• 제목/요약/키워드: diaphragmatic plication

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소아 심혈관수술 후의 횡격막마비 (Phrenic Nerve Paralysis after Pediatric Cardiovascular Surgery)

  • 윤태진
    • Journal of Chest Surgery
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    • 제25권12호
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    • pp.1542-1549
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    • 1992
  • From March 1986 to August 1992, 18 patients underwent diaphragmatic plication for the diaphragmatic paralyses complicating various pediatric cardiac procedures. Age at operation ranged from 16 day to 84 months with mean age of 11.8 months. In order of decreasing incidence, the primary cardiac procedures included modified Blalock-Taussig shunt [ 5 ], Arterial switch operation [ 4 ], modified Fontan operation [ 2 ], and others [ 7 ]. The suspicious causes of phrenic nerve injury included overzealous pericardial resection [ 7 ], direct trauma during the procedure [ 6 ], dissection of fibrous adhesion around the phrenic nerve [ 3 ] and unknown etiology [ 2 ]. The involved sides of diaphragm were right in 10, left in 7 and bilateral in one. The diagnosis was suspected by the elevation of hem-idiaphragm on chest x-ray and confirmed by fluoroscopy. The interval between primary operation and plication ranged from the day of operation to 38 postoperative days [mean : 14 days]. The method of plication were "Central pleating technique" described by Schwartz in 16 and other techniques in 2. Five patients expired after plication and the cause of death were not thought to be correlated directly with the plication itself. In the remaining 13 survivors, extubation or cessation of positive ventilation could be done between the periods of the day of plication and 14th postoperative days [mean; 3.8day]. We have made the following conclusions : 1] Phrenic nerve paralyses are relatively common complication after pediatric cardiac procedures and the causes of phrenic nerve injury are mostly preventable; 2] Phrenic nerve palsy is associated with corisiderable morbidity; 3] diaphragmatic plication is safe, reliable and can be applicable in patients who are younger age and require prolonged positive pressure ventilation.ntilation.

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Open Transthoracic Plication of the Diaphragm for Unilateral Diaphragmatic Eventration in Infants and Children

  • Alshorbagy, Ashraf;Mubarak, Yasser
    • Journal of Chest Surgery
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    • 제48권5호
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    • pp.307-310
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    • 2015
  • Background: To evaluate our experience of early surgical plication for diaphragmatic eventration (DE) in infancy and childhood. Methods: This study evaluated infants and children with symptomatic DE who underwent plication through an open transthoracic approach in our childhood development department between January 2005 and December 2012. Surgical plication was performed in several rows using polypropylene U-stitches with Teflon pledgets. Results: The study included 12 infants and children (7 boys and 5 girls) with symptomatic DE (9 congenital and 3 acquired). Reported symptoms included respiratory distress (91.7%), wheezing (75%), cough (66.7%), and recurrent pneumonia (50%). Preoperative mechanical ventilatory support was required in 41.7% of the patients. The mean length of hospital stay was $6.3{\pm}2.5days$. The mean follow-up period was $24.3{\pm}14.5months$. Preoperative symptoms were immediately relieved after surgery in 83.3% of patients and persisted in 16.7% of patients one year after surgery. All patients survived to the end of the two-year follow-up and none had recurrence of DE. Conclusion: Early diagnosis and surgical plication of the diaphragm for symptomatic congenital or acquired diaphragmatic eventration offers a good clinical outcome with no recurrence.

Clinical evaluation and surgical intervention for diaphragmatic eventration mimicking peritoneopericardial hernia in a cat

  • Min-Jung Ko;Kyoung-Min Song;Hun-Young Yoon
    • Journal of Veterinary Science
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    • 제25권2호
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    • pp.19.1-19.6
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    • 2024
  • A 2-year-old spayed female British Shorthair cat presented with an increased frequency and duration of cough since infant period. Based on radiographic, ultrasonographic, and computed tomography findings, peritoneopericardial diaphragmatic hernia was considered so that repair surgery was planned. During celiotomy, lax diaphragm was identified instead of defect. Transabdominal diaphragmatic plication was performed to resolve lax diaphragm and to prevent recurrence by overlapping relatively normal part of diaphragm. Diagnosed with diaphragmatic eventration postoperatively, the cat showed improvement in clinical signs and imaging results. Transabdominal diaphragmatic plication is a suitable treatment; the patient maintained normally during a 14-month follow-up period.

