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Stereotactic Radiosurgery for Cavernous Sinus Versus Noncavernous Sinus Dural Arteriovenous Fistulas: Outcomes and Outcome Predictors
YC. Hung, N. Mohammed, KN. Kearns, CJ. Chen, RM. Starke, H. Kano, J. Lee, D. Mathieu, AM. Kaufmann, WG. Wang, IS. Grills, CP. Cifarelli, J. Vargo, T. Chytka, L. Janouskova, CE. Feliciano, R. Rodriguez-Mercado, LD. Lunsford, JP. Sheehan,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
Grantová podpora
U54 GM104942
NIGMS NIH HHS - United States
Health & Medicine (ProQuest) od 2010-01-01 do Před 1 rokem
Odkazy
PubMed
31384943
DOI
10.1093/neuros/nyz260
Knihovny.cz E-zdroje
- MeSH
- cévní malformace centrálního nervového systému patologie radioterapie MeSH
- dospělí MeSH
- kohortové studie MeSH
- lidé středního věku MeSH
- lidé MeSH
- prognóza MeSH
- radiochirurgie metody MeSH
- retrospektivní studie MeSH
- senioři MeSH
- sinus cavernosus patologie MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
BACKGROUND: Dural arteriovenous fistulas (DAVFs) can be categorized based on location. OBJECTIVE: To compare stereotactic radiosurgery (SRS) outcomes between cavernous sinus (CS) and non-CS DAVFs and to identify respective outcome predictors. METHODS: This is a retrospective study of DAVFs treated with SRS between 1988 and 2016 at 10 institutions. Patients' variables, DAVF characters, and SRS parameters were included for analyses. Favorable clinical outcome was defined as angiography-confirmed obliteration without radiological radiation-induced changes (RIC) or post-SRS hemorrhage. Other outcomes were DAVFs obliteration and adverse events (including RIC, symptomatic RIC, and post-SRS hemorrhage). RESULTS: The overall study cohort comprised 131 patients, including 20 patients with CS DAVFs (15%) and 111 patients with non-CS DAVFs (85%). Rates of favorable clinical outcome were comparable between the 2 groups (45% vs 37%, P = .824). Obliteration rate after SRS was higher in the CS DAVFs group, even adjusted for baseline difference (OR = 4.189, P = .044). Predictors of favorable clinical outcome included higher maximum dose (P = .014) for CS DAVFs. Symptomatic improvement was associated with obliteration in non-CS DAVFs (P = .005), but symptoms improved regardless of whether obliteration was confirmed in CS DAVFs. Non-CS DAVFs patients with adverse events after SRS were more likely to be male (P = .020), multiple arterial feeding fistulas (P = .018), and lower maximum dose (P = .041). CONCLUSION: After SRS, CS DAVFs are more likely to obliterate than non-CS ones. Because these 2 groups have different total predictors for clinical and radiologic outcomes after SRS, they should be considered as different entities.
Department of Neurological Surgery Na Homolce Hospital Prague Czech Republic
Department of Neurological Surgery University of Manitoba Winnipeg Canada
Department of Neurological Surgery University of Miami Miami Florida
Department of Neurological Surgery University of Pennsylvania Philadelphia Pennsylvania
Department of Neurological Surgery University of Pittsburgh Pittsburgh Pennsylvania
Department of Neurological Surgery University of Puerto Rico San Juan Puerto Rico
Department of Neurological Surgery University of Virginia Charlottesville Virginia
Department of Neurological Surgery West Virginia University Morgantown West Virginia
Department of Radiation Oncology Beaumont Health System Royal Oak Michigan
Department of Radiation Oncology West Virginia University Morgantown West Virginia
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- $a Hung, Yi-Chieh $u Division of Neurosurgery, Department of Surgery, Chi-Mei Medical Center, Tainan, Taiwan. Department of Recreation and Healthcare Management, Chia Nan University of Pharmacy and Science, Tainan, Taiwan. Department of Neurological Surgery, University of Virginia, Charlottesville, Virginia.
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- $a Stereotactic Radiosurgery for Cavernous Sinus Versus Noncavernous Sinus Dural Arteriovenous Fistulas: Outcomes and Outcome Predictors / $c YC. Hung, N. Mohammed, KN. Kearns, CJ. Chen, RM. Starke, H. Kano, J. Lee, D. Mathieu, AM. Kaufmann, WG. Wang, IS. Grills, CP. Cifarelli, J. Vargo, T. Chytka, L. Janouskova, CE. Feliciano, R. Rodriguez-Mercado, LD. Lunsford, JP. Sheehan,
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- $a BACKGROUND: Dural arteriovenous fistulas (DAVFs) can be categorized based on location. OBJECTIVE: To compare stereotactic radiosurgery (SRS) outcomes between cavernous sinus (CS) and non-CS DAVFs and to identify respective outcome predictors. METHODS: This is a retrospective study of DAVFs treated with SRS between 1988 and 2016 at 10 institutions. Patients' variables, DAVF characters, and SRS parameters were included for analyses. Favorable clinical outcome was defined as angiography-confirmed obliteration without radiological radiation-induced changes (RIC) or post-SRS hemorrhage. Other outcomes were DAVFs obliteration and adverse events (including RIC, symptomatic RIC, and post-SRS hemorrhage). RESULTS: The overall study cohort comprised 131 patients, including 20 patients with CS DAVFs (15%) and 111 patients with non-CS DAVFs (85%). Rates of favorable clinical outcome were comparable between the 2 groups (45% vs 37%, P = .824). Obliteration rate after SRS was higher in the CS DAVFs group, even adjusted for baseline difference (OR = 4.189, P = .044). Predictors of favorable clinical outcome included higher maximum dose (P = .014) for CS DAVFs. Symptomatic improvement was associated with obliteration in non-CS DAVFs (P = .005), but symptoms improved regardless of whether obliteration was confirmed in CS DAVFs. Non-CS DAVFs patients with adverse events after SRS were more likely to be male (P = .020), multiple arterial feeding fistulas (P = .018), and lower maximum dose (P = .041). CONCLUSION: After SRS, CS DAVFs are more likely to obliterate than non-CS ones. Because these 2 groups have different total predictors for clinical and radiologic outcomes after SRS, they should be considered as different entities.
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- $a Mohammed, Nasser $u Department of Neurological Surgery, University of Virginia, Charlottesville, Virginia.
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