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Peak Plasma Concentration of Azithromycin and Treatment Responses in Mycobacterium avium Complex Lung Disease

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dc.contributor.author신성재-
dc.date.accessioned2017-10-26T07:56:11Z-
dc.date.available2017-10-26T07:56:11Z-
dc.date.issued2016-
dc.identifier.issn0066-4804-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/152708-
dc.description.abstractMacrolides, such as azithromycin (AZM) and clarithromycin, are the cornerstones of treatment for Mycobacterium avium complex lung disease (MAC-LD). Current guidelines recommend daily therapy with AZM for cavitary MAC-LD and intermittent therapy for noncavitary MAC-LD, but the effectiveness of these regimens has not been thoroughly investigated. This study evaluated associations between microbiological response and estimated peak plasma concentrations (Cmax) of AZM. The AZM Cmax was measured in patients receiving daily therapy (250 mg of AZM daily, n = 77) or intermittent therapy (500 mg of AZM three times weekly, n = 89) for MAC-LD and daily therapy for Mycobacterium abscessus complex LD (MABC-LD) (250 mg of AZM daily, n = 55). The AZM Cmax was lower with the daily regimen for MAC-LD (median, 0.24 μg/ml) than with the intermittent regimen for MAC-LD (median, 0.65 μg/ml; P < 0.001) or daily therapy for MABC-LD (median, 0.53 μg/ml; P < 0.001). After adjusting for confounding factors, AZM Cmax was independently associated with favorable microbiological responses in MAC-LD patients receiving a daily regimen (adjusted odds ratio [aOR], 1.58; 95% confidence interval [CI], 1.01 to 2.48; P = 0.044) but not an intermittent regimen (aOR, 0.85; 95% CI, 0.58 to 1.23, P = 0.379). With the daily AZM-based multidrug regimen for MAC-LD, a low AZM Cmax was common, whereas a higher AZM Cmax was associated with favorable microbiologic responses. The results also suggested that the addition of rifampin may lower AZM Cmax When a daily AZM-based multidrug regimen is used for treating severe MAC-LD, such as cavitary disease, the currently recommended AZM dose might be suboptimal. (This study has been registered at ClinicalTrials.gov under identifier NCT00970801.).-
dc.description.statementOfResponsibilityopen-
dc.publisherAmerican Society for Microbiology-
dc.relation.isPartOfANTIMICROBIAL AGENTS AND CHEMOTHERAPY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAged-
dc.subject.MESHAnti-Bacterial Agents/blood-
dc.subject.MESHAnti-Bacterial Agents/pharmacokinetics*-
dc.subject.MESHArea Under Curve-
dc.subject.MESHAzithromycin/blood-
dc.subject.MESHAzithromycin/pharmacokinetics*-
dc.subject.MESHDrug Administration Schedule-
dc.subject.MESHEthambutol/blood-
dc.subject.MESHEthambutol/pharmacokinetics*-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHLung/drug effects-
dc.subject.MESHLung/microbiology-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHModels, Statistical*-
dc.subject.MESHMycobacterium avium Complex/drug effects-
dc.subject.MESHMycobacterium avium Complex/growth & development-
dc.subject.MESHMycobacterium avium-intracellulare Infection/blood-
dc.subject.MESHMycobacterium avium-intracellulare Infection/drug therapy*-
dc.subject.MESHMycobacterium avium-intracellulare Infection/microbiology-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHRifampin/blood-
dc.subject.MESHRifampin/pharmacokinetics*-
dc.subject.MESHSputum/microbiology-
dc.titlePeak Plasma Concentration of Azithromycin and Treatment Responses in Mycobacterium avium Complex Lung Disease-
dc.typeArticle-
dc.publisher.locationUnited States-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Microbiology-
dc.contributor.googleauthorByeong-Ho Jeong-
dc.contributor.googleauthorKyeongman Jeon-
dc.contributor.googleauthorHye Yun Park-
dc.contributor.googleauthorSeong Mi Moon-
dc.contributor.googleauthorSu-Young Kim-
dc.contributor.googleauthorSoo-Youn Lee-
dc.contributor.googleauthorSung Jae Shin-
dc.contributor.googleauthorCharles L. Daley-
dc.contributor.googleauthorWon-Jung Koh-
dc.identifier.doi10.1128/AAC.00770-16-
dc.contributor.localIdA02114-
dc.relation.journalcodeJ00189-
dc.identifier.eissn1098-6596-
dc.identifier.pmid27480854-
dc.contributor.alternativeNameShin, Sung Jae-
dc.contributor.affiliatedAuthorShin, Sung Jae-
dc.citation.volume60-
dc.citation.number10-
dc.citation.startPage6076-
dc.citation.endPage6083-
dc.identifier.bibliographicCitationANTIMICROBIAL AGENTS AND CHEMOTHERAPY, Vol.60(10) : 6076-6083, 2016-
dc.date.modified2017-10-24-
dc.identifier.rimsid39717-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Microbiology (미생물학교실) > 1. Journal Papers

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