冠状动脉旁路术同期瓣膜手术的体会

目的 介绍冠状动脉旁路术(CABG)同时行心脏瓣膜手术的体会。方法 45例患者,平均年龄59岁(42～75岁);心功能(NYHA)Ⅱ级7例、Ⅲ级30例、Ⅳ级8例;二尖瓣病变30例、主动脉病变7例、联合瓣膜病变8例,均伴有单支或多支冠状动脉病变。手术在中度低温体外循环下完成。心脏停跳后,先作静脉桥的远端吻合,然后置换瓣膜。心脏复苏后完成大隐静脉与升主动脉的吻合,或在升主动脉1次阻断下完成。乳内动脉的吻合在换瓣后心脏复苏前完成。本组6例行二尖瓣成形,31例行机械瓣置换,8例行进口生物瓣置换。结果 本组患者无手术死亡。术后呼吸机使用时间平均18．7h,ICU监护1．8d。住院时间平均9．2d。随访6个月～4年患者无死亡,心功能Ⅰ级35例、Ⅱ级10例。结论 冠状动脉旁路移植术同时行瓣膜手术是安全、有效的。     

成人小主动脉瓣环患者的心瓣膜置换术

目的总结成人小主动脉瓣环行心瓣膜置换术的临床经验，以提高手术效果。方法对26例成人小主动脉瓣环患者行人工机械瓣膜置换术，单纯主动脉瓣置换17例，二尖瓣、主动脉瓣双瓣膜置换9例。采用Manougnian法主动脉瓣环加宽7例，瓣膜侧倾缝合置换主动脉瓣膜6例，瓣环上主动脉瓣置换13例，在双瓣膜置换中均先置换主动脉瓣后再置换二尖瓣。结果26例患者中无手术死亡，术后随访时间6～48个月（12±3个月），心功能均明显改善（Ⅰ级10例、Ⅱ级16例），无远期死亡。术后主动脉瓣有效瓣口面积指数（EOAI）1．02～1．44cm^2／m^3（〉0．85cm^2／m^3），无瓣膜-患者不匹配现象（PPM）。结论主动脉瓣病变伴小主动脉瓣环的成人患者行心瓣膜置换，选择新型人工瓣膜行瓣环上主动脉瓣置换是理想的选择，瓣膜侧倾缝合是可选择的方法，二尖瓣、主动脉瓣双瓣膜置换时先置换主动脉瓣可降低手术操作难度，大部分患者无需行瓣环扩大术。     

缺血性二尖瓣关闭不全的外科治疗

目的总结缺血性二尖瓣关闭不全的外科治疗经验.方法 12例缺血性二尖瓣关闭不全患者,其中二尖瓣大量反流9例,中量反流3例,均有心肌梗死史,术前心功能Ⅱ级4例,Ⅲ级4例,Ⅳ级4例,均接受冠状动脉旁路移植术和同期保留二尖瓣和瓣下结构的二尖瓣置换术.结果 1例术后并发肺部感染死亡,其余患者均痊愈出院,出院时心功能为Ⅰ～Ⅱ级.随访3～59个月,无远期死亡,亦无抗凝和机械瓣膜引起的并发症,患者心功能仍为Ⅰ～Ⅱ级.术后早期超声心动图检查示左心室舒张期末内径和左心房舒张期末内径均较术前缩小(P<0.05).结论缺血性心脏病伴缺血性中至重度二尖瓣反流行冠状动脉旁路移植术加二尖瓣置换术疗效可靠.     

