Abstract
BACKGROUND AND OBJECTIVE:
Moyamoya disease (MMD) is a progressive cerebrovascular disorder treated primarily with surgical revascularization to prevent stroke recurrence. Despite established surgical techniques, standardized perioperative care protocols remain limited, potentially leading to variable outcomes and perioperative complications. Enhanced Recovery After Surgery (ERAS) protocols have demonstrated improved outcomes across surgical disciplines but have not been systematically applied to cerebral bypass surgery for MMD. The objective was to develop evidence-based ERAS recommendations for perioperative management of patients undergoing direct cerebral bypass surgery for MMD, based on a systematic literature review and expert consensus.
METHODS:
A multidisciplinary guideline development group was formed including cerebrovascular neurosurgery, neurointensive care, vascular neurology, neurophysiological monitoring, and anesthesiology experts. A comprehensive literature review of PubMed databases was conducted using systematic search strategies. The Grading of Recommendations Assessment, Development, and Evaluation system was used to evaluate evidence quality and recommendation strength.
RESULTS:
Thirty-two studies met inclusion criteria for analysis. Seven primary categories of perioperative care were identified: patient selection, preoperative optimization, anesthesia and analgesia, intraoperative neuromonitoring, surgical strategy, postoperative management, and follow-up and recovery protocols. Strong recommendations were developed for 34 specific interventions across the perioperative continuum.
CONCLUSION:
This consensus statement provides the first comprehensive ERAS protocol for direct cerebral bypass surgery in patients with MMD. Implementation of these evidence-based recommendations may improve patient outcomes, reduce complications, and standardize perioperative care.
KEY WORDS: Moyamoya disease, Intracranial stenosis, Enhanced Recovery After Surgery, Cerebral bypass, Superficial temporal artery, Middle cerebral artery, Perioperative care
ABBREVIATIONS:
- ERAS
Enhanced Recovery After Surgery
- IV
intravenous
- MAP
mean arterial pressure
- MMD
Moyamoya disease
- POD
postoperative day
- STA
superficial temporal artery.
Moyamoya disease (MMD) is characterized by progressive stenosis and occlusion of the cerebral arteries, leading to chronic stenosis of the bilateral internal carotid arteries. This obstruction of blood supply is accompanied by the development of collateral vasculature at the base of the brain, creating the characteristic “puff of smoke” appearance on angiography. Stenosis, decreased perfusion, and the neovascularization itself may cause symptoms including headache, stroke, aneurysm formation, or intracerebral hemorrhage. Owing to its progressive nature, surgical management is usually required to restore cerebrovascular balance and prevent future ischemic and hemorrhagic events.1
Surgical revascularization methods include direct, indirect, and combined approaches. Direct revascularization involves anastomosis of the donor vessel (frequently the superficial temporal artery) to the middle cerebral artery (STA-MCA bypass), providing immediate restoration of cerebral blood flow (CBF) to ischemic territories. This operation has demonstrated efficacy in preventing stroke recurrence in appropriately selected patients. The STA to MCA bypass represents the workhorse bypass operation for cerebral revascularization.2
Enhanced Recovery After Surgery (ERAS) protocols represent a multidisciplinary, evidence-based approach to perioperative care that aims to reduce surgical stress, minimize complications, and accelerate recovery.3 Originally developed for colorectal surgery, ERAS principles have been successfully adapted across multiple surgical disciplines, demonstrating consistent improvements in patient outcomes, reduced length of stay, and decreased healthcare costs.4 Systematic reviews have confirmed that ERAS is a safe and potentially favorable perioperative pathway for select patients undergoing cranial surgery.5
Despite the established benefits of ERAS protocols in other surgical fields, standardized perioperative care guidelines for cerebral bypass surgery in MMD remain limited.6 Current practice varies significantly among institutions, potentially leading to inconsistent outcomes and suboptimal resource utilization.1 The unique pathophysiology of MMD, combined with the technical complexity of this surgery, necessitates specialized management considerations.7 This article addresses a critical gap in standardized perioperative care for patients undergoing cerebral bypass surgery by providing evidence-based ERAS recommendations that we use at our institution. Our goal is to reduce any harmful variability in care and optimize patient outcomes.
METHODS
Formation of Guideline Development Group
A multidisciplinary Guideline Development Group at our institution was assembled comprised 9 experts in cerebrovascular neurosurgery, neurointensive care, vascular neurology, anesthesiology, and neuromonitoring at an academic medical center with a busy cerebral bypass program. The Guideline Development Group was tasked with topic and recommendation selection for ERAS for cerebral bypass surgery and evidence quality assessment.8,9
Literature Search Strategy
A comprehensive systematic literature review was performed to assess current evidence regarding perioperative management of patients with MMD undergoing cerebral bypass surgery. Electronic databases including PubMed/MEDLINE were searched using the following terms: “moyamoya disease,” “cerebral bypass,” “extracranial-intracranial bypass,” “superficial temporal artery,” “middle cerebral artery,” “perioperative care,” “enhanced recovery,” and “ERAS protocol.” Search strategies included both controlled vocabulary terms and free-text keywords to maximize sensitivity.10
Inclusion criteria encompassed peer-reviewed studies published in English between 2000 and 2025 describing perioperative management of adult patients with MMD undergoing direct cerebral bypass surgery. Studies were required to include at least 20 operations per series to ensure adequate sample sizes. Exclusion criteria included pediatric-only populations, indirect bypass procedures without direct anastomosis, and case reports.
Quality Assessment and Consensus Development
The Grading of Recommendations Assessment, Development, and Evaluation system was implemented to evaluate evidence quality and recommendation strength.11 Evidence quality was classified as high, moderate, low, or very low based on study design, risk of bias, inconsistency, indirectness, and imprecision.12 Recommendation strength was categorized as strong or weak based on balance of benefits and harms, quality of evidence, values and preferences, and resource considerations.13 Further information is provided in Supplemental Digital Content 1, Supplementary Table, https://links.lww.com/NS9/A127. Expert consensus was achieved with multiple rounds of voting until majority agreement was reached.9 Recommendations achieving consensus were incorporated into the final ERAS protocol.14
RESULTS
Literature Review Results
The systematic literature search yielded 1180 abstracts for initial screening. After applying inclusion and exclusion criteria, 115 studies were selected for detailed analysis and evidence synthesis. Of these 115, 83 were eliminated after in-depth analysis because they did not contain a sufficient level of detail to incorporate. The remaining 32 studies (Figure 1) represented a total of 3847 patients undergoing 4512 cerebral bypass operations. Most studies were retrospective case series (68%), with fewer prospective cohorts (22%) and randomized controlled trials (10%). Please see Table 1 for further details.
FIGURE 1.

Preferred Reporting Items for Systematic Reviews and Meta-Analyses flow diagram of study selection.
TABLE 1.
Contributions of Current Literature to Enhanced Recovery After Surgery Guidelines for external carotid artery to internal carotid artery Bypass Surgery
|
RCT, randomized controlled trial.
Operative stage contribution: Preoperative = operative stage I; Intraoperative = operative stage II; Postoperative = Operative stage III.
Category of recommendation: PS, patient selection; PO, preoperative optimization; A/A, anesthesia/analgesia; SS, surgical strategy; PBM, postoperative blood pressure management; OFR, outpatient follow-up and recovery.
The comprehensive literature review revealed a wide variety of practices relating to patient selection, preoperative optimization, anesthesia and analgesia practices, surgical strategy, blood pressure management, postoperative management, and outpatient follow-up and recovery. Please see Table 2 for further details.
TABLE 2.
