...
首页> 外文期刊>Journal of aerosol medicine and pulmonary drug delivery >Multisite comparison of mucociliary and cough clearance measures using standardized methods
【24h】

Multisite comparison of mucociliary and cough clearance measures using standardized methods

机译:使用标准化方法对粘液纤毛和止咳措施的多点比较

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

Background: A standardized protocol for measuring mucociliary (MCC) and cough clearance (CC) was developed and tested at the University of North Carolina at Chapel Hill, NC (UNC), Johns Hopkins University (JHU), and the University of Pittsburgh (Pitt). Methods: A total of 50 healthy nonsmoking adults with normal lung function were studied at the three sites: 30 [21 males/9 females (21M/9F)] at UNC, 10 (6M/4F) at JHU, and 10 (4M/6F) at Pitt. Subjects inhaled an aerosol of 99mtechnetium sulfur colloid in 0.9% saline (mass median aerodynamic diameter=5.4 μm) under controlled breathing conditions (500 mL/sec, 30 breaths/min) by following a metronome and flow signal from a commercial dosimeter. Following inhalation, subjects sat in front of a gamma camera as sequential lung images were acquired for 60 min. Subjects then coughed 60 times, and images were acquired after each set of 20 coughs, i.e., at 70, 80, and 90 min. Subjects returned to the laboratory approximately 24 hr later for a final image of residual lung activity. Initial aerosol distribution was measured as a central/peripheral (C/P) ratio of activity. MCC/CC was expressed as the area under the retention versus time curve over 90 min (AUC90). Results: A multivariate analysis of clearance versus time with site and C/P as covariates showed no significant site-specific differences. Interestingly, MCC/CC was greater in females (n=19) versus males (n=31), with AUC90=0.84±0.11 and 0.90±0.07, respectively (p=0.03), for the combined data set from all sites (not significant for any given site). There were no gender differences for either C/P ratio or 24-hr clearance. Conclusions: This standardized protocol may prove beneficial in multicenter trials for testing new therapies that are designed to improve MCC/CC.
机译:背景:北卡罗来纳州北卡罗来纳大学教堂山分校(UNC),约翰霍普金斯大学(JHU)和匹兹堡大学(匹兹堡)制定并测试了用于测量粘液纤毛(MCC)和咳嗽清除率(CC)的标准化协议。 )。方法:在这三个地点对总共50名健康正常的非吸烟健康成年人进行了研究:在UNC,30名[21名男性/ 9名女性(21M / 9F)],在JHU,10名(6M / 4F),以及10名(4M / 6楼)。通过遵循商业剂量计的节拍器和流量信号,受试者在受控的呼吸条件下(500 mL / sec,30呼吸/ min)吸入0.9%盐水(质量中位数空气动力学直径= 5.4μm)中的99m net硫胶体气雾剂。吸入后,将受试者坐在伽马相机前,获取60分钟的连续肺图像。然后受试者咳嗽60次,每组20次咳嗽后即70、80和90分钟后获取图像。受试者大约在24小时后返回实验室,以获取残留肺活动的最终图像。初始气溶胶分布以活动的中心/外围(C / P)比进行测量。 MCC / CC表示为90分钟内保留时间对时间曲线下的面积(AUC90)。结果:清除率与时间的多变量分析以位点和C / P为协变量,显示无明显的位点特异性差异。有趣的是,对于来自所有地点的合并数据集,女性(n = 19)的MCC / CC高于男性(n = 31),分别为AUC90 = 0.84±0.11和0.90±0.07(p = 0.03)。对于任何给定的网站都是重要的)。 C / P比值或24小时通关率没有性别差异。结论:该标准化方案可能在多中心试验中证明有益,这些试验用于测试旨在改善MCC / CC的新疗法。

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