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研究结果显示心脏手术并发症与基因缺陷有关
发表:(2006-02-04 05:41);  最后修改:2006-05-17 08:48;  栏目:[临床进展]
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武汉协和医院日前公布了一项历时4年的研究结果:心脏手术后出现的水肿、器官功能衰竭等并发症,是由于患者缺失C4A基因所致,而向缺失者输入含有这种基因的血浆,可大大降低并发症的发生。

  据该院麻醉科教授张诗海介绍,在很多心脏手术中,都需要给患者建立血液体外循环系统,即让机器代替心脏工作。但这会引发部分患者术后严重并发症——毛细血管渗漏综合征,即患者血管中的水分渗透到血管之外,使得患者出现水肿、器官功能衰竭,甚至导致死亡。

  协和医院研究发现,所有发生毛细血管渗漏综合征的患者,其体内均缺失一种叫C4A的人体免疫基因。由于大部分人都拥有该基因,研究者大胆推想,把含有这种基因的血浆输送到缺失患者体内。医院在2001年至2005年就诊的3000多名心脏病患者中,挑选出116名有基因缺陷患者,并将其分为两组,一组在术前补充含有这种基因的血浆,另一组不补充。结果没有补充的一组100%出现并发症,而后者仅2人出现并发症,约占3.4%。

  这一成果已被世界医学权威杂志——英国的《柳叶刀》刊登,并引起世界医学界的关注。由于操作简单,这一方法已运用于临床,100多位患者已从中受益,为患者节省了约三分之一的医疗费用。

Lancet. 2005 Aug 13-19;366(9485):556-62.

Capillary leak syndrome in children with C4A-deficiency undergoing cardiac surgery with cardiopulmonary bypass: a double-blind, randomised controlled study.

Zhang S, Wang S, Li Q, Yao S, Zeng B, Ziegelstein RC, Hu Q.

Department of Anaesthesiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China.


BACKGROUND: Capillary leak syndrome is a life-threatening complication after cardiopulmonary bypass (CPB), with an incidence of about 4-37% in children worldwide. On the basis of previous results, we undertook a randomised controlled study to investigate the priming with plasma rich in the C4A isotype of complement component 4 on the incidence of capillary leak syndrome in children with C4A deficiency. METHODS: In a hospital in Wuhan, China, we randomly assigned 116 neonates, infants, and children lacking complement component C4A to receive C4A-free or C4A-rich plasma priming (n=58 each, 20 mL/kg). The primary outcome was capillary leak syndrome, identified as an increased transvascular escape rate of Evans blue dye from plasma. Concentrations of activated complement components C4 and C3, inflammatory mediators interleukin 6, interleukin 8, tumour necrosis factor (TNF) alpha, plasma protein, and PaO2/F(I)O2 ratios (ratio of the partial arterial pressure of oxygen to the fractional concentration of oxygen in inspired air) were measured before and 4 h after CPB. Analysis was by intention to treat. FINDINGS: Three (5%) patients given C4A-rich plasma priming had capillary leak syndrome compared with 56 (97%) given C4A-free plasma (p<0.0001). At 4 h after CPB, activated C4, interleukin 6, interleukin 8, and TNFalpha concentrations were higher, whereas PaO2/F(I)O2 ratios and plasma protein concentrations were significantly lower in the C4A-free group than changes in the C4A-rich group. Activated C3 rose equally in both groups. Activated C4 significantly correlated with interleukin 6, interleukin 8, and TNFalpha concentrations; PaO2/F(I)O2 ratios; and the escape rate of Evans blue dye at 4 h after CPB. Two patients in the C4A-free group died of respiratory and renal failure on day 3 after CPB. INTERPRETATION: In paediatric patients with C4A deficiency, C4A-rich plasma priming reduces the incidence of CPB-related capillary leak syndrome by blocking the activated C4 increase and attenuating the systemic inflammatory response after CPB.
 
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