1998
DOI: 10.1046/j.1537-2995.1998.381098440853.x
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Mini‐pool screening by nucleic acid testing for hepatitis B virus, hepatitis C virus, and HIV: preliminary results

Abstract: It is feasible to incorporate NAT-based screening of mini-pools into the routine virus diagnostics of a large blood transfusion service. It remains to be determined whether screening blood donations by NAT will indeed increase the safety of blood supply.

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Cited by 66 publications
(44 citation statements)
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“…Group testing has a rich history dating back to the works of Watson [1] and Dorfman [2]. Today, group testing is exploited in a variety of areas including epidemiology, genetics, blood-bank screening, drug discovery, biology, and plant pathology [3-9]. Depending on the application, group testing may be used simply to estimate the proportion of positives or to classify each individual item as positive or negative.…”
Section: Introductionmentioning
confidence: 99%
“…Group testing has a rich history dating back to the works of Watson [1] and Dorfman [2]. Today, group testing is exploited in a variety of areas including epidemiology, genetics, blood-bank screening, drug discovery, biology, and plant pathology [3-9]. Depending on the application, group testing may be used simply to estimate the proportion of positives or to classify each individual item as positive or negative.…”
Section: Introductionmentioning
confidence: 99%
“…The FDA requires a 95‐percent detection limit of at least 100 copies per mL for both HCV and HIV NAT blood screening assays and a sensitivity of at least 5000 copies per mL per donation when MP‐NAT is performed. Anticipating these developments, the blood transfusion organizations have introduced or are in the process of implementing MP‐NAT of blood donations for the presence of HCV RNA, HIV RNA, and HBV DNA 1‐5 . With the introduction of NAT, there was an urgent need for standardization to allow interlaboratory comparison of NAT assays.…”
mentioning
confidence: 99%
“…They claim that this low rate is due to single‐donation testing and that pool PCR testing, in contrast, results in a contamination rate between 3.5 and 5.0 percent. For reference, they cite studies by our group 2 and by Cardoso et al 3 In fact, however, the contamination rate of our HCV pool PCR as described in Roth et al 2 was only 0.4 percent. Although not explicitly demonstrated, the HCV‐specific false‐positive data may be easily deduced from the figure, which shows the numbers of PCR‐confirmed and ‐false‐positive values for each virus over time (Fig.…”
mentioning
confidence: 77%