High frequency chest wall oscillation for asthma and chronic obstructive pulmonary disease exacerbations: a randomized sham-controlled clinical trial

被引:21
作者
Mahajan, Amit K. [2 ]
Diette, Gregory B. [3 ]
Hatipoglu, Umur [4 ,5 ,6 ]
Bilderback, Andrew [3 ]
Ridge, Alana [3 ]
Harris, Vanessa Walker [3 ]
Dalapathi, Vijay [2 ]
Badlani, Sameer [7 ]
Lewis, Stephanie [1 ]
Charbeneau, Jeff T. [1 ]
Naureckas, Edward T. [2 ]
Krishnan, Jerry A. [1 ]
机构
[1] Univ Illinois, Sect Pulm Crit Care Sleep & Allergy, Dept Med, Chicago, IL 60612 USA
[2] Univ Chicago, Sect Pulm & Crit Care, Dept Med, Chicago, IL 60637 USA
[3] Johns Hopkins Univ, Div Pulm & Crit Care Med, Dept Med, Baltimore, MD 21205 USA
[4] Mercy Hosp, Dept Med, Chicago, IL 60617 USA
[5] Med Ctr, Chicago, IL 60617 USA
[6] Cleveland Clin, Respiratory Inst, Cleveland, OH 44195 USA
[7] Univ Chicago, Sect Hosp Med, Chicago, IL 60637 USA
关键词
asthma; chronic obstructive pulmonary disease; high frequency chest wall oscillation; airway mucus clearance;
D O I
10.1186/1465-9921-12-120
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
100201 [内科学];
摘要
Background: High frequency chest wall oscillation (HFCWO) is used for airway mucus clearance. The objective of this study was to evaluate the use of HFCWO early in the treatment of adults hospitalized for acute asthma or chronic obstructive pulmonary disease (COPD). Methods: Randomized, multi-center, double-masked phase II clinical trial of active or sham treatment initiated within 24 hours of hospital admission for acute asthma or COPD at four academic medical centers. Patients received active or sham treatment for 15 minutes three times a day for four treatments. Medical management was standardized across groups. The primary outcomes were patient adherence to therapy after four treatments (minutes used/60 minutes prescribed) and satisfaction. Secondary outcomes included change in Borg dyspnea score (>= 1 unit indicates a clinically significant change), spontaneously expectorated sputum volume, and forced expired volume in 1 second. Results: Fifty-two participants were randomized to active (n = 25) or sham (n = 27) treatment. Patient adherence was similarly high in both groups (91% vs. 93%; p = 0.70). Patient satisfaction was also similarly high in both groups. After four treatments, a higher proportion of patients in the active treatment group had a clinically significant improvement in dyspnea (70.8% vs. 42.3%, p = 0.04). There were no significant differences in other secondary outcomes. Conclusions: HFCWO is well tolerated in adults hospitalized for acute asthma or COPD and significantly improves dyspnea. The high levels of patient satisfaction in both treatment groups justify the need for sham controls when evaluating the use of HFCWO on patient-reported outcomes. Additional studies are needed to more fully evaluate the role of HFCWO in improving in-hospital and post-discharge outcomes in this population.
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页数:7
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