Endoscopic Lung Volume Reduction Using Endobronchial Valves in Patients with Severe Emphysema and Very Low FEV

被引:25
作者
Trudzinski, Franziska C. [1 ]
Hoeink, Anna J. [5 ]
Leppert, Daniela [2 ]
Fahndrich, Sebastian [1 ]
Wilkens, Heinrike [1 ]
Graeter, Thomas P. [6 ]
Langer, Frank [3 ]
Bals, Robert [1 ]
Minko, Peter [4 ]
Lepper, Philipp M. [1 ]
机构
[1] Univ Saarland, Med Ctr, Dept Internal Med Pneumol Allergol & Crit Care Me, Kirrberger Str 1, DE-66421 Homburg, Germany
[2] Univ Saarland, Med Ctr, Dept Nucl Med, Homburg, Germany
[3] Univ Saarland, Med Ctr, Dept Thorac & Cardiovasc Surg, Homburg, Germany
[4] Univ Saarland, Med Ctr, Dept Diagnost & Intervent Radiol, Homburg, Germany
[5] HELIOS Klinikum Krefeld, Dept Diagnost & Intervent Radiol, Krefeld, Germany
[6] Klinikum Lowenstein, Dept Thorac & Vasc Surg, Lowenstein, Germany
关键词
Endoscopic lung volume reduction; Endobronchial valves; Severe emphysema; MINIMAL IMPORTANT DIFFERENCE; COLLATERAL VENTILATION; TREATMENT TRIAL; SURGERY; PERFORMANCE; THERAPY; COPD; STANDARDIZATION; ATELECTASIS;
D O I
10.1159/000448761
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Patients with a forced expiratory volume in 1 s (FEV1) below 20% of the predicted normal values (pred.) and either homogeneous emphysema or low diffusing capacity for carbon monoxide (DLCO) have a high risk for adverse events including death when undergoing surgical lung volume reduction. Objectives: We hypothesized that selected patients can benefit from endoscopic lung volume reduction (eLVR) despite a very low FEV1. Methods: This study is a retrospective analysis of consecutive patients with severe airflow obstruction, an FEV1 <= 20% of pred., and low DLCO who were treated by eLVR with endobronchial valves (EBV) between June 2012 and January 2015. Pre- and post-interventional lung function parameters, the 6-min walking test (6-MWT) distance, adverse events, and follow-up were recorded. Results: In 20 patients, there was an overall improvement in lung function with an increase in FEV1 (16.97-21.03% of pred.) and a decrease in residual volume (322-270% of pred.) and total lung capacity (144-129.06% of pred.). The 6-MWT distance improved (from 239 +/- 77 to 267 +/- 97 m overall, and from 184 +/- 50 to 237 +/- 101 m if patients developed an atelectasis of the target lobe). Pneumothorax occurred in 5 of the 20 patients (25%). 30-day mortality was 0%, and all patients survived to discharge. Conclusions: The patients benefitted moderately from EBV treatment despite an initially low FEV1. Some patients improved remarkably. EBV treatment in patients with an FEV1 <= 20% of pred. is generally feasible and safe. The greatest risk is pneumothorax with prolonged chest tube duration. (C) 2016 S. Karger AG, Basel
引用
收藏
页码:258 / 265
页数:8
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