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Clinical effect of right subaxillary small incision approach on children with congenital heart disease 右腋下小切口入路治疗儿童先天性心脏病的临床疗效
Q4 Medicine Pub Date : 2020-01-05 DOI: 10.3760/CMA.J.ISSN.2095-428X.2020.01.011
Penggao Wang, Yu Zhang, Zhongjian Chen, Yazhou Cui, Wenbo Yu, Xiangyang Dong
Objective To analyze the clinical effect of right subaxillary small incision approach on children with congenital heart disease (CHD). Methods Eighty-six patients with CHD admitted to Henan Children′s Hospital from January 2015 to September 2017 were enrolled in this study.The patients were randomly divided into the control group and the observation group with 43 cases each group.The control group underwent sternal median incision, and the observation group underwent right subaxillary small incision.The total effective rate, incision satisfaction, general conditions of surgery (cardiopulmonary bypass time, operation time, aortic occlusion time, intraoperative blood loss), postoperative related conditions (thoracic drainage volume, postoperative monitoring time, postoperative assisted ventilation time, hospitalization time, hospitalization expenses), Wong-Baker facial expression scale (FPS-R) score, as well as the respiratory function index including the levels of peak inspiratory pressure (PIP) and alveolar-arterial oxygen pressure difference [p(A-a) (O2)]after anesthesia (T1), after operation (T2), at admission to intensive care unit (T3) and before extubation (T4) and complication rate between 2 groups were compared. Results (1)The incision satisfaction in the observation group [90.70% (39/43 cases)] was higher than that in the control group [62.79% (27/43 cases)], and the difference was statistically significant (χ2=9.382, P=0.002). (2)There was no significant difference in the the extracorporeal circulation time, operation time and aortic block time between the two groups [observation group: (68.94±8.26) min, (2.33±0.21) h, (28.79±7.32) min; control group: (67.11±9.11) min, (2.25±0.31) h, (30.02±6.88) min] (P>0.05). (3)The intraoperative blood loss [(89.87±11.25) mL] in the observation group was less than that in the control group [(105.91±31.01) mL], which difference was statistically significant (t=3.189, P=0.002). (4)Also there was significant difference in postoperative monitoring time, postoperative assisted ventilation time, hospitalization time, thoracic drainage volume and hospitalization expenses between the two groups (the observation group: postoperative monitoring time (30.55±10.39) h, postoperative assisted ventilation time [(9.68±2.19) h, hospitalization time (9.61±2.17) d, thoracic drainage volume (90.36±26.14) mL, hospitalization expenses (36 956.15±1 097.84) yuan; the control group: (41.39±9.93) h, (12.72±3.81) h, (12.33±3.15) d, (163.24±29.36) mL and (45 271.97±1 134.55) yuan] (t=4.946, 4.536, 4.663, 12.157, 34.540, all P 0.05). There was no significant difference in the complication rate between the observation group [6.98% (3/43 cases)] and the control group [4.65% (2/43 cases)] (χ2=0.000, P>0.05). Conclusions Right subaxillary small incision approach does not affect the respiratory function of children with CHD, which can improve the satisfaction of incision, reduce the amount of blood loss, accelerate
