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Early experience with automatic pressure-controlled cerebrospinal fluid drainage during thoracic endovascular aortic repair.
Kotelis, Drosos; Bianchini, Claudio; Kovacs, Bence; Müller, Thomas; Bischoff, Moritz; Böckler, Dittmar.
Afiliación
  • Kotelis D; Department of Vascular and Endovascular Surgery, Heidelberg University Hospital, Heidelberg, Germany drosos.kotelis@med.uni-heidelberg.de.
  • Bianchini C; Department of Vascular and Endovascular Surgery, Heidelberg University Hospital, Heidelberg, Germany.
  • Kovacs B; Department of Vascular and Endovascular Surgery, Heidelberg University Hospital, Heidelberg, Germany.
  • Müller T; Department of Anesthesiology, Heidelberg University Hospital, Heidelberg, Germany.
  • Bischoff M; Department of Vascular and Endovascular Surgery, Heidelberg University Hospital, Heidelberg, Germany.
  • Böckler D; Department of Vascular and Endovascular Surgery, Heidelberg University Hospital, Heidelberg, Germany.
J Endovasc Ther ; 22(3): 368-72, 2015 Jun.
Article en En | MEDLINE | ID: mdl-25862367
ABSTRACT

PURPOSE:

To report initial experience with automatic pressure-controlled cerebrospinal fluid drainage (CSFD) during thoracic endovascular aortic repair (TEVAR).

METHODS:

A prospective nonrandomized study enrolled 30 consecutive patients (median age 68 years, range 42-89; 18 men) who underwent TEVAR between March 2012 and July 2013 and were considered to be at high risk for postoperative spinal cord ischemia (SCI), fulfilling 2 of the following criteria stent-graft length >20 cm, left subclavian artery coverage, and previous infrarenal aortic repair. All patients received perioperative CSFD via the LiquoGuard system. The protocol aimed for a CSF pressure of 10 mm Hg and duration of CSFD of 3 or 7 days in asymptomatic or symptomatic patients, respectively. Muscle strength of the lower extremities was assessed with the Oxford muscle strength grading scale.

RESULTS:

Completion of the CSFD protocol was achieved in 26 (87%) of 30 patients. CSFD was prematurely stopped due to catheter dislocation in 1 patient and bloody spinal fluid in 3 patients. CSFD was performed for a median of 3 days (range 1-7). Median total CSFD volume was 714 mL (range 13-2369), with a median 192 mL drained per 24 hours. The SCI rate was 3% (1/30). CSFD-related complications were observed in 33% of the patients 1 fatal intracranial hemorrhage, 3 bloody spinal fluid episodes, 3 persistent CSF leaks requiring epidural blood patch, and 3 post lumbar puncture headaches. Mortality during a median follow-up of 16 months (range 10-25) was 3% (1/30).

CONCLUSION:

Prophylactic CSFD was associated with a low SCI rate in a high-risk patient collective undergoing TEVAR. Monitoring and drainage by an automatic modus was feasible, reproducible, and reliable but associated with relevant drainage-associated complications.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Aorta Torácica / Presión del Líquido Cefalorraquídeo / Drenaje / Implantación de Prótesis Vascular / Isquemia de la Médula Espinal / Procedimientos Endovasculares Tipo de estudio: Diagnostic_studies / Etiology_studies / Evaluation_studies / Observational_studies / Risk_factors_studies Límite: Aged80 Idioma: En Revista: J Endovasc Ther Asunto de la revista: ANGIOLOGIA Año: 2015 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Aorta Torácica / Presión del Líquido Cefalorraquídeo / Drenaje / Implantación de Prótesis Vascular / Isquemia de la Médula Espinal / Procedimientos Endovasculares Tipo de estudio: Diagnostic_studies / Etiology_studies / Evaluation_studies / Observational_studies / Risk_factors_studies Límite: Aged80 Idioma: En Revista: J Endovasc Ther Asunto de la revista: ANGIOLOGIA Año: 2015 Tipo del documento: Article País de afiliación: Alemania