Evidence map›Paper›PMID 38317784›Full record

ArticleOTO open

Evaluating Sinus Microbiology by Transplant Status in Persons With Cystic Fibrosis: A Matched Cohort Study.

Ranjani Somayaji, Christina S Thornton, Nicola Acosta, Kristine Smith, Jessica Clark, Linda Fatovich, Mitesh V Thakrar, Michael D Parkins

Abstract read
In one paragraph

Article in OTO open. 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. Review
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.

Ranjani SomayajiDepartment of Microbiology, Immunology and Infectious Diseases, Cumming School of Medicine University of Calgary Calgary Canada.ORCID https://orcid.org/0000-0003-3731-9675
Christina S ThorntonDepartment of Microbiology, Immunology and Infectious Diseases, Cumming School of Medicine University of Calgary Calgary Canada.
Nicola AcostaDepartment of Microbiology, Immunology and Infectious Diseases, Cumming School of Medicine University of Calgary Calgary Canada.
Kristine SmithDepartment of Otolaryngology-Head and Neck surgery University of Utah Salt Lake City Utah USA.
Jessica ClarkDepartment of Surgery, Otolaryngology-Head and Neck Surgery, Cumming School of Medicine University of Calgary Calgary Canada.
Linda FatovichDepartment of Medicine, Cumming School of Medicine, Alberta Health Services University of Calgary Calgary Canada.
Mitesh V ThakrarDepartment of Medicine, Cumming School of Medicine, Alberta Health Services University of Calgary Calgary Canada.
Michael D ParkinsDepartment of Microbiology, Immunology and Infectious Diseases, Cumming School of Medicine University of Calgary Calgary Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Sinus disease is prevalent in persons with cystic fibrosis (PwCF) and may be a reservoir of airway infection in postlung transplant (pTx) patients. The microbial composition of cystic fibrosis sinuses and its associations with chronic rhinosinusitis (CRS) is relatively unexplored. We aimed to examine the sinus and lower airway microbiome and their associations with CRS in PwCF and pTxPwCF. Study Design: Prospective single-centre study. Setting: A total of 31 sex and age (±2 years) matched PwCF and pTxPwCF. Methods: Demographic and clinical data along with sinus swabs and sputum were collected. CRS was assessed using Sinonasal Outcome Test-22 (SNOT-22) (patient reported outcome) and Lund-McKay (computed tomography sinus) scores. Samples underwent MiSeq Illumina sequencing of the universal 16S ribosomal RNA gene. Results: A total of 31 PwCF (15 pTxPwCF) were included. Aggregate airways microbiome composition was dominated by Conclusion: Sinus and airway microbiomes differed in PwCF and pTxPwCF, but the prevalent organisms remained consistent. Elucidating the relationship of the microbiome with clinical status to better understand when to intervene accordingly is needed to optimize sinus disease management in PwCF.

Indexed as

cystic fibrosislung transplantmicrobiomemicrobiotasinus

Identifiers

PMID38317784
PMCPMC10840018

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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.