成人主动脉缩窄的临床特点和外科矫正

目的探讨成人主动脉缩窄的临床特点和外科治疗方法。方法40例成人主动脉缩窄患者行手术矫治，其中心脏不停跳手术28例，常规体外循环下手术12例。行主动脉狭窄段切开、人工血管补片扩大术12例，人工血管置换术15例，锁骨下动脉降主动脉旁路移植术1例，采用人工血管行胸一腹主动脉旁路移植术9例，经心包后径路行升主动脉一降主动脉旁路移植术3例。结果全组无手术死亡，几种术式术后均无脑部和脊髓等神经系统并发症。术后36例得到随访，平均随访12个月。36例患者上、下肢血压差均小于10mmHg（1kPa－7．5mmHg）。超声心动图和超高速CT检查提示人工血管血流通畅，无假性动脉瘤形成。结论成人主动脉缩窄的外科术式有多种选择，掌握好手术适应证，根据患者的具体病理生理状况选择合适的手术方式可获得满意的治疗效果。     

非体外循环下成人复杂型主动脉缩窄的解剖矫治

目的为提高成人复杂型主动脉缩窄的矫治效果,探讨其最佳外科治疗策略。方法回顾性分析北京阜外心血管病医院2005年1月至2008年12月在非体外循环下一期解剖矫治7例成人复杂型主动脉缩窄患者的临床资料,其中男5例,女2例;年龄16~41岁,平均年龄24.4岁。合并主动脉弓发育不良2例,主动脉弓部动脉瘤1例,胸降主动脉瘤3例（其中合并B型主动脉夹层1例）,主动脉缩窄手术后再狭窄1例。全组患者术前均通过彩色超声心动图、CT或磁共振成像确诊。均在全身麻醉常温非体外循环下手术,手术入路为胸骨正中切口1例,左后外侧切口6例;解剖矫治为：主动脉弓补片加宽4例,降主动脉人工血管置换3例（其中1例同期行腹主动脉置换,1例B型主动脉夹层同期植入支架象鼻）。结果全组无手术死亡,无严重手术并发症。随访7例,随访时间6~49个月,平均随访20.1个月,无远期死亡,无主动脉缩窄复发二次手术患者。有1例术后出现声音嘶哑,随访11个月时声音嘶哑未改善。结论非体外循环下对成人复杂型主动脉缩窄行一期解剖矫治是安全可行的,近、远期效果良好。     

升主动脉-降主动脉心包内旁路术治疗成人主动脉缩窄及主动脉弓中断合并心脏畸形的临床分析

目的探讨经正中切口行升主动脉-降主动脉心包内旁路术治疗成人主动脉缩窄及主动脉弓中断合并心脏畸形的技术要点。方法 2010年4月至2015年1月2例成人主动脉缩窄和1例成人主动脉弓中断合并心脏畸形患者行手术治疗,其中男2例,女1例;年龄35.6(27~46)岁。患者的疾病包括先天性主动脉弓缩窄、二尖瓣前叶脱垂伴中度关闭不全1例,先天性主动脉瓣二瓣化畸形伴主动脉瓣重度关闭不全、升主动脉瘤及主动脉弓缩窄1例,先天性主动脉瓣二瓣化畸形伴主动脉瓣轻度狭窄、房间隔缺损(继发孔)及主动脉弓中断(A型)1例。患者均在升主动脉及股动脉,上下腔静脉插管建立体外循环,经正中切口行升主动脉-降主动脉心包内旁路术及合并心脏畸形矫治手术。结果本组无围术期死亡病例,术后患者症状明显好转,出院随访2~59个月,除1例患者仍有上肢高血压需服用药物控制外,其他患者血压恢复到正常水平,术后下肢乏力症状消失。主动脉CTA检查示人工血管通畅,无人工血管扭曲压缩及假性动脉瘤形成等并发症。结论经正中切口行升主动脉-降主动脉心包内旁路术治疗成人主动脉缩窄及主动脉弓中断,同时行合并心脏畸形矫治的一期手术,患者手术安全及疗效确切,临床可选择性应用。     

