首页> 外文期刊>International journal of dermatology >A comparative study between the efficacy of oral cimetidine and low-dose systemic meglumine antimoniate (MA) with a standard dose of systemic MA in the treatment of cutaneous leishmaniasis
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A comparative study between the efficacy of oral cimetidine and low-dose systemic meglumine antimoniate (MA) with a standard dose of systemic MA in the treatment of cutaneous leishmaniasis

机译:口服西咪替丁和低剂量全身性葡甲胺氯胺酸(MA)与标准剂量的全身性MA治疗皮肤利什曼病的疗效比较研究

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Cutaneous leishmaniasis (CL) is a major world health problem, which is increasing in incidence. Pentavalent antimonials have been considered as standard treatment for leishmaniasis. Many studies are performed to find an effective and safe treatment for patients with CL. The aim of this study was to compare the effect of oral cimetidine and low-dose systemic meglumine antimoniate (MA) with standard dose of systemic MA in the treatment of CL. This study was, to our knowledge, the first to show the effect of combination therapy oral cimetidine and MA in the treatment of CL all over the world. In this randomized double-blind placebo-controlled clinical trial, 120 patients with suspected CL were referred to the Aleppo University Hospital Clinic; 90 of these patients with the clinical and parasitological diagnosis of CL were recruited and were randomly divided into three treatment groups of 30 subjects each. Group A was treated with MA 60mg/kg/d IM and oral placebo. Groups B and C received MA 30mg/kg/d IM and oral cimetidine 1200mg/d, MA 30mg/kg/d IM and oral placebo, respectively. The duration of treatment was three weeks for all groups. The effectiveness of the treatment was classified in three levels as complete response, partial response, and no response. Data were analyzed by SPSS 19 using KI square, Mann-Whitney, Kaplan-Mayer, and ANOVA tests. At the end of the study (12weeks), the rate of complete response was 91.11% in the first group, and 84.66% and 78.33% in groups B and C, respectively (P<0.05). The highest response rate was for the group treated with a standard dose of systemic MA and placebo. Our results showed that although oral cimetidine and low-dose systemic MA had less efficacy in comparison to a standard dose of systemic MA in the treatment of CL, it still can be considered as a replacement therapy in high-risk patients (such as patients with heart, kidney, and/or liver disease) under close supervision of physicians.
机译:皮肤利什曼病(CL)是世界主要的健康问题,其发病率正在增加。五价锑已被认为是利什曼病的标准治疗方法。进行了许多研究,以寻找一种有效且安全的CL患者治疗方法。这项研究的目的是比较口服西咪替丁和小剂量全身性葡甲胺氯胺酸(MA)与标准剂量的全身性MA治疗CL的效果。就我们所知,这项研究是第一个显示口服西咪替丁和MA联合治疗在全世界治疗CL的效果的研究。在这项随机双盲安慰剂对照临床试验中,将120例疑似CL患者转诊至阿勒颇大学医院诊所;招募了其中90名具有CL临床和寄生虫学诊断的患者,并将其随机分为三个治疗组,每组30名。 A组用MA 60mg / kg / d IM和口服安慰剂治疗。 B组和C组分别接受MA 30mg / kg / d IM和口服西咪替丁1200mg / d,MA 30mg / kg / d IM和口服安慰剂。所有组的治疗时间均为三周。治疗的有效性分为完全缓解,部分缓解和无缓解三个级别。使用KI平方,Mann-Whitney,Kaplan-Mayer和ANOVA测试,通过SPSS 19分析数据。在研究结束时(12周),第一组的完全缓解率分别为91.11%,B和C组的完全缓解率分别为84.66%和78.33%(P <0.05)。最高反应率是使用标准剂量的全身性MA和安慰剂治疗的组。我们的结果表明,尽管口服西咪替丁和低剂量全身性MA与标准剂量的全身性MA相比在CL的治疗中疗效较差,但仍可被视为高危患者(如心脏,肾脏和/或肝脏疾病)在医生的密切监督下。

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