Evidence map›Paper›PMID 21755300›Full record

ArticleDigestive diseases and sciences2012

Clinical significance of discordant positive hepatitis C virus transcription-mediated amplification following end of treatment response.

Anisha Thadani, Jennifer Harley, Jonah Rubin, Edward Lebovics

Abstract readEvaluation Study
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In one paragraph

Article in Digestive diseases and sciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Anisha ThadaniSarah C Upham Division of Gastroenterology and Hepatobiliary Diseases, New York Medical College, Munger Pavilion, Suite 206, Valhalla, NY 10595, USA.
Jennifer Harley
Jonah Rubin
Edward Lebovics

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPolymerase chain reaction (PCR) assays are the standard for detecting hepatitis C virus viremia. The transcription-mediated amplification (TMA)-based assay is more sensitive.

methodsWe retrospectively reviewed the charts of patients with a post-end of treatment (EOT) PCR-/TMA+ result to assess the clinical significance of a positive TMA result after a PCR negative EOT response or sustained viral response (SVR). Patients were divided into Group 1: PCR-/TMA+ after EOT response but during 24 week follow-up (n = 4); and Group 2: PCR-/TMA+ after SVR (n = 11).

resultsAll Group 1 patients achieved SVR. No Group 2 patients became PCR positive or had a rise in ALT. The TMA subsequently became negative in 6/7 patients with follow-up evaluation.

conclusionsA discordant positive TMA post-EOT response or SVR did not seem to be clinically significant. This finding supports the possibility that patients with SVR have an acquired immune surveillance that prevents low-level viremia from progressing to clinical relapse.

Indexed as

Antiviral AgentsDisease ProgressionFollow-Up StudiesGenotypeHepacivirusHepatitis C, ChronicHumansNucleic Acid Amplification TechniquesRecurrenceRetrospective StudiesRNA, ViralSensitivity and SpecificityTreatment OutcomeAntiviral AgentsRNA, Viral

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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.