De Wet Charl J, Affleck David G, Jacobsohn Eric, Avidan Michael S, Tymkew Heidi, Hill Laureen L, Zanaboni Paul B, Moazami Nader, Smith Jennifer R
Department of Anesthesiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
J Thorac Cardiovasc Surg. 2004 Apr;127(4):1058-67. doi: 10.1016/j.jtcvs.2003.11.035.
The purpose of this study was to describe our institutional experience in using inhaled prostacyclin as a selective pulmonary vasodilator in patients with pulmonary hypertension, refractory hypoxemia, and right heart dysfunction after cardiothoracic surgery.
Between February 2001 and March 2003, cardiothoracic surgical patients with pulmonary hypertension (mean pulmonary artery pressure >30 mm Hg or systolic pulmonary artery pressure >40 mm Hg), hypoxemia (PaO(2)/fraction of inspired oxygen <150 mm Hg), or right heart dysfunction (central venous pressure >16 mm Hg and cardiac index <2.2 L.min(-1).m(-2)) were prospectively administered inhaled prostacyclin at an initial concentration of 20,000 ng/mL and then weaned per protocol. Hemodynamic variables were measured before the initiation of inhaled prostacyclin, 30 to 60 minutes after initiation, and again 4 to 6 hours later.
One hundred twenty-six patients were enrolled during the study period. At both time points, inhaled prostacyclin significantly decreased the mean pulmonary artery pressure without altering the mean arterial pressure. The average length of time on inhaled prostacyclin was 45.6 hours. There were no adverse events attributable to inhaled prostacyclin. The average cost for inhaled prostacyclin was 150 US dollars per day. Compared with nitric oxide, which costs 3000 US dollars per day, the potential cost savings over this period were 681,686 US dollars.
Inhaled prostacyclin seems to be a safe and effective pulmonary vasodilator for cardiothoracic surgical patients with pulmonary hypertension, refractory hypoxemia, or right heart dysfunction. Overall, inhaled prostacyclin significantly decreases mean pulmonary artery pressures without altering the mean arterial pressure. Compared with nitric oxide, there is no special equipment required for administration or toxicity monitoring, and the cost savings are substantial.
本研究的目的是描述我们机构在心胸外科手术后肺动脉高压、难治性低氧血症和右心功能不全患者中使用吸入性前列环素作为选择性肺血管扩张剂的经验。
在2001年2月至2003年3月期间,对患有肺动脉高压(平均肺动脉压>30 mmHg或收缩期肺动脉压>40 mmHg)、低氧血症(动脉血氧分压/吸入氧分数<150 mmHg)或右心功能不全(中心静脉压>16 mmHg且心脏指数<2.2 L·min⁻¹·m⁻²)的心胸外科手术患者前瞻性地给予初始浓度为20,000 ng/mL的吸入性前列环素,然后根据方案逐渐减量。在开始吸入性前列环素之前、开始后30至60分钟以及4至6小时后再次测量血流动力学变量。
在研究期间共纳入126例患者。在两个时间点,吸入性前列环素均显著降低平均肺动脉压,而不改变平均动脉压。吸入性前列环素的平均使用时间为45.6小时。没有可归因于吸入性前列环素的不良事件。吸入性前列环素的平均费用为每天150美元。与每天花费3000美元的一氧化氮相比,在此期间潜在的成本节约为681,686美元。
吸入性前列环素似乎是治疗患有肺动脉高压、难治性低氧血症或右心功能不全的心胸外科手术患者的一种安全有效的肺血管扩张剂。总体而言,吸入性前列环素显著降低平均肺动脉压,而不改变平均动脉压。与一氧化氮相比,给药或毒性监测不需要特殊设备,并且成本节约显著。