胆道闭锁Kasai术后中医证候暨中药干预治疗的临床研究
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摘要
【研究目的】
     观察、分析胆道闭锁Kasai术后的中医证候分布规律,探讨胆道闭锁Kasai术后的中医病因病机及治疗法则;观察中医药干预治疗胆道闭锁Kasai术后的临床疗效。
     【研究方法】
     1.胆道闭锁中医证候研究:以面对面的调查方法收集胆道闭锁Kasai术后的临床资料,统计分析胆道闭锁Kasai术后的中医证候分布规律,分析可能的发病因素及其与证候的关系,进一步探讨道闭锁Kasai术后的中医病因病机及治疗法则。
     2.观察以健脾化湿、温阳活血法的中药治疗胆道闭锁Kasai术后患儿的中医证候积分、肝功能指标及身高体重、生活质量情况,以评价其临床疗效。
     【研究结果】
     1.胆道闭锁中医证候研究
     1.1胆道闭锁术后主要症状为:肝功能异常、黄疸、便溏、疲倦乏力、纳差、胁下肿块、腹胀膨隆等;舌质主要表现为舌质淡,或舌体胖有齿印;舌苔多见厚腻白苔,或有灰黑苔;指纹表现多为淡红、达气关,或淡滞兼见。
     1.2胆道闭锁术后与气血阴阳虚证的关系:胆道闭锁术后多有气虚表现,出现频率为90.2%,阳虚者次之,为46.3%,血虚及阴虚者较少。气虚证及阳虚证可以单独存在,亦可以与其它虚证相兼存在。相兼证中以气虚+阳虚最多,占31.8%。Logistic回归分析显示:手术次数为血虚证的影响因素,手术次数为2次的患儿多有血虚表现;胆管炎为血虚证、阴虚证的影响因素,有胆管炎发生者,阴虚证、血虚证的比例越大;性别、手术日龄为阳虚的影响因素,阳虚证中男孩占73.6%,比例明显高于女孩,手术日龄越小,阳虚证患儿比例越大。
     1.3胆道闭锁术后与五脏的关系:胆道闭锁术后有脾虚表现者最多,占92.7%,其中脾气虚证为主要证候,占58.5%,脾阳虚证占36.6%;肾虚表现者次之,肾气虚证占29.3%,肾阳虚证占21.9%;肺虚者第三,为17.1%。脾虚、肾虚可以单独存在,亦可以与其它虚证相兼存在。Logistic回归分析显示:过敏史是肺虚的影响因素,有过敏史患儿出现肺虚证的比例越大。就诊年龄为肺虚、肾虚的影响因素,就诊年龄越大,肾虚、肺虚证越多。
     1.4胆道闭锁术后与实证的关系:胆道闭锁术后实证41例均有湿邪,湿邪分寒湿、湿热,以寒湿为主,占85.4%,且多见有气滞、血瘀表现,分布占90.2%、90.2%。气滞证均与其他实证相兼出现,且以气滞+血瘀+寒湿证为主,占75.7%。各种实证广泛分布于气血阴阳虚证的各种组合中,并与脾、肾、肺虚证相兼并存。以脾虚(寒)湿困、气滞血瘀最多见,20例,占48.8%。Logistic回归分析显示:胆管炎为血瘀证的影响因素,有胆管炎发生者,血瘀证比例越大。
     1.5证候相关性:结果显示气血阴阳虚证、五脏虚证与实证相互相关、相互影响,使胆道闭锁术后的证候表现虚实兼夹、错综复杂。
     2.健脾化湿、温阳活血法治疗胆道闭锁Kasai术后的临床观察
     2.1中医证候积分观察:结果显示经健脾化湿、温阳活血法中药干预治疗后,胆道闭锁Kasai术后患儿的各主要症状均有较好的改善,且随着疗程的增加,各症状改善的有效率逐渐增加。其中黄疸改善最快,经第1个疗程后有效率已达56.25%,经3个疗程治疗后,黄疸消退有效率达100%;食欲、精神、大便情况经第2个疗程治疗后明显改善;腹胀、胁下肿块、青筋暴露等症状改善较慢,经第3疗程之后有效率明显提高。
     2.2胆道闭锁Kasai术后患儿中药治疗前后肝功能情况:结果显示经中药治疗1个疗程后,总胆红素TB、直接胆红素DB、胆汁酸TBA、谷丙转氨酶ALT、谷草转氨酶AST、谷氨酰转肽酶GGT即明显逐渐下降,随着疗程的增加,其中总胆红素TB、直接胆红素DB在第3个疗程后均已降至正常范围,胆汁酸TBA、谷丙转氨酶ALT、谷草转氨酶AST经3个疗程后接近正常范围。碱性磷酸酶ALP下降较慢,经中药治疗2个疗程后才显示较治疗前有统计学差异(p<0.05)。
     2.3胆道闭锁Kasai术后中药干预治疗后生长发育情况:16例胆道闭锁术后患儿经中药干预治疗后,除有2例身高较正常偏低、1例体重较正常偏低外,其余均生长发育良好,15例IBM指标均正常。
