Fu Keng Seng, Wong Pei Yin, Hiew Fu Liong
Department of Neurology, Hospital Kuala Lumpur, Kuala Lumpur, Wilayah Persekutuan, Malaysia.
BMJ Neurol Open. 2020 Jan 30;2(1):e000020. doi: 10.1136/bmjno-2019-000020. eCollection 2020.
Therapeutic plasma exchange (TPE) for semi-critical neurological manifestations can be managed in non-acute setting instead of critical care unit. In 2014, we established a non-acute neurology TPE unit for semi-critical haemodynamically stable patients. In this study, we aimed to evaluate the technical and safety parameters from the first 3 years of service.
We analysed prospectively collected TPE data for patients treated with centrifugation TPE at our non-acute neurology TPE unit in Kuala Lumpur Hospital between May 2015 and June 2018.
A total of 245 TPE procedures were performed in 55 patients for nine neurological indications, predominantly the central nervous system (79%). Twenty four per cent (n=13) had category I and 73% (n=40) had category II indication (American Society for Apheresis (ASFA) 2019). Others (4%) were not in ASFA indications. Neuromyelitis optica spectrum disorders accounted for half (51%) of the total patients. Twenty-three (41.8%) patients experienced adverse events, with hypotensive episodes being the the most common (n=12/55, 21.8%). Five (9.1%) patients had catheter-related blood stream infection, correlating with higher exchange plasma volume (p=0.023). Symptomatic hypocalcaemia was less common (n=5/55, 9.1%) and allergic reaction to human albumin was rare (n=1/55, 1.8%). Four technical errors detected. Three involved centrifugation sets manufacturing defects and one involved error in centrifugation set installation. Seven (2.9%) procedures were terminated: 5 for adverse effects and 2 for technical errors.
Performing TPE among semi-critical patients with neurology manifestations in basic non-acute set-up proved safe, with predictable complications. This set-up reduced the reliance on critical care services for TPE procedures.
对于半危急神经学表现的治疗性血浆置换(TPE)可在非急症环境中进行管理,而非在重症监护病房。2014年,我们为血流动力学稳定的半危急患者设立了一个非急症神经学TPE单元。在本研究中,我们旨在评估该单元运营头3年的技术和安全参数。
我们前瞻性分析了2015年5月至2018年6月在吉隆坡医院非急症神经学TPE单元接受离心式TPE治疗的患者的TPE数据。
共对55例患者进行了245次TPE治疗,涉及9种神经学指征,主要为中枢神经系统疾病(79%)。24%(n = 13)的患者符合I类指征,73%(n = 40)的患者符合II类指征(美国单采学会(ASFA)2019年标准)。其他(4%)患者不符合ASFA指征。视神经脊髓炎谱系障碍患者占总患者数的一半(51%)。23例(41.8%)患者发生不良事件,其中低血压发作最为常见(n = 12/55,21.8%)。5例(9.1%)患者发生导管相关血流感染,与较高的置换血浆量相关(p = 0.023)。症状性低钙血症较少见(n = 5/55,9.1%),对人白蛋白的过敏反应罕见(n = 1/55,1.8%)。检测到4起技术错误。3起涉及离心设备制造缺陷,1起涉及离心设备安装错误。7例(2.9%)治疗终止:5例因不良反应,2例因技术错误。
在基本非急症环境中对有神经学表现的半危急患者进行TPE治疗被证明是安全的,并发症可预测。这种设置减少了TPE治疗对重症监护服务的依赖。