Pirozyński Michał, Skucha Wojciech, Słomiński Marek, Chyczewska Elzbieta, Malinowski Janusz, Nowak Dariusz, Bartmińiski Wojciech, Pachocki Robert
Klinika Anestezjologii i Intensywnej Terapii CMKP, Warszawie.
Pol Merkur Lekarski. 2005 Aug;19(110):139-43.
The aim of the work was evaluation of efficacy of fenspiride b.i.d. on the number of exacerbations and the time to the first exacerbation in patients with chronic bronchitis.
Randomized, multicentre study controlled versus placebo was carried out in 12 centers in Poland. All patients, 89 females and 68 males aged between 20 and 74, were treated with fenspiride at the dose of 160 mg/day for a period of 6 months. The following symptoms were recorded every month in order to evaluate the therapeutic efficacy: sputum quality and quantity, cough intensity, dyspnea and bronchospasm. Based on these symptoms diagnosis of exacerbation was performed according to American Thoracic Society criteria.
Quality and quantity of sputum and cough significantly improved in the fenspiride group (comparing to the placebo group p= 0.027 and p = 0.049 adequately for sputum and cough). A significant difference between groups was observed in the number of exacerbation episodes and their duration. In the fenspiride group there were 0.53 episodes of exacerbation compared with 1.12 episodes in the placebo group (p = 0.038). Mean duration of exacerbation was 3.3 days in the fenspiride group and 7.3 days in the placebo treated patients (p = 0.034). Time to the first exacerbation differed between groups, but this difference was not statistically significant. Number of side effects observed did not differ between groups.
Fenspiride treatment was assessed as relatively effective in terms of influence on exacerbations, and well tolerated during six month therapy.
本研究旨在评估每日两次服用芬司匹利对慢性支气管炎患者急性加重次数及首次急性加重时间的疗效。
在波兰的12个中心进行了一项随机、多中心、对照安慰剂的研究。所有患者,共89名女性和68名男性,年龄在20至74岁之间,接受剂量为160毫克/天的芬司匹利治疗,为期6个月。为评估治疗效果,每月记录以下症状:痰液质量和数量、咳嗽强度、呼吸困难和支气管痉挛。根据这些症状,依据美国胸科学会标准进行急性加重的诊断。
芬司匹利组的痰液质量和数量以及咳嗽症状均有显著改善(与安慰剂组相比,痰液和咳嗽的p值分别为0.027和0.049)。两组在急性加重发作次数及其持续时间方面存在显著差异。芬司匹利组的急性加重发作次数为0.53次,而安慰剂组为1.12次(p = 0.038)。芬司匹利组急性加重的平均持续时间为3.3天,安慰剂治疗患者为7.3天(p = 0.034)。两组首次急性加重的时间有所不同,但差异无统计学意义。两组观察到的副作用数量无差异。
就对急性加重的影响而言,芬司匹利治疗被评估为相对有效,且在六个月的治疗期间耐受性良好。