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首页> 外文期刊>Retina >Incidence of hemorrhagic complications after intravitreal bevacizumab (avastin) or ranibizumab (lucentis) injections on systemically anticoagulated patients.
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Incidence of hemorrhagic complications after intravitreal bevacizumab (avastin) or ranibizumab (lucentis) injections on systemically anticoagulated patients.

机译:系统性抗凝患者玻璃体内注射贝伐单抗(avastin)或兰尼单抗(lucentis)注射后出血并发症的发生率。

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PURPOSE: To assess the risk of hemorrhagic complications when performing intravitreal injections on systemically anticoagulated patients. METHODS: A single-center retrospective case series of 520 consecutive patients (675 eyes) receiving 3,106 antivascular endothelial growth factor injections. Patients on the systemic anticoagulants Coumadin (warfarin sodium) or Plavix (clopidogrel bisulfate) were identified, as well as patients on aspirin. Demographic parameters were recorded, as well as relevant anticoagulant medications, preoperative/postoperative best-corrected visual acuities and intraocular pressures, previous ocular surgery, relative ocular diagnoses, and injection complications. RESULTS: Of all patients, 104 were on Coumadin (134 eyes; 548 injections), 90 were on Plavix (123 eyes; 523 injections), 7 were on both Coumadin and Plavix (8 eyes; 33 injections), and 319 were not anticoagulated (400 eyes; 2002 injections). Also, 1,254 injections were on patients taking aspirin. There were no hemorrhagic complications (choroidal hemorrhage, vitreous hemorrhage, or increased submacular hemorrhage) noted in the Plavix (P = 1.0000; 95% confidence interval = 0.0000-0.0088), Coumadin (P = 1.0000; 95% confidence interval = 0.0000-0.0084), or aspirin (P = 1.0000; 95% confidence interval = 0.0000-0.0037) groups. CONCLUSION: The risk of hemorrhagic complications in systemically anticoagulated patients receiving intravitreal injections is extremely low. Because of the demonstrated thromboembolic risk of stopping anticoagulant therapy, we recommend that patients continue their current regiment without cessation.
机译:目的:评估全身抗凝患者玻璃体内注射时出血并发症的风险。方法:520例(675眼)连续患者接受3106例抗血管内皮生长因子注射,进行了单中心回顾性病例研究。确定了全身抗凝剂香豆素(华法林钠)或Plavix(氯吡格雷硫酸氢盐)的患者以及阿司匹林的患者。记录人口统计学参数,以及相关的抗凝药物,术前/术后最佳矫正视力和眼压,既往的眼科手术,相对的眼科诊断和注射并发症。结果:所有患者中,104例接受香豆素(134眼; 548针),90例接受Plavix(123眼; 523针),7例香豆素和普拉维(8眼; 33针),319例未抗凝。 (400眼; 2002年注射)。此外,阿司匹林患者也接受了1,254次注射。 Plavix(P = 1.0000; 95%置信区间= 0.0000-0.0088),Coumadin(P = 1.0000; 95%置信区间= 0.0000-0.0084)中未发现出血并发症(脉络膜出血,玻璃体出血或黄斑下出血增加) )或阿司匹林(P = 1.0000; 95%置信区间= 0.0000-0.0037)组。结论:接受玻璃体内注射的全身抗凝患者出血并发症的风险极低。由于已证明有停止栓塞治疗的血栓栓塞风险,因此我们建议患者继续目前的治疗方案,不要停止治疗。

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