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Microsurgery versus embolization: different risk factors for short- and longterm outcomes of patients with ruptured aneurysms

ABSTRACT

Purpose:

To evaluate the risk factors for poor outcomes after surgical and endovascular treatment of aneurysmal subarachnoid hemorrhage (aSAH).

Methods:

Patients with ≥ 18-years of age and aSAH were included, while patients who died within 12 h of admission or lost follow-up were excluded. All participants underwent standardized clinical and radiological assessment on admission and were reassessed at discharge and at 6-months follow-up using the Glasgow Outcome Scale (GOS).

Results:

Death at discharge was associated with female gender, anterior communication artery (ACoA) aneurysm location and presence of atherosclerotic plaque in the surgical group, and with age in the endovascular group. Both groups had clinical condition on follow-up associated with mFisher score on admission and hypertension. GOS on follow-up was also associated with presence of atherosclerotic plaque and multiple aneurysms in surgical group, and with age in endovascular group.

Conclusions:

Subjects treated surgically are prone to unfavorable outcomes if atherosclerotic plaques and multiple aneurysms are present. In patients with endovascular treatment, age was the main predictor of clinical outcome.

Key words
Intracranial Aneurysm; Subarachnoid Hemorrhage; Plaque; Atherosclerotic; Aneurysms; Follow-Up Studies; Prognosis

Introduction

Subarachnoid hemorrhage (SAH) is a subset of stroke that occurs in relatively young patients and that have poor prognosis in most cases: about 50% dies in the first month and 40% of those who survive remains functionally dependent11 Lawton MT, Vates GE. Subarachnoid hemorrhage. N Engl J Med. 2017;377(3):257–66. https://doi.org/10.1056/NEJMcp1605827
https://doi.org/10.1056/NEJMcp1605827...
,22 Nieuwkamp DJ, Setz LE, Algra A, Linn FH, de Rooij NK, Rinkel GJ. Changes in case fatality of aneurysmal subarachnoid haemorrhage over time, according to age, sex, and region: A meta-analysis. Lancet Neurol. 2009;8(7):635–42. https://doi.org/10.1016/s1474-4422(09)70126-7
https://doi.org/10.1016/s1474-4422(09)70...
. SAH secondary to rupture of intracranial aneurysms, the aneurysmal subarachnoid hemorrhage (aSAH), accounts for 80% of nontraumatic SAH cases11 Lawton MT, Vates GE. Subarachnoid hemorrhage. N Engl J Med. 2017;377(3):257–66. https://doi.org/10.1056/NEJMcp1605827
https://doi.org/10.1056/NEJMcp1605827...
,22 Nieuwkamp DJ, Setz LE, Algra A, Linn FH, de Rooij NK, Rinkel GJ. Changes in case fatality of aneurysmal subarachnoid haemorrhage over time, according to age, sex, and region: A meta-analysis. Lancet Neurol. 2009;8(7):635–42. https://doi.org/10.1016/s1474-4422(09)70126-7
https://doi.org/10.1016/s1474-4422(09)70...
and its management may be endovascular or surgical.

For the last two decades, the treatment of SAH secondary to aneurysm rupture has changed due to the increasingly use of endovascular coiling, especially after the results of the International Subarachnoid Aneurysm Trial (ISAT)33 Molyneux A, Kerr R, Stratton I, Sandercock P, Clarke M, Shrimpton J, Holman R; International Subarachnoid Aneurysm Trial (ISAT) Collaborative Group. International Subarachnoid Aneurysm Trial (ISAT) of neurosurgical clipping versus endovascular coiling in 2143 patients with ruptured intracranial aneurysms: A randomised trial. Lancet. 2002;360(9342):1267–74. https://doi.org/10.1016/s0140-6736(02)11314-6
https://doi.org/10.1016/s0140-6736(02)11...
. The ISAT demonstrated that endovascular treatment of patients with ruptured intracranial aneurysms and good clinical condition on admission leads to better short and long-term outcomes than surgical clipping33 Molyneux A, Kerr R, Stratton I, Sandercock P, Clarke M, Shrimpton J, Holman R; International Subarachnoid Aneurysm Trial (ISAT) Collaborative Group. International Subarachnoid Aneurysm Trial (ISAT) of neurosurgical clipping versus endovascular coiling in 2143 patients with ruptured intracranial aneurysms: A randomised trial. Lancet. 2002;360(9342):1267–74. https://doi.org/10.1016/s0140-6736(02)11314-6
https://doi.org/10.1016/s0140-6736(02)11...
,44 Molyneux AJ, Birks J, Clarke A, Sneade M, Kerr RS. The durability of endovascular coiling versus neurosurgical clipping of ruptured cerebral aneurysms: 18 year follow-up of the UK cohort of the International Subarachnoid Aneurysm Trial (ISAT). Lancet. 2015;385(9969):691–7. https://doi.org/10.1016/S0140-6736(14)60975-2
https://doi.org/10.1016/S0140-6736(14)60...
.

