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目的 总结杂交技术经胸肺动脉瓣球囊扩张成形术治疗室间隔完整型肺动脉闭锁的即刻疗效及近、中期随访结果.方法 2005年3月至2010年3月,采用超声引导经胸肺动脉瓣球囊扩张成形术治疗室间隔完整型肺动脉膜性闭锁30例,年龄1天~48个月,平均(4.59±3.21)个月.胸骨正中切口,于右室流出道距离肺动脉瓣环下约2 cm缝荷包线,然后置入导丝.在超声引导下置入穿刺鞘管.确认穿刺针对准膜性闭锁的瓣膜后,在钢丝引导下放入球囊扩张管进行扩张,超声提示肺动脉瓣开放满意.<3个月病婴行改良Blalock-Taussig(B-T)体肺分流术,并同期行动脉导管结扎术.>3个月病婴行球囊扩张术后,如血氧饱和度改善明显,不常规行改良B-T分流术,并保留动脉导管开放,如血氧饱和度改善不明显,则考虑行改良B-T分流术,结扎或保留动脉导管.>5个月病儿行球囊扩张后血氧饱和度改善不满意,且重度右心发育不良,则选择双向Glenn术.结果 30例行球囊扩张均取得成功,同期行动脉导管结扎术25例,改良B-T分流术8例,双向Glenn术2例.均未出现严重并发症.1例术后因低氧血症,术后第3天行动脉导管结扎术和改良B-T分流术;余者术后血流动力学稳定,顺利出院.术后随访1.5~62.0个月,平均(18.7±17.2)个月.血氧饱和度由术前0.73±0.08上升至0.94±0.04,心功能Ⅰ级.院外死亡5例,25例生长发育良好.结论 杂交技术经胸肺动脉瓣球囊扩张成形术是一种治疗新生儿及婴幼儿室间隔完整型肺动脉膜性闭锁的安全、有效的方法.Abstract: Objective In patients with pulmonary atresia and intact ventricular septum ( PAIVS) without right ventricular-dependent coronaries, catheter techniques including the use of a sniff wire, lasers, and radiofrequency have been the most widely used initial therapy. However, percutaneous perforation and balloon valvuloplasty were associated with higher rate of procedural failure and serious complications. Methods We report our experience with a hybrid approach for pulmonary atresia with intact ventricular septum, combining surgery and interventional catheterization techniques. Between March 2005 and March 2010, hybrid procedure was carried out successfully in 30 newboms and infants with favorable anatomy. The age ranged from 1 day to 48 months with a mean of (4.59 ±3.21) months. The heart was exposed through median sternotomy. A pursestring suture was placed in the right ventricular outflow tract 2 cm away from the pulmonary trunk. Then a 16-gauge intravenous catheter was punctured through the right ventrical and perforated the atretic PV with the guidance of echocardiography. A guide wire was then inserted into the sheath and used to guide the balloon across the PV. Sequential dilations were performed until a full opening of the PV with the guidance of epicardial echocardiography. In patients < 3 months PDA ligation was performed followed by modified Blalock-Taussig (B-T) shunt. In patients > 3 months PDA ligation was not performed. A modified B-T shunt was inserted if severe systemic oxygen desaturation occurred after PDA ligation. Bidirectional Glenn shunt was performed for severe hypoplasia. Hybrid procedure was achieved in all patients. The simultaneous procedures included 25 cases of PDA ligation. 6 newborns underwent modified B-T shunt placement (3.5 to 5 mm) after pulmonary valvuloplasty and PDA ligation, and 2 patients > 1 month underwent modified B-T shunt. Another 2 patients were selected for univentricular palliative surgery because of a diminutive monopartite right ventricle and bidirectional Glenn procedure was performed. No pericardial effusion or cardiac tamponade was observed in all patients. Another case without PDA