正中切口解剖外旁路移植术一期治疗主动脉缩窄合并心脏畸形

目的总结正中切口解剖外旁路移植术一期治疗主动脉缩窄合并心脏畸形的外科治疗经验,以提高手术疗效。方法1997年7月至2008年7月,采用正中切口解剖外旁路移植术一期治疗主动脉缩窄合并心脏畸形31例,其中男20例,女11例;年龄31．9±11．7岁。合并的心脏畸形包括：主动脉瓣狭窄或关闭不全22例,二尖瓣狭窄或关闭不全9例,动脉导管未闭5例,升主动脉瘤4例,室间隔缺损3例,冠心病2例。解剖外旁路移植术包括升主动脉-腹主动脉旁路移植术22例,升主动脉-心包后降主动脉旁路移植术9例。同期手术包括主动脉瓣置换术16例,主动脉根部置换术6例,二尖瓣成形或置换术9例,升主动脉置换或成形术4例,动脉导管未闭缝合术5例,室间隔缺损修补术3例,冠状动脉旁路移植术2例。结果住院死亡1例（3．2％）,术后39d死于感染性中毒性休克。术后上、下肢收缩压压差较术前明显下降（13．7±10．2mmHg vs．64．2±25．3mmHg,P〈0．05）。随访27例,随访时间4～73个月,无晚期死亡、与人工血管相关的并发症和再次手术患者。结论正中切口解剖外旁路移植术是一期治疗成人及青少年主动脉缩窄合并心脏畸形的一种安全有效的手术方法。升主动脉腹主动脉旁路移植术及升主动脉-心包后降主动脉旁路移植术均可获得满意疗效。     

升主动脉-降主动脉人工血管旁路移植术在复杂主动脉缩窄中的应用5例

目的探讨正中开胸行升主动脉-降动脉人工血管旁路移植术治疗复杂主动脉缩窄的手术细节。方法 5例复杂型主动脉缩窄患者正中开胸行升主动脉-降主动脉旁路手术,其中4例行膈肌上吻合(其中1例经左心缘路径,3例经右心缘路径),1例行膈肌下吻合。分别观察术后上下肢压差及并发症情况。结果 5例患者均无死亡,术后上下肢压差均降低至20 mmHg以下,恢复可,术后并发症包括咳嗽1例及黑朦2例。结论正中开胸行升主动脉-降动脉人工血管旁路移植术治疗主动脉缩窄效果可,但手术细节对术后并发症的影响仍需进一步研究。     

升主动脉至胸降主动脉人工血管转流在主动脉缩窄外科治疗中的应用

目的：分析总结使用升主动脉至胸降主动脉人工血管转流术治疗成人型主动脉缩窄10例临床病例资料,探讨升主动脉至胸降主动脉人工血管转流术在临床中治疗主动脉缩窄的意义。方法中国医学科学院、北京协和医院心脏外科2006年1月-2015年12月共收治成人主动脉缩窄患者10例,其中男性患者7例,女性患者3例,年龄14~35岁,中位年龄27岁,其中1例合并主动脉瓣二瓣畸形及主动脉根部瘤样扩张,余均为单纯主动脉缩窄。10例患者静息情况下测量上下肢压差均大于20 mmHg (1 mmHg=0.133 kPa),术前评估无明确手术禁忌。10例均在体外循环下行升主动脉至胸降主动脉人工血管转流术,合并主动脉瓣二瓣畸形及主动脉根部扩张的患者,同时行Bentall术。结果无围术期死亡及大出血、脊髓缺血性损害等严重并发症,嘱托患者出院后3~6个月门诊复查,复测上下肢压差均小于20 mmHg,CTA结果提示未见动脉瘤、人工血管血栓形成等表现。结论利用人工血管从升主动脉转流至降主动脉是治疗胸主动脉缩窄的有效方法。     