Following studies have investigated the subpopulations in which coiling or clipping would be more beneficial. According to Pierot et al.55 Pierot L, Cognard C, Anxionnat R, Ricolfi F; CLARITY Investigators. Ruptured intracranial aneurysms: Factors affecting the rate and outcome of endovascular treatment complications in a series of 782 patients (CLARITY study). Radiology. 2010;256(3):916–23. https://doi.org/10.1148/radiol.10092209
https://doi.org/10.1148/radiol.10092209...
, risk factors for procedural complications during endovascular coiling include aneurysm’s size, neck size and location, age, smoking and hypertension. Nguyen et al.66 Nguyen TN, Raymond J, Guilbert F, Roy D, Bérubé MD, Mahmoud M, Weill A. Association of endovascular therapy of very small ruptured aneurysms with higher rates of procedure-related rupture. J Neurosurg. 2008;108(6):1088–92. https://doi.org/10.3171/JNS/2008/108/6/1088
https://doi.org/10.3171/JNS/2008/108/6/1...
studied the use of endovascular treatment in very small aneurysms and found that this procedure is five times more likely to results in procedure-related rupture when performed in aneurysms < 3 mm than in larger lesions.

Even though the risk factors for poor outcomes after the surgical treatment of ruptured aneurysms are well known (which include severity of the initial event, rebleeding, perioperative medical management, and the timing and technical success of aneurysm treatment), evidence regarding the risk factors for poor outcomes after endovascular coiling is still lacking. Therefore, considering the importance of comparing the different risk factor to better indicate the treatment, the aim of this study is to assess risk factors for poor outcomes after surgical and endovascular treatment of ruptured intracranial aneurysms.

Methods

This prospective cohort study was performed in Central Institute of Clinical Hospital from School of Medicine, University of São Paulo (HC-FMUSP), and was approved by the Ethics and Research Committee of HC-FMUSP. All methods were performed in accordance with the relevant guidelines and regulations. Each patient was fully informed about the study and provided informed consent as approved by the local Institutional Review Board.

Patient selection

This study enrolled patients from HC-FMUSP Division of Neurological Surgery between January 2018 and November 2019. Patients were eligible for enrollment if they were 18 years of age or older and admitted in the emergence department of the Central Institute of HC-FMUSP with diagnosis of ruptured aneurysm. Patients who died within the first 12 h after admission or lost follow-up after hospital discharge were excluded.

Data collection

Participants’ characteristics assessed included age, gender, hypertension, diabetes mellitus, smoking, alcohol abuse and previous SAH. The clinical condition at admission was assessed through the Hunt–Hess scale (HH). The radiological assessment included the modified Fisher classification (mFisher) on admission, multiple aneurysms, aneurysm’s location and size, and presence of atherosclerotic plaque in intracranial arteries. Time from ictus until intervention, clinical and surgical complication during in-hospital stay were also assessed. The patients were followed for 6 months and evaluated using the Glasgow Outcome Scale (GOS). The follow-up consultations were carried out at the HC-FMUSP Vascular Neurosurgery Clinic or by phone calls.

Statistical analysis

Descriptive statistics were applied to describe the clinical and demographic characteristics of the patients studied. Continuous variables were described as mean (standard deviation) or median (interquartile distance), as appropriate under normal data analysis. Categorical data were described as frequencies (valid percentage). Logistic regression was used to assess predictors of poor outcomes in short-term outcomes (clinical and surgical complications). Predictors of long-term outcomes (GOS) were assessed through ordered logistic regression. A two-tailed alpha level of 5% was adopted. The analyses were performed using the Stata software, version 17.0. Data from microsurgical and endovascular group were analyzed separately and the results were subsequently compared and discussed.

Results

A total of 112 patients were included. Seventy-six were submitted to microsurgical treatment and thirty-six to endovascular treatment (Fig. 1). The overall comparison between groups demonstrated no significant difference in terms of death at discharge (p = 0.06) and GOS in the follow-up (p = 0.44).

