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Diseases2

Death Emergencies

Analytical, Diagnostic and Therapeutic Techniques and Equipment33

Human Experimentation Therapeutic Human Experimentation Nontherapeutic Human Experimentation Patient Selection Clinical Trials as Topic Research Design Questionnaires Randomized Controlled Trials as Topic Prospective Studies AIDS Serodiagnosis Control Groups Risk Assessment Records as Topic Pilot Projects Surgical Procedures, Operative Clinical Trials, Phase I as Topic Surgical Procedures, Elective Clinical Trials, Phase IV as Topic Treatment Outcome Embryo Disposition Cross-Sectional Studies Sensitivity and Specificity Medical Records Focus Groups Data Collection Genetic Testing Interviews as Topic Feasibility Studies Reproducibility of Results Clinical Protocols Donor Selection Mass Screening Risk Factors

Psychiatry and Psychology28

Mental Competency Disclosure Comprehension Personal Autonomy Refusal to Participate Confidentiality Paternalism Decision Making Researcher-Subject Relations Truth Disclosure Physician-Patient Relations Duty to Warn Communication Morals Treatment Refusal Health Knowledge, Attitudes, Practice Trust Ethics Attitude Attitude to Health Parents Mental Recall Professional-Family Relations Behavioral Research Attitude of Health Personnel Focus Groups Family Duty to Recontact

Phenomena and Processes2

Sensitivity and Specificity Pregnancy

Disciplines and Occupations13

Human Experimentation Therapeutic Human Experimentation Nontherapeutic Human Experimentation Biomedical Research Genetic Research Research Design Emergency Medicine General Surgery Empirical Research Research Anesthesiology Behavioral Research Qualitative Research

Anthropology, Education, Sociology and Social Phenomena41

Informed Consent Consent Forms Presumed Consent Parental Consent Mental Competency Third-Party Consent Disclosure Personal Autonomy Confidentiality Patient Rights Informed Consent By Minors Patient Advocacy Patient Education as Topic Truth Disclosure Privacy Child Advocacy Duty to Warn Liability, Legal Government Regulation Treatment Refusal Malpractice Public Opinion Jurisprudence Therapeutic Misconception Genetic Privacy Defensive Medicine Internationality Human Rights Judicial Role Freedom Parents United States Office of Research Integrity Compensation and Redress War Crimes Access to Information Federal Government Family Cultural Diversity Physician Impairment Social Justice Duty to Recontact

Technology, Industry, Agriculture2

Audiovisual Aids Multimedia

Humanities22

Ethics, Research Personal Autonomy Ethics, Medical Beneficence Ethics Committees, Research Ethics, Clinical Bioethical Issues Helsinki Declaration Conflict of Interest Ethical Review Ethics Committees Morals Moral Obligations Bioethics Therapeutic Misconception Codes of Ethics Ethics, Professional Therapeutic Equipoise Ethics Principle-Based Ethics Social Responsibility Social Justice

Information Science17

Disclosure Questionnaires Communication Documentation Audiovisual Aids Multimedia Records as Topic Information Dissemination Access to Information Medical Records Focus Groups Data Collection Interviews as Topic Pamphlets Communication Barriers Journalism, Medical Editorial Policies

Named Groups11

Research Subjects Minors Legal Guardians Research Personnel Persons Vulnerable Populations Mentally Ill Persons Patients Pregnant Women Parents Tissue Donors

Health Care89

Informed Consent Consent Forms Presumed Consent Parental Consent Mental Competency Third-Party Consent Ethics, Research Personal Autonomy Ethics, Medical Ethics Committees, Research Biological Specimen Banks Confidentiality Patient Rights Informed Consent By Minors Patient Advocacy Ethics, Clinical Patient Selection Patient Participation Clinical Trials as Topic Patient Education as Topic Physician-Patient Relations Privacy Child Advocacy Helsinki Declaration Conflict of Interest Ethical Review Questionnaires Duty to Warn Ethics Committees Liability, Legal Professional Staff Committees Government Regulation Tissue and Organ Procurement Tissue Banks Treatment Refusal Randomized Controlled Trials as Topic Malpractice Prospective Studies Voluntary Programs Bioethics Health Knowledge, Attitudes, Practice Jurisprudence Codes of Ethics Ethics, Professional Ethics Genetic Privacy Defensive Medicine Risk Assessment Selection Bias Human Rights Guidelines as Topic Attitude to Health Patient Satisfaction Records as Topic Pilot Projects Freedom Clinical Trials, Phase I as Topic United States Office of Research Integrity Clinical Trials, Phase IV as Topic Patient Identification Systems Compensation and Redress Treatment Outcome Cross-Sectional Studies Sensitivity and Specificity Medical Records Attitude of Health Personnel Focus Groups Data Collection Institute of Medicine (U.S.)Genetic Testing Practice Guidelines as Topic Federal Government Interviews as Topic Legislation, Medical Educational Status Clinical Trials Data Monitoring Committees Feasibility Studies Physician Impairment Reproducibility of Results Clinical Protocols Consumer Participation Hospitals, Teaching Donor Selection Emergencies Forms and Records Control Mass Screening Risk Factors Social Justice Duty to Recontact

Geographicals4

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