Cargando…

Chlorhexidine oral rinses for symptomatic COPD: a randomised, blind, placebo-controlled preliminary study

OBJECTIVES: Determine the effect of twice-daily chlorhexidine oral rinses on oral and lung microbiota biomass and respiratory symptoms. SETTING: Single centre. PARTICIPANTS: Participants were aged 40–85 with chronic obstructive pulmonary disease (COPD) and chronic productive cough or COPD exacerbati...

Descripción completa

Detalles Bibliográficos
Autores principales: Pragman, Alexa A, Fieberg, Ann M, Reilly, Cavan S, Wendt, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8672026/
https://www.ncbi.nlm.nih.gov/pubmed/34903538
http://dx.doi.org/10.1136/bmjopen-2021-050271
_version_ 1784615274206461952
author Pragman, Alexa A
Fieberg, Ann M
Reilly, Cavan S
Wendt, Christine
author_facet Pragman, Alexa A
Fieberg, Ann M
Reilly, Cavan S
Wendt, Christine
author_sort Pragman, Alexa A
collection PubMed
description OBJECTIVES: Determine the effect of twice-daily chlorhexidine oral rinses on oral and lung microbiota biomass and respiratory symptoms. SETTING: Single centre. PARTICIPANTS: Participants were aged 40–85 with chronic obstructive pulmonary disease (COPD) and chronic productive cough or COPD exacerbation within the last year. Exclusions included antibiotics in the previous 2 months and/or those with less than four teeth. Forty-four participants were recruited and 40 completed the study. INTERVENTION: Participants were randomised 1:1 to twice-daily 0.12% chlorhexidine oral rinses versus placebo for 2 months along with daily diaries. St. George’s Respiratory Questionnaire (SGRQ), blood tests, oral rinse and induced sputum were collected at randomisation and the final visit. PRIMARY AND SECONDARY OUTCOMES: Primary outcome was a change in oral and sputum microbiota biomass. Secondary outcomes included: sputum and oral microbiota Shannon and Simpson diversity and taxonomy; inflammatory markers; Breathlessness, Cough and Sputum Scale and SGRQ scores. RESULTS: Neither the oral microbiota nor the sputum microbiota biomass decreased significantly in those using chlorhexidine compared with placebo (oral microbiota mean log(10) difference (SE)=−0.103 (0.23), 95% CI −0.59 to 0.38, p=0.665; sputum microbiota 0.80 (0.46), 95% CI −0.15 to 1.75, p=0.096). Chlorhexidine decreased both oral and sputum microbiota alpha (Shannon) diversity (linear regression estimate (SE) oral: −0.349 (0.091), p=0.001; sputum −0.622 (0.169), p=0.001). Chlorhexidine use did not decrease systemic inflammatory markers compared with placebo (C reactive protein (chlorhexidine 1.8±7.5 vs placebo 0.4±6.8, p=0.467), fibrinogen (22.5±77.8 vs 10.0±77.0, p=0.406) or leucocytes (0.2±1.8 vs 0.5±1.8, p=0.560)). Chlorhexidine use decreased SGRQ scores compared with placebo (chlorhexidine −4.7±8.0 vs placebo 1.7±8.9, p=0.032). CONCLUSIONS: We did not detect a significant difference in microbiota biomass due to chlorhexidine use. Chlorhexidine decreased oral and sputum microbiota alpha diversity and improved respiratory health-related quality of life compared with placebo. TRIAL REGISTRATION: NCT02252588.
format Online
Article
Text
id pubmed-8672026
