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dc.contributor.author김태형-
dc.date.accessioned2018-02-15T08:39:49Z-
dc.date.available2018-02-15T08:39:49Z-
dc.date.issued2011-08-
dc.identifier.citationINTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE, 권: 15, 호: 8, 페이지: 1104-1110en_US
dc.identifier.issn1027-3719-
dc.identifier.urihttp://www.ingentaconnect.com/content/iuatld/ijtld/2011/00000015/00000008/art00017-
dc.description.abstractSETTING: Eleven referring hospitals in South Korea. OBJECTIVE: To compare therapeutic responses in chronic obstructive pulmonary disease (COPD) subgroups, classified by diffusing capacity of the lung for carbon monoxide (DL(CO)) and lung volume. DESIGN: A total of 130 stable male COPD patients were classified into four subgroups according to baseline DL(CO) and residual volume/total lung capacity (RV/TLC) ratio. We compared therapeutic responses to short acting beta(2)-agonist (SABA) and 3-month combined inhalation of long-acting beta(2)-agonist (LABA) and corticosteroid among patients with these subgroups. RESULTS: Among the 130 COPD patients, 41 (31.5%) had normal DL(CO) and RV/TLC, 28 (21.5%) low DL(CO) and normal RV/TLC, 31 (23.8%) normal DL(CO) and high RV/TLC, and 30 (23.1%) low DL(CO) and high RV/TLC. The normal DL(CO)/high RV/TLC subgroup showed a significantly larger flow response (changes in forced expiratory volume in 1 s) to salbutamol than the normal DL(CO)/RV/TLC subgroups, and a larger volume response (changes in forced vital capacity) than the two normal RV/TLC subgroups. The normal DL(CO)/high RV/TLC subgroup also showed significantly larger flow and volume response to 3-month combined inhalation of LABA and corticosteroid than the two normal RV/TLC subgroups. CONCLUSION: COPD subgroups classified by DLco and RV/TLC may have different pulmonary function responses to pharmacological treatment.en_US
dc.description.sponsorshipThis study was supported by a grant from the Korea Healthcare Technology R&D Project, Ministry for Health, Welfare and Family Affairs, Republic of Korea (A102065) and by the Asan Institute for Life Science (07-057).JBS has been an investigator in a government-sponsored study (2006-2008 Korea Science and Engineering Foundation).YMO has been an investigator in university-sponsored studies (Asan Institute for Life Science, University of Ulsan College of Medicine) and an industry-sponsored study (MSD Korea and Astra-Zeneca Korea), and has participated as a speaker at scientific meetings organised and financed by various pharmaceutical companies (Handok, GlaxoSmithKline, AstraZeneca Korea, MSD Korea and Boehringer Ingelheim) and a magazine company (Korea Doctors' Weekly).SDL serves as a consultant to GlaxoSmithKline, and has participated as a speaker at scientific meetings organised and financed by various pharmaceutical companies (GlaxoSmithKline, AstraZeneca Korea and Boehringer Ingelheim).en_US
dc.language.isoenen_US
dc.publisherINT UNION AGAINST TUBERCULOSIS LUNG DISEASE (I U A T L D), 68 BOULEVARD SAINT-MICHEL,, 75006 PARIS, FRANCEen_US
dc.subjectCOPDen_US
dc.subjectdiffusing capacityen_US
dc.subjectemphysemaen_US
dc.subjectlung volumeen_US
dc.titleDifferent therapeutic responses in chronic obstructive pulmonary disease subgroupsen_US
dc.typeArticleen_US
dc.relation.no8-
dc.relation.volume15-
dc.identifier.doi10.5588/ijtld.10.0553-
dc.relation.page1104-1110-
dc.relation.journalINTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE-
dc.contributor.googleauthorRa, Seung Won-
dc.contributor.googleauthorLee, J. S.-
dc.contributor.googleauthorHuh, J. W.-
dc.contributor.googleauthorOh, Y-M.-
dc.contributor.googleauthorLee, S-D.-
dc.contributor.googleauthorChae, E. J.-
dc.contributor.googleauthorSeo, J. B.-
dc.contributor.googleauthorRa, S. W.-
dc.contributor.googleauthorLee, J-H.-
dc.contributor.googleauthorKim, T-H.-
dc.relation.code2011204354-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.piddrterry-
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COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
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