Your browser doesn't support javascript.
loading
Clinical Outcomes of Arteriovenous Fistula Treatment Using the Penumbra SMART COIL System: A Subgroup Analysis from the Multicenter SMART Registry.
Abdelsalam, Ahmed; Silva, Michael; Park, Min S; Eatz, Tiffany; Schirmer, Clemens M; Sanikommu, Sai; Wu, Eva M; Bellon, Richard J; Burks, Joshua D; Spiotta, Alejandro M; Starke, Robert M.
Afiliación
  • Abdelsalam A; Department of Neurological Surgery, University of Miami, Miami, Florida, USA. Electronic address: aaa824@miami.edu.
  • Silva M; Department of Neurological Surgery, University of Miami, Miami, Florida, USA.
  • Park MS; Department of Neurological Surgery, University of Virginia, Charlottesville, Virginia, USA.
  • Eatz T; Department of Neurological Surgery, University of Miami, Miami, Florida, USA.
  • Schirmer CM; Department of Neurosurgery, Geisinger Commonwealth School of Medicine, Wilkes-Barre, Pennsylvania, USA.
  • Sanikommu S; Department of Neurological Surgery, University of Miami, Miami, Florida, USA.
  • Wu EM; Department of Neurological Surgery, University of Miami, Miami, Florida, USA.
  • Bellon RJ; Department of Radiology, Swedish Medical Center, Englewood, Colorado, USA.
  • Burks JD; Department of Neurological Surgery, University of Miami, Miami, Florida, USA.
  • Spiotta AM; Department of Neurosurgery, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Starke RM; Department of Neurological Surgery, University of Miami, Miami, Florida, USA.
World Neurosurg ; 2024 Jul 08.
Article en En | MEDLINE | ID: mdl-38986948
ABSTRACT

BACKGROUND:

Endovascular embolization procedures are typically the primary treatment modality for arteriovenous fistula (AVF). The objective of this subset analysis was to evaluate the prospective long-term clinical outcomes of AVF patients treated with the SMART COIL System.

METHODS:

Patients who had AVFs and underwent endovascular coiling using the Penumbra SMART COIL system were part of a subset analysis within the SMART registry. The SMART registry is a postmarket registry that is prospective, multicenter, and single-arm in design. After the treatment, these patients were monitored for a period of 12 ± 6 months.

RESULTS:

A total of 41 patients were included. No patients (0/41) had a procedural device-related serious adverse event (SAE). Reaccess involving a guidewire due to catheter kickout was unnecessary for 85.4% (35/41) of the patients. Complete occlusion after the procedure was achieved in 87.8% (36/41) of patients. The periprocedural SAE rate was 2.4% (1/41), and no periprocedural deaths occurred (0/41). During the follow-up period, there were instances of retreatment in 3.4% (1/29) of patients. At 1 year, the lesion occlusion was better or stable in 93.3% (28/30) of patients. The rate of SAE from 24 hours to 1 year (±6 months) following the procedure was 26.8% (11/41). The 1-year all-cause mortality rate stood at 2.4% (1/41), and at the 1-year follow-up, 90.9% (20/22) of patients had a modified Rankin Scale score within the range of 0 to 2.

CONCLUSIONS:

The coiling procedure for AVFs using the SMART COIL System proved to be safe and effective at the 1-year follow-up.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: World Neurosurg Asunto de la revista: NEUROCIRURGIA Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: World Neurosurg Asunto de la revista: NEUROCIRURGIA Año: 2024 Tipo del documento: Article