A prospective long-term study of 220 patients with a retrievable vena cava filter for secondary prevention of venous thromboembolism

A prospective long-term study of 220 patients with a retrievable vena cava filter for secondary prevention of venous thromboembolism
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DOI:
10.1378/chest.06-0631
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发表时间:
2007-01-01
期刊:
影响因子:
9.6
通讯作者:
Barral, Fabrice Guy
Barral, Fabrice Guy
中科院分区:
医学1区
文献类型:
--
作者:
Mismetti, Patrick;Rivron-Guillot, Karine;Barral, Fabrice Guy

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背景资料:直接和长期的临床事件与可回收的过滤器(ALN过滤器; ALN植入物Chiralcicaux; Ghisonaccia,法国)的放置和取出仍然在很大程度上unknow.Methods:这是一项前瞻性队列研究,随访18个月。结果:1999年4月至2005年6月期间,在我院放射科有220例患者需要置入ALN滤器(平均年龄,70.8岁),随访中位持续时间为338.5天(范围,1至561天); 148例患者(67.3%)完成了18个月的随访。无患者无法接受随访。所有患者都有急性或既往静脉血栓栓塞。主要适应症为尽管进行了充分抗凝治疗但仍复发性静脉血栓栓塞(10.9%)、一过性出血事件(21.8%)、明确的抗凝治疗禁忌症(26.8%)或因大手术、重大创伤或侵入性操作而必须停止抗凝治疗(37.7%)。98.6%的患者成功插入滤器,11.8%的患者发生即刻并发症。滤器植入的中位持续时间为166天(第一至第三四分位数,34至478天)。同时,17.0%(217例患者中的37例)至少发生1起静脉血栓栓塞事件。在中位数为51天(范围,6至352天)后,25.3%的患者尝试回收滤器; 92.7%的患者首次尝试成功取出滤器。结论:滤器可以很容易地插入并在插入后一年内成功取出。其预防肺栓塞的安全性和有效性应在随机研究中进行适当评估。
Background: The immediate and long-term clinical events associated with the placement and removal of a retrievable filter (ALN filter; ALN Implants Chirurgicaux; Ghisonaccia, France) remain largely unknown.Methods: This was a prospective cohort study with an 18-month follow-up. All consecutive patients scheduled for placement of an ALN filter between April 1999 and June 2005 in the Radiology Department of our hospital were included.Results: During the study period, placement of an ALN filter was indicated in 220 patients (mean age, 70.8 years), who were followed up for a median duration of 338.5 days (range, 1 to 561 days); 148 patients (67.3%) completed the 18-month follow-up. No patients were unavailable for follow-up. All patients had an acute or past venous thromboembolism. Main indications were recurrent venous thromboembolism despite adequate anticoagulation therapy (10.9%), transient bleeding event (21.8 %), definitive contraindication for anticoagulant therapy (26.8 %), or obligation to stop anticoagulant therapy due to major surgery, major trauma, or invasive procedure (37.7%). Filter insertion was successful in 98.6% of patients and resulted in an immediate complication in 11.8%. The median duration of filter implantation was 166 days (first to third quartiles, 34 to 478 days). Meanwhile, 17.0% (37 of 217 patients) had at least one venous thromboembolic event. Filter retrieval was attempted in 25.3% of patients after a median of 51 days (range, 6 to 352 days); removal was successful at the first attempt in 92.7% of patients.Conclusions: The filter could be easily inserted and successfully removed up to I year after insertion. Its safety and efficacy in preventing pulmonary embolism should be properly assessed in a randomized study.