Evidence map›Paper›PMID 31265759›Full record

ArticleTransfusion2019

Reassessment of hepatitis B virus window periods for two transcription-mediated amplification assays using screening data of South African blood donors.

Marion Vermeulen, Harry van Drimmelen, Charl Coleman, Wendy Sykes, Ravi Reddy, Michael Busch, Steve Kleinman, Nico Lelie

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Transfusion, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 4 countries.

Marion VermeulenSouth African National Blood Service (SANBS), Johannesburg, South Africa.ORCID 0000-0003-4383-4526
Harry van DrimmelenDDL Laboratories, Biologicals Quality Control, Heiloo, The Netherlands.
Charl ColemanSouth African National Blood Service (SANBS), Johannesburg, South Africa.
Wendy SykesSouth African National Blood Service (SANBS), Johannesburg, South Africa.
Ravi ReddySouth African National Blood Service (SANBS), Johannesburg, South Africa.
Michael BuschVitalant Research Institute (previously Blood Systems Research Institute), San Francisco, California.
Steve KleinmanUniversity of British Columbia, Victoria, British Columbia, Canada.
Nico LelieLelie Research, Alkmaar, The Netherlands.
South African National Blood Service · ZABlood Systems Research Institute · USDDL Diagnostic Laboratory · NLUniversity of British Columbia · CA

Funding

Research training in HIV-related transfusion medicine and hematology in South AfricaD43TW010345 · FIC · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI UTE JENTSCH, EDWARD L MURPHY · 2017 to 2026
$3.0M
FIC NIH HHS D43 TW010345
6 · The paper itself

Abstract

backgroundTranscription-mediated amplification assays for HBV DNA detection have transitioned from the Ultrio to the Ultrio Plus assay, which features increased analytic sensitivity due to inclusion of a target enhancer reagent. The impact on HBV detection for different categories of HBV infection has not been fully evaluated. STUDY DESIGN AND

methodsHepatitis B virus (HBV) DNA and hepatitis B surface antigen (HBsAg) detection rates as well as viral load (VL) distributions in HBV nucleic acid test (NAT)-yield samples were compared during 1 year of screening of South African blood donors with the Ultrio assay and the subsequent year by the Ultrio Plus version. HBV-DNA concentration at the HBsAg seroconversion point was established by regression analysis using a set of antibody to hepatitis B core antigen-negative acute viremic samples.

resultsUltrio Plus detected twofold more window-period (WP) NAT yield donations and 1.7-fold more occult HBV infections than Ultrio. The VL distribution data indicated that Ultrio not only missed samples of less than 100 copies/mL, but also a substantial number higher than this level. The VL at the HBsAg seroconversion point was estimated at 916 copies/mL, whereas the VL at the NAT-conversion points was calculated at 63 and 4.1 copies/mL for Ultrio and Ultrio Plus. This reduced the infectious WP (compared to HBsAg testing) by 10.3 and 20.4 days, respectively.

conclusionThe higher-than-expected increase in HBV-NAT yields after introduction of the Ultrio Plus assay is likely attributable to variable sensitivity of the former Ultrio assay for different HBV samples. Therefore, previously published HBV WP reduction and residual risk estimates based on analytical sensitivity of the Ultrio assay need to be revised.

Indexed as

Blood DonorsDiagnostic Tests, RoutineLimit of DetectionBlood BankingBlood BanksCalibrationDNA, ViralHepatitis BHepatitis B Surface AntigensHepatitis B virusHumansMass ScreeningPredictive Value of TestsReal-Time Polymerase Chain ReactionSensitivity and SpecificitySerologic TestsDNA, ViralHepatitis B Surface Antigens

Identifiers

PMID31265759
PMCPMC7384397
OpenAlexW2953446728

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.