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Effectiveness of proton pump inhibitor in unexplained chronic cough

BACKGROUND: Current guidelines recommend that patients with unexplained chronic cough undergo empirical proton pump inhibitor (PPI) treatment, but scientific evidence for this treatment is lacking. We investigated the effectiveness and appropriate dose of PPI therapy in chronic cough. METHODS: We in...

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Autores principales: Park, Hye Jung, Park, Yoo Mi, Kim, Jie-Hyun, Lee, Hye Sun, Kim, Hyung Jung, Ahn, Chul Min, Byun, Min Kwang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634560/
https://www.ncbi.nlm.nih.gov/pubmed/29016626
http://dx.doi.org/10.1371/journal.pone.0185397
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author Park, Hye Jung
Park, Yoo Mi
Kim, Jie-Hyun
Lee, Hye Sun
Kim, Hyung Jung
Ahn, Chul Min
Byun, Min Kwang
author_facet Park, Hye Jung
Park, Yoo Mi
Kim, Jie-Hyun
Lee, Hye Sun
Kim, Hyung Jung
Ahn, Chul Min
Byun, Min Kwang
author_sort Park, Hye Jung
collection PubMed
description BACKGROUND: Current guidelines recommend that patients with unexplained chronic cough undergo empirical proton pump inhibitor (PPI) treatment, but scientific evidence for this treatment is lacking. We investigated the effectiveness and appropriate dose of PPI therapy in chronic cough. METHODS: We included 27 patients with unexplained chronic cough after excluding subjects with positive response to postnasal drip medication. Subjects were randomized to a placebo, standard, and high dose of PPI groups with blinding. The drug or placebo was administered orally for 8 weeks, and the Leicester Cough Questionnaire (LCQ) score and visual analogue scale (VAS) scores were collected. RESULTS: The LCQ score in the PPI group significantly improved from 0 weeks (11.4 ± 1.4) to 4 weeks (14.8 ± 1.4) and to 8 weeks (17.1 ± 1.4), whereas that in the placebo group did not improve from 0 weeks (13.7 ± 1.1) to 8 weeks (11.8 ± 1.4); the difference between the 2 groups was significant (P < 0.001). In subgroup analysis according to reflux, significant improvements in the LCQ score were observed in the PPI group regardless of reflux (P < 0.001 in the reflux group and P < 0.001 in the no reflux group, respectively; P = 0.188 between the 2 groups). In addition, improvements in LCQ and VAS scores between the standard- and high-dose PPI groups were not significantly different; however, adverse reactions were induced by only the high dose (16.7%). CONCLUSIONS: The results of this pilot study support the empirical use of the standard dose of PPI for 8 weeks in patients suffering from unexplained chronic cough regardless of whether reflux is present. TRIAL REGISTRATION: ClinicalTrial.gov NCT01888549 www.clinicaltrials.gov; cris.nih.go.kr KCT0000543 cris.nih.go.kr/
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spelling pubmed-56345602017-10-30 Effectiveness of proton pump inhibitor in unexplained chronic cough Park, Hye Jung Park, Yoo Mi Kim, Jie-Hyun Lee, Hye Sun Kim, Hyung Jung Ahn, Chul Min Byun, Min Kwang PLoS One Research Article BACKGROUND: Current guidelines recommend that patients with unexplained chronic cough undergo empirical proton pump inhibitor (PPI) treatment, but scientific evidence for this treatment is lacking. We investigated the effectiveness and appropriate dose of PPI therapy in chronic cough. METHODS: We included 27 patients with unexplained chronic cough after excluding subjects with positive response to postnasal drip medication. Subjects were randomized to a placebo, standard, and high dose of PPI groups with blinding. The drug or placebo was administered orally for 8 weeks, and the Leicester Cough Questionnaire (LCQ) score and visual analogue scale (VAS) scores were collected. RESULTS: The LCQ score in the PPI group significantly improved from 0 weeks (11.4 ± 1.4) to 4 weeks (14.8 ± 1.4) and to 8 weeks (17.1 ± 1.4), whereas that in the placebo group did not improve from 0 weeks (13.7 ± 1.1) to 8 weeks (11.8 ± 1.4); the difference between the 2 groups was significant (P < 0.001). In subgroup analysis according to reflux, significant improvements in the LCQ score were observed in the PPI group regardless of reflux (P < 0.001 in the reflux group and P < 0.001 in the no reflux group, respectively; P = 0.188 between the 2 groups). In addition, improvements in LCQ and VAS scores between the standard- and high-dose PPI groups were not significantly different; however, adverse reactions were induced by only the high dose (16.7%). CONCLUSIONS: The results of this pilot study support the empirical use of the standard dose of PPI for 8 weeks in patients suffering from unexplained chronic cough regardless of whether reflux is present. TRIAL REGISTRATION: ClinicalTrial.gov NCT01888549 www.clinicaltrials.gov; cris.nih.go.kr KCT0000543 cris.nih.go.kr/ Public Library of Science 2017-10-10 /pmc/articles/PMC5634560/ /pubmed/29016626 http://dx.doi.org/10.1371/journal.pone.0185397 Text en © 2017 Park et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Park, Hye Jung
Park, Yoo Mi
Kim, Jie-Hyun
Lee, Hye Sun
Kim, Hyung Jung
Ahn, Chul Min
Byun, Min Kwang
Effectiveness of proton pump inhibitor in unexplained chronic cough
title Effectiveness of proton pump inhibitor in unexplained chronic cough
title_full Effectiveness of proton pump inhibitor in unexplained chronic cough
title_fullStr Effectiveness of proton pump inhibitor in unexplained chronic cough
title_full_unstemmed Effectiveness of proton pump inhibitor in unexplained chronic cough
title_short Effectiveness of proton pump inhibitor in unexplained chronic cough
title_sort effectiveness of proton pump inhibitor in unexplained chronic cough
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634560/
https://www.ncbi.nlm.nih.gov/pubmed/29016626
http://dx.doi.org/10.1371/journal.pone.0185397
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