• 제목/요약/키워드: myocardial bridge

검색결과 9건 처리시간 0.028초

흉통(胸痛)이 있는 심근교(myocardial bridge) 환자의 치험 1례 (A Case of Treating Chest Pain Associated with Myocardial Bridge)

  • 김보람;최동준;임성우
    • 대한중풍순환신경학회지
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    • 제10권1호
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    • pp.74-80
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    • 2009
  • Myocardial bridging, a congenital coronary anomaly, is present when a segment of a major epicardial coronary artery, runs intramurally through the myocardium. So with each systole, the coronary artery is compressed. It has been associated with angina, arrhythmia, myocardial infarction and sudden cardiac death. This is a case of a 39-year-old woman who was diagnosed myocardial bridge. She complained of recurrent chest pain, palpitation. We diagnosed her as Gyesimtong(JiXiTong, 悸心痛), and prescribed Jeongkicheonhyang-tang(正氣天香湯). After treatment, all of the symptoms had improved and have not recurred for 18 months. This case suggests that oriental medicine therapy can be applicable to improve in symptoms of myocardial bridge.

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심폐바이패스없이 관상동맥 심근교의 수술치험 -1례 보고- (Supra-Arterial Myotomy without Cardiopulmonary Bypass for Myocardial Bridging -One case report-)

  • 김재현;최세영;유영선;이광숙;윤경찬;박창권
    • Journal of Chest Surgery
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    • 제32권2호
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    • pp.181-184
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    • 1999
  • 심근교에 의한 관상동맥협착은 드문 질환으로 흉통, 심근경색 및 심실세동을 유발할 수 있다. 약물치료에 반응이 없는 심근교는 심근절개술의 적응이 된다. 저자들은 흉골부분절개술하 심폐바이패스없이 좌전하행지부위에 심근절개술을 성공적으로 시행하였기에 보고하는 바이다

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심근교(Myocardial Bridging)에 대한 수술적 치료 -2예 보고 (Surgery for Myocardial Bridging - A report of two cases -)

  • 김재현;오삼세;이길수;정인석;윤효철;김인섭;나찬영
    • Journal of Chest Surgery
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    • 제40권9호
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    • pp.629-632
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    • 2007
  • 심근교는 증상과 관련없이 우연히 발견되는 경우가 대부분이지만 드물게 협심증, 심근 경색, 심실성부정맥 등의 증상을 유발한다. 증상이 있는 심근교 환자에서 약물치료가 효과적이지 않을 경우 스텐트 삽입술, 동맥상부 심근 절개술 혹은 관상동맥우회술 등을 시행하고 있으나 명확한 치료지침은 없는 상태이다. 저자들이 경험한 심근교에 대한 수술 증례 2예를 문헌고찰과 함께 보고하는 바이다.

Delayed Repair of Ventricular Septal Rupture Following Preoperative Awake Extracorporeal Membrane Oxygenation Support

  • Park, Bong Suk;Lee, Weon Yong;Lim, Jung Hyeon;Ra, Yong Joon;Kim, Yong Han;Kim, Hyoung Soo
    • Journal of Chest Surgery
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    • 제50권3호
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    • pp.211-214
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    • 2017
  • Outcomes of ventricular septal rupture (VSR) as a complication of acute myocardial infarction are extremely poor, with an in-hospital mortality rate of 45% in surgically treated patients and 90% in patients managed with medication. Delaying surgery for VSR is a strategy for reducing mortality. However, hemodynamic instability is the main problem with this strategy. In the present case, venoarterial extracorporeal membrane oxygenation (ECMO) was used to provide stable hemodynamic support before the delayed surgery. Awake ECMO was also used to avoiding the complications of sedatives and mechanical ventilation. Here, we describe a successful operation using awake ECMO as a bridge to surgery.

