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重症肌无力(MG)是一种神经肌肉处乙酰胆碱传递障碍引起的一种慢性自身免疫性疾病。重症肌无力危象(MGC)是指重症肌无力患者急骤发生呼吸肌或(和)由延髓支配的肌肉严重无力导致呼吸、咳嗽困难和威胁患者生命安全的一种征象。现将我科(ICU)2014年8月至2015年4月收治的4例MGC合并呼吸衰竭患者的护理体会总结如下。1临床资料我院ICU病房共收治MGC患者10例,其中4例MGC患者合并呼吸衰竭。年龄47~59岁,男3例,女1例。3例行
Myasthenia Gravis (MG) is a chronic autoimmune disease caused by disorders of acetylcholine delivery at the neuromuscular. Myasthenia gravis crisis (MGC) is a sign of a sudden onset of respiratory muscle or / or myasthenia gravis in myasthenia gravis leading to severe breathing and coughing difficulties and threatening the patient’s life safety. Now my department (ICU) from August 2014 to April 2015 admitted 4 cases of MGC patients with respiratory failure nursing experience is summarized as follows. 1 clinical data ICU ward admitted to our hospital a total of 10 patients with MGC patients, including 4 cases of MGC patients with respiratory failure. Age 47 to 59 years old, 3 males and 1 female. 3 routine