scholarly journals PRIMARY CARDIAC ARREST IN A NOT-SO-ASYMPTOMATIC CARRIER OF DUCHENNE MUSCULAR DYSTROPHY

2019 ◽  
Vol 73 (9) ◽  
pp. 2330
Author(s):  
Brenden Boyle
2005 ◽  
pp. 1562
Author(s):  
Aruna Nathan ◽  
Arjunan Ganesh ◽  
Rodolfo I. Godinez ◽  
Susan C. Nicolson ◽  
William J. Greeley

1978 ◽  
Vol 93 (1) ◽  
pp. 88-90 ◽  
Author(s):  
Alan R. Seay ◽  
Fred A. Ziter ◽  
Joel A. Thompson

2001 ◽  
Vol 160 (9) ◽  
pp. 579-580 ◽  
Author(s):  
Tim P. Kerr ◽  
Andrew Durward ◽  
Shirley V. Hodgson ◽  
Elaine Hughes ◽  
Stephanie A. Robb

Author(s):  
Ji Hyoung Park ◽  
Kwang Ho Lee ◽  
Wi Kwang Wang ◽  
Hyun Kyo Lim

Duchenne muscular dystrophy (DMD) is a progressive myopathy. The development of respiratory therapy has increased the life expectancy of DMD patients. This change has increased the chances of anesthesia administration in DMD patients with advanced cardiomyopathy. We report a severe cardiomyopathy case in a 14-year-old boy with DMD, adrenal insufficiency, and severe mental retardation, who experienced a sudden cardiac arrest with successful resuscitation. The patient underwent feeding gastrostomy surgery to relieve recurrent aspiration pneumonia, during which cardiac index and heart rate decreased. Cardiomyopathy has emerged as a new challenge in DMD patients; it is important to maintain end organ perfusion by proper function of the left ventricle.


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