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        west china medical publishers
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        find Keyword "封堵器" 14 results
        • Clinical Feasibility of Percutaneous Closure for Subarterial Ventricular Septal Defect Using Asymmetric Occluder Device

          目的 觀察和評價采用偏心型封堵器導管介入治療干下型室間隔缺損的近期療效和安全性。 方法 2011年8月-12月,6例經無主動脈瓣脫垂的干下型室間隔缺損(直徑≤7 mm)患者(年齡>3歲)在雜交手術室接受介入治療。造影評估后,建立動靜脈軌道,在保留導絲的情況下置入合適型號的國產偏心型室間隔缺損封堵器,并于術后定期隨訪復查。 結果 6例患者缺損直徑4~7 mm(平均5.3 mm),其中5例成功地接受了導管介入封堵治療,置入封堵器直徑5~9 mm(平均6.4 mm)。僅1例因封堵器置入后出現主動脈瓣受壓影響關閉,即改由外科微創經胸封堵成功。所有患者在隨訪期內,無栓塞、殘余分流、瓣膜功能障礙、房室傳導阻滯、死亡等并發癥。 結論 無主動脈瓣脫垂的干下型室間隔缺損患者接受導管介入封堵治療是安全、可行的,且短期隨訪結果良好。

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        • 完全可降解封堵器治療膜周部室間隔缺損兩例

          Release date:2018-06-26 05:41 Export PDF Favorites Scan
        • Transcatheter occlusion of ventricular septal defects

          Objective To access the feasibility, effectiveness and safety of transcatheter closure of ventricular septal defects(VSD) in 17patients. Methods Seventeen patients, aged 4 23 years, were selected by transthoracic echocardiography. The location of VSD was perimembranous in 16 patients and was muscular in 1 patient. And 1 patient with aneurysm formation. All cases had no severe pulmonary hypertension or right to left shunt. Membranous VSD underwent transcatheter closure with Amplatzer membranous VSD occluder or membranous VSD occluder made in China. Muscular VSD was closed by Amplatzer patent ductus arteriosus occluder. Results The VSD diameter ranged from 2.3 10.5 mm(5.75±2.10 mm). The device diameter ranged from 412 mm (7.12±1.67 mm). After application of the prosthesis there was no residual shunt in all patients. One patient developed grade I atrioventricular block and complete right bundle branch block. Two patients developed right bundle branch block after 3 4 days. No other compli...更多cations were observed in 1 12 months follow up. Conclusion The transcatheter closure of VSD appears to be a safe and effective method.

          Release date:2016-08-30 06:27 Export PDF Favorites Scan
        • Clinical evaluation of endoscopic bronchial closure of central airway-pleural fistulas with the atrial septal defect occluders: long-term follow-up

          Objective To explore the safety and efficacy for patients with central airway-pleural fistula (APF) treated by atrial septal defect (ASD) occluder. Methods This was a retrospective study. Between January 2017 and October 2021, a total of 16 patients with postoperative APF were treated with ASD occluder through bronchoscope under local anesthesia combined with sedation. The efficacy and complication were recorded during and after the procedure. Results Sixteen patients were recruited in this study and the average age was 60.7 years (range 31 - 74 years). The main etiology for APF was lobectomy/segmentectomy (n=12), pneumonectomy (n=2), radical esophagectomy (n=1) or decortication for chronic empyema (n=1). Totally, 4 fistulas were located in right main bronchus, 3 in left main bronchus, 3 in right upper bronchus, 1 in right middle bronchus, 2 in right lower bronchus and 3 in left upper bronchus. The median diameter of APF was 7.8 mm (ranged from 4 to 18 mm) and the median diameter of ASD occluder inserted was 10.0 mm (ranged from 6 to 20 mm). Successful occlusion of APF was observed in 15 patients (15/16) and 1 patient died of multiple organ failure caused by bacteremia 14 days after the procedure. Fourteen patients were recruited for long-term follow-up, on a median follow-up period of 16.2 months (ranged from 3 to 46 months). There were 12 patients of complete remission and 2 patients of partial remission and only one patient took a second operation due to the enlargement of fistula and translocation of occluder. At follow-up, 4 patients died and the reasons were directly related to the primary etiology, and no patient died due to APF recurrence. Conclusion Endobronchial closure of central APF using ASD occluder is a minimally invasive but effective modality of treatment with satisfactory long-term outcome.