目的分析右腋下小切口入路治疗儿童先天性心脏病的临床疗效。方法对河南省儿童医院2015年1月至2017年9月收治的86例冠心病患者进行研究。将患者随机分为对照组和观察组,每组43例。对照组采用胸骨正中切口,观察组采用右腋下小切口。总有效率、切口满意度、手术一般情况(体外循环时间、手术时间、主动脉闭塞时间、术中失血量)、术后相关情况(胸腔引流量、术后监护时间、术后辅助通气时间、住院时间、住院费用),比较麻醉后(T1)、手术后(T2)、进入重症监护室(T3)和拔管前(T4)的Wong-Baker面部表情量表(FPS-R)评分、呼吸功能指数(包括峰值吸气压(PIP)和肺泡动脉氧压差[p(A-A)(O2)])和并发症发生率。结果(1)观察组切口满意度【90.70%(39/43例)】明显高于对照组【62.79%(27/43)】,差异有统计学意义(χ2=9.382,P=0.002),两组手术时间和主动脉阻断时间[观察组:(68.94±8.26)min,(2.33±0.21)h,(28.79±7.32)min;对照组:(67.11±9.11)min,差异有统计学意义(t=3.189,P=0.002)。(4)两组在术后监护时间、术后辅助通气时间、住院时间、胸腔引流量、住院费用等方面也有显著性差异(观察组:术后监测时间(30.55±10.39)h,术后辅助通气时间[(9.68±2.19)h,住院时间(9.61±2.17)d,胸腔引流量(90.36±26.14)mL,住院费用(36956.15±1097.84)元;对照组:(41.39±9.93)h,(12.72±3.81)h,[12.33±3.15)d,(163.24±29.36)mL,[45.271.97±134.55)元](t=4.946,4.536,4.663,12.157,34.540,均P 0.05)观察组并发症发生率[6.98%(3/43例)]与对照组[4.65%(2/43例)差异有统计学意义(χ2=0.000,P>0.05),减轻术后疼痛,减轻父母的经济负担。此外,术中熟练准确的操作可以减少或避免相关并发症的发生,确保手术安全。关键词:微创;胸骨正中切口;先天性心脏病;右腋下小切口;儿童;开放手术
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引用次数: 0
Progress of pulmonary artery denervation in treatment of pulmonary arterial hypertension 肺动脉去神经支配治疗肺动脉高压的进展
Q4 Medicine Pub Date : 2020-01-05 DOI: 10.3760/CMA.J.ISSN.2095-428X.2020.01.003
S. Pan
Pulmonary artery denervation (PADN) can block local sympathetic nerve of pulmonary artery, reduce the hemodynamic parameters of pulmonary arterial hypertension(PAH), attenuate pulmonary vascular remodeling, right ventricular hypertrophy and fibrosis, thus improving cardiac function.Early basic experiment has determined the position of sympathetic nerve of pulmonary artery in pulmonary endarterium and confirmed the safety and effectiveness of PADN in the animal model of PAH.PADN may play a role by inhibiting execssive activation of the sympathetic nervous system and renin-angiotension-aldosterone system.PADN has been applied to adult clinical research, and has achieved a good clinical effect.On this basis, the possibility of applying PADN to children′s PAH is being explored preliminarily. Key words: Pulmonary arterial hypertension; Pulmonary artery denervation; Autonomic nerve; Child
肺动脉去神经支配(PADN)可阻断肺动脉局部交感神经,降低肺动脉高压(PAH)血流动力学参数,减轻肺血管重构、右心室肥厚和纤维化,从而改善心功能。早期基础实验确定了肺动脉交感神经在肺动脉内膜的位置,证实了PADN在PAH动物模型中的安全性和有效性。PADN可能通过抑制交感神经系统和肾素-血管紧张-醛固酮系统的过度激活发挥作用。PADN已应用于成人临床研究,取得了良好的临床效果。在此基础上,对PADN应用于儿童多环芳烃的可能性进行了初步探讨。关键词:肺动脉高压;肺动脉去神经支配;自主神经;孩子
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引用次数: 0
Non-compaction of ventricular myocardium in children 儿童心室心肌不压实
Q4 Medicine Pub Date : 2020-01-05 DOI: 10.3760/CMA.J.ISSN.2095-428X.2020.01.020
Kaiyan Song, S. Nie
Non-compaction of ventricular myocardium (NVM), a rare congenital and inherited cardiomyopathy, is characterized by prominent trabeculations and deep intertrabecular recesses in communication with the ventricular cavity.NVM has diverse clinical presentations without specificity, of which the major characteristics are cardiac insufficiency, arrhythmias and thrombosis.Echocardiography and cardiac magnetic resonance imaging are necessary technologies to diagnose NVM.Symptomatic therapy is the only choice for most patients.Furthermore, if medical treatment fails, the heart transplantation could be performed.As a whole, NVM has a high mortality and entirely different prognosis, however, the prognosis of asymptomatic patients is relatively good. Key words: Non-compaction of ventricular myocardium; Cardiac insufficiency; Arrhythmia; Thrombosis