同期施行冠状动脉旁路移植术与心瓣膜手术

目的　为了提高同期施行冠状动脉旁路移植术 (CABG)与心瓣膜手术的疗效 ,降低死亡率 ,总结手术及围术期处理的经验。　方法　 2 4例患者中 ,二尖瓣病变 11例 ,主动脉瓣病变 3例 ,二尖瓣、主动脉瓣双瓣膜病变 10例。 1支冠状动脉病变 1例 ,2支 11例 ,3支 6例 ,另 6例为心瓣膜手术中发现左冠状动脉开口有阻塞 ,急症行 CABG。全组行二尖瓣成形术 2例 ,二尖瓣置换术 9例 ,主动脉瓣置换术 3例 ,二尖瓣、主动脉瓣双瓣膜置换术 10例 ;移植 1支血管 7例 ,2支 11例 ,3支 6例。　结果　术后早期 (30天内 )死亡 2例 ,分别死于低心排血量综合征和多器官功能衰竭。随访 2 2例 ,随访时间 8个月～ 7年 ,晚期死亡 1例 ,其余 2 1例心功能明显改善 ,心功能 (NYHA分级 ) 级 15例 , 级 5例 , 级 1例 ,心绞痛消失 7例。　结论　冠状动脉粥样硬化性心脏病和心脏瓣膜疾病并存时 ,应同期施行CABG和心瓣膜手术 ,彻底纠正心脏病变。术中加强心肌保护 ,尽量缩短心肌缺血时间 ;术后妥善处理心、肾等器官功能衰竭 ,是提高手术疗效的重要措施     

胸腔镜下二尖瓣生物瓣置换术32例分析

目的探讨胸腔镜下二尖瓣生物瓣置换的经验,评价其临床效果。方法回顾性分析2013年3～12月在广东省人民医院心血管外科行胸腔镜下二尖瓣生物瓣置换术32例患者的临床资料。其中男14例、女18例,年龄19～80（55.6±17.3）岁,体重37～78（55.7±9.7）kg,体表面积1.30～1.95（1.67±0.16）m^2;合并心房颤动5例,术前心功能分级（NYHA）Ⅱ级20例,Ⅲ级11例,Ⅳ级1例;二尖瓣风湿性病变16例,二尖瓣退行性病变11例,感染性心内膜炎4例,合并先天性心脏病1例。结果所有患者均行胸腔镜下二尖瓣生物瓣置换术,其中采用Medtronic HancockⅡ人工生物瓣27例,Medtronic Mosaic生物瓣5例。同期行三尖瓣成形术13例,房间隔缺损修补术1例。全组患者住院期间无死亡,均顺利出院,住院期间未并发低心排血量综合征及左心室破裂。术后复查心脏彩色超声心动图提示,所有患者人工二尖瓣功能良好,无瓣周漏发生。术后患者心功能较术前明显改善,心功能恢复至Ⅰ级9例,Ⅱ级17例,Ⅲ级6例。术后早期及术后3个月左心房内径及左心室舒张期末内径与术前相比均明显减小。而术后早期及术后3个月左心室射血分数（LVEF）与术前相比有所降低。结论胸腔镜下二尖瓣生物瓣置换术创伤小,并发症少,安全可行,使用特殊类型生物瓣可明显减小手术切口大小。     

全保留二尖瓣及瓣下结构在重症二尖瓣关闭不全患者二尖瓣置换术中的应用

目的探讨全保留二尖瓣及瓣下结构在重症二尖瓣关闭不全患者二尖瓣置换术中的应用经验,评价其临床效果。方法回顾性分析2011年6月至2013年1月在广东省人民医院心血管外科因重症二尖瓣关闭不全行全保留二尖瓣及瓣下结构二尖瓣置换术17例患者的临床资料,其中男14例,女3例;年龄38~82（63.41±11.82）岁;合并心房颤动13例;术前纽约心脏学会（NYHA）心功能分级Ⅲ级5例,Ⅳ级12例;缺血性二尖瓣关闭不全7例,退行性二尖瓣关闭不全9例,风湿性二尖瓣关闭不全1例。结果所有患者均行全保留二尖瓣及瓣下结构的二尖瓣置换术,同期行冠状动脉旁路移植术4例;其中生物瓣11例,机械瓣6例。全组患者住院期间无死亡,均顺利出院,住院期间未并发低心排血量综合征,无左心室破裂。17例患者均随访,随访时间2~25（16.44±5.02）个月。随访期间1例患者因术后2个月发生二尖瓣重度瓣周漏死亡。其余患者人工二尖瓣功能良好,无抗凝和瓣膜引起的并发症,心功能较术前明显改善,心功能NYHA分级恢复至Ⅰ级11例,Ⅱ级4例,Ⅲ级1例。术后早期及随访期间心胸比率、左心房内径、左心室舒张期末内径及收缩期末内径与术前相比均明显减小。而术后早期左心室射血分数（LVEF）与术前相比有所降低[（50.94%±8.78%）vs.（55.31%±10.44%）,P=0.04],术前LVEF与随访期间的差异无统计学意义[（55.31%±10.44%）vs.（56.13%±9.67%）,P=0.73],随访期间LVEF与术后早期相比显著增加[（56.13%±9.67%）vs.（50.94%±8.78%）,P=0.02]。术后早期与随访期间人工二尖瓣压力减半时间（PHT）差异无统计学意义[（95.06±19.00）ms vs.（94.56±19.19）ms,P=0.91]。结论全保留二尖瓣及瓣下结构在重症二尖瓣关闭不全患者二尖瓣置换术中应用安全有效,可以改善左心室重构及术后心功能。     

