística & dados numéricos , Humanos , Segurança do Paciente/legislação & jurisprudência , Segurança do Paciente/normas , Risco
8.
Int J Pharm Pract ; 26(6): 485-493, 2018 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-29349921

RESUMO

OBJECTIVES: To examine community pharmacists' perspectives on CMs regulation in New Zealand, where proposals for CMs regulations had recently been suspended and where, currently, CMs are only weakly regulated. METHODS: Qualitative, in-depth, semi-structured interviews with New Zealand practising community pharmacists are identified through purposive and convenience sampling. Data were analysed using a general inductive approach. KEY FINDINGS: Participants held mixed views regarding harmonisation of CMs regulations across Australia and NZ; some supported an NZ national regulatory framework for CMs, based on the Australian system. Participants recognised the current CMs regulatory framework in NZ as inadequate, that regulation was required to some extent, and that mandatory regulation was not necessarily required. A key reason given in support of CMs regulations was the need for greater assurances around quality of CMs. Participants also supported a regulatory framework that incorporated assessment of the safety of CMs, but were less convinced of the need for, or feasibility of, requiring evidence of efficacy from clinical trials. Participants believed that regulation of CMs practitioners, such as herbalists, and CMs retailers was important, although there were mixed views as to whether regulation should be statutory or whether self-regulation would be adequate. CONCLUSIONS: On the basis of these findings, pharmacists would be expected to welcome proposals for national regulations for CMs in NZ: such regulations should address concerns regarding product quality, inappropriate health claims and supporting evidence, and therefore should support pharmacists in meeting their obligations under the NZ Pharmacy Council's Code of Ethics.


Assuntos
Atitude do Pessoal de Saúde , Serviços Comunitários de Farmácia/organização & administração , Terapias Complementares/legislação & jurisprudência , Farmacêuticos/estatística & dados numéricos , Adulto , Idoso , Austrália , Terapias Complementares/efeitos adversos , Feminino , Pessoal de Saúde/legislação & jurisprudência , Humanos , Entrevistas como Assunto , Masculino , Pessoa de Meia-Idade , Nova Zelândia , Papel Profissional , Adulto Jovem
9.
Med Leg J ; 86(1): 23-31, 2018 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28967838

RESUMO

The development of statutory regulation of healthcare professionals first emerged in the 15th century in the UK. However, it was not until the 20th century that statutory regulation of complementary therapies emerged with the Osteopath and Chiropractors Acts. However, during that period, acupuncture failed to gain statutory regulation but was rather subject to the equivalent of trading standards. This review explores the background to this failure and the present need for statutory regulation. It draws comparisons with the need for regulation of hijama, another invasive therapy, for which there is at present no regulation. The benefits of the negative licensing model developed in Australia are considered.


Assuntos
Terapia por Acupuntura/tendências , Terapias Complementares/legislação & jurisprudência , Segurança do Paciente/legislação & jurisprudência , Austrália , Certificação/legislação & jurisprudência , Pessoal de Saúde/legislação & jurisprudência , Humanos
10.
J Midwifery Womens Health ; 62(3): 348-352, 2017 May.
Artigo em Inglês | MEDLINE | ID: mdl-28632953

RESUMO

This article provides information on recent changes in the US Food and Drug Administration (FDA) labeling and safety regulations for mifepristone (Mifeprex). The revised label now permits midwives, advanced practice nurses, and physician assistants to order and prescribe mifepristone, eliminating the requirement for physician supervision. The updated label also extends eligibility for use from 49 to 70 days' gestation and decreases the number of required visits from 3 to 2. The recommended dose of mifepristone has been reduced, and the dosage, timing, and route of administration for misoprostol have also been changed to reflect current research. These changes have implications for clinical practice and may lead to expanded access for women in the United States.


Assuntos
Abortivos Esteroides/administração & dosagem , Aborto Induzido/legislação & jurisprudência , Controle de Medicamentos e Entorpecentes , Regulamentação Governamental , Pessoal de Saúde/legislação & jurisprudência , Mifepristona/administração & dosagem , Misoprostol/administração & dosagem , Aborto Induzido/métodos , Rotulagem de Medicamentos/legislação & jurisprudência , Quimioterapia Combinada , Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos/prevenção & controle , Feminino , Idade Gestacional , Humanos , Tocologia/legislação & jurisprudência , Enfermeiros Obstétricos/legislação & jurisprudência , Profissionais de Enfermagem/legislação & jurisprudência , Assistentes Médicos/legislação & jurisprudência , Gravidez , Prática Profissional/legislação & jurisprudência , Estados Unidos , United States Food and Drug Administration
11.
Cas Lek Cesk ; 155(5): 263-266, 2016.
Artigo em Tcheco | MEDLINE | ID: mdl-27696892

