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Timing and driving components of the breathing strategy in children with cystic fibrosis during exercise.

机译:运动过程中囊性纤维化儿童呼吸策略的时机和驱动因素。

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The aim of this study was twofold: first, to determine the breathing strategies of children with cystic fibrosis (CF) during exercise, and secondly, to see if there was a correlation with lung function parameters. We determined the tension-time index of the inspiratory muscles (T(T0.1)) during exercise in nine children with CF, who were compared with nine healthy children with a similar age distribution. T(T0.1) was determined as followed T(T0.1) = P(0.1)/P(Imax) . T(I)/T(TOT), where P(0.1) is mouth occlusion pressure, P(Imax) is maximal inspiratory pressure, and T(I)/T(TOT) is the duty cycle. CF children showed a significant decrease of their forced expiratory volume in 1 sec (FEV(1)), forced vital capacity (FCV), and FEV(1)/FVC, whereas the residual volume to total lung capacity ratio (RV/TLC) ratio and functional residual capacity (FRC) were significantly increased (P < 0.001). Children with CF showed mild malnutrition assessed by actual weight expressed by percentage of ideal weight for height, age, and gender (weight/height ratio; 82.3 +/- 3.6%). Children with CF showed a significant reduction in their P(Imax) (69.3 +/- 4.2 vs. 93.8 +/- 7 cmH(2)O). We found a negative linear correlation between P(Imax) and weight/height only in children with CF (r = 0.9, P < 0.001). During exercise, P(0.1), P(0.1)/P(Imax), and T(T0.1) were significantly higher, for a same percent maximal oxygen uptake in children with CF. On the contrary, T(I)/T(TOT) ratio was significantly lower in children with CF compared with healthy children. At maximal exercise, children with CF showed a T(T0.1) = 0.16 vs. 0.14 in healthy children (P < 0.001). We observed at maximal exercise that P(0.1)/P(Imax) increased as FEV(1)/FVC decreased (r = -0.90, P < 0.001), and increased as RV/TLC increased (r = 0.92, P < 0.001) only in children with CF. Inversely, T(I)/T(TOT) decreased as FEV(1)/FVC decreased (r = 0.89, P < 0.001), and T(I)/T(TOT) decreased as RV/TLC increased (r = -0.94, P < 0.001). These results suggest that children with CF adopted a breathing strategy during exercise in limiting the increase of the duty cycle. Two determinants of this strategy were degrees of airway obstruction and hyperinflation. (c) 2005 Wiley-Liss, Inc.
机译:这项研究的目的是双重的:首先,确定运动过程中患有囊性纤维化(CF)的儿童的呼吸策略;其次,看是否与肺功能参数相关。我们确定了9名CF儿童的运动过程中吸气肌的张力时间指数(T(T0.1)),并与9名年龄分布相似的健康儿童进行了比较。确定T(T0.1)如下:T(T0.1)= P(0.1)/ P(Imax)。 T(I)/ T(TOT),其中P(0.1)是口腔阻塞压力,P(Imax)是最大吸气压力,T(I)/ T(TOT)是占空比。 CF儿童在1秒钟内表现出他们的强制呼气量(FEV(1)),强制肺活量(FCV)和FEV(1)/ FVC显着降低,而剩余容量与总肺活量之比(RV / TLC)比率和功能残余容量(FRC)显着增加(P <0.001)。患有CF的儿童显示出通过实际体重评估的轻度营养不良,实际体重以身高,年龄和性别的理想体重百分比表示(体重/身高比; 82.3 +/- 3.6%)。患有CF的儿童的P(Imax)显着降低(69.3 +/- 4.2 vs. 93.8 +/- 7 cmH(2)O)。我们发现仅在CF儿童中,P(Imax)与体重/身高之间呈负线性关系(r = 0.9,P <0.001)。在运动过程中,CF患儿最大摄氧量的百分比相同时,P(0.1),P(0.1)/ P(Imax)和T(T0.1)显着更高。相反,CF儿童的T(I)/ T(TOT)比健康儿童低得多。在最大程度的运动下,CF儿童的T(T0.1)= 0.16,而健康儿童的T(T0.1)= 0.14(P <0.001)。我们观察到在最大运动量下P(0.1)/ P(Imax)随着FEV(1)/ FVC的减少而增加(r = -0.90,P <0.001),并且随着RV / TLC的增加而增加(r = 0.92,P <0.001) )仅适用于CF儿童。相反,随着FEV(1)/ FVC的降低,T(I)/ T(TOT)降低(r = 0.89,P <0.001),并且随着RV / TLC的提高,T(I)/ T(TOT)降低(r =- 0.94,P <0.001)。这些结果表明,患有CF的儿童在运动中采取了呼吸策略,以限制工作周期的增加。该策略的两个决定因素是气道阻塞程度和过度充气。 (c)2005 Wiley-Liss,Inc.

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