High-Flow Oxygen and Bilevel Positive Airway Pressure for Persistent Dyspnea in Patients With Advanced Cancer: A Phase II Randomized Trial

被引:79
作者
Hui, David [1 ]
Morgado, Margarita [1 ]
Chisholm, Gary [2 ]
Withers, Laura [3 ]
Quan Nguyen [3 ]
Finch, Clarence [3 ]
Frisbee-Hume, Susan [1 ]
Bruera, Eduardo [1 ]
机构
[1] Univ Texas Houston, MD Anderson Canc Ctr, Dept Palliat Care & Rehabil Med, Houston, TX 77030 USA
[2] Univ Texas Houston, MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[3] Univ Texas Houston, MD Anderson Canc Ctr, Dept Resp Therapy, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
Dyspnea; positive-pressure respiration; neoplasms; oxygen; randomized controlled trial; high flow oxygen; bilevel positive airway pressure; ACUTE RESPIRATORY-FAILURE; PROGNOSTIC-FACTORS; NASAL OXYGEN; CARE; BREATHLESSNESS; VENTILATION; THERAPY;
D O I
10.1016/j.jpainsymman.2012.10.284
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Context. Dyspnea is one of the most distressing symptoms for cancer patients. The role of high-flow oxygen (HFO) and bilevel positive airway pressure (BiPAP) in the palliation of dyspnea has not been well characterized. Objectives. To determine the feasibility of conducting a randomized trial of HFO and BiPAP in cancer patients and examine the changes in dyspnea, physiologic parameters, and adverse effects with these modalities. Methods. In this randomized study (ClinicalTrials. gov Identifier: NCT01518140), we assigned hospitalized patients with advanced cancer and persistent dyspnea to either HFO or BiPAP for two hours. We assessed dyspnea with a numeric rating scale (NRS) and modified Borg scale (MBS) before and after the intervention. We also documented vital signs, transcutaneous carbon dioxide, and adverse effects. Results. Thirty patients were enrolled (1: 1 ratio) and 23 (77%) completed the assigned intervention. HFO was associated with improvements in both NRS (mean 1.9; 95% CI 0.4-3.4; P=0.02) and MBS (mean 2.1; 95% CI 0.6-3.5; P=0.007). BiPAP also was associated with improvements in NRS (mean 3.2; 95% CI 1.3-5.1; P=0.004) and MBS (mean 1.5; 95% CI -0.3, 3.2; P=0.13). There were no significant differences between HFO and BiPAP in dyspnea NRS (P=0.14) and MBS (P=0.47). Oxygen saturation improved with HFO (93% vs. 99%; P=0.003), and respiratory rate had a nonstatistically significant decrease with both interventions (HFO -3, P=0.11; BiPAP -2, P=0.11). No significant adverse effects were observed. Conclusion. HFO and BiPAP alleviated dyspnea, improved physiologic parameters, and were safe. Our results justify larger randomized controlled trials to confirm these findings. (C) 2013 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:463 / 473
页数:11
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