Surgical Outcomes of Pneumatic Compression Using Carbon Dioxide Gas in Thoracoscopic Diaphragmatic Plication

  • Ahn, Hyo Yeong;Kim, Yeong Dae;I, Hoseok;Cho, Jeong Su;Lee, Jonggeun;Son, Joohyung
    • Journal of Chest Surgery
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    • 제49권6호
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    • pp.456-460
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    • 2016
  • Background: Surgical correction needs to be considered when diaphragm eventration leads to impaired ventilation and respiratory muscle fatigue. Plication to sufficiently tense the diaphragm by VATS is not as easy to achieve as plication by open surgery. We used pneumatic compression with carbon dioxide ($CO_2$) gas in thoracoscopic diaphragmatic plication and evaluated feasibility and efficacy. Methods: Eleven patients underwent thoracoscopic diaphragmatic plication between January 2008 and December 2013 in Pusan National University Hospital. Medical records were retrospectively reviewed, and compared between the group using $CO_2$ gas and group without using $CO_2$ gas, for operative time, plication technique, duration of hospital stay, postoperative chest tube drainage, pulmonary spirometry, dyspnea score pre- and postoperation, and postoperative recurrence. Results: The improvement of forced expiratory volume at 1 second in the group using $CO_2$ gas and the group not using $CO_2$ gas was $22.46{\pm}11.27$ and $21.08{\pm}5.39$ (p=0.84). The improvement of forced vital capacity 3 months after surgery was $16.74{\pm}10.18$ (with $CO_2$) and $15.6{\pm}0.89$ (without $CO_2$) (p=0.03). During follow-up ($17{\pm}17$ months), there was no dehiscence in plication site and relapse. No complications or hospital mortalities occurred. Conclusion: Thoracoscopic plication under single lung ventilation using $CO_2$ insufflation could be an effective, safe option to flatten the diaphragm.

선천성 횡경막 이완증 2예 (Congenital Diaphragmatic Hernia - 2 cases report -)

  • 심재영
    • Journal of Chest Surgery
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    • 제20권4호
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    • pp.855-858
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    • 1987
  • Eventration of the diaphragm is a rare anomaly, the cause of which still is not understand completely. Recently we were experienced two cases of diaphragmatic eventration which were successfully treated with surgical diaphragmatic plication at the department of thoracic and cardiovascular surgery, college of medicine, chosun university. Specific complication were not noticed after surgical repair of diaphragmatic eventration with good results.

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신생아에서의 선천성 횡격막 내번증;치험 3례 (Congenital Diaphragmatic Eventration in Neonates -A Report of 3 cases-)

  • 최강주
    • Journal of Chest Surgery
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    • 제26권9호
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    • pp.730-734
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    • 1993
  • Three neonates with congenital diaphragmatic eventration underwent intrathoracic operation had marked improvements in symptoms postoperatively. Two were one day of ages, one was 1 month of age, and they were all female and had other congenital abnormalities of lung hypoplasia, cleft palate, nasal polyps and neonatal hepatitis. The right diaphragm was more affected than left as 2:1. The repair for diaphragmatic eventration was performed successfully by plication of remnant diaphragm, and there were no complications postoperatively.

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소아 심혈관 수술 후 발생한 횡격신경마비가 술후 호흡관리에 미치는 영향 (The Effect of Phrenic Nerve Paralysis After Pediatric Cardiac Surgery on Postoperative Respiratory Care)

  • 윤태진;이정렬
    • Journal of Chest Surgery
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    • 제29권10호
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    • pp.1118-1122
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    • 1996
  • 1990년 1월부터 1995년 12월가지 43명의 환아가 다양한 심혈관수술로 인해 유발된 횡격막 마비로횡 격막 습벽형성술을 시행 받았다. 환아의 평균연령은 11.1개월이었고, 남녀 비율은 31:12였다. 횡격막 마비의 원인이 된 수술로는 변형 Blalock-Taussig단락술 및 활로씨 4징증의 전교정술이 각각 7례로 가장 많았고, 기타 동맥 전환술 6례, 심실중격결손을 동반한 폐동맥 폐쇄증에서의 unifocalization 및 변형 Fontan수술, 심실중격결손 교정 등이 각각 3례씩이었다. 마비된 부위는 우측이 17례, 좌측이 23례, 양측성이 3례였으며, 원인은 대부분 과도한 심낭 절제 및 심낭 절개면 부위의 전기소작으로 추정되었다. 원인이 된 수술후 횡격막 습벽형성술까지의 기간은 수술 당일로부터 98일까지로 대부분 2주이내에 습 벽형성술이 이루어졌다 수술방법은 2례를 제외하고 모두 횡격막 신경분지를 피해서 횡격막을 접어주는 central pleating technique 이 적용되었다. 10명의 환아가 습벽형성술후 사망했으며(조기: 7, 만기: 3), 사망원인은 전례 에서 습벽 형성술과는 무관한 것으로 사료되 었다. 36명의 조기생존자들은 습벽 형성술후 1일에서 24일 사이에 양압호\ulcorner으로 부터 벗어날 수 있었다(평균 4.5일). 6명의 환아가 습벽 형성술후 8개 월에서 52개월 사이에 fluoroscopy를 시행하였으며, 대부분 횡격막의 위치 및 운동성이 양호하였다. 결 론적으로 불가역적인 횡격막 신경 손상이 없다면 횡격막 습벽형성술은 단기적으로는 환아의 양압호흡 의존기 간을 단축시키고 장기적으로는 횡격막 기능의 완전회복을 유도할 수 있다.

