de Oliveira Clark R M, Neto A Bakonyi, Bianchi E H, de Carvalho L R
Department of Surgery, Botucatu School of Medicine - Unesp, São Paulo State University, Botucatu - SP, Brazil.
Transplant Proc. 2010 Jan-Feb;42(1):87-91. doi: 10.1016/j.transproceed.2009.12.015.
We sought to establish an anesthetic protocol to evaluate the hemodynamic, metabolic, and electrolytic changes after graft reperfusion in pigs undergoing orthotopic intestinal transplant (ITx).
Fifteen pigs were distributed into two groups: GI (n = 6), without immunosuppression, and GII (n = 9), immunosuppressed before surgery with tacrolimus (0.3 mg/kg). The animals were premedicated at 1 hour before surgery with IM acepromazine (0.1 mg/kg), morphine (0.4 mg/kg), ketamine (10 mg/kg), and atropine (0.044 mg/kg IM). Anesthesia induction used equal proportions of diazepam and ketamine (0.1-0.15 mL/kg/IV) and for maintenance in IV infusion of xylazine (1 mg/mL), ketamine (2 mg/mL), and guaiacol glyceryl ether 5% (50 mg/mL), diluted in 250 mL of 5% glucose solution. In addition, recipient pigs were treated with isofluorane inhalation. Heart rate (HR), systolic (SAP), mean (MAP), and diastolic (DAP) arterial pressure, pulse oximetry, respiratory frequency (f), capnography, body temperature (T), blood gas analysis (pH, Paco(2), Pao(2), base excess, BE; Hco(3)(-), Sato(2)), serum potassium (K), calcium (Ca), sodium, hematocrit (Hct), and glucose (Glu) were measured at four times; M0: after incision (basal value); M1: 10 minutes before reperfusion; and M2 and M3: 10 and 20 minutes after graft reperfusion.
All groups behaved in a similar pattern. There was significant hypotension after graft reperfusion in GI and GII (M2 = 56.2 +/- 6.4 and M3 = 57.2 +/- 8.3 mm Hg and M2 = 65.7 +/- 10.2 and M3 = 67.8 +/- 16.8 mm Hg, respectively), accompanied by elevated HR. The ETco(2) was elevated at M2 (42 mm Hg) and M3 (40 mm Hg). Metabolic acidosis was observed after reperfusion, with significant increase in K levels.
The anesthetic protocol for donors and recipients was safe to perform the procedure, allowing control of hemodynamic and metabolic changes after reperfusion without differences regarding immunosuppression.
我们试图建立一种麻醉方案,以评估接受原位肠道移植(ITx)的猪在移植器官再灌注后的血流动力学、代谢和电解质变化。
15头猪被分为两组:GI组(n = 6),未进行免疫抑制;GII组(n = 9),术前用他克莫司(0.3 mg/kg)进行免疫抑制。动物在手术前1小时用肌肉注射乙酰丙嗪(0.1 mg/kg)、吗啡(0.4 mg/kg)、氯胺酮(10 mg/kg)和阿托品(0.044 mg/kg肌肉注射)进行术前用药。麻醉诱导使用等比例的地西泮和氯胺酮(0.1 - 0.15 mL/kg静脉注射),维持麻醉采用静脉输注稀释于250 mL 5%葡萄糖溶液中的赛拉嗪(1 mg/mL)、氯胺酮(2 mg/mL)和愈创甘油醚5%(50 mg/mL)。此外,受体猪采用异氟烷吸入治疗。在四个时间点测量心率(HR)、收缩压(SAP)、平均动脉压(MAP)和舒张压(DAP)、脉搏血氧饱和度、呼吸频率(f)、二氧化碳图、体温(T)、血气分析(pH、动脉血二氧化碳分压、动脉血氧分压、碱剩余、BE;碳酸氢根离子、氧饱和度)、血清钾(K)、钙(Ca)、钠、血细胞比容(Hct)和葡萄糖(Glu);M0:切开后(基础值);M1:再灌注前10分钟;M2和M3:移植器官再灌注后10分钟和20分钟。
所有组的表现模式相似。GI组和GII组在移植器官再灌注后均出现显著低血压(M2时分别为56.2 ± 6.4和M3时为57.2 ± 8.3 mmHg,M2时分别为65.7 ± 10.2和M3时为67.8 ± 16.8 mmHg),同时心率升高。呼气末二氧化碳分压(ETco₂)在M2(42 mmHg)和M3(40 mmHg)时升高。再灌注后观察到代谢性酸中毒,钾水平显著升高。
供体和受体的麻醉方案在实施该手术时是安全的,能够控制再灌注后的血流动力学和代谢变化,且在免疫抑制方面无差异。