室性心肌致密性不全(NVM)是一种罕见的先天性和遗传性心肌病,其特征是突出的小梁和与心室相通的深部小梁间凹陷。NVM临床表现多样,无特异性,主要特征为心功能不全、心律失常和血栓形成。超声心动图和心脏磁共振成像是诊断NVM的必要技术。症状治疗是大多数患者的唯一选择。此外,如果治疗失败,可以进行心脏移植。总体而言,NVM具有较高的死亡率和完全不同的预后,但无症状患者的预后相对较好。关键词:心室心肌不致密;心功能不全;心律失常;血栓形成
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引用次数: 0
Progress in diagnosis and treatment of heart failure in children 儿童心力衰竭的诊断和治疗进展
Q4 Medicine Pub Date : 2020-01-05 DOI: 10.3760/CMA.J.ISSN.2095-428X.2020.01.005
M. Qian
Heart failure is a complex clinical syndrome characterized by the heart losing the function of effective blood-pumping and venous return, which will cause a series of symptoms, and its clinical manifestations vary with the age of children.The main causes of heart failure in children are congenital heart disease and cardiomyopathy.Drug therapy for heart failure in children has gained rapid progression recently with Sacubitril/valsartan being a typical one, which was approved by Food and Drug Administration (FDA) in October 2019 for its effective use in symptomatic left ventricular dysfunction in children aged 1 year and above, marking that the drug therapy for heart failure in children stands at a new starting point.Implantable cardioverter defibrillator and cardiac resynchronization therapy are applicable to some patients with indications.Mechanical circulatory support is essential in the treatment of patients with cardiopulmonary failure, including extracorporeal membrane oxygenation and ventricular assist device, which is used as an important transition of short-term circulatory assisted transplantation.Pediatric heart transplantation is a treatment option for end-stage heart failure. Key words: Heart failure; Congenital heart disease; Pediatric intensive care; Progress
心力衰竭是一种复杂的临床综合征,其特征是心脏失去有效的血液泵送和静脉回流功能,会引起一系列症状,其临床表现随儿童年龄的不同而不同。儿童心力衰竭的主要原因是先天性心脏病和心肌病。近年来,儿童心力衰竭的药物治疗进展迅速,其中萨库必曲/缬沙坦是一种典型的药物,该药物于2019年10月被美国食品药品监督管理局(FDA)批准用于治疗1岁及以上儿童症状性左心室功能障碍,标志着儿童心力衰竭药物治疗站在了一个新的起点上。植入式心律转复除颤器和心脏再同步治疗适用于一些有适应症的患者。机械循环支持在心肺功能衰竭患者的治疗中至关重要,包括体外膜肺氧合和心室辅助装置,作为短期循环辅助移植的重要过渡。儿童心脏移植是治疗终末期心力衰竭的一种选择。关键词:心力衰竭;先天性心脏病;儿科重症监护;进度
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引用次数: 0
Case report of type I and cardiomyopathy in children with mucopolysaccharidosis and literature review 儿童粘多糖病I型和心肌病病例报告及文献复习
Q4 Medicine Pub Date : 2020-01-05 DOI: 10.3760/CMA.J.ISSN.2095-428X.2020.01.018
Han Zhang, Shiwei Yang
对2017年1月南京医科大学附属儿童医院收治的1例因心脏扩大就诊后检测发现黏多糖贮积症Ⅰ型患儿诊疗经过及预后情况进行整理,结合在中国期刊全文数据库、万方数据库、PubMed等图书馆检索到的相关文献,分析并总结儿童黏多糖贮积症I型并心肌病的诊治原则及预后。患儿,4个月7 d,因"心脏扩大"就诊,临床特殊有毛发浓密,反复呼吸道感染后经抗炎、强心等处理,基因结果提示IDUA基因出现2个杂合变异,考虑为黏多糖贮积症I型并心肌病,随访至出生后11个月患儿干细胞移植后因感染死亡。黏多糖贮积症I型为罕见病,既往无特异性治疗手段。目前治疗方法包括造血干细胞移植、酶替代疗法及基因治疗等。但对于黏多糖贮积症Ⅰ型更重要的是早期识别,以改善该病预后。
A case of type I mucopolysaccharide storage syndrome in children admitted to the Children's Hospital affiliated with Nanjing Medical University in January 2017 was analyzed and summarized based on the diagnosis, treatment, and prognosis of a child diagnosed with type I mucopolysaccharide storage syndrome due to cardiac enlargement. Relevant literature retrieved from the Chinese Journal Full Text Database, Wanfang Database, PubMed, and other libraries were used to analyze and summarize the diagnosis, treatment