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非转流下原位肝移植术中患者氧代谢的变化

时间:2010-08-24 11:35:34  来源:  作者:

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Changes in oxygen metabolism during orthotopic liver transplantation without venovenous bypass

黄素琴 祝胜美 吴健 何慧梁 陈益忠 冯智英 陈庆廉

HUANG SuqinZHU ShengmeiWU Jianet al.Department of AnesthesiaFirst Affiliated HospitalMedical CollegeZhejiang UniversityHangzhou 310003China

 

Abstract

  ObjectiveTo investigate the changes in oxygen metabolism during orthotopic liver transplantationOLRwithout venovenous bypass since dramatic circulatory changes may take place during operation.

  MethodsTwentyone patients with endstage liver disease18 males3 femalesaged 2061 yrs weighing 4486 kg undergoing OLT without venous bypass under general anesthesia were enroUed in this study.SG catheter was placed in the pulmonary artery via right internaljugular vein and both right and left radial artery were cannated. ECGSp02Prr C02 and nasopharyngeal temperature were continuously monitored during surgery. Anesthesia Was induced with midazolam 0.1 mg/kgetomidate 0.20.3 mg/kgfentanyl 510 μg/kg and vecuronium 0.080.1 mg/kgAfter tracheal intubation anesthesia Was maintained with isoflurane inhalation0.5%-1.0%)and continuous infusion of propofol at 24 mg/kg/h supplemented with intermittent i.v.boluses of midazolamfentanyl and vecuronium.A 14F nasogastric TRIPNGS tube was inserted in the stomach for measurement of gastric mucosal pH pHi.Blood samples were taken from radial and pulmonary artery for blood gas unalysis. Hemodynam icparametersblod gasesarterial and mixed venous and Psc02 were recorded and oxygen delivery DO2),oxygen consumptionVO2and pHi were calculated at 30 min after inductionT0baseline),when inferior vena cava and portal vein were clampedT1),5 min after unclam ping of inferior verla cava and portal veinT2),90 min after graft reperfusionT3and at the end of operationT4.

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  ResultsDO2 was significantly decreased at T1 while VO2 was significantly increased at T4 compared to baseline T0)(P<0.O1 or 0.05.PgCO2 and PgaC02 were both significantly increased at T12 and pHi and pHa were both significandy decreased at T14 compared to baselineP<O.05 or O.01.

  ConclusionThere are significant changes in oxygen metabolism and gastric mucosal pH during OLT without VenoVenous bypass and hemodynamicmonitoring is mandatory.

  Key wordsLiver transplantationOxygen consumptionGastric mucosa. 

 

  终末期肝病患者多伴随术前肝功能失代偿,以及由此导致的一系列的病理生理改变,而且原位肝移植手术复杂、出血多、时间长、内环境和循环系统变化急剧,可能导致机体组织的氧代谢障碍。本研究拟观察终末期肝病患者非转流下原位肝移植术中氧代谢的变化。

 

资料和方法

  拟行肝移植术的终末期肝病患者21例,男18例,女3例,年龄2061岁,体重4486kg。其中原发性肝癌6例,重症肝炎6例,肝炎后肝硬化7例,肝囊肿1例,胆汁性肝硬化1例。肝功能child C级的有12例,伴肝肾综合征4例,肝肺综合征2例,上消化道出血1例。入室后开放三条粗大(16号套管针)外周静脉。连接DatexOhmeda多功能监测仪连续监测心电图、脉搏氧饱和度、呼气末二氧化碳分压和鼻咽温度。麻醉诱导前行双侧桡动脉穿刺置管分别用于采动脉血样和监测动压脉。经右颈内静脉穿刺放入7F SwanGanz漂浮导管(Arrow公司,美国),持续有创监测平均动脉压(MAP)、肺动脉平均压(PAP)、中心静脉压(CVP)和肺毛细血管嵌锲压(PCWP)。静脉注射咪唑安定0.1 mg/kg1、依托咪酯0.20.3 mg/kg1、芬太尼510μg/kg1和维库溴铵0.080.1 mg/kg1 行全麻诱导,气管插管后间断吸入0.5%~1.0%异氟醚,异丙酚24 mg/kg1 /h1持续微泵输注,咪唑安定、芬太尼、维库溴铵间断静脉推注维持麻醉。麻醉诱导后经鼻向胃内置入14F TRIPNGS导管(Tonometries,美国)连接胃二氧化碳张力仪(DatexOhmeda,美国)测胃粘膜二氧化碳分压(PgCO2)。分别在全麻诱导后30 minT0)、门静脉阻断即刻(T1)、门静脉开放后5 minT2)、门静脉开放后90 minT3)、关腹时(T4)记录心率(HR)、MAPPAPCVPPCWP,同时行桡动脉和肺动脉血气分析,用热稀释法测定相应时点的心输出量(CO)。计算心脏指数(CI)、心搏量指数(SVI)、外周血管总阻力指数(SVRI)、肺血管总阻力指数(PVRI)、氧供(DO2)、氧耗(VO2)、氧供指数(DO2I)、氧耗指数(VO2I)、氧摄取率(ERO2)和PgCO2,根据HendersonHasselbalch[1]公式计算出胃粘膜内pH值(pHi)和胃粘膜与动脉血二氧化碳分压差(PgaCO2)。术中持续微泵输注多巴胺(2μg/kg1 /min1),门静脉阻断前开始持续微泵输注肾上腺素,同时在门静脉阻断和开放即刻均静脉注射肾上腺素,以维持收缩压在90 mill Hg1 kPa7.5 mm Hg)以上。

