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Recombinant streptokinase vs hydrocortisone suppositories in acute hemorrhoids: A randomized controlled trial

机译:重组痔链激酶与氢化可的松栓剂治疗急性痔的随机对照试验

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摘要

AIM: To compare the efficacy and safety of recombinant streptokinase (rSK) vs hydrocortisone acetate-based suppositories in acute hemorrhoidal disease.METHODS: A multicenter (11 sites), randomized (1:1:1), open, controlled trial with parallel groups was performed. All participating patients gave their written, informed consent. After inclusion, patients with acute symptoms of hemorrhoids were centrally randomized to receive, as outpatients, by the rectal route, suppositories of rSK 200000 IU of one unit every 8 h (first 3 units) and afterwards every 12 h until 8 administrations were completed (schedule A), one unit every 8 h until 6 units were completed (schedule B), or 25 mg hydrocortisone acetate once every 8 h up to a maximum of 24 administrations. Evaluations were performed at 3, 5, and 10 d post-inclusion. The main end-point was the 5th-day response (disappearance of pain and bleeding, and ≥ 70% reduction of the lesion size). Time to response and need for thrombectomy were secondary efficacy variables. Adverse events were also evaluated.RESULTS: Groups were homogeneous with regards to demographic and baseline characteristics. Fifth day complete response rates were 156/170 (91.8%; 95%CI: 87.3-96.2), 155/170 (91.2%; 95%CI: 86.6%-95.7%), and 46/170 (27.1%; 95%CI: 20.1%-34.0%) with rSK (schedule A and B) and hydrocortisone acetate suppositories, respectively. These 64.6% and 63.9% differences (95%CI: 56.7%-72.2% and 55.7%-72.0%) were highly significant (P < 0.001). This advantage was detected since the early 3rd day evaluation (68.8% and 64.1% vs 7.1% for the rSK and active control groups, respectively; P < 0.001) and was maintained even at the late 10th day assessment (97.1% and 93.5% vs 67.1% for rSK and hydrocortisone acetate, respectively; P < 0.001). Time to response was 3 d (95%CI: 2.9-3.1) for both rSK groups and 10 d (95%CI: 9.3-10.7) in the hydrocortisone acetate group. This difference was highly significant (P < 0.001). All subgroup stratified analyses (with or without thrombosis and hemorrhoid classification) showed a statistically significant advantage for the rSK groups. Thrombectomy was necessary in 4/251 and 14/133 patients with baseline thrombosis in the rSK and hydrocortisone acetate groups, respectively (P < 0.001). There were no adverse events attributable to the experimental treatment.CONCLUSION: rSK suppositories showed a significant advantage over a widely-used over-the-counter hydrocortisone acetate preparation for the treatment of acute hemorrhoidal illness, as well as having an adequate safety profile.
机译:目的:比较重组链激酶(rSK)和醋酸氢化可的松栓剂在急性痔疮中的疗效和安全性。方法:多中心(11个位点),随机(1:1:1)随机对照开放试验被执行了。所有参与的患者均签署了书面知情同意书。入院后,将具有痔疮急性症状的患者集中随机分配至门诊,通过直肠途径每8小时(前3个单位)接受rSK 200000 IU栓剂,随后每12小时接受一次,直至完成8次给药(计划A),每8小时1个单位,直到完成6个单位(计划B)为止,或者每8小时一次25毫克醋酸氢化可的松,最多24次给药。纳入后3、5和10 d进行评估。主要终点是第5天的反应(疼痛和出血消失,病灶缩小≥70%)。响应时间和需要进行血栓切除术是次要疗效变量。结果:各组在人口统计学和基线特征方面是同质的。第五天的完全缓解率为156/170(91.8%; 95%CI:87.3-96.2),155/170(91.2%; 95%CI:86.6%-95.7%)和46/170(27.1%; 95%) CI:20.1%-34.0%)分别含rSK(附表A和B)和醋酸氢化可的松栓剂。这些64.6%和63.9%的差异(95%CI:56.7%-72.2%和55.7%-72.0%)高度显着(P <0.001)。自第3天早期评估以来就检测到了这一优势(rSK和活动对照组分别为68.8%和64.1%对7.1%; P <0.001),甚至在10 <第一天评估(rSK和醋酸氢化可的松分别为97.1%和93.5%对67.1%; P <0.001)。两个rSK组的响应时间均为3 d(95%CI:2.9-3.1),而乙酸氢化可的松组的响应时间为10 d(95%CI:9.3-10.7)。这种差异非常显着(P <0.001)。所有亚组分层分析(有无血栓形成和痔疮分类)均显示rSK组具有统计学上的显着优势。 rSK组和醋酸氢化可的松组分别有基线血栓形成的4/251和14/133患者必须行血栓切除术(P <0.001)。结论:rSK栓剂在治疗急性痔疮疾病方面比广泛使用的非处方醋酸氢化可的松制剂具有明显优势,并且具有足够的安全性。

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