Hon Jennifer M L, Bhattacharya Jo J, Counsell Carl E, Papanastassiou Vakis, Ritchie Vaughn, Roberts Richard C, Sellar Robin J, Warlow Charles P, Al-Shahi Salman Rustam
Division of Clinical Neurosciences, Western General Hospital, University of Edinburgh, Edinburgh, UK.
Stroke. 2009 Jun;40(6):1980-5. doi: 10.1161/STROKEAHA.108.533034. Epub 2009 Apr 23.
Reported risks of hemorrhage from intracranial developmental venous anomalies (DVAs) vary, so we investigated this in a systematic review and population-based study.
We systematically reviewed the literature (Ovid Medline and Embase to November 7, 2007) and selected studies of >or=20 participants with >or=1 DVA(s) that described their clinical presentation and/or their clinical course over a specified follow-up period. We also identified every adult first diagnosed with a DVA in Scotland from 1999 to 2003 and followed them in a prospective, population-based study.
Of 2068 articles detected by the literature search, 15 met our inclusion criteria and described clinical presentation, 8 of which also described the clinical course of DVAs. In the 15 studies of 714 people first presenting with a DVA, 61% were incidental findings, the mode of presentation was unclear in 23%, 6% presented with nonhemorrhagic focal neurological deficit, 6% had caused symptomatic hemorrhage, 4% were associated with epileptic seizure, and <1% were associated with infarction. In studies of the clinical course of 422 people with a DVA, the hemorrhage rate after first presentation ranged from 0% to 1.28% per year. In the population-based study of 93 adults with DVAs, 98% were incidental, 1% presented with symptomatic hemorrhage, and 1% presented with an infarct, but there were no symptomatic hemorrhages or infarcts in 492 person-years of follow-up (0% per person-year; 95% CI, 0% to 0.7%).
Intracranial DVAs have a benign presentation and clinical course.
颅内发育性静脉异常(DVA)出血的报道风险不一,因此我们进行了一项系统评价和基于人群的研究来对此展开调查。
我们系统检索了文献(截至2007年11月7日的Ovid Medline和Embase),并选择了≥20名参与者且≥1个DVA的研究,这些研究描述了其临床表现和/或在特定随访期内的临床病程。我们还识别了1999年至2003年在苏格兰首次诊断为DVA的每一位成年人,并在一项前瞻性、基于人群的研究中对他们进行随访。
在文献检索中检测到的2068篇文章中,15篇符合我们的纳入标准并描述了临床表现,其中8篇还描述了DVA的临床病程。在对714例首次出现DVA的患者的15项研究中,61%为偶然发现,23%的表现方式不明确,6%表现为非出血性局灶性神经功能缺损,6%有症状性出血,4%与癫痫发作有关,<1%与梗死有关。在对422例患有DVA患者的临床病程研究中,首次出现症状后每年的出血率为0%至1.28%。在对93例患有DVA的成年人的基于人群的研究中,98%为偶然发现,1%表现为症状性出血,1%表现为梗死,但在492人年的随访中没有症状性出血或梗死(每人年0%;95%CI,0%至0.7%)。
颅内DVA具有良性的表现和临床病程。