Safety and Efficacy of Endobronchial Valve for Bronchoscopic Lung Volume Reduction Surgery: a Prospective Pilot Study

China-Japan Friendship Hospital10 enrolled

Overview

The goal of this pliot study al is to preliminarily evaluate the effectiveness and safety of transbronchial lung volume reduction surgery using the self-devloped endobronchial valves for chronic obstructive pulmonary disease patients with emphysema phenotype . The main questions it aims to answer are: Does self-devloped endobronchial valves improve the lung function、exercise capacity and symptons of participants? What surgery-related adverse events do participants have after transbronchial lung volume reduction surgery using the self-devloped endobronchial valves? Participants will: undergo transbronchial lung volume reduction surgery using the self-devloped endobronchial valves. receive follow-up before surgery (baseline) and 3 days, 4 weeks, 12weeks after surgery.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Emphysema Chronic Obstructive Pulmonary Disease

Interventions

Eligibility

Sex: ALLMin age: 40 YearsMax age: 85 Years

Medical Language ↔ Plain English

Inclusion Criteria: * 1\. Patients with chronic obstructive pulmonary disease based on GOLD diagnostic criteria; * 2\. Age range from 40 to 85 years old (including 40 and 85 years old); * 3\. BMI ≤ 35kg/m2; * 4\. 15% ≤ FEV1% pred ≤ 45%; * 5\. TLC\>100% pred, RV\>140% pred, and DLCO/red% ≥ 20%; * 6\. 100m ≤ 6WMD ≤ 500m after rehabilitation training; * 7\. Quit smoking for more than 4 months; * 8\. The evaluation result of pulmonary bypass ventilation function is negative; * 9\. Participants in this clinical trial requires the signing of an informed consent form by the individual or legal representative. Exclusion Criteria: * 1\. Being pregnant or breastfeeding; * 2\. PaCO2\>50mmHg and/or PaO2\<45mmHg; * 3\. Obvious bronchiectasis or other infectious lung diseases; * 4\. Hospitalization due to pulmonary infection or acute exacerbation of COPD within the past 12 months prior to baseline assessment twice or more times; * 5\. Coagulation dysfunction, platelet count\<60e+09/L; * 6\. Myocardial infarction or congestive heart failure within the past 24 weeks; * 7\. Previous lobectomy, LVRS or lung transplantation; * 8\. Anticoagulant therapy that cannot be stopped before surgery; * 9\. Uncontrolled pulmonary arterial hypertension (systolic pulmonary arterial pressure\>45mmHg) or lungs diagnosed within the past 12 weeks Arterial hypertension; * 10\. Left ventricular ejection fraction (LVEF) within the past 12 weeks is less than 45%; * 11\. Pulmonary nodules that require intervention; * 12\. Patients participating in other clinical trials; * 13\. Individuals with other contraindications to bronchial operations; * 14\. Other circumstances that the researcher deems unsuitable for participation in this clinical trial.