停循环技术应用于升主动脉-胸降主动脉人工血管旁路移植治疗主动脉缩窄

目的总结经单一胸部正中切口采用低温停循环技术行解剖外升主动脉-胸降主动脉人工血管旁路移植术治疗主动脉缩窄的经验。方法回顾性分析2009年12月至2018年5月我院连续12例主动脉缩窄患者的临床资料。其中男女各6例,年龄13～42岁,均有高血压症状,上下肢动脉收缩压差46～85(57.1±16.8)mm Hg。手术经胸部正中切口,采用体外循环及深低温停循环技术,行升主动脉-心包后胸降主动脉人工血管旁路移植术。结果人工血管平均直径14～20(17.2±1.8)mm,体外循环时间69～197(115.9±40.6)min,主动脉阻断时间41～142(69.8±30.7)min,深低温停循环时间9～27(16.8±4.1)min。所有患者均未输血,无严重并发症。术后上下肢动脉收缩压差值为–12～22(14.3±4.8)mm Hg,较术前显著下降(P0.01)。所有患者均康复出院,平均随访3～91(41.9±21.5)个月,随访期间仅1例患者术后需要服用1种降压药物,其余患者均正常。结论深低温停循环下经胸部切口行解剖外人工血管旁路移植术治疗主动脉缩窄安全有效,未来需要更多病例进一步验证。     

降主动脉-升主动脉吻合术矫治婴儿期主动脉缩窄合并心内畸形15例

目的探讨降主动脉-升主动脉吻合术治疗婴儿期主动脉缩窄合并主动脉弓发育不良及心内畸形的疗效。方法选取2011-05—2015-05间治疗的主动脉缩窄合并主动脉弓发育不良、心内畸形的患儿15例。患儿均采用胸骨正中切口、开胸后先游离出主动脉弓、头臂干、动脉导管、弓降部等血管。建立体外循环、选择性脑灌注下行降主动脉-升主动脉端侧吻合术,恢复全身灌注后完成心内畸形的矫治。体外循环时间86~132 min,主动脉阻断时间51~94 min。结果术后早期死亡2例,低心排出量综合征6例,室上性心动过速6例,肺炎7例。13例患儿随访2个月~3 a,无死亡及再次主动脉狭窄。结论降主动脉-升主动脉吻合术治疗婴儿期主动脉缩窄合并主动脉弓发育不良及心内畸形的临床效果满意。     

常温非体外循环下全胸腹主动脉替换术

目的 总结常温非体外循环下全胸腹主动脉替换术(total thoracoabdominal aortic aneurysm repair,tTAAAR)的手术方式和早期治疗效果.方法 2009年2月至2010年12月,共完成41例全胸腹主动脉替换术,其中27例CrawfordⅡ型胸腹主动脉瘤(thoracoabdominal aortic aneurysm,TAAA)患者接受常温非体外循环tTAAAR治疗.男18例,女9例;平均年龄(41.85 ±10.11)岁.手术经左侧胸腹联合切口、腹膜外入路,常温非体外循环下建立降主动脉→双侧髂动脉旁路循环,然后采用分段阻断法,重建T6～T12肋间动脉及内脏血管.结果 所有患者均完成手术,降主动脉阻断(13.78 ±3.77) min.脊髓缺血( 19.19±3.93) min,内脏缺血(25.19 ±5.88) min.1例患者术中死亡,其余患者均生存.术后永久性脊髓损伤2例,呼吸系统并发症3例.结论 中国全胸腹主动脉瘤患者应早期积极治疗,常温非体外循环下的全胸腹主动脉替换术是一种安全、有效的治疗策略.     

