• 대한치과마취과학회지
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• 제12권2호
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• pp.99-104
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• 2012

Anticoagulation therapy with warfarin sodium is used to reduce the risk of thromboembolic events in patients with valvular heart disease, prosthetic heart valve, recurrent myocardiac infarction, etc. To keep anticoagulation state and minimize bleeding risk, patients with high risk of thromboembolism have been usually hospitalized for heparinization before oral surgery like extraction. However, this protocol requires time and high expense because of the long period of hospitalization and this is why low-molecular-weight heparin (LMWH) therapy is receiving attention in medical field as well as dentistry. LMWH has several advantages over unfractionated heparin (UFH) including predictable anticoagulant response which makes coagulation monitoring unnecessary in most patients and longer half-life than heparin which enables the patients to give themselves a subcutaneous injection once or twice daily. These advantages of LMWH make patients get oral surgery on an outpatient basis so that they can save time and cost. This case report introduces the use of LMWH in dental surgery and suggests proper use of LMWH. Though LMWH bridging therapy is widely used most of the previous studies are observational studies. Therefore randomized controlled trials are necessary to evaluate the safety and efficacy of LMWH bridging therapy.

• Journal of Chest Surgery
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• 제36권10호
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• pp.759-765
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• 2003

대동맥궁 차단증을 동반한 동맥간은 매우 중한 자연경과를 갖고 있는 희귀한 선천성 심장 기형이다. 생후 25일,체중 3.1 kg의 신생아에서 정중흉골절개술에 의한 일차 완전교정술을 시행하였다. A형 대동맥궁 차단증은 하행대동맥을 원위부 상행대동맥에 직접 문합하였으며, 폐동맥을 동맥간으로부터 분리하여 동맥간의 앞쪽에 위치한 다음 처리하지 않은 무판막 자가심낭도관을 사용하여 우심실 유출로를 재건하였다. 성공적 교정술 후 약 1년간의 양호한 추적결과를 경험하였기에 보고하는 바이다.

• Journal of Chest Surgery
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• 제18권2호
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• pp.293-298
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• 1985

Cor triatriatum is a rare congenital malformation of the heart in which a septum stretches in a transverse plane through the left atrium, thus creates two left atrial subchambers. The upper one connects with the pulmonary veins, and the lower connects with the left ventricles. Due to the rarity of, and difficulty in diagnosing car triatriatum, data on the surgery of the disease are of necessity and very limited. A case of cor triatriatum combined with atrial septal defect and persistent left superior vena cava was experienced in November, 1984 in Chonnam University Medical School. There was a transverse septum in the left atrium below atrial septal defect, all pulmonary veins were drained into the upper chamber of the left atrium which connected with the right atrium via atrial septal defect and the lower chamber via an oval opening[8mm] in the abnormal septum and the lower chamber was connected with the left atrial appendage, and the left ventricle via mitral valve. There was persistent left superior vena cava drained to left atrium and coronary sinus. The abnormal transverse septum within the left atrium was completely excised and the atrial septal defect was repaired with Woven Dacron patch. The post-operative course was not eventful and the patient was discharged to home with good result on the 15th postoperative day, and has been in good condition upto now.

• Journal of Chest Surgery
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• 제43권3호
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• pp.308-311
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• 2010

성인에서 종종 대동맥 축착증은 다른 심장 내 질환과 동반된다. 이러한 환자들에서 가장 적절한 수술적 방법을 결정하는 것은 매우 어렵다. 저자들은 대동맥 축착증 및 대동맥 판막부전을 동반한 대동맥근부 확장병변을 가진 환자에서, Bentall 수술 및 상행 대동맥-하행 대동맥간 우회로술을 정중 흉골절개를 통해 동시에 시행하였기에 보고하는 바이다.

• Journal of Chest Surgery
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• 제14권3호
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• pp.302-306
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• 1981

Aorticopulmonary window is a rare anomaly among congenital heart disease. Various terms have been suggested including A-P window, A-P fenestration, fistula, aorticseptal defect etc. The defect lies usually between the left side of the ascending aorta and right wall of the pulmonary artery just anterior to the origin of the right main pulmonary artery. We have experienced one case of aorticopulmonary septal defect which was diagnosed as V5D with pulmonary hypertension in 1 4/12 year old, 7.2 Kg, male patient. Operation was done under the hypothermic cardiopulmonary bypass using 5t. Thomas cardioplegic solution. Vertical right ventriculotomy over the anterior wall of RVOT revealed no defect in the ventricular septum, and incision was extended up to the main pulmonary artery to find the source of massive regurgitation of blood through MPA. Finger tip compression of the aorticopulmanary window was replaced with Foley bag catheter balloon, and the $7{\times}10$ mm aorticoseptal defect located 15mm above the pulmonic valve was sutured continuously wih 3-0 nylon suture during azygos flow of cardiopulmonary cannula which was located distal to the window resulted massive air pumping systemically, and temporary reversal of pumping was tried to minimize cerebral air embolism. Remained procedure was done as usual, and pump off was smooth and uneventful. Postoperatively, patient was attacked frequent opistotonic seizure with no recovery sign mentally and p.hysically. Vital signs were gradually worsen with peripheral cyanosis and oliguria, and cardiac activity was arrested 1485 minutes after operation. Autopsy was performed to find the sutured window and massive edema of the brain.