     2.4胆道闭锁Kasai术后中药干预治疗后生活质量评价情况:16例胆道闭锁术后经中药干预治疗后,除有2例因反复发生胆管炎,对生活评价质量为稍差外,其余评价生活质量为“很好”者4例,评价为“一般”者10例。绝大部分患儿能如正常儿童一样生活和学习,其中有7例3岁以上患儿已上幼儿园,1例11岁患儿在读小学,学习成绩优良。
     【研究结论】
     1.胆道闭锁Kasai术后中医证候特点为:虚证以脾气虚、脾肾阳虚多见,实证以气滞、寒湿、血瘀为主;各种证候相互相关、相互影响,常相兼出现,病性属虚实夹杂;其病位主要在肝胆、脾、肾、肺;主要病性要素为:湿、气虚、阳虚、气滞、血瘀;常见证型为:脾虚湿困、气滞血瘀;胆道闭锁Kasai术后的中医病因病机可概括为“湿、滞、瘀、虚”。
     2.健脾化湿、温阳活血法中药干预治疗可改善患儿的各主要症状及肝功能指标,从而进一步改善患儿的生长发育情况及生活质量。
Objective
     1.The objective of this research is to investigate the regularities of distribution on TCM syndrome of biliary atresia after Kasai operation, and further to discuss Chinese medicine cause and pathogenesis and therapy method about biliary atresia after Kasai operation.
     2. The objective of the research is also to observe the clinical effect of the treatment with traditional Chinese medicine to biliary atresia after Kasai operation.
     Method
     1. Study on TCM syndrome of biliary atresia after Kasai operation:Firstly, We collect the clinical data on TCM syndrome of biliary atresia after Kasai operation through the investigation method by face to face. Secondly, we analyse the regularities of distribution on TCM syndrome of biliary atresia after Kasai operation, and then according to the result we try to discuss the Chinese medicine cause and pathogenesis about the disease. Lastly, we advance some Chinese therapy method about biliary atresia after Kasai operation.
     2. We treat the children of biliary atresia after Kasai operation with Chinese medicine by tonifying spleen and resolving dampness, warming yang and invigorate the circulation of blood. And then we record the integral of TCM syndrome, the index of liver function, height and weight before and after the therapy with Chinese medicine. Lastly, we can estimate the clinical effect of the Chinese medicine used to treat the children of biliary atresia after Kasai operation.
