By Ana Espino | Published on July 28, 2025 | 3 min read
#HepatitisC #Immunity
#InfectiousDiseases #Diagnosis
Hepatitis C remains a major global
health issue, with nearly 50 million people infected worldwide. Although highly
effective treatments are now available,
screening continues to be a weak link
in the care cascade—especially among vulnerable populations such as people who
inject drugs (PWID), who are the main at-risk group.
Despite universal access to
direct-acting antivirals (DAAs),
screening and treatment rates are declining.
The standard diagnostic pathway—based on venous blood draws and delayed
results—often leads to
loss to follow-up, particularly among PWID. In this context,
rapid point-of-care tests offer a promising alternative. However, their
specificity remains limited: a significant number of positive results concern
patients who have already cleared the infection, leading to unnecessary
confirmatory RNA testing. This
hampers the operational efficiency of screening
campaigns, especially in resource-limited settings. The current challenge is
therefore to balance speed, simplicity, and reliability.
This study assessed whether
reading
the OraQuick rapid test at 5 minutes—rather than the recommended 20
minutes—could
reduce unnecessary RNA tests without missing active infections.
Can 5 minutes be enough for accurate screening?
In this study, 298 participants with a history of injecting drug use and no prior treatment with DAAs were included. Each participant underwent an OraQuick rapid test, with two reading times — at 5 minutes and then at 20 minutes — followed by a confirmatory RNA test (GeneXpert or laboratory-based). The performance of the 5-minute reading was compared to the 20-minute reading and RNA results to assess the device’s sensitivity, specificity, and predictive values. At 5 minutes, the test detected 97.5% of individuals who were truly viremic (high sensitivity), but with a specificity limited to 37%.
Compared to the standard 20-minute read,
the 5-minute
interpretation reduced unnecessary RNA confirmatory tests by 13%. However, this
approach
missed 2.5% of viremic cases. Most of the positive results that
appeared only at 20 minutes were in patients with
resolved infections, who
still had antibodies but no active virus.
These findings suggest the
benefit
of a dual-read strategy: use the 5-minute result to immediately guide RNA
testing in positive cases, and rely on the 20-minute read to identify resolved
infections that don’t require confirmation.
Speed or accuracy: why not both?
Hepatitis C remains a significant
chronic infection worldwide, particularly among high-risk groups like PWID. The
key challenge is
improving screening within these populations while
avoiding
unnecessary and costly diagnostic steps.
This study aimed to determine
whether
accelerating the OraQuick test read time to 5 minutes could optimize
screening without compromising the identification of active cases. The results
show that a
shorter read time significantly reduces unnecessary RNA confirmatory
testing while maintaining
excellent sensitivity for detecting viremic
infections. This balance between speed and accuracy is especially relevant for
low-resource settings, mobile units, or community-based services.
However, several limitations hinder
full optimization of this strategy. Additional studies are needed to
evaluate
the impact of the slight sensitivity loss at 5 minutes and to account for the
highly variable post-infection profiles in target populations. Moreover,
performance data from newer-generation, even faster tests remain to be
assessed.
Integrating rapid reads, reflex RNA testing, and “test-and-treat”
models could
greatly improve hepatitis C management among marginalized
groups—provided this approach is validated across diverse clinical contexts.
Read next: Hepatitis: when the virus writes its own rules
About the author – Ana EspinoPhD in Immunology, specialized in Virology
As a scientific writer, Ana is passionate about bridging the gap between research and real-world impact. With expertise in immunology, virology, oncology, and clinical studies, she makes complex science clear and accessible. Her mission: to accelerate knowledge sharing and empower evidence-based decisions through impactful communication.