Status Epilepticus in a Patient with Amyotrophic Lateral Sclerosis

被引:1
|
作者
Dag, Ersel [1 ]
Sahin, Oruc [1 ]
Gokce, Burcu [1 ]
Erdemoglu, Ali Kemal [1 ]
机构
[1] Kirikkale Univ, Fac Med, Dept Neurol, TR-71100 Kirikkale, Turkey
来源
关键词
Amyotrophic lateral sclerosis; status epilepticus;
D O I
10.5152/jaemcr.2014.76476
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Introduction: Amyotrophic Lateral Sclerosis, the most common and well-known form of motor neuron disease, is characterized by progressive degeneration of upper and lower motor neurons. Respiratory failure and aspiration due to respiratory muscle weakness is the most common causes of mortality in patients with amyotrophic lateral sclerosis. Status epilepticus is the second most frequent neurological emergency with a risk of major morbidity or mortality. Status epilepticus, due to causes such as prolonged seizures, respiratory distress, acidosis, hypoglycemia, and hypotension may lead to mortality. Case Report: A forty-eight year old male patient had been followed for 4 years with a diagnosis of amyotrophic lateral sclerosis and was referred to our clinic with the diagnosis of status epilepticus. The refractory status epilepticus patient was treated with a diagnosis of respiratory failure and the need for mechanical ventilation evolved. Conclusion: We report the development of status epilepticus in a patient with amyotrophic lateral sclerosis, and in addition to the appropriate anti-epileptic medication, ventilator support and intensive care was needed, emphasizing the life-saving procedure.
引用
收藏
页码:5 / 7
页数:3
相关论文
共 50 条
  • [1] MANAGEMENT OF THE PATIENT WITH AMYOTROPHIC LATERAL SCLEROSIS
    BLOUNT, M
    BRATTON, C
    LUTTRELL, N
    NURSING CLINICS OF NORTH AMERICA, 1979, 14 (01) : 157 - 171
  • [2] Health Status Perspectives in Amyotrophic Lateral Sclerosis
    Pinto, Susana
    de Carvalho, Mamede
    NEURODEGENERATIVE DISEASES, 2017, 17 (06) : 323 - 329
  • [3] Amyotrophic lateral sclerosis (ALS) - Patient decongestion
    Tanant, V.
    REANIMATION, 2011, 20 (02): : S510 - S511
  • [4] Nutritional Care of the Patient with Amyotrophic Lateral Sclerosis
    Dobak, Stephanie
    PRACTICAL GASTROENTEROLOGY, 2022, 46 (04) : 60 - 67
  • [5] Anesthetic management of the patient with amyotrophic lateral sclerosis
    Prabhakar, Amit
    Owen, Christopher Paul
    Kaye, Alan David
    JOURNAL OF ANESTHESIA, 2013, 27 (06) : 909 - 918
  • [6] Amyotrophic lateral sclerosis (ALS) in patient with dermatomyositis
    Papastergios, C.
    Chlopicki, B.
    Bergelin-Axelsson, M.
    EUROPEAN JOURNAL OF NEUROLOGY, 2017, 24 : 292 - 292
  • [7] PATIENT RESISTANCE AND PROGNOSIS IN AMYOTROPHIC LATERAL SCLEROSIS
    MULDER, DW
    HOWARD, FM
    MAYO CLINIC PROCEEDINGS, 1976, 51 (09) : 537 - 541
  • [8] Use of Sugammadex in a Patient with Amyotrophic Lateral Sclerosis
    Kelsaka, Ebru
    Karakaya, Deniz
    Zengin, Eyup Cagatay
    MEDICAL PRINCIPLES AND PRACTICE, 2013, 22 (03) : 304 - 306
  • [9] Amyotrophic lateral sclerosis in a patient with Kartagener syndrome
    Yamashita, Satoshi
    Migita, Akie
    Hayashi, Kenyu
    Hirahara, Tomoo
    Kimura, En
    Maeda, Yasushi
    Hirano, Teruyuki
    Uchino, Makoto
    AMYOTROPHIC LATERAL SCLEROSIS, 2010, 11 (04): : 402 - 404
  • [10] COMPLEX TREATMENT OF AMYOTROPHIC LATERAL SCLEROSIS PATIENT
    Bialkowska, Joanna
    Mroczkowska, Dorota
    Huflejt, Margaret E.
    Wojtkiewicz, Joanna
    Siwek, Tomasz
    Barczewska, Monika
    Maksymowicz, Wojciech
    ACTA CLINICA CROATICA, 2019, 58 (04) : 757 - 766