Why the study?
Perioperative low-dose aspirin management strategies to minimize both hemorrhagic and thromboembolic complications during open craniotomy surgery lacked information.
Does perioperative aspirin continuation compared to discontinuation affect the risk of hemorrhagic complications and MACCEs in patients undergoing clipping surgery for unruptured intracranial aneurysms?
Does perioperative aspirin continuation compared to discontinuation affect the risk of hemorrhagic complications and MACCEs in patients undergoing clipping surgery for unruptured intracranial aneurysms?
Perioperative aspirin continuation during intracranial aneurysm clipping increases intracranial hemorrhage risk, but discontinuation increases MACCE risk in patients requiring secondary prevention, suggesting early resumption is indicated for high-risk patients.
Answers are grounded in this paper and cite their sources.
Aspirin continuation may increase ICH risk while discontinuation raises MACCEs in secondary prevention; leaves optimal perioperative strategy open for randomized trials.
BACKGROUND AND OBJECTIVE: Perioperative low-dose aspirin (ASA) management for open craniotomy surgery lacked information. We analyze to establish the perioperative ASA strategy to minimize both hemorrhagic and thromboembolic complications. METHODS: The investigators designed a multicenter retrospective study, which included patients scheduled to have clipping surgery for unruptured intracranial aneurysm. The incidence and risk factors were analyzed for postoperative hemorrhagic complications and major cardio- and cerebrovascular events (MACCEs) within 1 month postoperation. RESULTS: This study included 503 long-term ASA users of 3654 patients at three tertiary centers. The incidence of hemorrhagic complications and MACCEs was 7.4% (37/503) and 8.8% (44/503), respectively. Older age (>70 years, odds ratio [OR]: 2.928, 95% CI [1.337-6.416]), multiple aneurysms operation (OR: 2.201, 95% CI [1.017-4.765]), large aneurysm (>10 mm, OR: 4.483, 95% CI [1.485-13.533]), and ASA continuation (OR: 2.604, 95% CI [1.222-5.545]) were independent risk factors for postoperative hemorrhagic complications. Intracranial hemorrhage was the only type of hemorrhagic complication that increased in the ASA continuation group (10.6% vs 2.9%, P = .001). Between the ASA continuation and discontinuation groups, the overall incidence of MACCEs was not significantly different (log-rank P = .8). In the subgroup analysis, ASA discontinuation significantly increased the risk of MACCEs in the secondary prevention group (adjusted hazard ratio: 2.580, 95% CI [1.015-6.580]). CONCLUSION: ASA continuation increased the risk of postoperative intracranial hemorrhage. Simultaneously, ASA discontinuation was the major risk factor for postoperative MACCEs in the high-risk group. Without evidence of intracranial hemorrhage, early ASA resumption was indicated (a total cessation duration <7-10 days) in the secondary prevention group.
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Han et al. (2023) studied this question.
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