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Code of Ethics for the Australasian Menopause Society

Introduction

The Australasian Menopause Society is a professional organization whose members have the privileges and responsibilities ceded to professionals.

Professionals have specialized knowledge and skills which they are expected to exercise with competence and objectivity. Balancing these privileges are the responsibilities to adhere to the norms of professional behaviour.

Professional societies represent their members to the public and there are expectations by the public that these Societies will identify, disseminate and enforce the professional norms of their membership.

Codes of ethics have aspirational features identifying high standards of professional behaviour. They also include educational features indicating to members what would be the collective expectations of individual behaviour. Also included will be regulatory features indicating and supporting the appropriate roles of behaviour and issuing sanctions on occasion for violations.

This code of ethics has been developed by the board of the Australasian Menopause Society from templates developed for the Endocrine Society and the Royal Australasian College of Physicians (seeAppendix 1)。该代码被视为将修订并修改为道德问题的生命文件。

Executive Summary of the Code of Ethics

The Code is divided into two sections, the Responsibilities of the Society and the Responsibilities of the Members.

社会的责任are to conduct the affairs of the Society in an ethical and prudent manner. It should be careful to maintain its independence from industry support and to ensure that its educational presentations remain objective and complete. The Society should be careful in endorsing or marketing products and services not of its own design. The Society's principal function is to disseminate knowledge about menopause science and practice. It must ensure that meetings, publications and courses given the Society's imprimatur remain of the highest quality. The Society has a responsibility to teach professional ethics and to respond to ethical dilemmas, as they become apparent.

The responsibilities of the Australasian Menopause Society membersinclude respect for colleagues, including their work and their reputations, the honest performance and reporting of research and the honouring of predecessors and collaborators. This also includes appropriate sharing of research tools. Responsibilities involve high standards of research on humans, including respect for research subjects, informed consent, maintenance of privacy and confidentiality, ethical approval of the research design, and honest reporting of adverse results. Research employing animals should include respect for animals as sentient creatures.

那些追求临床实践有应答sibility to treat their patients with respect and within their scope of expertise, including obtaining informed consent when appropriate. They should avoid or disclose conflicts of interest and maintain patient privacy and confidentiality in the clinical setting. They must keep adequate records and inform patients of clinical developments. They must remain informed of developments in their field of expertise from objective and complete sources. Physicians should be cautious in accepting gifts from pharmaceutical and device companies because these gifts may be intended to influence opinion. Physicians are obliged to use their expertise to participate in decision-making regarding the distribution of resources in medicine for the benefit of patients, both as individuals and as groups.

I. Responsibilities of the Society as an organization

一个。Responsibilities of the Society: General

The Australasian Menopause Society shall discharge its responsibilities to support menopause research, education, and clinical practice with excellence, openness and the highest integrity. The Society has a responsibility to promote high quality science and collegiality among its members and to protect member privacy. The Annual Scientific Meeting and other educational programs of the Society shall be conducted so as to provide the highest quality of objective information.

1. The Society shall not allow its objectivity to be influenced by corporate or other sources of income. Dualities of interest shall be disclosed in a timely and comprehensive manner.

2.协会应提供审慎的资金管理,并通过定期审核验证。审计报告应提供给会员。

3. The management of the Society shall be subject to regular performance review by Board.

4. Members shall be kept informed of the activities of the Society and the affairs of the Society shall be open to the members, including the activities of its Committees.

5. Member privacy and confidentiality shall be maintained in accordance with Australian privacy legislation.

6. The Society shall conduct fair and democratic elections and ensure democratic decision-making among its Committees.

7.社会应为成员提供表达其关注的机制。对成员提出的问题的及时和建设性反应应成为重要的社会职能。

8.社会应及时及时地对与更年期有关的研究和实践讨论期间提出的关注和问题提供及时的回应。

9. The Society shall strive to ensure that there are no barriers to any of its activities as a result of affiliation, sex, ethnicity or disability by encouraging diversity in all activities and all Committees.

10. Society participation is based on volunteer efforts. While time commitments may be expected, members shall not be expected to incur significant financial expenses in their service to the Society. Service to the Society should not be based on economic considerations.