ligation underwent a modified B-T shunt because of hypoxemia three days after hybrid procedure, and the rest patients were discharged without any further surgical intervention.During the follow-up period of 1.5 to 62.0 months, 5 patients died. 25 (83.3%) survived and were all in New York Heart Association functional class 1. Peripheral oxygen saturation increased from 0.73 ± 0.08 to 0.94 ± 0.04 (P < 0.05). One patient remains in a single-ventricle pathway, whereas 24 patients achieved a two-ventricle circulation. Results Conclusion Perventricular balloon pulmonary valvuloplasty using a hybrid approach is a safe and feasible procedure for patients with PAIVS. 相似文献
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目的探讨适当的手术方式,评价手术矫治室间隔完整的肺动脉闭锁的临床疗效。方法1992年1月至2004年8月手术治疗17例室间隔完整的肺动脉闭锁病儿,男9例,女8例;年龄15d~12岁,平均(25.5±7.9)个月;体重3.5~28.0kg,平均(7.8±5.4)kg。其中根治手术10例,三尖瓣Z值-2.3~1.2,平均(-0.78±0.34),肺动脉发育指数149.53~297.89mm2/m2,平均(206.35±82.15)mm2/m2,其中2例病儿因严重低氧血症术后次日加行体肺分流手术;生理矫治手术6例,Z值-6.1~0.2,平均(-2.7±0.92),肺动脉发育指数39.88~218.29mm2/m2,平均(131.85±72.93)mm2/m2,包括双向格林手术2例,体肺动脉分流手术1例,右室流出道重建合并体肺动脉分流术3例;一个半心室矫治术1例,首先行双向格林手术,2年后行房间隔缺损修补术,动脉导管结扎术和右室流出道重建术。结果围术期死亡3例(16.67%),2例为先行根治术次日加行体肺分流手术者,1例为右室流出道重建合并体肺动脉分流术者。术后并发症低心排综合征3例,低氧血症3例,乳糜胸1例,右心衰3例,余者均顺利康复。结论合并室间隔完整的肺动脉闭锁是一种少见的先天性心脏病,依照右心室大小、三尖瓣环大小、肺动脉发育情况及冠状动脉解剖等采用适当的手术方式可取得满意的治疗效果。 相似文献
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目的总结室间隔完整型肺动脉闭锁(pulmonary atresia with intact ventricular septum,PA/IVS)的个体化外科治疗策略和中期随访结果。方法回顾性分析2008年1月至2018年12月我院收治151例PA/IVS患儿的临床资料。将患儿分为两组:一期根治组26例,其中男17例、女9例,平均年龄(14.7±13.2)个月;分期手术组125例,其中男72例、女53例,平均年龄(6.4±6.3)个月。比较两组临床结果。结果全组术后随访1~11年,死亡18例,失访19例,1年、5年和10年的生存率分别为90.2%、87.0%和85.2%。其中,一期根治组死亡2例,分期手术组初期手术后死亡12例,初期手术后已行终期手术的患儿死亡4例,三尖瓣Z值(P=0.013)和右室重度发育不良(P=0.025)是影响PA/IVS患儿术后死亡的危险因素。分期手术最后完成终期手术58例,终期手术(含一期根治)占55.6%(84/151)。全组中期随访手术再干预共5例,其余患者均恢复良好,心功能分级仅2例为Ⅲ级,余均为Ⅰ~Ⅱ级。结论依据不同患儿右心室发育程度、就诊年龄以及有无冠状动脉畸形等制定个体化的外科治疗策略,可明显提高PA/IVS患儿的手术成功率,早期完成右室减压手术有利于提高双心室修补机会。 相似文献
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目的 比较经导管介入治疗与外科手术的室间隔完整型肺动脉瓣闭锁(pulmonary valveatresia with intact ventricular septum,PA/IVS)临床治疗效果,探讨PA/IVS安全、有效的首期治疗方法 .方法 2006年1月至2009年5月,收治25例PA/IVS病儿中男20例,女5例.首期治疗年龄2天~8个月.体重2.1~6.7 kg.超声心动图提示右室三部分存在,右室轻~中度发育不良(三尖瓣Z值在-2~1.5),无右室依赖型冠状循环.经导管介入治疗(介入组)8例,外科手术(手术组)17例.结果 两组成功率分别为88%和94%,两组各死亡1例.两组术后残余肺动脉瓣狭窄(PS)程度无明显差异,介入组机械通气时间及术后住院时间较之手术组短.全组随访3~36个月,介入组术后1例再次行球囊扩张,手术组术后行PS外科矫治和PS球囊扩张各1例,2例等待球囊扩张术.全组21例获双心室循环,介入组与手术组各1例因右心功能不全拟行双向格林手术.结论 对于右室轻~中度发育不良的PA/IVS,经导管介入治疗可以取代外科手术作为首期治疗方法 . 相似文献
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目的 比较经导管介入治疗与外科手术的室间隔完整型肺动脉瓣闭锁(pulmonary valveatresia with intact ventricular septum,PA/IVS)临床治疗效果,探讨PA/IVS安全、有效的首期治疗方法 .方法 2006年1月至2009年5月,收治25例PA/IVS病儿中男20例,女5例.首期治疗年龄2天~8个月.体重2.1~6.7 kg.超声心动图提示右室三部分存在,右室轻~中度发育不良(三尖瓣Z值在-2~1.5),无右室依赖型冠状循环.经导管介入治疗(介入组)8例,外科手术(手术组)17例.结果 两组成功率分别为88%和94%,两组各死亡1例.两组术后残余肺动脉瓣狭窄(PS)程度无明显差异,介入组机械通气时间及术后住院时间较之手术组短.全组随访3~36个月,介入组术后1例再次行球囊扩张,手术组术后行PS外科矫治和PS球囊扩张各1例,2例等待球囊扩张术.全组21例获双心室循环,介入组与手术组各1例因右心功能不全拟行双向格林手术.结论 对于右室轻~中度发育不良的PA/IVS,经导管介入治疗可以取代外科手术作为首期治疗方法 . 相似文献