RESUMO

As military and prison chaplains have been active in the military or prison service for many years, nowadays, hospital chaplains have been active in many hospitals in the Czech Republic, too. The work of hospital chaplains, however, still lacks the necessary legislative framework and being embodied in law, which brings some drawbacks. These include primarily non-participation of the ministry of health as a contractual partner in the agreement on spiritual care in health care, the lack of a framework that would arrange the status of chaplains among other health professionals and the related uncertainty regarding career and competency profile of a chaplain.Moreover, the ministry has not set clear rules for the work of chaplains in hospitals, and due to this fact, it has created the space for providing this service also by unqualified persons. This may ultimately have a negative impact on patients. It is therefore the responsibility of the hospital management to arrange that only professional hospital chaplains sent to hospitals on the basis of an agreement between the hospital and the relevant church work there.Key words: hospital chaplain, spiritual assistant, health care system, legislation.


Assuntos
Serviço Religioso no Hospital/legislação & jurisprudência , Clero/legislação & jurisprudência , Pessoal de Saúde/legislação & jurisprudência , Religião e Medicina , República Tcheca , Humanos , Espiritualidade
17.
J Calif Dent Assoc ; 42(1): 19-23, 2014 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25080685

RESUMO

Recent federal health care legislation contains explicit and implicit drivers for medical-dental collaboration. These laws implicitly promote health care evolution through value-based financing, "big data" and health information technology, increased number of care providers and a more holistic approach. Additional changes--practice aggregation, consumerism and population health perspectives--may also influence dental care. While dentistry will likely lag behind medicine toward value-based and accountable care organizations, dentists will be affected by changing consumer expectations.


Assuntos
Atenção à Saúde/legislação & jurisprudência , Relações Interprofissionais , Equipe de Assistência ao Paciente , Patient Protection and Affordable Care Act/legislação & jurisprudência , Criança , Proteção da Criança/legislação & jurisprudência , Participação da Comunidade , Comportamento Cooperativo , Coleta de Dados/legislação & jurisprudência , Assistência Odontológica/legislação & jurisprudência , Pessoal de Saúde/legislação & jurisprudência , Saúde Holística/legislação & jurisprudência , Humanos , Informática Médica/legislação & jurisprudência , Saúde Bucal/legislação & jurisprudência , Atenção Primária à Saúde/legislação & jurisprudência , Prática Profissional , Saúde Pública/legislação & jurisprudência , Estados Unidos , Aquisição Baseada em Valor/legislação & jurisprudência
19.
Orv Hetil ; 155(15): 575-81, 2014 Apr 13.
Artigo em Húngaro | MEDLINE | ID: mdl-24704769

RESUMO

This paper aims to present factual information and to suggest possible solutions regarding some of the recent questions which have arisen regarding the regulation of traditional Chinese medicine in Hungary. According to current legislation "traditional Chinese doctors", who are the most highly trained professionals in this field, are not allowed to practice Chinese medicine and acupuncture in Hungary. This situation cannot be explained by their educational background, as they receive thorough training in both Chinese medicine and modern medical sciences. Furthermore, this legislation is not supported by any EU standard: Traditional Chinese medicine professionals can practice Chinese medicine and acupuncture in a number of European countries within a legal and regulated framework. Different kinds of healthcare professionals may practice Chinese medicine and acupuncture in the UK - this could be a good example for Hungarian regulation. The five-year bachelor level traditional Chinese medicine training at the Faculty of Health Sciences, Semmelweis University and the increasing number of locally trained traditional Chinese medicine professionals could be a good basis for laying the groundwork of the new system.


Assuntos
Terapia por Acupuntura , Pessoal de Saúde/legislação & jurisprudência , Legislação Médica , Medicina Tradicional Chinesa , Educação Profissionalizante , União Europeia , Humanos , Hungria , Legislação Médica/normas , Legislação Médica/tendências , Reino Unido
20.
Cad. naturol. terap. complem ; 3(4): 89-94, 2014.
Artigo em Português | MTYCI | ID: biblio-879124

RESUMO

Em entrevista realizada por Isadora F. B. O. Alves, em 01 e 02 de junho de 2014, Kalil Mondadori, na função de Presidente da Associação Brasileira de Naturologia ­ ABRANA ­ e Flavia Placeres, Presidente da Associação Paulista de Naturologia ­ APANAT ­ fazem revelações importantes para a construção da história da inserção da Naturologia no universo das práticas trabalhistas voltadas para a saúde.(AU)


Assuntos
Humanos , Naturologia , Sociedades/legislação & jurisprudência , Brasil , Pessoal de Saúde/legislação & jurisprudência
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