     Result
     1. Study on TCM syndrome of biliary atresia after Kasai operation:The main syndrome of biliary atresia after Kasai operation is that:abnormal liver function、jaundice、loose stool、fatigue、poor diet、phyma below the costal region、enlarged abdomen, etc. The tongue manifestation is pale tongue, or corpulent tongue with casts of the teeth; and with white or grey tongue fur. The characteristic of TCM syndrome about biliary atresia after Kasai operation: asthenia syndrome is mamily from qi deficiency type, yang deficiency type and spleen deficiency type; sthenia-syndrome is mamily from Stagnation of Qi, Stagnation of Blood, Cold and Dampness type.These types of syndrome are interrelated and influenced each other, and will appear simultaneously. The nature of this disease is deficiency and excess interlaced each other. The location of disease can be in liver,gall, spleen, kidney or lung.The key element of the nature about this disease is dampness, blood stasis, stagnation of qi.The most common type of syndrome is spleen dysfunction due to dampness, qi and blood stasis. The Chinese medicine cause and pathogenesis about biliary atresia after Kasai operation can be summarized by "dampness、stagnate、stagnate、asthenia".
     2. Chinese medicine through tonifying spleen and resolving dampness,warming yang and invigorate the circulation of blood can alleviate the symptom and the index of liver function. And the the symptoms like jaundice, anorexia, weary and stool will be better faster, but the the symptoms like abdominal distension, phyma below the costal region, blue veins stand out on belly will be alleviated slowly. The index of liver function like total bilirubin, direct bilirubin have delined after the third course of treatment. The index of liver function like alkaline phosphatase(ALP) decreased moe slowly. Most of the children of biliary atresia after Kasai operation can grow and live like normal children.
     Conclusion
     1. The characteristic of TCM syndrome about biliary atresia after Kasai operation:asthenia syndrome is mamily from qi deficiency type, yang deficiency type and spleen deficiency type. Sthenia-syndrome is mamily from stagnation of qi, stagnation of blood, cold and dampness type.These types of syndrome are interrelated and influenced each other, and appear simultaneously. The nature of this disease is deficiency and excess interlaced each other. The location of this disease can be liver, gall, spleen, kidney or lung. The key element of the nature about this disease is dampness, blood stasis, stagnation of qi. The most common type of syndrome is spleen sysfunction due to sampness, qi and blood stasis. The Chinese medicine cause and pathogenesis about biliary atresia after Kasai operation can be summarized by "dampness、stagnate、stagnate、asthenia".
     2. Chinese medicine through tonifying spleen and resolving dampness, warming yang and invigorate the circulation of blood can alleviate the symptom and the index of liver function, and then improve thelevel of grouth and life quality.
引文
[1]Sokol RI, Mack C, Narkew cz MR, etal. Pathogenesis and outcome of biliary atresia:Current concepts. J Pediatr Gastroenterol Nutr,2003,37:4-21.
    [2]Perlmutter DH, Shephercl R. Extrahepatic biliary atresia:A disease or a phenoltype Hepatology,2002,35:1297-1304.
    [3]黄磊,魏明发.胆道闭锁的基因学研究进展.中华小儿外科杂志,2007,2:216~218.
    [3]Mack CL, Sokol RI. Unraveling the pathogenesis and etiology of biliary atresia Pediatr Res,2005,57:87-94.
    [4]Clotman F, Lannoy VJ, Reber M, et al. neonecut transcription actor HNF6 is required for normal development of the biliary tract. Development,2002,129: 1819-1828.
    [5]Bezerra JA, Taog, Ryckman FC, etal. Genetic induetion of proinflammatory immunity in children with biliary atresia Lancet.2002,23:1653-1659.
    [6]Choe BH, Kim KM, Kwon S, et al. The pattern of differentially expressed genes in biliary atresia. J Korean Med Sci,2003,18:392-396.
    [7]Leonhardt J, Stanulla M. Wasielewski R, et al. Gene expression profile of the infective murine model for biliary atresia. Pediatr Surg Int,2006,22: 84-89.
    [8]Paul K,Tam H.Cholangitis Mter Hepatic Portoentemstomy For Biliary Atresia: A Multivariate Analysis Of Risk Factors. J Pediatr,2003,142:566-571.
    [9]Peterson C, Biemanns D, Kuske M, et al. New aspects in a murine model for extrahepatic biliary atresia[J]. J Pediatr Surg,1997,32(8):1190-1195.
