This is a single-arm, exploratory study to evaluate the value of transarterial CT angiography applying Nexaris Angio-CT in the interventional treatment of massive hemoptysis
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Transarterial catheter-directed CT angiography during interventional treatment of hemoptysis
Union Hospital affiliated to Tongji Medical College of Huazhong University of Science and Technology
Wuhan, Hubei, China
The accuracy rate of transarterial CT angiography in the identification of culprit vessel
The accuracy rate of transarterial CT angiography in the identification of culprit vessel, by calculating the matching rate between Angio-CT and selective angiography findings.
Time frame: Intraoperative phase
In-hospital clinical success
either the complete cessation of hemoptysis or a clinically significant reduction in bleeding, defined as ≤ 5 mL/24 hours of blood-tinged sputum or fresh blood during the hospitalization period.
Time frame: During the postoperative hospitalization period (i.e., the period after bronchial artery embolization until discharge)
Early hemoptysis recurrence rate
Recurrence rate of hemoptysis within 3 months after treatment
Time frame: 3 months after treatment
Technical success rate
Technical success is defined as complete cessation of target blood flow confirmed by DSA
Time frame: Intraoperative phase
Radiation exposure
Radiation exposure data were systematically collected from structured radiation dose reports. For Angio-CT scans, radiation exposure was quantified using the volume CT dose index (CTDIvol) and dose-length product (DLP). For digital subtraction angiography (DSA) and fluoroscopy, air kerma (AK) and dose-area product (DAP) were utilized as metrics.
Time frame: Intraoperative phase
The amount of contrast agent consumed
The amount of contrast agent consumed during treatment
Time frame: Intraoperative phase
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Adverse events
AEs were monitored and classified according to the Common Terminology Criteria for Adverse Events (CTCAE), version 5.0. The CTCAE system grades AEs on a 5-point scale, with grade ≥ 3 denoting a serious AE.
Time frame: Intraoperative phase and during 3 months after treatment