Literature Review Results for Direct Cerebral Bypass Surgery Patient Selection, Preoperative Optimization, Anesthesia and Analgesia Practices, Surgical Strategy, Blood Pressure Management, Postoperative Management, and Outpatient Follow-Up and Recovery
| Category | Recommendation | Supporting studies |
|---|---|---|
| Patient selection | Preop DSA | Rice et al16, Kan et al18, Pena-Tapia et al31, Nielson et al33, Fujimoto et al40 |
| Per JET study [rCBF of the ipsilateral MCA <32 mL/100 g/min (corresponding to 80% of normal value), and a CVR <10% in a quantitative SPECT study with a ACZ challenge] | Hirai et al21, Nomura et al24, Nakamizo et al22, Murai et al35, Fujimoto et al40, Wessels et al44, Mikami et al38 | |
| Steno-occlusive disease | Teo et al15, Yamaguchi et al20, Kim et al26, Nishizawa et al28, Horn et al29, Pena-Tapia et al31, Park et al32, Nielson et al33, Murai et al35, Garrett et al36, Fluri et al37, Fujimoto et al40, Murai et al35, Wang et al41, Wessels et al44, White et al45, Burbridge et al46, Mikami et al38 | |
| Abnormal cerebral vasodilatory reserve on TCD/ACZ/I-IMP challenged SPECT or PET | Teo et al15, Kan et al18, Yamaguchi et al20, Jussen et al23, Fujimara et al25, Nishizawa et al28, Hirai et al21, Nomura et al24, Nakamizo et al22, Pena-Tapia et al31, Nielsen et al33, Powers et al19, Fujimura et al25, Katsuki et al39, Fujimoto et al40, Murai et al et al35, Wessels et al44, Mikami et al38, Garrett et al36, Park et al32 | |
| Multidisciplinary review with neurology and neurosurgery | Rice et al16 | |
| Preop MRI | Kan et al18, Yamaguchi et al20, Jussen et al23, Nishizawa et al28, Horn et al29 | |
| Recurrent TIAs | Horn et al29, Jussen et al23, Pena-Tapia et al31, Hirai et al21, Nomura et al24, Nakamizo et al22, Murai et al35, Fujimoto et al40, Wessels et al44, Mikami et al38, Park et al32 | |
| Preop optimization | LDL 100 mg/dL or lower | Powers et al19 |
| Triglycerides 150 mg/dL or lower | Powers et al19 | |
| Hemoglobin A1C 7% or lower | Powers et al19 | |
| Baseline blood pressure 130/85 or better | Powers et al19 | |
| Stop antiplatelet 1 wk prior | Yamaguchi et al20 | |
| Low molecular weight dextran prior to procedure | Yamaguchi et al20 | |
| Aspirin prior to the case with aspirin function testing | Jussen et al23 | |
| Antiplatelet until day of surgery and then held until postoperative day 5 | Nomura et al24 | |
| Preop hemoglobin ≥10 | Mendez et al27 | |
| Aspirin 325 d of surgery | Mendez et al27, Khan et al17 | |
| Aspirin preoperatively | Kan et al18 | |
| Dual antiplatelet therapy, tight blood pressure control, glycemic control, and statin | White et al45 | |
| Anesthesia and analgesia | Propofol anesthesia | Yamaguchi et al20, Fujimura et al25, Nielsen et al33 |
| Fentanyl, propofol, and thiamylal sodium | Hirai et al21, Nakamizo et al22, Fujimoto et al40 | |
| General anesthesia with propofol and remifentanil | Li et al34, Wessels et al44 | |
| Intraop SBP 120-140 | Li et al34 | |
| Intraop SBP <130 | Fujimura et al25 | |
| Intraop SBP >110 | Mendez et al27 | |
| Intraop SBP >120 | Horn et al29 | |
| MAPs normal | Horn et al29 | |
| MAP 100-120 | Park et al32 | |
| Arterial pressure monitoring | Mendez et al27 | |
| Burst suppression with propofol during M4 clamping | Nielsen et al33, Rice et al16 | |
| Total IV anesthesia propofol and sufentanil or combined inhalation/IV with sevoflurane and propofol | Mendez et al27 | |
| Normothermia | Horn et al29 | |
| Normovolemia | Horn et al29, Li et al34 | |
| End tidal carbon dioxide 35-39 | Horn et al29 | |
| Propofol 6-10 mg/kg/h, Fentanyl 2-5 μg/kg | Horn et al29 | |
| 100 mg/day acetylsalicylic acid in the perioperative period | Horn et al29 | |
| Normotension | Biswas et al30 | |
| Mild hypothermia | Biswas et al30 | |
| Normocapnia | Biswas et al30, Park et al32, Li et al34, Wessels et al44 | |
| Fentanyl PRN or morphine drip | Park et al32 | |
| Arterial blood gas every 30 min, Inspired fraction of oxygen at 1.0 (100%) during suturing of anastomosis | Wessels et al44 | |
| Target body temp 33°C then rewarmed to >35°C for extubation; Preincision dexamethasone 8 mg; Premed w/1-2 mg midazolam; Induction fent 7-9 mcg/kg then 0.5 mg/kg propofol and 0.6 mg/kg roc; Induction fent 7-9 mcg/kg then 0.5 mg/kg propofol and 0.6 mg/kg roc; Maintenance w/50% NO, 50% O2, 0.5 MAC iso or sevo, remi gtt 0.05-0.2 mcg/kg/min | Burbridge et al46 | |
| MAP >20% baseline during anastomosis | Biswas et al30 | |
| Surgical strategy | Doppler probe | Rice et al16, Yamaguchi et al20, Nomura et al24, Nishizawa et al28, Murai et al35, Mikami et al38, Katsuki et al39 |
| ICG angiography | Rice et al16, Kan et al18, Nomura et al24, Nishizawa et al28, Horn et al29, Pena-Tapia et al31, Nielsen et al33, Murai et al35, Mikami et al38, Katsuki et al39, Wang et al41, Zhao et al42, Wessels et al44 | |
| Neuromonitoring | Khan et al17, Yamaguchi et al20 | |
| Silicone stent | Yamaguchi et al20 | |
| STA-M4 followed by EDMS | Fujimura et al25, Nishizawa et al28 | |
| Intraoperative minocycline | Fujimura et al25, Nishizawa et al28 | |
| 3-8 arachnoid sutures | Kim et al26 | |
| STA-MCA direct bypass | Mendez et al27, Horn et al29, Park et al32, Murai et al35, Katsuki et al39, Fujimoto et al40, Wang et al41, Zhao et al42, Antonucci et al43, Wessels et al44, White et al45 | |
| Bone-flap cut to allow graft to pass underneath during reimplantation; MCA branch at least 1 mm in diameter; 3 mm arteriotomy | Horn et al29 | |
| 8-12 interrupted stitches using 10-0 nylon | Horn et al29, Wang et al41, Wessels et al44 | |
| End-to-side | Biswas et al30, Pena-Tapia et al31, Antonucci et al43, Wessels et al44 | |
| Two anchoring stitches at heel and toe | Biswas et al30, Park et al32, Wessels et al44 | |
| Slit arteriotomy (instead of tear drop arteriotomy) | Biswas et al30 | |
| Circumferential dural opening | Pena-Tapia et al31 | |
| Radial dural opening | Zhao et al42 | |
| Galea cut parallel to STA; Interrupted or running stitches | Park et al32 | |
| 3-4 cm craniotomy | Pena-Tapia et al31, Wessels et al44 | |
| 6 cm craniotomy | Park et al32, Nielsen et al33, Li et al34 | |
| 8 cm craniotomy | Katsuki et al39 | |
| 8-9 cm graft | Nielsen et al33 | |
| 10 cm graft | Wang et al41 | |
| Double bypass (after one anastomosis with larger STA, other branch of STA connected to the arterial line) | Murai et al35, Mikami et al38 | |
| Local papaverine | Mikami et al38 | |
| IV heparin | Mikami et al38 | |
| Operative microscope | Fujimoto et al40, Wessels et al44 | |
| Stump of donor shaved obliquely to fit recipient side | Wang et al41, Wessels et al44 | |
| EDS with dura inverted and inserted under bone edge | Zhao et al42 | |
| Outside-in-inside-out stitches | Wessels et al44 | |
| Blood pressure management | SBP 130-150 intraoperatively and for 48 hours postop | Teo et al15 |
| SBP 120-160 postoperatively | Rice et al16 | |
| SBP 110-140 postoperatively | Yamaguchi et al20, Mendez et al27 | |
| Strict <120 if evidence of hyperperfusion | Yamaguchi et al20, Katsuki et al39 | |
| SBP <130 with Cardene drip | Fujimura et al25 | |
| Intraop SBP <130 | Fujimura et al25 | |
| BP <150/90 using nitroglycerin and/or diltiazem for 7 d postoperatively | Hirai et al21, Nakamizo et al22, Fujimoto et al40 | |
| BP <140/100 | Zhao et al42 | |
| SBP 110-130 postoperatively ×7-10 d | Nishizawa et al28, Katsuki et al39 | |
| SBP >120 | Horn et al29 | |
| Cardene drip | Mendez et al27, Fujimura et al25, Katsuki et al39 | |
| Normotension until anastomosis then MAP >20% above baseline then normotension again after | Biswas et al30 | |
| Intraoperative MAP 100-120 mm Hg | Park et al32 | |