11. The Society shall organize its activities to recognize the diverse professional needs of its members.

b.Responsibilities of the Society: Relations with Industry

科学社会和工业有互惠互利的关系,在该关系中,社会为其科学会议获得了可观的财政支持。相反,行业有一个无与伦比的机会,可以向复杂而敏感的受众展示其进步。该协会需要阐明并定期更新与行业资金有关的政策。这包括在确定科学内容(包括选择会议和演讲者)中对独立性的全面披露和维护。即使有保障措施,会议(和会议)似乎仍然受到商业企业的影响。

Meetings

Sources of commercial funding should not influence the scientific, educational, or public policy decisions of the Society.

一个。商业支持者不得以任何方式控制社会的任何计划,尤其是那些经过持续医学教育学分认证的计划,内容,发言人的选择或执行。

b. The display of commercial products or services in exhibit hall areas at Society meetings, symposium or social event sponsorship do not imply warranty, endorsement or approval of these products or services, nor effectiveness, quality or safety. The display of misleading data shall not be countenanced. Neither shall commercial sponsorships influence the subject matter of the Annual Meeting.

c. Complete disclosure of commercial support is required for all Society-sponsored activities, as well as a balanced and objective presentation of data related to commercial products. Speakers are required to indicate at the time of their presentations any dualities of interest, including any relationship to the session sponsor.

d. The Society will instruct program directors, speakers and commercial sponsors about these policies prior to every presentation.

e。适当的社会委员会将制定提名继续教育计划的主席的政策。会议主席(或委员会)将确定会议的内容,并在委员会的批准下邀请发言人。将明确要求演讲者确保与有争议的问题相关的平衡演示,包括表现出特定疗法的优势和缺点。

c.Responsibilities of the Society: Endorsements

As a professional organization the Society may take positions intended to inform the public and/or educate legislators regarding specific issues related to menopause. Pivotal to this responsibility, the Society may act to promote the study, or increase awareness, of specific medical conditions.

在这种情况下,在可能的情况下,社会不得支持特定的治疗,以避免损害其客观性和信誉。此外,这种支持不应为特定的quid pro quo. Any such statements shall undergo formal internal review for their impact on the integrity of the Society.

d.Responsibilities of the Society: 营销

1. The Society shall not participate in the marketing of health-related products with the exception of its own journals, educational materials and programs.

2. The Society may make available to its members specific goods or services as a benefit (as in discounts or group availability), that may raise money for the Society, provided that the rationale of the endorsement and the benefit to the Society members are fully disclosed in advance.

e。Responsibilities of the Society:制裁

On occasion, the professional behaviour of a member might be such as to warrant a sanction by the Society. Such decisions require an unequivocal demonstration of professional behaviour that is unethical or illegal. Such decisions also require the administration of a due process procedure by the Society.

ii。澳大利亚更年期社会成员的责任beplay官网地址

A.Responsibility to Colleagues

1. Members shall treat their colleagues with respect and promote collegiality.

2. Members shall promote the educational and professional growth of their colleagues and trainees.

3.成员应适当地归因于同事的成就和工作,包括初级医生,学员和医学生。

4. Clinically related commercial ventures with colleagues shall maintain patient welfare as the top priority, not financial gain or academic promotion.

5.成员应向适当的当局报告威胁研究完整性,医学界或患者福利的完整性的同事的行为。

6. Members who supervise trainees shall disclose to them their financial interests in projects directly involving the trainee's academic program. It is suggested that mentor-trainee relationships that involve these financial interests be delineated and approved by the institution's leadership.

B. Research (General)

成员of the Australasian Menopause Society are expected to conduct themselves according to the highest standards of professional behaviour in both research and clinical care. They should engage in responsible performance and reporting of research. They should behave in a collegial manner and share intellectual property appropriately.

1. Performance and reporting of research. Scientific studies must be carried out with rigor and honesty. Data should be reported fully and truthfully.

2. To the extent possible, experimental results and analyses should be submitted promptly for publication. However, there are cases in which competitive and/or patent issues based on a proprietary interest in a new finding may require some delay in submission; this delay should be minimized. Dissemination of the results of negative studies is also important. To this end members conducting research should register their research with The Cochrane Collaboration or other appropriate bodies so that a record of unpublished results may be maintained.

