• 한국환경생태학회지
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• 제36권3호
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• pp.350-357
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• 2022

본 연구에서는 국립공원에서 자연의 소리는 생태계의 구성요소임과 동시에 탐방객들이 공원을 체험하는 중요한 요소이다. 따라서 국립공원 내 소음 분포 특성을 파악하고 자연의 음환경(Soundscape) 보존 및 복원을 위한 노력은 국립공원 관리 차원에서 중요한 과제 중 하나이다. 그러나 여전히 국내 국립공원에서는 소음 관리 및 음환경 보존에 대한 관심이 미약한 것이 사실이다. 무등산국립공원은 호남지역에서 가장 중요한 자연보호지역 중 하나로 계절별 동물이 우는 소리, 물소리, 바람 소리 등 탐방객들에게 자연의 소리를 제공할 수 있는 최적의 장소이지만 대도시에 인접해 있고 공원 내부로 도로 및 대규모 시설지가 인접해있는 등 소음이 발생하여 공원 내 음환경에 위협이 되고 있는 상황이다. 따라서 본 연구는 소음지도, 탐방로 소리등급도, 주요 지점의 음환경 녹음 데이터, 소리자원 분포도 등의 분석을 통해 무등산국립공원 내 소리 분포 특성을 파악하고 광범위한 소음의 영향을 나타냄으로써 음환경 관리의 필요성을 시사하고 있다는 중요성을 지니고 있다. 반면 본 연구에서는 연구 인력과 장비의 한계로 인하여 소음지도, 탐방로 소리등급도, 소리자원 분포도의 속성 데이터 수집 기간이 상이한 점이 한계점으로 남는다. 그러나 본 연구의 결과는 탐방 만족도 및 자연의 음환경 보존 등을 목표로 향후 지속적인 음환경 보존 및 관리를 위해 활용될 수 있는 기초자료가 될 것으로 판단된다.

• 대한음성학회:학술대회논문집
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• 대한음성학회 2007년도 한국음성과학회 공동학술대회 발표논문집
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• pp.3-23
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• 2007

King Sejong the Great, his students in Jip-hyeun-jeon school and Choe Sejin, their successor of the sixteenth century, indicated Middle Korean had three distinctive pitches, low, high, and rising (phyeong-, geo-, sang-sheong). Thanks to $Hun-min-jeng-{\emptyset}eum$ as well as its Annotation and side-dots literatures in fifteenth and sixteenth centuries, we can compare Middle Korean with Hamgyeong dialect, Gyeongsang dialect, and extant tone dialects with joint preservers of what was probably the tonal system of unitary mother Korean language. What is most remarkable about middle Korean phonetic work is its manifest superiority in conception and execution as anything produced in the present day linguistic scholarship. But at this stage in linguistics, prior to the technology and equipment needed for the scientific analysis of sound waves, auditory description was the only possible frame for an accurate and systematic classification. And auditory phonetics still remains fundamental in pitch description, even though modern acoustic categories may supplement and supersede auditory ones in tonological analysis. Auditory phonetics, however, has serious shortcoming that its theory and practice are too subject to be developed into the present century science. With joint researchers, I am developping a new pitch scale. It is a semiautomatic auditory grade pitch analysis program. The result of our labor will give a significant breakthrough to upgrade our component in linguistics.

• Journal of Chest Surgery
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• 제12권3호
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• pp.281-288
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• 1979