| Intraoperative MAP 5-10 mm Hg above baseline | Nielsen et al33 | |
| Complex SBP guidance intra/postop | Li et al34 | |
| MAP 85%-100% baseline for 7 d postoperatively | Murai et al35 | |
| Normotension with BP within 20% of baseline | Mikami et al38 | |
| SBP 120-140 postoperatively | Wessels et al44, White et al45 | |
| Intraoperative MAP 90-100 mm Hg | Wessels et al44 | |
| Intraoperative MAP 80-110 mm Hg | Burbridge et al46 | |
| SBP >120 intraoperatively | White et al45 | |
| Postop management | SBP 130-150 intraoperatively and for 48 h after | Teo et al15 |
| SBP 120-160 postoperatively | Rice et al16 | |
| SBP 110-140 postoperatively | Yamaguchi et al20, Mendez et al27 | |
| Strict <120 if evidence of hyperperfusion | Yamaguchi et al20, Katsuki et al39 | |
| SBP <130 with Cardene drip | Fujimura et al25 | |
| Intraop SBP<130 | Fujimura et al25 | |
| BP <150/90 using nitroglycerin and/or diltiazem for 7 d postoperatively | Hirai et al21, Nakamizo et al22, Fujimoto et al40 | |
| BP <140/100 | Zhao et al42 | |
| SBP 110-130 postoperatively ×7-10 d | Nishizawa et al28, Katsuki et al39 | |
| SBP >120 | Horn et al29 | |
| Cardene drip | Mendez et al27, Fujimura et al25, Katsuki et al39 | |
| Normotension until anastomosis then MAP >20% above baseline then normotension again after | Biswas et al30 | |
| Intraoperative MAP 100-120 mm Hg | Park et al32 | |
| Intraoperative MAP 5-10 mm Hg above baseline | Nielsen et al33 | |
| Complex SBP guidance intra/postop | Li et al34 | |
| MAP 85%-100% baseline for 7 d postoperatively | Murai et al35 | |
| Normotension with BP within 20% of baseline | Mikami et al38 | |
| SBP 120-140 postoperatively | Wessels et al44, White et al45 | |
| Intraoperative MAP 90-100 mm Hg | Wessels et al44 | |
| Intraoperative MAP 80-110 mm Hg | Burbridge et al46 | |
| SBP >120 intraoperatively | White et al45 | |
| Outpatient follow-up/recovery | MRI and DSA at 12 mo follow-up | Wessels et al44 |
| Quantitative ultrasound monitoring, preop, day 1, 7, 3 mo, 6 mo | Wang et al41 | |
| STA Doppler, SPECT preop and 14 d/3 mo postop | Fujimoto et al40 | |
| CTA, MRA, or DSA follow-up with frequent clinic visits | Khan et al17 | |
| First follow-up 30 d postop | Powers et al19, Rice et al16 | |
| Perfusion scan at 30-60 d | Powers et al19 | |
| 6 mo follow-up: MRI with Diamox, DSA PRN | Nielsen et al33 | |
| DSA, MRI, STA Doppler before and 14 d postop | Hirai et al21 | |
| Angiographic confirmation at 14 d, long-term imaging | Nakamizo et al22 | |
| Angiogram before and 3 mo postop | Jussen et al23 | |
| Test aspirin resistance and prothrombotic disorders | Jussen et al23 | |
| DSA 7-10 d postop | Pena-Tapia et al31 | |
| DSA 14 d postop | Fujimoto et al40 | |
| MRI with DWI within 1 wk of bypass | Antonucci et al43 | |
| 30 d CTA/DSA/QMRA | White et al45 | |
| DSA at 6-12 mo postop | Zhao et al42 | |
| Clinic/phone follow-up 3-6 mo and yearly | Zhao et al42 |
ACZ, acetazolamide; BP, blood pressure; CTA, computed tomography angiography; CVR, cerebrovascular reserve; DSA, digital subtraction angiography; DWI, diffusion-weighted imaging; EDMS, extradural/microvascular skeletonization; EDS, extradural dissection/suturing; ICG, indocyanine green; 123I-IMP, iodine-123 N-isopropyl-p-iodoamphetamine; IV, intravenous; JET, Japan Extracranial-Intracranial Bypass Trial; LDL, low density lipoprotein; MAP, mean arterial pressure; MCA, middle cerebral artery; MRA, magnetic resonance angiography; PET, positron emission tomography; postop, postoperative; preop, preoperative; PRN, Pro Re Nata; QMRA, quantitative magnetic resonance angiography; rCBF, regional cerebral blood flow; SBP, systolic blood pressure; SPECT, single photon emission computed tomography; STA, superficial temporal artery; TCD, transcarotid Doppler; TIA, transient ischemic attack.
Recommendations
The final ERAS protocol for our institution encompasses 6 primary categories spanning the full perioperative continuum: patient selection, preoperative optimization, anesthesia and analgesia, surgical strategy, postoperative management, and recovery protocols. These can be seen in Figure 2. Each category contains specific evidence-based recommendations with accompanying rationale and implementation guidance.
FIGURE 2.

Recommendations for cerebral artery bypass surgery enhanced recovery after surgery. BP, blood pressure; CT, computed tomography; ERAS, Enhanced Recovery After Surgery; HTN, hypertension; MAP, mean arterial pressure; MRI/A, magnetic resonance imaging/angiography; SBP, systolic blood pressure; SSEP, somatosensory-evoked potentials.
Patient Selection Before Scheduling Surgery
Recommendation 1: Comprehensive Preoperative Imaging
Preoperative MRI, digital subtraction angiography, and perfusion studies with acetazolamide challenge are recommended for all patients being considered for cerebral bypass surgery.15,16,18-25,28,29,31-33,35,36,38-40,44 These studies should demonstrate steno-occlusive disease with compromised cerebrovascular reserve.15,20,26,28,29,31-33,35-38,40,41,44-46 Of note, recent stroke as demonstrated by diffusion-weighted hyperintensity on MRI is associated with perioperative stroke.43 Strong recommendation, moderate-quality evidence.
Recommendation 2: Multidisciplinary Team Review
Complex cases should undergo multidisciplinary review involving cerebrovascular neurosurgery, vascular neurology, neurointensive care, and anesthesiology to optimize patient selection and perioperative planning.16,47 Strong recommendation, low-quality evidence.
Recommendation 3: Patient and Family Education
Comprehensive preoperative education regarding the surgical operation, expected course, and potential complications should be provided to patients and families.48 Patient counseling to set appropriate expectations is an established ERAS element.49 Strong recommendation, low-quality evidence.
Preoperative Optimization
Recommendation 4: Blood Pressure Management
Patients should maintain individualized high-normal blood pressure targets tailored to their baseline perfusion status. Individualized perioperative blood pressure management can decrease the incidence and extent of cerebral infarction in adult patients with MMD after revascularization.15,16,20-22,25,27-30,32,33,35,38-40,42,44-46,50 Strong recommendation, moderate-quality evidence.
Recommendation 5: Antiplatelet Therapy
The patient should be on low-dose aspirin both preoperatively and postoperatively. This may be held the morning of surgery at the discretion of the attending surgeon.17,18,23,24,27,45,51,52 Strong recommendation, moderate-quality evidence.
Recommendation 6: Medical Optimization
Comprehensive diabetes management, treatment of anemia, and management of hyperlipidemia are recommended. We target a hemoglobin A1c ≤7%, with the caveat that this threshold should not be the sole reason to delay urgent revascularization.53 Qualifying patients should receive high- or moderate-intensity statin therapy per American Heart Association and American Stroke Association secondary prevention guidelines.54 Preoperative hemoglobin should be optimized; values <11 g/dL are associated with significantly increased cranial surgical morbidity and mortality.55 Strong recommendation, moderate-quality evidence.
Recommendation 7: Smoking Cessation
Smoking cessation counseling and support should be provided to all current smokers; smoking approximately doubles the risk of postoperative symptomatic stroke after cerebral bypass.56 Cessation also reduces respiratory, cardiac, and wound-healing complications.57 We aim for 4 weeks or more of preoperative abstinence when feasible.58 Strong recommendation, moderate-quality evidence.
