Zezos P, Papaioannou G, Nikolaidis N, Patsiaoura K, Papageorgiou A, Vassiliadis T, Giouleme O, Evgenidis N
2nd Propaedeutic Department of Internal Medicine, Division of Gastroenterology, 'Hippokration' General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Aliment Pharmacol Ther. 2006 May 15;23(10):1443-53. doi: 10.1111/j.1365-2036.2006.02870.x.
Heparin could be beneficial to the treatment of active ulcerative colitis because of its anticoagulant, anti-inflammatory and immunomodulatory properties.
To evaluate the tolerability, safety and efficacy of low-molecular-weight heparin as adjuvant therapy in patients with active ulcerative colitis.
Thirty-four adult patients with active ulcerative colitis were consecutively included in a prospective, randomized, comparative study, and were treated for 12 weeks. Eighteen patients in the 'standard therapy' group were treated with aminosalicylates and weekly tapered corticosteroids. Sixteen patients in the 'heparin therapy' group were treated with standard therapy plus enoxaparin 100 Anti-Xa IU/kg/day subcutaneously.
Seventeen patients in the 'standard therapy' group and 15 patients in the 'heparin therapy' group completed the study. Tolerability and compliance to therapy were excellent and no withdrawals were noted because of complications. There was a significant improvement in the disease severity in both groups (P<0.001), without any difference between them (P=not significant). Both treatment groups showed similar proportions of disease improvement (65% and 73%, respectively; P=not significant). There were no significant differences in inflammation (fibrinogen, ESR, CRP) and coagulation (thrombin-antithrombin complex, F1+2, D-dimers) parameters during and at the end of the study between treatment groups.
Adjuvant administration of low-molecular heparin in patients with active ulcerative colitis is safe and well tolerated, but no additive benefit over standard therapy for ulcerative colitis was noted.
肝素因其抗凝、抗炎和免疫调节特性,可能对活动性溃疡性结肠炎的治疗有益。
评估低分子量肝素作为活动性溃疡性结肠炎患者辅助治疗的耐受性、安全性和疗效。
34例成年活动性溃疡性结肠炎患者连续纳入一项前瞻性、随机、对照研究,治疗12周。“标准治疗”组的18例患者接受氨基水杨酸类药物治疗,并每周递减剂量使用皮质类固醇。“肝素治疗”组的16例患者接受标准治疗加皮下注射依诺肝素100抗Xa国际单位/千克/天。
“标准治疗”组的17例患者和“肝素治疗”组的15例患者完成了研究。治疗的耐受性和依从性良好,未因并发症而退出研究。两组疾病严重程度均有显著改善(P<0.001),但两组之间无差异(P=无显著性)。两个治疗组疾病改善的比例相似(分别为65%和73%;P=无显著性)。治疗组之间在研究期间和结束时的炎症(纤维蛋白原、血沉、C反应蛋白)和凝血(凝血酶-抗凝血酶复合物、F1+2、D-二聚体)参数无显著差异。
活动性溃疡性结肠炎患者辅助使用低分子肝素是安全且耐受性良好的,但未发现其对溃疡性结肠炎的治疗比标准治疗有额外益处。