使用树脂微球进行钇-90放射性栓塞且不常规栓塞胃十二指肠动脉
Yttrium-90 Radioembolization with Resin Microspheres without Routine Embolization of the Gastroduodenal Artery.
作者信息
Ward Thomas J, Louie John D, Sze Daniel Y
机构信息
Division of Interventional Radiology, H-3646 Stanford University Medical Center, 300 Pasteur Drive, Stanford, CA 94305-5642.
Division of Interventional Radiology, H-3646 Stanford University Medical Center, 300 Pasteur Drive, Stanford, CA 94305-5642.
出版信息
J Vasc Interv Radiol. 2017 Feb;28(2):246-253. doi: 10.1016/j.jvir.2016.09.002. Epub 2016 Nov 22.
PURPOSE
To evaluate safety of resin microsphere radioembolization (RE) without prophylactic embolization of the gastroduodenal artery (GDA).
MATERIALS AND METHODS
Between July 2013 and April 2015, all patients undergoing RE with resin microspheres for liver-dominant metastatic disease were treated without routine embolization of the GDA. Selective embolization of distal hepaticoenteric vessels was performed if identified by digital subtraction angiography, cone-beam computed tomography, or technetium-99m macroaggregated albumin scintigraphy. Resin microspheres were administered using 5% dextrose flush distal to the origin of the GDA in lobar or segmental fashion, with judicious use of an antireflux microcatheter in recognized high-risk situations. Gastrointestinal toxicity was evaluated by the performing physician for at least 3 months.
RESULTS
RE with resin microspheres was performed in 62 patients undergoing 69 treatments. During planning angiography, embolization of 0 or 1 vessel (median, 1; range, 0-4) was performed in 86% of patients, most commonly the right gastric and supraduodenal arteries. Prophylactic embolization of the GDA was performed in only 2 patients (3%). In 6 treatments (9%), adjunctive embolization was required immediately before RE, and an antireflux microcatheter was used in 14% of treatments. Clinical follow-up was available in 60 of 62 patients (median, 134 d; range, 15-582 d). No signs or symptoms of gastric or duodenal ulceration were observed.
CONCLUSIONS
RE using resin microspheres without embolization of the GDA can be performed safely.
目的
评估不预防性栓塞胃十二指肠动脉(GDA)的树脂微球放射性栓塞(RE)的安全性。
材料与方法
2013年7月至2015年4月期间,所有因肝转移为主的疾病接受树脂微球RE治疗的患者均未常规栓塞GDA。如果通过数字减影血管造影、锥形束计算机断层扫描或锝-99m大颗粒白蛋白闪烁显像发现肝肠远端血管,则进行选择性栓塞。树脂微球通过在GDA起源远端使用5%葡萄糖冲洗以叶或段的方式给药,在公认的高风险情况下谨慎使用抗反流微导管。由执行医师评估至少3个月的胃肠道毒性。
结果
62例患者接受了69次树脂微球RE治疗。在计划血管造影期间,86%的患者栓塞了0或1支血管(中位数为1;范围为0 - 4),最常见的是胃右动脉和十二指肠上动脉。仅2例患者(3%)进行了GDA的预防性栓塞。在6次治疗(9%)中,RE前立即需要辅助栓塞,14%的治疗中使用了抗反流微导管。62例患者中有60例有临床随访(中位数为134天;范围为15 - 582天)。未观察到胃或十二指肠溃疡的体征或症状。
结论
不栓塞GDA使用树脂微球进行RE可以安全实施。