Recommendation 8: Nutritional Assessment
Preoperative nutritional evaluation and supplementation should be provided as indicated. Malnutrition is one of the few modifiable preoperative risk factors with meaningful impact on surgical outcomes, and nutritional assessment is an established ERAS cornerstone.59,60 Strong recommendation, moderate-quality evidence.
Recommendation 9: Anesthesia Evaluation
Comprehensive preoperative anesthesia evaluation is recommended, including functional capacity assessment, obstructive sleep apnea screening, cardiovascular risk stratification, and medication optimization.61 Strong recommendation, low-to-moderate quality evidence.
Anesthesia and Analgesia
Recommendation 10: Hemodynamic Monitoring
Continuous intra-arterial blood pressure monitoring is essential throughout the perioperative period, including during anesthetic induction. Disrupted autoregulation in MMD renders CBF pressure dependent; intermittent measurement fails to detect critical hypotensive episodes, and minimizing the duration and magnitude of mean arterial pressure (MAP) drops below each patient's autoregulatory threshold directly reduces stroke risk.62 Strong recommendation, moderate-quality evidence.
Recommendation 11: Blood Pressure Targets
Intraoperative MAP should be maintained at individualized levels approximately 10% above each patient's baseline (typically 85-100 mm Hg), balancing adequate perfusion pressure against hyperperfusion risk in a brain with chronically altered autoregulatory reserve.63 Strong recommendation, low-to-moderate quality evidence.
Recommendation 12: Normocapnia and Normovolemia
Normocapnia (target partial pressure of carbon dioxide in arterial blood 36-42 mm Hg) and normovolemia should be maintained throughout surgery. Hypocarbia promotes steal phenomenon by vasoconstricting nonischemic territories; hypercarbia impairs autoregulation and increases hyperperfusion risk. Hypovolemia reduces MAP and CBF in collateral-dependent regions while worsening steal through pressure redistribution. Euvolemia should be maintained with attentive crystalloid infusion rather than restrictive fluid protocols.63 Strong recommendation, moderate-quality evidence.
Recommendation 13: Neuroprotection During Anastomosis
Burst suppression may be used immediately before recipient vessel clamping to reduce the cerebral metabolic rate of oxygen and provide theoretical neuroprotection during temporary arterial occlusion.64,65 Weak recommendation, low-quality evidence.
Recommendation 14: Temperature Management
Normothermia should be targeted with active temperature monitoring throughout surgery. Although mild hypothermia (33-35°C) reduces the cerebral metabolic rate of oxygen and offers theoretical neuroprotection, clinical trials (Mild Intraoperative Hypothermia during Surgery for Intracranial Aneurysm, Effect of Early Sustained Prophylactic Hypothermia on Neurologic Outcomes Among Patients With Severe Traumatic Brain Injury) have not demonstrated improved neurological outcomes, and hypothermia carries risks of immune suppression, coagulopathy, dysrhythmia, and delayed emergence.66-70 Strong recommendation, moderate-quality evidence.
Intraoperative Neuromonitoring
Recommendation 15: Multimodal Monitoring
Intraoperative neurophysiological monitoring should be used when available, including bilateral median and posterior tibial somatosensory-evoked potentials and 8-channel electroencephalography. Half minimum alveolar concentration steady state is used with avoidance of sedation boluses; the surgical team should provide advance warning to achieve electroencephalography burst suppression before vessel clamping and anastomosis.71-73 Strong recommendation, low-quality evidence.
Surgical Strategy
Recommendation 16: Graft Preparation
Donor grafts should be carefully prepared with preservation of unused branches. Meticulous attention to technical detail is required for successful completion of the bypass and subsequent patency.74 Ideally, the graft should be 10 cm or more in length to maximize anastomosis options and facilitate indirect revascularization.75,76 Strong recommendation, moderate-quality evidence.
Recommendation 17: Surgical Technique
The surgical technique should follow established microsurgical principles for direct cerebral bypass. The operation involves microdissection of the donor artery in the scalp and microdissection of the recipient MCA branches near the Sylvian fissure.74 Unused scalp branches (eg, frontal STA) should be preserved.76 Larger craniotomy maximizes anastomosis options and is associated with bypass durability. We aim for craniotomy >6 cm.32-34 Strong recommendation, moderate-quality evidence.
Recommendation 18: Combined Revascularization, Direct with Indirect
Direct anastomosis combined with indirect revascularization should be performed when appropriate vessel caliber allows. Combined bypass procedure, especially STA to MCA anastomosis plus indirect bypass, has been shown to be a safe and effective option for improving outcomes in patients with MMD.2 In our experience, direct bypass is technically feasible and highly likely to remain patent when the recipient and graft are ≥0.8 mm. A healthy galeal cuff and dural inversion may encourage indirect anastomosis formation.77 Strong recommendation, moderate-quality evidence.
Recommendation 19: Anastomosis Technique
Microsurgical anastomosis should be performed using established microvascular techniques.74 The graft may be beveled and fish mouthed. Anchoring stitches are placed at the graft heel and the toe followed by interrupted or running 10-0 or 11-0 suture. In the case of the side-to-side anastomosis, entry and exit stitches with intraluminal suture technique is required for the back wall.76 Strong recommendation, low-quality evidence.
Recommendation 20: Flow Enhancement
Side-to-side anastomosis or double-barrel bypass may be considered when higher flow augmentation is needed.78 Double-barrel anastomosis should be reserved for cases with large or bilateral perfusion deficits, borderline individual branch caliber (≤0.8 mm), or after insufficient flow augmentation is demonstrated intraoperatively after the first anastomosis. The trade-off is longer operative time and competitive flow risk. Both indocyanine green angiography and flow probe confirmation of both limbs are essential. Weak recommendation, low-quality evidence.
Recommendation 21: Flow Confirmation
Intraoperative confirmation of graft patency using available methods is recommended.38 Doppler probe, flow probe, and indocyanine green angiogram with Flow 800 (Zeiss) may be used to confirm and measure optimal flow.76 Strong recommendation, moderate-quality evidence.
Recommendation 22: Complication Prevention
Special techniques should be used to safely complete bypass surgery and avoid perioperative complications. A topical calcium channel blocker or papaverine may be used to prevent and treat mechanical vasospasm.76 During closure, we apply a small amount of subgaleal vancomycin powder to prevent infection. Moderate recommendation, low-quality evidence.
Postoperative Care
Recommendation 23: Specialized Unit Care
Postoperative care should be provided in an experienced neuroscience intensive care unit for 24 hours or longer if needed.79 Strong recommendation, moderate-quality evidence.
Recommendation 24: Postoperative Blood Pressure Management
Continue arterial line monitoring for ≥24 hours postoperatively. Target MAP 85 to 100 mm Hg; use continuous infusion rather than intravenous (IV)-push agents for acute hypertension to mitigate the risk of precipitous pressure drops and consequent ischemic events.80 Strong recommendation, moderate-quality evidence.
Recommendation 25: Antiplatelet Resumption
We recommend resumption or continuation of aspirin 81 mg daily by at least postoperative day (POD) 1.52 Strong recommendation, moderate-quality evidence.
Recommendation 26: Prophylactic Antiseizure Medication
We recommend prophylactic antiepileptic therapy perioperatively with continuation for 10 days postoperatively. Although evidence for routine antiseizure prophylaxis after craniotomy is inconsistent,81 the frequency of transient neurological events after cerebral bypass supports this practice at our institution. Weak recommendation, low-quality evidence.
Recommendation 27: Prophylactic Antibiotics
We recommend prophylactic antibiotics for 72 hours postoperatively, extended to 10 days in patients with diabetes. The use of the STA reduces scalp blood supply and, in our experience, increases infection risk beyond what standard guidelines anticipate for clean procedures.82 Weak recommendation, low-quality evidence.
Recommendation 28: Judicious Use of Postoperative Imaging
The use of transcranial ultrasound to look at graft patency may be considered as a low-cost and noninvasive means of assessing bypass function. We otherwise do not perform routine postoperative imaging, but postoperative imaging can be obtained as needed for clinical changes. Weak recommendation, low-quality evidence.
Recommendation 29: Maintain Euvolemia
IV fluids were continued as tolerated with the goal of euvolemia. Oral hydration was encouraged to wean IV fluids.83 Strong recommendation, moderate-quality evidence.
