Treatment of Advanced Emphysema with Emphysematous Lung Sealant (AeriSeal®)

被引:100
作者
Herth, F. J. F. [1 ]
Gompelmann, D. [1 ]
Stanzel, F. [2 ]
Bonnet, R. [3 ]
Behr, J. [4 ]
Schmidt, B. [5 ]
Magnussen, H. [6 ]
Ernst, A. [1 ,7 ]
Eberhardt, R. [1 ]
机构
[1] Univ Klinikum Heidelberg, Thoraxklin, Heidelberg, Germany
[2] Lungenklin Hemer, Hemer, Germany
[3] Zent Klin Bad Berka GmbH, Klin Pneumol, Bad Berka, Germany
[4] Klinikum Grosshadern LMU, Med Klin & Poliklin 1, Munich, Germany
[5] Charite, Med Klin Schwerpunkt Infektiol & Pneumol, Berlin, Germany
[6] Krankenhaus Grosshansdorf, Zentrum Pneumol & Thoraxchirurg GmbH, Grosshansdorf, Germany
[7] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
关键词
Lung volume reduction; Emphysema therapy; Bronchoscopic lung volume reduction; Interventional pulmonology; Emphysematous lung sealant; VOLUME-REDUCTION SURGERY; OUTCOMES; TRIAL; VALVE;
D O I
10.1159/000322649
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: This report summarizes initial tests of an emphysematous lung synthetic polymer sealant (ELS) designed to reduce lung volume in patients with advanced emphysema. Objectives: The primary study objective was to define a therapeutic strategy to optimize treatment safety and effectiveness. Methods: ELS therapy was administered bronchoscopically to 25 patients with heterogeneous emphysema in an open-label, noncontrolled study at 6 centers in Germany. Treatment was performed initially at 2-4 subsegments. After 12 weeks, patients were eligible for repeat therapy to a total of 6 sites. Safety and efficacy were assessed after 6 months. Responses were evaluated in terms of changes from baseline in lung physiology, functional capacity, and health-related quality of life. Follow-up is available for 21 of 25 patients. Results: Treatment was well tolerated. There were no treatment-related deaths (i.e. within 90 days of treatment), and an acceptable short-and long-term safety profile. Physiological and clinical benefits were observed at 24 weeks. Efficacy responses were better among Global Initiative for Chronic Obstructive Lung Disease (GOLD) stage III patients [n = 14; change in residual volume/total lung capacity (Delta RV/TLC) = -7.4 +/- 10.3%; Delta forced expiratory volume in 1 s (Delta FEV(1)) = +15.9 +/- 22.6%; change in forced vital capacity (Delta FVC) = +24.1 +/- 22.7%; change in carbon monoxide lung diffusion capacity (Delta DLCO) = +19.3 +/- 34.8%; change in 6-min walk test (Delta 6MWD) = +28.7 +/- 59.6 m; change in Medical Research Council Dyspnea (Delta MRCD) score = -1.0 +/- 1.04 units; change in St. George's Respiratory Questionnaire (Delta SGRQ) score = -9.9 +/- 15.3 units] than for GOLD stage IV patients (n = 7; Delta RV/TLC = -0.5 +/- 6.4%; Delta FEV 1 = +2.3 +/- 12.3%; Delta FVC = +2.6 +/- 21.1%; Delta DLCO = -2.8 +/- 17.2%; Delta 6MWD = +28.3 +/- 58.4 m; Delta MRCD = 0.3 +/- 0.81 units; Delta SGRQ = -6.7 +/- 7.0 units). Conclusions: ELS therapy shows promise for treating patients with advanced heterogeneous emphysema. Additional studies to assess responses in a larger cohort with a longer follow-up are warranted. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:36 / 45
页数:10
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