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目的 比较经导管介入治疗与外科手术的室间隔完整型肺动脉瓣闭锁(pulmonary valveatresia with intact ventricular septum,PA/IVS)临床治疗效果,探讨PA/IVS安全、有效的首期治疗方法 .方法 2006年1月至2009年5月,收治25例PA/IVS病儿中男20例,女5例.首期治疗年龄2天~8个月.体重2.1~6.7 kg.超声心动图提示右室三部分存在,右室轻~中度发育不良(三尖瓣Z值在-2~1.5),无右室依赖型冠状循环.经导管介入治疗(介入组)8例,外科手术(手术组)17例.结果 两组成功率分别为88%和94%,两组各死亡1例.两组术后残余肺动脉瓣狭窄(PS)程度无明显差异,介入组机械通气时间及术后住院时间较之手术组短.全组随访3~36个月,介入组术后1例再次行球囊扩张,手术组术后行PS外科矫治和PS球囊扩张各1例,2例等待球囊扩张术.全组21例获双心室循环,介入组与手术组各1例因右心功能不全拟行双向格林手术.结论 对于右室轻~中度发育不良的PA/IVS,经导管介入治疗可以取代外科手术作为首期治疗方法 . 相似文献
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目的讨论体-肺动脉分流术的手术方式,评价其治疗效果。方法自2003年9月至2005年5月对10例伴有室间隔缺损的肺动脉闭锁患者施行了体-肺动脉分流术,6例手术为右锁骨下动脉与右肺动脉吻合术,3例行升主动脉和右肺动脉人工血管连接术,1例3个月行中心分流术。结果10例手术均顺利完成,患者右上臂无缺血及运动障碍。末梢血氧饱和度由术前的(60±11)%上升至术后的(90±3)%。紫绀显著减轻,活动耐力明显增强,能从事正常的学习与生活。术后随访3~18个月,心功能Ⅰ级8例,Ⅱ级2例。McGoon指数由术前的0.91±0.15增至术后的1.15±0.20。NaKata指数由术前的(92±41)mm2/m2增至术后的(121±38)mm2/m2。结论体-肺动脉分流术是治疗伴有室间隔缺损且左右肺动脉发育较差的肺动脉闭锁的一种较好的姑息性手术。 相似文献
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Pulmonary atresia with intact ventricular septum is difficult to manage, and the surgical procedures are associated with high
mortality and morbidity. The lesion is morphologically heterogeneous, with varying degrees of right ventricular and tricuspid
valve hypoplasia. Aberrations of the coronary circulation are common. A single approach is impractical because the wide spectrum
of right heart morphology makes a uniform surgical approach impossible. Anatomical criteria, such as the degree of tricuspid
valve or right ventricular hypoplasia or whether a right ventricular infundibulum is present, have been used to assign the
infants to single-ventricular or biventricular repair tracks. If the patient is considered a candidate for biventricular repair,
right ventricular decompression, either alone or combined with a systemic-pulmonary artery shunt, is performed, whereas only
a systemic-pulmonary artery shunt is performed in a candidate for single-ventricular repair. Several authors reported that
the Z-value of the tricuspid valve diameter could be a guide to the initial procedure; however, poor interobserver reproducibility
and wide normal ranges are serious limitations. Definitive operations, including biventricular repair, one-and-a-half ventricular
repair, or Fontan-type operation, are performed to eliminate cyanosis. The most important problem when planning a strategy
for a definitive repair is the fact that right ventricular growth and its contribution to pulmonary flow is difficult to predict
before the operation. The management protocol should be determined by the precisely estimated morphology of the right ventricle
and tricuspid valve, and the adequacy of the protocol should be analyzed based on surgical outcomes.
