长期抗栓治疗对下肢近端深静脉血栓形成患者血栓后综合征发展的影响

A. Petrikov, D. Dudin, S. Zaitsev, V. Eirikh, V. Belykh, Y. Shoikhet
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引用次数: 2

摘要

本文致力于血栓后综合征(PTS)的发生率和严重程度,在长期抗血栓华法林和舒洛地特(SD)治疗(ATT)的背景下,既往近侧深静脉血栓形成(DVT)患者PTS发展的优势比(OR),并适当考虑到本年度临床显著出血(CSB)的安全性和发展。共有130例18至69岁的急性近端DVT患者被纳入比较前瞻性研究。第一组包括64名患者(31名男性和33名女性),接受维生素K拮抗剂(华法林)治疗。II组包括66名患者(37名男性和29名女性),他们在完成一个疗程的标准ACT(急性期过渡到AVK的肝素)后3个月内接受舒洛地特治疗。研究参数包括OR、患者的PTS发生率和严重程度(按Villalta评分)、华法林和舒洛地特持续ATT背景下12个月PTS发生率。研究证实,与华法林标准治疗相比,近端DVT患者在完成一个标准ACT疗程后一年内延长舒洛地特ATT治疗可使PTS临床症状的发生减少22.2%。同时,在接受舒洛地特治疗的患者中,发生近端静脉血栓形成的严重形式PTS发生率较低,为17.8%。因此,延长舒洛地特ATT与PTS及其严重形式的发展风险降低1.7倍相关。因此,对于近端深静脉血栓形成的患者,长期使用舒洛地特一年,可作为华法林的替代方案,并与较低的PTS发生率相关,包括其严重形式。长时间的舒洛地特ATT是安全的,在这一年中不会引起临床显著的出血并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The influence of prolonged antithrombotic therapy on the development of post-thrombotic syndrome in patients with proximal deep vein thrombosis of the lower limbs
The article is devoted to the incidence and severity of post-thrombotic syndrome (PTS), the odds ratio (OR) of PTS development in patients with previous proximal deep vein thrombosis (DVT) against the background of prolonged antithrombotic warfarin and sulodexide (SD) therapy (ATT) with due account for safety and development of clinically significant bleeding (CSB) during the year. A total of 130 patients aged 18 to 69 years with acute proximal DVT were enrolled in the comparative prospective study. Group I included 64 patients (31 men and 33 women), who received vitamin K antagonists (warfarin) therapy. Group II included 66 patients (37 men and 29 women), who received sulodexide in 3 months after completing a course of standard ACT (heparins in the acute period with the transition to AVK). The studied parameters included OR, incidence and severity of PTS in patients according to the Villalta scale, and the incidence rate of PTS against the background of prolonged warfarin and sulodexide ATT in 12 months’ time. It was established that the prolonged sulodexide ATT within one year after completing a course of standard ACT in patients with proximal DVT reduced the development of clinical signs of PTS by 22.2% compared to the standard warfarin therapy. At the same time, there is a lower incidence of severe forms of PTS in patients, who underwent proximal venous thrombosis, 17.8% against the background of sulodexide treatment. Thus, the prolonged sulodexide ATT is associated with a 1.7-fold decrease in the risk of the development of both PTS and its severe forms. Therefore, the prolonged use of sulodexide for one year in patients, who underwent proximal DVT, provides an alternative to warfarin and is associated with a lower incidence of PTS, including its severe forms. The prolonged sulodexide ATT is safe and does not cause the development of clinically significant hemorrhagic complications during the year.
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