Clin Lab. 2022 Jul 1;68(7). doi: 10.7754/Clin.Lab.2021.211051.
Severe hypertriglyceridemia (sHTG) is an independent risk factor of atherosclerotic heart disease (ASHD) and acute pancreatitis (AP). The aim was to evaluate the efficacy and safety of DFPP in sHTG patients (TG > 1,000 mg/dL).
This was a prospective single-center study in which patients with severe symptomatic drug and diet refractory HTG were recruited. Peripheral venous access of upper extremities was used for DFPP. Blood flow rate was 100 - 120 mL/min and plasma separation rate was 800 - 1,000 mL/h. Plasma volume to treat in each case was calculated with the Kaplan formula. Anticoagulation was achieved by low molecular weight heparin. Treatment goal was triglyceride level decreased to normal (< 1.7 mmol/L). Epidemiological data, lipid, hematological parameters as well as side effects were evaluated before and after DFPP.
Seven patients (6 males and 1 female) were consecutively enrolled to this trial. There was diabetes mellitus type 2 in four patients and obesity-associated nephropathy in one patient. The mean age was 42.5 years. The average TG level before plasmapheresis was 17.41 mmol/L (range 10.93 - 26.33 mmol/L). After one session, the levels of triglyceride, total cholesterol, LDL-c, HDL-c decreased significantly by 58.3%, 43.2%, 41.9%, 20.7%, respectively. The mean number of treatment sessions was 1.5 (range 1 - 3). DFPP was well-tolerated. Except for transient decrease of albumin, globulin and fibrinogen, liver and renal functions, hematological parameters did not change significantly.
According to our own experience, DFPP may be used safely and effectively in sHTG patients at risk of acute coronary events and AP. However, further randomized controlled trials are necessary to explore the long-term effect.
重度高甘油三酯血症(sHTG)是动脉粥样硬化性心脏病(ASHD)和急性胰腺炎(AP)的独立危险因素。本研究旨在评估 DFP 在 sHTG 患者(TG>1000mg/dL)中的疗效和安全性。
这是一项前瞻性单中心研究,纳入了患有严重症状性药物和饮食难治性 HTG 的患者。采用上肢外周静脉通路进行 DFP。血流速度为 100-120ml/min,血浆分离速度为 800-1000ml/h。根据 Kaplan 公式计算每个病例的血浆治疗量。采用低分子肝素抗凝。治疗目标是将甘油三酯水平降至正常(<1.7mmol/L)。在 DFP 前后评估流行病学数据、血脂、血液学参数以及副作用。
本试验连续纳入了 7 名患者(6 名男性和 1 名女性)。其中 4 例患有 2 型糖尿病,1 例患有肥胖相关性肾病。平均年龄为 42.5 岁。血浆置换前平均甘油三酯水平为 17.41mmol/L(范围 10.93-26.33mmol/L)。单次治疗后,甘油三酯、总胆固醇、LDL-c、HDL-c 水平分别显著下降 58.3%、43.2%、41.9%、20.7%。治疗次数平均为 1.5 次(范围 1-3 次)。DFP 耐受性良好。除白蛋白、球蛋白和纤维蛋白原的短暂下降外,肝肾功能、血液学参数无明显变化。
根据我们的经验,DFP 可安全、有效地用于有发生急性冠脉事件和 AP 风险的 sHTG 患者。但需要进一步的随机对照试验来探讨其长期疗效。