Figure 1
Flowchart of patient selection.

Microsurgical group

The microsurgical group had a mean age (SD) of 55.69 ± 12.43 and included 54 (71%) females, 22 (28.9%) males, 39 (51.3%) patients with hypertension, 18 (23.6%) with diabetes mellitus, 7 (9.2%) with a previous SAH, 9 (11.8%) with alcohol abuse and 30 (39.4%) were smokers (Tables 1 and 2). The median (interquartile range, IQR) period between ictus and surgery was 5 ± 9 days. Fifty-three (69.7%) patients had HH ≤ 2 on admission and 23 (30.2%) HH > 2 on admission.

Table 1
Demographic characteristics and its respective association with GOS score in follow-up.
Table 2
Demographic characteristics and its respective association with death at discharge.

The median (IQR) size (i.e., the largest dimension) of the aneurysms was 6±5 mm, 19 (25%) patients had atherosclerotic plaque, 12 (15.7%) patients had multiple aneurysms. MFisher was assessed on 75 patients: 20 (26.6%) had mFisher 0–2, 26 (34.6%) had mFisher 3, 29 (38.6%) had mFisher 4. Regarding the ruptured aneurysm location: n = 27 (35.5%) were in PCoA, n = 24 (31.5%) were in MCA, n = 12 (15.7%) were in anterior communication artery (ACoA), n = 5 (6.5%) were in ICA and n = 8 (10.5%) were in other arteries, which included ACA, PICA, pericallosal, AICA, ophthalmic, vertebral and basilar arteries (Tables 3 and 4).

Table 3
Radiological features and GOS in follow-up.
Table 4
Radiological features and death at discharge. mFisher was assessed in 75 patientsfrom the microsurgical group and 34 patients from the endovascular group.

Eighteen (23.6%) patients were dead at discharge. Among the 58 patients followed 6 months later, 4 (6.8%) died after discharge (GOS 1), 2 (3.4%) presented severe disability (GOS 3), 14 (24.1%) had minor neurologic deficits (GOS 4) and 38 (65.5%) returned to their original functional level (GOS 5) (Table 5). The statistical analysis revealed that hypertension (p = 0.03; 95% confidence interval [CI] = 0.12–2.62), mFisher 3 (p = 0.02; 95% CI = 0.33–6.19), presence of atherosclerotic plaque (p = 0.03; 95% CI = 0.09–2.80) and multiple aneurysms (p = 0.03; 95% CI = 0.10–4.05) were associated with GOS in the follow-up. Female gender (odds ratio [OR] = 0.25; p = 0.03; 95% CI = 0.072–0.92), ACoA location (OR = 14935.17; p = 0.01; 95% CI = 4.86–4.58) and presence of atherosclerotic plaque (OR = 179.22; p = 0.02; 95% CI = 2.03–15789.2) were associated with death at discharge.

Table 5
Short and long-term outcomes.

The endovascular group had a mean age (SD) of 58.39 (14.3) and included 25 (69.4%) females, 11 males (30.5%), 19 (52.7%) patients with hypertension, 10 (27.7%) with diabetes mellitus, 5 (13.8%) with a previous SAH, 7 (19.4%) with alcohol abuse and 9 (25%) were smokers (Tables 1 and 2). The median (IQR) period between ictus and surgery was 5 ± 5 days. Twenty-two (61.1%) patients had HH ≤ 2 on admission and 14 (38.8%) HH > 2 on admission.

The median (IQR) size (i.e., the largest dimension) of the aneurysms was 5±5 mm, n = 12 (33.3%) patients had atherosclerotic plaque, n = 6 (16.6%) patients had multiple aneurysms. MFisher was assessed on 34 patients: n = 7 (20.5%) had mFisher 0–2, n = 9 (26.4%) mFisher 3, n = 18 (52.9%) mFisher 4. Regarding the ruptured aneurysm location: n = 5 (13.8%) were in PCoA, n = 3 (8.3%) were in MCA, n = 8 (22.2%) were in ACoA, n = 9 (25%) were in ICA and n = 11 (30.5%) were in other arteries, which included ACA, PICA, Pericallosal, AICA, Ophthalmic, vertebral and basilar arteries (Tables 3 and 4).

Eleven (30.5%) patients were dead at discharge. Among the remaining 25 patients who were followed 6 months later, 4 (16%) had died during the follow-up period (GOS 1), 5 (20%) presented severe disability (GOS 3), 4 (16%) had minor neurologic deficits (GOS 4) and 12 (48%) had returned to their original functional level (GOS 5) (Table 5).

