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Annals of Thoracic Surgery Short Reports
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    • Congenital & Pediatric Case Report
      Open Access

      Azygos Vein Patch for Enlarging Anastomosis of Ascending Aorta and Neoaorta After Norwood Procedure

      Annals of Thoracic Surgery Short Reports
      Vol. 1Issue 1p96–98Published online: November 30, 2022
      • Shiori Kimura
      • Yasutaka Hirata
      • Miyuki Shibata
      • Minoru Ono
      Cited in Scopus: 0
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        Pericardium and polytetrafluoroethylene are popular patch materials, although they have some deficits in use for thin and small vessels. We present a case of post-Norwood hypoplastic left heart syndrome that required enlargement of the anastomosis between the native ascending aorta and the neoaorta at the time of a bidirectional Glenn procedure. The azygos vein was a useful material for patch augmentation of a hypoplastic ascending aorta.
        Azygos Vein Patch for Enlarging Anastomosis of Ascending Aorta and Neoaorta After Norwood Procedure
      • Congenital & Pediatric Short Report
        Open Access

        Mitral Valve Operation After Tetralogy of Fallot Repair: Early and Late Outcomes

        Annals of Thoracic Surgery Short Reports
        Vol. 1Issue 1p65–69Published online: November 24, 2022
        • Sepideh Jahanian
        • Joseph A. Dearani
        • Pouya Hemmati
        • Elizabeth H. Stephens
        • Hartzell V. Schaff
        • Heidi M. Connolly
        • and others
        Cited in Scopus: 0
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          There is a paucity of data regarding reoperation for mitral valve (MV) disease after tetralogy of Fallot (TOF) repair. We aimed to characterize this population and to analyze outcomes.
          Mitral Valve Operation After Tetralogy of Fallot Repair: Early and Late Outcomes
        • Congenital & Pediatric Short Report
          Open Access

          Trends in the Hospital Care of Neonates With Hypoplastic Left Heart Syndrome in the United States

          Annals of Thoracic Surgery Short Reports
          Vol. 1Issue 1p70–73Published online: November 24, 2022
          • Jason W. Greenberg
          • Farhan Zafar
          • Alia Dani
          • David S. Winlaw
          • Haleh C. Heydarian
          • Samuel P. Hanke
          • and others
          Cited in Scopus: 0
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            Surgical outcomes of first-stage palliation for hypoplastic left heart syndrome (HLHS) are vastly improved from prior eras and are well described, but rates and determinants of nonsurgical management are understudied, particularly on the national scale.
          • Congenital & Pediatric Case Report
            Open Access

            Traumatic Hemomediastinum and Hemothorax in a Patient With Totally Corrected Tetralogy of Fallot

            Annals of Thoracic Surgery Short Reports
            Vol. 1Issue 1p91–93Published online: November 17, 2022
            • Yuki Matsumura
            • Sho Inomata
            • Hikaru Yamaguchi
            • Masayuki Watanabe
            • Yuki Ozaki
            • Satoshi Muto
            • and others
            Cited in Scopus: 0
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            An 18-year-old Japanese youth was transferred to our emergency department because of a traffic accident. He had a past history of total correction for tetralogy of Fallot as an infant. Chest computed tomography revealed hemomediastinum and hemothorax. In an emergency operation, massive bleeding from the mediastinum was observed. Bleeding arose from the torn Blalock-Taussig shunt and right subclavian artery. Hemostasis was achieved by clipping the shunt and suturing the subclavian artery. This is a rare case of a patient with hemomediastinum caused by torn Blalock-Taussig shunt after a high-impact accident who survived it by operation.
            Traumatic Hemomediastinum and Hemothorax in a Patient With Totally Corrected Tetralogy of Fallot
          • Congenital & Pediatric Case Report
            Open Access

            Modified Blalock-Thomas-Taussig Shunt Using Femoral Artery Homograft

            Annals of Thoracic Surgery Short Reports
            Vol. 1Issue 1p94–95Published online: November 8, 2022
            • Sandy Zhang
            • Suneet Bhansali
            • Jaclyn McKinstry
            • Prema Ramaswamy
            • Kristen Thomas
            • Michael Martinez
            • and others
            Cited in Scopus: 0
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              Modified Blalock-Thomas-Taussig shunts are typically performed with biosynthetic polytetrafluoroethylene grafts. However, biologic conduits are being increasingly investigated. We herein report a case in which a femoral artery homograft was effectively used as material for a Blalock-Thomas-Taussig shunt.
              Modified Blalock-Thomas-Taussig Shunt Using Femoral Artery Homograft
            • Congenital & Pediatric Case Report
              Open Access

              Virtual Imaging for a Complex Case of Previous Coarctation Repair

              Annals of Thoracic Surgery Short Reports
              Vol. 1Issue 1p77–80Published online: October 12, 2022
              • Yuji Matsubayashi
              • Kenichi Kamiya
              • Tomoaki Suzuki
              • Shunta Miwa
              • Yotaro Mori
              • Masahide Enomoto
              • and others
              Cited in Scopus: 0
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              • Video
              Repeated surgical procedures for previous aortic coarctation is challenging. Three-dimensional imaging may be useful to visualize the complex anatomy more clearly than with computed tomography imaging, possibly leading to better outcomes. To evaluate the feasibility and efficacy of virtual imaging for preoperative planning of thoracic aortic surgery in this case, we used Vesalius 3D software, 3-dimensional image processing software, and detailed anatomic exploration. This technology may serve to optimize anatomically complex thoracic aortic surgery.
              Virtual Imaging for a Complex Case of Previous Coarctation Repair
            • Congenital & Pediatric Case Report
              Open Access

