Online ISSN: 2187-2988 Print ISSN: 0911-1794
特定非営利活動法人日本小児循環器学会 Japanese Society of Pediatric Cardiology and Cardiac Surgery
Pediatric Cardiology and Cardiac Surgery 41(1): 51-57 (2025)
doi:10.9794/jspccs.41.51

症例報告Case Report

先天性心疾患乳児に対するAvalon Elite Bi-Caval Dual Lumen Catheterを用いたV-V ECMOの使用経験Avalon Elite Bi-Caval Dual Lumen Catheter to Facilitate Veno-Venous Extracorporeal Membrane Oxygenation in a Cardiac Infant with Limited Vascular Access: A Case Report

1北海道立子ども総合医療・療育センター小児循環器内科Department of Pediatric Cardiology, Hokkaido Medical Center for Child Health and Rehabilitation ◇ Hokkaido, Japan

2北海道立子ども総合医療・療育センター集中治療科Department of Pediatric Intensive Care Unit, Hokkaido Medical Center for Child Health and Rehabilitation ◇ Hokkaido, Japan

3北海道立子ども総合医療・療育センター臨床工学部Department of Clinical Engineering, Hokkaido Medical Center for Child Health and Rehabilitation ◇ Hokkaido, Japan

4北海道立子ども総合医療・療育センター新生児科Department of Neonatology, Hokkaido Medical Center for Child Health and Rehabilitation ◇ Hokkaido, Japan

受付日:2024年8月5日Received: August 5, 2024
受理日:2024年11月18日Accepted: November 18, 2024
発行日:2025年2月28日Published: February 28, 2025
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Avalon Elite® Bi-Caval Dual Lumen Catheter(Avalon DLC)は1本のカニューレでV-V体外式膜型人工肺(Veno-venous extracorporeal membrane oxygenation: V-V ECMO)の送血と脱血が可能なデバイスであるが,先天性心疾患児に対する使用報告はない.症例はCantrell症候群,ファロー四徴症,左上大静脈遺残と診断された生後3か月,体重3.5 kgの男児.臍帯ヘルニア,横隔膜ヘルニアと気管軟化症に対して多期的腹壁閉鎖術,横隔膜縫縮術と気管切開術を施行した.生後3か月時から低酸素血症が顕在化し,心臓MRI検査で肺体血流比=0.4と低肺血流状態であり,Blalock–Taussig shunt手術が必要と判断した.腹壁の術創と気管切開孔が胸骨と近接し術後縦隔炎が懸念されたため,正中切開を選択せず左側開胸での手術を計画した.しかし,術側肺の圧排が更に酸素化を悪化させるため,手術執刀前にV-V ECMOの導入を計画した.静脈の解剖学的特徴から,カニューレを経皮的に挿入できる部位は右内頚静脈のみであった.右内頸静脈からAvalon DLC 13 Frを挿入してV-V ECMOを使用し,良好な酸素化を得た.手術終了時にV-V ECMOを合併症なく離脱することが可能であった.先天性心疾患と多発奇形がある場合,バスキュラーアクセスに制限があることがあり,導入時の選択としてAvalon DLCは一候補になりうる.

The Avalon Elite® bi-caval dual lumen catheter (Avalon DLC) enables veno-venous extracorporeal membrane oxygenation (V-V ECMO) with a single cannula. There are no reports of using this catheter in infants with congenital heart disease in Japan. We report a 3-month-old boy who weighed 3.5 kg and was diagnosed with Cantrell syndrome, tetralogy of Fallot, and persistent left superior vena cava. He underwent multistage abdominal wall closure, diaphragmatic suture, and tracheostomy for omphalocele, diaphragmatic hernia, and tracheomalacia. At 3 months of age, hypoxemia appeared and cardiac magnetic resonance imaging showed low pulmonary blood flow with a Qp/Qs ratio of 0.4, indicating the need for Blalock–Taussig shunt surgery. There was concern regarding postoperative mediastinitis because of the proximity of the abdominal wound and tracheostomy site to the sternum. Therefore, a left-sided thoracotomy was planned instead of a median sternotomy. However, compression of the lung on the operative side was expected to further worsen oxygenation, and we planned to introduce V-V ECMO before surgery. The right internal jugular vein was the only site where a cannula could be inserted percutaneously owing to the anatomical characteristics of the vessels. A 13 Fr Avalon DLC was inserted through the right internal jugular vein, and V-V ECMO was used to achieve good oxygenation. The Avalon DLC may be useful in infants with congenital heart disease and multiple malformations who require ECMO.

Key words: extracorporeal membrane oxygen; dual lumen catheter; Veno-venous dual lumen cannula; Cantrell syndrome

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This page was last modified on 2025-05-26T08:37:23.000+09:00


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