L. Tortolero, J. Nuño, P. Luengo, L. Gajate, A. Buenadicha, A. Serrano, F. Liaño, R. Peromingo, P. L. Hervás
{"title":"免疫抑制治疗对肝移植后神经系统并发症的影响","authors":"L. Tortolero, J. Nuño, P. Luengo, L. Gajate, A. Buenadicha, A. Serrano, F. Liaño, R. Peromingo, P. L. Hervás","doi":"10.31487/j.nnb.2020.02.14","DOIUrl":null,"url":null,"abstract":"Background: Neurological complications (NC) after liver transplantation (LT) are frequent, appearing in\nup to 60% of patients. Etiology is often related to immunosuppressant neurotoxicity and opportunistic\ninfections. The use of basiliximab allows for less toxic immunosuppressive therapies. The aim of this study\nwas to evaluate the neurological complications present during the first 30 days after LT and to evaluate its\nrelationship with renal function, immunosuppressive therapy, and mortality.\nMethods: A total of 231 recipients were included in the retrospective, longitudinal, and nonrandomized\nstudy under 2 different immunosuppression protocols (with -group B- or without basiliximab -group A-).\nResults: NC were present in 14.3% of patients (n: 33), the average age of these patients was 55.4 years. The\nincidence of NC was significantly higher in group A than in group B (19.5% vs. 9.3% p <0.05), with no\ndifferences in the incidence of infection or rejection between both groups. The incidence of acute renal\nfailure, the need for renal replacement therapy, the days of admission to the ICU, the days of hospital\nadmission, as well as mortality during admission and one year after LT were higher among patients with\nNC. However, when analyzing patients with a neurological complication, patients in group A had a higher\nincidence of complications than in group B.\nConclusion: The use of immunosuppressive therapies that apply lower doses of anticalcineurinics and with\na later onset, classically called nephroprotective as used in group B, could also be neuroprotective, reducing\nthe appearance of neurological complications and, therefore, morbidity. These findings most be verified in\nstudies with a larger number of patients and randomized.","PeriodicalId":19179,"journal":{"name":"Neurology and Neurobiology","volume":"13 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Neurological Complications after Liver Transplantation According to Immunosuppressive Therapy\",\"authors\":\"L. Tortolero, J. Nuño, P. Luengo, L. Gajate, A. Buenadicha, A. Serrano, F. Liaño, R. Peromingo, P. L. Hervás\",\"doi\":\"10.31487/j.nnb.2020.02.14\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Neurological complications (NC) after liver transplantation (LT) are frequent, appearing in\\nup to 60% of patients. Etiology is often related to immunosuppressant neurotoxicity and opportunistic\\ninfections. The use of basiliximab allows for less toxic immunosuppressive therapies. The aim of this study\\nwas to evaluate the neurological complications present during the first 30 days after LT and to evaluate its\\nrelationship with renal function, immunosuppressive therapy, and mortality.\\nMethods: A total of 231 recipients were included in the retrospective, longitudinal, and nonrandomized\\nstudy under 2 different immunosuppression protocols (with -group B- or without basiliximab -group A-).\\nResults: NC were present in 14.3% of patients (n: 33), the average age of these patients was 55.4 years. The\\nincidence of NC was significantly higher in group A than in group B (19.5% vs. 9.3% p <0.05), with no\\ndifferences in the incidence of infection or rejection between both groups. The incidence of acute renal\\nfailure, the need for renal replacement therapy, the days of admission to the ICU, the days of hospital\\nadmission, as well as mortality during admission and one year after LT were higher among patients with\\nNC. However, when analyzing patients with a neurological complication, patients in group A had a higher\\nincidence of complications than in group B.\\nConclusion: The use of immunosuppressive therapies that apply lower doses of anticalcineurinics and with\\na later onset, classically called nephroprotective as used in group B, could also be neuroprotective, reducing\\nthe appearance of neurological complications and, therefore, morbidity. 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引用次数: 0
摘要
背景:肝移植(LT)术后神经系统并发症(NC)较为常见,发生率高达60%。病因常与免疫抑制神经毒性和机会性感染有关。使用basiliximab允许毒性较小的免疫抑制疗法。本研究的目的是评估肝移植后前30天出现的神经系统并发症,并评估其与肾功能、免疫抑制治疗和死亡率的关系。方法:在2种不同的免疫抑制方案(B组或A组)下,共有231名接受者被纳入回顾性、纵向和非随机研究。结果:14.3%的患者(33例)存在NC,这些患者的平均年龄为55.4岁。A组NC发生率显著高于B组(19.5% vs. 9.3% p <0.05),两组间感染和排斥发生率无差异。nc患者的急性肾功能衰竭发生率、肾脏替代治疗需求、入住ICU天数、住院天数以及入院期间和术后1年的死亡率均高于nc患者。然而,当分析有神经系统并发症的患者时,a组患者的并发症发生率高于B组。结论:使用免疫抑制疗法,使用低剂量的抗胆碱尿素和较晚的起病时间,通常被称为肾保护疗法,如B组所使用的,也可以起到神经保护作用,减少神经系统并发症的出现,从而降低发病率。这些发现大多在有大量患者和随机的研究中得到证实。
Neurological Complications after Liver Transplantation According to Immunosuppressive Therapy
Background: Neurological complications (NC) after liver transplantation (LT) are frequent, appearing in
up to 60% of patients. Etiology is often related to immunosuppressant neurotoxicity and opportunistic
infections. The use of basiliximab allows for less toxic immunosuppressive therapies. The aim of this study
was to evaluate the neurological complications present during the first 30 days after LT and to evaluate its
relationship with renal function, immunosuppressive therapy, and mortality.
Methods: A total of 231 recipients were included in the retrospective, longitudinal, and nonrandomized
study under 2 different immunosuppression protocols (with -group B- or without basiliximab -group A-).
Results: NC were present in 14.3% of patients (n: 33), the average age of these patients was 55.4 years. The
incidence of NC was significantly higher in group A than in group B (19.5% vs. 9.3% p <0.05), with no
differences in the incidence of infection or rejection between both groups. The incidence of acute renal
failure, the need for renal replacement therapy, the days of admission to the ICU, the days of hospital
admission, as well as mortality during admission and one year after LT were higher among patients with
NC. However, when analyzing patients with a neurological complication, patients in group A had a higher
incidence of complications than in group B.
Conclusion: The use of immunosuppressive therapies that apply lower doses of anticalcineurinics and with
a later onset, classically called nephroprotective as used in group B, could also be neuroprotective, reducing
the appearance of neurological complications and, therefore, morbidity. These findings most be verified in
studies with a larger number of patients and randomized.