scholarly journals Association of Schistosomiasis with False-Positive HIV Test Results in an African Adolescent Population

2010 ◽  
Vol 48 (5) ◽  
pp. 1570-1577 ◽  
Author(s):  
D. B. Everett ◽  
K. J. Baisely ◽  
R. McNerney ◽  
I. Hambleton ◽  
T. Chirwa ◽  
...  
2012 ◽  
Vol 5 (1) ◽  
Author(s):  
Steven Baveewo ◽  
Moses R Kamya ◽  
Harriet Mayanja-Kizza ◽  
Robin Fatch ◽  
David R Bangsberg ◽  
...  

2007 ◽  
Vol 45 (1) ◽  
pp. 139-140 ◽  
Author(s):  
A. Salinas ◽  
M. Gorgolas ◽  
M. Fernandez-Guerrero

2012 ◽  
Vol 2012 ◽  
pp. 1-4 ◽  
Author(s):  
Tamara T. Chao ◽  
Jeanne S. Sheffield ◽  
George D. Wendel ◽  
M. Qasim Ansari ◽  
Donald D. McIntire ◽  
...  

2018 ◽  
Vol 5 (9) ◽  
Author(s):  
Joanne D Stekler ◽  
Lauren R Violette ◽  
Lisa Niemann ◽  
Vanessa M McMahan ◽  
David A Katz ◽  
...  

Abstract Regular HIV testing is required to ensure the safety of HIV pre-exposure prophylaxis (PrEP). We describe and discuss a series of false-positive HIV test results from an individual receiving PrEP. The expansion of PrEP will likely result in greater numbers of false-positive test results that may pose challenges for interpretation.


PLoS ONE ◽  
2021 ◽  
Vol 16 (1) ◽  
pp. e0245189
Author(s):  
Michael A. Linström ◽  
Wolfgang Preiser ◽  
Nokwazi N. Nkosi ◽  
Helena W. Vreede ◽  
Stephen N. J. Korsman ◽  
...  

Automated testing of HIV serology on clinical chemistry analysers has become common. High sample throughput, high HIV prevalence and instrument design could all contribute to sample cross-contamination by microscopic droplet carry-over from seropositive samples to seronegative samples resulting in false positive low-reactive results. Following installation of an automated shared platform at our public health laboratory, we noted an increase in low reactive and false positive results. Subsequently, we investigated HIV serology screening test results for a period of 21 months. Of 485 initially low positive or equivocal samples 411 (85%) tested negative when retested using an independently collected sample. As creatinine is commonly requested with HIV screening, we used it as a proxy for concomitant clinical chemistry testing, indicating that a sample had likely been tested on a shared high-throughput instrument. The contamination risk was stratified between samples passing the clinical chemistry module first versus samples bypassing it. The odds ratio for a false positive HIV serology result was 4.1 (95% CI: 1.69–9.97) when creatinine level was determined first, versus not, on the same sample, suggesting contamination on the chemistry analyser. We subsequently issued a notice to obtain dedicated samples for HIV serology and added a suffix to the specimen identifier which restricted testing to a dedicated instrument. Low positive and false positive rates were determined before and after these interventions. Based on measured rates in low positive samples we estimate that before the intervention, of 44 117 HIV screening serology samples, 753 (1.71%) were false positive, declining to 48 of 7 072 samples (0.68%) post-intervention (p<0.01). Our findings showed that automated high throughput shared diagnostic platforms are at risk of generating false-positive HIV test results, due to sample contamination and that measures are required to address this. Restricting HIV serology samples to a dedicated platform resolved this problem.


Author(s):  
Rosemary A. Audu ◽  
Rosemary N. Okoye ◽  
Chika K. Onwuamah ◽  
Fehintola A. Ige ◽  
Adesola Z. Musa ◽  
...  

Background: In order to scale up access to HIV counselling and testing in Nigeria, an HIV diagnostic algorithm based on rapid testing was adopted. However, there was the need to further evaluate the testing strategy in order to better assess its performance, because of the potential for false positivity.Objectives: The objective of this study was to compare positive HIV test results obtained from the approved rapid testing algorithm with results from western blot tests performed on samples from the same patient.Methodology: A retrospective review was conducted of HIV screening and confirmatory results for patients seen between 2007 and 2008. Rapid test and western blot results were extracted and compared for concordance. Discordant results were further reviewed using a combination of HIV-1 RNA viral load and CD4+ cell count test results and clinical presentation from medical records.Results: Analysis of 2228 western blot results showed that 98.3% (n = 2191) were positive for HIV-1, 0.4% (n = 8) were positive for HIV-2 and 0.3% (n = 7) were dual infections (positive for both HIV-1 and HIV-2); 0.6% (n = 13) were indeterminate and 0.4% (n = 9) were negative. Further investigation of the 13 indeterminate results showed nine to be HIV-1 positive and four to be HIV-negative, for a total of 13 negative results. The positive predictive value of the HIV counselling and testing algorithm was 99.4%.Conclusion: Using the rapid testing algorithm alone, false positives were detected. Therefore, effective measures such as training and retraining of staff should be prioritised in order to minimise false-positive diagnoses and the associated potential for long-term psychological and financial impact on the patients.


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