    [10]冯杰雄,李民驹,蔡挺,等.轮状病毒致新生鼠胆管损伤的机制.中华小儿外科杂志,2003,24(3):264-267.
    [11]马亚贞,汤绍涛,童强松.轮状病毒致胆道闭锁动物模型的建立.中华小儿外科杂志,2007,28(12):659-661.
    [12]冯杰雄.病毒感染与胆道闭锁的关系,实用儿科临床杂志,2007,22(12):1761-1763
    [13]孟庆娅,詹江华.胆道闭锁病因学研究进展.天津医药,2008,36(10):826-827.
    [14]万里飞,关智平,温德儒.先天性胆道闭锁患儿的维生素D代谢及佝偻病防治.儿科临床杂志,1996,14(6):384-386.
    [15]李桂生.胆道闭锁诊治现状与展望.临床外科杂志,2004,12(5):266.
    [16]Chen SM, ChangMH, Du JC, etal. Screening for biliary atresia by infant.2008, 12(5):66.
    [17]邓玉华,张明满.胆道闭锁最新进展.实用儿科临床杂志,2009,24(11):869-872.
    [18]刘钧澄,李桂生,司徒升,等.影响胆道闭锁早期诊治的原因分析.中华小儿外科杂志,2002,23(3):220-221.
    [19]陈文娟,何静波,胡原.超声检查在先天性胆道闭锁的诊断及鉴别中的应用价值.中国超声医学杂志,2006.22(12):932-934.
    [20]Nadel HR. Hepatobiliary scintingraphy in children[J]. Semin Nucl Med,1996,26(1):25-42.
    [21]Dillon PW, Owings E, Cilley R, et al. Immunosuppression as adjuvant therapy for biliary atresia. J Pediatr Surg,2001,36:80-85.
    [22]McKiernan PJ, Baker AJ, Lloyd C,etal. British paediatric surveillanceunitstudy of biliary atresia Qutcome at 13 years[J] J Pediatr Gastroenterol NutrJ 2009.48(1):78-81.
    [23]Wildhaber BE, Maino P, MayrJ, etal. B; iliary atresia Swiss national study 1994-2004[J]. Pediatr Gastroenterol NutrJ.2008,46(3):299-307.
    [24]SantosJL Yieling CO, Meurer L, etal. The extent of biliary proliferation in liverbiopsies from patients with biliary atresia at portoenterostomy is associated with the postoperative prognosis[J]J Pediatr Surg.2009,44(4): 695-701.
    [25]Lee H, Hirose S, Bratton B, et al. Initial experience with complex laparoscopic biliary surgery in children:Biliary atresia and choledochal cyst. Pediatr Surg,2004,39:804-807.
    [26]Fouquet V, Alves A, Branchereau S, etal. Long-term outcome of pediatric liver transplantation for biliary atresia:A 10-year follow-up in a single center. Liver Transpl,2005,11:152-160.
    [27]李栋林,徐晓活.活体肝移植治疗100例胆道闭锁症患儿的长期随访报告.中华移植杂志(电子版),2007,1(1):59.
    [28]古维李.小儿活体肝移植的现状.实用儿科临床杂志,2003,18:510-513.
    [29]张金哲.小儿胆道闭锁与移植.实用儿科临床杂志,2003,18:501.
    [30]郑珊.胆道闭锁的治疗现状.实用儿科临床杂志,2007,22(23):1767-1768.
    [31]冯大军.胆道闭锁肝门空肠吻合术后早期胆管炎的防治.硕士学位论文,20070525.
    [32]李桂生.胆道闭锁诊治现状与展望.临床外科杂志,2004,12(5):266.
    [33]Davenport M. Biliary atresia. Semin Pediatr Surg,2005,14(1):42-48.
    [28]刘钧澄,李桂生,钟思陶.胆道闭锁葛西手术后肝脏病理变化.中华小儿外科杂志,1994,15(6):332-334.