非缺血性心脏瓣膜疾病合并冠心病同期手术治疗的临床分析

目的 总结非缺血性心脏瓣膜疾病合并冠心病同期手术患者的临床特征和手术效果,以提高手术疗效. 方法 2000年1月至2007年6月同期手术治疗105例非缺血性心脏瓣膜疾病合并冠心病患者,年龄36～79岁(61.96±7.61岁),其中风湿性心瓣膜疾病59例,退行性二尖瓣病变24例,老年性钙化性主动脉瓣病变13例;其它主动脉瓣病变9例.术前行冠状动脉造影明确诊断98例,术中探查发现冠心病7例.全组均行冠状动脉旁路移植术,共移植血管216支(2.06支/例),同期行二尖瓣置换术36例,二尖瓣成形术15例,主动脉瓣置换术43例,双瓣膜置换术11例. 结果 术后住院死亡6例(5.7%,6/105).死于严重低心排血量3例,肾功能衰竭2例,术后心脏骤停并发多器官功能衰竭1例.术后随访93例,随访时间1个月至7年,失访6例.无晚期死亡患者.心功能分级(NYHA)Ⅰ级25例,Ⅱ级53例,Ⅲ级10例,Ⅳ级5例.1例患者活动后仍有心绞痛存在. 结论 非缺血性心脏瓣膜疾病合并冠心病患者绝大多数无典型的心绞痛症状,50岁以上的患者必须行冠状动脉造影检查,对有冠心病易患因素者,应积极作冠状动脉造影检查;冠心病所致的心肌缺血可明显加重心脏瓣膜疾病所引起的心肌损害,术中心肌保护尤为重要;正确评价术前左心功能低下的患者是选择手术治疗的难点,更是影响手术效果的关键因素.     

左心房折叠术在二尖瓣病变合并巨大左心房治疗中的应用

目的探讨左心房折叠术治疗二尖瓣病变合并巨大左心房的临床应用效果.方法回顾性分析23例收缩末期左心房内径为(129±37)mm (92～250 mm)、行左心房折叠术的二尖瓣手术患者的临床资料.22例选用人工机械瓣膜置换,1例为生物瓣置换,同期行左心房折叠术.术前心功能NYHA分级,Ⅲ级15例,Ⅳ级8例;术前心胸比为0.79±0.10.单纯二尖瓣置换术18例,其中行三尖瓣成形术10例;双瓣膜置换和三尖瓣成形术5例,其中二次手术2例, 术中行心房纤颤射频消融术2例.结果术后低心排出量综合征3例(13%),呼吸衰竭2例(9%).早期死亡3例(13%),其中2例为低心排出量综合征、1例为脑梗死.术后失访2例,术后1年意外死亡1例,平均随访(44±39)个月,17例生存患者心功能Ⅰ级14例、Ⅱ级3例;术后心胸比为0.68±0.11,较术前明显缩小(t=3.80,P=0.000).结论在瓣膜病手术的同时对巨大左心房症行左心房折叠术,可减少术后并发症,术后效果良好.     

