TY - JOUR
T1 - Consortium for Dural Arteriovenous Fistula Outcomes Research (CONDOR)
T2 - rationale, design, and initial characterization of patient cohort
AU - the Consortium for Dural Arteriovenous Fistula Outcomes Research
AU - Guniganti, Ridhima
AU - Giordan, Enrico
AU - Chen, Ching Jen
AU - Abecassis, Isaac Josh
AU - Levitt, Michael R.
AU - Durnford, Andrew
AU - Smith, Jessica
AU - Samaniego, Edgar A.
AU - Derdeyn, Colin P.
AU - Kwasnicki, Amanda
AU - Alaraj, Ali
AU - Potgieser, Adriaan R.E.
AU - Sur, Samir
AU - Chen, Stephanie H.
AU - Tada, Yoshiteru
AU - Winkler, Ethan
AU - Phelps, Ryan R.L.
AU - Lai, Pui Man Rosalind
AU - Du, Rose
AU - Abla, Adib
AU - Satomi, Junichiro
AU - Starke, Robert M.
AU - van Dijk, J. Marc
AU - Amin-Hanjani, Sepideh
AU - Hayakawa, Minako
AU - Gross, Bradley A.
AU - Fox, W. Christopher
AU - Bulters, Diederik
AU - Kim, Louis J.
AU - Sheehan, Jason
AU - Lanzino, Giuseppe
AU - Piccirillo, Jay F.
AU - Kansagra, Akash P.
AU - Zipfel, Gregory J.
AU - Raman, Hari
AU - Lipsey, Kim
AU - Brinjikji, Waleed
AU - Vine, Roanna
AU - Cloft, Harry J.
AU - Kallmes, David F.
AU - Pollock, Bruce E.
AU - Link, Michael J.
AU - Patibandla, Mohana Rao
AU - Ding, Dale
AU - Buell, Thomas
AU - Paisan, Gabriella
AU - Meyer, R. Michael
AU - Kelly, Cory
AU - Duffill, Jonathan
AU - Ditchfield, Adam
AU - Millar, John
AU - Macdonald, Jason
AU - Polifka, Adam J.
AU - Laurent, Dimitri
AU - Hoh, Brian
AU - Lockerman, Ashley
AU - Lunsford, L. Dade
AU - Jankowitz, Brian T.
AU - Gutierrez, Santiago Ortega
AU - Hasan, David
AU - Roa, Jorge A.
AU - Rossen, James
AU - Guerrero, Waldo
AU - McGruder, Allen
AU - Charbel, Fady T.
AU - Aletich, Victor A.
AU - Rose-Finnell, Linda
AU - Peterson, Eric C.
AU - Yavagal, Dileep R.
AU - Kanematsu, Yasuhisa
AU - Yamamoto, Nobuaki
AU - Kinouchi, Tomoya
AU - Korai, Masaaki
AU - Yamaguchi, Izumi
AU - Yamamoto, Yuki
AU - Lawton, Michael
AU - Rutkowski, Martin
AU - Aziz-Sultan, M. Ali
AU - Patel, Nirav
AU - Frerichs, Kai U.
