Journals / Ankara Üniversitesi Tıp Fakültesi Mecmuası / 2018 / Cilt: 71 - Sayı: 1

Anesthesia Management of Duchenne Muscular Dystrophy with Complete Atrioventricular Block in Angiography Laboratory

Av Tam Blok Gelișen Duchenne Musküler Distrofi Tanılı Olgunun Anjiografi Laboratuvarındaki Anestezi Yönetimi

Pages
87–90
Publication Date
2022-10-10
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this ar-ticle we aimed to present anesthetical management of implantation of permanent pacemaker to a patient with Duchenne Muscular Dystrophy who had a temporary transvenous pacemaker for complete atrioventricular block.

📌 3 Key Takeaways

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Objective & Hypothesis:Duchenne muscular distrophy is an X-linked, recessive, inherited genetic disorder, which is seen in 1/3500 of the population and characterized by progressive muscle degeneration and cont-ractures.
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Key Findings & Data:As well as muscle weakness is the main problem; respiratory infections are frequent due to the difficulty of coughing and expectoration caused by the retension of respiratory muscles.
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Conclusion & Impact:In this ar-ticle we aimed to present anesthetical management of implantation of permanent pacemaker to a patient with Duchenne Muscular Dystrophy who had a temporary transvenous pacemaker for complete atrioventricular block.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Duchenne muscular distrophy is an X-linked, recessive, inherited genetic disorder, which is seen in 1/3500 of the population and characterized by progressive muscle degeneration and cont-ractures. As well as muscle weakness is the main problem; respiratory infections are frequent due to the difficulty of coughing and expectoration caused by the retension of respiratory muscles. Due to the cardiomyopathy, cardiac problems such as ventricular dilatation, conduc-tion defects, supraventricular or ventricular arrhytmias, myocardial necrosis, anesthesia mana-gement is special. Inhalational anesthetics and depolarizing neuromuscular blocking agents may cause fatal complications such as malignant hyperthermia and rhabdomyolysis. In this ar-ticle we aimed to present anesthetical management of implantation of permanent pacemaker to a patient with Duchenne Muscular Dystrophy who had a temporary transvenous pacemaker for complete atrioventricular block.

Özet

Duchenne Musküler Distrofi X’e bağlı resesif kalıtımla aktarılan, 1/3500 sıklıkta gözlenen prog-resif kas dejenerasyonu ve kontraktürler ile karakterize genetik bir hastalıktır. Kas güçsüzlüğü temel problem olmakla birlikte; solunum kaslarının tutulması sonucu öksürme ve ekspektoras-yon güçlüğü nedeni ile solunum yolu enfeksiyonları sıktır. Kardiyomiyopati nedeniyle ventrikü-ler dilatasyon, iletim kusurları, supraventriküler veya ventriküler aritmiler, miyokardiyal nekroz gibi kardiyak problemler görülebileceği için anestezi yönetimi özellik göstermektedir. İnhalas-yon anestezikleri ve depolarizan kas gevșetici ajanlar, malign hipertermi ve rabdomiyoliz gibi mortal komplikasyonlara neden olabilir. Bu makalemizde AV tam blok nedeniyle geçici transve-nöz pacemakerın, kalıcı pacemaker ile değiștirilmesi planlanan Duchenne Musküler Distrofi ta-nılı olguda uyguladığımız anestezi yöntemini sunmayı hedefledik.

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Cite This Article

BERMEDE, A. O., BAYTAŞ, V., KARABAK, P., ŞAŞAL, G., DENKER, Ç., VURGUN, V. K. (2022). Anesthesia Management of Duchenne Muscular Dystrophy with Complete Atrioventricular Block in Angiography Laboratory. Ankara Üniversitesi Tıp Fakültesi Mecmuası, Cilt: 71 - Sayı: 1, 87–90. https://ajindex.com/articles/443653

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References (1)

  1. Kocabas S, Yedicocuklu D, Askar F, et al. Anesthetic management of a child with Duchenne muscular dystrophy undergo-ing correction of Fallot’s Tetralogy. Pedi-atric Anesthesia 2008; 18: 448-450. 15. Frankowski GA, Johnson JO, Tobias JD. Rapacuronium administration to two children with Duchenne’s muscular dyst-rophy. Anesth Analg 2000; 91: 27-28. 14. Shin HH, Park DH, Lee C, et al. Anesthe-sia for a 10-year-old boy with Duchenne muscular dystrophy syndrome: A case re-port. Korean J Anesthesiol 2008; 55: 217-220. 13. Girshin M, Mukherjee J, Clowney R, et al. The postoperative cardiovascular arrest of a 5-year-old male: an initial presentation of Duchenne’s muscular dystrophy. Paediatr Anaesth 2006; 16: 170-173. 12. Birnkrat DJ, Panitch HB, Benditt JO, et al. American collage of chest physicians con-sensus statement on the respiratory and re-lated management of patients with Duc-henne muscular dystrophy undergoing anesthesia or sedation. Chest 2007; 132: 1977-1986. 11. Wick S, Muenster T, Schmidt J, et al. On-set and duration of rocuronium-induced neuromuscular blockade in patients with Duchenne muscular dystrophy. Anesthe-siology 2005; 102: 915-919. 10. Epstein AE, DiMarco JP, Ellenbogen KA, et al. 2012 ACCF/AHA/HRS focused update incorporated into the ACCF/AHA/HRS 2008 guidelines for device-based therapy of cardiac rhythm abnormalities: a report of the American College of Cardiology Foundation/Ameri-can Heart Association Task Force on Practice Guidelines and the Heart Rhythm Society. J Am Coll Cardiol 2013; 61: e6-75. 9. Finsterer J, Stöllberger C. The heart in hu-man dystrophinopathies. Cardiology 2003; 99: 1-19. 8. Fayssoil A, Nardi O, Orlikowski D, et al. Cardiomyopathy in Duchenne muscular dystrophy: pathogenesis and therapeutics. Heart Fail Rev 2010; 15: 103-107. 7. Obata R, Yasumi Y, Suzuki A, et al. Rhab-domyolysis in association with Duc-henne’s muscular dystrophy. Can J Anesth 1999; 46: 564-566. 6. Mavrogeni S, Markousis-Mavrogenis G, Papavasiliou A, et al. Cardiac involvement in Duchenne and Becker muscular dyst-rophy. World J Cardiol 2015; 7: 410-414. 5. Finder JD, Birnkrant D, Carl J, et al. Res-piratory care of the patient with Duchenne muscular dystrophy: ATS consensus state-ment. Am J Respir Crit Care Med 2004; 170: 456-465. 4. Birnkrant DJ, Bushby KM, Amin RS, et al. The respiratory management of patients with duchenne muscular dystrophy: a DMD care considerations working group specialty article. Pediatr Pulmonol 2010; 45: 739-748. 3. Ba