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高剂量沙美特罗治疗囊性纤维化的有效性和耐受性

Effectiveness and tolerability of high-dose salmeterol in cystic fibrosis.

作者信息

Hordvik Nancy L, Sammut Paul H, Judy C Gerald, Colombo John L

机构信息

Department of Pediatric Pulmonology, University of Nebraska Medical Center, Omaha, Nebraska 68198, USA.

出版信息

Pediatr Pulmonol. 2002 Oct;34(4):287-96. doi: 10.1002/ppul.10162.

Abstract

The efficacy and tolerability of high-dose salmeterol (100 mcg, BID) and albuterol (2.5 mg, BID) were compared with those of albuterol (2.5 mg, BID) in outpatients with cystic fibrosis in a randomized, double-blind, double-dummy, placebo-controlled, crossover study with both short- (4 weeks of each) and long-term (24 weeks of each) treatment periods. The primary outcome measure was the difference in mean change in forced expired volume in 1 sec (FEV(1)) from baseline to the end of each treatment, and secondary measures included changes in forced vital capacity (FVC), forced expiratory flow between 25-75% of FVC (FEF(25-75)), patient-rated weekly symptom scores, number of extra (rescue) albuterol treatments, and number of antibiotic treatments. Tolerability was evaluated by changes in vital signs and adverse events.Thirty-six out of 44 patients enrolled finished the short-term treatment period, and 19 out of 23 who continued the study also finished the long-term treatment period. There was no significant difference in the mean % change in FEV(1) from baseline to completion of 4 weeks with each drug in the short-term treatment period (0.1% vs. 0.06%, albuterol vs. salmeterol; respectively). In the long-term treatment period, there was a significant decrease from baseline in FEV(1) with albuterol vs. salmeterol, as measured after both 12 and 24 weeks of each treatment (-6.2% vs. 1.8%, P = 0.013 after 12 weeks, and -6.5% vs. 1.7%, P = 0.002, after 24 weeks, respectively). In both treatment periods, salmeterol was well-tolerated. While there were more rescue treatments per patient per week with albuterol than with salmeterol treatment in both the short- and long-term periods (0.67 vs. 0.40 and 1.76 vs. 0.74, respectively), rescue treatments were needed significantly more often for only the long-term period with albuterol compared to salmeterol (P = 0.022). Also, there were more antibiotic interventions with albuterol than with salmeterol treatment in both the short- and long-term periods (25 vs. 10 and 56 vs. 42, respectively); however, antibiotics were needed significantly more often for only the short-term period (P = 0.011). In addition, there was a significantly higher symptom score with albuterol vs. salmeterol treatment during the second half of the long-term period (1.24 vs. 0.89, P = 0.001).In conclusion, long-term high-dose salmeterol was equally safe and was associated with better pulmonary function, fewer interventions, and fewer respiratory symptoms compared to standard therapy with albuterol in a population of outpatients with mild to moderate CF.

摘要

在一项针对囊性纤维化门诊患者的随机、双盲、双模拟、安慰剂对照、交叉研究中,比较了高剂量沙美特罗(100微克,每日两次)和沙丁胺醇(2.5毫克,每日两次)与沙丁胺醇(2.5毫克,每日两次)的疗效和耐受性,该研究包括短期(每种治疗4周)和长期(每种治疗24周)治疗期。主要结局指标是从基线到每种治疗结束时1秒用力呼气容积(FEV(1))的平均变化差异,次要指标包括用力肺活量(FVC)、FVC的25%-75%之间的用力呼气流量(FEF(25-75))、患者每周症状评分、额外(急救)沙丁胺醇治疗次数以及抗生素治疗次数。通过生命体征变化和不良事件评估耐受性。44名入组患者中有36名完成了短期治疗期,继续研究的23名患者中有19名也完成了长期治疗期。在短期治疗期,每种药物从基线到4周治疗结束时FEV(1)的平均变化百分比无显著差异(沙丁胺醇为0.1%,沙美特罗为0.06%)。在长期治疗期,每种治疗12周和24周后测量,沙丁胺醇组的FEV(1)较基线显著下降,而沙美特罗组则不然(12周后分别为-6.2%对1.8%,P = 0.013;24周后分别为-6.5%对1.7%,P = 0.002)。在两个治疗期,沙美特罗耐受性良好。在短期和长期治疗期,沙丁胺醇治疗的每位患者每周急救治疗次数均多于沙美特罗治疗(分别为0.67对0.40和1.76对0.74),但仅在长期治疗期,沙丁胺醇组急救治疗的需求显著多于沙美特罗组(P = 0.022)。此外,在短期和长期治疗期,沙丁胺醇治疗的抗生素干预次数均多于沙美特罗治疗(分别为25对10和56对42);然而,仅在短期治疗期抗生素的需求显著更多(P = 0.011)。此外,在长期治疗期的后半段,沙丁胺醇治疗的症状评分显著高于沙美特罗治疗(1.24对0.89,P = 0.001)。总之,在轻度至中度CF门诊患者中,与沙丁胺醇标准治疗相比,长期高剂量沙美特罗同样安全,且与更好的肺功能、更少的干预措施和更少的呼吸道症状相关。

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