Lanciego Carlos, Toledano Nicolás, De Miguel Silvia, Perea Miguel, Padilla Manuel, Rodriguez-Merlo Rufo, Dávila Julio, Ibarburen Cristina, Cano Cristóbal, García Isaac Ruíz, García Lorenzo García
Vascular Interventional Radiology Unit, Hospital Virgen de la Salud, Toledo, Spain.
J Vasc Interv Radiol. 2003 Nov;14(11):1417-25. doi: 10.1097/01.rvi.0000096763.74047.ef.
To evaluate in a prospective, multicenter setting the long-term effectiveness of polyurethane stents in the percutaneous management of epiphora.
Patients (n = 426; age range, 19-88 years, mean, 48; 91 men, 335 women) with severe epiphora had stents (470 eyes/496 stents) inserted to treat unilateral or bilateral and complete or partial obstruction of the nasolacrimal system. The etiology of the obstruction was idiopathic in 280 cases (59.5%) and chronic dacryocystitis in 190 (40.4%). The stent set designed by Song was used in all patients, and the original technique was slightly modified by us and conducted on an outpatient basis.
The initial technical success rate of stent placement was 95%. The average time of the procedure was 6 minutes (range, 3-70). Resolution of epiphora was complete in 452 eyes and partial in 18. On follow-up (mean, 24 months; range, 1 week to 67 months), 340 of 496 stents remained patent (68.5%). Segregating primary patency by year of follow-up, the rates were 75.6%, 68.4%, 64.8%, 60.1%, and 59.2% in the first, second, third, fourth, and the current (67 months) years, respectively. Minor complications such as moderate pain (21 cases), epistaxis (75 cases), palpebral edema and hematoma (31 cases), and headache (four cases) and two acute dacryocystitis events were recorded. Of the 156 obstructed stents, 114 were withdrawn, and 49 of these patients remained asymptomatic for a mean of 27 months (secondary patency, 31.4%). After stent removal, the sac configuration was unchanged in 93 (81.5%), contracted in 11 (9.6%), and widened in 10 (8.8%) cases.
The procedure is simple and safe, both in stent insertion and in withdrawal when occluded. The success rate was >75% in the short term and >55% in the long term. Although not totally without concerns, the technique is attractive for most patients who prefer not to undergo surgery or are unsuitable surgical candidates. Stent failure does not preclude subsequent treatment options and is an excellent first-line treatment of epiphora.
在一项前瞻性、多中心研究中评估聚氨酯支架在经皮治疗泪溢中的长期有效性。
426例(年龄范围19 - 88岁,平均48岁;男性91例,女性335例)严重泪溢患者接受支架植入(470只眼/496个支架),以治疗鼻泪系统的单侧或双侧、完全或部分阻塞。阻塞病因中,280例(59.5%)为特发性,190例(40.4%)为慢性泪囊炎。所有患者均使用宋氏设计的支架套装,我们对原技术稍作修改并在门诊进行操作。
支架置入的初始技术成功率为95%。手术平均时间为6分钟(范围3 - 70分钟)。452只眼泪溢完全缓解,18只眼部分缓解。随访(平均24个月;范围1周 - 67个月)时,496个支架中有340个保持通畅(68.5%)。按随访年份划分初次通畅率,第1、2、3、4年及当前(67个月)的通畅率分别为75.6%、68.4%、64.8%、60.1%和59.2%。记录到一些轻微并发症,如中度疼痛(21例)、鼻出血(75例)、睑水肿和血肿(31例)、头痛(4例)以及2例急性泪囊炎事件。在156个阻塞的支架中,114个被取出,其中49例患者在取出后平均27个月无症状(二次通畅率31.4%)。取出支架后,93例(81.5%)泪囊形态无变化,11例(9.6%)缩小,10例(8.8%)扩大。
该手术无论是支架置入还是阻塞时取出都简单且安全。短期成功率>75%,长期成功率>55%。尽管并非毫无问题,但该技术对大多数不愿接受手术或不适合手术的患者具有吸引力。支架失败并不排除后续治疗选择,是泪溢的一种优秀一线治疗方法。