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After reading the news article below, what are the types of considerations must be used during
epidemiological investigations involving patient data?
http://www.medicalnewstoday.com/articles/137993.php
Solution
Ethical health research and privacy protections both provide valuable benefits to
society. Health research is vital to improving human health and health care—and protecting
individuals involved in research from harm and preserving their rights is essential to the conduct
of ethical research. The primary justification for protecting personal privacy is to protect the
interests of individuals. In contrast, the primary justification for collecting personally identifiable
health information for health research is to benefit society. But it is important to stress that
privacy also has value at the societal level because it permits complex activities, including
research and public health activities, to be carried out in ways that protect individuals’ dignity. It
is also important to note that health research can benefit individuals, for example, when it
facilitates access to new therapies, improved diagnostics, and more effective ways to prevent
illness and deliver care. The U.S. Department of Health and Human Services (HHS) developed a
set of federal standards for protecting the privacy of personal health information under the Health
Insurance Portability and Accountability Act of 1996 (HIPAA).1 The HIPAA Privacy Rule set
forth detailed regulations regarding the types of uses and disclosures of individuals’ personally
identifiable health information—called “protected health information”—permitted by “covered
entities” (health plans, health care clearing houses, and health care providers who transmit
information in electronic form in connection with transactions for which HHS has adopted
standards under HIPAA).2 A major goal of the Privacy Rule is to ensure that individuals’ health
information is properly protected while allowing the flow of information needed to promote
high-quality health care. The Privacy Rule also set out requirements for the conduct of health
research. The Institute of Medicine (IOM) Committee on Health Research and the Privacy of
Health Information (the committee) was charged with two principal tasks3: (1) to assess whether
the HIPAA Privacy Rule is having an impact on the conduct of health research, defined broadly
to include biomedical research, epidemiological studies, and health services research, as well as
studies of behavioral, social, and economic factors that affect health; and (2) to propose
recommendations to enable the efficient and effective conduct of important health research while
maintaining or strengthening the privacy protections of personally identifiable health
information.

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After reading the news article below, what are the types of con.pdf

  • 1. After reading the news article below, what are the types of considerations must be used during epidemiological investigations involving patient data? http://www.medicalnewstoday.com/articles/137993.php Solution Ethical health research and privacy protections both provide valuable benefits to society. Health research is vital to improving human health and health care—and protecting individuals involved in research from harm and preserving their rights is essential to the conduct of ethical research. The primary justification for protecting personal privacy is to protect the interests of individuals. In contrast, the primary justification for collecting personally identifiable health information for health research is to benefit society. But it is important to stress that privacy also has value at the societal level because it permits complex activities, including research and public health activities, to be carried out in ways that protect individuals’ dignity. It is also important to note that health research can benefit individuals, for example, when it facilitates access to new therapies, improved diagnostics, and more effective ways to prevent illness and deliver care. The U.S. Department of Health and Human Services (HHS) developed a set of federal standards for protecting the privacy of personal health information under the Health Insurance Portability and Accountability Act of 1996 (HIPAA).1 The HIPAA Privacy Rule set forth detailed regulations regarding the types of uses and disclosures of individuals’ personally identifiable health information—called “protected health information”—permitted by “covered entities” (health plans, health care clearing houses, and health care providers who transmit information in electronic form in connection with transactions for which HHS has adopted standards under HIPAA).2 A major goal of the Privacy Rule is to ensure that individuals’ health information is properly protected while allowing the flow of information needed to promote high-quality health care. The Privacy Rule also set out requirements for the conduct of health research. The Institute of Medicine (IOM) Committee on Health Research and the Privacy of Health Information (the committee) was charged with two principal tasks3: (1) to assess whether the HIPAA Privacy Rule is having an impact on the conduct of health research, defined broadly to include biomedical research, epidemiological studies, and health services research, as well as
  • 2. studies of behavioral, social, and economic factors that affect health; and (2) to propose recommendations to enable the efficient and effective conduct of important health research while maintaining or strengthening the privacy protections of personally identifiable health information.