Levofloxacin versus clarithromycin in COPD exacerbation: focus on exacerbation-free interval
Antibiotic treatment of bacterial exacerbation of chronic obstructive pulmonary disease (COPD) shows some immediate clinical benefits and may also minimise the frequency of further recurrences. Patients (n=511) were enrolled into a randomised double-blind multicentric study comparing the exacerbatio...
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Veröffentlicht in: | The European respiratory journal 2004-12, Vol.24 (6), p.947-953 |
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creator | Lode, H Eller, J Linnhoff, A Ioanas, M Evaluation of Therapy-Free Interval in COPD Patients Study Group |
description | Antibiotic treatment of bacterial exacerbation of chronic obstructive pulmonary disease (COPD) shows some immediate clinical benefits and may also minimise the frequency of further recurrences. Patients (n=511) were enrolled into a randomised double-blind multicentric study comparing the exacerbation-free interval (EFI), efficacy and safety of 7-day levofloxacin versus 10-day clarithromycin in patients with COPD exacerbation. Patients were monitored over a 1-yr period. A total of 434 patients (per protocol population) received the medication for > or =5 days. The median EFI in the per protocol population was 300 days for levofloxacin and 350 days for clarithromycin. For patients with a new documented exacerbation during follow-up (n=223), the median EFI was 100.5 days in the levofloxacin group and 95 days for clarithromycin. No significant differences in EFI between groups could be observed when stratifying the study population according to microbial aetiology and severity of bronchial obstruction. Levofloxacin and clarithromycin showed similar clinical success rates. The bacteriological success rate was significantly higher in the levofloxacin group. Both antibiotics were well tolerated. In summary, levofloxacin was associated with a significantly higher bacteriological eradication rate but similar exacerbation-free interval in patients with chronic obstructive pulmonary disease exacerbation compared to clarithromycin. |
doi_str_mv | 10.1183/09031936.04.00009604 |
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Patients (n=511) were enrolled into a randomised double-blind multicentric study comparing the exacerbation-free interval (EFI), efficacy and safety of 7-day levofloxacin versus 10-day clarithromycin in patients with COPD exacerbation. Patients were monitored over a 1-yr period. A total of 434 patients (per protocol population) received the medication for > or =5 days. The median EFI in the per protocol population was 300 days for levofloxacin and 350 days for clarithromycin. For patients with a new documented exacerbation during follow-up (n=223), the median EFI was 100.5 days in the levofloxacin group and 95 days for clarithromycin. No significant differences in EFI between groups could be observed when stratifying the study population according to microbial aetiology and severity of bronchial obstruction. Levofloxacin and clarithromycin showed similar clinical success rates. The bacteriological success rate was significantly higher in the levofloxacin group. Both antibiotics were well tolerated. In summary, levofloxacin was associated with a significantly higher bacteriological eradication rate but similar exacerbation-free interval in patients with chronic obstructive pulmonary disease exacerbation compared to clarithromycin.</description><identifier>ISSN: 0903-1936</identifier><identifier>EISSN: 1399-3003</identifier><identifier>DOI: 10.1183/09031936.04.00009604</identifier><identifier>PMID: 15572537</identifier><language>eng</language><publisher>Leeds: Eur Respiratory Soc</publisher><subject>Administration, Oral ; Adult ; Anti-Bacterial Agents - adverse effects ; Anti-Bacterial Agents - therapeutic use ; Antibacterial agents ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Bacterial Infections - drug therapy ; Biological and medical sciences ; Chronic obstructive pulmonary disease, asthma ; Clarithromycin - adverse effects ; Clarithromycin - therapeutic use ; Disease Progression ; Double-Blind Method ; Female ; Germany ; Humans ; Levofloxacin ; Male ; Medical sciences ; Middle Aged ; Ofloxacin - adverse effects ; Ofloxacin - therapeutic use ; Pharmacology. 