Evidence map›Paper›PMID 36490265›Full record

ArticlePloS one2022

A quality improvement study on the relationship between intranasal povidone-iodine and anesthesia and the nasal microbiota of surgery patients.

Eric N Hammond, Ashley E Kates, Nathan Putman-Buehler, Lauren Watson, Jared J Godfrey, Nicole Brys, Courtney Deblois, Andrew J Steinberger, Madison S Cox, Joseph H Skarlupka and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

14 authors at 2 institutions in 1 country.

Eric N HammondInstitute for Clinical and Translational Research, University of Wisconsin-Madison, Madison, WI, United States of America.ORCID 0000-0003-2239-0727
Ashley E KatesDivision of Infectious Disease, Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States of America.
Nathan Putman-BuehlerDepartment of Biochemistry, College of Agricultural and Life Sciences, University of Wisconsin-Madison, Madison, WI, United States of America.ORCID 0000-0003-2398-2265
Lauren WatsonSSM Health, St. Mary's Hospital, Madison, WI, United States of America.
Jared J GodfreyDivision of Infectious Disease, Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States of America.
Nicole BrysWaisman Center, University of Wisconsin-Madison, Madison, WI, United States of America.
Courtney DebloisDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI, United States of America.ORCID 0000-0002-1049-7212
Andrew J SteinbergerDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI, United States of America.
Madison S CoxDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI, United States of America.ORCID 0000-0001-7092-2754
Joseph H SkarlupkaDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI, United States of America.
Ambar HaleemDivision of Infectious Disease, Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States of America.
Michael L BentzDivision of Plastic and Reconstructive Surgery and Urology, Department of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States of America.
Garret SuenDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI, United States of America.
Nasia SafdarDivision of Infectious Disease, Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States of America.
University of Wisconsin–Madison · USSt. Mary's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe composition of the nasal microbiota in surgical patients in the context of general anesthesia and nasal povidone-iodine decolonization is unknown. The purpose of this quality improvement study was to determine: (i) if general anesthesia is associated with changes in the nasal microbiota of surgery patients and (ii) if preoperative intranasal povidone-iodine decolonization is associated with changes in the nasal microbiota of surgery patients. MATERIALS AND

methodsOne hundred and fifty-one ambulatory patients presenting for surgery were enrolled in a quality improvement study by convenience sampling. Pre- and post-surgery nasal samples were collected from patients in the no intranasal decolonization group (control group, n = 54). Pre-decolonization nasal samples were collected from the preoperative intranasal povidone-iodine decolonization group (povidone-iodine group, n = 97). Intranasal povidone-iodine was administered immediately prior to surgery and continued for 20 minutes before patients proceeded for surgery. Post-nasal samples were then collected. General anesthesia was administered to both groups. DNA from the samples was extracted for 16S rRNA sequencing on an Illumina MiSeq.

resultsIn the control group, there was no evidence of change in bacterial diversity between pre- and post-surgery samples. In the povidone-iodine group, nasal bacterial diversity was greater in post-surgery, relative to pre-surgery (Shannon's Diversity Index (P = 0.038), Chao's richness estimate (P = 0.02) and Inverse Simpson index (P = 0.027). Among all the genera, only the relative abundance of the genus Staphylococcus trended towards a decrease in patients after application (FDR adjusted P = 0.06). Abundant genera common to both povidone-iodine and control groups included Staphylococcus, Bradyrhizobium, Corynebacterium, Dolosigranulum, Lactobacillus, and Moraxella.

conclusionsWe found general anesthesia was not associated with changes in the nasal microbiota. Povidone-iodine treatment was associated with nasal microbial diversity and decreased abundance of Staphylococcus. Future studies should examine the nasal microbiota structure and function longitudinally in surgical patients receiving intranasal povidone-iodine.

Indexed as

Anti-Infective Agents, LocalPovidone-IodineAdministration, IntranasalBacteriaHumansNoseQuality ImprovementRNA, Ribosomal, 16SStaphylococcusAnti-Infective Agents, LocalPovidone-IodineRNA, Ribosomal, 16S

Identifiers

PMID36490265
PMCPMC9733847
OpenAlexW4311677615

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.