The statistical analysis revealed that age (p = 0.01; 95% CI = 0.23–0.02) hypertension (p = 0.001; 95% CI = 2.09–8.02) and mFisher 3 (p = 0.03; 95% CI = 11.12–0.52) were associated with clinical outcome in follow-up. Age (OR = 1.11; p = 0.039; 95% CI = 1.00–1.23) was also associated with death at discharge.

Discussion

In this study, death at discharge was associated with female gender, ACoA aneurysm location and presence of atherosclerotic plaque in patients surgically treated, while only age was associated with the same outcome in patients who underwent the endovascular procedure. Both groups had clinical condition on 6 months of follow-up associated with mFisher score on admission and hypertension. Additionally, the multivariate analysis demonstrated that the presence of atherosclerotic plaque on imaging and multiple aneurysms could predict clinical long-term outcomes in patients treated surgically, while only age was associated with long-term outcomes in the endovascular group.

Studies have shown that higher mFisher grade and hypertension are associated with poor long-term outcomes in patients with aSAH, regardless of the type of treatment77 Eskesen V, Rosenørn J, Schmidt K, Rønde F. Pre-existing arterial hypertension in subarachnoid haemorrhage: An unfavourable prognostic factor. Br J Neurosurg. 1987;1(4):455–61. https://doi.org/10.3109/02688698708999636
https://doi.org/10.3109/0268869870899963...
1111 Zheng K, Zhong M, Zhao B, Chen SY, Tan XX, Li ZQ, Xiong Y, Duan CZ. Poor-grade aneurysmal subarachnoid hemorrhage: Risk factors affecting clinical outcomes in intracranial aneurysm patients in a multi-center study. Front Neurol. 2019;10:123. https://doi.org/10.3389/fneur.2019.00123
https://doi.org/10.3389/fneur.2019.00123...
. The same pattern was observed in this study. Premorbid hypertension is an independent risk factor for increased severity of aSAH, rebleeding, hydrocephalus, mortality, and disability77 Eskesen V, Rosenørn J, Schmidt K, Rønde F. Pre-existing arterial hypertension in subarachnoid haemorrhage: An unfavourable prognostic factor. Br J Neurosurg. 1987;1(4):455–61. https://doi.org/10.3109/02688698708999636
https://doi.org/10.3109/0268869870899963...
1313 De Marchis GM, Lantigua H, Schmidt JM, Lord AS, Velander AJ, Fernandez A, Falo MC, Agarwal S, Connolly ES Jr, Claassen J, Mayer SA. Impact of premorbid hypertension on haemorrhage severity and aneurysm rebleeding risk after subarachnoid haemorrhage. J Neurol Neurosurg Psychiatry. 2014;85(1):56–9. https://doi.org/10.1136/jnnp-2013-305051
https://doi.org/10.1136/jnnp-2013-305051...
. The association between poor prognosis and female gender is likely due to the higher risk of vasospasm after aSAH in females1414 Brisman JL, Song JK, Newell DW. Cerebral aneurysms. N Engl J Med. 2006;355:928–39. https://doi.org/10.1056/NEJMra052760
https://doi.org/10.1056/NEJMra052760...
.

The association between systemic hypertension and intracranial aneurysm formation and ruptured is well established, but the mechanism behind this association is not fully understood. The link between systemic hypertension and IA might be the renin-angiotensin system (RAS). RAS plays an important role in vasorelaxation/vasoconstriction, vascular remodeling, and maintenance of arterial wall integrity1515 Nuki Y, Tsou TL, Kurihara C, Kanematsu M, Kanematsu Y, Hashimoto T. Elastase-induced intracranial aneurysms in hypertensive mice. Hypertension. 2009;54(6):1337–44. https://doi.org/10.1161/HYPERTENSIONAHA.109.138297
https://doi.org/10.1161/HYPERTENSIONAHA....
1717 Ohkuma H, Suzuki S, Fujita S, Nakamura W. Role of a decreased expression of the local renin-angiotensin system in the etiology of cerebral aneurysms. Circulation. 2003;108(7):785–7. https://doi.org/10.1161/01.CIR.0000087339.31094.3C
https://doi.org/10.1161/01.CIR.000008733...
. Zheng et al.1212 Zheng J, Xu R, Liu G, Guo Z, Sun X. Effect of premorbid hypertension control on outcome of patients with aneurysmal subarachnoid hemorrhage. Acta Neurochir (Wien). 2018;160(12):2401–7. https://doi.org/10.1007/s00701-018-3699-1
https://doi.org/10.1007/s00701-018-3699-...
retrospectively studied hypertensive patients with aSAH and showed that those treated with angiotensin-converting enzyme inhibitors and angiotensin receptor blockers suffered from less amount of aneurysmal bleeding than the patients treated with other types of antihypertensive drugs.