          Release date:2023-10-10 01:39 Export PDF Favorites Scan
        • Application of different types of congenital heart disease occluder in bronchopleural fistula

          ObjectiveTo introduce implantation methods of different types of congenital heart disease occluder for the treatment of bronchopleural fistula (BPF) and its preliminary efficacy.MethodsThree patients who diagnosed with BPF and treated by congenital heart disease occluder were reviewed. The clinical data was analyzed after comprehensively reviewing of relevant literature.ResultsAll the three patients were treated with postoperative BPF and empyema. The diameter of the fistula ranged from 3 to 8 mm. We used occlusive devices for congenital heart diseases such as atrial septum (ASD), ventricular septum (VSD) defect or patent ductus arteriosus (PDA), respectively. After treatment, all three patients were cured of BPF and empyema caused by BPF in a short time, and the thoracic drainage tube was successfully removed. During the follow-up period from 7 to 25 months, no significant long-term complications were observed.ConclusionThe use of ASD, VSD and PDA occluder for the treatment of BPF with a fistula more than 3 mm is effective and safe.

          Release date:2021-02-08 08:11 Export PDF Favorites Scan
        • 應用Amplatzer封堵器治療動脈導管未閉

          目的 評價Amplatzer封堵器在動脈導管未閉(PDA)介入治療中的安全性和療效. 方法 自2000年9月開始應用Amplatzer封堵器治療30例PDA患者,在術后24小時、1個月、3個月行超聲心動圖檢查,觀察封堵效果及有無并發癥. 結果 PDA最窄處直徑為2.5~12.0mm,平均5.3mm;1例伴有重度肺動脈高壓的粗大PDA采用Amplatzer房間隔缺損封堵器治療,余29例用Amplatzer PDA封堵器.29例術后24小時、1例48小時時彩色多普勒超聲心動圖檢查均未見殘余分流,1例術后早期發生機械性溶血.隨訪中,未出現封堵器移位、殘余分流和再通. 結論 應用Amplatzer封堵器治療PDA是一種安全有效的非外科手術方法,適應證廣、技術成功率高、近期療效滿意,遠期效果尚需進一步觀察.

          Release date:2016-08-30 06:31 Export PDF Favorites Scan
        • Current situation and prospect of interventional therapy for congenital heart disease in China

          Transcatheter intervention for congenital heart disease has been developed for 40 years in China, it has experienced the transition of learning to self-dependent innovation, and witnessed the intervention therapy system starting from scratch and gradually reaching the top level and gaining high achievements in the world scale. With the continuous development of interventional technology and devices, cutting-edge ideas and viewpoints are constantly discussed. This review summarized the development of intervention techniques and devices, hoping to provide some experience for the further development of transcatheter interventions for congenial heart disease.

          Release date:2022-10-26 01:37 Export PDF Favorites Scan
        • Efficacy and safety of ultrasound-guided percutaneous retrograde closure of patent ductus arteriosus

