Artigo Acesso aberto Revisado por pares

Arteriopathy Diagnosis in Childhood Arterial Ischemic Stroke

2014; Lippincott Williams & Wilkins; Volume: 45; Issue: 12 Linguagem: Inglês

10.1161/strokeaha.114.007404

ISSN

1524-4628

Autores

Max Wintermark, Nancy K. Hills, Gabrielle deVeber, A. James Barkovich, Mitchell S.V. Elkind, Katherine Sear, Guangming Zhu, Carlos Leiva‐Salinas, Qinghua Hou, Michael M. Dowling, Timothy J. Bernard, Neil Friedman, Rebecca Ichord, Heather J. Fullerton, Susan Benedict, Christine K. Fox, Warren Lo, Marilyn A. Tan, Mark T. Mackay, Adam Kirton, Marta Hernández, Peter Humphreys, Lori C. Jordan, Sally Sultan, Michael J. Rivkin, Mubeen F. Rafay, Luigi Titomanlio, Gordana Kovačević, Jerome Y. Yager, Catherine Amlie‐Lefond, Nomazulu Dlamini, John Condie, E. Ann Yeh, Rachel Kneen, Bruce Björnson, Paola Pergami, Li Zou, Jorina Elbers, Abdalla Abdalla, Anthony K.C. Chan, Osman Farooq, Mingming J. Lim, Jessica L. Carpenter, Steven G. Pavlakis, Virginia Wong, Rob Forsyth,

Tópico(s)

Renal and Vascular Pathologies

Resumo

Background and Purpose— Although arteriopathies are the most common cause of childhood arterial ischemic stroke, and the strongest predictor of recurrent stroke, they are difficult to diagnose. We studied the role of clinical data and follow-up imaging in diagnosing cerebral and cervical arteriopathy in children with arterial ischemic stroke. Methods— Vascular effects of infection in pediatric stroke, an international prospective study, enrolled 355 cases of arterial ischemic stroke (age, 29 days to 18 years) at 39 centers. A neuroradiologist and stroke neurologist independently reviewed vascular imaging of the brain (mandatory for inclusion) and neck to establish a diagnosis of arteriopathy (definite, possible, or absent) in 3 steps: (1) baseline imaging alone; (2) plus clinical data; (3) plus follow-up imaging. A 4-person committee, including a second neuroradiologist and stroke neurologist, adjudicated disagreements. Using the final diagnosis as the gold standard, we calculated the sensitivity and specificity of each step. Results— Cases were aged median 7.6 years (interquartile range, 2.8–14 years); 56% boys. The majority (52%) was previously healthy; 41% had follow-up vascular imaging. Only 56 (16%) required adjudication. The gold standard diagnosis was definite arteriopathy in 127 (36%), possible in 34 (9.6%), and absent in 194 (55%). Sensitivity was 79% at step 1, 90% at step 2, and 94% at step 3; specificity was high throughout (99%, 100%, and 100%), as was agreement between reviewers (κ=0.77, 0.81, and 0.78). Conclusions— Clinical data and follow-up imaging help, yet uncertainty in the diagnosis of childhood arteriopathy remains. This presents a challenge to better understanding the mechanisms underlying these arteriopathies and designing strategies for prevention of childhood arterial ischemic stroke.

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