• 대한한방내과학회지
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• 제22권3호
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• pp.463-469
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• 2001

Valvular heart disease is one of the main current of cardiac problems and has many problems must be solved by sequelae and complications, etc. Rheumatic Mitral Stenosis is mainly attacked by rheumatic fever and developed by process of treatment of mitral valve or formation of trace. The purpose of this study is to examine the efficacy of oriental treatment for Cerebral Infarction with Rheumatic Mitral Stenosis. At the time of visiting ER, he was shown the symptoms of dull mentality, Rt. hemiplegia, global aphasia, dysphagia, chest discomfort, insomnia, dyspnea, etc, It showed that Atrial fibrillation in EKG monitoring, Atrial fibrillation, Rheumatic Mitral Stenosis, Ejection-Fraction slope 60% in Cardiac echography, Lt. atrial hypertrophy, Rt. atrial hypertrophy, Rt. ventricular hypertrophy with pulmonary congestion in chest X-ray. From the view of oriental diagnostic criteria. We classified the patient's clinical conditions and treated accordingly. As a result of treatment, symptoms were markedly improved and he was discharged. Further elaboration of oriental diagnostic classification could possibly lead to the fundamental treatment.

• Korean Circulation Journal
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• 제53권3호
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• pp.134-150
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• 2023

Ventricular septal defects (VSDs) are the most common kind of congenital heart disease and, if indicated, surgical closure has been accepted as a gold-standard treatment. However, as less-invasive methods are preferred, percutaneous device closure has been developed. After the first VSD closure was performed percutaneously by Lock in 1988, both techniques and devices have developed consistently. A perventricular approach for closure of muscular VSD in small patients and the closure of perimembranous VSD using off-label devices are key remarkable developments. Even though the Amplatzer membranous VSD occluder (Abbott) could not be approved for use due to the high complete atrioventricular conduction block rate, other new devices have shown good results for closure of perimembranous VSDs. However, the transcatheter technique is slightly complicated to perform, and concerns about conduction problems after VSD closure with devices remain. There have been a few reports demonstrating successful closure of subarterial-type VSDs with Amplatzer devices, but long-term issues involving aortic valve damage have not been explored yet. In conclusion, transcatheter VSD closure should be accepted as being as effective and safe as surgery but should only be performed by experienced persons and in specialized institutes because the procedure is complex and requires different techniques. To avoid serious complications, identifying appropriate patient candidates for device closure before the procedure is very important.

• Journal of Chest Surgery
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• 제37권10호
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• pp.833-838
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• 2004

배경: 선천성 이엽성 대동맥판막질환에 대한 성형술은 술 후 조기 성적에서는 매우 우수하다고 알려져 있으나 중기 및 장기 성적에 대해서는 논란이 되고 있는 실정이다. 대상 및 방법: 판막 성형술의 중기 성적을 알아보기 위해 1994년부터 2003년까지 선천성 이엽성 대동맥판막질환으로 판막성형술을 시행받은 22명의 환자들의 임상기록 및 심초음파 검사들을 후향적으로 분석하였다. 결과: 남자가 17명, 여자가 5명이었으며 평균 연령은 41$\pm$14세였다. 이엽성 판막의 폐쇄부전이 대부분(91%=20/22)의 환자에서 주 병변이었다. 수술 방법들로는 붙어 있는 공통 판막엽의 해리(release)가 19예(86%)에서 시행되었으며, 이탈된 판막엽에 대한 수술로는 채기 절제 및 일차봉합술이 11예(50%), 판엽줄임술(plication) 후 심막으로 보강한 것이 6예(27%), 판막엽만 줄인 3예(14%)가 있었다. 두꺼워진 판막엽을 깎은 것이(slicing) 12예(55%)에서 사용되었으며, 교련부위의 성형술은 8예(36%), 교련부위절개술이 6예(27%)에서 시행되어 평균 환자당 2.8개의 술식이 사용되었다. 수술 사망은 없었으며 모든 환자를 술 후 평균 38$\pm$17개월간 추적 관찰하였다. 추적기간 중 1명의 환자가 술 후 2개월에 성형술 봉합의 풀림에 의한 급성 대동맥판막 폐쇄부전으로 대동맥 판막 치환술을 받았다. 환자들의 기능적 상태는 (NYHA functional class)는 술 전 평균 1.9$\pm$0.6에서 술 후 1.2$\pm$0.5로 의미있게 개선되었으며(p<0.01), 심초음파 검사상 좌심실의 수축기말/이완기말 용적도 각각 45$\pm$9 mm, 67$\pm$10 mm에서 37$\pm$10 mm, 56$\pm$10 mm로 의미있게 줄어들었다(p<0.05). 대동맥 판막의 폐쇄부전 정도는 술 전 3.1$\pm$1.2에서 심폐기 이탈 직후에 0.9$\pm$0.7로 의미있게 줄었으나 추적 관찰 중 1.8$\pm$1.1로 증가하는 양상을 보였다. 중등도 이상의 폐쇄부전이 없이 생존할 확률은 술 후 1년에 89.7%, 3년에 89.7%, 4년에 39.9%로 나타나 중기 이후에 판막기능의 악화가 빨라지는 경향을 보였다. 결론: 선천성 이엽성 대동맥판막질환 성형술의 중기 성적은 임상적으로는 초기의 우수한 상태를 유지하였으나, 성형된 대동맥 판막의 장기적 내구성은 장담할 수 없었다.

