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Karahalios, Katherine

https://orcid.org/0000-0002-0425-8020

Mayo Clinic

Barrow Neurological Institute

Citations 2

Cerebrospinal Fluid Biomarkers for Diagnosis and the Prognostication of Acute Ischemic Stroke: A Systematic Review
Adeleye, Olufunmilola , Winkler, Ethan A. , Hartke, Joelle N., Karahalios, Katherine , Mihaljević, Sandra, Rani, Anupama , Raikwar, Sudhanshu P. , Rulney, Jarrod, Scherschinski, Lea , Ducruet, Andrew F. , Albuquerque, Felipe C. , Lawton, Michael T. , Raikwar, Sudhanshu , Scherschinski, Lea , Adeleye, Olufunmilola , Naik, Anant , Koester, Stefan Wolfgang , Desai, Shashvat M. , Catapano, Joshua S , Jadhav, Ashutosh P. , Jha, Ruchira Menka

International Journal of Molecular Sciences | June 30, 2023 | Volume: 24 | Issue: 13 | Pages: 10902

10.3390/ijms241310902 Get It

Despite the high incidence and burden of stroke, biological biomarkers are not used routinely in clinical practice to diagnose, determine progression, or prognosticate outcomes of acute ischemic stroke (AIS). Because of its direct interface with neural tissue, cerebrospinal fluid (CSF) is a potentially valuable source for biomarker development. This systematic review was conducted using three databases. All trials investigating clinical and preclinical models for CSF biomarkers for AIS diagnosis, prognostication, and severity grading were included, yielding 22 human trials and five animal studies for analysis. In total, 21 biomarkers and other multiomic proteomic markers were identified. S100B, inflammatory markers (including tumor necrosis factor-alpha and interleukin 6), and free fatty acids were the most frequently studied biomarkers. The review showed that CSF is an effective medium for biomarker acquisition for AIS. Although CSF is not routinely clinically obtained, a potential benefit of CSF studies is identifying valuable biomarkers from the pathophysiologic microenvironment that ultimately inform optimization of targeted low-abundance assays from peripheral biofluid samples (e.g., plasma). Several important catabolic and anabolic markers can serve as effective measures of diagnosis, etiology identification, prognostication, and severity grading. Trials with large cohorts studying the efficacy of biomarkers in altering clinical management are still needed.
Microsurgical Obliteration of Craniocervical Junction Dural Arteriovenous Fistulas: Multicenter Experience
Salem, Mohamed M. , Srinivasan, Visish M. , Ravindran, Krishnan , Yang, Kaiyun , Karahalios, Katherine , Raygor, Kunal P. , Naylor, Ryan M. , Tavakoli, Samon , Abdelsalam, Ahmed , Chen, Stephanie H. , Jankowitz, Brian T. , Başkaya, Mustafa K. , Cherian, Jacob , Kim, Louis J. , Starke, Robert M., Kan, Peter , Dehdashti, Amir R. , Abla, Adib A. , Lawton, Michael T. , Burkhardt, Jan‐Karl , Abla, Adib , Burkhardt, Jan‐Karl , Tonetti, Daniel A. , Taussky, Philipp , Catapano, Joshua S , Grandhi, Ramesh , Mascitelli, Justin R , Gompel, Jamie J. Van , Couldwell, William T. , Kim, Louis J. , Cohen‐Gadol, Aaron

Neurosurgery | December 15, 2022 | Volume: 92 | Issue: 1 | Pages: 205-212

10.1227/neu.0000000000002196 Get It

BACKGROUND: Dural arteriovenous fistulas (dAVFs) located at craniocervical junction are extremely rare (1%-2% of intracranial/spinal dAVFs). Their angio-architectural complexity renders endovascular embolization to be challenging given multiple small feeders with risk of embolysate reflux into vertebral artery and limited transvenous access. The available literature discussing microsurgery for these lesions is limited to few case reports. OBJECTIVE: To report a multicenter experience assessing microsurgery safety/efficacy. METHODS: Prospectively maintained registries at 13 North American centers were queried to identify craniocervical junction dAVFs treated with microsurgery (2006-2021). RESULTS: Thirty-eight patients (median age 59.5 years, 44.7% female patients) were included. The most common presentation was subarachnoid/intracranial hemorrhage (47.4%) and myelopathy (36.8%) (92.1% of lesions Cognard type III-V). Direct meningeal branches from V3/4 vertebral artery segments supplied 84.2% of lesions. All lesions failed (n = 5, 13.2%) or were deemed inaccessible/unsafe to endovascular treatment. Far lateral craniotomy was the most used approach (94.7%). Intraoperative angiogram was performed in 39.5% of the cases, with angiographic cure in 94.7% of cases (median imaging follow-up of 9.2 months) and retreatment rate of 5.3%. Favorable last follow-up modified Rankin Scale of 0 to 2 was recorded in 81.6% of the patients with procedural complications of 2.6%. CONCLUSION: Craniocervical dAVFs represent rare entity of lesions presenting most commonly with hemorrhage or myelopathy because of venous congestion. Microsurgery using a far lateral approach provides robust exposure and visualization for these lesions and allows obliteration of the arterialized draining vein intradurally as close as possible to the fistula point. This approach was associated with a high rate of angiographic cure and favorable clinical outcomes.