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一项关于腔静脉滤器预防近端深静脉血栓形成患者肺栓塞的临床试验。腔静脉阻断预防肺栓塞风险研究组。

A clinical trial of vena caval filters in the prevention of pulmonary embolism in patients with proximal deep-vein thrombosis. Prévention du Risque d'Embolie Pulmonaire par Interruption Cave Study Group.

作者信息

Decousus H, Leizorovicz A, Parent F, Page Y, Tardy B, Girard P, Laporte S, Faivre R, Charbonnier B, Barral F G, Huet Y, Simonneau G

机构信息

Clinical Pharmacology Unit, Bellevue Hospital, Saint-Etienne, France.

出版信息

N Engl J Med. 1998 Feb 12;338(7):409-15. doi: 10.1056/NEJM199802123380701.

Abstract

BACKGROUND

The efficacy and safety of vena caval filters in the prevention of pulmonary embolism in patients with proximal deep-vein thrombosis is still a matter of debate.

METHODS

Using a two-by-two factorial design, we randomly assigned 400 patients with proximal deep-vein thrombosis who were at risk for pulmonary embolism to receive a vena caval filter (200 patients) or no filter (200 patients), and to receive low-molecular-weight heparin (enoxaparin, 195 patients) or unfractionated heparin (205 patients). The rates of recurrent venous thromboembolism, death, and major bleeding were analyzed at day 12 and at two years.

RESULTS

At day 12, two patients assigned to receive filters (1.1 percent), as compared with nine patients assigned to receive no filters (4.8 percent), had had symptomatic or asymptomatic pulmonary embolism (odds ratio, 0.22; 95 percent confidence interval, 0.05 to 0.90). At two years, 37 patients assigned to the filter group (20.8 percent), as compared with 21 patients assigned to the no-filter group (11.6 percent), had had recurrent deep-vein thrombosis (odds ratio, 1.87; 95 percent confidence interval, 1.10 to 3.20). There were no significant differences in mortality or the other outcomes. At day 12, three patients assigned to low-molecular-weight heparin (1.6 percent), as compared with eight patients assigned to unfractionated heparin (4.2 percent), had had symptomatic or asymptomatic pulmonary embolism (odds ratio, 0.38; 95 percent confidence interval, 0.10 to 1.38).

CONCLUSIONS

In high-risk patients with proximal deep-vein thrombosis, the initial beneficial effect of vena caval filters for the prevention of pulmonary embolism was counterbalanced by an excess of recurrent deep-vein thrombosis, without any difference in mortality. Our data also confirmed that low-molecular-weight heparin was as effective and safe as unfractionated heparin for the prevention of pulmonary embolism.

摘要

背景

下腔静脉滤器在预防近端深静脉血栓形成患者发生肺栓塞方面的疗效和安全性仍存在争议。

方法

采用二乘二析因设计,我们将400例有发生肺栓塞风险的近端深静脉血栓形成患者随机分为两组,一组接受下腔静脉滤器植入(200例患者),另一组不接受滤器植入(200例患者);同时将这些患者分为两组,一组接受低分子量肝素(依诺肝素,195例患者),另一组接受普通肝素(205例患者)。在第12天和两年时分析复发性静脉血栓栓塞、死亡和大出血的发生率。

结果

在第12天,接受滤器植入的2例患者(1.1%)发生了有症状或无症状的肺栓塞,而未接受滤器植入的9例患者(4.8%)发生了有症状或无症状的肺栓塞(优势比为0.22;95%置信区间为0.05至0.90)。在两年时,滤器植入组的37例患者(20.8%)发生了复发性深静脉血栓形成,而未接受滤器植入组的21例患者(11.6%)发生了复发性深静脉血栓形成(优势比为1.87;95%置信区间为1.10至3.20)。在死亡率和其他结局方面无显著差异。在第12天,接受低分子量肝素的3例患者(1.6%)发生了有症状或无症状的肺栓塞,而接受普通肝素的8例患者(4.2%)发生了有症状或无症状的肺栓塞(优势比为0.38;95%置信区间为0.10至1.38)。

结论

在高危近端深静脉血栓形成患者中,下腔静脉滤器预防肺栓塞的初始有益作用被复发性深静脉血栓形成的增加所抵消,死亡率无差异。我们的数据还证实,低分子量肝素在预防肺栓塞方面与普通肝素一样有效和安全。

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