A randomized trial of the effects of nebulized albuterol on pulmonary edema in brain-dead organ donors.

A randomized trial of the effects of nebulized albuterol on pulmonary edema in brain-dead organ donors.
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DOI:
10.1111/ajt.12564
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发表时间:
2014-03
期刊:
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
影响因子:
--
通讯作者:
California Transplant Donor Network
California Transplant Donor Network
中科院分区:
其他
文献类型:
--
作者:
Ware LB;Landeck M;Koyama T;Zhao Z;Singer J;Kern R;Neidlinger N;Nguyen J;Johnson E;Janz DR;Bernard GR;Lee JW;Matthay MA;California Transplant Donor Network

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Donor lung utilization rates are persistently low primarily due to donor lung dysfunction. We hypothesized that a treatment that enhances the resolution of pulmonary edema by stimulating the rate of alveolar fluid clearance would improve donor oxygenation and increase donor lung utilization. We conducted a randomized, blinded, placebo-controlled trial of aerosolized albuterol (5 mg q4h) versus saline placebo during active donor management in 506 organ donors. The primary outcome was change in oxygenation (PaO2/FiO2) from enrollment to organ procurement. The albuterol (n=260) and placebo (n=246) groups were well matched for age, gender, ethnicity, smoking, and cause of brain death. The change in PaO2/FiO2 from enrollment to organ procurement did not differ between treatment groups (p=0.54) nor did donor lung utilization (albuterol 29% vs. placebo 32%, p=0.44). Donors in the albuterol vs. placebo group were more likely to have the study drug dose reduced (13% vs. 1%, p<0.001) or stopped (8% vs. 0%, p<0.001) for tachycardia. In summary, treatment with high dose inhaled albuterol during the donor management period did not improve donor oxygenation or increase donor lung utilization but did cause tachycardia. High dose aerosolized albuterol should not be used in donors to enhance the resolution of pulmonary edema.
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