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Diseases4

Neoplasms HIV Infections Death Emergencies

Analytical, Diagnostic and Therapeutic Techniques and Equipment43

Human Experimentation Therapeutic Human Experimentation Nontherapeutic Human Experimentation Research Design Clinical Trials as Topic Patient Selection Questionnaires Randomized Controlled Trials as Topic Prospective Studies Risk Assessment Data Collection Control Groups AIDS Serodiagnosis Treatment Outcome Reproducibility of Results Cross-Sectional Studies Records as Topic Interviews as Topic Risk Factors Surgical Procedures, Operative Sensitivity and Specificity Pilot Projects Surgical Procedures, Elective Clinical Trials, Phase IV as Topic Clinical Trials, Phase I as Topic Embryo Disposition Medical Records Genetic Testing Clinical Protocols Feasibility Studies Mass Screening Retrospective Studies Focus Groups Magnetic Resonance Imaging Incidental Findings Stem Cell Research Therapies, Investigational Logistic Models Cohort Studies Health Care Surveys Statistics, Nonparametric Donor Selection Follow-Up Studies

Psychiatry and Psychology35

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

Phenomena and Processes3

Sensitivity and Specificity Time Factors Pregnancy

Disciplines and Occupations26

Human Experimentation Research Therapeutic Human Experimentation Nontherapeutic Human Experimentation Genetic Research Research Design Biomedical Research Nursing Research Health Services Research Behavioral Research Qualitative Research Translational Medical Research Empirical Research Community-Based Participatory Research Clinical Nursing Research Emergency Medicine General Surgery Dental Research Anesthesiology Pediatrics Psychiatry Medical Oncology Stem Cell Research Public Health Genetics, Medical Neurosurgery

Anthropology, Education, Sociology and Social Phenomena48

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 Government Regulation Duty to Warn Liability, Legal Treatment Refusal Public Opinion Therapeutic Misconception Malpractice Jurisprudence Genetic Privacy Human Rights Defensive Medicine Parents Access to Information Internationality United States Office of Research Integrity National Institutes of Health (U.S.)Freedom Judicial Role Compensation and Redress Federal Government War Crimes Family Cultural Diversity Developing Countries International Cooperation United States Dept. of Health and Human Services Socioeconomic Factors Physician Impairment Organizational Policy Duty to Recontact Culture Social Justice

Technology, Industry, Agriculture2

Audiovisual Aids Multimedia

Humanities25

Ethics, Research Personal Autonomy Ethics, Medical Beneficence Ethics Committees, Research Ethics, Clinical Bioethical Issues Conflict of Interest Helsinki Declaration Ethical Review Ethics Committees Morals Moral Obligations Bioethics Therapeutic Misconception Ethics, Professional Ethics Codes of Ethics Therapeutic Equipoise Social Responsibility Principle-Based Ethics History, 20th Century Knowledge Religion and Medicine Social Justice

Information Science22

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

Named Groups14

Research Subjects Minors Research Personnel Legal Guardians Persons Vulnerable Populations Mentally Ill Persons Patients Parents Pregnant Women Tissue Donors Physicians Infant, Newborn Volunteers

Health Care113

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

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Informed Consent Consent Forms Presumed Consent Parental Consent Ethics, Research Mental Competency Human Experimentation Third-Party Consent Research Subjects Research Disclosure Therapeutic Human Experimentation Nontherapeutic Human Experimentation Comprehension Personal Autonomy Ethics, Medical Genetic Research Beneficence Minors Biological Specimen Banks Ethics Committees, Research Research Design Confidentiality Refusal to Participate Research Personnel Biomedical Research Patient Rights Paternalism Informed Consent By Minors Research Support as Topic Ethics, Clinical Patient Advocacy Decision Making Clinical Trials as Topic Patient Selection Researcher-Subject Relations Patient Participation Legal Guardians Bioethical Issues Nursing Research Patient Education as Topic Truth Disclosure Privacy Physician-Patient Relations Questionnaires Conflict of Interest Child Advocacy Helsinki Declaration United States Health Services Research Communication Government Regulation Tissue Banks Duty to Warn Ethical Review Professional Staff Committees Ethics Committees Morals Behavioral Research Liability, Legal Moral Obligations Tissue and Organ Procurement Randomized Controlled Trials as Topic Qualitative Research Treatment Refusal Public Opinion Translational Medical Research Bioethics Health Knowledge, Attitudes, Practice Persons Prospective Studies Empirical Research Vulnerable Populations Great Britain Guidelines as Topic Therapeutic Misconception Trust Documentation Information Dissemination Ethics, Professional Ethics Risk Assessment Codes of Ethics Malpractice Attitude Audiovisual Aids Jurisprudence Voluntary Programs Community-Based Participatory Research Attitude to Health Genetic Privacy Therapeutic Equipoise Data Collection Social Responsibility Control Groups Mentally Ill Persons AIDS Serodiagnosis Selection Bias Multimedia Treatment Outcome

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