Heslet Lars, Nielsen Jorn Dalsgaard, Levi Marcel, Sengeløv Henrik, Johansson Pär I
Department of Intensive Care ITA 4131, University Hospital of Copenhagen, Rigshospitalet, Blegdamsvej 9, DK 2100 Denmark.
Crit Care. 2006;10(6):R177. doi: 10.1186/cc5132.
Diffuse alveolar hemorrhage (DAH) is a serious pulmonary complication seen in patients with autoimmune disorders and patients treated with chemotherapy or after hematopoietic stem cell transplantation. The clinical management of DAH is complex and the condition has a high mortality rate. Tissue factor is expressed in the lung alveoli during inflammation and therefore pulmonary administration of human recombinant activated factor VIIa (rFVIIa) could be a rational treatment option.
Six patients with acute, bronchoscopically confirmed DAH from a single intensive care unit university hospital center were included in the study of acute DAH in critically ill patients. The patients were treated with intrapulmonary administration of 50 microg/kg rFVIIa in 50 ml of sodium chloride by bronchoalveolar lavage (BAL) with 25 ml in each of the main bronchi, which was repeated after 24 hours in case of treatment failure.
An excellent response, defined as complete and sustained hemostasis after a single dose of rFVIIa, was seen in three patients. A good response, meaning that sustained hemostasis was achieved by a repeated rFVIIa administration, was seen in the remaining three patients. In one of these patients, the BAL treatment was repeated twice; in another patient, the second dose of rFVIIa was administered by nebulizer after extubation after the initial BAL. The hemostatic effect was statistically significant (p = 0.031). The oxygenation capacity, as reflected by the PaO2/FiO2 (arterial oxygen pressure/inspiratory fractional oxygen content) ratio, increased significantly (p = 0.024) in all six patients following the local rFVIIa therapy.
Symptomatic therapy of DAH after intrapulmonary administration of one or more doses of rFVIIa was found to have a good to excellent hemostatic effect in six consecutive patients with DAH. The intrapulmonary administration of rFVIIa seemed to have a high benefit-to-risk ratio. Larger series should confirm the safety of this approach.
弥漫性肺泡出血(DAH)是自身免疫性疾病患者以及接受化疗或造血干细胞移植后的患者中出现的一种严重肺部并发症。DAH的临床管理较为复杂,且该病症死亡率较高。炎症期间肺组织中会表达组织因子,因此肺部给予人重组活化因子VIIa(rFVIIa)可能是一种合理的治疗选择。
来自一家大学医院重症监护病房的6例经支气管镜确诊为急性DAH的患者被纳入重症患者急性DAH的研究。患者通过支气管肺泡灌洗(BAL)在50ml氯化钠中肺内给予50μg/kg rFVIIa,每个主支气管注入25ml,若治疗失败则在24小时后重复。
3例患者出现良好反应,定义为单次给予rFVIIa后实现完全且持续的止血。其余3例患者出现较好反应,即通过重复给予rFVIIa实现持续止血。其中1例患者BAL治疗重复了两次;另1例患者在初次BAL后拔管时通过雾化器给予第二剂rFVIIa。止血效果具有统计学意义(p = 0.031)。局部rFVIIa治疗后,所有6例患者的氧合能力(以PaO2/FiO2(动脉血氧分压/吸入氧分数)比值反映)显著提高(p = 0.024)。
在连续6例DAH患者中,肺内给予一剂或多剂rFVIIa后进行DAH的对症治疗被发现具有良好至优异的止血效果。肺内给予rFVIIa似乎具有较高的效益风险比。更大规模的系列研究应证实该方法的安全性。