  统计学处理 计量资料以均数±标准差(x±s)表示,采用SPSS 11.0软件包进行分析,组内比较采用双因素方差分析,P<0.05为差异有显著性。

 

结 果

  与T0比较,T14HR增快(P<0 01),T1MAPCVPPCWPPAPCOCISVI下降,SVRI升高(P<0.050.01),T2PAPPCWPCOCI上升(P<0.05),T3MAPSVI下降(P<0.05),T1DO2DO2I下降,ERO2增高(P<0.01),T4VO2VO2I增加(P<0.05),T1 pHi下降(P<0.01),T1T2PgCO2PgaCO2均增高(P<0.050.01)。见表1

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讨 论

  原位肝移植术患者病情危重,手术操作复杂,术中有大量的血液丢失和相应的容量置换,采用非转流术式时,无肝期内脏器官及下肢淤血。门静脉和下腔静脉开放后,肝脏和其它内脏器官再灌注可导致血液动力学不稳定,引起全身和局部组织氧代谢异常。在本研究中血液动力学表现为无肝期SVICOCICVPPAPPAWP急剧下降,这是由于回心血量急剧减少所致。同时,HRSVRI增加,MAP基本保持稳定,这与使用肾上腺素有关;f1静脉和下腔静脉开放后,CO和各压力指标均增加,这是由于回心血量骤增所致。随着时间推移血液动力学状态逐渐得到改善并与无肝前期相近。Carmichael[2]等的研究结果与本研究的一致。

  DO2VO2作为全身组织氧代谢监测的指标,可作为评价危重患者机体功能改善的重要标志[34],被认为是肝移植术中一个重要的监测指标[56]

  本研究显示,门静脉和下腔静脉阻断即刻DO2显著下降。这是由于回心血量减少和CO降低的结果。由于无肝期全身VO2并不减少[27],因此ERO2增加,以保证有充足的氧维持重要器官的有氧代谢。本组患者在门静脉阻断前即开始持续应用肾上腺素,使HR明显增快,MAP维持相对稳定,在一定程度上阻止了DO2的过度降低,使得门腔静脉阻断对全身的影响降低。门静脉开放后的Do2基本恢复至无肝前期水平,是CO增加和血液动力学改善的结果。新肝后期(关腹时)随着新肝血流的再灌注和肝功能的逐渐恢复,以及原来在无肝期因缺血、淤血而处于低灌注、低氧代谢的组织器官血供恢复后有氧代谢增强,导致了氧耗量增加。

  DO2VO2作为机体氧代谢监测的指标,反映的是全身微循环和氧代谢状态。Steib[8]观察到肝移植时尽管维持足够的全身DO2和灌注压,仍存在组织氧合受损的情况。胃肠粘膜是缺氧时最容易和最先被累及的部位,因而pHi值是较敏感的局部组织氧代谢指标,能够及时反映内脏器官灌注及氧合状态,有助于较早的发现内脏微循环灌注不足及缺氧。本研究发现无肝期的PgCO2升高、pHi下降,其原因是门腔静脉阻断导致胃肠道血流减少、局部粘膜缺血缺氧;新肝期PsCO2PgaCO2迅速恢复至无肝前期水平但,phi仍较低,提示胃肠粘膜仍存在代谢性酸中毒。其可能与以下因素有关:尽管门静脉开放后D02VO2已恢复至无肝前期水平,但胃肠道血流分布不均仍存在[9];无肝期胃肠道形成的氧债的偿还有一个过程;肾上腺素使内脏血流减少,对组织氧合产生不利影响[1011]Welte[9]的研究结果与此一致。

  综上所述,非转流下原位肝移植术患者无肝期后存在明显氧代谢障碍,其对手术预后的影响值得进一步研究。

 

参考文献

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2. Carmichael FJLindop MJFarman JV.Anesthasia for hepatic transplantationcardiovascular and metablic alteration and their management.Anesth Analg198564108116.

3. Lugo GArizpe DDominguez Get a1.Relationship between oxygen consumption and oxygen delivery during anesthesia in highrisk patients.Crit Care Med1993216469.

4. Shibutani KKomatsu TKubal Ket al.Critical level of oxygen delivery in anesthetized man.Crit Care Med198311640643.

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5. Steltzer HHiesmayr MTuchy G. et al. Perioperative liver graft functionthe role of oxygen transport and utilization. Anesth Analg199376574579.

6. 黄文起,黑子青,汪凡,等.原位肝移植术围术期机体组织氧供氧耗的变化.中华麻醉学杂志,200020588590.

7. Leach RMTreacher DF.The pulmonary physician in critical care.2oxygen delivery and consumption in the critically il1.Thorax200257170177.

8. Steib AFreys GGohard Ret al.Tissue oxygenation during liver transplantation.Crit Care Med199220977983.

9. Welte M Pichler BGroh Jet a1.Perioperative mucosal pH and splanchnlc endotoxin concentration in orthotopic liver transplantation.Br J anaesth .1996.769098.

10. Silva EDeBaeker DCreteur Jet a1.Efects of vasoactive drugs on gastric intramucosal pH.Crit Care Med19982617491758.

11. Meier Hellmann AReinhart KBredle DLet al.Epinephrine impairs splanchnic perfusion in septic shock.Crit Care Med199725399404.

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