Sample Nursing Essay Paper on Ethics in Health Care

Ethics in Health Care

Community Engagement in Health Care

            Ethics in health care is necessary, and health professionals should take care of health information for patients. Pursuing alternative community engagement is necessary. Consultation with the commonwealth may be significant depending on the nature of the choice. While individual consultation is necessary, consultation with community members is a wee of gaining public surveillance. It is important to find ways of responding to views of the community who may find it difficult to attend meetings and are not familiar with the patient’s representative. The emphasis on community engagement will encourage health professionals and policy makers to create new opportunities as they face new challenges (Hatcher, 2012). . These opportunities improve the consent process, identify ethical pitfalls and create processes for resolving ethical problems when they arise. The community also gains a higher profile creating goodwill.

Effects of Conducting research using my Medical Records without My Consent

            Examining and using patients records of past illness without their consent is unethical in healthcare. The high value should be placed on protecting the privacy, confidentiality and security of a patient’s information (Robichau, 2014). .Privacy is a crucial and valuable component of human wellbeing. Respecting privacy gives humans their moral uniqueness. Privacy is important as it facilitates values such as personal autonomy, individuality, respect, and worth as people.

            First, If and when my medical records were examined and included in research without my consent, I would feel embarrassed and discriminated. Without my consent and assurance of privacy, I may not be able to disclose complete sensitive information even to my physician. It is important for doctors to ensure privacy in health care to enhance autonomy and preventing embarrassment and discrimination (Robichau, 2014). 

            Secondly, my relationship with other people will be ruined. Although some people emphasize the need to maintain close relationships, others take a wider view of it as being essential for the maintenance of a variety of social relationships (Shelton, Freeman, Fish, Bachman, & Richardson, 2015). It will alter my relationship with different people such as physician or boss. For instance, I would share certain information with my boss than I would with my doctor.

Loss of trust

            Lack of confidentiality in health care diminishes physician’s patient relationship. I would less likely share confidential information with my doctor and impact negatively on my care. A trusting environment is crucial for the patient to disclose information that may bring about stigma such as issues on reproduction, sexual, public and psychiatrist problems. To ensure trust, doctors must seek the consent of patients before using their health records information in research.

Stigmatization

            Also, disclosing my health information without my consent, it can invite social stigma and discrimination. Since each will be aware of my health status, I will be forced to separate from my colleagues. It is as a result of discrimination from the community as a whole. Stigmatization, in turn, leads to emotional torture.

Lack of public confidence

            Also, uninformed consent may also reduce public trust in health. Disclosing of my health information will reduce my confidence in the doctor. Lack of confidence, in turn, lead to a lack of trust in the health care as a whole I will believe that each physician in the health care is not worth trusting due to the information used in research without my consent. Public confidence is crucial for any patient as it improves the relationship between the doctors and the patients.

Conclusion

Ethics plays a significant role in health care. It is important to disclose patient’s information for research with the consent of the patients. Community engagement in health is necessary to gain insights hence practice of diverse activities in the health care.

References

Shelton, A., Freeman, B., Fish, A., Bachman, J., & Richardson, L. (2015). American Journal of    Critical Care, 24(2), 148-155. doi: 10.4037/ajcc2015983

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Robichau, B. P. (2014). Healthcare information privacy and security: Regulatory compliance and data security in the age of electronic health records.

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Hatcher, J. A., & Bringle, R. G. (2012). Understanding service-learning and community    engagement: Crossing boundaries through research. Charlotte, N.C: Information Age        Pub.

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