Alternatives to nucleic acid testing in the blood transfusion service

Since October 2013, French Polynesia has experienced the largest documented outbreak of Zika virus (ZIKAV) infection. To prevent transmission of ZIKAV by blood transfusion, specific nucleic acid testing of blood donors was implemented. From November 2013 to February 2014: 42 (3%) of 1,505 blood donors, although asymptomatic at the time of blood donation, were found positive for ZIKAV by PCR. Our results serve to alert blood safety authorities about the risk of post-transfusion Zika fever.

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Low risk of SARS-CoV-2 in blood transfusion

PLoS ONE ◽

10.1371/journal.pone.0249069 ◽

2021 ◽

Vol 16 (4) ◽

pp. e0249069

Author(s):

Michael Owusu ◽

Augustina Angelina Sylverken ◽

Philip El-Duah ◽

Nana Kwame Ayisi-Boateng ◽

Richmond Yeboah ◽

...

Keyword(s):

Nucleic Acid ◽

Blood Transfusion ◽

Developed Countries ◽

Viral Rna ◽

Acid Extraction ◽

Cross Sectional ◽

Global Challenge ◽

Predominant Symptom ◽

Blood Transfusion Service ◽

Novel Coronavirus

Background The novel coronavirus disease (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), continues to remain a global challenge. There is emerging evidence of SARS-CoV-2 virus found in the blood of patients from China and some developed countries. However, there is inadequate data reported in Ghana and other parts of Africa, where blood transfusion service heavily relies on voluntary and replacement blood donors. This study aimed to investigate whether plasma of infected individuals could pose significant transfusion transmitted risk of COVID-19 in Ghanaian populations. Methods This cross-sectional retrospective study was conducted at the Kumasi Centre for Collaborative Research into Tropical Medicine (KCCR), KNUST, Ghana. Study subjects comprised contacts of COVID-19 individuals, those with classical symptoms of COVID-19 and individuals who had recovered based on the new Ghana discharge criteria. Whole blood, sputum or deep coughed saliva samples were collected and transported to KCCR for SARS-CoV-2 testing. Viral nucleic acid was extracted from sputum/nasopharyngeal samples using Da An Gene column based kit and from plasma using LBP nucleic acid extraction kit. Real-Time PCR was performed specifically targeting the ORF1ab and Nucleocapsid (N) genomic regions of the virus. Results A total of 97 individuals were recruited into the study, with more than half being males (58; 59.7%). The mean age of all subjects was 33 years (SD = 7.7) with minimum being 22 years and maximum 56 years. Majority (76; 78.4%) of all the subjects were asymptomatic, and among the few symptomatic subjects, cough (10; 10.3%) was the most predominant symptom. Of the 97 sputum samples tested, 79 (81.4%) were positive for SARS-CoV-2. We identified SARS-CoV-2 viral RNA in the plasma of 1 (1.03%) subject who had clinically recovered. Conclusion This study reports the identification of SARS-CoV-2 viral RNA in a convalescent individual in Ghana. Due to the low prevalence observed and the marginal cycling thresholds associated, the risk of transfusion transmission of SARS-CoV-2 is negligible. Well-powered studies and advanced diagnostics to determine infectious viremia is recommended to further evaluate the potential risk of hematogenous transmission among recovered patients.

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Fourth-Generation ELISA Screening of Blood Donors: A Reliable Alternative to Nucleic Acid Testing

Journal of BioMedical Research and Clinical Practice ◽

10.46912/jbrcp.214 ◽

2021 ◽

Vol 4 (1) ◽

pp. 97-104

Author(s):

Z Ayuba ◽

OD Damulak ◽

L Salawu ◽

ED Jatau ◽

J Jasini ◽

...

