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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The European respiratory journal 2004-12, Vol.24 (6), p.947-953
Hauptverfasser: Lode, H, Eller, J, Linnhoff, A, Ioanas, M, Evaluation of Therapy-Free Interval in COPD Patients Study Group
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 953
container_issue 6
container_start_page 947
container_title The European respiratory journal
container_volume 24
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
format Article
fullrecord <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1183_09031936_04_00009604</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>15572537</sourcerecordid><originalsourceid>FETCH-LOGICAL-c411t-eafcffe8e4aba813df20517bb35c2abfa264e4c9867c8a4b811c91c016b32f993</originalsourceid><addsrcrecordid>eNpVkFtLAzEQhYMotlb_gci--Lg1s8lmN75JvUKhPuibEGbTxG7ZS0m21f57s7SlOAwMHL5zYA4h10DHADm7o5IykEyMKR_TMFJQfkKGwKSMGaXslAx7JO6ZAbnwfkkpCM7gnAwgTbMkZdmQfE3NprVV-4u6bKKNcX7tI12hK7uFa-ttr4adzN4fIxMg4wrsyra5j2yrA9o2_-TYOmOCoTNug9UlObNYeXO1vyPy-fz0MXmNp7OXt8nDNNYcoIsNWm2tyQ3HAnNgc5vQFLKiYKlOsLCYCG64lrnIdI68yAG0BB2-KVhipWQjwne52rXeO2PVypU1uq0Cqvqy1KEsRbk6lBVsNzvbal3UZn407dsJwO0eQK-xsg4bXfojJxiDTMCRW5Tfi5_SGeVrrKoQC8q4ZcKVUJJn7A--74B1</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Levofloxacin versus clarithromycin in COPD exacerbation: focus on exacerbation-free interval</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Lode, H ; Eller, J ; Linnhoff, A ; Ioanas, M ; Evaluation of Therapy-Free Interval in COPD Patients Study Group</creator><creatorcontrib>Lode, H ; Eller, J ; Linnhoff, A ; Ioanas, M ; Evaluation of Therapy-Free Interval in COPD Patients Study Group ; Evaluation of Therapy-Free Interval in COPD Patients Study Group ; the Evaluation of Therapy-Free Interval in COPD Patients Study Group</creatorcontrib><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 &gt; 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. Drug treatments ; Pneumology ; Prospective Studies ; Pulmonary Disease, Chronic Obstructive - complications ; Pulmonary Disease, Chronic Obstructive - microbiology ; Statistics, Nonparametric ; Treatment Outcome</subject><ispartof>The European respiratory journal, 2004-12, Vol.24 (6), p.947-953</ispartof><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-eafcffe8e4aba813df20517bb35c2abfa264e4c9867c8a4b811c91c016b32f993</citedby><cites>FETCH-LOGICAL-c411t-eafcffe8e4aba813df20517bb35c2abfa264e4c9867c8a4b811c91c016b32f993</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16331761$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15572537$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Levofloxacin versus clarithromycin in COPD exacerbation: focus on exacerbation-free interval</title><title>The European respiratory journal</title><addtitle>Eur Respir J</addtitle><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 &gt; 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 &gt; 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.</abstract><cop>Leeds</cop><pub>Eur Respiratory Soc</pub><pmid>15572537</pmid><doi>10.1183/09031936.04.00009604</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0903-1936
ispartof The European respiratory journal, 2004-12, Vol.24 (6), p.947-953
issn 0903-1936
1399-3003
language eng
recordid cdi_crossref_primary_10_1183_09031936_04_00009604
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-16T06%3A16%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Levofloxacin%20versus%20clarithromycin%20in%20COPD%20exacerbation:%20focus%20on%20exacerbation-free%20interval&rft.jtitle=The%20European%20respiratory%20journal&rft.au=Lode,%20H&rft.aucorp=Evaluation%20of%20Therapy-Free%20Interval%20in%20COPD%20Patients%20Study%20Group&rft.date=2004-12-01&rft.volume=24&rft.issue=6&rft.spage=947&rft.epage=953&rft.pages=947-953&rft.issn=0903-1936&rft.eissn=1399-3003&rft_id=info:doi/10.1183/09031936.04.00009604&rft_dat=%3Cpubmed_cross%3E15572537%3C/pubmed_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/15572537&rfr_iscdi=true