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Reduced risk of venous thromboembolism with the use of intermittent pneumatic compression after craniotomy: a randomized controlled prospective study.
Prell, Julian; Schenk, Grit; Taute, Bettina-Maria; Scheller, Christian; Marquart, Christian; Strauss, Christian; Rampp, Stefan.
Afiliación
  • Prell J; Departments of1Neurosurgery and.
  • Schenk G; Departments of1Neurosurgery and.
  • Taute BM; 2Angiology, University of Halle, Germany.
  • Scheller C; Departments of1Neurosurgery and.
  • Marquart C; Departments of1Neurosurgery and.
  • Strauss C; Departments of1Neurosurgery and.
  • Rampp S; Departments of1Neurosurgery and.
J Neurosurg ; : 1-7, 2018 Mar 01.
Article en En | MEDLINE | ID: mdl-29600912
ABSTRACT
OBJECTIVEThe term "venous thromboembolism" (VTE) subsumes deep venous thrombosis (DVT) and pulmonary embolism. The incidence of DVT after craniotomy was reported to be as high as 50%. Even clinically silent DVT may lead to potentially fatal pulmonary embolism. The risk of VTE is correlated with duration of surgery, and it appears likely that it develops during surgery. The present study aimed to evaluate intraoperative use of intermittent pneumatic compression (IPC) of the lower extremity for prevention of VTE in patients undergoing craniotomy.METHODSA total of 108 patients undergoing elective craniotomy for intracranial pathology were included in a single-center controlled randomized prospective study. In the control group, conventional compression stockings were worn during surgery. In the treatment group, IPC of the calves was used in addition. The presence of DVT was evaluated by Doppler sonography pre- and postoperatively.RESULTSIntraoperative use of IPC led to a significant reduction of VTE (p = 0.029). In logistic regression analysis, the risk of VTE was approximately quartered by the use of IPC. Duration of surgery was confirmed to be correlated with VTE incidence (p < 0.01); every hour of surgery increased the risk by a factor of 1.56.CONCLUSIONSIntraoperative use of IPC significantly lowers the incidence of potentially fatal VTE in patients undergoing craniotomy. The method is easy to use and carries no additional risks.■ CLASSIFICATION OF EVIDENCE Type of question therapeutic; study

design:

randomized controlled trial; evidence class I.Clinical trial registration no. DRKS00011783 (https//www.drks.de).
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Idioma: En Año: 2018 Tipo del documento: Article