Health intervention in the context of Infectious disease (medical specialty)


Health intervention in the context of Infectious disease (medical specialty)

⭐ Core Definition: Health intervention

A public health intervention is any effort, policy, or program intended to improve mental and physical health at the population level. Interventions involve social movements that strive to support public health at different levels of society. Public health interventions may be run by a variety of organizations, including governmental health departments and non-governmental organizations (NGOs). Interventions can be personal, community-level, national, and global. Common types of interventions include screening programs, vaccination, food and water supplementation, and health promotion. Common issues that are the subject of public health interventions include obesity, drug, tobacco, and alcohol use, and the spread of infectious disease, e.g. HIV. Public health interventions are distinct from healthcare interventions in terms of their scope, methods, and objectives. Specifically, public health information tends to focus on population-level information and preventative measures while healthcare interventions tend to focus on the individual. Though, both are highly interconnected and necessarily complementary.

A policy may meet the criteria of a public health intervention if it prevents disease on both the individual and community level and has a positive impact on public health.

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Health intervention in the context of Beneficence (ethics)

Beneficence in general means "active well-doing". Duties of beneficence form a part of various religious and secular ethical theories. As an applied ethical concept relating to research, beneficence means that researchers should have the welfare of the research participant as a goal of any clinical trial or other research study. The antonym of this term, maleficence, describes a practice that opposes the welfare of any research participant. According to the Belmont Report, researchers are required to follow two moral requirements in line with the principle of beneficence: do not harm, and maximize possible benefits for research while minimizing any potential harm on others.

The idea that medical professionals and researchers would always practice beneficence seems natural to most patients and research participants, but in fact, every health intervention or research intervention has potential to harm the recipient. There are many different precedents in medicine and research for conducting a cost–benefit analysis and judging whether a certain action would be a sufficient practice of beneficence, and the extent to which treatments are acceptable or unacceptable is under debate.

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Health intervention in the context of Phases of clinical research

The phases of clinical research are the stages in which scientists conduct experiments with a health intervention to obtain sufficient evidence for a process considered effective as a medical treatment. For drug development, the clinical phases start with testing for drug safety in a few human subjects, then expand to many study participants (potentially tens of thousands) to determine if the treatment is effective. Clinical research is conducted on drug candidates, vaccine candidates, new medical devices, and new diagnostic assays.

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