Audie L Murphy Division, The University of Texas Health Science Center at San Antonio, Texas, USA.
Int J Chron Obstruct Pulmon Dis. 2009;4:245-51. doi: 10.2147/copd.s4862. Epub 2009 Jul 20.
COPD exacerbations are responsible for the morbidity and mortality of this disease. The relationship between exacerbations and patient-related clinical outcomes is not clearly understood.
A retrospective analysis of two 1-year, placebo-controlled clinical trials with tiotropium 18 microg daily was conducted to examine relationships between exacerbations and other clinical outcomes. The relationship between FEV(1), St. George's Respiratory Questionnaire (SGRQ), and the transition dyspnea index (TDI) were examined based on the frequency of exacerbations (0, 1, 2, >2).
921 patients participated in the trials (mean age 65 years, mean FEV(1) = 1.02 L (39% predicted). The percent change from baseline in FEV(1) in the tiotropium group was +12.6%, +12.0%, +2.1% and +8.9%; and in the placebo group was -3.4%, -3.4%, -5.7% and -6.7% for exacerbation frequencies of 0, 1, 2, >2, respectively. Compared with baseline, the largest improvement in SGRQ occurred in patients with no exacerbations. In the placebo group, there was a significant association between an increased frequency of exacerbations and worsening SGRQ scores. A reduction in exacerbation rates of 4.4% to 42.0% such as that shown in this study cohort was associated with meaningful changes in questionnaire based instruments.
In the placebo-treated patients increased frequency of exacerbations was associated with larger decrements in FEV(1), TDI, and SGRQ. A reduction in the frequency of exacerbations is associated with changes that are considered meaningful in these clinical outcomes.
COPD 加重是导致该病发病率和死亡率的原因。加重与患者相关临床结局之间的关系尚不清楚。
对噻托溴铵 18μg/d 进行的两项为期 1 年、安慰剂对照临床试验进行回顾性分析,以检查加重与其他临床结局之间的关系。根据加重的频率(0、1、2、>2),检查 FEV1、圣乔治呼吸问卷(SGRQ)和呼吸困难指数(TDI)之间的关系。
921 例患者参与了这些试验(平均年龄 65 岁,平均 FEV1 为 1.02L(预测值的 39%)。噻托溴铵组的 FEV1 从基线的变化百分比分别为+12.6%、+12.0%、+2.1%和+8.9%;而安慰剂组则为-3.4%、-3.4%、-5.7%和-6.7%,分别为加重频率为 0、1、2、>2。与基线相比,无加重患者的 SGRQ 改善最大。在安慰剂组中,加重频率增加与 SGRQ 评分恶化之间存在显著相关性。如本研究队列所示,将加重发生率降低 4.4%至 42.0%与问卷评估工具的显著变化相关。
在接受安慰剂治疗的患者中,加重频率增加与 FEV1、TDI 和 SGRQ 更大的下降相关。降低加重频率与这些临床结局中认为有意义的变化相关。