LifeServe Blood Center is your non-profit, community-based blood center that has served the needs of local hospitals and patients in our regions for more than 75 years. As one of the 15 largest blood centers in the country, LifeServe is the sole provider of blood and blood products to more than 160 hospitals primarily in Iowa, Nebraska and South Dakota.
LifeServe is regulated by the U.S. Food and Drug Administration (FDA), which is responsible for regulatory oversight of the U.S. blood supply. The FDA enforces standards for blood collection and for the manufacturing of blood products.
In 2023, the FDA updated their policy on recommendations for evaluating donor eligibility using individual assessment of health and history to reduce the risk of HIV transmission by blood and blood products. The questions are the same for every donor, regardless of sexual orientation, sex or gender. The overall assessment is that these changes will make the blood supply safer with risk assessment of all donors’ sexual activity, not just one group.
The specific changes to the Donor History Questionnaire (DHQ) or QuickPass are:
- In the past three months, have you “had sexual contact with a new partner?”
- In the past three months, have you “had sexual contact with more than one partner?”
- “Are you pregnant now?”
- “Have you ever been pregnant?”
If the donor answers yes to either question regarding sexual contact, they will be asked about the type of sexual contact (anal sex) to determine the risk of newly acquired transfusion-transmitted infection.
IDA Changes FAQ
Human blood cannot be manufactured which means we need more than 100,000 community members to donate each year to ensure local hospital patients have the blood products they need, when they need them. Fewer than three percent of eligible donors donate on a regular basis. With the FDA’s guidance, there is potential for the quantity of eligible donors to increase through the reduction of unnecessary deferrals.