Department of Neurology, University Hospitals of Leicester, Leicester, UK.
J Neurol Sci. 2011 Sep 15;308(1-2):124-7. doi: 10.1016/j.jns.2011.05.035. Epub 2011 Jun 15.
The incidence and determinants of thromboembolic complications (TEC) of intravenous immunoglobulin (IVIg) therapy in patients with dysimmune neuropathy are uncertain.
We performed a retrospective study of patients with dysimmune neuropathy seen at our institution and treated with IVIg, over a 24-month period.
Sixty-two patients were treated with a total of 616 courses of IVIg. TEC occurred in 7 patients. In 5, these occurred within 14 days after IVIg infusion ("early TEC"). Early TEC were significantly more frequent after courses administered to IVIg-naïve patients (3/25 vs. 2/591 courses; p<0.001), but incidences were comparable in newly- vs. previously-treated patients (3/25 vs. 2/44 patients; p=0.34). Early TEC included 2 cases of myocardial infarction, one of acute coronary syndrome, one of deep vein thrombosis (DVT) with pulmonary embolism and one of isolated DVT. Mean dose per course was comparable in affected and unaffected patients (p=0.47), but administration of daily doses ≥ 35 g correlated significantly with occurrence of early TEC (p=0.028). Previous coronary disease (p=0.037) and immobility at time of treatment (p=0.049) were independent predictors of early TEC. Patients with early TEC had significantly more risk factors (p<0.001), and were significantly more likely to have ≥ 4 risk factors (p=0.006), than those without early TEC.
The risk of TEC with IVIg is not negligible in patients with neuropathy. Although higher with a first-ever infusion, the general risk may be comparable in IVIg-naïve and previously-treated patients. Administration of daily doses ≥ 35 g of IVIg may carry a greater risk of early TEC. Coronary disease, immobility at time of treatment, presence of ≥ 4 risk factors, should lead to caution and consideration of alternative treatments.
静脉注射免疫球蛋白(IVIg)治疗免疫性神经病患者的血栓栓塞并发症(TEC)的发生率和决定因素尚不确定。
我们对在我院就诊并接受 IVIg 治疗的免疫性神经病患者进行了一项回顾性研究,研究时间为 24 个月。
62 例患者共接受了 616 次 IVIg 治疗。7 例患者发生 TEC。其中 5 例发生在 IVIg 输注后 14 天内(“早期 TEC”)。IVIg 初治患者中早期 TEC 发生率明显更高(3/25 与 2/591 疗程;p<0.001),但新治与既往治疗患者发生率相似(3/25 与 2/44 例患者;p=0.34)。早期 TEC 包括 2 例心肌梗死、1 例急性冠脉综合征、1 例深静脉血栓形成(DVT)伴肺栓塞和 1 例孤立性 DVT。受影响和未受影响患者的每疗程平均剂量无差异(p=0.47),但每日剂量≥35 g 与早期 TEC 的发生显著相关(p=0.028)。既往冠心病(p=0.037)和治疗时的不活动(p=0.049)是早期 TEC 的独立预测因素。发生早期 TEC 的患者具有更多的危险因素(p<0.001),并且发生≥4 个危险因素的可能性显著更高(p=0.006),而非早期 TEC 患者。
免疫性神经病患者使用 IVIg 时 TEC 的风险不容忽视。尽管首次输注时风险较高,但 IVIg 初治和既往治疗患者的总体风险可能相似。每日剂量≥35 g 的 IVIg 给药可能会增加早期 TEC 的风险。冠心病、治疗时不活动、存在≥4 个危险因素,应引起警惕并考虑替代治疗。