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FDA’s Blood Ban Reversal for Gay Men, Explained
The United States Food and Drug Administration announced on May 11, 2023, that it has officially from donating blood under many circumstances on May 11, 2023. The ban was in the early days of the AIDS epidemic, but for years medical professionals and gay-rights advocates have argued that the ban is no longer medically justifiable and that it unnecessarily discriminates against .
is a health policy researcher at the University of California, Los Angeles, who studies HIV treatment and prevention. She explains the history of the ban and the reasoning behind its long-awaited reversal.
1. When and why did the ban begin?
When the FDA in 1983 for men who have sex with men, there were good reasons for broad regulations to ensure the safety of the blood supply. At the start of the AIDS epidemic, public health officials were dealing with an unknown virus that was spread through unknown means. Researchers a year later, in 1984, and it took another year to approve the first test to screen blood donations for HIV in 1985.
Despite the ban on blood donations from men who have sex with men, there was some small risk that failures in and could lead to transmission of HIV or other diseases from blood transfusion. But over the years, scientific advancements and strict protocols have helped to nearly through blood. In fact, the last documented transmission of HIV through the a U.S. donor’s blood product .
Starting in 2013, the U.S. government began implementing a the safety of the U.S. blood supply for a variety of different pathogens, including HIV.
2. Why lift the ban now?
While the blood donation ban—as well as many other —was reasonable at the time, the science has changed. Researchers and public health officials have gained a better understanding of how HIV is transmitted and the risks associated with different activities. Given today’s knowledge, many that the benefits of the ban no longer outweigh the hit to the blood supply or the harm caused by what is a discriminatory rule.
The FDA has been slowly working toward this change. In December 2015, the organization took a big step by allowing men who have sex with men to donate blood if they haven’t had . That period was in April 2020, during the height of the COVID-19 pandemic, to help fight a .
While a step in the right direction, these updates didn’t change the blunt assessment by the FDA that men who have sex with men are performing high-risk sexual behaviors and are themselves high-risk donors. Researchers and gay-rights advocates have long argued that and fail to realistically consider the differences in risk associated with the type of sex, type of relationship, number of partners and frequency of sexual encounters.
The FDA’s latest go a long way toward improving clarity about what makes a person a high-risk donor and remove the blanket categorization of prospective donors based on their gender and sexual orientation alone.
Under the new guidelines, there is a way to differentiate between individuals who are monogamous and those who are not, as well as between those who have not engaged in anal sex in the prior three months and those who have. The recommendation now suggests that blood donor history questionnaires be used to evaluate an individual’s risk, rather than a reliance on broad categorizations. If the assessment finds an individual to be high-risk, then the guidelines recommend that person be prevented from donating blood for three months.
3. What effect could this have on the blood supply?
The FDA’s latest move represents a seismic shift for men who have sex with men as well as for the .
According to recent research, a conservative estimate suggests that the lifting of the ban will lead to a . With the ongoing blood shortage, that increase could help save more than a million lives. In addition, removing gender and sexual orientation from the risk assessment for blood donation will take the U.S. one step further in addressing stigma and discrimination against men who have sex with men.
This article was originally published by . It has been published here under a Creative Commons license.
Ayako Miyashita
is an adjunct professor at the UCLA Luskin School of Public Affairs, Department of Social Welfare. As co-director for the Southern California HIV/AIDS Policy Research Center (SCHPRC), Professor Miyashita collaborates on interdisciplinary research with community and academic partners to bring the most relevant and timely evidence to bear on California’s efforts to develop and maintain efficient, cost-effective, and accessible programs and services to people living with or at risk for HIV, viral hepatitis, sexually transmitted infections and overdose. Her research interests focus on HIV and other related health disparities at the intersection of race/ethnicity, sexual and gender identity, and migrant status.
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