Evidence map›Paper›PMID 36016828›Full record

ArticleInternational journal of clinical practice2022

An Analysis of Predictive Sample-to-Cutoff Index for HIV Infection Confirmation Using Elecsys® HIV Combi PT Assay.

Xiaohong Xia, Xiang Zhang, Jun Zhou, Mengying Zhang

Open access · goldAbstract read
In one paragraph

Article in International journal of clinical practice, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Xiaohong XiaDepartment of Laboratory Medicine, Branch of National Clinical Research Center for Laboratory Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.ORCID https://orcid.org/0000-0002-6375-0955
Xiang ZhangDepartment of Infection Management, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.ORCID https://orcid.org/0000-0003-4462-3798
Jun ZhouDepartment of Laboratory Medicine, Branch of National Clinical Research Center for Laboratory Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.ORCID https://orcid.org/0000-0002-0716-3967
Mengying ZhangDepartment of Laboratory Medicine, Branch of National Clinical Research Center for Laboratory Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.ORCID https://orcid.org/0000-0001-8405-3377
National Center for Clinical Laboratories · CNJiangsu Province Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Early and rapid diagnosis is crucial in HIV preventing and treatment. However, the false-positive rate (FPR) by 4-th generation detection assays was high in low-HIV-prevalence regions. Objectives: To analyze the relation between sample-to-cutoff index (COI) and HIV confirmatory results, and to explore a new COI threshold in our own laboratory to predict HIV infection. Methods: We retrospectively analyzed primarily reactive results by Elecsys® HIV combi PT assays and their confirmatory results by western blot (WB) at Nanjing Center for Disease Control and Prevention (CDC). The mean COI values of true positive (TP), false positive (FP), and indeterminate groups were compared, and receiver operating characteristic curve (ROC) analysis was performed to determine the optimal COI value for predicting HIV infection. Results: Totally 150,980 HIV serological results were reviewed, and 305 (0.2%) were primarily reactive. There are 82 (26.89%) true positives, 210 (71.92%) false positives, and 11 indeterminate samples confirmed by WB tests, and another 2 patients rejected WB tests. Mean COI values of TP (643.5) were greatly higher than that of FP (3.174) ( Conclusions: By adjusting the COI threshold, the FP samples can be reduced and the efficiency of screening assays can be increased, which can save much additional reagent and staff costs and much time for delivery of HIV test results.

Indexed as

HIV-1HIV InfectionsHIV AntibodiesHumansImmunoassayRetrospective StudiesSensitivity and SpecificityHIV Antibodies

Identifiers

PMID36016828
PMCPMC9385312
OpenAlexW4290988912

What OpenQuestion holds

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LicenceCC BY
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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.