二尖瓣脱垂合并感染性心内膜炎的临床分析

目的总结二尖瓣脱垂（mitral valve prolapse,MVP）合并感染性心内膜炎（infeclous endoearditis,IE）的临床特点、手术时机和手术前后超声心动图的特点。方法2000年6月至2007年12月我科共收治原发性MVP合并IE患者45例,术前心功能分级（NYHA）Ⅱ级15例,Ⅲ级21例,Ⅳ级9例。术前血培养阳性率为40％,最常见的为草绿色链球菌（38．9％）。术前超声心动图检查发现腱索断裂3例,急性左心功能衰竭9例,有脑血管意外6例。术中根据瓣膜质量和损伤情况,行二尖瓣成形术5例,二尖瓣置换术35例;同期行主动脉瓣置换术6例,三尖瓣成形术19例,冠状动脉旁路移植术1例。结果术前死亡5例,3例死于脑血管意外,2例死于多器官功能衰竭;术后早期死亡1例,死于肾功能衰竭;长期生存39例,术后随访6个月～8年（平均2．7年）,无晚期死亡,超声心动图复查未见心内膜炎复发及瓣周漏。结论MVP合并IE的临床特点为起病隐匿,心力衰竭、体循环栓塞（尤其脑栓塞）等并发症的发生率较高。对中至重度关闭不全的MVP合并IE患者应早期治疗。     

CABG同期瓣膜置换的外科治疗

目的总结瓣膜置换术同期冠状动脉旁路移植在新疆地区的应用经验。方法1995年4月～2004年4月对402例冠心病行外科治疗，其中对62例瓣膜置换术同期冠状动脉旁路移植(CABG)。双瓣置换10例，单瓣置换术52例；其中二尖瓣成形术2例。结果随访62例，10d～9年无早、远期死亡，无抗凝所致并发症发生。结论CABG与瓣膜置换同期进行是安全有效的外科手段，在新疆地区进一步开展对挽救此类重症患者生命是积极有效的方法。     

Celiac Disease and Metabolic Bone Disease

Celiac disease is a common autoimmune gastrointestinal disorder affecting multiple organs, precipitated in genetically vulnerable persons by the ingestion of gluten. Gluten is poorly digested and is presented to the intestinal mucosa as a large polypeptide. Binding to human leukocyte antigen-DQ2 and human leukocyte antigen-DQ8 molecules on antigen-presenting cells stimulates cellular and humeral immune reactions. Although common serological tests are available to diagnose celiac disease, the diagnosis of celiac disease is often delayed or missed because of lack of recognition as the disease presentation in adults is highly variable and may be asymptomatic. Celiac disease is a common secondary cause of metabolic bone disease and delayed treatment with gluten-free diet affects bone mineral density and fracture risk, so it is crucial to diagnose and treat celiac disease promptly. In this article, we will review recent studies of celiac disease in adults and provide practical, easily accessible information for busy clinicians.     

Joint Disease in End-Stage Renal Disease

The joint diseases that are encountered in chronic dialysis have been reviewed. There are two general categories: de novo disease and arthropathy anteceding ESRD. The de novo joint diseases include categories that are probably the direct result of ESRD. Microcrystalline CaOHapatite and CaPPD arthritis is associated with hyperparathyroidism and a high Ca X P. Aluminum phosphate joint disease is the result of aluminum toxicity. Both types have severe disease of the adjacent bone: osteitis fibrosa with CaOHapatite-CaPPD arthropathy and osteomalacia with aluminum phosphate. Calcium oxalate joint disease probably results from renal oxalate retention in ESRD and conversion of ascorbate to oxalate. The evidence for uric acid arthropathy in the absence of primary gout or lead toxicity is not convincing. Amyloid is the most frequent cause of the carpal tunnel syndrome and is related to retention of β-2 microglobulin. Infective arthritis may be Seen, often occumng as a result of bacteremia from an infected fistula site. A degenerative arthritis different from osteoarthritis has also been described. Pathologic fractures can occur with both amyloid deposition in bone and aluminum osteomalacia. Long-term steroid therapy can lead to avascular necrosis of femoral or humeral heads. Diabetes mellitus with neuropathy can give rise to a very destructive Charcot joint. Tendon ruptures occur, but the mechanism is obscure.
It is most important that the nephrologist work closely with the rheumatologist. Carefbl and sophis ticated examination of synovial fluid and tissue is mandatory in the microcrystalling diseases. Immunohistochemical methods may be required, particularly for tissue removed during decompression of the median nerve. Together the subspecialists can establish the diagnosis and determine the appropriate therapy for the iarge number of joint disorders to which the dialysis patient is subject.     