For years, physicians and anatomists have been interested in the heart that has one functioning ventricle. Various terms have been suggested for this entity including single ventricle, common ventricle, double-inlet left ventricle, cor biatriatum triloculare, and primitive ventricle. In this report, the term "single ventricle" is utilized as suggested by Van Praagh, and is defined as that congenital cardiac anomaly in which a common or separate atrioventricular valves open into a ventricular chamber from which both great arterial trunks emerge. An outlet chamber, or infundibulum, may or may not be present and give rise to the origin of either of the great arteries. This definition excludes the entity of mitral and tricuspid atresia. An 11 year old cyanotic boy was admitted chief complaints of exertional dyspnea and frequent upper respiratory infection since 2 weeks after birth. He was diagnosed as inoperable cyanotic congenital heart disease, and remained without any corrective treatment up to his age of 11 year when he suffered from aggravation of symptoms and signs of congestive heart failure for 2 months before this admission. On 22nd of May 1979, he was admitted for total corrective operation under the impression of tricuspid atresia suggested by a pediatrician. Physical check revealed deep cyanosis with finger and toe clubbing, and grade V systolic ejection murmur with single second heart sound was audible at the left 3rd intercostal space. Development was moderate in height [135 cm] and weight[28Kg]. Routine lab findings were normal except increased hemoglobin [21.1gm%], hematocrit [64 %], and left axis deviation with left ventricular hypertrophy on EKG. Cardiac catheterization and angiography revealed 1-transposition of aorta, pulmonic valvular stenosis, double inlet of a single ventricle with d-loop, and normal atriovisceral relationship [Type III C solitus according to the classification of Van Praagh]. At operation, longitudinal incision at the outflow tract of right ventricle in between the right coronary artery and its branch [LAD from RCA] revealed high far anterior aortic valve which had fibrous continuity with mitral annulus, and pulmonic valve was stenotic up to 4 mm in diameter positioned posterolaterally to the aorta. Ventricular septum was totally defective, and one markedly hypertrophied moderator band originated from crista supraventricularis was connected down to the imaginary septum of the ventricular cavity as a pseudoseptum of the ventricle. Size of the defect was 3X3 cm2 in total. Patch closure of the defect with a Teflon felt of 3.5 x 4 cm2 was done with interrupted multiple sutures after cut off of the moderator band, which was resutured to the artificial septum after reconstruction of the ventricular septum. Pulmonic valvotomy was done from 4 mm to 11 mm in diameter thru another pulmonary arteriotomy incision, and right ventriculotomy wound was closed reconstructing the right ventricular outflow tract with pericardial autograft of 3 x 4 cm2. Atrial septal defect of 2 cm in diameter was closed with 3-0 Erdeck suture, and atrial wall was sutured also when rectal temperature reached from 24`C to 35.5`C. Complete A-V block was managed with temporary external pacemaker with a pacing rate of 110/min. thru myocardial wire, and arterial blood pressure of 80/50 mmHg was maintained with Isuprel or Dopamine dripping under the CVP of 25-cm saline. Consciousness was recovered one hour after the operation when his blood pressure reached 100 /70 mmHg, but vital signs were not stable, and bleeding from the pericardial drainage and complete anuria were persisted until his heart could not capture the pacemaker impulse, and patient died of low output syndrome 320 min after the operation.

• Journal of Chest Surgery
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• 제12권3호
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• pp.289-296
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• 1979

For years, physicians and anatomists have been interested in the heart that has one functioning ventricle. Various terms have been suggested for this entity including single ventricle, common ventricle, double-inlet left ventricle, cor biatriatum triloculare, and primitive ventricle. In this report, the term "single ventricle" is utilized as suggested by Van Praagh, and is defined as that congenital cardiac anomaly in which a common or separate atrioventricular valves open into a ventricular chamber from which both great arterial trunks emerge. An outlet chamber, or infundibulum, may or may not be present and give rise to the origin of either of the great arteries. This definition excludes the entity of mitral and tricuspid atresia. An 11 year old cyanotic boy was admitted chief complaints of exertional dyspnea and frequent upper respiratory infection since 2 weeks after birth. He was diagnosed as inoperable cyanotic congenital heart disease, and remained without any corrective treatment up to his age of 11 year when he suffered from aggravation of symptoms and signs of congestive heart failure for 2 months before this admission. On 22nd of May 1979, he was admitted for total corrective operation under the impression of tricuspid atresia suggested by a pediatrician. Physical check revealed deep cyanosis with finger and toe clubbing, and grade V systolic ejection murmur with single second heart sound was audible at the left 3rd intercostal space. Development was moderate in height [135 cm] and weight[28Kg]. Routine lab findings were normal except increased hemoglobin [21.1gm%], hematocrit [64 %], and left axis deviation with left ventricular hypertrophy on EKG. Cardiac catheterization and angiography revealed 1-transposition of aorta, pulmonic valvular stenosis, double inlet of a single ventricle with d-loop, and normal atriovisceral relationship [Type III C solitus according to the classification of Van Praagh]. At operation, longitudinal incision at the outflow tract of right ventricle in between the right coronary artery and its branch [LAD from RCA] revealed high far anterior aortic valve which had fibrous continuity with mitral annulus, and pulmonic valve was stenotic up to 4 mm in diameter positioned posterolaterally to the aorta. Ventricular septum was totally defective, and one markedly hypertrophied moderator band originated from crista supraventricularis was connected down to the imaginary septum of the ventricular cavity as a pseudoseptum of the ventricle. Size of the defect was 3X3 cm2 in total. Patch closure of the defect with a Teflon felt of 3.5 x 4 cm2 was done with interrupted multiple sutures after cut off of the moderator band, which was resutured to the artificial septum after reconstruction of the ventricular septum. Pulmonic valvotomy was done from 4 mm to 11 mm in diameter thru another pulmonary arteriotomy incision, and right ventriculotomy wound was closed reconstructing the right ventricular outflow tract with pericardial autograft of 3 x 4 cm2. Atrial septal defect of 2 cm in diameter was closed with 3-0 Erdeck suture, and atrial wall was sutured also when rectal temperature reached from 24`C to 35.5`C. Complete A-V block was managed with temporary external pacemaker with a pacing rate of 110/min. thru myocardial wire, and arterial blood pressure of 80/50 mmHg was maintained with Isuprel or Dopamine dripping under the CVP of 25-cm saline. Consciousness was recovered one hour after the operation when his blood pressure reached 100 /70 mmHg, but vital signs were not stable, and bleeding from the pericardial drainage and complete anuria were persisted until his heart could not capture the pacemaker impulse, and patient died of low output syndrome 320 min after the operation.