Although the neurological status on admission is considered the most important predictor for aSAH outcome, this study found no association between initial HH scores and short- or long-term outcomes for both groups1010 Jaja BN, Lingsma H, Schweizer TA, Thorpe KE, Steyerberg EW, Macdonald RL; SAHIT collaboration. Prognostic value of premorbid hypertension and neurological status in aneurysmal subarachnoid hemorrhage: Pooled analyses of individual patient data in the SAHIT repository. J Neurosurg. 2015;122(3):644–52. https://doi.org/10.3171/2014.10.JNS132694
https://doi.org/10.3171/2014.10.JNS13269...
,1818 Connolly ES Jr, Rabinstein AA, Carhuapoma JR, Derdeyn CP, Dion J, Higashida RT, Hoh BL, Kirkness CJ, Naidech AM, Ogilvy CS, Patel AB, Thompson BG, Vespa P; American Heart Association Stroke Council; Council on Cardiovascular Radiology and Intervention; Council on Cardiovascular Nursing; Council on Cardiovascular Surgery and Anesthesia; Council on Clinical Cardiology. Guidelines for the management of aneurysmal subarachnoid hemorrhage: A guideline for healthcare professionals from the American Heart Association/American Stroke Association. Stroke. 2012;43(6):1711–37. https://doi.org/10.1161/STR.0b013e3182587839
https://doi.org/10.1161/STR.0b013e318258...
,1919 Steiner T, Juvela S, Unterberg A, Jung C, Forsting M, Rinkel G; European Stroke Organization. European Stroke Organization guidelines for the management of intracranial aneurysms and subarachnoid haemorrhage. Cerebrovasc Dis. 2013;35(2):93–112. https://doi.org/10.1159/000346087
https://doi.org/10.1159/000346087...
. On the other hand, age seemed to be the main predictor of poor outcomes in patients who underwent embolization. In fact, older age has been previously associated with increased mortality and discharge to long-term facilities in patients with SAH2020 Brinjikji W, Lanzino G, Rabinstein AA, Kallmes DF, Cloft HJ. Age-related trends in the treatment and outcomes of ruptured cerebral aneurysms: A study of the nationwide inpatient sample 2001-2009. AJNR Am J Neuroradiol. 2013;34(5):1022–7. https://doi.org/10.3174/ajnr.A3321
https://doi.org/10.3174/ajnr.A3321...
2323 Shirao S, Yoneda H, Kunitsugu I, Ishihara H, Koizumi H, Suehiro E, Nomura S, Kato S, Fujisawa H, Suzuki M. Preoperative prediction of outcome in 283 poor-grade patients with subarachnoid hemorrhage: A project of the Chugoku-Shikoku Division of the Japan Neurosurgical Society. Cerebrovasc Dis. 2010;30(2):105–13. https://doi.org/10.1159/000314713
https://doi.org/10.1159/000314713...
. Proust et al.2424 Proust F, Gérardin E, Derrey S, Lesvèque S, Ramos S, Langlois O, Tollard E, Bénichou J, Chassagne P, Clavier E, Fréger P. Interdisciplinary treatment of ruptured cerebral aneurysms in elderly patients. J Neurosurg. 2010;112(6):1200–7. https://doi.org/10.3171/2009.10.JNS08754
https://doi.org/10.3171/2009.10.JNS08754...
assessed clinical outcomes of elderly patients (70 years or older) with ruptured intracranial aneurysms after the surgical or endovascular treatment, concluding that age exceeding 75 years was associated with functional dependence for groups.