Outcomes of Coronary Artery Bypass Grafting after Extracorporeal Life Support in Patients with Cardiac Arrest or Cardiogenic Shock

  • Kim, Younghwan;Cho, Yang-Hyun;Yang, Ji-Hyuk;Sung, Kiick;Lee, Young Tak;Kim, Wook Sung;Lee, Heemoon;Cho, Su Hyun
    • Journal of Chest Surgery
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    • 제52권2호
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    • pp.70-77
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    • 2019
  • Background: Extracorporeal life support (ECLS) is used as a bridge to revascularization in high-risk patients with ischemic heart disease. We reviewed our experiences of coronary artery bypass grafting (CABG) after ECLS in patients with cardiac arrest or refractory cardiogenic shock. Methods: We retrospectively reviewed 4,616 patients who underwent CABG at our institution between May 2006 and February 2017. We identified patients who underwent CABG following ECLS for cardiogenic shock or cardiac arrest. Twenty-three patients (0.5% of all CABG cases) were enrolled in the analysis. Their median age was 65 years (Q1-Q3, 58-77 years). Nine patients (39.1%) were diagnosed with ST-elevation myocardial infarction. Mechanical complications after acute myocardial infarction, including acute mitral regurgitation, left ventricular rupture, and ventricular septal defect, occurred in 9 patients (39.1%). Results: The median time from cardiopulmonary resuscitation to ECLS initiation was 25 minutes (Q1-Q3, 18.5-28.5 minutes). Conventional CABG was performed in 10 patients (43.5%) who underwent concomitant intracardiac procedures. Postoperative ECLS was required in 16 patients (69.5%). The rate of successful ECLS weaning was 91.3% (n=21). There were 6 early mortalities (26.1%). Conclusion: CABG after ECLS was very rare in real-world circumstances. Although the early mortality rate was high, the risk of mortality may be acceptable under such devastating circumstances.

말기 심부전 환자에서 심장이식의 교량으로서 좌심실 축소술 - 중례보고 - (Partial Left Ventriculectomy as a Bridge to Cardiac Transplantation in a Patient of End-Stage Heart Failure -Case Report-)

  • 전양빈;이창하;이재웅;박철현;박국양
    • Journal of Chest Surgery
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    • 제35권9호
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    • pp.672-674
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    • 2002
  • 확장성 심근병증과 말기 심부전으로 진단된 40세 남자환자가 1997년 7월 좌심실 축소술(partial left ventriculectomy)을 시행하고 18개월 후 1999년 1월 심장 이식술을 시행하였다 좌심실 축소술 시행후 3개월에 시행한 심초음파 소견상 좌심실 구출율은 26%에서 42.6%로 증가하였고, 확장기 좌심실크기는 71 mm에서 45mm로 감소하여 심초음파로 측정한 심박출량 및 심박출지수는 각각 3.95 L/min, 2.28 L/min/m$^2$이었다. 술 후 11개월뒤 심초음파상 좌심실 크기가 56/51 mm(확장기/수축기 직경)로 증가하고 좌심실 구출율은 17%로 감소하여 약물을 더 증량하고 18개월째에 공여심장이 제공되어 심장이식을 시행하였다. 1, 3, 6개월만에 3회 시행한 심근 조직검사상 ISHLT(International Society of Heart and Lung Transplantation) 분류상 la로 판정됐고 현재까지 거부반응으로 인한 치료는 필요하지 않았다. 말기 심부전을 동반한 확장성 심근병증 환자에서 심장 이식을 기다리는 동안 좌심실 축소술이 성공적인 교량역할을 했기에 이를 보고하는 바이다.

성인용 공기구동식 심실보조장치의 모의순환실험 (In Vitro Test of an Adult-Sized Pneumatic Type Ventricular Assist Device)

  • 김상현;장병철;김원기;김남현;조범구
    • 대한의용생체공학회:의공학회지
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    • 제14권2호
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    • pp.163-167
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    • 1993
  • We developed a ventricular assist device(VAD) to be used as a bridge to heart transplantation or a circulatory assist device for patients with end-stage heart disease or poor myocardial function after cardiac surgery. It is a pneumatic and diaphragm-type VAD and its stroke volume is 90 cc. The upper housing and diaphragm is made of a segmented polyurethane and the lower back plate is made of a polycarbonate. Two Carbomedics$^R$ mechanical valves are used as inlet and outlet valves. It was tested in vitro and the cardiac output of the VAD was 7 L/min at a heart rate of 70 bpm. The line pressure from a pressure transducer inserted in the pneumatic line was recorded and compared with the ideal pressure tracing.