principles, and prognosis of type I mucopolysaccharide storage syndrome in children with cardiomyopathy. The child, aged 4 months and 7 days, was diagnosed with "cardiac enlargement" and had a clinical condition characterized by dense hair. After repeated respiratory infections and anti-inflammatory and cardiac strengthening treatments, the genetic results showed two heterozygous variants in the IDUA gene. They were considered to have type I mucopolysaccharide storage syndrome and cardiomyopathy. They were followed up until 11 months after birth and died due to infection after stem cell transplantation. Mucopolysaccharide storage syndrome type I is a rare disease with no specific treatment in the past. The current treatment methods include hematopoietic stem cell transplantation, enzyme replacement therapy, and gene therapy. But for mucopolysaccharide storage disease type I, early identification is more important to improve the prognosis of the disease.
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引用次数: 0
Significance of serum glutamate acid levels in children with retinopathy of prematurity and its effect on prognosis 早产儿视网膜病变患儿血清谷氨酸水平的变化及其对预后的影响
Q4 Medicine Pub Date : 2020-01-05 DOI: 10.3760/CMA.J.ISSN.2095-428X.2020.01.013
Xiang Lei, Zhanrong Li, Yanping Liu
Objective To investigate the relationship between serum glutamate levels and severity of retinopathy of prematurity (ROP) in children and its impact on the prognosis. Methods A total of 92 children with ROP who were screened and treated at Henan Provincial Eye Hospital from June 2017 to June 2018 and 50 healthy preterm infants screened at Henan Provincial Eye Hospital were selected for clinical control study.Ninety-two children with ROP were divided into the mild ROP group and the severe ROP group according to the stage of lesions, and they were divided into the progressive group and the spontaneous regression group according to whether the disease was progressive.The severity of ROP and prognosis were analyzed by measuring serum glutamate levels in 1 week and 6 weeks after birth. Results The serum glutamate concentration in the severe ROP group was the highest in the first week after birth[(122.08±14.55) mmol/L] and in the 6th week after birth [(107.13±13.20) mmol/L], followed by the mild ROP group[(98.60±14.48) mmol/L, (85.41±14.49) mmol/L] separately, and the lowest in the control group[(68.52±7.69) mmol/L, (54.97±6.31) mmol/L] separately, and there were significant differences among the 3 groups (all P<0.05). Pearson correlation analysis showed that serum glutamate concentration was positively correlated with the severity of ROP at 1 week and 6 weeks after birth (r=0.869, 0.875, all P<0.05). The levels of serum glutamate at the first week after birth and at the 6th week after birth in the progressive group [(107.18±17.62) mmol/L, (92.94±16.21) mmol/L]were significantly higher than those in the spontaneous regression group[(131.53±10.22) mmol/L, (118.82±8.18) mmol/L], and there were significant differences between the 2 groups (all P<0.05). The area under the curve(AUC) values of serum glutamate concentration at 1 week after birth and 6 weeks after birth were 0.855 and 0.936, respectively, according to the receiver operating characteristic(ROC) curve, while the optimal