升主动脉粥样硬化患者的冠状动脉旁路移植

目的 总结冠状动脉粥样硬化性心脏病合并升主动脉粥样硬化患者冠状动脉旁路移植手术的特点。方法 22例患者中,13例采用非体外循环、心脏不停跳下冠状动脉旁路移植术(59％);9例采用低温体外循环(41％),其中5例在深低温、低流量并间断停循环条件下不阻断升主动脉行旁路-升主动脉近端吻合。结果 20例康复出院,术后早期死亡2例;并发症有肺部感染、心绞痛、室颤、急性心肌梗死和血胸,无神经系统并发症。结论 减少术中升主动脉操作是防止升主动脉损伤和减少并发症的关键。应用带蒂动脉旁路、旁路远端序贯吻合和近端Y形吻合可避免或减少旁路-升主动脉吻合;低温体外循环加左心室引流时,可不阻断升主动脉行旁路远端吻合;深低温、低流量并间断停循环下行旁路-升主动脉吻合,可避免阻断和部分阻断升主动脉,利于控制并发症。     

主动脉缩窄的诊断和外科矫正

外科矫正主动脉缩窄２１例。术前漏诊３例。手术分别在浅低温、左心转流、体外循环或常温下进行，共采用８种术式。结果：ｌ８例术后上、下肢压差消失。２１例均痊愈出院，随访１～８年，仅２例成年病人仍有高血压。结论：上肢高血压而下肢低血压或存在差异性发绀者应疑诊本病。病人应于学龄前接受手术。多数可常温阻断主动脉行矫正术，术后应药物控制高血压。     

Hypothermic circulatory arrest does not increase the risk of ascending thoracic aortic aneurysm resection.

OBJECTIVE: The purpose of this study was to investigate the safety and efficacy of a period of deep hypothermic circulatory arrest (DHCA) during elective replacement of the ascending thoracic aorta. SUMMARY BACKGROUND DATA: DHCA has been implemented in ascending thoracic aortic aneurysm resection whenever the anatomy or pathology of the aorta or arch vessels prevents safe or adequate cross-clamping. Profound hypothermia and retrograde cerebral perfusion have been shown to be neurologically protective during ascending aortic replacement under circulatory arrest. METHODS: The authors conducted a retrospective analysis of 91 consecutive patients who underwent repair of chronic ascending thoracic aortic aneurysms from 1986 to present. The authors hypothesized that patients undergoing DHCA with or without retrograde cerebral perfusion during aneurysm repair were at no greater operative risk than patients who received aneurysm resection while on standard cardiopulmonary bypass. RESULTS: There were no significant differences in hospital mortality, stroke rate, or operative morbidity between patients repaired on DHCA when compared to those repaired on cardiopulmonary bypass. CONCLUSIONS: DHCA with or without retrograde cerebral perfusion does not result in increased morbidity or mortality during the resection of ascending thoracic aortic aneurysms. In fact, this technique may prevent damage to the arch vessels in select cases and avoid the possible complications associated with cross-clamping a friable or atherosclerotic aorta.     

The use of pulmonary autograft patch for type A aortic interruption and Swiss-cheese ventricular septal defect (VSD)

The surgical management of the aortic arch pathologies is controversial. Primary anastomosis and patch aortoplasties combined with end-to-end anastomosis have some complications like recurrence and aneurysm formation. Surgical repair of apical muscular (Swiss-cheese) defects is also still under debate. A 6-year-old patient with diagnosis of type A aortic arch interruption and Swiss-cheese ventricular septal defect (VSD) underwent successful intracardiac repair and aortic arch reconstruction. Aortic arch reconstruction was done by end-to-side anastomosis of distal aortic archus and thoracic aorta without cardiopulmonary bypass. The anterior side of the anastomosis was augmented by using pulmonary autograft patch and this patch was extended to the inferior surface of the archus aorta. Swiss-cheese VSD was repaired with a single patch using septal obliteration technique via transatrial approach. Pulmonary autograft patch aortoplasty and end-to-side anastomosis may be an alternative surgical management for surgical repair and it may be done without the need for cardiopulmonary bypass. In these patients associated multiple apical muscular VSDs can be repaired with a single patch, septal obliteration technique.     