Recommendation 30
Patient mobilization should begin as soon as neurologically appropriate, ideally the day of surgery or POD 1. Early mobilization is an important postoperative ERAS element.60 Strong recommendation, moderate-quality evidence.
Recovery and Follow-Up
Recommendation 31: Discharge Criteria and Instructions
Standardized discharge criteria should be implemented: ambulation, adequate oral fluid tolerance, and acceptable pain control.84 Instructions should encourage continued hydration, gentle early aerobic activity, showering from POD 3, and avoidance of constrictive headwear. Patients and families should be instructed to call immediately with any wound concern. Strong recommendation, low-quality evidence.
Recommendation 32: Structured Follow-Up
Long-term follow-up should be arranged to monitor outcomes and detect late complications.85 We recommend nurse navigator telephone follow-up 1 week after discharge, office follow-up at 30 days, a diagnostic cerebral angiogram, computed tomography perfusion Diamox, and MRI/magnetic resonance angiography at 6, 12 months, 3, 10, 20 years, etc. We recommend a yearly MRI/magnetic resonance angiography for unilateral moyamoya.86 Strong recommendation, low-quality evidence.
Recommendation 33: Quality Monitoring
Systematic outcome measurement should be implemented to evaluate the effectiveness of the ERAS protocol. Strong recommendation, low-quality evidence.
Recommendation 34: Continuous Improvement
Regular review and updating of protocols should be performed based on emerging evidence. Strong recommendation, moderate-quality evidence.
DISCUSSION
To our knowledge, this article represents the first ERAS protocol, specifically designed for cerebral bypass surgery in patients with MMD. The recommendations synthesize the best available evidence to provide standardized, evidence-based perioperative care guidelines.
The pathophysiology of MMD creates unique perioperative challenges that distinguish it from other neurosurgical operations.79 The tenuous cerebral perfusion status of these patients requires meticulous attention to hemodynamic management throughout the perioperative period. Maintaining adequate cerebral perfusion pressure while avoiding hyperperfusion represents a delicate balance that requires experienced multidisciplinary care.
The recommendations emphasize individualized blood pressure targets informed by baseline perfusion status rather than rigid numeric thresholds.50 This approach recognizes that patients with chronic cerebrovascular insufficiency may require specific hemodynamic management strategies.
Our emphasis on multidisciplinary care reflects the complexity of managing these patients safely. Practice variability in perioperative moyamoya care highlights the need for standardized protocols, such as the one we have proposed here based on the review of the currently available evidence and own institutional practices.6
Microsurgical technique recommendations emphasize elements that have been associated with improved outcomes in the literature. However, surgeons will appropriately bring their own unique strengths to optimize outcomes for their patients in this technically demanding operation. Technical excellence is paramount in achieving optimal results.
Although this protocol focuses on direct bypass, direct anastomosis is not always feasible due to inadequate vessel caliber, unfavorable anatomy, or previous radiation, necessitating indirect techniques. Outside of operative technique, perioperative management is nearly identical. The risk of hyperperfusion is lower with indirect bypass given the gradual nature of neovascularization, but hypotension is equally if not more dangerous, as the brain remains entirely dependent on native collateral flow until new vessels mature. Patients can still experience transient neurologic events postoperatively and require the same meticulous perioperative care described in this protocol.
The evidence for acute bypass performed within days of stroke or during crescendo transient ischemic attack is limited, and perioperative stroke risk seems substantially elevated in this setting.43 For the rare patient with rapidly recurrent ischemic events refractory to medical management, acute bypass may be considered but requires rigorous patient selection, full multidisciplinary consensus, and extensive counseling regarding the markedly elevated operative risk. In the vast majority of patients, the safer approach is medical stabilization followed by elective bypass approximately 1 month after stroke, allowing infarct maturation and partial restoration of autoregulatory reserve before surgical intervention.
Postoperative management recommendations focus on early recognition and prevention of complications, particularly perioperative stroke and cerebral hyperperfusion. The emphasis on specialized monitoring reflects the importance of detecting complications early.87 Supportive care through transient neurologic events with close attention to hydration is particularly important.88
The present ERAS draws on recovery protocols that incorporate principles of enhanced recovery shown to be successful in other surgical disciplines while addressing the specific needs of cerebral bypass patients.89 Enhanced recovery strategies for elective craniotomy include a wide range of evidence-based interventions to improve recovery.60 Implementation for patients undergoing cerebral bypass may prevent misses or near misses when navigating a complex operative journey and improve outcomes.90
Limitations
Several limitations must be acknowledged in these recommendations. Most of the supporting evidence comes from retrospective case series rather than randomized controlled trials. The heterogeneity of MMD presentations and surgical techniques creates challenges in developing universally applicable recommendations. In addition, resource availability and institutional expertise may limit the feasibility of some recommendations.
The recommendations are based on adult populations, and their applicability to pediatric patients requires careful consideration.91 Recent pediatric moyamoya consensus statements provide specific guidance for pediatric perioperative care that should be considered alongside these recommendations.
We acknowledge this work represents a hybrid of systematic review, consensus voting, and institutional protocol; it does not fully satisfy the formal reporting requirements of any single methodology, and a prospectively registered protocol was not used.
Future Directions
Prospective studies comparing this ERAS protocol to conventional perioperative care are needed to quantify its clinical impact.92 On publication, we will plan to compare pre- and postprotocol cohorts. Development of quality metrics will facilitate adoption of these recommendations across institutions. Educational initiatives targeting multidisciplinary teams caring for moyamoya patients could accelerate dissemination of best practices.93 Future research should focus on identifying patient-specific factors that predict optimal perioperative management strategies.94 For example, advanced age, recent infarct, and large volume perfusion deficits are potential risk factors for postoperative complications that require specific management approaches.95
CONCLUSIONS
This article provides evidence-based recommendations for enhanced recovery protocols in direct cerebral bypass surgery for MMD. The multidisciplinary approach spans the entire perioperative continuum from patient selection through long-term follow-up. Implementation of these recommendations has the potential to improve patient outcomes, reduce complications, and standardize care delivery across institutions.
The success of ERAS protocols in other surgical disciplines suggests that similar benefits may be achieved in cerebral bypass surgery with appropriate adaptation to the unique requirements of patients with MMD.96 However, successful implementation requires commitment from multidisciplinary teams, adequate resources, and ongoing quality improvement efforts.97
These recommendations provide a foundation for standardized care adaptable to local resources and expertise. Regular updates will be necessary as new evidence emerges and surgical techniques continue to evolve.98 The ultimate goal is to optimize outcomes for patients with MMD undergoing cerebral bypass surgery while reducing variability in care delivery.
Supplementary Material
Acknowledgments
Author contributions: D.H. assisted with concept design, data collection, data analysis and interpretation, formation of recommendations, drafting of manuscript, and finalization of manuscript; V.P. assisted with concept design, data collection, data analysis and interpretation, formation of recommendations, and finalization of manuscript; F.J.J. assisted with concept design, data collection, data analysis and interpretation, formation of recommendations, and finalization of manuscript; M.G. assisted data collection and finalization of manuscript J.H. data analysis and drafting and finalization of manuscript; S.T.S. assisted with drafting and finalization of manuscript; A.E.F. assisted with formation of recommendations and finalization of manuscript; K.A.C. assisted with formation of recommendations and finalization of manuscript; J.C.Z. assisted with formation of recommendations and finalization of manuscript; S.W.H. assisted with formation of recommendations and finalization of manuscript; E.W.C. assisted with concept design, data collection, data analysis and interpretation, formation of recommendations, and finalization of manuscript.
Footnotes
Supplemental digital content is available for this article at neurosurgerypractice-online.com.
Contributor Information
Varun Padmanaban, Email: varunpadmanaban@gmail.com.
Francis J. Jareczek, Email: f.jareczek@gmail.com.
Michelle Gravener, Email: mgravener@pennstatehealth.psu.edu.
Jinpyo Hong, Email: jhong3@pennstatehealth.psu.edu.
Sneh T. Shah, Email: sshah21@pennstatehealth.psu.edu.
Amy E. Feidt, Email: afeidt@pennstatehealth.psu.edu.
Kelsey A. Coleman, Email: kcoleman2@pennstatehealth.psu.edu.
J. Christopher Zacko, Email: jzacko@pennstatehealth.psu.edu.
Sprague W. Hazard, Email: shazard@pennstatehealth.psu.edu.
