Coimbra Raul, Razuk-Filho Alvaro, Yada-Langui Margareth M, Rocha-E-Silva Mauricio
Division of Trauma, Department of Surgery, University of California San Diego School of Medicine, San Diego, California 92103-8896, USA.
Anesth Analg. 2004 May;98(5):1439-46, table of contents. doi: 10.1213/01.ane.0000111106.98535.fd.
The role of pentoxifylline (PTX) as a resuscitation adjunct in hemorrhagic shock is unclear. PTX infusion into the pulmonary artery and its effects on cardiac performance and oxygen utilization have not been defined. We hypothesized that pulmonary PTX is superior to systemic PTX or lactated Ringer's (LR) solution alone. The effects of LR solution, systemic PTX, and pulmonary PTX on cardiac performance and oxygen utilization in a hemorrhagic shock model in dogs were compared. Animals were bled to a mean arterial blood pressure (MAP) of 40 mm Hg maintained for 30 min and randomized into 3 resuscitation groups: LR solution (2x shed blood), systemic PTX (10 mg/kg bolus i.v.) in addition to LR solution (2x shed blood) + PTX (5 mg/kg for 45 min i.v.), and pulmonary PTX (10 mg/kg bolus + 5 mg/kg for 45 min via a pulmonary artery catheter) plus LR solution (2x shed blood, i.v.). Arterial blood gases, hemoglobin levels, MAP, cardiac index, systemic vascular resistance index, pulmonary vascular resistance index, oxygen delivery, oxygen consumption, and oxygen extraction ratio (O(2)ER) were measured serially. No differences in blood loss, hemoglobin, and MAP were observed. Pulmonary PTX increased cardiac index to levels more than baseline (P = 0.012) and decreased systemic vascular resistance index and pulmonary vascular resistance index to levels less than baseline (P < 0.0001). Pulmonary PTX increased oxygen delivery and oxygen consumption to baseline levels. Postresuscitation O(2)ER levels in LR-treated animals remained more than baseline (P < 0.0001). Systemic and pulmonary PTX significantly decreased O(2)ER compared with shock levels. PTX resuscitation is superior compared with LR solution alone. Intraarterial pulmonary PTX administration is safe, and improves cardiac performance as well as O(2) utilization.
This study shows that a novel route (via the pulmonary circulation) used to administer pentoxifylline after hemorrhagic shock leads to superior cardiac performance in comparison with administration via lactated Ringer's solution or i.v. systemic pentoxifylline.
己酮可可碱(PTX)作为出血性休克复苏辅助药物的作用尚不清楚。向肺动脉输注PTX及其对心脏功能和氧利用的影响尚未明确。我们假设肺动脉内给予PTX优于全身给予PTX或单独使用乳酸林格氏液(LR)。比较了LR溶液、全身PTX和肺动脉PTX对犬出血性休克模型心脏功能和氧利用的影响。将动物放血至平均动脉血压(MAP)为40mmHg并维持30分钟,然后随机分为3个复苏组:LR溶液(2倍失血量)、除LR溶液(2倍失血量)外的全身PTX(静脉推注10mg/kg)+PTX(静脉输注5mg/kg,持续45分钟),以及肺动脉PTX(通过肺动脉导管静脉推注10mg/kg+持续45分钟静脉输注5mg/kg)加LR溶液(2倍失血量,静脉输注)。连续测量动脉血气、血红蛋白水平、MAP、心脏指数、全身血管阻力指数、肺血管阻力指数、氧输送、氧消耗和氧摄取率(O₂ER)。在失血量、血红蛋白和MAP方面未观察到差异。肺动脉PTX使心脏指数增加至高于基线水平(P = 0.012),并使全身血管阻力指数和肺血管阻力指数降低至低于基线水平(P < 0.0001)。肺动脉PTX使氧输送和氧消耗增加至基线水平。LR治疗动物复苏后的O₂ER水平仍高于基线(P < 0.0001)。与休克水平相比,全身和肺动脉PTX显著降低了O₂ER。PTX复苏优于单独使用LR溶液。动脉内肺动脉给予PTX是安全的,并可改善心脏功能以及氧利用。
本研究表明,与通过乳酸林格氏液或静脉全身给予己酮可可碱相比,出血性休克后通过一种新途径(经肺循环)给予己酮可可碱可导致更好的心脏功能。