Joint Disease in End-Stage Renal Disease

The joint diseases that are encountered in chronic dialysis have been reviewed. There are two general categories: de novo disease and arthropathy anteceding ESRD. The de novo joint diseases include categories that are probably the direct result of ESRD. Microcrystalline CaOHapatite and CaPPD arthritis is associated with hyperparathyroidism and a high Ca X P. Aluminum phosphate joint disease is the result of aluminum toxicity. Both types have severe disease of the adjacent bone: osteitis fibrosa with CaOHapatite-CaPPD arthropathy and osteomalacia with aluminum phosphate. Calcium oxalate joint disease probably results from renal oxalate retention in ESRD and conversion of ascorbate to oxalate. The evidence for uric acid arthropathy in the absence of primary gout or lead toxicity is not convincing. Amyloid is the most frequent cause of the carpal tunnel syndrome and is related to retention of β-2 microglobulin. Infective arthritis may be Seen, often occumng as a result of bacteremia from an infected fistula site. A degenerative arthritis different from osteoarthritis has also been described. Pathologic fractures can occur with both amyloid deposition in bone and aluminum osteomalacia. Long-term steroid therapy can lead to avascular necrosis of femoral or humeral heads. Diabetes mellitus with neuropathy can give rise to a very destructive Charcot joint. Tendon ruptures occur, but the mechanism is obscure. It is most important that the nephrologist work closely with the rheumatologist. Carefbl and sophis ticated examination of synovial fluid and tissue is mandatory in the microcrystalling diseases. Immunohistochemical methods may be required, particularly for tissue removed during decompression of the median nerve. Together the subspecialists can establish the diagnosis and determine the appropriate therapy for the iarge number of joint disorders to which the dialysis patient is subject.     

Simultaneous Development of Dieterich Disease and Freiberg Disease

Dieterich disease is an uncommon arthropathy of the hand, with few studies published. This lesion shares a similar etiopathogenesis with Freiberg disease, although the association of both conditions has only been described once. We report a 65-year-old man consulting for inflammatory pain in his right hand of 1 month's duration and also in his right foot of 4 months' duration. The rheumatology department was consulted to rule out systemic disease because the synovitis had occurred simultaneously in 2 different locations. The plain radiography and magnetic resonance imaging findings supported the diagnosis of Dieterich disease and Freiberg disease, although only increased uptake was found on scintigraphy in the affected zones. Few studies have been published about Dieterich disease, most in case report form. To our knowledge, only 1 study has described the association of Dieterich disease and Freiberg disease. Surgical treatment has been described when conservative management is unsuccessful, with multiple techniques used. The present case is the first in which Dieterich disease and Freiberg disease manifested simultaneously in the initial painful inflammatory phase.     

Castleman病

Castleman病（Castleman disease,CD）亦称巨大淋巴结增生症,是一种少见的淋巴组织增生性疾病。由Castleman等在1954年首次以病理现象报道,1956年定义。1972年Keller等首次描述其浆细胞分型,1978年Gaba等报道了首例多中心型CD。临床上分为局灶型（localize Castleman disease,LCD）与多中心型（multicentric Castleman disease,MCD）。CD临床表现复杂,影像学亦无特异性表现,若临床医生缺乏对CD的认识,很难早期发现并诊断,甚至漏诊、误诊。治疗亦需根据临床及病理分型区别对待。