Flow-Diverter Devices for Intracranial Aneurysms: Systematic Review and Meta-analysis

被引:140
|
作者
Arrese, Ignacio [1 ]
Sarabia, Rosario [1 ]
Pintado, Rebeca [1 ]
Delgado-Rodriguez, Miguel [2 ]
机构
[1] Hosp Univ Rio Hortega, Unit Vasc Neurosurg, Valladolid, Spain
[2] Univ Jaen, Dept Prevent Med, Jaen, Spain
关键词
Aneurysms; Brain; Endovascular procedures; Flow diverter; Stents; PIPELINE EMBOLIZATION DEVICE; ENDOVASCULAR TREATMENT; NATURAL-HISTORY; PARENT ARTERY; FOLLOW-UP; EXPERIENCE; STENT; TRIAL; RECONSTRUCTION; MANAGEMENT;
D O I
10.1227/01.neu.0000430297.17961.f1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND: Although the introduction of flow-diverter devices (FDDs) has aroused great enthusiasm, the level of evidence supporting their use has not been systematically evaluated. OBJECTIVE: To report a systematic review of medical literature up to May 2012 on FDDs to assess the morbidity, case fatality rate, and efficacy of FDDs for intracranial aneurysms. METHODS: The literature was searched by using MEDLINE, Embase, and all Evidence-Based Medicine in the OVID database. Eligibility criteria were studies including at least 10 patients, reporting duration of follow-up and number of patients lost to follow-up, and documenting the rate of aneurysm occlusion and death and neurological complications. The endpoints were angiographic success, early and late mortality, and neurological morbidity. RESULTS: Fifteen studies were analyzed consisting of 897 patients with 1018 aneurysms. The mean value of methodological quality score was 14.4 using the STROBE score. The early mortality rate was 2.8% (95% confidence interval [CI]: 1.7-3.8; I-2 = 93.4%) and the late mortality rate was 1.3% (95% CI: 0.2-2.3; I-2 = 36.9%). The early neurological morbidity rate was 7.3% (95% CI: 5.7-9; I-2 = 91.8%) and the late morbidity rate was 2.6% (95% CI: 1.1-4; I-2 = 81.3%). The Egger test for early and late morbidity and aneurysm occlusion was <0.001. CONCLUSION: With the available data from the studies, both heterogeneity and publication biases imply that the current clinical use of FDDs is not supported by high-quality evidence. In the absence of reliable evidence, the use of FDDs in patients eligible for more conventional treatments should be restricted to controlled clinical trials.
引用
收藏
页码:193 / 199
页数:7
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