critical values of serum glutamate concentration at 1 week and 6 weeks after birth were 117.83 mmol/L (sensitivity was 0.909, specificity was 0.728) and 106.69 ng/L (sensitivity was 1.000, specificity was 0.790), respectively. Conclusions The serum glutamate concentration was positively correlated with the severity of ROP infants in 1 week and 6 weeks after birth.The optimal threshold of serum glutamate concentration in 1 week and 6 weeks after birth was more sensitive and specific in predicting the progression of retinopathy, and had higher value in evaluating the prognosis of the infants. Key words: Retinopathy of prematurity; Glutamate; Progression; Prognosis
目的探讨血清谷氨酸水平与儿童早产儿视网膜病变(ROP)严重程度的关系及其对预后的影响。方法选择2017年6月至2018年6月在河南省眼科医院筛查治疗的92例ROP患儿和在河南省眼部医院筛查的50例健康早产儿进行临床对照研究。92例ROP患儿根据病变分期分为轻度ROP组和重度ROP组,根据病情是否进展分为进展组和自发消退组。通过测量出生后1周和6周的血清谷氨酸水平来分析ROP的严重程度和预后。结果重度ROP组的血清谷氨酸浓度在出生后第一周最高[(122.08±14.55)mmol/L],在出生后第六周最高[[(107.13±13.20)mmol/L],其次是轻度ROP组[(98.60±14.48)mmol/L,(85.41±14.49)mmol/L,Pearson相关分析显示,出生后1周和6周血清谷氨酸浓度与ROP的严重程度呈正相关(r=0.869,0.875,均P<0.05),进展组出生后第1周和出生后第6周的血清谷氨酸水平[(107.18±17.62)mmol/L、(92.94±16.21)mmol/L明显高于自然回归组[(131.53±10.22)mmol/L、[(118.82±8.18)mmol/L],两组间差异有统计学意义(均P<0.05),根据受试者操作特性(ROC)曲线,出生后1周和6周血清谷氨酸浓度的最佳临界值分别为117.83mmol/L(灵敏度为0.909,特异度为0.728)和106.69ng/L(灵敏度为1.000,特异性为0.790)。结论出生后1周和6周血清谷氨酸浓度与ROP的严重程度呈正相关。出生后1周和6周血清谷氨酸浓度的最佳阈值在预测视网膜病变进展方面更为敏感和特异,在评估婴儿预后方面具有更高的价值。关键词:早产儿视网膜病变;谷氨酸;进展;预后
{"title":"Significance of serum glutamate acid levels in children with retinopathy of prematurity and its effect on prognosis","authors":"Xiang Lei, Zhanrong Li, Yanping Liu","doi":"10.3760/CMA.J.ISSN.2095-428X.2020.01.013","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.2095-428X.2020.01.013","url":null,"abstract":"Objective \u0000To investigate the relationship between serum glutamate levels and severity of retinopathy of prematurity (ROP) in children and its impact on the prognosis. \u0000 \u0000 \u0000Methods \u0000A total of 92 children with ROP who were screened and treated at Henan Provincial Eye Hospital from June 2017 to June 2018 and 50 healthy preterm infants screened at Henan Provincial Eye Hospital were selected for clinical control study.Ninety-two children with ROP were divided into the mild ROP group and the severe ROP group according to the stage of lesions, and they were divided into the progressive group and the spontaneous regression group according to whether the disease was progressive.The severity of ROP and prognosis were analyzed by measuring serum glutamate levels in 1 week and 6 weeks after birth. \u0000 \u0000 \u0000Results \u0000The serum glutamate concentration in the severe ROP group was the highest in the first week after birth[(122.08±14.55) mmol/L] and in the 6th week after birth [(107.13±13.20) mmol/L], followed by the mild ROP group[(98.60±14.48) mmol/L, (85.41±14.49) mmol/L] separately, and the lowest in the control group[(68.52±7.69) mmol/L, (54.97±6.31) mmol/L] separately, and there were significant differences among the 3 groups (all P<0.05). Pearson correlation analysis showed that serum glutamate concentration was positively correlated with the severity of ROP at 1 week and 6 weeks after birth (r=0.869, 0.875, all P<0.05). The levels of serum glutamate at the first week after birth and at the 6th week after