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Analysis of ischemic cerebral lesions using 3.0-T diffusion-weighted imaging and magnetic resonance angiography after revascularization surgery for ischemic disease
Authors:Yasuo Murai  Takayuki Mizunari  Ryo Takagi  Yasuo Amano  Sunao Mizumura  Yuichi Komaba  Seiji Okubo  Shiro Kobayashi  Akira Teramoto
Affiliation:1. Department of Neurosurgery, Nippon Medical School, Tokyo, Japan;2. Department of Neurosurgery, Nippon Medical School Chiba Hokuso Hospital, Chiba, Japan;3. Department of Internal Medicine, Division of Neurology, Nephrology, and Rheumatology, Nippon Medical School, Tokyo, Japan;4. Department of Radiology, Nippon Medical School, Tokyo, Japan
Abstract:

Background

Cerebral revascularization surgery (CRS) is increasingly recognized as an important component in the treatment of complex cerebral vascular disease and tumors. CRS requires that the incidence of perioperative neurological complications should be minimized, because CRS for ischemic disease is often not the goal of treatment, but rather a prophylactic surgery. CRS carries the risk of focal postoperative neurological deficits. Little has been established concerning mechanisms of post-CRS ischemia. We used 3.0-T diffusion-weighted magnetic resonance imaging (DWI) and magnetic resonance angiography (MRA) to analyze the incidence and mechanism of ischemic lesions.

Methods

We studied the anterior circulation territory after 20 CRS procedures involving 33 vascular anastomosis procedures (13 double anastomoses and 7 single anastomoses) in 12 men and 8 women between June 2007 and October 2011. The operations included single or double superficial temporal artery–middle cerebral artery (STA–MCA) anastomosis to treat internal carotid artery/MCA occlusions or severe MCA stenosis. A combined STA–MCA anastomosis and indirect bypass were performed for moyamoya disease. Postoperative DWI and MRA were obtained in all patients between 24 and 96 h after surgery to detect thromboembolism, hypoperfusion, or procedural ischemic complications and vasospasms of the donor STA.

Results

Follow-up DWI and MRA were carried out 1.8 ± 0.6 days after CRS (range, 1–4 days). Temporary occlusion time for anastomoses averaged 18.9 min (range, 16–32 min). Asymptomatic new hyperintensities occurred in the ipsilateral hemisphere of 2 patients on postoperative DWI (10% patients/6.0% anastomoses), and 1 moyamoya patient (5.0% patients/3.0% anastomoses) developed a symptomatic hyperintensity in the ipsilateral occipital lobe in response to the operation. Two abnormal small (<5 mm) cortical DWI lesions were caused by sacrifices of a small branch of the recipient MCA.

Conclusion

This study is the first postoperative 3.0-T DWI study of CRS and related clinical events. The incidence of symptomatic postoperative DWI abnormalities was restricted to 1 moyamoya patient representing 5.0% of total patients and 3.0% anastomoses. Although some postoperative DWI abnormalities occurred, CRS was found to be safe with a low risk of symptomatic ischemia.
Keywords:AC, aneurismal clipping   ACZ, acetazolamide   ADC, apparent diffusion coefficient   CVRC, cerebrovascular reserve capacity   CI, cerebral infarction   CRS, cerebral vascular reconstructive surgery   DWI, diffusion-weighted magnetic resonance imaging   F, female   ICA, internal carotid artery   ICO, internal carotid artery occlusion   M, male   MCA, middle cerebral artery   MCO, middle cerebral artery occlusion   MCS, middle cerebral artery stenosis   MMD, moyamoya disease   MRA, magnetic resonance angiography   mRS, modified Rankin Scale   MRI, magnetic resonance Imaging   STA, superficial temporal artery
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