Pritha Ariana, Medha Tanisha N, Garg Ravindra K
Neurosciences, The University of New Mexico, Albuquerque, USA.
Medicine, University of New Mexico, Albuquerque, USA.
Cureus. 2022 Aug 25;14(8):e28389. doi: 10.7759/cureus.28389. eCollection 2022 Aug.
Subacute sclerosing panencephalitis (SSPE) is a progressive, disabling, and deadly neurological disorder related to measles (rubeola) infection occurring primarily in children. The slow but persistent viral infection occurs in children or young adults and affects their central nervous system (CNS). There have been plenty of reports on SSPE throughout the world, but it is considered a rare disease in developed countries. This research focuses on comparing the current treatments available to prolong the life of patients for over three years after the onset of SSPE. The goal was to identify possible patterns or trends among the treatments in order to find the best possible method to lengthen a patient's life. The results indicated that interferon alpha, inosine pranobex, and ribavirin display the most effective treatment plan and indicate the most potential in discovering a more effective therapeutic for SSPE.
亚急性硬化性全脑炎(SSPE)是一种进行性、致残性且致命的神经系统疾病,主要发生于儿童,与麻疹(风疹)感染有关。这种缓慢但持续的病毒感染发生在儿童或年轻人身上,并影响他们的中枢神经系统(CNS)。全世界有大量关于SSPE的报道,但在发达国家它被认为是一种罕见疾病。本研究着重比较目前可延长SSPE发病后患者生命三年以上的现有治疗方法。目的是确定治疗方法中可能存在的模式或趋势,以便找到延长患者生命的最佳方法。结果表明,α干扰素、异丙肌苷和利巴韦林展现出最有效的治疗方案,并且在发现更有效的SSPE治疗方法方面显示出最大潜力。