N1 - Publisher Copyright:
© AANS 2022
PY - 2022/4
Y1 - 2022/4
N2 - OBJECTIVE Cranial dural arteriovenous fistulas (dAVFs) are rare lesions, hampering efforts to understand them and improve their care. To address this challenge, investigators with an established record of dAVF investigation formed an international, multicenter consortium aimed at better elucidating dAVF pathophysiology, imaging characteristics, natural history, and patient outcomes. This report describes the design of the Consortium for Dural Arteriovenous Fistula Outcomes Research (CONDOR) and includes characterization of the 1077-patient cohort. METHODS Potential collaborators with established interest in the field were identified via systematic review of the literature. To ensure uniformity of data collection, a quality control process was instituted. Data were retrospectively obtained. RESULTS CONDOR comprises 14 centers in the United States, the United Kingdom, the Netherlands, and Japan that have pooled their data from 1077 dAVF patients seen between 1990 and 2017. The cohort includes 359 patients (33%) with Borden type I dAVFs, 175 (16%) with Borden type II fistulas, and 529 (49%) with Borden type III fistulas. Overall, 852 patients (79%) presented with fistula-related symptoms: 427 (40%) presented with nonaggressive symptoms such as tinnitus or orbital phenomena, 258 (24%) presented with intracranial hemorrhage, and 167 (16%) presented with nonhemorrhagic neurological deficits. A smaller proportion (224 patients, 21%), whose dAVFs were discovered incidentally, were dataasymptomatic. Many patients (85%, 911/1077) underwent treatment via endovascular embolization (55%, 587/1077), surgery (10%, 103/1077), radiosurgery (3%, 36/1077), or multimodal therapy (17%, 184/1077). The overall angiographic cure rate was 83% (758/911 treated), and treatment-related permanent neurological morbidity was 2% (27/1467 total procedures). The median time from diagnosis to follow-up was 380 days (IQR 120-1038.5 days). CONCLUSIONS With more than 1000 patients, the CONDOR registry represents the largest registry of cranial dAVF patient data in the world. These unique, well-annotated data will enable multiple future analyses to be performed to better understand dAVFs and their management.
AB - OBJECTIVE Cranial dural arteriovenous fistulas (dAVFs) are rare lesions, hampering efforts to understand them and improve their care. To address this challenge, investigators with an established record of dAVF investigation formed an international, multicenter consortium aimed at better elucidating dAVF pathophysiology, imaging characteristics, natural history, and patient outcomes. This report describes the design of the Consortium for Dural Arteriovenous Fistula Outcomes Research (CONDOR) and includes characterization of the 1077-patient cohort. METHODS Potential collaborators with established interest in the field were identified via systematic review of the literature. To ensure uniformity of data collection, a quality control process was instituted. Data were retrospectively obtained. RESULTS CONDOR comprises 14 centers in the United States, the United Kingdom, the Netherlands, and Japan that have pooled their data from 1077 dAVF patients seen between 1990 and 2017. The cohort includes 359 patients (33%) with Borden type I dAVFs, 175 (16%) with Borden type II fistulas, and 529 (49%) with Borden type III fistulas. Overall, 852 patients (79%) presented with fistula-related symptoms: 427 (40%) presented with nonaggressive symptoms such as tinnitus or orbital phenomena, 258 (24%) presented with intracranial hemorrhage, and 167 (16%) presented with nonhemorrhagic neurological deficits. A smaller proportion (224 patients, 21%), whose dAVFs were discovered incidentally, were dataasymptomatic. Many patients (85%, 911/1077) underwent treatment via endovascular embolization (55%, 587/1077), surgery (10%, 103/1077), radiosurgery (3%, 36/1077), or multimodal therapy (17%, 184/1077). The overall angiographic cure rate was 83% (758/911 treated), and treatment-related permanent neurological morbidity was 2% (27/1467 total procedures). The median time from diagnosis to follow-up was 380 days (IQR 120-1038.5 days). CONCLUSIONS With more than 1000 patients, the CONDOR registry represents the largest registry of cranial dAVF patient data in the world. These unique, well-annotated data will enable multiple future analyses to be performed to better understand dAVFs and their management.
KW - consortium
KW - dural arteriovenous fistula
KW - natural history
KW - treatment
KW - vascular disorders
UR - http://www.scopus.com/inward/record.url?scp=85128161285&partnerID=8YFLogxK
U2 - 10.3171/2021.1.JNS202790
DO - 10.3171/2021.1.JNS202790
M3 - Article
C2 - 34507282
AN - SCOPUS:85128161285
SN - 0022-3085
VL - 136
SP - 951
EP - 961
JO - Journal of neurosurgery
JF - Journal of neurosurgery
IS - 4
ER -