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흉강경하 횡경막 주름성형술: 작업창없이 3개의 포트를 이용한 수술법 (Thoracoscopic Diaphragmatic Plication Using Three 5 mm Ports)

  • 김도형;김길동;황정주;최진호;이준완
    • Journal of Chest Surgery
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    • 제43권5호
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    • pp.513-517
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    • 2010
  • 배경: 횡경막 내장전위증의 치료를 위해 흉강경을 이용한 횡격막 주를 성형술은 효과적인 방법이다. 그러나, 기존 흉강경을 이용한 횡경막 주름 성형술은 여러 가지 문제점을 가지고 있다. 본 저자들은 Head up position, $CO_2$ 삽입 및 Figure of eight 봉합법을 이용하여 수술 술기를 단순화하여 기존 흉강경의 단점을 개선하고자 하였다. 대상 및 방법: 2005년 3월부터 2009년 9월까지 횡경막 내장전위증으로 수술을 받은 9명의 환자를 대상으로 후향적 연구를 시행하였다. 평균 연령은 $38.5{\pm}53.0$세(범위, 2~76세)였으며 남자 4명, 여자 5명이었다. 결과: 평균 수술 시간은 $46.7{\pm}15.9$분(범위, 30~85분)이었다. 수술 중 사망은 없었다. 합병증으로는 7일 이상의 지속적 공기 누출 1예, 폐부종(Re-expansion pulmonary edema)으로 3일간 호흡기 사용 1예가 있었다. 평균 재원일 수는 $6.22{\pm}2.04$일(범위, 4~11일)이었다. 수술 후 추적 관찰 기간(평균 $27.2{\pm}11.6$개월, 범위 2~43개월) 동안 1예에서만 수술 직후 횡경막 위치에 비해 2.5 cm 이상 상승을 보였다. 호흡 곤란 증상을 보이는 환자는 없었다. 결론: 저자들의 변형 술식에 의해 횡격막 내장전위증 환자에서 단지 수술창의 사용없이 3개의 5 mm 포트를 이용하여 횡격막 주름 성형술이 가능하였다. 횡경막 내장 전위증 환자에서 흉강경을 이용한 방법이 현재 널리 사용되고 있는 개흉을 이용한 방법보다 유용한 수술 방법으로 생각된다.

고양이에서의 선천성 식도열공허니아 1예 (Congenital Esophageal Hiatal Hernia in a Cat)

  • 정성목;정언승;김순영;최성천;손혜정;이충호;양정환;김완희;서민호
    • 한국임상수의학회지
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    • 제18권1호
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    • pp.61-64
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    • 2001
  • A 1.2 kg, five-month-old, female domestic short-hair cat was referred to Seoul National University Veterinary Medical Teaching Hospital with a history of vomiting immediatley after eating. Clinical signs were depression, anorexia, severe dehydration and vomiting since weaning. According to history taking, physical examination, complete blood count, serum chemical profile and contrast radiographic study, it was diagnosed as congenital sliding esophageal hiatal hernia. Diaphragmatic plication, esophagopexy and left-sided belt-loop gastropexy were performed. Ranitidine (2 mg/kg, IV, q12h) and sucralfate suspension (20 mg/kg, PO, q6h) were administered with low-fat liquified diet to treat reflux esophagitis. Clinical signs related to esophageal hiatal hernia disappeared immediately after surgical treatment and did not recur for 4 months.

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응급 수술을 요하는 선천성 횡경막 내번증 1예 (A Case of Congenital Diaphragmatic Eventration Requiring Emergency Operation)

  • 이석열;이승진;박형주;이철세;이길노
    • Advances in pediatric surgery
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    • 제10권2호
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    • pp.142-144
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    • 2004
  • A one day old female infant was brought to the emergency room suffering from shortness of breath. An x-ray revealed the gastrointestinal tract in the right thoracic cavity. An emergency operation demonstrated eventration of the diaphragm, and a plication was performed. The baby was discharged without complication and has been followed up in the out patient clinic. Congenital diaphragmatic eventuation requiring emergency operation is rare.

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