主-肺动脉间隔缺损的外科治疗

目的探讨主肺动脉间隔缺损的外科治疗。方法１９８３年１月至１９９６年１２月间,手术治疗主肺动脉间隔缺损患者５例,其中男２例,女３例;年龄６～３４岁（平均１７４岁）。按Ｍｏｒｉ分型：Ⅰ型２例,Ⅱ型２例,Ⅲ型１例。缺损直径１０～３０ｃｍ。手术均在全身麻醉、中度低温、体外循环下进行。３例经肺动脉切口,２例经主动脉切口,以绦纶毡片修补。结果５例均痊愈出院,术后随访１０个月～１２年,情况良好。结论本病确诊后应尽早手术,手术方法宜采用体外循环下修补,主动脉切口优于肺动脉切口,以补片修补可防止大血管腔狭窄及术后再通     

Mitral valve replacement with the beating heart technique in a patient with previous bypass graft from ascending to descending aorta due to aortic coarctation

BACKGROUND AND AIM: Conventional mitral valve replacement (MVR) is carried out under cardioplegic arrest with cross-clamping of the ascending aorta during cardiopulmonary bypass. In this case, MVR was performed with on-pump beating heart technique without cross-clamping the aorta because of the diffuse adhesion around the ascending aorta, and tube graft presence between ascending and descending aortas. METHODS: A 47-year-old female patient had aorto-aortic bypass graft from ascending aorta to descending aorta with median sternotomy and left thoracotomy in single stage because of aortic coarctation 2 years ago in our cardiac center. She was admitted to the hospital with palpitation and dyspnea on mild exertion. Transthoracic echocardiography revealed 4th degree mitral insufficiency. RESULTS: MVR was carried out through remedian sternotomy with on-pump beating heart technique without cross-clamping the aorta. CONCLUSIONS: MVR with on-pump beating heart technique offers a safe approach when excessive dissection is required to place cross-clamp on the ascending aorta.     

Primary repair of traumatic aortic rupture: a preferred approach.

Eighty patients with traumatic rupture of the thoracic aorta were treated. Seven patients died during the initial resuscitation. Forty-three patients underwent surgical repair using the clamp-and-sew technique; 14 patients had a heparin-bonded shunt placed, and 16 patients were repaired using cardiopulmonary bypass. An interposition Dacron graft was used in only 19 patients (26%). The last 32 consecutive patients underwent primary repair of the ruptured aorta. Overall mortality was 19.2% (14 of 80); 9 of 14 patients (64%) had laparotomies along with the aortic repair, and 13 of 14 patients (92%) had three or more associated major injuries. Paraplegia occurred in four cases (5.6%). Traumatic aortic rupture remains a difficult surgical problem. Primary repair, without graft interposition, is the preferred technique and can be accomplished even when the two aortic ends have retracted several centimeters.     

Surgical management of aortopulmonary window.

OBJECTIVE: Aortopulmonary window is a rare congenital malformation involving a window-like communication between the ascending aorta and the pulmonary artery. Here, we present our experience regarding the surgical repair of an aortopulmonary window, and also assess the long-term outcome. METHODS: Thirteen children with an aortopulmonary window associated with various congenital lesions underwent a repair of the defect. The age at operation ranged from 3 days to 1 year (median age, 19 days). The patient's weight ranged from 2.1 to 7.0 kg (mean weight, 3.6 kg). The associated lesions included an interrupted aortic arch (5 patients), a ventricular septal defect (2), an atrial septal defect (1), mitral valve regurgitation (1), and tricuspid atresia [Ic] with mitral valve regurgitation (1). The aortopulmonary window was repaired with a cardiopulmonary bypass in 11 patients, and 2 patients were ligated without a cardiopulmonary bypass. RESULTS: One patient associated with tricuspid atresia died (mortality rate of 7.7%). There has been no late death during a mean follow-up of 7 years and 3 months. CONCLUSIONS: The surgical results for an aortopulmonary window are encouraging, even if such patients are associated with major cardiac anomalies and an interrupted aortic arch. Most have shown a good long-term outcome.     

