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舒张功能障碍中的吸气肌无力。

Inspiratory muscle weakness in diastolic dysfunction.

作者信息

Lavietes Marc H, Gerula Christine M, Fless Kristin G, Cherniack Neil S, Arora Rohit R

机构信息

University Hospital #I354, 100 Bergen St, Newark, NJ 07103, USA.

出版信息

Chest. 2004 Sep;126(3):838-44. doi: 10.1378/chest.126.3.838.

Abstract

OBJECTIVES

To test the hypothesis that patients with well-documented diastolic dysfunction (DD) in the setting of normal systolic function will have inspiratory muscle weakness when compared to normal control subjects, and will experience dyspnea and tachypnea during exercise.

BACKGROUND

Respiratory muscle weakness has been described in patients with (systolic) congestive heart failure; however, whether or not patients with DD may present with the findings of congestive heart failure is not known.

METHODS

We selected for study 14 patients with DD previously referred for cardiopulmonary evaluation whose diagnosis had been confirmed by data obtained at cardiac catheterization. Seven control subjects matched for age, sex, and weight were recruited from the hospital community. Subjects performed both basic pulmonary function tests and tests of muscle strength: handgrip strength (Hgr), and maximal subatmospheric static inspiratory muscle pressure (Pimax). Subjects then performed a graded exercise test on a bicycle ergometer. Minute ventilation, oxygen consumption, carbon dioxide production, and heart rate were monitored continuously. Echocardiography was performed three times: before exercise, at a selected submaximal exercise level (20% of a predicted maximal workload), and at maximal exercise. Subjects rated their degree of dyspnea using the Borg scale at the same three time intervals.

RESULTS

Pimax was - 102 +/- 17 cm H(2)O in control subjects, and - 77 +/- 19 cm H(2)O in patients with DD (p = 0.013) [mean +/- SD]. Hgr was similar between the groups. At the selected submaximal exercise level, patients with DD rated dyspnea to be 2.6 +/- 2.2 Borg scale units (control subjects, 0.5 +/- 0.8 Borg scale units). Hey plots described a rapid, shallow breathing pattern in patients with DD during exercise. Patients with DD and control subjects achieved similar maximal work loads.

CONCLUSION

Patients with DD have diminished Pimax, adopt a rapid, shallow breathing pattern during exercise, and experience dyspnea at low work loads when compared to matched control subjects.

摘要

目的

检验以下假设:与正常对照受试者相比,收缩功能正常但有充分记录的舒张功能障碍(DD)患者会出现吸气肌无力,并且在运动期间会出现呼吸困难和呼吸急促。

背景

已有研究描述了(收缩性)充血性心力衰竭患者存在呼吸肌无力;然而,DD患者是否会出现充血性心力衰竭的表现尚不清楚。

方法

我们选择了14例先前因心肺评估而转诊的DD患者,其诊断已通过心导管检查获得的数据得到证实。从医院社区招募了7名年龄、性别和体重相匹配的对照受试者。受试者进行了基本肺功能测试和肌肉力量测试:握力(Hgr)和最大负压静态吸气肌压力(Pimax)。然后,受试者在自行车测力计上进行分级运动测试。连续监测每分通气量、耗氧量、二氧化碳产生量和心率。在运动前、选定的次最大运动水平(预测最大工作量的20%)和最大运动时进行三次超声心动图检查。受试者在相同的三个时间间隔使用Borg量表对其呼吸困难程度进行评分。

结果

对照受试者的Pimax为-102±17cmH₂O,DD患者为-77±19cmH₂O(p = 0.013)[平均值±标准差]。两组之间的Hgr相似。在选定的次最大运动水平,DD患者将呼吸困难评为2.6±2.2 Borg量表单位(对照受试者为0.5±0.8 Borg量表单位)。Hey图描述了DD患者在运动期间快速、浅呼吸模式。DD患者和对照受试者达到了相似的最大工作量。

结论

与匹配的对照受试者相比,DD患者的Pimax降低,在运动期间采用快速、浅呼吸模式,并且在低工作量时出现呼吸困难。

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