birth in the progressive group [(107.18±17.62) mmol/L, (92.94±16.21) mmol/L]were significantly higher than those in the spontaneous regression group[(131.53±10.22) mmol/L, (118.82±8.18) mmol/L], and there were significant differences between the 2 groups (all P<0.05). The area under the curve(AUC) values of serum glutamate concentration at 1 week after birth and 6 weeks after birth were 0.855 and 0.936, respectively, according to the receiver operating characteristic(ROC) curve, while the optimal critical values of serum glutamate concentration at 1 week and 6 weeks after birth were 117.83 mmol/L (sensitivity was 0.909, specificity was 0.728) and 106.69 ng/L (sensitivity was 1.000, specificity was 0.790), respectively. \u0000 \u0000 \u0000Conclusions \u0000The serum glutamate concentration was positively correlated with the severity of ROP infants in 1 week and 6 weeks after birth.The optimal threshold of serum glutamate concentration in 1 week and 6 weeks after birth was more sensitive and specific in predicting the progression of retinopathy, and had higher value in evaluating the prognosis of the infants. \u0000 \u0000 \u0000Key words: \u0000Retinopathy of prematurity; Glutamate; Progression; Prognosis","PeriodicalId":9843,"journal":{"name":"中华实用儿科临床杂志","volume":"35 1","pages":"50-53"},"PeriodicalIF":0.0,"publicationDate":"2020-01-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47610857","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Progress in application of implantable cardioverter defibrillators in children 植入式心律转复除颤器在儿童中的应用进展
Q4 Medicine Pub Date : 2020-01-05 DOI: 10.3760/CMA.J.ISSN.2095-428X.2020.01.004
Cong Liu, Lin Liu, S. Zeng
Implantable cardioverter defibrillator (ICD) plays an irreplaceable role in preventing sudden cardiac death.There has been a continuous increase in the implantation rate of ICD in children along with technologic improvement.However, the choice of indication, device and implantation approaches of ICD still faces great challenges due to the particularity of children.Related issues on the clinical application of ICD in children, including common diseases, indications and the clinical application of ICD, are reviewed in this paper. Key words: Cardiology; Sudden cardiac death; Implantable cardioverter defibrillator; Child
植入式心律转复除颤器(ICD)在预防心源性猝死方面发挥着不可替代的作用。随着技术的进步,儿童ICD的植入率不断提高。然而,由于儿童的特殊性,ICD的适应症、装置和植入方法的选择仍然面临着巨大的挑战。本文综述了ICD在儿童临床应用中的相关问题,包括常见疾病、适应症和ICD的临床应用。关键词:心脏病学;心脏性猝死;植入式心律转复除颤器;儿童
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引用次数: 0
Prognosis and risk factors of tricuspid regurgitation after transcatheter closure of perimembranous ventricular septal defects in children 儿童膜周室间隔缺损经导管闭合后三尖瓣反流的预后及危险因素
Q4 Medicine Pub Date : 2020-01-05 DOI: 10.3760/CMA.J.ISSN.2095-428X.2020.01.012
Y. Deng, W. Zhao, L. Fu, Jie Shen, Yi-wei Chen, W. Ji, D. Zhu, Fen Li