• Journal of Chest Surgery
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• 제43권6호
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• pp.614-618
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• 2010

배경: 단독 대동맥판막 폐쇄부전증(AR) 환자에서 단독 대동맥판막 치환술 후 좌심실질량 감소의 정도를 평가하고자 하였다. 대상 및 방법: 2002년부터 2007년까지 대동맥판막 폐쇄부전증으로 단순 대동맥판막 치환술을 시행한 20명을 대상으로 수술 전과 수술 후 1년에 심초음파 검사결과를 후향적으로 조사하였다. 대상환자는 남자 12명, 여자 8명, 평균연령 $55.8{\pm}11.8$세, 평균체표면적 $1.64{\pm}0.19m^2$이었다. 대조군은 심초음파상 병변이 발견되지 않은 비슷한 나이의 41명을 대상으로 하였다. 대동맥판막 치환술 이외의 복합시술을 시행한 환자와 감염성 심내막염 환자는 제외하였다. 결과: 수술에 사용된 판막의 종류는 조직판막이 7명, 기계판막이 13명에서 사용되었으며 크기는 21 mm가 3명, 23 mm가 13명 그리고 25 mm가 4명에서 사용되었다. 수술 후 좌심실질량계수(LVMI, $125.5{\pm}42g/m^2$)는 술전에 비해 유의하게 감소하였으나($212.3{\pm}80g/m^2$, p=0.000) 대조군($80.5{\pm}15.9g/m^2$, p=0.000)에 비해 높았다. 수술 전후의 심실중격(확장기/수축기: $13.5{\pm}3.4mm/17.1{\pm}4.1mm$)과 좌심실 후벽(확장기/수축기: $12.9{\pm}3.4mm/16.7{\pm}3.4mm$)의 두께는 수술 전에 비해 일부 감소가 있었으나 통계적으로 유의하지 않았으며 각각 대조군(확장기/수축기 $8.6{\pm}1.4mm/12.1{\pm}1.7mm$, 확장기/수축기 $8.4{\pm}1.4mm/13.2{\pm}1.9mm$)보다 유의하게 높았다(p < 0.001). 결론: 단독 대동맥판막 폐쇄부전으로 단독 대동맥판막 치환술 시행 1년 후 주로 좌심실용적의 감소에 의한 LVMI의 유의한 감소가 있었으나 대조군에 비해서는 여전히 높았다.

• Journal of Chest Surgery
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• 제14권3호
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• pp.260-267
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• 1981

Left atrial myxoma is a rare disease and its recurrence is reported to be always possible whenever primary excision is incomplete. Cardiac Myxoma is rare disease of the heart, and it has a little chance of recurrence. We experienced a patient of recurrent left atrial myxoma who was 31 years old, had been gotten excision of Lt. atrial myxoma when she was 28 years of her age. She was gotten mitral valve replacement simultaneously during 2nd operation with difficulty. So we report this case with the review of the literatures. [KTCS 1981;3:260-267]Surgical Treatment of Acute Pyogenic Pericarditis followed the Sepsis Ki Woo Shin, M.D.,* Ho Wan Lee, M.D.* and Dong Jun Lee, M.D.* Two cases of acute pyogenic pericarditis are, one case, 12-year-old male patient, followed the bacteremia of pneumonia and other case, 9 year old female patient, followed the bacteremia of osteomyelitis. After the confirmed diagnosis by pericardial aspiration, the emergency pericardial window was made to relief the severe cardiogenic symptoms. The general symptoms were improved immediately, but 40 days and 15 days after pericardiostomy, in each case, the sign and symptoms of cardiac compression were seen with recurrent cardiac tamponade. Pericardiectomy with median sternotomy was performed in each case and thereafter the patients were discharged without any problems.