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Patients (n=511) were enrolled into a randomised double-blind multicentric study comparing the exacerbation-free interval (EFI), efficacy and safety of 7-day levofloxacin versus 10-day clarithromycin in patients with COPD exacerbation. Patients were monitored over a 1-yr period. A total of 434 patients (per protocol population) received the medication for > or =5 days. The median EFI in the per protocol population was 300 days for levofloxacin and 350 days for clarithromycin. For patients with a new documented exacerbation during follow-up (n=223), the median EFI was 100.5 days in the levofloxacin group and 95 days for clarithromycin. No significant differences in EFI between groups could be observed when stratifying the study population according to microbial aetiology and severity of bronchial obstruction. Levofloxacin and clarithromycin showed similar clinical success rates. The bacteriological success rate was significantly higher in the levofloxacin group. Both antibiotics were well tolerated. In summary, levofloxacin was associated with a significantly higher bacteriological eradication rate but similar exacerbation-free interval in patients with chronic obstructive pulmonary disease exacerbation compared to clarithromycin.</description><subject>Administration, Oral</subject><subject>Adult</subject><subject>Anti-Bacterial Agents - adverse effects</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Antibacterial agents</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Bacterial Infections - drug therapy</subject><subject>Biological and medical sciences</subject><subject>Chronic obstructive pulmonary disease, asthma</subject><subject>Clarithromycin - adverse effects</subject><subject>Clarithromycin - therapeutic use</subject><subject>Disease Progression</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Germany</subject><subject>Humans</subject><subject>Levofloxacin</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Ofloxacin - adverse effects</subject><subject>Ofloxacin - therapeutic use</subject><subject>Pharmacology. Drug treatments</subject><subject>Pneumology</subject><subject>Prospective Studies</subject><subject>Pulmonary Disease, Chronic Obstructive - complications</subject><subject>Pulmonary Disease, Chronic Obstructive - microbiology</subject><subject>Statistics, Nonparametric</subject><subject>Treatment Outcome</subject><issn>0903-1936</issn><issn>1399-3003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkFtLAzEQhYMotlb_gci--Lg1s8lmN75JvUKhPuibEGbTxG7ZS0m21f57s7SlOAwMHL5zYA4h10DHADm7o5IykEyMKR_TMFJQfkKGwKSMGaXslAx7JO6ZAbnwfkkpCM7gnAwgTbMkZdmQfE3NprVV-4u6bKKNcX7tI12hK7uFa-ttr4adzN4fIxMg4wrsyra5j2yrA9o2_-TYOmOCoTNug9UlObNYeXO1vyPy-fz0MXmNp7OXt8nDNNYcoIsNWm2tyQ3HAnNgc5vQFLKiYKlOsLCYCG64lrnIdI68yAG0BB2-KVhipWQjwne52rXeO2PVypU1uq0Cqvqy1KEsRbk6lBVsNzvbal3UZn407dsJwO0eQK-xsg4bXfojJxiDTMCRW5Tfi5_SGeVrrKoQC8q4ZcKVUJJn7A--74B1</recordid><startdate>20041201</startdate><enddate>20041201</enddate><creator>Lode, H</creator><creator>Eller, J</creator><creator>Linnhoff, A</creator><creator>Ioanas, M</creator><creator>Evaluation of Therapy-Free Interval in COPD Patients Study Group</creator><general>Eur Respiratory Soc</general><general>Maney</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20041201</creationdate><title>Levofloxacin versus clarithromycin in COPD exacerbation: focus on exacerbation-free interval</title><author>Lode, H ; Eller, J ; Linnhoff, A ; Ioanas, M ; Evaluation of Therapy-Free Interval in COPD Patients Study Group</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-eafcffe8e4aba813df20517bb35c2abfa264e4c9867c8a4b811c91c016b32f993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Administration, Oral</topic><topic>Adult</topic><topic>Anti-Bacterial Agents - adverse effects</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Antibacterial agents</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Bacterial Infections - drug therapy</topic><topic>Biological