Nonpenetrating trauma to the thoracic aorta

Twenty-seven patients underwent surgical repair for nonpenetrating injuries of the thoracic aorta. Emergency operation was performed in 19 patients with acute aortic injury and there were 12 survivors. Left heart bypass (LHB), external shunts, and simple aortic cross-clamping were methods employed during repair. All operative deaths occurred in the left heart bypass group. Morbidity, hospital stay, operative time, and blood loss all were markedly less in patients repaired with an external shunt or simple cross-clamping. Systemic heparinization related adversely to mortality and morbidity. Eight patients had repair of chronic post-traumatic descending aortic aneurysms. One of these had previous repair elsewhere with paraplegia and subsequent mycotic aneurysm at the graft repair site. He presented to us with massive hemoptysis. Surgical correction in the chronic group was performed using either left heart bypass, external shunt, or simple aortic cross-clamp with graft interposition. The only death occurred in a patient repaired on left heart bypass.     

婴幼儿室间隔缺损合并动脉导管未闭的外科治疗

目的　探讨婴幼儿室间隔缺损 (VSD)合并动脉导管未闭 (PDA)的外科治疗经验。方法　回顾性分析 44例VSD伴PDA婴幼病儿的临床特征、手术过程、围术期处理与转归。结果　婴幼儿VSD合并PDA者易早期产生重度肺动脉高压和心功能不全。手术死亡 2例 ,病死率 4 5 %。结论　VSD伴PDA婴幼病儿宜在 1岁前手术治疗 ,PDA可根据病情分期或一期手术 ,PDA恰当处理与术后转归关系密切 ,术后呼吸功能不全是死亡的主要原因。围术期应注意心功能保护 ,加强呼吸道管理及营养支持 ,预防和治疗肺动脉高压危象。     

Anatomically positioned aorta ascending-descending bypass grafting via left posterolateral thoracotomy for reoperation of aortic coarctation.

OBJECTIVE: Operation for aortic recoarctation and/or residual hypoplastic arch represents a surgical challenge because of surrounding scar tissue in the coarctation area, hazard of spinal cord ischemia due to aortic cross-clamping, laceration of the recurrent nerve, and the choice of the best approach. We demonstrate the first results of an anatomically guided technique via the prior left thoracotomy approach without establishment of cardiopulmonary bypass. METHODS: Since 1989, five patients underwent anatomically positioned ascending-descending bypass grafting for treatment of recoarctation. Indication was a non-dilatable hypoplastic aortic arch segment; in two cases an additional isthmic restenosis was present. Inclusion criteria for our technique was an aorta ascending diameter large enough to allow partial clamping. Primary repair of aortic coarctation was end-to-end anastomosis in four patients and patch angioplasty in one. Mean age at primary repair was 5.5 years and at reoperation 16.1 years. Systolic pressure gradients at rest ranged from 35 to 70 mmHg; upper extremity hypertension was present in all patients. Operative technique consisted of performing a dacron or PTFE aorta ascending-descending bypass graft parallel to the aortic arch, size 18 or 20 mm in diameter, via the prior left thoracotomy. RESULTS: There were no intraoperative complications and all patients survived. Postoperative complications were left lung atelectasis with necessity of reintubation, pericardial effusion, and transient left diaphragm elevation, each in one patient. After 7-90 months all patients are free of symptoms, have normal blood pressure (with two patients being under anti-hypertensive medication), and have no echocardiographically measurable pressure gradients. CONCLUSIONS: Anatomically positioned aorta ascending-descending bypass grafting via the prior left posterolateral thoracotomy without cardiopulmonary bypass is a safe and efficient method for operation of complex recoarctation in patients with an acceptable size of the aorta ascendens.