          ObjectiveTo evaluate the efficacy and safety of transcatheter closure of patent ductus arteriosus (PDA) with transthoracic echocardiography (TTE).MethodsFrom February 2016 to November 2018, 98 patients of pure PDA were selected, including 43 patients of funnel type and 55 patients of tube type. There were 38 males and 60 females at age of 2-48 (9.8±10.4) years. All patients underwent TTE-guided retrograde closure of the PDA through the femoral artery to establish a femoral-abdominal aorta-thoracic aorta-ductus arteriosus-aorta-right ventricle trajectory.Under the guidance of TTE, a suitable closure umbrella was placed through the femoral artery. One month, 3 months, 6 months, 12 months after the surgery, the patients received out-patient clinical follow-up.ResultsNinety eight patients were successfully occluded by TTE. The occluder was replaced many times in an adult PDA patient, but finally it was successfully plugged. The operation time was 33.2±5.8 min. The lumbar diameter was 12±6 mm. And the postoperative murmur disappeared. Ultrasound showed no shunt between the aorta and the pulmonary artery, and the postoperative hospital stay was 3-4 days. No shunt signal was found in 1, 3, 6, 12 months follow-up. Left atrial anteroposterior diameter (25.8±6.1 mm vs. 30.6±8.4 mm) and left ventricular end diastolic diameter (38.5±9.1 mm vs. 45.2±11.5 mm) were significantly smaller (P < 0.05).ConclusionTTE-guided transcatheter closure of PDA via femoral artery is a safe and effective method to avoid the damage of X-ray and contrast medium. The prospect of clinical application is good.

          Release date:2019-12-13 03:50 Export PDF Favorites Scan
        • Influencing factors and outcomes of atrial septal defect or ventricular septal defect occlusion guided by echocardiography

          Objective To analyze the influencing factors and outcomes of atrial septal defect (ASD) and ventricular septal defect (VSD) occlusion guided by echocardiography. Methods We retrospectively analyzed the clinical data of 188 patients receiving transthoracic and percutaneous transcatheter closure of ASD and VSD from July 2009 to July 2017 in our department, including 74 males and 114 females, aged 13.48±13.53 years ranging from 1 to 65 years. Results Fifty-three ASD patients accepted transthoracic closure surgery, of whom 4 patients were difficult to close and 6 patients failed to close; 24 patients underwent percutaneous transcatheter ASD occlusion surgery, of whom 3 were difficult to close and 1 failed in occlusion; 108 VSD patients implemented transthoracic closure surgery, of whom 10 patients were difficult to close and 5 patients failed in closure; 9 VSD patients underwent percutaneous transcatheter closure, of whom 5 failed and then was converted to transthoracic closure. Our study showed that too large or too small aperture was the independent risk factor. Two kinds of closure surgery had their own advantages and disadvantages. The special type of VSD was the influencing factor of transthoracic closure. Conclusion When the ASD diameter≥25 mm, transthoracic closure is the best choice to avoid the use of large occluder. When the ASD diameter<25 mm, percutaneous closure surgery is the best choice. When the ASD diameter≥35 mm, it is best to give up the closure operation. Technical improvements can significantly raise the closure success rate of the subarterial VSD. For the entry diameter>10 mm and membranous aneurysm with multi-break, occlusion surgery should be avoided in VSD.

          Release date:2018-11-27 04:47 Export PDF Favorites Scan
        • Clinical Outcomes of Transesophageal Echocardiography-guided Occlusion of Infundibular Ventricular Septal Defect via Minithoracotomy

          ObjectiveTo investigate clinical outcomes and safety of transesophageal echocardiography (TEE)-guided occlusion of infundibular ventricular septal defect (VSD) via minithoracotomy. MethodsClinical data of 21 pediatric patients with infundibular VSD who underwent TEE-guided occlusion via minithoracotomy in Children's Hospital of Hebei Province from January to June 2013 were retrospectively analyzed. There were 10 male and 11 female patients with their age of 8-24 (16±8) months and body weight of 9±3 kg. The size of VSD was 4.5±2.5 mm. TEE was used to evaluate the position of the occluder, its influence on the atrioventricular valves and aortic valve, and the presence of residual shunt. ResultsThere was no perioperative death or complication. VSD occlusion was successfully performed in 20 out of 21 patients (95.2%). One patient received conversion to open VSD repair under extracorporeal circulation because VSD size was too big. Mean time of delivery of occluders was 32±16 minutes, the size of the occluders was 5±3 mm, and length of hospital stay was 6-8 days. All the patients were followed up for 3-6 months after discharge. During follow-up, echocardiography showed clear echo and normal position of the occluders, and there was no mild or more severe residual shunt or valvular regurgitation. ConclusionTEE-guided occlusion of infundibular VSD via minithoracotomy is easy to perform and safe with satisfactory clinical outcomes.

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