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1.
Rev. bras. cir. cardiovasc ; 37(3): 306-314, May-June 2022. tab
Article in English | LILACS-Express | LILACS | ID: biblio-1376553

ABSTRACT

ABSTRACT Introduction: Functional tricuspid regurgitation (TR) is known to complicate adult atrial septal defect (ASD), but its management is still under debate. We reviewed our experience in ASD surgery, focusing on associated functional TR and its treatment. Methods: This retrospective study (2005-2019) included 206 consecutive adult ASD surgical cases without associated valve pathology, except functional TR. Variables were statistically compared on TR classes and surgery-defined groups. Results: Mean age of the patients was 40.3±13 years; 19.9% had sinus venosus syndrome. TR severity was directly related to age, pulmonary systolic pressure, right ventricular and tricuspid annulus diameters, and heart failure class. TR ≥ 2 was found in 134 (65%) patients, while TR ≥ 3 in 56 (27.2%) patients. Tricuspid surgery was associated to shunt closure in 66 (32%) patients, almost all through valve repair; indication was directly related to age, right ventricular and tricuspid annulus diameters, and heart failure class ≥ 3. Tricuspid surgery was more efficient than isolated shunt closure in decreasing TR (79±23% vs. 36±26%; P=1.8 E-18). Device closure availability (last four years of the study) was associated with 1/3 reduction of surgical cases but increased the share of cases with TR>2 (> 51% vs. < 31%; P<0.05). Conclusion: In the era of device closure, surgery for adult ASD is less frequent, but the share of significant TR cases is in net increase. To avoid long-term postoperative TR, we plead for valve repair in all patients with severe TR and for considering repair in moderate TR at risk of persistence.

2.
The Korean Journal of Thoracic and Cardiovascular Surgery ; : 57-60, 2018.
Article in English | WPRIM | ID: wpr-742320

ABSTRACT

Left main bronchus compression occasionally occurs in patients with cardiac disease. A 19-month-old female patient weighing 6.7 kg was admitted for recurrent pneumonia and desaturation. She had an a trial septal defect (AS D) with a right aortic arch. Her left main bronchus had been compressed between the enlarged right pulmonary artery (RPA) and the descending thoracic aorta for 14 months. We conducted ASD closure and RPA anterior translocation via sternotomy. The left main bronchus compression was relieved despite the medium-term duration of compression.


Subject(s)
Female , Humans , Infant , Aorta, Thoracic , Bronchi , Heart Defects, Congenital , Heart Diseases , Pneumonia , Pulmonary Artery , Sternotomy
3.
Journal of Genetic Medicine ; : 20-23, 2018.
Article in English | WPRIM | ID: wpr-715205

ABSTRACT

Point mutations in the human cardiac homeobox gene NKX2.5 are associated with familial atrial septal defect (ASD), atrioventricular (AV) conduction disturbance, as well as sudden cardiac death. To date, more than 60 NKX2.5 mutations have been documented, but there are no reports in Korea. We are reporting the first Korean family with ASD and AV block associated with a novel mutation in the NKX2.5 coding region. A 9-year-old boy presented with a slow and irregular pulse, and was diagnosed with secundum ASD and first degree AV block. The boy's father, who had a history of ASD correction surgery, presented with second degree AV block and atrial fibrillation. The boy's brother was also found to have secundum ASD and first degree AV block. There were two sudden deaths in the family. Genetic testing revealed a novel mutation of NKX2.5 in all affected members of the family.


Subject(s)
Child , Humans , Male , Atrial Fibrillation , Atrioventricular Block , Clinical Coding , Death, Sudden , Death, Sudden, Cardiac , Fathers , Genes, Homeobox , Genetic Testing , Heart Septal Defects, Atrial , Korea , Point Mutation , Siblings
4.
The Korean Journal of Thoracic and Cardiovascular Surgery ; : 378-381, 2017.
Article in English | WPRIM | ID: wpr-139845

ABSTRACT

Patients with an atrial septal defect (ASD) and severe pulmonary arterial hypertension (PAH) are considered ineligible for defect closure surgery because of the risk of right ventricular decompensation and death after the operation. We report the case of a patient with large ASD and severe PAH who was able to undergo defect closure surgery successfully following long-term use of combined oral sildenafil and beraprost.