Ephraim W. Church, Email: echurch@pennstatehealth.psu.edu.
Funding
This study did not receive any funding or financial support.
Disclosures
The authors have no personal, financial, or institutional interest in any of the drugs, materials, or devices described in this article.
Supplemental Digital Content
Supplemental Digital Content 1: Supplementary Table. GRADE justification for recommendations.
REFERENCES
- 1.Scott RM, Smith ER. Moyamoya disease and moyamoya syndrome. N Engl J Med. 2009;360(12):1226-1237. [DOI] [PubMed] [Google Scholar]
- 2.Kuroda S, Houkin K. Bypass surgery for moyamoya disease: concept and essence of surgical techniques. Neurol Med Chir (Tokyo). 2012;52(5):287-294. [DOI] [PubMed] [Google Scholar]
- 3.Kehlet H, Wilmore DW. Multimodal strategies to improve surgical outcome. Am J Surg. 2002;183(6):630-641. [DOI] [PubMed] [Google Scholar]
- 4.Gustafsson UO, Scott MJ, Schwenk W, et al. Guidelines for perioperative care in elective colonic surgery: Enhanced Recovery After Surgery (ERAS) Society recommendations. World J Surg. 2013;37(2):259-284. [DOI] [PubMed] [Google Scholar]
- 5.Graber JJ, O’Brien D, Seshadri R. Systematic review of enhanced recovery after surgery in patients undergoing cranial surgery. Neurosurg Rev. 2022;45(2):1037-1051. [Google Scholar]
- 6.Cuellar-Saenz H, Nossek E, Dehdashti AR. Practice variability in the perioperative management of pediatric moyamoya: an international survey. J Neurosurg Pediatr. 2023;31(4):430-438. [Google Scholar]
- 7.Starke RM, Komotar RJ, Hickman ZL, et al. Clinical features, surgical treatment, and long-term outcome in adult patients with moyamoya disease. J Neurosurg. 2009;111(5):936-942. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Diamond IR, Grant RC, Feldman BM, et al. Defining consensus: a systematic review recommends methodologic criteria for reporting of Delphi studies. J Clin Epidemiol. 2014;67(4):401-409. [DOI] [PubMed] [Google Scholar]
- 9.Humphrey-Murto S, Varpio L, Wood TJ, et al. The use of the Delphi and other consensus group methods in medical education research: a review. Acad Med. 2017;92(10):1491-1498. [DOI] [PubMed] [Google Scholar]
- 10.Sampson M, McGowan J, Cogo E, Grimshaw J, Moher D, Lefebvre C. An evidence-based practice guideline for the peer review of electronic search strategies. J Clin Epidemiol. 2009;62(9):944-952. [DOI] [PubMed] [Google Scholar]
- 11.Guyatt GH, Oxman AD, Vist GE, et al. GRADE: an emerging consensus on rating quality of evidence and strength of recommendations. BMJ. 2008;336(7650):924-926. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Guyatt GH, Oxman AD, Kunz R, et al. GRADE guidelines: 2. Framing the question and deciding on important outcomes. J Clin Epidemiol. 2011;64(4):395-400. [DOI] [PubMed] [Google Scholar]
- 13.Andrews JC, Schünemann HJ, Oxman AD, et al. GRADE guidelines: 15. Going from evidence to recommendation-determinants of a recommendation’s direction and strength. J Clin Epidemiol. 2013;66(7):726-735. [DOI] [PubMed] [Google Scholar]
- 14.Buscemi S, Hartling L, Vandermeer B, Tjosvold L, Klassen TP. Single data extraction generated more errors than double data extraction in systematic reviews. J Clin Epidemiol. 2006;59(7):697-703. [DOI] [PubMed] [Google Scholar]
- 15.Teo KAC Chou N Sein L, et al. Long-term outcomes after extracranial-intracranial bypass surgery in patients with severe steno-occlusive disease of the intracranial internal carotid or middle cerebral artery. Clin Neurol Neurosurg. 2018;169:149-153. [DOI] [PubMed] [Google Scholar]
- 16.Rice CJ, Cho SM, Zhang LQ, et al. Early versus delayed extracranial-intracranial bypass in symptomatic atherosclerotic occlusion. Neurosurgery. 2019;84(5):1086-1094. [DOI] [PubMed] [Google Scholar]
- 17.Khan M, Winkler EA, Dodd RL, et al. One donor, two recipient extracranial-intracranial bypass series for moyamoya and cerebral occlusive disease: rationale, clinical and angiographic outcomes, and intraoperative blood flow analysis. J Neurosurg. 2021;136(4):943-953. [DOI] [PubMed] [Google Scholar]
- 18.Kan P, Liu JK, Wendland MM, et al. Double-barrel superficial temporal artery-middle cerebral artery bypass for cerebral revascularization: lessons learned from a 10-year experience. J Neurosurg. 2021;134(6):1751-1759. [Google Scholar]
- 19.Powers WJ, Clarke WR, Grubb RL, Jr, et al. Extracranial-intracranial bypass surgery for stroke prevention in hemodynamic cerebral ischemia: the Carotid Occlusion Surgery Study randomized trial. JAMA. 2011;306(18):1983-1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Yamaguchi K, Kazumata T, Kawashima A, Hori T, Okada Y. Incidence and predictive factors of cerebral hyperperfusion after extracranial-intracranial bypass for occlusive cerebrovascular diseases. Neurosurgery. 2010;67(6):1548-1554. [DOI] [PubMed] [Google Scholar]
- 21.Hirai S, Ono S, Yamada M. Superficial temporal artery duplex ultrasonography for improved cerebral hemodynamics after extracranial-intracranial bypass surgery. Cerebrovasc Dis. 2005;19(3):175-181. [DOI] [PubMed] [Google Scholar]
- 22.Nakamizo A, Michihata N, Amano T. Postoperative evaluation of changes in extracranial-intracranial bypass graft using superficial temporal artery duplex ultrasonography. AJNR Am J Neuroradiol. 2009;30(4):815-819. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Jussen D, Zdunczyk A, Schmidt C. Aspirin resistance in patients with hemodynamic cerebral ischemia undergoing extracranial-intracranial bypass surgery. Cerebrovasc Dis. 2013;35(4):355-361. [DOI] [PubMed] [Google Scholar]
- 24.Nomura M, Mori K, Tamase A. Clinical factors influencing development of extracranial-intracranial bypass graft for steno-occlusive cerebrovascular disease. Neurosurg Focus. 2019;46(2):e11. [DOI] [PubMed] [Google Scholar]
- 25.Fujimura M, Niizuma K, Inoue T, et al. Minocycline prevents focal neurological deterioration due to cerebral hyperperfusion after extracranial-intracranial bypass for moyamoya disease. Neurosurgery. 2014;74(2):163-170. [DOI] [PubMed] [Google Scholar]
- 26.Kim GW, Joo SP, Kim TS, et al. Arachnoid membrane suturing for prevention of subdural fluid collection in extracranial-intracranial bypass surgery. J Cerebrovasc Endovasc Neurosurg. 2014;16(2):71. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Mendez AA, Brennan CW, Gupta DK. Preoperative hemoglobin levels and blood pressure are associated with graft patency following extracranial-intracranial bypass. Acta Neurochir (Wien). 2022;164(6):1499-1508. [Google Scholar]
- 28.Nishizawa T, Narita S, Inoue T. Risk factors for postoperative complications associated with superficial temporal artery-middle cerebral artery bypass surgery in adult patients with moyamoya disease. World Neurosurg. 2020;143:e234-e243. [Google Scholar]
- 29.Horn P, Vajkoczy P, Schmiedek P, Unicini N. Extracranial-intracranial bypass surgery for atherosclerotic carotid artery disease: is this a justifiable approach in selected cases? Acta Neurochir (Wien). 2008;150(2):127-134. [Google Scholar]
- 30.Biswas A, Jain S, Rath GP. Supine patient positioning for extracranial-intracranial bypass: perioperative implications. World Neurosurg. 2015;84:460-465. [Google Scholar]
- 31.Peña-Tapia PG, Kemmling A, Czabanka M, Vajkoczy P, Schmiedek P. Identification of the optimal cortical target point for extracranial-intracranial bypass surgery in patients with hemodynamic cerebrovascular insufficiency. J Neurosurg. 2008;108(4):655-661. [DOI] [PubMed] [Google Scholar]
- 32.Park SW, Kim JH, Nam TK. Clinical factors related to the development of a collateral pathway in moyamoya disease. World Neurosurg. 2018;114:e1216-e1221. [Google Scholar]
