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Safety and timing of early therapeutic anticoagulation therapy after craniotomy.
Wilson, John M; Shelvin, Kierany B; Lawhon, Sarah E; Crabill, George A; Hayden, Ellery A; Velander, Alan J.
Afiliación
  • Wilson JM; Department of Neurosurgery, Louisiana State University Health Sciences Center New Orleans, New Orleans, Louisiana, United States.
  • Shelvin KB; Department of Neurosurgery, Louisiana State University Health Sciences Center New Orleans, New Orleans, Louisiana, United States.
  • Lawhon SE; Department of Neurosurgery, Louisiana State University Health Sciences Center New Orleans, New Orleans, Louisiana, United States.
  • Crabill GA; Department of Neurosurgery, Louisiana State University Health Sciences Center New Orleans, New Orleans, Louisiana, United States.
  • Hayden EA; Department of Neurosurgery, Louisiana State University Health Sciences Center New Orleans, New Orleans, Louisiana, United States.
  • Velander AJ; Department of Neurosurgery, Louisiana State University Health Sciences Center New Orleans, New Orleans, Louisiana, United States.
Surg Neurol Int ; 15: 31, 2024.
Article en En | MEDLINE | ID: mdl-38468647
ABSTRACT

Background:

To date, there are few guidelines and studies to guide the timing of initiation of therapeutic anticoagulation (AC) after craniotomy. The goal of this study was to assess the timing, safety, and outcomes of patients following the administration of therapeutic AC after craniotomy.

Methods:

A retrospective case-control study was performed evaluating all craniotomy patients from August 2017 to July 2021. Cases were selected if they received therapeutic AC within ten days of craniotomy. Nineteen out of 1013 craniotomy patients met the inclusion criteria. Indications for therapeutic AC were diverse, including deep venous thrombosis, pulmonary embolism, dural venous sinus thrombosis, mechanical heart valve, and left ventricular thrombus.

Results:

The mean and median time to therapeutic AC were 5.35 and 5 days, respectively. Three patients developed intracerebral hemorrhage (ICH) that was stable on repeat imaging and did not require any surgical intervention or result in new neurologic deficits. There was no significant association between therapeutic AC and postoperative ICH (P = 0.067).

Conclusion:

This study demonstrated that the initiation of therapeutic AC in postoperative craniotomy patients from postoperative days 2 to 10 did not result in any major complications. A prospective study is warranted to clarify the indications and safety of therapeutic AC after craniotomy.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Surg Neurol Int Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Surg Neurol Int Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos