...
首页> 外文期刊>Indian Journal of Pediatrics >Montelukast — evaluation in 6 to 14 years old children with persistent asthma — pediatric montelukast study group
【24h】

Montelukast — evaluation in 6 to 14 years old children with persistent asthma — pediatric montelukast study group

机译:孟鲁司特-对6至14岁持续性哮喘患儿的评估-小儿孟鲁司特研究组

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Objective : The suffering of children with asthma as a persistent illness is present in approximately 10% of the total population. The prevalent treatment regimens available has been the inhaled coticosteroids and short acting bronchodialators. Though the therapies are rational and well accepted but at the cost of side effects on chronic use. The changing definitions and guidelines with regard to asthma have given a classified slot to newer treatments like leukotriene receptor antagonists (LTRAs). The aim of the present study was to study the efficacy and tolerability of montelukast in the treatment of Indian pediatric patients aged 6 to 14 years with chronic asthma.Methods: It was a prospective, open, non-comparative multicentric study. 881 Children (Mean age 11.83± 3.12 years) were included. Patients fulfilling the inclusion criteria were given one mouth dissolving 5 mg montelukast tablet daily in the evening for 30 days.Results : There was an overall improvement in all the efficacy parameters. The daytime total asthma score decreased from 9.55 ± 1.52 to 3.59 ±2.10. The average number of asthma attacks over the last 4 weeks decreased from 1.14± 1.19 to 0.28±0.57. The number of nocturnal awakenings fell from 1.54±0.78 to 0.43±0.54. FEV, (L) (Predicted J improved by 21.18%). PEFR (LJmin.) improved by 34.69%). Approximately 45% physicians rated the treatment as excellent, 30% as very good, 18% as good, 7% as fair and none as poor.Conclusion: Montelukast administered once daily improved efficacy end-points and was well tolerated in pediatric patients with chronic persistent asthma establishing itself as a valuable treatment option to current asthma therapies in 6 to 14 years old patients.
机译:目的:约有10%的人口患有哮喘病作为持续性疾病。可用的流行治疗方案是吸入的类固醇和短效支气管扩张药。尽管疗法是合理的并且被广泛接受,但是以长期使用的副作用为代价。关于哮喘的不断变化的定义和指南已经为白三烯受体拮抗剂(LTRAs)等较新的治疗方法分类。本研究的目的是研究孟鲁司特在印度小儿6至14岁的慢性哮喘患者中的疗效和耐受性。方法:这是一项前瞻性,开放性,非对照性多中心研究。包括881名儿童(平均年龄11.83±3.12岁)。符合入组标准的患者每天晚上用一只嘴溶解5 mg孟鲁司特片,持续30天。结果:所有功效参数均得到总体改善。白天的总哮喘评分从9.55±1.52降低至3.59±2.10。最近4周的平均哮喘发作次数从1.14±1.19降至0.28±0.57。夜间觉醒次数从1.54±0.78降至0.43±0.54。 FEV,(L)(预测的J提高了21.18%)。 PEFR(LJmin。)提高了34.69%。大约45%的医生将治疗评为极好,30%的非常好,18%的好,7%的公平,没有差的结论。结论:孟鲁司特每天给药一次可改善疗效终点,并且对慢性儿科患者耐受良好持续性哮喘已成为6至14岁患者目前哮喘治疗的重要治疗选择。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号