Evidence map›Paper›PMID 33453673›Full record

ArticleDiagnostic microbiology and infectious disease2021

Impact of hematocrit on point-of-care C-reactive protein-based tuberculosis screening among people living with HIV initiating antiretroviral therapy in Uganda.

Sandra Z Mwebe, Christina Yoon, Lucy Asege, Martha Nakaye, Jane Katende, Alfred Andama, Adithya Cattamanchi, Fred C Semitala

Abstract readComparative Study
In one paragraph

Article in Diagnostic microbiology and infectious disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
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.

Sandra Z MwebeInfectious Diseases Research Collaboration, Kampala, Uganda.
Christina YoonDivision of Pulmonary and Critical Care Medicine, University of California San Francisco, San Francisco, USA.
Lucy AsegeInfectious Diseases Research Collaboration, Kampala, Uganda.
Martha NakayeInfectious Diseases Research Collaboration, Kampala, Uganda.
Jane KatendeMakerere University Joint AIDS Program (MJAP), Kampala, Uganda.
Alfred AndamaInfectious Diseases Research Collaboration, Kampala, Uganda; Department of Internal Medicine, Makerere University College of Health Sciences, Kampala, Uganda.
Adithya CattamanchiDivision of Pulmonary and Critical Care Medicine, University of California San Francisco, San Francisco, USA.
Fred C SemitalaInfectious Diseases Research Collaboration, Kampala, Uganda; Makerere University Joint AIDS Program (MJAP), Kampala, Uganda; Department of Internal Medicine, Makerere University College of Health Sciences, Kampala, Uganda. Electronic address: semitala@gmail.com.

Funding

Virology CoreP30AI027763 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI STEVEN Grant DEEKS · 1988 to 2026
$93.6M
Evaluation of novel tuberculosis screening strategies for people living with HIVK23AI114363 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI YOON, CHRISTINA · 2014 to 2018
$943k
Point-of-care C-reactive protein-based tuberculosis screening among people living with HIV: planning a comparative effectiveness trialR34AI134589 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI YOON, CHRISTINA · 2017 to 2017
$236k
NIAID NIH HHS K23 AI114363NIAID NIH HHS P30 AI027763NIAID NIH HHS R34 AI134589
6 · The paper itself

Abstract

Point-of-care C-reactive protein (POC CRP) testing is a potential tuberculosis (TB) screening tool for people living with HIV (PLHIV). Unlike lab-based assays, POC assays do not routinely adjust CRP levels for hematocrit, potentially resulting in TB screening status misclassification. We compared the diagnostic accuracy of unadjusted and hematocrit-adjusted POC CRP for culture-confirmed TB among PLHIV with CD4 cell-count ≤350 cells/uL initiating antiretroviral therapy (ART) in Uganda. We prospectively enrolled consecutive adults, measured POC CRP (Boditech; normal <8 mg/L), collected two spot sputum specimens for comprehensive TB testing, and extracted pre-ART hematocrit from clinic records. Of the 605 PLHIV included, hematocrit-adjusted POC CRP had similar sensitivity (80% vs 81%, difference +1% [95% CI -3 to +5], P= 0.56) and specificity (71% vs 71%, difference 0% [95% CI -1 to +1], P= 0.56) for culture-confirmed TB, relative to unadjusted POC CRP. When used for TB screening, POC CRP may not require adjustment for hematocrit. However, larger studies may be required if differences close to the clinically meaningful threshold are to be detected.

Indexed as

AdultAntiretroviral Therapy, Highly ActiveCD4 Lymphocyte CountC-Reactive ProteinCross-Sectional StudiesFemaleHematocritHIV InfectionsHumansMaleMass ScreeningPoint-of-Care SystemsProspective StudiesSensitivity and SpecificityTuberculosisTuberculosis, PulmonaryC-Reactive ProteinC-reactive proteinHaematocritPLHIVPoint of careScreeningTuberculosis

Identifiers

PMID33453673
PMCPMC8915862

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.