Objective To investigate the incidence and prognosis of tricuspid regurgitation after transcatheter closure of perimembranous ventricular septal defects in pediatric patients as well as the risk factors of regurgitation occurrence or aggravation. Methods Clinical data of 1 108 patients who underwent percutaneous closure in Shanghai Children′s Medical Center, School of Medicine, Shanghai Jiaotong University from January 2011 to January 2017 was analyzed retrospectively, and the prognosis and risk factors of postoperative tricuspid regurgitation and aggravation were also analyzed. Results Mild tricuspid regurgitation occurred in 24 cases after surgery with the incidence of 2.1%.Among 5 cases with mild or above preoperative tricuspid regurgitation, the regurgitation was alleviated after surgery in 4 cases.No severe tricuspid regurgitation requiring surgical intervention occurred in any patient during follow-up.Univariate analysis showed that intervention time (P<0.05) and residual shunt (P<0.05) were risk factors for mild or above tricuspid regurgitation after intervention.Binary regression analysis indicated that the size of the occluder (mm) (OR=1.48, 95%CI: 1.13-1.90) and residual shunt (OR=6.53, 95%CI: 1.69-25.30) were risk factors for tricuspid regurgitation after intervention (all P<0.05). Conclusions There is a certain incidence of tricuspid regurgitation after transcatheter closure of perimembranous ventricular septal defects, but most tricuspid regurgitation do not need surgical intervention.The intervention time, size of occluder and residual shunt are risk factors of intraoperatively or postoperatively tricuspid regurgitation. Key words: Ventricular septal defects; Tricuspid regurgitation; Septal occlude device; Retrospective study
目的探讨小儿经导管膜周室间隔缺损闭合术后三尖瓣反流的发生率、预后及反流发生或加重的危险因素。方法回顾性分析2011年1月至2017年1月在上海交通大学医学院上海儿童医学中心行经皮缝合术的1 108例患者的临床资料,分析术后三尖瓣反流加重的预后及危险因素。结果术后发生轻度三尖瓣反流24例,发生率为2.1%。5例术前有轻度及以上三尖瓣反流,术后4例反流缓解。随访期间未发生需要手术干预的严重三尖瓣反流。单因素分析显示,干预时间(P<0.05)和残留分流(P<0.05)是干预后轻度及以上三尖瓣反流发生的危险因素。二元回归分析显示,封堵器大小(mm) (OR=1.48, 95%CI: 1.13 ~ 1.90)和残留分流器(OR=6.53, 95%CI: 1.69 ~ 25.30)是干预后三尖瓣反流发生的危险因素(均P<0.05)。结论经导管封堵膜周室间隔缺损后三尖瓣反流发生率一定,但多数三尖瓣反流不需要手术干预。介入时间、闭塞器大小、分流器残留是术中、术后三尖瓣反流发生的危险因素。关键词:室间隔缺损;三尖瓣返流;鼻中隔闭塞装置;回顾性研究
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引用次数: 0
Influence of cardiopulmonary bypass on postoperative brain cognitive function of children with congenital heart disease 体外循环对先天性心脏病患儿术后大脑认知功能的影响
Q4 Medicine Pub Date : 2020-01-05 DOI: 10.3760/CMA.J.ISSN.2095-428X.2020.01.019
K. Xiang, Haisong Bu, Jiarong Li
Congenital heart disease (CHD) is the most common congenital malformation disease in infants.With the rapid development of clinical treatment, the survival rate of children with CHD increased significantly.However, postoperative complications in children with CHD, including heart failure, heart arrythmia, pulmonary hypertension and brain cognitive dysfunction, are another challenge, among which, brain cognitive dysfunction has been gradually recognized and valued by scholars.At present, the effect of cardiopulmonary bypass on brain cognitive function of children with CHD has been studied by a variety of research methods, including molecular biological technique, magnetic resonance imaging technique, optical imaging technology, brain electrical activity monitoring technology and nervous development scale.Varying degrees of brain cognitive dysfunction will occur in children with CHD after heart surgery, which is closely associated with many factors such as systemic inflammatory response related to cardiopulmonary bypass, cerebral ischemia-reperfustion injury, the duration of cardiopulmonary bypass, aortic cross clamp time, deep hypothermia circulatory arrest time, dynamic changes of temperature, degree of hemodilution and blood gas management strategy.The influence of cardiopulmonary bypass on postoperative brain cognitive function in children with CHD is reviewed in this paper, in order to provide reference for clinical diagnosis and treatment, and to improve the prognosis of children with CHD. Key words: Cardiopulmonary bypass; Brain cognitive function; Congenital heart disease
