Goss Selena G, Alcantara Sean D, Todd George J, Lantis John C
Dept of Vascular Surgery, St. Luke's-Roosevelt Hospital Center, 1090 Amsterdam Avenue, Suite 7A, New York, NY 10025 USA.
J Invasive Cardiol. 2015 Sep;27(9):423-8.
The preponderance of existing literature for the treatment of Paget-Schroetter syndrome (PSS) advocates clot lysis followed by thoracic outlet decompression (TOD). We postulate that long-term anticoagulation has equal outcomes to more invasive and costly surgical intervention, and review our experience with non-operative management of PSS.
A retrospective review was conducted, examining patients between 1994-2014. Forty patients were identified with PSS, and 27 of these patients had sufficient follow-up for this analysis. Charts were reviewed for details of clinical presentation, disease course, interventions, duration of oral anticoagulation, ultrasound reports, and symptoms at long-term follow-up.
With a mean follow-up of 54.3 months, 23/27 patients (85%) were asymptomatic after non-operative therapy. In this cohort, 16/27 patients (59%) underwent catheter-directed thrombolysis. Average treatment course with oral anticoagulation was 8.6 months. Four patients (15%) remained symptomatic at follow-up. Two patients (7%) underwent thoracic outlet decompression at another institution, with good results. At least partial recanalization of vessels was documented in 25/27 patients (93%), although recanalization did not correlate with symptoms at long-term follow-up.
Based upon equivalent functional results, non-operative management appears to offer similar outcomes for some patients with PSS. We propose a patient-tailored approach to the treatment of PSS, in which patients presenting acutely undergo catheter-directed thrombolysis, followed by a 6-12 month course of oral anticoagulation. Persistent symptoms, recurrent disease, lengthy duration of symptoms prior to diagnosis, and identifiable structural abnormalities may be factors predictive of poor outcomes after non-operative intervention.
现有关于佩吉特 - 施罗特综合征(PSS)治疗的文献大多主张先进行血栓溶解,然后行胸廓出口减压术(TOD)。我们推测长期抗凝治疗与更具侵入性且费用更高的手术干预效果相当,并回顾我们对PSS非手术治疗的经验。
进行了一项回顾性研究,研究对象为1994年至2014年间的患者。确定了40例PSS患者,其中27例患者有足够的随访时间用于此次分析。查阅病历以获取临床表现、疾病进程、干预措施、口服抗凝治疗持续时间、超声报告以及长期随访时的症状等详细信息。
平均随访54.3个月,27例患者中有23例(85%)在非手术治疗后无症状。在该队列中,27例患者中有16例(59%)接受了导管定向溶栓治疗。口服抗凝治疗的平均疗程为8.6个月。4例患者(15%)在随访时仍有症状。2例患者(7%)在另一机构接受了胸廓出口减压术,效果良好。27例患者中有25例(93%)记录到血管至少部分再通,尽管再通与长期随访时的症状无关。
基于同等的功能结果,非手术治疗似乎为一些PSS患者提供了相似的疗效。我们提出一种针对PSS的个体化治疗方法,即急性发病的患者先接受导管定向溶栓治疗,随后进行6至12个月的口服抗凝治疗。持续症状、疾病复发、诊断前症状持续时间长以及可识别的结构异常可能是预测非手术干预后预后不良的因素。