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Heterogeneity of the efficacy of the 23-valent pneumococcal polysaccharide vaccine caused by various underlying conditions of chronic pulmonary disease in older patients: prospective cohort study

OBJECTIVE: To determine the ideal conditions for use of the 23-valent pneumococcal polysaccharide vaccine (PPV23) in older outpatients with chronic pulmonary diseases. DESIGN: Prospective cohort study. PARTICIPANTS: 1378 outpatients with chronic pulmonary diseases ≥60 years of age. INTERVENTION: Par...

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Autores principales: Inoue, Satoshi, Watanuki, Yuji, Kaneko, Tetsuji, Sato, Takashi, Miyazawa, Naoki, Kaneko, Takeshi, Ishigatsubo, Yoshiaki, Morita, Satoshi, Natsumeda, Yutaka, Mizushima, Shunsaku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3191416/
https://www.ncbi.nlm.nih.gov/pubmed/22021764
http://dx.doi.org/10.1136/bmjopen-2011-000105
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author Inoue, Satoshi
Watanuki, Yuji
Kaneko, Tetsuji
Sato, Takashi
Miyazawa, Naoki
Kaneko, Takeshi
Ishigatsubo, Yoshiaki
Morita, Satoshi
Natsumeda, Yutaka
Mizushima, Shunsaku
author_facet Inoue, Satoshi
Watanuki, Yuji
Kaneko, Tetsuji
Sato, Takashi
Miyazawa, Naoki
Kaneko, Takeshi
Ishigatsubo, Yoshiaki
Morita, Satoshi
Natsumeda, Yutaka
Mizushima, Shunsaku
author_sort Inoue, Satoshi
collection PubMed
description OBJECTIVE: To determine the ideal conditions for use of the 23-valent pneumococcal polysaccharide vaccine (PPV23) in older outpatients with chronic pulmonary diseases. DESIGN: Prospective cohort study. PARTICIPANTS: 1378 outpatients with chronic pulmonary diseases ≥60 years of age. INTERVENTION: Participants were educated about PPV23, and those who responded affirmatively were vaccinated between August and November 2002. The participants who chose no intervention served as controls. The prevaccine period was defined as August 2001 to August 2002. Participants were followed for 2 years from December 2002 or until death. MAIN OUTCOME MEASURES: Events of interest included the first episode of bacterial (including pneumococcal) pulmonary infection (primary endpoint) and death of any cause (secondary endpoint). RESULTS: Frequent episodes of pulmonary infection during the prevaccine period significantly decreased event-free survival during the 2-year observation period (p<0.001). Chronic respiratory failure was associated with a decreased event-free survival only when the pulmonary infection episode did not occur in the prevaccine period (p<0.001). No significant differences in event-free survival were observed between the vaccinated and unvaccinated group during analysis of the entire cohort. In the Cox proportional hazards regression model, event-free survival decreased significantly when pulmonary infection occurred in the prevaccine period. In the subgroup analysis, the first episode of bacterial pulmonary infection (but not death of any cause) was reduced significantly by PPV23 only in patients with chronic respiratory failure who had no episodes of pulmonary infection during the prevaccine period (p=0.019). CONCLUSION: The efficacy of PPV23 against pulmonary infection and death of any cause might be unachievable if pulmonary infection occurs during the prevaccine period. PPV23 needs to be given to older patients with chronic pulmonary disease at an earlier time in which infectious complications in the lung have not yet occurred.
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spelling pubmed-31914162011-10-13 Heterogeneity of the efficacy of the 23-valent pneumococcal polysaccharide vaccine caused by various underlying conditions of chronic pulmonary disease in older patients: prospective cohort study Inoue, Satoshi Watanuki, Yuji Kaneko, Tetsuji Sato, Takashi Miyazawa, Naoki Kaneko, Takeshi Ishigatsubo, Yoshiaki Morita, Satoshi Natsumeda, Yutaka Mizushima, Shunsaku BMJ Open Infectious Diseases OBJECTIVE: To determine the ideal conditions for use of the 23-valent pneumococcal polysaccharide vaccine (PPV23) in older outpatients with chronic pulmonary diseases. DESIGN: Prospective cohort study. PARTICIPANTS: 1378 outpatients with chronic pulmonary diseases ≥60 years of age. INTERVENTION: Participants were educated about PPV23, and those who responded affirmatively were vaccinated between August and November 2002. The participants who chose no intervention served as controls. The prevaccine period was defined as August 2001 to August 2002. Participants were followed for 2 years from December 2002 or until death. MAIN OUTCOME MEASURES: Events of interest included the first episode of bacterial (including pneumococcal) pulmonary infection (primary endpoint) and death of any cause (secondary endpoint). RESULTS: Frequent episodes of pulmonary infection during the prevaccine period significantly decreased event-free survival during the 2-year observation period (p<0.001). Chronic respiratory failure was associated with a decreased event-free survival only when the pulmonary infection episode did not occur in the prevaccine period (p<0.001). No significant differences in event-free survival were observed between the vaccinated and unvaccinated group during analysis of the entire cohort. In the Cox proportional hazards regression model, event-free survival decreased significantly when pulmonary infection occurred in the prevaccine period. In the subgroup analysis, the first episode of bacterial pulmonary infection (but not death of any cause) was reduced significantly by PPV23 only in patients with chronic respiratory failure who had no episodes of pulmonary infection during the prevaccine period (p=0.019). CONCLUSION: The efficacy of PPV23 against pulmonary infection and death of any cause might be unachievable if pulmonary infection occurs during the prevaccine period. PPV23 needs to be given to older patients with chronic pulmonary disease at an earlier time in which infectious complications in the lung have not yet occurred. BMJ Group 2011-07-18 /pmc/articles/PMC3191416/ /pubmed/22021764 http://dx.doi.org/10.1136/bmjopen-2011-000105 Text en © 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
spellingShingle Infectious Diseases
Inoue, Satoshi
Watanuki, Yuji
Kaneko, Tetsuji
Sato, Takashi
Miyazawa, Naoki
Kaneko, Takeshi
Ishigatsubo, Yoshiaki
Morita, Satoshi
Natsumeda, Yutaka
Mizushima, Shunsaku
Heterogeneity of the efficacy of the 23-valent pneumococcal polysaccharide vaccine caused by various underlying conditions of chronic pulmonary disease in older patients: prospective cohort study
title Heterogeneity of the efficacy of the 23-valent pneumococcal polysaccharide vaccine caused by various underlying conditions of chronic pulmonary disease in older patients: prospective cohort study
title_full Heterogeneity of the efficacy of the 23-valent pneumococcal polysaccharide vaccine caused by various underlying conditions of chronic pulmonary disease in older patients: prospective cohort study
title_fullStr Heterogeneity of the efficacy of the 23-valent pneumococcal polysaccharide vaccine caused by various underlying conditions of chronic pulmonary disease in older patients: prospective cohort study
title_full_unstemmed Heterogeneity of the efficacy of the 23-valent pneumococcal polysaccharide vaccine caused by various underlying conditions of chronic pulmonary disease in older patients: prospective cohort study
title_short Heterogeneity of the efficacy of the 23-valent pneumococcal polysaccharide vaccine caused by various underlying conditions of chronic pulmonary disease in older patients: prospective cohort study
title_sort heterogeneity of the efficacy of the 23-valent pneumococcal polysaccharide vaccine caused by various underlying conditions of chronic pulmonary disease in older patients: prospective cohort study
topic Infectious Diseases
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3191416/
https://www.ncbi.nlm.nih.gov/pubmed/22021764
http://dx.doi.org/10.1136/bmjopen-2011-000105
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