Evidence map›Paper›PMID 32140752›Full record

ArticleInternational urogynecology journal2020

A revalidation and critique of assumptions about urinary sample collection methods, specimen quality and contamination.

Linda Collins, Sanchutha Sathiananthamoorthy, Jennifer Rohn, James Malone-Lee

Abstract read
In one paragraph

Article in International urogynecology journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. 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

4 authors.

Linda CollinsSchool of Nursing, Kingston University, Frank Lampl Building, Kingston Hill Campus, London, UK. l.collins@sgul.kingston.ac.uk.ORCID 0000-0002-9826-5749
Sanchutha SathiananthamoorthyDepartment of Renal Medicine, Division of Medicine, University College London, London, UK.
Jennifer RohnDepartment of Renal Medicine, Division of Medicine, University College London, London, UK.
James Malone-LeeDepartment of Renal Medicine, Division of Medicine, University College London, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introduction and hypothesisMidstream urine (MSU) is key in assessing lower urinary tract syndrome (LUTS), but contingent on some assumptions. The aim of this study was to compare the occurrence of contamination and the quality of substrates obtained from four different collections: MSU, catheter specimen urine (CSU), a commercial MSU collecting device (Peezy) and a natural void. Contamination was quantified by differential, uroplakin-positive, urothelial cell counts.

methodsThis was a single blind, crossover study conducted in two phases. First, we compared the MSU with CSU using urine culture, pyuria counts and differential counting of epithelial cells after immunofluorescence staining for uroplakin III (UP3). Second, we compared the three non-invasive (MSU, Peezy MSU™, natural void) methods using UP3 antibody staining only.

resultsThe natural void was best at collecting bladder urinary sediment, with the majority of epithelial cells present derived from the urinary tract. CSU sampling missed much of the urinary sediment and showed sparse culture results. Finally, the MSU collection methods did not capture much of the bladder sediment.

conclusionWe found little evidence for contamination with the four methods. Natural void was the best method for harvesting shed urothelial cells and white blood cells. It provides a richer sample of the inflammatory exudate, including parasitised urothelial cells and the microbial substrate. However, if the midstream sample is believed to be important, the MSU collection device is advantageous.

Indexed as

PyuriaUrinary Tract InfectionsCross-Over StudiesHumansSingle-Blind MethodUrinalysisUrineUrine Specimen CollectionCatheterMidstreamPeezySampleUrineUTI

Identifiers

PMID32140752
PMCPMC7270983

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