C. Responsibility to Review

成员have a responsibility to review articles submitted to scientific journals as well as research grant applications.

1. Reviewers should demonstrate respect for scientific inquiry, knowledge of the discipline and willingness to provide judgment of publications in a fair and impartial manner.

2. When the request for review is made, reviewers have an obligation to inform the editor or manager immediately of actual or perceived conflicts of interest and to recuse themselves from the review, preferably without reading the submission.

3.审稿人有义务保持通讯的隐私和机密性。

D. Research Tools

Sharing of materials should be a goal of investigators, applied to the extent it is practical. It is desirable to encourage agreements and basic guidelines for the transfer of research tools and the Society encourages dissemination of research tools without legal agreements whenever possible.

E.人类​​研究:调查员责任

Research involving humans includes direct interaction with individual persons, and the acquisition or use of personal data from participants. All research must be justifiable in terms of its potential contribution to new knowledge, must be based on a thorough study of the existing literature, and must incorporate clearly stated hypotheses, methods and assessment of risks and discomfort to participants. Studies should be properly statistically powered and include appropriate controls.

1. Members are responsible for ensuring that the welfare, rights, beliefs and customs of research participants are fully respected. They must give full informed consent to the proposed research.

2. Members have a responsibility to ensure that the risk of harm or discomfort to participants in research is minimized. This responsibility exceeds that of any commitment to the goals or potential benefits of knowledge.

3. Members should honour their commitment to obtain new knowledge and communicate it to other researchers and society. This commitment should prevail over other motivations for conducting research, including economic or academic benefit.

4. All research involving humans must be conducted or supervised by individuals with the appropriate skill and experience in the conduct of human research.

5. Adequate resources must be available for the proper conduct of the research, and provision must be made for adverse events.

6. Participants in research should be indemnified against costs associated with any injury related to the study and should be informed of the terms of this indemnity in their consent process.

7. Proper provision must be made for the secure storage of data obtained in the conduct of the work. Data should be safely stored for a specified period to allow verification of results and assessment of adverse events following administration of drugs.

8. While full reports of the research should be published, the confidentiality of individual participants must be maintained.

9. Where developing results suggest that the risks associated with a particular research project are significantly greater than originally anticipated,urgent IRB review should be requested, the participants notified and the research stopped.

F. Human Research: Informed Consent

Informed consent is a practical application of respect for a person. Consent should be directly obtained from subjects with decision-making capacity.

在进行涉及人类受试者的研究之前,必须获得每个参与者的同意。这涉及提供适合其知识,教育和理解的水平,语言和形式的足够信息。应在以下情况下披露与研究相关的目的,方法,需求,风险(身体,社会心理,经济和家庭)以及不适,在此情况下,有关是否参与的选择可以摆脱强制,压力或过度诱因。目的是理解参与者,而不是调查人员的教学法案。

G. Human Research: Privacy and Confidentiality

保护机密性是医学的重要价值,但不是绝对的价值。涉及人类受试者的研究应尊重参与者的隐私以及根据澳大利亚隐私法规在研究过程中获得的任何数据的机密性。

H. Human Research: Clinical Trials

A clinical trial is a research study directed to the examination of a new therapy on persons. It may involve new drugs, devices or procedures for which limited efficacy and safety data are available. A trial may require the involvement of individuals with specific conditions that may make them especially vulnerable. The participants in clinical trials are usually committed individuals who are making sacrifices and taking risks in the interest of science. They must be treated with the utmost respect. Clinical trials provide potential for divergence among the interests of the investigator, the sponsor, and the patient. On the part of the clinician, conflicts of interest include career enhancement and financial gain versus adequate concern for the needs and rights of the patient.

Investigators should make their own decisions as to whether a clinical trial is well designed and ethical by understanding the literature and by ensuring adherence to the rules.

I. Ethics of Clinical Practice

1. Responsibilities to patients

(a)无论他们的社会,财务或医疗状况如何,生活方式或性偏好,都应尊重患者。

(b) Physicians must practise within their scope of expertise. Patients with conditions outside of this scope should, if possible, be referred to others with appropriate competence.

