World Journal for Pediatric and Congenital Heart Surgery最新文献_第5页

Konno-Rastan Operation in a Patient With Dextrocardia and Situs Inversus. 在一名右心室突出和心功能不全患者身上实施的 Konno-Rastan 手术

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World Journal for Pediatric and Congenital Heart Surgery Pub Date : 2023-07-01 Epub Date: 2023-06-06 DOI: 10.1177/21501351231174824

Alwaleed Al-Dairy, Bairak Salameh, Hadeel Badran, Hasan Hasan, Lujain Alkyakhii

引用次数: 0

Prevalence and Pattern of Congenital Heart Diseases in School Children in Dongguan, China. 中国东莞学龄儿童先天性心脏病的患病率和模式。

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World Journal for Pediatric and Congenital Heart Surgery Pub Date : 2023-07-01 Epub Date: 2023-03-17 DOI: 10.1177/21501351231163133

GuanYang Kang, JianMin Xiao, Jieying Wang, HuiQing Zhang

{"title":"Prevalence and Pattern of Congenital Heart Diseases in School Children in Dongguan, China.","authors":"GuanYang Kang, JianMin Xiao, Jieying Wang, HuiQing Zhang","doi":"10.1177/21501351231163133","DOIUrl":"10.1177/21501351231163133","url":null,"abstract":"Background: To determine the prevalence and pattern of congenital heart disease (CHD) among elementary school children in Dongguan, China.Methods: Between November 2011 and November 2012, 540,574 school children from 449 elementary schools were screened for CHD by trained doctors in Dongguan. The school children who were suspected to have CHD were referred to a pediatric cardiologist and/or an echocardiographer for a complete evaluation.Results: The total prevalence of CHD was 2.14 per 1,000 school children (1,157/540,574). The most common form of CHD was isolated ventricular septal defect (37.77%; 437/1,157), followed by isolated atrial septal defect (20.22%; 234/1,157) and patent ductus arteriosus (9.94%; 115/1,157). With respect to sex, CHD was equally distributed between males and females.Conclusion: Our data show that the prevalence of CHD in Dongguan is not as high as expected and that isolated ventricular septal defect is the predominant pathology. Echocardiography plays a crucial role in the diagnosis of CHD.","PeriodicalId":23974,"journal":{"name":"World Journal for Pediatric and Congenital Heart Surgery","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9788624","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

Spontaneous Hemopericardium Complicated by Tamponade in a Child With Moderate Hemophilia A: Case-Based Review. 中度血友病 A 患儿自发性血心包并发心肌填塞：基于病例的综述》（Spontaneous Hemopericardium Complicated by Tamponade in a Child with Moderate Hemophilia A: Case-Based Review.

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World Journal for Pediatric and Congenital Heart Surgery Pub Date : 2023-07-01 Epub Date: 2023-04-26 DOI: 10.1177/21501351231168868

Seyfeddine Zayani, Farah Thabet, Majdi Ben Massoud, Chokri Chouchane, Habib Gamra, Slaheddine Chouchane

{"title":"Spontaneous Hemopericardium Complicated by Tamponade in a Child With Moderate Hemophilia A: Case-Based Review.","authors":"Seyfeddine Zayani, Farah Thabet, Majdi Ben Massoud, Chokri Chouchane, Habib Gamra, Slaheddine Chouchane","doi":"10.1177/21501351231168868","DOIUrl":"10.1177/21501351231168868","url":null,"abstract":"Hemophilia A is the most common severe innate bleeding disorder. It is an X-linked recessive inherited bleeding disorder characterized by a qualitative and/or quantitative deficiency of factor VIII. The clinical manifestation of this disease is hemorrhaging that can affect every organ, in particular joints (hemarthrosis) and muscles (hematoma). Some serious but rare hemorrhages can be life-threatening, in particular hemorrhage of the central nervous system and hemopericardium. We report a rare case of spontaneous hemopericardium complicated by tamponade in a child with moderate hemophilia A treated with Factor VIII replacement infusion and pericardial drainage, with a favorable outcome. To our knowledge, this is the second case described in the literature of spontaneous hemopericardium occurring in a child with hemophilia A. Our case suggests that a dose of 50 IU/kg/8 h of factor VIII maintained for up to one day after removal of the pericardial drain seems to be sufficient to ensure correct hemostasis, though further evidence is needed to confirm this impression.","PeriodicalId":23974,"journal":{"name":"World Journal for Pediatric and Congenital Heart Surgery","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9791572","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