    [34]Petersen C, Bruns E, Kuske M, et al. Treatment of extrahepatic biliary atresia with interferon-alpha in a murine infectious model. Pediatr Res,1997,42:623-628.
    [35]Hsieh CS, Huang CC, Huang LT, et al. Glucocorticoid treatment downregulate chemokine expression of BA cterial cholangitis in cholestatic rats. J Pediatr Surg,2004,39:10-15.
    [36]Petersen C, Biermanns D, Kuske M, et al. New aspects in a murine model for extrahepatic biliary atresia. J Pediatr Surg 1997,32:1190-1195.
    [37]Ohi R. Surgery for biliary atresia. Liver,2001,21(3):175-182.
    [38]朱坚,韩天权.胆道闭锁患儿Kasai术后远期预后研究.临床小儿外科杂志,2005,4(6):401-402.
    [39]ShinkaiM Qhhama Y. Take H, etal. Long term outcome of children with biliary atresia who were not transplanted after the Kasai operation> 20 year experience at a children's hospital[J]. Pediatr Gastroenterol Nutr.2009,48 (1):443-450.
    [40]Hung PY, Chen CC, Chen WJ, etal. Long term prognosis of patients with biliary atresia a 25 year summary[J]. J Pediatr Gastroenterol Nutr, J 2006,42(2):190-195.
    [41]Kuroda T, Saeki M, Moriakawa N, etal. Management of adult biliary atresia patients. Should hardwork and pregnancy be discouraged[J]Pediatr Surg,2007,42(12):2106-2109.
    [42]彭春辉,陈亚军.胆道闭锁Kasai手术预后的影响因素.实用儿科临床杂志,2010,25(23):1835-1838
    [43]柯礼业,韩树堂,黄疸的中医证治沿革.中医学报,2010,3(2):356-358.
    [44]姜德友,韩洁茹,黄疸病源流考,中华中医药学刊,2009,27(1):16-18.
    [45]陈兆洋.黄疸病机从瘀论探析,广西中医药,2010,24(3):39-40.
    [45]陈兆洋.黄疸病机从瘀论探析,广西中医药,2010,24(3):39-40.
    [46]汪承柏.凉血活血通腑利胆对重度黄疸肝炎的退黄作用机制的探讨.中医杂志,1986;27(4):31.
    [47]唐智敏,余绍源.浅议中医对黄疸病的认识及其辨治大法.湖北中医杂志,2001,23(8):15-16.
    [48]金庆丰.中西医结合治疗肝硬变476例.北京中医杂志,1991(3):25-27.
    [49]胡军勇,陈金亮.肝纤维化的中医病机和治法探讨.时珍国医国.2008,19(2): 134-136
    [51]唐智敏,茹清静,张振鄂.肝血瘀阻与肝纤维化关系的临床研究.中国中西医结合杂志,1997,17(2):81-89.
    [52]宋家武,李绍白,张文英.血府逐瘀汤抗大鼠肝纤维化作用的研究.中西医结合肝病杂志,1997,7(1):38-40.
    [53]孙克伟,褚裕义,陈翔,等.大黄(庶虫)虫丸抗大鼠免疫性肝纤维化研究.中西医结合肝病杂志,1997,7(1):90-92.
    [54]北京中医医院编.关幼波临床经验选[M].北京:人民卫生出版社,1979,127-1541.
    [55]王伯祥.中医肝胆病学,北京:中国医药科技出版社,1993,629-6311.
    [56]王暴魁,谢宁,姜德友,等.张琪治疗肝炎后肝硬化经验.中医杂志,1996,37(4):202-2031.
    [57]王伯祥.中医肝胆病学,北京:中国医药科技出版社,1993,619-6211.
    [58]卢方,吴允华.中西医结合治疗肝硬化腹水56例.辽宁中医杂志,1998,25(7):319-3201.
    [59]郭福定,周俊.辨证分型治疗肝硬化浅识.实用中医内科杂志,2006,20(2):1411.
    [60]张琴,刘平.肝硬化黄疸中医证型研究.中西医结合肝病杂志2001,11(3):139-141.