The aneurysm location and size are also important factors when choosing between the two procedures. Some studies indicate that PCoA and MCA location are risk factors for intraprocedural rupture and poor outcomes when coiled55 Pierot L, Cognard C, Anxionnat R, Ricolfi F; CLARITY Investigators. Ruptured intracranial aneurysms: Factors affecting the rate and outcome of endovascular treatment complications in a series of 782 patients (CLARITY study). Radiology. 2010;256(3):916–23. https://doi.org/10.1148/radiol.10092209
https://doi.org/10.1148/radiol.10092209...
,2525 Kocur D, Przybyłko N, Bażowski P, Baron J. Rupture during coiling of intracranial aneurysms: Predictors and clinical outcome. Clin Neurol Neurosurg. 2018;165:81–7. https://doi.org/10.1016/j.clineuro.2018.01.006
https://doi.org/10.1016/j.clineuro.2018....
. On the other hand, endovascular approach of lesions < 3 mm is more prone to evolve to intraprocedural rupture66 Nguyen TN, Raymond J, Guilbert F, Roy D, Bérubé MD, Mahmoud M, Weill A. Association of endovascular therapy of very small ruptured aneurysms with higher rates of procedure-related rupture. J Neurosurg. 2008;108(6):1088–92. https://doi.org/10.3171/JNS/2008/108/6/1088
https://doi.org/10.3171/JNS/2008/108/6/1...
. In this study, the aneurysm size and location were not associated with outcomes in the endovascular group, which most likely reflect the limited sample size than the absence of association per se. Additionally, most aneurysms were bigger than 3 mm, limiting the analysis. However, the surgical group had a positive association between death at discharge and ACoA aneurysm location.

The presence of atherosclerotic plaque on imaging was associated to poor clinical outcomes 6-months later in the group treated surgically. The pathophysiology behind the unfavorable outcomes of patients treated with aneurysms treated via surgery when compared with those treated via embolization was not yet clarified or even sufficiently investigated. The finding of this study suggest that the surgical treatment may lead to the inadvertent mobilization of intravascular atherosclerotic plaques, leading to microembolization and microinfarcts.

Multiple aneurysms were also predictors of poor outcomes in follow-up. Few studies have evaluated the impact of multiple lesions on long-term outcomes, most of them suggest that patients with unruptured multiple lesions do not have increased risk of rupture or poor clinical outcomes2626 Asiltürk M, Abdallah A. Clinical outcomes of multiple aneurysms microsurgical clipping: Evaluation of 90 patients. Neurol Neurochir Pol. 2018;52(1):15–24. https://doi.org/10.1016/j.pjnns.2017.09.005
https://doi.org/10.1016/j.pjnns.2017.09....
, 2727 Lee YJ, Parreira T, Matouk CC, Menezes R, Mandell DM, terBrugge KG, Willinsky RA, Krings T. Clinical characteristics and preferential location of intracranial mirror aneurysms: A comparison with non-mirror multiple and single aneurysms. Neuroradiology. 2015;57(1):35–40. https://doi.org/10.1007/s00234-014-1437-9
https://doi.org/10.1007/s00234-014-1437-...
. However, as this study investigated a subset of subjects who already suffered the rupture, it suggests that, once evolving with aSAH, cases of multiple aneurysms have higher risk of unfavorable outcomes.

Limitations

This study presents limitations that should be considered aiming a proper interpretation. First, the results’ analysis is limited by the small sample size, especially in the endovascular group. Second, the loss of follow-up, due to impossibility of following long-distance patients and giving up the participation in the study, limited the long-term analysis. Finally, the inconsistent results regarding the association of aneurysm size and location with clinical outcomes may be explained by the treatment selection bias.

Conclusions

Premorbid hypertension and severity of aSAH on imaging are predictors of poor outcomes, regardless of the type o treatment undergone. Subjects treated surgically are more susceptible to unfavorable outcomes if atherosclerotic plaques are present on imaging. This finding suggests that the vessel manipulation during the surgical procedure may cause inadvertent mobilization of atherosclerotic lesions, leading to detachment of microemboli into the cerebral circulation. Studies about pathophysiology of this process, which may explain the better results of endovascular procedures in many cases, are still lacking. Multiple aneurysms in the context of aSAH were associated with poor outcomes when treated surgically. In patients who underwent endovascular treatment, age was the main predictor of clinical outcome.

Acknowledgments

Not applicable.

  • Research performed at Department of Neurological Surgery, School of Medicine, Hospital das Clínicas, Universidade de São Paulo, Sao Paulo (SP), Brazil.
  • Data availability statement

    Data will be available upon request.
  • Funding

    Not applicable.

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    » https://doi.org/10.3171/JNS/2008/108/6/1088
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Publication Dates

  • Publication in this collection
    28 Nov 2022
  • Date of issue
    2022

History

  • Received
    23 Apr 2022
  • Reviewed
    25 June 2022
  • Accepted
    26 July 2022
Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia https://actacirbras.com.br/ - São Paulo - SP - Brazil
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