Subject(s)
Humans , Heart Defects, Congenital , Heart Septal Defects, Atrial , Hypertension , Hypertension, Pulmonary , Sildenafil Citrate
5.
The Korean Journal of Thoracic and Cardiovascular Surgery ; : 378-381, 2017.
Article in English | WPRIM | ID: wpr-139844

ABSTRACT

Patients with an atrial septal defect (ASD) and severe pulmonary arterial hypertension (PAH) are considered ineligible for defect closure surgery because of the risk of right ventricular decompensation and death after the operation. We report the case of a patient with large ASD and severe PAH who was able to undergo defect closure surgery successfully following long-term use of combined oral sildenafil and beraprost.


Subject(s)
Humans , Heart Defects, Congenital , Heart Septal Defects, Atrial , Hypertension , Hypertension, Pulmonary , Sildenafil Citrate
6.
The Korean Journal of Thoracic and Cardiovascular Surgery ; : 421-426, 2016.
Article in English | WPRIM | ID: wpr-25162

ABSTRACT

BACKGROUND: Median sternotomy is the standard approach for atrial septal defect (ASD) closure. However, minimally invasive cardiac surgery (MICS) has been introduced at many centers in adult/grown-up congenital heart patients. We retrospectively reviewed the results of right anterolateral thoracotomy compared with conventional median sternotomy (CMS) for ASD closure at Seoul National University Hospital. METHODS: We retrospectively analyzed 60 adult patients who underwent isolated ASD closure from January 2004 to December 2013 (42 in the CMS group, 18 in the MICS group). Preoperative, operative, and postoperative data were collected and compared between the 2 groups. RESULTS: The MICS group was younger (44.6 years vs. 32.4 years, p=0.002) and included more females (66.7% vs. 94.4%, p=0.025) than the CMS group. Operation time (188.4 minutes vs. 286.7 minutes, p<0.001), cardiopulmonary bypass time (72.7 minutes vs. 125.8 minutes, p<0.001), and aortic cross-clamp time (25.5 minutes vs. 45.6 minutes, p<0.001) were significantly longer in the MICS group. However, there were no significant differences in morbidity and mortality between groups. Only chest tube drainage in the first 24 hours (627.1 mL vs. 306.1 mL, p<0.001) exhibited a significant difference. CONCLUSION: MICS via right anterolateral thoracotomy is an alternative choice for ASD closure. The results demonstrated similar morbidity and mortality between groups, and favored MICS in chest tube drainage in the first 24 hours.


Subject(s)
Adult , Female , Humans , Cardiopulmonary Bypass , Chest Tubes , Drainage , Heart , Heart Defects, Congenital , Heart Septal Defects, Atrial , Minimally Invasive Surgical Procedures , Mortality , Retrospective Studies , Seoul , Sternotomy , Thoracic Surgery , Thoracotomy
7.
Academic Journal of Second Military Medical University ; (12): 301-304, 2014.
Article in Chinese | WPRIM | ID: wpr-839101

ABSTRACT

Objective To explore the changes of plasma coupling factor 6 (CF6) in children with large atrial septal defect and different degrees of pulmonary hypertension. Methods A total of 160 patients with large atrial septal defect and different degrees of pulmonary hypertension from January 2010 to August 2012 were retrospectively analyzed. The age of the patients ranged from 4 to 16 (mean 9. 7 ± 2. 1) months old, and the weight ranged from 3. 5to8. 3 (mean 6. 9 ±2. 1) kg. The participants were divided into three groups: atrial septal defect without pulmonary artery hypertension (control group, n = 41); atrial septal defect with pulmonary artery hypertension, but not to a severe degree (A group, n = 76); and atrial septal defect with severe pulmonary artery hypertension (B group, n = 43). The plasma CF6 levels were determined and compared by radioimmunoassay between different groups; the relation of CF6 levels with degree of pulmonary artery hypertension was analyzed. Results The plasma CF6 level was (198. 5±43. 7) pg/mL in the control group, (167. 7±89. 8) pg/mL in A group, and (304. 4±80. 7) pg/mL in B group, showing no significant difference between control group and A group (P>0. 05), but with that in B group being significantly higher than those of control group andA group (P<0. 01). We also found that the ratio of systolic pulmonary artery pressure to systolic blood pressure was positively correlated with plasma levll of CF6 in atrial septal defect children withsevere pulmonary artery hypertension (r = 0. 781, P < 0. 01). Conclusion The plasma CF6 levll is obviously increased in children with large atrial septal defect and severe pulmonary artery hypertension. CF6 may be one of the reasons for severe pulmonary artery hypertension.