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BMJ Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-86720262021-12-28 Chlorhexidine oral rinses for symptomatic COPD: a randomised, blind, placebo-controlled preliminary study Pragman, Alexa A Fieberg, Ann M Reilly, Cavan S Wendt, Christine BMJ Open Infectious Diseases OBJECTIVES: Determine the effect of twice-daily chlorhexidine oral rinses on oral and lung microbiota biomass and respiratory symptoms. SETTING: Single centre. PARTICIPANTS: Participants were aged 40–85 with chronic obstructive pulmonary disease (COPD) and chronic productive cough or COPD exacerbation within the last year. Exclusions included antibiotics in the previous 2 months and/or those with less than four teeth. Forty-four participants were recruited and 40 completed the study. INTERVENTION: Participants were randomised 1:1 to twice-daily 0.12% chlorhexidine oral rinses versus placebo for 2 months along with daily diaries. St. George’s Respiratory Questionnaire (SGRQ), blood tests, oral rinse and induced sputum were collected at randomisation and the final visit. PRIMARY AND SECONDARY OUTCOMES: Primary outcome was a change in oral and sputum microbiota biomass. Secondary outcomes included: sputum and oral microbiota Shannon and Simpson diversity and taxonomy; inflammatory markers; Breathlessness, Cough and Sputum Scale and SGRQ scores. RESULTS: Neither the oral microbiota nor the sputum microbiota biomass decreased significantly in those using chlorhexidine compared with placebo (oral microbiota mean log(10) difference (SE)=−0.103 (0.23), 95% CI −0.59 to 0.38, p=0.665; sputum microbiota 0.80 (0.46), 95% CI −0.15 to 1.75, p=0.096). Chlorhexidine decreased both oral and sputum microbiota alpha (Shannon) diversity (linear regression estimate (SE) oral: −0.349 (0.091), p=0.001; sputum −0.622 (0.169), p=0.001). Chlorhexidine use did not decrease systemic inflammatory markers compared with placebo (C reactive protein (chlorhexidine 1.8±7.5 vs placebo 0.4±6.8, p=0.467), fibrinogen (22.5±77.8 vs 10.0±77.0, p=0.406) or leucocytes (0.2±1.8 vs 0.5±1.8, p=0.560)). Chlorhexidine use decreased SGRQ scores compared with placebo (chlorhexidine −4.7±8.0 vs placebo 1.7±8.9, p=0.032). CONCLUSIONS: We did not detect a significant difference in microbiota biomass due to chlorhexidine use. Chlorhexidine decreased oral and sputum microbiota alpha diversity and improved respiratory health-related quality of life compared with placebo. TRIAL REGISTRATION: NCT02252588. BMJ Publishing Group 2021-12-13 /pmc/articles/PMC8672026/ /pubmed/34903538 http://dx.doi.org/10.1136/bmjopen-2021-050271 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Infectious Diseases
Pragman, Alexa A
Fieberg, Ann M
Reilly, Cavan S
Wendt, Christine
Chlorhexidine oral rinses for symptomatic COPD: a randomised, blind, placebo-controlled preliminary study
title Chlorhexidine oral rinses for symptomatic COPD: a randomised, blind, placebo-controlled preliminary study
title_full Chlorhexidine oral rinses for symptomatic COPD: a randomised, blind, placebo-controlled preliminary study
title_fullStr Chlorhexidine oral rinses for symptomatic COPD: a randomised, blind, placebo-controlled preliminary study
title_full_unstemmed Chlorhexidine oral rinses for symptomatic COPD: a randomised, blind, placebo-controlled preliminary study
title_short Chlorhexidine oral rinses for symptomatic COPD: a randomised, blind, placebo-controlled preliminary study
title_sort chlorhexidine oral rinses for symptomatic copd: a randomised, blind, placebo-controlled preliminary study
topic Infectious Diseases
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8672026/
https://www.ncbi.nlm.nih.gov/pubmed/34903538
http://dx.doi.org/10.1136/bmjopen-2021-050271
work_keys_str_mv AT pragmanalexaa chlorhexidineoralrinsesforsymptomaticcopdarandomisedblindplacebocontrolledpreliminarystudy
AT fiebergannm chlorhexidineoralrinsesforsymptomaticcopdarandomisedblindplacebocontrolledpreliminarystudy
AT reillycavans chlorhexidineoralrinsesforsymptomaticcopdarandomisedblindplacebocontrolledpreliminarystudy
AT wendtchristine chlorhexidineoralrinsesforsymptomaticcopdarandomisedblindplacebocontrolledpreliminarystudy