Rationale: The Chartis® ( Pulmonx, CA, USA) measurement system is a tool to assess interlobar collateral ventilation during bronchoscopy. Assessing collateral ventilation is important when you intend to treat a patient with endobronchial valves. Chartis measurement of collateral ventilation can be performed under both conscious sedation as well as general anesthesia. There is no consensus on what is the preferred method of anesthesia for Chartis measurements in the literature. Objective: In this project we want to investigate whether there is a difference in Chartis measurement outcomes between these two methods of anesthesia: conscious sedation and general anesthesia. Study design: This study will be a single center observational study Study population: The study population exists of patients with severe emphysema who undergo collateral ventilation assessment before bronchoscopic lung volume reduction treatment with one-way endobronchial valves. Intervention: All patients will undergo two subsequent Chartis measurements. The first measurement will be performed with the patient undergoing conscious sedation and the second measurement with the patient under general anesthesia. Main study parameters/endpoints: Our primary outcome measure is the failure rate of the Chartis collateral ventilation measurement under general anesthesia versus conscious sedation.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
30
All patients will undergo two subsequent Chartis measurements. The first measurement will be performed with the patient undergoing conscious sedation and the second measurement with the patient under general anesthesia.
University Medical Center Groningen
Groningen, Netherlands
Failure rate
The failure rate of the Chartis collateral ventilation measurement under general anesthesia versus conscious sedation.
Time frame: Baseline
Chartis measurement duration
To compare the duration of Chartis measurement in patients undergoing conscious sedation versus general anesthesia.
Time frame: Baseline
Physician feasibility
To investigate qualitative assessment feasibility for the physician in patients undergoing conscious sedation or general anesthesia.
Time frame: Baseline
Influence severity on outcome
To investigate the influence of severity of disease in patients undergoing conscious sedation or general anesthesia.
Time frame: Baseline
Influence collateral ventilation status on outcome
To investigate outcome difference in collateral ventilation status in patients undergoing conscious sedation versus general anesthesia
Time frame: Baseline
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