• 대한관절경학회지
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• 제10권1호
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• pp.70-76
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• 2006

목적: 금속 봉합 나사못을 이용한 견관절 습관성 전방 탈구 수술 후, 여러 원인에 의하여 발생한 금속 봉합 나사 못 돌출 합병증을 보고하고 발생 원인, 임상 양상 및 관절경적 치료에 대하여 알아보고자 하였다. 대상 및 방법: 견관절 습관성 전방 탈구로 봉합 나사못을 이용한 Bankart 수술을 시행 받은 후 운동시 들리는 관절내 마찰음 및 통증 또는 불안정성을 호소하며 내원하여 관절경 재수술을 시행받은 환자 5명을 대상으로 하였다. 처음 수술 이후 재수술까지의 평균 기간은 5.2개월이었다. 환자들은 관절경 재수술시 봉합 나사못의 돌출이 확인되었으며 관절경 술식을 이용하여 돌출 봉합 나사못을 제거하였다. 결과: 주 증상은 4명에서 통증을 동반한 관절내 마찰음이었으며 이 마찰음은 외전 및 외회전시 분명하게 들렸다. 1명은 통증과 함께 견관절 불안정성을 호소하였다. 견관절 운동 범위는 외회전만 약간 감소되었을 뿐 거의 정상 소견을 나타내었다. 돌출되었던 봉합 나사못의 위치는 5시 방향 1명, 4시 방향 2명, 2시 및 3시 방향 각각 1명씩이었다. 그 중 2명은 전방 관절와연에서 5 mm 정도 내측 관절면 위에 위치하였다. 나머지 3명은 올바른 위치에 삽입되어 있었으나 나사못 주변의 연골 마모 및 골소실이 관찰되었다. 재수술시 5명 모두 상완골두에 연골 손상이 발견되었으며 1명은 관절와에도 연골 결손이 동반되었다. 재수술 후 2년째 추시 결과 재탈구나 불안정성을 보이는 환자는 없었으며 통증에 대한 VAS 점수는 수술 전 3.4에서 수술 후 1.2로 감소되었다. Constant 점수는 수술 전 65점에서 수술 후 89점으로 증가하였으며 ASES 점수도 수술 전 67점에서 수술후 88점으로 증가하였다. 결론: 봉합 나사못 합병증으로 인한 증상은 불안정성을 동반하지 않는 경우가 많으며 대부분 재활 운동 시점부터 증상이 나타나지만 정상적인 수술 후 통증과 구분이 어려운 경우가 많다 그러나 돌출된 봉합 나사못은 상완골두 연골의 파괴를 유발하는 심각한 합병증을 초래하므로 봉합 나사못 돌출이 의심되면 관절경을 통하여 관절내의 변화를 관찰하며 돌출된 봉합 나사못을 다시 삽입하거나 제거하여야 한다. 봉합 나사못 제거에 본 수술 방법을 사용하면 용이하게 봉합 나사못 제거가 가능하리라 사료된다.