Perfusion Strategy to Prevent Right Ventricular Decompression on Cardiopulmonary Bypass During Extracardiac Fontan for Right Ventricle-Dependent Coronary Circulation. 心外方坦术治疗右心室依赖性冠状动脉循环时防止心肺旁路右心室减压的灌注策略。

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World Journal for Pediatric and Congenital Heart Surgery Pub Date : 2023-07-01 Epub Date: 2023-04-02 DOI: 10.1177/21501351231162894

Reena Khantwal Joshi, Neeraj Aggarwal, Mridul Agarwal, Siddartha C Rudrappa, Raja Joshi

引用次数: 0

Modification of the Warden Procedure for Surgical Repair of Partial Anomalous Pulmonary Venous Connection. 修改部分异常肺静脉连接手术修复的 Warden 程序。

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World Journal for Pediatric and Congenital Heart Surgery Pub Date : 2023-07-01 Epub Date: 2023-05-15 DOI: 10.1177/21501351231168830

Mark H D Danton, Emeka B Kesieme

引用次数: 0

Identifying Anomalies of Systemic Venous Drainage: Systemic Venous Anomalies; Atrial Morphology. 识别全身静脉引流异常：全身静脉异常；心房形态。

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World Journal for Pediatric and Congenital Heart Surgery Pub Date : 2023-07-01 Epub Date: 2023-03-15 DOI: 10.1177/21501351231158539

Madan M Maddali, Hamood N Al Kindi, Pranav Subbaraya Kandachar, Abdulla Al Farqani, Khalid S Al Alawi, Faiza Al Kindi, Salim Nasser Al-Maskari, Diane E Spicer, Robert Henry Anderson

{"title":"Identifying Anomalies of Systemic Venous Drainage: Systemic Venous Anomalies; Atrial Morphology.","authors":"Madan M Maddali, Hamood N Al Kindi, Pranav Subbaraya Kandachar, Abdulla Al Farqani, Khalid S Al Alawi, Faiza Al Kindi, Salim Nasser Al-Maskari, Diane E Spicer, Robert Henry Anderson","doi":"10.1177/21501351231158539","DOIUrl":"10.1177/21501351231158539","url":null,"abstract":"So as to produce totally anomalous systemic venous connection, all of the systemic venous tributaries, along with the coronary sinus, should be connected with the morphologically left atrium. Previous descriptions of this rare constellation of anomalous connections of the systemic venous tributaries of the heart have been compromised by the inclusion of individuals having isomeric atrial appendages. In these settings, most frequently, the totally, or almost totally, anomalous systemic venous connections are associated with a sinus venosus defect. It is the anomalous pulmonary venous connections that then create a venovenous bridge, which permits the systemic venous tributaries to drain into the morphologically left atrium, even though they may be predominantly connected to the right atrium. More rarely, it is feasible for the primary atrial septum to develop so as to leave the systemic venous sinus in direct connection with the body of the morphologically left, rather than the morphologically right, atrium. We report a series of patients potentially falling into the category of anomalous systemic venous connections. The findings show a spectrum from partially to totally anomalous connections, with some better interpreted on the basis of anomalous drainage. Included in our cases, nonetheless, is an autopsied example of totally anomalous systemic venous connection produced by an abnormal location of the primary atrial septum. We discuss the potential morphogenesis for this finding. We emphasize the distinction that needs to be made between anomalous systemic venous connections and anomalous systemic venous drainage.","PeriodicalId":23974,"journal":{"name":"World Journal for Pediatric and Congenital Heart Surgery","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10164695","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

Novel Diabolo Configuration of a Large Covered Stent to Treat Cyanosis Related to Pulmonary Arteriovenous Malformations. 治疗肺动静脉畸形相关性青紫症的新型双螺旋结构大型有盖支架。

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World Journal for Pediatric and Congenital Heart Surgery Pub Date : 2023-07-01 Epub Date: 2023-03-27 DOI: 10.1177/21501351231162958

Sarosh P Batlivala, Amr Matoq, Shabana Shahanavaz

引用次数: 0

Severe Aortic Root Dilatation in a Patient With Larsen Syndrome. 一名拉森综合征患者的主动脉根部严重扩张

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World Journal for Pediatric and Congenital Heart Surgery Pub Date : 2023-07-01 Epub Date: 2023-03-08 DOI: 10.1177/21501351231155868

Ruth Eletta, Abinash Pandey, Tarathya Dharmasaputra, Marcial Moreno, Yonna Oparaugo, Tk Susheel Kumar, Susan Beker

引用次数: 0

Invited Commentary: Achieving Post-Bypass Hemostasis in Young Children: At What Cost? 特邀评论：实现幼童搭桥后止血：代价是什么？