(c) The religious and cultural values of patients shall be respected.

(d) Physicians must maintain (or offer alternative) avenues of communication and/or access for patients after normal business hours and during holidays or vacations.

(e) Conflicts of interest, that is, circumstances in which the physician has a financial interest in clinical or research ventures, must not be allowed to pose a threat to patient welfare, and shall be identified and disclosed.

(f)与患者,员工和学生的性关系在道德上不当。

(g) Privacy and confidentiality shall be maintained in patient relations. Conversations about specific patients should be held in private only with parties relevant to the care of the patient. Clinical records must also be held confidential and should not be released without the explicit or implicit permission of the patient, except when required by law.

(h) Confidentiality may be breached when required by law, such as reporting of certain infections (TB, syphilis) or the possibility of child, spousal or elder abuse.

2. Consent

(a) While the ordinary practices of medicine including history taking, physical examination and provision of advice and medications involve the implicit consent of the patient, invasive procedures require explicit written consent. There are other practices that may require explicit informed consent, for example, using medications in an off label manner, especially when the risks are significant.

(b)获得同意并不总是直接的:例如,它可能受到疾病的性质或患者理解的能力的限制。由于医生及其患者之间经常建立的密切关系,还必须谨慎行事以避免不适当的影响。

3. Reporting

(a) Medical practitioners have an obligation to ensure that all diagnoses, opinions and results of studies are recorded and followed up appropriately. A medical practitioner is obliged to attempt to inform a patient of significant results of tests.

(b) Physicians have a responsibility to use existing, approved drugs in the most effective and appropriate way, to monitor their use, to report adverse reactions and to keep up to date with scientific developments.

4. Clinical decision-making

As far as possible, clinical decision should be based on evidence as well as experience. However, evidence can vary in quality and may itself be subject to ethical values, either in relation to its acquisition or its application. Physicians have the responsibility to assess critically the nature of evidence on which their decisions are based and to remain aware that ethics and evidence cannot be separated.

5.礼物

Manufacturers may wish to offer physicians many gifts and members should be very sensitive to the potential influences these gifts may carry. Acceptable gifts include books, simple diagnostic kits or equipment etc.

6. Expenses/Honoraria

After careful consideration and if one's academic independence can be preserved and respected, it is appropriate to accept reasonable travel/accommodation and sustenance expenses together with an honorarium commensurate with lost income to participate in research or educational fora. Such support should be acknowledged openly at the fora. The presenter should not be involved in the promotion of the sponsor's product and the lecture or presentation should be appropriate and the same as if the topic was presented to any independent peer reviewed meeting.

7. Clinical Innovation

Recognizing that the boundary between clinical practice and research may be blurred, it is important that clinicians be committed to careful evaluation of new or potentially new treatments that are tried in the course of clinical practice. If clinical observation suggests that a new therapy may have promise, a more systematic evaluation of this therapy may be initiated. This systematic evaluation constitutes experimental therapy (or research). In this case, the clinician must ensure that appropriate procedures for ethical review and consent are followed.

8. New Technologies

Physicians must become sensitive to new approaches to organizing health care on patient management, privacy and confidentiality all of which present new ethical dilemmas. In light of the potential for electronic breaches, physicians need to remain protective of their patients' privacy.

9. Political role

Physicians play an important role in determining the distribution of health care resources. Doctors are always under an obligation to exercise restraint and responsibility in the use of society's resources. However, physicians are not simply agents required to carry out mandates regarding health care. For the benefit of their patients and of society they must use their knowledge and expertise to take initiatives to influence health care policy development and implementation.

Appendix 1

Stanley C Korenman, M.D. Chair
道德咨询委员会成员:医学博士Mark Ba​​ch;马萨诸塞州卡特里娜·布拉姆斯泰特(Katrina Bramstedt);保罗·科姆萨罗夫(Paul Komesaroff),医学博士;琼·拉科斯基(Joan Lakoski)博士;凯瑟琳·摩尔(Katherine Moore),博士;罗伯特·斯佩斯(Robert Speth)博士。

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Cointent Updated January 2008

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