Evidence map›Paper›PMID 28236807›Full record

ArticleJournal of medical case reports2017

Pediatric tuberculosis-human immunodeficiency virus co-infection in the United Kingdom highlights the need for better therapy monitoring tools: a case report.

Dimitrios Evangelopoulos, Elizabeth Whittaker, Isobella Honeyborne, Timothy D McHugh, Nigel Klein, Delane Shingadia

Abstract readCase Reports
In one paragraph

Article in Journal of medical case reports, 2017. 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. Culture-Free Enumeration ofMicroorganisms · 2022
    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

6 authors.

Dimitrios EvangelopoulosCentre for Clinical Microbiology, University College London, London, NW3 2PF, UK. dimitrios.evangelopoulos@crick.ac.uk.ORCID http://orcid.org/0000-0003-0472-7576
Elizabeth WhittakerDepartment of Academic Paediatrics, Imperial College London, London, W2 1PG, UK.
Isobella HoneyborneCentre for Clinical Microbiology, University College London, London, NW3 2PF, UK.
Timothy D McHughCentre for Clinical Microbiology, University College London, London, NW3 2PF, UK.
Nigel KleinInstitute of Child Health and Great Ormond Street Hospital for Children, London, WC1N 3JH, UK.
Delane ShingadiaDepartment of Paediatric Infectious Diseases, Great Ormond Street Hospital for Children, London, WC1N 3JH, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTuberculosis is an infection that requires at least 6 months of chemotherapy in order to clear the bacteria from the patient's lungs. Usually, therapeutic monitoring is dependent on smear microscopy where a decline in acid-fast bacilli is observed. However, this might not be indicative of the actual decline of bacterial load and thus other tools such as culture and molecular assays are required for patient management. CASE PRESENTATION: Here, we report the case of a 12-year-old Black African boy co-infected with tuberculosis and human immunodeficiency virus who remained smear culture positive and liquid culture negative for a prolonged period of time following chemotherapy. In order to determine whether there was any live bacteria present in his specimens, we applied the newly developed molecular bacterial load assay that detects the presence of 16S ribosomal ribonucleic acid derived from the bacteria. Using this methodology, we were able to quantify his bacterial load and inform the management of his treatment in order to reduce the disease burden. Following this intervention he went on to make a complete recovery.

conclusionsThis case report highlights the value of improved biomarkers for monitoring the treatment of tuberculosis and the role of molecular assays such as the molecular bacterial load assay applied here. The molecular bacterial load assay detects bacterial ribonucleic acid which corresponds closely with the number of live bacilli as compared with polymerase chain reaction that detects deoxyribonucleic acid and may include dead bacteria.

Indexed as

Bacterial LoadBiomarkersChildCoinfectionHIV InfectionsHumansMaleRadiographyRNA, Ribosomal, 16SSputumTuberculosis, PulmonaryUnited KingdomBiomarkersRNA, Ribosomal, 16SCase reportChildhood tuberculosisClinical decisionsMolecular bacterial loadRapid assayTuberculosis treatment monitoring

Identifiers

PMID28236807
PMCPMC5326674

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Registered trials

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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.