Perioperative Low-Dose Aspirin Management for Planned Clipping Surgery: When, How Long, and With What Precautions?

Hyun Jin Han1, Junhyung Kim2, Chang Ki Jang3

  • 1Department of Neurosurgery, Severance Hospital, Yonsei University College of Medicine, Seoul , Republic of Korea.

Neurosurgery
|October 6, 2023
PubMed

Insights

Continuing low-dose aspirin (ASA) increases intracranial hemorrhage risk after craniotomy. However, stopping ASA significantly raises major adverse cardiovascular and cerebrovascular events (MACCEs) in secondary prevention patients.

Area of Science:

  • Neurosurgery
  • Cardiology
  • Pharmacology

Background:

  • Management of low-dose aspirin (ASA) during open craniotomy surgery is not well-defined.
  • There is a need to balance hemorrhagic and thromboembolic risks in these patients.

Purpose of the Study:

  • To analyze perioperative low-dose aspirin (ASA) management strategies for open craniotomy.
  • To minimize both hemorrhagic and thromboembolic complications in patients undergoing clipping surgery for unruptured intracranial aneurysms.

Main Methods:

  • A multicenter retrospective study including 3654 patients undergoing clipping surgery for unruptured intracranial aneurysms.
  • Analysis of postoperative hemorrhagic complications and major cardio- and cerebrovascular events (MACCEs) within one month.
  • Identification of risk factors for these complications.

Main Results:

  • Among 503 long-term ASA users, hemorrhagic complications occurred in 7.4% and MACCEs in 8.8%.
  • Independent risk factors for hemorrhage included older age, multiple aneurysms, large aneurysm size, and continued ASA use.
  • ASA continuation significantly increased intracranial hemorrhage risk (10.6% vs 2.9%), while discontinuation increased MACCEs in secondary prevention patients.

Conclusions:

  • Continuing ASA elevates the risk of postoperative intracranial hemorrhage.
  • Discontinuing ASA is a major risk factor for MACCEs in high-risk patients.
  • Early ASA resumption (cessation <7-10 days) is recommended for secondary prevention patients without intracranial hemorrhage evidence.
Abstract

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