García-de-Lorenzo Abelardo, López-Martínez Jorge, Planas Mercé, Chacón Pilar, Montejo Juan C, Bonet Alfonso, Ortiz-Leyba Carlos, Sánchez-Segura Juan M, Ordóñez Javier, Acosta Jose, Grau Teodoro, Jiménez Francisco J
Intensive Care Unit, Hospital Universitario La Paz, Madrid, Spain.
JPEN J Parenter Enteral Nutr. 2003 May-Jun;27(3):208-15. doi: 10.1177/0148607103027003208.
A concentrated fat emulsion (Intralipid 30%) with a phospholipid/triglyceride ratio of 0.04 was tested for clinical tolerance and metabolic effects in the short-term parenteral nutrition of septic and trauma critically ill patients and compared with Intralipid 20% (phospholipid/triglyceride ratio of 0.06).
This was a prospective, randomized, multicenter study in the intensive care units in 10 university hospitals, including 90 adult patients in 2 groups: 55 septic and 35 trauma patients. Patients in each group were randomly divided into 2 subgroups according to the fat emulsions administered (1.4 g/kg per day) as part of the calories for at least 6 days of continuous total parenteral nutrition (TPN). One subgroup was treated with 30% long-chain triglycerides (phospholipid/ triglyceride ratio: 0.04) and the other with 20% long-chain triglycerides (phospholipid/triglyceride ratio: 0.06). The parenteral nutrition formula was isocaloric and isonitrogenous with 0.25 g of nitrogen/kg per day and 40% of the nonprotein calories as fat. Clinical tolerance was assessed during the study. At baseline and after 3 and 6 days of TPN, the following biochemical parameters were measured: prealbumin, retinol-binding protein, serum albumin, hematologic, hepatic and renal function variables, triglycerides, phospholipids, total and free cholesterol, nonesterified cholesterol, nonesterified fatty acids, and lipoproteins.
At baseline, no differences in age, gender, severity of the condition [Acute Physiology and Chronic Health Evaluation (APACHE II) score], or clinical chemistry were found between the subgroups. The levels of plasma proteins studied and the renal, hematologic, or hepatic function variables did not vary during the study period. Total cholesterol increased significantly, owing to esterified cholesterol, with 20% long-chain triglyceride in septic patients (baseline: 2.1 +/- 0.8 mmol/L, day 6: 2.8 +/- 0.6 mmol/L, p = .026). In septic patients receiving 20% long-chain triglycerides, plasma triglycerides had a similar behavior (baseline: 1.4 +/- 0.6 mmol/L, day 3: 2.2 +/- 0.8 mmol/L, p < .05). The very-low-density lipoprotein content of cholesterol, triglycerides, and phospholipids showed a tendency to decrease in septic patients treated with 30% long-chain triglycerides (NS). None of the emulsions induced the synthesis of lipoprotein X.
Our results indicate that while both fat emulsions used in the TPN of critically ill patients are clinically safe, the 30% long-chain triglyceride fat emulsion with a phospholipid/triglyceride ratio of 0.04 causes fewer lipid metabolic disturbances.
对一种磷脂/甘油三酯比例为0.04的浓缩脂肪乳剂(英脱利匹特30%)在脓毒症和创伤重症患者短期肠外营养中的临床耐受性和代谢影响进行了测试,并与英脱利匹特20%(磷脂/甘油三酯比例为0.06)进行比较。
这是一项在10所大学医院重症监护病房进行的前瞻性、随机、多中心研究,包括90例成年患者,分为2组:55例脓毒症患者和35例创伤患者。每组患者根据给予的脂肪乳剂(每天1.4 g/kg)随机分为2个亚组,作为连续全肠外营养(TPN)至少6天热量的一部分。一个亚组接受30%长链甘油三酯(磷脂/甘油三酯比例:0.04)治疗,另一个亚组接受20%长链甘油三酯(磷脂/甘油三酯比例:0.06)治疗。肠外营养配方为等热量、等氮量,每天0.25 g氮/kg,40%的非蛋白热量为脂肪。在研究期间评估临床耐受性。在TPN基线时以及3天和6天后,测量以下生化参数:前白蛋白、视黄醇结合蛋白、血清白蛋白、血液学、肝功能和肾功能变量、甘油三酯、磷脂、总胆固醇和游离胆固醇、非酯化胆固醇、非酯化脂肪酸和脂蛋白。
在基线时,各亚组之间在年龄、性别、病情严重程度[急性生理与慢性健康评估(APACHE II)评分]或临床化学方面未发现差异。所研究的血浆蛋白水平以及肾功能、血液学或肝功能变量在研究期间没有变化。在脓毒症患者中,由于酯化胆固醇,总胆固醇显著升高,使用20%长链甘油三酯(基线:2.1±0.8 mmol/L,第6天:2.8±0.6 mmol/L,p = 0.026)。在接受20%长链甘油三酯的脓毒症患者中,血浆甘油三酯有类似变化(基线:1.4±0.6 mmol/L,第3天:2.2±0.8 mmol/L,p < 0.05)。在接受30%长链甘油三酯治疗的脓毒症患者中,极低密度脂蛋白中的胆固醇、甘油三酯和磷脂含量有下降趋势(无统计学意义)。两种乳剂均未诱导脂蛋白X的合成。
我们的结果表明,虽然用于重症患者TPN的两种脂肪乳剂在临床上都是安全的,但磷脂/甘油三酯比例为0.04的30%长链甘油三酯脂肪乳剂引起的脂质代谢紊乱较少。