and medical sciences</topic><topic>Chronic obstructive pulmonary disease, asthma</topic><topic>Clarithromycin - adverse effects</topic><topic>Clarithromycin - therapeutic use</topic><topic>Disease Progression</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>Germany</topic><topic>Humans</topic><topic>Levofloxacin</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Ofloxacin - adverse effects</topic><topic>Ofloxacin - therapeutic use</topic><topic>Pharmacology. Drug treatments</topic><topic>Pneumology</topic><topic>Prospective Studies</topic><topic>Pulmonary Disease, Chronic Obstructive - complications</topic><topic>Pulmonary Disease, Chronic Obstructive - microbiology</topic><topic>Statistics, Nonparametric</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lode, H</creatorcontrib><creatorcontrib>Eller, J</creatorcontrib><creatorcontrib>Linnhoff, A</creatorcontrib><creatorcontrib>Ioanas, M</creatorcontrib><creatorcontrib>Evaluation of Therapy-Free Interval in COPD Patients Study Group</creatorcontrib><creatorcontrib>Evaluation of Therapy-Free Interval in COPD Patients Study Group</creatorcontrib><creatorcontrib>the Evaluation of Therapy-Free Interval in COPD Patients Study Group</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>The European respiratory journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lode, H</au><au>Eller, J</au><au>Linnhoff, A</au><au>Ioanas, M</au><au>Evaluation of Therapy-Free Interval in COPD Patients Study Group</au><aucorp>Evaluation of Therapy-Free Interval in COPD Patients Study Group</aucorp><aucorp>the Evaluation of Therapy-Free Interval in COPD Patients Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Levofloxacin versus clarithromycin in COPD exacerbation: focus on exacerbation-free interval</atitle><jtitle>The European respiratory journal</jtitle><addtitle>Eur Respir J</addtitle><date>2004-12-01</date><risdate>2004</risdate><volume>24</volume><issue>6</issue><spage>947</spage><epage>953</epage><pages>947-953</pages><issn>0903-1936</issn><eissn>1399-3003</eissn><abstract>Antibiotic treatment of bacterial exacerbation of chronic obstructive pulmonary disease (COPD) shows some immediate clinical benefits and may also minimise the frequency of further recurrences. Patients (n=511) were enrolled into a randomised double-blind multicentric study comparing the exacerbation-free interval (EFI), efficacy and safety of 7-day levofloxacin versus 10-day clarithromycin in patients with COPD exacerbation. Patients were monitored over a 1-yr period. A total of 434 patients (per protocol population) received the medication for > or =5 days. The median EFI in the per protocol population was 300 days for levofloxacin and 350 days for clarithromycin. For patients with a new documented exacerbation during follow-up (n=223), the median EFI was 100.5 days in the levofloxacin group and 95 days for clarithromycin. No significant differences in EFI between groups could be observed when stratifying the study population according to microbial aetiology and severity of bronchial obstruction. Levofloxacin and clarithromycin showed similar clinical success rates. The bacteriological success rate was significantly higher in the levofloxacin group. 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subjects | Administration, Oral Adult Anti-Bacterial Agents - adverse effects Anti-Bacterial Agents - therapeutic use Antibacterial agents Antibiotics. Antiinfectious agents. Antiparasitic agents Bacterial Infections - drug therapy Biological and medical sciences Chronic obstructive pulmonary disease, asthma Clarithromycin - adverse effects Clarithromycin - therapeutic use Disease Progression Double-Blind Method Female Germany Humans Levofloxacin Male Medical sciences Middle Aged Ofloxacin - adverse effects Ofloxacin - therapeutic use Pharmacology. Drug treatments Pneumology Prospective Studies Pulmonary Disease, Chronic Obstructive - complications Pulmonary Disease, Chronic Obstructive - microbiology Statistics, Nonparametric Treatment Outcome |
title | Levofloxacin versus clarithromycin in COPD exacerbation: focus on exacerbation-free interval |
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