8.
Korean Journal of Pediatrics ; : 297-303, 2014.
Article in English | WPRIM | ID: wpr-18400

ABSTRACT

Transcatheter closure of atrial septal defects has become a popular procedure. The availability of a preprocedural imaging study is crucial for a safe and successful closure. Both the anatomy and morphology of the defect should be precisely evaluated before the procedure. Three-dimensional (3D) echocardiography and cardiac computed tomography are helpful for understanding the morphology of a defect, which is important because different defect morphologies could variously impact the results. During the procedure, real-time 3D echocardiography can be used to guide an accurate closure. The safety and efficiency of transcatheter closures of atrial septal defects could be improved through the use of detailed imaging studies.


Subject(s)
Echocardiography , Echocardiography, Three-Dimensional , Heart Septal Defects, Atrial , Tomography Scanners, X-Ray Computed , Vascular Access Devices
9.
The Korean Journal of Thoracic and Cardiovascular Surgery ; : 280-282, 2014.
Article in English | WPRIM | ID: wpr-215827

ABSTRACT

Atrial septal defect (ASD) is one of the most common congenital heart defects in adults. Surgical repair is the most common treatment approach, but device closure has recently become widely performed in accordance with the trend toward less invasive surgical approaches. Although surgery is recommended when ASD is accompanied by atrial fibrillation, this study reports a case in which a complete cure was achieved by closure of a device and totally thoracoscopic ablation.


Subject(s)
Adult , Humans , Atrial Fibrillation , Heart Defects, Congenital , Heart Septal Defects, Atrial , Minimally Invasive Surgical Procedures
10.
The Korean Journal of Thoracic and Cardiovascular Surgery ; : 340-345, 2013.
Article in English | WPRIM | ID: wpr-67175

ABSTRACT

BACKGROUND: This study aims to evaluate whether or not the method of right vertical axillary minithoracotomy (RVAM) is preferable to and as reliable as conventional sternotomy surgery, and also assesses its cosmetic results. METHODS: Thirty-three patients (7 males, 26 females) with atrial septal defect were admitted to the Cardiovascular Surgery Clinic of Cukurova University from December 2005 until January 2010. The patients' ages ranged from 3 to 22. Patients who underwent vertical axillary minithracotomy were assigned to group I, and those undergoing conventional sternotomy, to group II. Group I and group II were compared with regard to the preoperative, perioperative and postoperative variables. Group I included 12 females and 4 males with an average age of 16.5+/-9.7. Group II comprised 14 female and 3 male patients with an average age of 18.5+/-9.8 showing similar features and pathologies. The cases were in Class I-II according to the New York Heart Association (NYHA) Classification, and patients with other cardiac and systemic problems were not included in the study. The ratio of the systemic blood flow to the pulmonary blood flow (Qp/Qs) was 1.8+/-0.2. The average pulmonary artery pressure was 35+/-10 mmHg. Following the diagnosis, performing elective surgery was planned. RESULTS: No significant difference was detected in the average time of the patients' extraportal circulation, cross-clamp and surgery (p>0.05). In the early postoperative period of the cases, the duration of mechanical ventilator support, the drainage volume in the first 24 hours, and the hospitalization time in the intensive care unit were similar (p>0.05). Postoperative pains were evaluated together with narcotic analgesics taken intravenously or orally. While 7 cases (43.7%) in group I needed postoperative analgesics, 12 cases (70.6%) in group II needed them. No mortality or major morbidity has occurred in the patients. The incision style and sizes in all of the patients undergoing RVAM were preserved as they were at the beginning. Furthermore, the patients of group I were mobilized more quickly than the patients of group II. The patients of group I were quite pleased with the psychological and cosmetic results. No residual defects have been found in the early postoperative period and after the end of the follow-up periods. All of the patients achieved functional capacity per NYHA. No deformation of breast growth has been detected during 18 months of follow-up for the group I patients, who underwent RVAM. CONCLUSION: To conclude, the repair of atrial septal defect by RVAM, apart from the limited working zone for the surgeon in these pathologies as compared to sternotomymay be considered in terms of the outcomes, and early and late complications. And this has accounted for less need of analgesics and better cosmetic results in recent years.


Subject(s)
Female , Humans , Male , Analgesics , Breast , Drainage , Follow-Up Studies , Heart , Heart Septal Defects, Atrial , Hospitalization , Intensive Care Units , Narcotics , New York , Pain, Postoperative , Postoperative Period , Pulmonary Artery , Sternotomy , Ventilators, Mechanical
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