Q67.4 Q87.8
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients diagnosed with lymphatic, arteriovenous or venous malformation of the face and having undergone image-guided treatment by sclerotherapy or embolization in the form of one or more sessions in the period from 01/01/2017 to 12/30/2021. - Patients who have received the above procedures with the following sclerotherapy/embolization agents: Polidocanol, (gelled) alcohol, EVOH-based liquid embolization agents (EVOH = ethylene vinyl alcohol copolymer), bleomycin, OK 432 (picibanil), doxycycline, STS (sodium tetradecyl sulfate).
Exclusion criteria
Exclusion criteria: - Patients with lymphatic, arteriovenous or venous malformation without facial involvement. - Patients who have received other image-guided interventional procedures, e.g., electrosclerotherapy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Retrospective evaluation of image-guided interventional treatments of venous and arteriovenous malformations of the face. | — |
Secondary
| Measure | Time frame |
|---|---|
| - Analysis of technical success after image-guided, interventional treatment of lymphatic, arteriovenous and venous malformations of the face (successful performance of the procedures) - Analysis of devascularization of malformations after image-guided interventional treatment of lymphatic, arteriovenous and venous malformations of the face (grading of devascularization based on pre- and post-interventional imaging) - Analysis of complication rate after image-guided interventional treatment of lymphatic, arteriovenous, and venous malformations of the face (periinterventional and postinterventional complications < 30 days). | — |
Countries
Germany
Contacts
Klinik und Poliklinik für Radiologie Klinikum der Universität München Campus Großhadern