Keyword(s):

Nucleic Acid ◽

Blood Transfusion ◽

Blood Donors ◽

Nucleic Acid Amplification ◽

Fourth Generation ◽

Research Centre ◽

Nucleic Acid Amplification Testing ◽

Resource Limited ◽

Blood Transfusion Service ◽

P24 Antigen

The gold standard for HIV screening of blood donors is individual nucleic acid amplification testing (NAT). However, individual NAT testing is cost-prohibitive, especially in a resource-limited setting. The fourth-generation ELISA that detects both p24 antigen and antibody to HIV-1 and 2 has been recommended as the minimum test for HIV to enhance blood transfusion safety and can be an alternative to NAT testing in resource-limited settings. The aim was to assess the performance of a fourth-generation ELISA in use at a regional blood transfusion service using nucleic acid amplification testing on units of screened blood negative to HIV. The study was a cross-sectional study conducted at the National Blood Transfusion Service center and the Plateau State Virology Research Centre, both in Jos, Nigeria. Between August and October 2016, one thousand and eighteen voluntary blood donors were recruited consecutively and had their samples tested using fourth-generation ELISA. One thousand p24 antigen-negative samples were pooled for NAT in an aliquot of 50 samples. All the pools of fifty samples of 1,000 HIV p24 antigen-antibody negative donor blood screened by the fourth-generation ELISA tested negative for HIV RNA on nucleic acid amplification. The yield of pooled NAT for HIV after a fourth-generation ELISA screening of blood donors was found to be zero in this study, thus establishing the fourth-generation ELISA's reliability. Therefore, we recommend adopting the fourth-generation ELISA test as a minimum requirement for blood donor screening.

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West Nile virus blood transfusion-related infection despite nucleic acid testing

Transfusion ◽

10.1111/j.0041-1132.2004.04130.x ◽

2004 ◽

Vol 44 (12) ◽

pp. 1695-1699 ◽

Cited By ~ 44

Author(s):

Alexandre Macedo de Oliveira ◽

Brady D. Beecham ◽

Susan P. Montgomery ◽

Robert S. Lanciotti ◽

Jeffrey M. Linnen ◽

...

Keyword(s):

West Nile Virus ◽

Nucleic Acid ◽

Blood Transfusion ◽

Nucleic Acid Testing ◽

West Nile

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Elevated white blood cell count does not predict Clostridium difficile nucleic acid testing results

Clinical Infectious Diseases ◽

10.1093/cid/ciab106 ◽

2021 ◽

Author(s):

Dustin E Bosch ◽

Patrick C Mathias ◽

Niklas Krumm ◽

Andrew Bryan ◽

Ferric C Fang ◽

...

Keyword(s):

Nucleic Acid ◽

Clostridium Difficile ◽

Blood Cell ◽

Cell Count ◽

Prognostic Marker ◽

White Blood Cell Count ◽

White Blood Cell ◽

Inpatient Setting ◽

Nucleic Acid Testing ◽

Blood Cell Count

Abstract Background An elevated white blood cell count (>15 thousand/μL) is an established prognostic marker in patients with Clostridium difficile infection (CDI). Small observational studies have suggested that a markedly elevated WBC should prompt consideration of CDI. However, there is limited evidence correlating WBC elevation with the results of C. difficile nucleic acid testing (NAAT). Methods Retrospective review of laboratory testing, outcomes, and treatment of 16,568 consecutive patients presenting to 4 hospitals over four years with NAAT and WBC testing on the same day. Results No significant relationship between C. difficile NAAT results and concurrent WBC in the inpatient setting was observed. Although an elevated WBC did predict NAAT results in the outpatient and emergency department populations (p<0.001), accuracy was poor, with receiver-operator areas under the curve of 0.59 and 0.56. An elevated WBC (>15 thousand/μL) in CDI was associated with a longer median hospital length of stay (15.5 vs. 11.0 days, p<0.01), consistent with leukocytosis as a prognostic marker in CDI. NAAT-positive inpatients with elevated WBC were more likely to be treated with metronidazole and/or vancomycin (relative ratio 1.2, 95% confidence interval 1.1–1.3) and die in the hospital (relative ratio 2.9, 95% CI 2.0–4.3). Conclusions Although WBC is an important prognostic indicator in patients with CDI, an isolated WBC elevation has low sensitivity and specificity as a predictor of fecal C. difficile NAAT positivity in the inpatient setting. A high or rising WBC in isolation is not a sufficient indication for CDI testing.

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