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Assessing time to pulmonary function benefit following antibiotic treatment of acute cystic fibrosis exacerbations

BACKGROUND: Cystic Fibrosis (CF) is a life-shortening genetic disease in which ~80% of deaths result from loss of lung function linked to inflammation due to chronic bacterial infection (principally Pseudomonas aeruginosa). Pulmonary exacerbations (intermittent episodes during which symptoms of lung...

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Autores principales: VanDevanter, Donald R, O'Riordan, Mary A, Blumer, Jeffrey L, Konstan, Michael W
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959026/
https://www.ncbi.nlm.nih.gov/pubmed/20925941
http://dx.doi.org/10.1186/1465-9921-11-137
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author VanDevanter, Donald R
O'Riordan, Mary A
Blumer, Jeffrey L
Konstan, Michael W
author_facet VanDevanter, Donald R
O'Riordan, Mary A
Blumer, Jeffrey L
Konstan, Michael W
author_sort VanDevanter, Donald R
collection PubMed
description BACKGROUND: Cystic Fibrosis (CF) is a life-shortening genetic disease in which ~80% of deaths result from loss of lung function linked to inflammation due to chronic bacterial infection (principally Pseudomonas aeruginosa). Pulmonary exacerbations (intermittent episodes during which symptoms of lung infection increase and lung function decreases) can cause substantial resource utilization, morbidity, and irreversible loss of lung function. Intravenous antibiotic treatment to reduce exacerbation symptoms is standard management practice. However, no prospective studies have identified an optimal antibiotic treatment duration and this lack of objective data has been identified as an area of concern and interest. METHODS: We have retrospectively analyzed pulmonary function response data (as forced expiratory volume in one second; FEV(1)) from a previous blinded controlled CF exacerbation management study of intravenous ceftazidime/tobramycin and meropenem/tobramycin in which spirometry was conducted daily to assess the time course of pulmonary function response. RESULTS: Ninety-five patients in the study received antibiotics for at least 4 days and were included in our analyses. Patients received antibiotics for an average of 12.6 days (median = 13, SD = 3.2 days), with a range of 4 to 27 days. No significant differences were observed in mean or median treatment durations as functions of either treatment group or baseline lung disease stage. Average time from initiation of antibiotic treatment to highest observed FEV(1 )was 8.7 days (median = 10, SD = 4.0 days), with a range of zero to 19 days. Patients were treated an average of 3.9 days beyond the day of peak FEV(1 )(median = 3, SD = 3.8 days), with 89 patients (93.7%) experiencing their peak FEV(1 )improvement within 13 days. There were no differences in mean or median times to peak FEV(1 )as a function of treatment group, although the magnitude of FEV(1 )improvement differed between groups. CONCLUSIONS: Our results suggest that antibiotic response to exacerbation as assessed by pulmonary function is essentially complete within 2 weeks of treatment initiation and relatively independent of the magnitude of pulmonary function response observed.
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spelling pubmed-29590262010-10-22 Assessing time to pulmonary function benefit following antibiotic treatment of acute cystic fibrosis exacerbations VanDevanter, Donald R O'Riordan, Mary A Blumer, Jeffrey L Konstan, Michael W Respir Res Research BACKGROUND: Cystic Fibrosis (CF) is a life-shortening genetic disease in which ~80% of deaths result from loss of lung function linked to inflammation due to chronic bacterial infection (principally Pseudomonas aeruginosa). Pulmonary exacerbations (intermittent episodes during which symptoms of lung infection increase and lung function decreases) can cause substantial resource utilization, morbidity, and irreversible loss of lung function. Intravenous antibiotic treatment to reduce exacerbation symptoms is standard management practice. However, no prospective studies have identified an optimal antibiotic treatment duration and this lack of objective data has been identified as an area of concern and interest. METHODS: We have retrospectively analyzed pulmonary function response data (as forced expiratory volume in one second; FEV(1)) from a previous blinded controlled CF exacerbation management study of intravenous ceftazidime/tobramycin and meropenem/tobramycin in which spirometry was conducted daily to assess the time course of pulmonary function response. RESULTS: Ninety-five patients in the study received antibiotics for at least 4 days and were included in our analyses. Patients received antibiotics for an average of 12.6 days (median = 13, SD = 3.2 days), with a range of 4 to 27 days. No significant differences were observed in mean or median treatment durations as functions of either treatment group or baseline lung disease stage. Average time from initiation of antibiotic treatment to highest observed FEV(1 )was 8.7 days (median = 10, SD = 4.0 days), with a range of zero to 19 days. Patients were treated an average of 3.9 days beyond the day of peak FEV(1 )(median = 3, SD = 3.8 days), with 89 patients (93.7%) experiencing their peak FEV(1 )improvement within 13 days. There were no differences in mean or median times to peak FEV(1 )as a function of treatment group, although the magnitude of FEV(1 )improvement differed between groups. CONCLUSIONS: Our results suggest that antibiotic response to exacerbation as assessed by pulmonary function is essentially complete within 2 weeks of treatment initiation and relatively independent of the magnitude of pulmonary function response observed. BioMed Central 2010 2010-10-06 /pmc/articles/PMC2959026/ /pubmed/20925941 http://dx.doi.org/10.1186/1465-9921-11-137 Text en Copyright ©2010 VanDevanter et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
VanDevanter, Donald R
O'Riordan, Mary A
Blumer, Jeffrey L
Konstan, Michael W
Assessing time to pulmonary function benefit following antibiotic treatment of acute cystic fibrosis exacerbations
title Assessing time to pulmonary function benefit following antibiotic treatment of acute cystic fibrosis exacerbations
title_full Assessing time to pulmonary function benefit following antibiotic treatment of acute cystic fibrosis exacerbations
title_fullStr Assessing time to pulmonary function benefit following antibiotic treatment of acute cystic fibrosis exacerbations
title_full_unstemmed Assessing time to pulmonary function benefit following antibiotic treatment of acute cystic fibrosis exacerbations
title_short Assessing time to pulmonary function benefit following antibiotic treatment of acute cystic fibrosis exacerbations
title_sort assessing time to pulmonary function benefit following antibiotic treatment of acute cystic fibrosis exacerbations
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959026/
https://www.ncbi.nlm.nih.gov/pubmed/20925941
http://dx.doi.org/10.1186/1465-9921-11-137
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