    [61]卢良威,娄国强.肝纤维化的证治规律研究,浙江中医学院学报,2004,28(4):94-95.
    [62]刘路明,邓淑玲,辛俊平.肝硬化中医证型研究及其临床意义.中国热带医学,2007,7(4):658-660
    [63]王继,陈俊红,李兵顺,等.活血、益气、软坚不同中医治则逆转大鼠肝纤维化的实验观察.中国中医基础学杂志,2006.12(6):420-422.
    [64]卢良威,张永生.活血渗湿法抗肝纤维化探究.浙江中医学院学报,2000,24(1):9-10.
    [65]黄彬,周大桥.软肝冲剂治疗肝纤维化的临床研究.新中医,2000,32(10)34-35.
    [66]刘平,胡义杨,徐列明.肝硬化“虚损生积”病机理论溯源及其临床意义.中国实验方剂学杂志,1997,3(4):20-25.
    [67]王拥泽,杨宏志,杨沛华.川芎嗪抗肝纤维化作用机制研究.河北中医药学报,2006,21(3):8-9.
    [68]陈在忠,王红.川芎嗪抗肝纤维化作用的实验研究.中西医结合肝病杂志,2007,7(3):156-158.
    [69]郭一民,曾英坚.清热祛湿解毒法全程干预对慢性乙型肝炎肝纤维化的影响.江苏中医药,2009,41(9):27-28.
    [70]周晴,杨悦娅.张云鹏解毒为先治疗肝病的临证思辨特点.辽宁中医杂志.2010, 37(7): 1216-1218.
    [71]李卓玲,李西坡,尚勇.调肝解毒丸治疗慢性肝纤维化48例报告.甘肃中医,2006,19(6):19.
    [72]于世瀛,贲长恩,杨美娟.清热利湿方药抗肝纤维化的形态学和免疫组织化学定量研究.北京中医药大学学报,1997,20(10):28-32.
    [73]孙玉凤,姚希贤,崔东来.益肝煎剂抗肝纤维化的临床研究.河北中医,2002,24(11):808-810.
    [74]邝卫红.鳖甲煎汤抗肝纤维化的血清学研究.广州中医药大学报,2004,21(6):420-423.
    [75]刘光伟,王春芳,王灵台,等.补肾健脾法治疗慢性肝病理论探析.中医研究.2010,23(11):13-14.
    [76]史海立.赵庆华.从中医“治未病”谈肝硬化的防治.辽宁中医杂志.2009,35(8):1298-1299.
    [77]千叶庸夫.汉方方剂在胆道闭锁症术后的使用经验.日本东洋医学杂志,1993,43(5): 100.
    [78]千叶庸夫.胆道闭锁Kasai术后脾功能亢进的汉方治疗.日本东洋医学杂志,1997,47(5):845-849.
    [79]高荣慧编译.汉方在儿外科中的应用.国外医学中医中药分册,2003,25(4):217-218.
    [80]郭锦章.中医治验小儿先天性胆道闭锁.安徽中医学院学报,1984,(1):50-51.
    [81]黄磊,冯杰雄,魏明发.茵栀黄注射液在胆道闭锁患儿手术前后的辅助治疗效果.实用儿科临床杂志,2007,22(11):811-822.
    [82]姜之炎,姜永红,石李.益气祛瘀通络法治疗胆道闭锁Kasai术后20例临床观察.中国中医药信息杂志,2008,15(11):79-80.
    [83]姜之炎,郑珊,石李.胆闭通络方结合西药治疗胆道闭锁Kasai术后临床疗效观察.上海中医药杂志,2010,44(6):92-92.
    [84]柳静,陈芳,闫慧敏,等.胆道闭锁患儿术后的中药干预治疗.实用儿科临床杂志,2009,24(23):1838-1840.
    [85]赖东兰.许华教授治疗小儿胆道闭锁Kasai术后经验介绍.新中医,2011,43(5):172-173

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