This review was submitted at the invitation of the editorial committee. 相似文献
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目的分析经右心室流出道肺动脉瓣球囊成形术(surgical balloon valvuloplasty,SBV)进行右心室减压联合个体化分流手术治疗室间隔完整型肺动脉闭锁(pulmonary atresia with intact ventricular septum,PA/IVS)的中远期疗效。方法回顾性分析2005年1月至2017年12月在本中心接受SBV治疗的91例PA/IVS患者的临床资料,其中男52例(57.1%)、女39例(42.9%),中位年龄3个月(1 d,24个月),中位体重4.1(2.5,12.0)kg。结果所有患者均行SBV,其中62例患者同期行其他外科手术,包括动脉导管未闭(patent ductus arteriosus,PDA)结扎术33例;PDA结扎术+改良Blalock-Taussig分流术23例;PDA结扎术+双向格林手术6例。没有早期死亡。中位随访时间8.8(2.5,13.4)年,4例(4.4%)失访。随访患者中,7例(8.0%)患者死亡,1例(1.1%)患者因肺动脉瓣狭窄再次行SBV。在随访中,5例(5.7%)行一个半心室矫治术,2例(2.3%)行Fontan手术;平均三尖瓣Z值为?1.7±1.5,较术前明显增加(t=5.587,P<0.001)。结论通过SBV联合个体化分流手术策略治疗PA/IVS是安全、有效的,大多数患儿可达到双心室矫治,避免单心室姑息治疗。 相似文献
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Pulmonary atresia with intact ventricular septum (PAIVS) is sometimes associated with coronary artery anomalies, including
right ventricle (RV)-to-coronary artery fistulas (sinusoidal communications), coronary artery stenoses, and coronary artery
occlusions. In some cases, the coronary circulation depends entirely or partly on the desaturated systemic venous blood supply
from the RV. Under these circumstances, decompression of the RV can result in fatal myocardial ischemia. A 6-month-old boy,
diagnosed with PAIVS associated with sinusoidal communications, underwent a bidirectional cavopulmonary shunt procedure under
venoarterial cardiopulmonary bypass (CPB). During CPB, to prevent RV decompression, we maintained right atrial pressure above
5 mmHg and used a pump perfusion rate of 30%–40% of the calculated value based on body surface area. Although electrocardiography
showed slight ST depression and bradycardia, myocardial contractility after weaning from CPB was adequate to maintain the
circulation with the administration of dobutamine and atrial pacing. In patients with PAIVS and RV-dependent coronary circulation,
it is important to maintain coronary artery perfusion throughout the period of anesthesia. 相似文献
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Shigemitsu Iwai Hidefumi Kishimoto Hiroaki Kawata 《The Japanese Journal of Thoracic and Cardiovascular Surgery》2005,53(7):400-403
We repaired a case of pulmonary atresia with intact ventricular septum in which the blood supply to the left anterior descending
coronary artery depended on the right ventricle. At the time of a bidirectional Glenn operation, total cardiopulmonary bypass
with venous drainage from the right atrium was performed in order to evaluate the safety of right ventricular decompression
required for a planned Fontan operation. We confirmed the dependence of the coronary perfusion on the right ventricle by demonstrating
transient depression of the ST segment in the epicardial electrocardiogram during temporary decompression of the right ventricle.