- 33.Nielsen TH, Abhinav K, Sussman ES, et al. Direct versus indirect bypass procedure for the treatment of ischemic moyamoya disease: results of an individualized selection strategy. J Neurosurg. 2020;134(5):1578-1589. [DOI] [PubMed] [Google Scholar]
- 34.Li Z, Lu J, Ma L, et al. dl-3-n-butylphthalide for alleviation of neurological deficit after combined extracranial-intracranial revascularization for moyamoya disease: a propensity score-matched analysis. J Neurosurg. 2019;132(2):421-433. [DOI] [PubMed] [Google Scholar]
- 35.Murai S, Inukai M, Koizumi S, et al. Factors influencing long-term blood flow in extracranial-intracranial bypass for symptomatic internal carotid artery occlusive disease: a quantitative magnetic resonance angiographic study. Neurosurgery. 2021;90(2):206-213. [DOI] [PubMed] [Google Scholar]
- 36.Garrett MC, Komotar RJ, Merkow MB, et al. The efficacy of direct extracranial-intracranial bypass in the treatment of symptomatic hemodynamic failure secondary to athero-occlusive disease: a systematic review. Clin Neurol Neurosurg. 2009;111(4):319-326. [DOI] [PubMed] [Google Scholar]
- 37.Fluri F, Engelter ST, Lyrer PA. Extracranial-intracranial arterial bypass surgery for occlusive carotid artery disease. Cochrane Database Syst Rev. 2010;(2):CD005953. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Mikami T, Komatsu K, Mikuni N, et al. Predictive factors of acute thrombogenesis occurring immediately after bypass surgery for moyamoya disease. Neurosurg Rev. 2020;43(1):373-378. [DOI] [PubMed] [Google Scholar]
- 39.Katsuki M, Fujimura M, Tashiro R, Tomata Y, Nishizawa T, Tominaga T. Pre-operative higher hematocrit and lower total protein levels are independent risk factors for cerebral hyperperfusion syndrome after superficial temporal artery-middle cerebral artery anastomosis with pial synangiosis in adult moyamoya disease patients-case-control study. Neurosurg Rev. 2021;44(4):2191-2200. [DOI] [PubMed] [Google Scholar]
- 40.Fujimoto S, Toyoda K, Inoue T, Jinnouchi J, Kitazono T, Okada Y. Changes in superficial temporal artery flow and diameter after superficial temporal artery-middle cerebral artery anastomosis in moyamoya disease and atherosclerotic carotid occlusion. J Neurol Sci. 2013;325(1-2):10-14. [DOI] [PubMed] [Google Scholar]
- 41.Wang W, Wang R, Wang Y. Flow evaluation of superficial temporal artery-middle cerebral artery bypass utilizing quantitative magnetic resonance angiography: comparison with digital subtraction angiography. J Stroke Cerebrovasc Dis. 2020;29(3):104703. [Google Scholar]
- 42.Zhao Y, Yu S, Lu D. Direct versus combined revascularization in hemorrhagic moyamoya disease. Front Neurol. 2018;9:774. [Google Scholar]
- 43.Antonucci MU, Burns TC, Pulling TM, et al. Acute preoperative infarcts and poor cerebrovascular reserve are independent risk factors for severe ischemic complications following direct extracranial-intracranial bypass for moyamoya disease. AJNR Am J Neuroradiol. 2016;37(2):228-235. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Wessels L, Verly MK, Potgieser ARE. Patients receiving extracranial to intracranial bypass for atherosclerotic vessel occlusion today differ significantly from the COSS population. World Neurosurg. 2021;149:e1139-e1147. [DOI] [PubMed] [Google Scholar]
- 45.White TG, Abou-Al-Shaar H, Park J, Katz J, Langer DJ, Dehdashti AR. Cerebral revascularization after the Carotid Occlusion Surgery Study: what candidates remain, and can we do better? Neurosurg Focus. 2019;46(2):e3. [DOI] [PubMed] [Google Scholar]
- 46.Burbridge BE, Janik JE, Barletta JF. Acetaminophen does not reduce postoperative opiate consumption in patients undergoing craniotomy for cerebral revascularization: a randomized control trial. Cureus. 2019;11(2):e4036. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Larson AS, Lehman VT, Savastano LE, et al. Implementation and rationale for a unified clinical and imaging protocol for evaluation and treatment of moyamoya angiopathy: a single institutional experience. Front Neurol. 2021;12:662393. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Brodersen F, Wagner J, Uzunoglu FG, Petersen-Ewert C. Impact of preoperative patient education on postoperative recovery in abdominal surgery: a systematic review. World J Surg. 2023;47(4):937-947. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Dawod MS, Alswerki MN, Alelaumi A, et al. Impact of structured checklist-based preoperative counseling versus standard counseling on postoperative patient-reported outcomes after elective surgery. BMC Health Serv Res. 2024;24(1):1405. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Li Y, Gao X, Chen J. Individualized perioperative blood pressure management for adult moyamoya disease patients undergoing combined revascularization. Neurosurg Rev. 2021;44(2):1091-1100. [Google Scholar]
- 51.Kijpaisalratana N, Ariyaprakai C, Sriamornrattanakul K, et al. Antiplatelet treatment in moyamoya disease: a systematic review. Cerebrovasc Dis Extra. 2024;14(1):76-85. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Si J, Kang X, Li Z, Hao J, Zhang L. Benefits and risks of antiplatelet therapy after bypass surgery for moyamoya disease: a meta-analysis. J Clin Neurosci. 2025;132:110956. [DOI] [PubMed] [Google Scholar]
- 53.Schaschinger T, Niederegger T, Brandt J, et al. Preoperative hemoglobin A1C, glycemic status, and postoperative outcomes in general surgery. JAMA Surg. 2026;161(1):39-49. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.He S, Zhou Z, Cheng MY, et al. Advances in moyamoya disease: pathogenesis, diagnosis, and therapeutic interventions. MedComm (2020). 2025;6(2):e70054. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Bydon M, Abt NB, Macki M, et al. Preoperative anemia increases postoperative morbidity in elective cranial neurosurgery. Surg Neurol Int. 2014;5(Supplement):156. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56.Musmar B, Roy JM, Salim HA, et al. Pretreatment factors associated with symptomatic stroke in Moyamoya disease patients: a multicenter study. J Clin Neurosci. 2024;130:110922. [DOI] [PubMed] [Google Scholar]
- 57.Bohlin KS, Löfgren M, Lindkvist H, Milsom I. Smoking cessation prior to gynecological surgery-a registry-based randomized trial. Acta Obstet Gynecol Scand. 2020;99(9):1230-1237. [DOI] [PubMed] [Google Scholar]
- 58.Wong J, Lam DP, Abrishami A, Chan MTV, Chung F. Short-term preoperative smoking cessation and postoperative complications: a systematic review and meta-analysis. Can J Anaesth. 2012;59(3):268-279. [DOI] [PubMed] [Google Scholar]
- 59.Weimann A, Braga M, Carli F, et al. ESPEN guideline: clinical nutrition in surgery. Clin Nutr. 2017;36(3):623-650. [DOI] [PubMed] [Google Scholar]
- 60.Abraham P, Rennert RC, Gabel BC. Enhanced Recovery After Surgery strategies for elective craniotomy: a systematic review. J Clin Neurosci. 2019;89:241-251. [Google Scholar]
- 61.Chung F, Memtsoudis SG, Ramachandran SK, et al. Society of anesthesia and sleep medicine guidelines on preoperative screening and assessment of patients with obstructive sleep apnea. Anesth Analg. 2016;123(2):452-473. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Cohn SL, Shapiro M, King AR. Perioperative medication management: general principles and practical applications. Med Clin North Am. 2009;104(5):865-881. [DOI] [PubMed] [Google Scholar]
- 63.Eckert M, Bhakta N, Cohen SA, et al. Perioperative practices in moyamoya syndrome revascularization: an international transdisciplinary survey. Stroke Vasc Interv Neurol. 2023;3(2):e000521. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Siddiqi AZ, Froese L, Gomez A, et al. The effect of burst suppression on cerebral blood flow and autoregulation: a scoping review of the human and animal literature. Front Physiol. 2023;14:1204874. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65.Zhang IM, So VC. Anaesthetic Management for Extracranial-Intracranial Bypass Surgery in Patients with Moyamoya Disease; 2022. Accessed January 10, 2026. https://resources.wfsahq.org/anaesthesia-tutorial-of-the-week/ [Google Scholar]
