scholarly journals Surgical management of severe scoliosis with high-risk pulmonary dysfunction in Duchenne muscular dystrophy

2009 ◽  
Vol 34 (3) ◽  
pp. 401-406 ◽  
Author(s):  
Masashi Takaso ◽  
Toshiyuki Nakazawa ◽  
Takayuki Imura ◽  
Naonobu Takahira ◽  
Moritoshi Itoman ◽  
...  
PEDIATRICS ◽  
2018 ◽  
Vol 142 (Supplement 2) ◽  
pp. S82-S89 ◽  
Author(s):  
Susan D. Apkon ◽  
Ben Alman ◽  
David J. Birnkrant ◽  
Robert Fitch ◽  
Robert Lark ◽  
...  

2021 ◽  
Vol 9 ◽  
Author(s):  
Ahmed K. Bamaga ◽  
Fouad Alghamdi ◽  
Nahla Alshaikh ◽  
Waleed Altwaijri ◽  
Fahad A. Bashiri ◽  
...  

Background: The coronavirus disease 2019 (COVID-19) pandemic has caused overwhelming challenges in healthcare worldwide. During such an outbreak, some needs of high-risk groups who require regular follow-ups and long-term management are not met. The vulnerable populations include patients with Duchenne muscular dystrophy (DMD). Duchenne muscular dystrophy is characterized by respiratory complications caused by muscle weakness. Hence, patients with this condition are at high risk of severe diseases including COVID-19.Methods: To standardize care and provide optimal treatment to DMD patients in Saudi Arabia during the COVID-19 pandemic, a panel of experts including neurologists and pediatricians consolidated recommendations for healthcare professionals and caregivers.Results: During this pandemic, substituting unnecessary clinic visits with virtual clinic services was highly recommended, if possible, without compromising clinical outcomes. Duchenne muscular dystrophy patients with respiratory complications should be closely monitored, and those with cardiovascular complications must continue taking angiotensin-converting enzyme inhibitors or angiotensin receptor blockers. Moreover, individualized home-based rehabilitation management was preferred. Glucocorticoid and new gene correction therapies should be continued. However, new gene correction therapy must be post-poned in newly diagnosed patients. A multidisciplinary decision was required before the initiation of hydroxychloroquine based on the COVID-19 treatment protocol.Conclusion: COVID-19 has caused challenges and transformed access to health care. However, these limitations have provided opportunities for the health care system to adapt. Further, telemedicine has become a reliable platform for follow-up appointments that should be conducted by a multidisciplinary team including physicians, dieticians, and physical therapists.


2021 ◽  
Author(s):  
Keisuke Okuno ◽  
Daisuke Kawaba ◽  
Atsushi Maejima ◽  
Sosuke Kakee ◽  
Noriyuki Namba

Spine ◽  
2002 ◽  
Vol 27 (18) ◽  
pp. 2072-2079 ◽  
Author(s):  
Dilip K. Sengupta ◽  
S. H. Mehdian ◽  
Jeffrey R. McConnell ◽  
Stephen M. Eisenstein ◽  
John K. Webb

2010 ◽  
Vol 124 (12) ◽  
pp. 1333-1336 ◽  
Author(s):  
C Desvant ◽  
D Chevalier ◽  
G Mortuaire

AbstractIntroduction:The development of a tracheo-arterial fistula is a rare but severe complication of tracheotomy. The reported patient presented with such a fistula involving an aberrant right subclavian artery, termed an arteria lusoria, an aortic arch abnormality which is usually asymptomatic.Case report:A 30-year-old man was admitted to our institution for bleeding through his tracheotomy. He had been treated for advanced Duchenne muscular dystrophy, involving invasive assisted ventilation, since the age of 10 years. Surgical exploration and computed tomography scanning revealed a tracheo-arterial fistula involving an aberrant right subclavian artery, associated with severe scoliosis. Emergency, transient haemostasis was achieved by over-inflation of the tracheostomy tube cuff. Aneurysm ablation was successfully achieved as the result of an endovascular interventional radiology procedure.Discussion:Arteria lusoria is one of the most common aortic arch abnormalities. The occurrence of an aneurysm of this artery in a tracheotomised patient has not previously been described. In Duchenne muscular dystrophy patients, spinal deformities may result in thoracic compression, which may alter the anatomical relations of mediastinal vessels. Such deformities are slowly progressive. Thus, vigilance is required in the long term management of Duchenne muscular dystrophy patients with a tracheostomy.


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