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Maintenance of perioperative antiplatelet and anticoagulant therapy for vitreoretinal surgery

机译:玻璃体视网膜手术围术期抗血小板和抗凝治疗的维持

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Background The objective of this study was to prospectively assess the risk of bleeding from vitreoretinal surgery in a continuous unbiased cohort of patients taking unsuspended antiplatelet or anticoagulant therapy. Design Prospective hospital-based study. Participants Eighty-five patients taking unsuspended aspirin, clopidogrel and/or warfarin therapy undergoing all forms of vitreoretinal surgery at The Mater Misericordiae University and The Mater Private Hospital, Dublin, Ireland. Methods Consecutive patients undergoing vitreoretinal surgery taking unsuspended antiplatelet or anticoagulant therapy over a 1-year period were included in this prospective study to evaluate the intraoperative and postoperative bleeding complications. Main Outcome Measures The intraoperative and postoperative bleeding rates. Results One hundred and seven vitreoretinal procedures were performed on 85 patients taking unsuspended antiplatelet or anticoagulant therapy. The intraoperative bleeding rate was 23%, the majority of which consisted of mild bleeding into the vitreous cavity during vitrectomy. The postoperative bleeding rate was 22%, consisting of 3.7% anterior chamber haemorrhage, 11% dispersed vitreous cavity haemorrhage, 4.7% dense vitreous cavity haemorrhage, 0.9% subretinal haemorrhage and 1.9% localized choroidal haemorrhage. The single greatest significant independent predictor of intraoperative bleeding was proliferative diabetic retinopathy and of postoperative bleeding was the presence of diabetes mellitus. Conclusions There were no cases of uncontrolled intraoperative haemorrhage or serious postoperative choroidal haemorrhage. Mild haemorrhagic oozing during vitrectomy and dispersed vitreous cavity haemorrhage postoperatively were common. For the majority of patients taking antiplatelet or anticoagulant medication, these agents can be safely continued in the vitreoretinal surgical perioperative period.
机译:背景技术这项研究的目的是前瞻性评估连续连续无偏倚接受抗血小板或抗凝治疗的患者在玻璃体视网膜手术中出血的风险。设计基于医院的前瞻性研究。参加研究的八十五名接受非悬浮阿司匹林,氯吡格雷和/或华法林治疗的患者在爱尔兰的都柏林的Mater Misericordiae大学和Mater私立医院接受了各种形式的玻璃体视网膜手术。方法该前瞻性研究纳入了连续1年接受玻璃体视网膜手术的患者,接受无悬浮抗血小板或抗凝治疗,以评估术中和术后出血并发症。主要观察指标术中及术后出血率。结果对85例接受非悬浮抗血小板或抗凝治疗的患者进行了107次玻璃体视网膜手术。术中出血率为23%,其中大部分是在玻璃体切割术中玻璃体腔内轻微出血。术后出血率为22%,包括3.7%的前房出血,11%的分散性玻璃体腔出血,4.7%的致密性玻璃体腔出血,0.9%的视网膜下出血和1.9%的局部脉络膜出血。术中出血的最大的独立预测因素是增生性糖尿病视网膜病变,术后出血是糖尿病的存在。结论没有发生术中失控或严重的术后脉络膜出血的病例。玻璃体切除术中轻度的渗血和术后玻璃体腔出血的扩散是常见的。对于大多数服用抗血小板药或抗凝药的患者,在玻璃体视网膜手术围手术期可以安全地继续使用这些药物。

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