HIV is a complex and multifaceted entity, especially in terms of the biopsychosocial model of disease. For decades, its biological characteristics have consistently outstripped our human ability to understand its molecular and pathogenic complexities. The psychosocial, legal and ethical implications are equally devastating, requiring concerted global debates and commitments on the subject of human rights. While the Universal Declaration of Human Rights (UDHR) was adopted as an instrument that guarantees and safeguards the inherent dignity and equality of every being, and as a framework for bettering the relationship between a government and its citizenry, the translation of the declaration into practical law, and its subsequent implementation, has suffered continual debates, hitches and neglect worldwide. [1] To what extent has Nigeria implemented policies protecting any of the 'rights' it purports to defend? It is evident that in Nigeria, HIV-positive people are denied employment and even access to healthcare on the basis of stigmatisation. [2] Mandatory HIV testing as a prerequisite for surgery, and even worse, the refusal of treatment to patients infected with the virus, is ethically unacceptable worldwide. [3] In India, such practice was criticised and said to have no public health justification, as it has the potential to drive vulnerable and possibly HIV-positive people out of HIV/AIDS intervention programmes. [4] Thomas [3] showed that even when the government had issued guidelines in compliance with the UDHR charter, they were rarely enforced, resulting in the widespread practice of mandatory HIV testing, with practitioners maintaining that the risk of transmission is not zero, despite universal precautions. While surgeons could argue the case on the basis of their risk of infection, mandatory testing leads to stigmatisation and discrimination. Conversely, in the developed world, many clients treat infected health practitioners with distrust, a situation that led the American College of Surgeons (ACS) to release a guideline to resolve the stalemate. [5] This study assessed the practice of mandatory HIV testing, HIV testing without consent and disclosure of test results in Nigeria.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.