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World Journal for Pediatric and Congenital Heart Surgery Pub Date : 2023-07-01 DOI: 10.1177/21501351231174826

Susan Nicholson

{"title":"Invited Commentary: Achieving Post-Bypass Hemostasis in Young Children: At What Cost?","authors":"Susan Nicholson","doi":"10.1177/21501351231174826","DOIUrl":"10.1177/21501351231174826","url":null,"abstract":"Young children requiring bypass often develop coagulopathy resulting in major postoperative blood loss. Increased post-bypass bleeding and donor exposures are independently associated with adverse outcomes. When transfusion of hemostatic blood products fails to reduce bleeding to an acceptable level, rescue therapies including prothrombin complex concentrates (PCCs), and/or recombinant activated factor VII are being given \"off-label\" with increasing frequency. A number of studies attempting to determine the safety and efficacy of PCCs in neonates and young children are being published. These studies are most commonly retrospective, observational, performed in a single center with varying doses, indications for, and timing of administration in a small number of patients with varying results. The results of these individual studies are questionable and are not to be generalized to other center's patients. Because factor VIII inhibitor bypassing activity (FEIBA) contains the activated form of factor VII and factor X there are concerns regarding the potential for thrombotic events in a population with a known risk of postoperative thromboembolism. Currently, there is no validated assay with which to measure the efficacy of FEIBA in vivo to determine dose titration. Well-designed multicenter randomized control trials are needed to determine the optimal dose and risk-benefit of PCCs after pediatric cardiac surgery. Until such data are available the decision to give a procoagulant to neonates and young children after bypass needs to be made when the consequences of blood loss and replacement pose more risk than the risk of thrombotic complications from the drug.","PeriodicalId":23974,"journal":{"name":"World Journal for Pediatric and Congenital Heart Surgery","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9795383","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

Preoperative Computed Tomographic Angiography Can Predict Need for Branch Pulmonary Artery Intervention in Patients With Ductal-Dependent Pulmonary Blood Flow. 术前计算机断层血管造影可以预测导管依赖性肺血流患者是否需要肺动脉分支介入治疗。

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World Journal for Pediatric and Congenital Heart Surgery Pub Date : 2023-05-01 DOI: 10.1177/21501351221151050

Kirsten Graff, Anthony M Hlavacek, Nicholas Aizcorbe, Scott M Bradley, Shahryar M Chowdhury

{"title":"Preoperative Computed Tomographic Angiography Can Predict Need for Branch Pulmonary Artery Intervention in Patients With Ductal-Dependent Pulmonary Blood Flow.","authors":"Kirsten Graff, Anthony M Hlavacek, Nicholas Aizcorbe, Scott M Bradley, Shahryar M Chowdhury","doi":"10.1177/21501351221151050","DOIUrl":"https://doi.org/10.1177/21501351221151050","url":null,"abstract":"Background: Neonates with ductal-dependent pulmonary blood flow (DD-PBF) are at risk for pulmonary artery (PA) stenosis. The objective of this study was to identify preoperative cardiovascular computed tomography angiography (CTA) measures that are associated with the need for branch PA intervention.Methods: We identified neonates with DD-PBF who underwent preoperative CTA at our center and were followed for 24 months. The primary outcome was requiring intervention for branch PA stenosis at the initial or subsequent procedure. Patients were divided into three groups: 1) No PA intervention, 2) Initial PA intervention, and 3) Remote PA intervention. Measurements of the branch PAs and patent ductus arteriosus (PDA) were made prospectively.Results: Forty patients were included, 7 (18%) did not receive a PA intervention, 23 (58%) were in the initial PA intervention group, and 10 (25%) were in the remote PA intervention group. The distance from PA bifurcation to the largest diameter of the PA that receives the PDA showed a difference between the no-intervention group versus the initial and remote intervention groups (0.8 mm [IQR 0.7, 2.0], 8.2 mm [IQR 1.9, 13.7], 8.5 mm [IQR 6.5, 11.1], respectively, P = .02). The receiver operating characteristic curve showed a distance >2.2 mm had a sensitivity = 91% and specificity = 86% in predicting the need for PA intervention.Conclusion: The distance from the PA bifurcation to the largest diameter of the branch PA that accepts the PDA on preoperative CTA is highly predictive of the need for initial or remote PA intervention in this group. Preoperative CTA should be considered for risk stratification in neonates undergoing intervention for DD-PBF.","PeriodicalId":23974,"journal":{"name":"World Journal for Pediatric and Congenital Heart Surgery","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9414153","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