To prevent ischemic myocardial damage, we then performed an extracardiac Fontan operation with a temporary venous shunt and
without cardiopulmonary bypass. 相似文献
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目的评价非体外循环下肺动脉瓣切开术在室间隔完整型肺动脉闭锁(PA/IVS)初期手术治疗中的疗效。方法回顾性分析2013年1月至2019年9月于我院行非体外循环下右心室减压术的61例PA/IVS患儿的临床资料,男37例、女24例,年龄29.7(2.0~86.0)d,体重4.1(2.5~6.9)kg。其中39例行非体外循环下肺动脉瓣切开术(直视切开组),22例行经右心室肺动脉瓣穿刺球囊扩张成形术(镶嵌治疗组)。比较两组患儿术后死亡率、早期再干预率以及终期手术情况等。结果全组共2例死亡,死亡率3.3%(2/61),直视切开组和镶嵌治疗组各死亡1例,两组死亡率差异无统计学意义(2.6%vs.4.5%,P=0.68)。两组在早期再干预率(5.3%vs.19.0%,P=0.09)、气管插管时间[(56.0±25.9)h vs.(62.0±28.9)h,P=0.41]、ICU滞留时间[(4.7±2.9)d vs.(5.5±2.2)d,P=0.23]、住院时间[(3.9±0.9)d vs.(4.3±1.1)d,P=0.38]等方面差异无统计学意义。随访时间45.3(4.0~84.0)个月,共5例失访。随访期间,直视切开组17例患者无需再手术,13例已完成终期手术,镶嵌治疗组7例患者无需再手术,8例完成终期手术,两组心功能分级(NYHA)均为Ⅰ~Ⅱ级。结论非体外循环下肺动脉瓣切开术与镶嵌治疗相比同样具有操作简便、手术时间短、手术成功率高等特点,且因更经济实惠及再干预率相对偏低,可能更易于临床推广应用。 相似文献
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Motoyuki Hisagi Yasuyuki Suzuki Shisei Nakayama 《The Japanese Journal of Thoracic and Cardiovascular Surgery》2003,51(1):25-28
Pulmonary atresia with intact ventricular septum (PA-IVS) is very difficult to treat due to the variety of right ventricular
hypoplasia and coronary artery anomalies. Biventricular repair is viewed as possible in patients with mild right ventricular
hypoplasia but not in those with severe right ventricular hypoplasia or with sinusoidal communication. We report a case of
a 17-day-old boy with PA-IVS and severe right ventricular hypoplasia and large sinusoidal communications. We successfully
conducted biventricular repair, ligated coronary artery and right ventricular fistulas, and implemented right ventricular
outflow tract reconstruction. He now enjoys good health and attends elementary school. Sinusoidal communications are not always
a limiting factor in biventricular repair for PA-IVS if the right ventricle can be decompressed without inviting ventricular
dysfunction by ligating fistulas. 相似文献