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공압식 심실보조장치의 개발 및 동물실험 (Development and Animal Tests of Pneumatic Ventricular Assist Device)

  • 박영환;김상현
    • Journal of Chest Surgery
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    • 제30권3호
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    • pp.247-252
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    • 1997
  • 심장이식시에 가교 역할을 담당하거나 수술 후 심부전에 빠진 심장을 보조할 공압식 심실보조장치를 개발하여 동물실험을 시행하였다. 실험 에 이용한 심실보조장치는 소아용과 성 인용의 두 가지 종류로서 박동장이 각각 34cc와 70cc이다. 심실 재료는 폴리우레탄으로 제작하여 항혈전성을 높였다. 총 10마리의 동물실험을 시행하였다. 심실보조장치의 혈액펌프는 좌심방과 대동맥에 연결관을 이용하여 이식하였다. 심실보조장치의 평균 박출량은 펌프 박동수가 60회일 때 성 인의 경우 2.38 L/min였고 소아용의 경우 0.41 L/min였다. 생존시간은 최고 26시간이었다. 가장 큰 합병증은 출혈이었고 주 사망원인은 심부전 및 폐부전이었다. 심실보조장치 자체 에 대한 결함때문에 일어난 실패는 없었다. 현재까지의 실험 결과를 토대로 심실보조장치를 발전시키면 임상에서도 사용 가능할 것으로 보인다.

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공압식 심실 보조기의 동물실험 (Animal Experiment of the Pneumatic Ventrivular Assist Device)

  • 박성식;김삼현;서필원;최창휴;이상훈;이혁수;황승옥;안혁
    • Journal of Chest Surgery
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    • 제32권12호
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    • pp.1065-1077
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    • 1999
  • Background : Ventricular assist devices(VADs) are being used for patients in postcvardiotomy cardiogenic shock status bridge to cardiac transplant settings and in post-myocardial infarction cardiogenic shock. The VAD which was developed at the Deparment of medical engineering in Dankook University College of Medicine was a pneumatically driven device and can maintain pulsatile flow. The goal of this study is to develop animal experimental models using the VAD and to clarify the reliability and hemodynamic property adequacy of end organ perfusion durability and severity of thrombotic-hemolytic tendency of the device. Material and Method : The pneumatic VAD was applied to 8 adult female lambs, We examined some hemodynamic parameters such as arterial blood pressure pulmonary capillary wedge pressure(pcwp) pulmonary artery pressure(PAP) left atrial pressure hour urine output cardiac index VAD flow EKG to determine the reliability of the VAD and hemodynamic compatibility of the experimental animals within 24 hours of experiment. We also observed the end organ perfusion durability of the VAD and thrombotic-hemolytic property of the VAD after 24 hours of VAD insertion. Result: We could monitor all hemodynamic parameters including pcwp PAP cardiac index EKG, adn hour urine as true clinical settings. We observed that the reliability of the VAD was excellent and the hemodynamic property of the experimental animal and end organ perfusion were adequate within 24 hours of experiment. In four lambs surviving 24 hours after insertion the reliability of the VAD and end organ perfusion were excellent and no thrombotic-hemolytic tendency was noted. However after 15 days of experiment the diaphragm of the VAD was torn and it was recommende that the durability of the VAD should be extended. Conclusion : e conclude that the pneumatic VAD developed at Dankook University Biomedical Engineering has good hemodynamic property and low thromboembolic tendency and presents adequate end organ perfusion but we noted that the durability of the device should be expanded further. It will be possible to do more reliable experiment in the future according to the animal experimental method developed in this study especially with the heart failure models.

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