Evidence map›Paper›PMID 32171668›Full record

ArticleJournal of pediatric urology2020

A cross-sectional analysis of the urine microbiome of children with neuropathic bladders.

Catherine S Forster, Karuna Panchapakesan, Crystal Stroud, Payal Banerjee, Heather Gordish-Dressman, Michael H Hsieh

Open access · greenAbstract read
In one paragraph

Article in Journal of pediatric urology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

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  19. IntravesicalTopics in spinal cord injury rehabilitation · 2023
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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

6 authors at 1 institution in 1 country.

Catherine S ForsterDepartment of Pediatrics, Children's National Hospital, Washington, DC, USA. Electronic address: csforster@childrensnational.org.
Karuna PanchapakesanCenter for Genetic Medicine, Children's Research Institute, Children's National Hospital, Washington D.C, USA.
Crystal StroudCenter for Genetic Medicine, Children's Research Institute, Children's National Hospital, Washington D.C, USA.
Payal BanerjeeCenter for Genetic Medicine, Children's Research Institute, Children's National Hospital, Washington D.C, USA.
Heather Gordish-DressmanCenter for Genetic Medicine, Children's Research Institute, Children's National Hospital, Washington D.C, USA.
Michael H HsiehDepartment of Surgery, Children's National Hospital, Washington, DC, USA.
Children's National · US

Funding

NCATS NIH HHS L30 TR001292
6 · The paper itself

Abstract

backgroundDistinguishing a urinary tract infection (UTI) from asymptomatic bacteriuria (ASB) in children with neuropathic bladders is difficult. Currently used markers of infection, such as the routine urinalysis, lack specificity for UTI in this population. The urinary microbiome may help differentiate these states.

objectiveThe objective of this work was to describe the baseline microbiome in children with neuropathic bladders, and to determine if differences exist among the urine microbiomes of children with neuropathic bladders who have negative urine cultures, ASB, or UTI. STUDY

designThis is a cross-sectional study of children with neuropathic bladders who use clean intermittent catheterization for bladder management who had a urine culture sent as part of clinical management. Residual urine, initially collected via catheter for urine culture, was obtained for use in this work. Microbial DNA was isolated, and the V4 region of the 16SrRNA gene sequenced. The relative abundance of each bacteria was measured in each group. Alpha diversity, measured by Chao1 and the Shannon Diversity Index, was also measured in each group. PERMANOVA was used to compare the microbiota between groups.

results36 children with neuropathic bladders were included in this study (UTI = 11, ASB = 19, negative cultures = 4). The most abundant bacteria were unspecified Enterobacteriaceae, Klebsiella, Staphylococcus, Streptococcus, and Enterococcus. Children who catheterize their urethra have a higher proportion of Staphylococcus, while the urine microbiome of those who catheterize through a Mitrofanoff consists predominantly of members of the family Enterobacteriaceae. Given the low numbers of patients with Mitrofanoffs and augmented bladders, we did not statistically compare the urine microbiomes between these patients. There was no difference in either alpha diversity or the overall microbiota between children with neuropathic bladders with UTI, ASB, and negative cultures. DISCUSSION: In this pilot cohort of children with neuropathic bladders, bacteria that are members of the family Enterobacteriaceae are the most predominant bacteria in the urine microbiomes. There was no difference in the urine microbiome between those with UTI, ASB, and negative cultures. Route of catheterization may affect the composition of the urine microbiome, although due to limited sample size, this was not confirmed statistically.

conclusionThere was no difference in the urine microbiome between patients with negative urine cultures, ASB, and UTI. Further work is needed to determine if the urine microbiome varies based on either the route of catheterization or the presence of augmented bladder.

Indexed as

BacteriuriaMicrobiotaUrinary Bladder, NeurogenicUrinary Tract InfectionsChildCross-Sectional StudiesHumansMaleUrineNeuropathic bladderPediatricsUrinary tract infectionUrine microbiome

Identifiers

PMID32171668
PMCPMC7434660
OpenAlexW3007644669

What OpenQuestion holds

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Read underepoch 390

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.