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Effectiveness and safety of micronized purified flavonoid fraction for the treatment of concomitant varicose veins of the pelvis and lower extremities

机译:微粉化纯化的黄酮级分配治疗骨盆和下肢伴随静脉曲张的有效性和安全性

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Objective: Concomitant varicose veins of the pelvis (VVP) and lower extremities (VVLE) frequently coexist. This study evaluated the effectiveness and safety of micronized purified flavonoid fraction (MPFF) in the treatment of patients with both conditions. Methods: Female outpatients with concomitant VVP and VVLE received MPFF 1000 mg once daily for 2 months (Group 1), or 1000 mg twice daily for 1 month followed by 1000 mg once daily for 1 month (Group 2), based on pelvic pain intensity. Change in pain intensity during treatment was evaluated on a 10 cm visual analog scale. All patients underwent transvaginal and transabdominal duplex ultrasound scanning, radionuclide phlebography of the lower extremities, and emission computer tomography of the pelvic veins at inclusion and end of treatment. Results: In Group 1 (N = 35), MPFF was associated with a twofold reduction in pain syndrome severity (pelvic, perineal and lower leg pain) in all patients after 1 month, and a reduction in chronic pelvic pain (CPP) from 3.4 +/- 1.2 to 0.83 +/- 0.18 cm at 2 months. Leg pain significantly decreased from 2.8 +/- 0.6 at baseline to 0.94 +/- 0.11 after 2 months. In Group 2 (N = 30), MPFF decreased CPP severity from 6.3 +/- 0.8 to 1.2 +/- 0.12, perineal pain from 3.6 +/- 0.9 to 0.88 +/- 0.22 and leg pain from 4.6 +/- 0.5 to 0.9 +/- 0.1. Radionuclide phlebography confirmed the clinical improvement in both treatment groups, with a substantial increase in linear blood flow velocity in the internal iliac veins (similar to 10% in Group 1 and 35% in Group 2) and a reduction in mean transit times of the radiopharmaceutical. MPFF also reduced blood stasis in the pelvic venous plexuses. Gastralgias were reported in two patients but resolved rapidly and did not lead to treatment withdrawal. Conclusion: Phlebotropic treatment with MPFF is an effective and safe method of conservative therapy in patients with concomitant VVP and VVLE.
机译:目的:伴随骨盆(VVP)和下肢(VVLE)的静脉曲张经常共存。该研究评估了微粉化纯化的黄酮级分数(MPFF)治疗两种条件患者的有效性和安全性。方法:具有伴随的VVP和VVLE的女性门诊患者每天一次接受MPFF 1000毫克2个月(第1组),或每日两次,每天两次,后跟1000mg每日一次(第2组),基于骨盆疼痛强度。在10cm的视觉模拟规模上评估治疗过程中疼痛强度的变化。所有患者均接受了经病和转龙腹双相超声扫描,放射性核素噬菌体的下肢脊布,以及骨盆静脉的排放计算机断层扫描,含有和结束治疗。结果:在第1组(n = 35)中,在1个月后,所有患者的疼痛综合征严重程度(骨盆,会阴和小腿疼痛)的双重降低有关,以及3.4的慢性骨盆疼痛(CPP)减少2个月+/- 1.2至0.83 +/- 0.18厘米。腿部疼痛在2个月后,基线在2.8 +/- 0.6下显着降低至0.94 +/- 0.11。在第2组(N = 30)中,MPFF从6.3 +/- 0.8降至1.2 +/- 0.12,从3.6 +/- 0.9到0.88 +/- 0.22,从4.6 +/- 0.5到0.88 +/- 0.5到0.9 +/- 0.1。放射性核素噬菌体噬菌体证实了两种治疗组的临床改善,内部髂静脉的线性血流速度大幅增加(类似于第1组和第2组中的35%),并且放射性药物的平均分流时间减少。 MPFF还减少了盆腔静脉丛中的血瘀。在两个患者中报告了Gastralgias,但迅速解决,并且不会导致治疗戒断。结论:用MPFF进行静脉分析治疗是伴随VVP和VVLE患者的有效和安全的保守疗法方法。

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