              Direct Hepatic Vein Connection to Left Atrium Without Congenital Anomaly in Adult Heart Disease

              Annals of Thoracic Surgery Short Reports
              Vol. 1Issue 1p81–84Published online: October 12, 2022
              • Soo Jin Park
              • Sung-Ho Jung
              Cited in Scopus: 0
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                Anomalous hepatic venous connection without other cardiac anomalies is a rare condition but does not have high clinical significance. We describe a patient in whom a portion of the left hepatic vein was directly connected to the left atrium, without intracardiac or extracardiac anomalies. A left-to-right shunt with tricuspid regurgitation and atrial fibrillation occurred from right atrial volume overload. Shunt ligation with tricuspid valvuloplasty and a maze procedure were performed as a treatment.
                Direct Hepatic Vein Connection to Left Atrium Without Congenital Anomaly in Adult Heart Disease
              • Congenital & Pediatric Case Report
                Open Access

                Intraoperative Stent Placement for the Treatment of Congenital Pulmonary Vein Atresia

                Annals of Thoracic Surgery Short Reports
                Vol. 1Issue 1p85–87Published online: September 14, 2022
                • Ryan Callahan
                • Rebecca S. Beroukhim
                • Christopher W. Baird
                Cited in Scopus: 0
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                  A 2-month-old infant presenting with failure to thrive was found to have right upper and right lower pulmonary vein atresia and underwent 2 failed transcatheter recanalization attempts. A hybrid intervention including pulmonary vein identification, ostial resection, venoplasty, and intraoperative stent placement is described and 2.5 years of subsequent follow-up is presented.
                  Intraoperative Stent Placement for the Treatment of Congenital Pulmonary Vein Atresia
                • Congenital & Pediatric Case Report
                  Open Access

                  Totally 3D Endoscopic Repair of Double-Chambered Right Ventricle

                  Annals of Thoracic Surgery Short Reports
                  Vol. 1Issue 1p88–90Published online: September 14, 2022
                  • Riku Kato
                  • Soh Hosoba
                  • Daichi Fukumi
                  • Toshiaki Ito
                  Cited in Scopus: 0
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                  • Video
                  Double-chambered right ventricle (DCRV) is a rare malformation that may develop after ventricular septal defect (VSD) closure. We describe a case of a 34-year-old women who underwent VSD closure in her infancy with a small Y-collar incision. She developed dyspnea on exertion and was recommended for surgery. She desired minimally invasive surgery for a cosmetic reason. We performed a totally 3e-dimensional endoscopic minimally invasive repair of DCRV. Endoscopic repair of DCRV after VSD closure for an adult is possible with an excellent view.
                  Totally 3D Endoscopic Repair of Double-Chambered Right Ventricle
                • Congenital & Pediatric How To Do It
                  Open Access

                  “Invisible” Incision: Modified Horizontal Right Axillary Mini-Thoracotomy for Pediatric Cardiac Surgery

                  Annals of Thoracic Surgery Short Reports
                  Vol. 1Issue 1p99–101Published online: August 8, 2022
                  • Naruhito Watanabe
                  • Ashley Hapak
                  • Teimour Nasirov
                  Cited in Scopus: 0
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                  • Video
                  Median sternotomy has been the standard surgical approach for pediatric cardiac surgery. The downside is that it leaves a notable and visible scar. Right axillary mini-thoracotomy provides a more aesthetically pleasing incision in addition to an earlier recovery time for patients. However, this contemporary thoracotomy provides a smaller and deeper view of the heart that can make the procedure more difficult. This report describes the modified techniques used to provide an excellent surgical exposure through the right axillary mini-thoracotomy, which also allows patients to have an “invisible” incision.
                  “Invisible” Incision: Modified Horizontal Right Axillary Mini-Thoracotomy for Pediatric Cardiac Surgery
                • Congenital & Pediatric Case Report
                  Open Access

                  Intra-atrial Approach for Infracardiac Total Anomalous Pulmonary Venous Connection

                  Annals of Thoracic Surgery Short Reports
                  Vol. 1Issue 1p74–76Published online: July 21, 2022
                  • Makoto Nakamura
                  • Kazuyoshi Kanno
                  • Masahiko Nishioka
                  Cited in Scopus: 0
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                    Patients with total anomalous pulmonary venous connection have various forms of pulmonary veins. Because pulmonary vein obstruction is a major and critical complication, it is necessary to create as large an anastomosis as possible while considering the positional relationship with the left atrium. Here, we report the case of a female neonate diagnosed with infracardiac total anomalous pulmonary venous connection and hypoplastic common pulmonary vein. The operation was performed by a sutureless technique in the intra-atrium.
                    Intra-atrial Approach for Infracardiac Total Anomalous Pulmonary Venous Connection
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