先天性心脏病(CHD)是婴幼儿最常见的先天性畸形疾病。随着临床治疗的快速发展,儿童冠心病的生存率显著提高。然而,儿童冠心病的术后并发症,包括心力衰竭、心律失常、肺动脉高压和脑认知功能障碍是另一个挑战,其中脑认知功能障碍已逐渐被学者们所认识和重视。目前,通过分子生物学技术、磁共振成像技术、光学成像技术、脑电活动监测技术、神经发育量表等多种研究方法研究体外循环对冠心病儿童脑认知功能的影响。冠心病患儿心脏手术后会出现不同程度的脑认知功能障碍,这与体外循环相关的全身炎症反应、脑缺血再灌注损伤、体外循环持续时间、主动脉交叉夹持时间、深低温循环停搏时间、体温动态变化、血液稀释程度、血气管理策略等诸多因素密切相关。本文就体外循环对冠心病患儿术后脑认知功能的影响进行综述,以期为临床诊断和治疗提供参考,改善冠心病患儿预后。关键词:体外循环;脑认知功能;先天性心脏病
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引用次数: 0
Clinical analysis of rapid thrombocytopenia after percutaneous transcatheter closure of arteries in children 儿童经皮动脉闭塞术后快速血小板减少的临床分析
Q4 Medicine Pub Date : 2020-01-05 DOI: 10.3760/CMA.J.ISSN.2095-428X.2020.01.014
Z. Ji, Na Liu, G. Luo, Zhen Bing
目的 探讨经皮动脉导管介入封堵术后血小板快速减少的临床特点、发病机制和防治措施。 方法 选择2017年1月至2018年12月青岛市妇女儿童医院心脏中心共实施经皮动脉导管介入封堵手术121例,其中6例术后发生血小板快速减少,回顾分析其相关临床资料,总结血小板快速减少发生的危险因素、临床特点、可能机制和防治措施。 结果 6例患儿血小板减少发生时间为术后第3-5天,血小板下降最低值为19×109/L,血小板恢复时间为术后7~20 d。造影测量动脉导管内径为4.0~4.5 mm,4例选用美国AGA公司生产规格9-PDA-0810堵闭器,2例选用上海形状记忆公司生产规格0810PDA堵闭器。骨髓学检查提示3例患儿骨髓产板型巨核细胞减少,免疫治疗后恢复良好。所有患儿血小板计数在出院时恢复正常。出院随访6~14个月,所有患儿血小板计数维持正常。 结论 经皮动脉导管介入封堵术后需警惕血小板快速减少,多无严重并发症发生,预后良好,免疫机制可能参与其中,需进一步研究。
Objective To explore the clinical characteristics, pathogenesis, and prevention and treatment measures of rapid platelet reduction after percutaneous arterial catheter occlusion. Method: From January 2017 to December 2018, the Heart Center of Qingdao Women and Children's Hospital conducted a total of 121 cases of percutaneous arterial catheter occlusion surgery. Among them, 6 cases experienced rapid thrombocytopenia after surgery. The relevant clinical data were retrospectively analyzed, and the risk factors, clinical characteristics, possible mechanisms, and prevention and treatment measures for rapid thrombocytopenia were summarized. The occurrence time of thrombocytopenia in 6 children was 3-5 days after surgery, and the lowest value of thrombocytopenia was 19 × 109/L, platelet recovery time is 7 to 20 days after surgery. The diameter of the arterial catheter measured by angiography was 4.0-4.5 mm. Four cases used the 9-PDA-0810 occluder produced by AGA Company in the United States, and two cases used the 0810 PDA occluder produced by Shanghai Shape Memory Company. Bone marrow examination showed a decrease in the production of plate type megakaryocytes in the bone marrow of 3 children, and they recovered well after immunotherapy. All pediatric platelet counts returned to normal upon discharge. During a follow-up period of 6-14 months after discharge, all patients maintained normal platelet counts. Conclusion: After percutaneous arterial catheter occlusion, it is necessary to be vigilant for rapid platelet reduction, with no serious complications, a good prognosis, and possible involvement of immune mechanisms. Further research is needed.
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中华实用儿科临床杂志
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