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NAT yield in blood donors: An observational study
Ankit Sharma1, Sunita Bundas1, Rashmi Parashar2
1Department of Immunohematology and Transfusion Medicine, SMS Medical College and Hospital, Jaipur, Rajasthan, India.
Individual donation nucleic acid testing (ID-NAT) detected viral transfusion-transmissible infections (TTIs) in 0.09% of blood donors. This sensitive method identified infections missed by traditional screening, enhancing blood safety.
Area of Science:
- Transfusion Medicine
- Virology
- Public Health
Background:
- Individual donation nucleic acid testing (ID-NAT) is a highly sensitive method for detecting viral transfusion-transmissible infections (TTIs).
- Traditional screening methods like ELISA may miss infections in non-seroconverting or delayed seroconverting donors.
- Enhancing blood safety through advanced screening technologies is crucial for public health.
Purpose of the Study:
- To analyze the results of ID-NAT in a tertiary care center in North India.
- To evaluate the yield of ID-NAT across different donor demographics, including age, gender, and blood group.
- To assess the effectiveness of ID-NAT in identifying viral infections missed by conventional screening.
Main Methods:
- A retrospective analysis of ID-NAT results was conducted.
- Data from 18,313 apparently healthy adult blood donors were collected between June 2019 and December 2021.
- Donors were tested using ID-NAT, and results were analyzed based on year, viral markers, and donor characteristics.
Main Results:
- The overall NAT yield was 1 in 1017 (0.09%).
- Specific NAT yields were: HBV 1 in 1077, HCV 1 in 18313, and no HIV yield.
- NAT yield varied annually, with rates of 1 in 754 (2019), 1 in 2368 (2020), and 1 in 741 (2021).
Conclusions:
- ID-NAT significantly enhances blood safety by detecting infections missed by ELISA, particularly occult hepatitis B.
- The study highlights the importance of ID-NAT in identifying non-seroconverting or delayed seroconverting infections.
- Implementing ID-NAT is essential for a comprehensive strategy to prevent transfusion-transmitted viral infections.
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