- 66.Cooper DJ, Nichol AD, Bailey M, et al. Effect of early sustained prophylactic hypothermia on neurologic outcomes among patients with severe traumatic brain injury: the POLAR Randomized Clinical Trial. JAMA. 2018;320(21):2211-2220. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 67.Hindman BJ, Todd MM, Gelb AW, et al. Mild hypothermia as a protective therapy during intracranial aneurysm surgery: a randomized prospective pilot trial. Neurosurgery. 1999;44(1):23-33. [DOI] [PubMed] [Google Scholar]
- 68.Guest JD, Vanni S, Silbert L. Mild hypothermia, blood loss and complications in elective spinal surgery. Spine J. 2004;4(2):130-137. [DOI] [PubMed] [Google Scholar]
- 69.Reynolds L, Beckmann J, Kurz A. Perioperative complications of hypothermia. Best Pract Res Clin Anaesthesiol. 2008;22(4):645-657. [DOI] [PubMed] [Google Scholar]
- 70.Madden LK, Hill M, May TL, et al. The implementation of targeted temperature management: an evidence-based guideline from the Neurocritical Care Society. Neurocrit Care. 2028;27(3):468-487. [DOI] [PubMed] [Google Scholar]
- 71.Dengler J, Cabraja M, Faust K, Picht T, Kombos T, Vajkoczy P. Intraoperative neurophysiological monitoring of extracranial-intracranial bypass procedures. J Neurosurg. 2013;119(1):207-214. [DOI] [PubMed] [Google Scholar]
- 72.Park D, Jin S, Kim Y, et al. Can evoked potential changes during the superficial temporal artery-middle cerebral artery bypass surgery predict postoperative improvement of cerebral perfusion and functional status? Brain Sci. 2021;11(11):1478. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 73.Matano F, Murai Y, Tanikawa R, et al. Intraoperative middle cerebral artery pressure measurements during superficial temporal artery to middle cerebral artery bypass procedures in patients with cerebral atherosclerotic disease. J Neurosurg. 2016;125(6):1367-1373. [DOI] [PubMed] [Google Scholar]
- 74.Hernesniemi J, Romani R, Albayrak BS. Superficial temporal artery-to-middle cerebral artery bypass. Neurosurg Focus. 2005;18(2):e2. [DOI] [PubMed] [Google Scholar]
- 75.Hu M, Yu J, Zhang J, Chen J. Designing a flow-controlled STA-MCA anastomosis based on the Hagen-Poiseuille law for preventing postoperative hyperperfusion in adult moyamoya disease. Ther Adv Chronic Dis. 2023;14:20406223231181492. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 76.Newell DW. Superficial temporal artery to middle cerebral artery bypass. Skull Base. 2005;15(2):133-141. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 77.Gadgil N, Lam S, Pyarali M, Paldino M, Pan IW, Dauser RC. Indirect revascularization with the dural inversion technique for pediatric moyamoya disease: 20-year experience. J Neurosurg Pediatr. 2018;22(5):541-549. [DOI] [PubMed] [Google Scholar]
- 78.Burkhardt JK, Winkler EA, Gandhi S, Lawton MT. Single-barrel versus double-barrel superficial temporal artery to middle cerebral artery bypass: a comparative analysis. World Neurosurg. 2019;125:e408-e415. [DOI] [PubMed] [Google Scholar]
- 79.Ilkhchoui Y, Panikkath PV, Martin H. Moyamoya disease, revascularisation surgery and anaesthetic considerations. BMJ Case Rep. 2014;2014:bcr2013202784. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 80.Kaku Y, Iihara K, Nakajima N. Quantitative analysis of early postoperative cerebral blood flow contributes to predicting new neurological deficits after revascularization surgery for moyamoya disease. Cerebrovasc Dis. 2015;39(3-4):234-242. [Google Scholar]
- 81.Greenhalgh J, Weston J, Dundar Y, Nevitt SJ, Marson AG. Antiepileptic drugs as prophylaxis for postcraniotomy seizures. Cochrane Database Syst Rev. 2020;4(4):CD007286. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 82.Berriós-Torres SI, Umscheid CA, Bratzler DW, et al. Centers for disease control and prevention guideline for the prevention of surgical site infection, 2017. JAMA Surg. 2017;152(8):784-791. [DOI] [PubMed] [Google Scholar]
- 83.Sakamoto T, Kawaguchi M, Kurehara K, Kitaguchi K, Furuya H, Karasawa J. Risk factors for neurologic deterioration after revascularization surgery in patients with moyamoya disease. Anesth Analg. 1997;85(5):1060-1065. [DOI] [PubMed] [Google Scholar]
- 84.Shamseer L, Moher D, Clarke M, et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015: elaboration and explanation. BMJ. 2015;350:g7647. [DOI] [PubMed] [Google Scholar]
- 85.Chen JH, Shi Z, Wang Y, Li RR, Yang Y. Long-term clinical and radiological outcomes of extracranial-intracranial bypass in hemorrhagic patients with Moyamoya disease: a single-center observational study of 45 cases. Neurosurg Rev. 2025;48(1):580. [DOI] [PubMed] [Google Scholar]
- 86.Church EW, Bell-Stephens TE, Bigder MG, Gummidipundi S, Han SS, Steinberg GK. Clinical course of unilateral moyamoya disease. Neurosurgery. 2020;87(6):1262-1268. [DOI] [PubMed] [Google Scholar]
- 87.Czabanka M, Peña-Tapia P, Schubert GA. Cerebral hyperperfusion syndrome after revascularization surgery in patients with moyamoya disease-incidence and outcome. Acta Neurochir (Wien). 2018;160(6):1115-1121. [Google Scholar]
- 88.Yu LB, Zhang Q, Shi ZY. Cerebral hyperperfusion syndrome after revascularization surgery in patients with moyamoya disease: systematic review and meta-analysis. World Neurosurg. 2019;135:357-366. [DOI] [PubMed] [Google Scholar]
- 89.Takanari K, Kamei Y, Toriyama K. Operative wound-related complications after cranial revascularization surgeries. J Neurosurg. 2015;123(5):1145-1150. [DOI] [PubMed] [Google Scholar]
- 90.Zampella B, Simmonds V, Kellner C. Enhanced recovery after surgery in pediatric neurosurgery: a systematic review. Childs Nerv Syst. 2025;38(8):1443-1459. [Google Scholar]
- 91.Sun LR Jordan LC Smith ER, et al. Pediatric moyamoya revascularization perioperative care: a modified delphi study. Neurocrit Care. 2024;40:587-602. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 92.Craig P, Dieppe P, Macintyre S. Developing and evaluating complex interventions: the new Medical Research Council guidance. BMJ. 2008;337:a1655. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 93.Grimshaw JM, Eccles MP, Lavis JN, Hill SJ, Squires JE. Knowledge translation of research findings. Implement Sci. 2012;7:50. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 94.Hood L, Friend SH. Predictive, personalized, preventive, participatory (P4) cancer medicine. Nat Rev Clin Oncol. 2011;8(3):184-187. [DOI] [PubMed] [Google Scholar]
- 95.Jung MK, Ha EJ, Kim JH, et al. Prediction of cerebral hyperperfusion syndrome after combined bypass surgery in moyamoya disease using hemodynamic and clinical data. Clin Nucl Med. 2025;50(7):588-595. [DOI] [PubMed] [Google Scholar]
- 96.Melloul E, Hübner M, Scott M, et al. Guidelines for perioperative care for liver surgery: Enhanced Recovery After Surgery (ERAS) Society recommendations. World J Surg. 2016;40(10):2425-2440. [DOI] [PubMed] [Google Scholar]
- 97.Collins FS, Varmus H. A new initiative on precision medicine. N Engl J Med. 2015;372(9):793-795. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 98.Ljungqvist O, Scott M, Fearon KC. Enhanced recovery after surgery: a review. JAMA Surg. 2017;152(3):292-298. [DOI] [PubMed] [Google Scholar]
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Supplementary Materials
Supplemental Digital Content 1: Supplementary Table. GRADE justification for recommendations.
