Yeo Tsin W, Lampah Daniel A, Gitawati Retno, Tjitra Emiliana, Kenangalem Enny, Granger Donald L, Weinberg J Brice, Lopansri Bert K, Price Ric N, Celermajer David S, Duffull Stephen B, Anstey Nicholas M
International Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
PLoS One. 2008 Jun 11;3(6):e2347. doi: 10.1371/journal.pone.0002347.
L-arginine infusion improves endothelial function in malaria but its safety profile has not been described in detail. We assessed clinical symptoms, hemodynamic status and biochemical parameters before and after a single L-arginine infusion in adults with moderately severe malaria.
In an ascending dose study, adjunctive intravenous L-arginine hydrochloride was infused over 30 minutes in doses of 3 g, 6 g and 12 g to three separate groups of 10 adults hospitalized with moderately severe Plasmodium falciparum malaria in addition to standard quinine therapy. Symptoms, vital signs and selected biochemical measurements were assessed before, during, and for 24 hours after infusion. No new or worsening symptoms developed apart from mild discomfort at the intravenous cannula site in two patients. There was a dose-response relationship between increasing mg/kg dose and the maximum decrease in systolic (rho = 0.463; Spearman's, p = 0.02) and diastolic blood pressure (r = 0.42; Pearson's, p = 0.02), and with the maximum increment in blood potassium (r = 0.70, p<0.001) and maximum decrement in bicarbonate concentrations (r = 0.53, p = 0.003) and pH (r = 0.48, p = 0.007). At the highest dose (12 g), changes in blood pressure and electrolytes were not clinically significant, with a mean maximum decrease in mean arterial blood pressure of 6 mmHg (range: 0-11; p<0.001), mean maximal increase in potassium of 0.5 mmol/L (range 0.2-0.7 mmol/L; p<0.001), and mean maximal decrease in bicarbonate of 3 mEq/L (range 1-7; p<0.01) without a significant change in pH. There was no significant dose-response relationship with blood phosphate, lactate, anion gap and glucose concentrations. All patients had an uncomplicated clinical recovery.
CONCLUSIONS/SIGNIFICANCE: Infusion of up to 12 g of intravenous L-arginine hydrochloride over 30 minutes is well tolerated in adults with moderately severe malaria, with no clinically important changes in hemodynamic or biochemical status. Trials of adjunctive L-arginine can be extended to phase 2 studies in severe malaria.
ClinicalTrials.gov NCT00147368.
输注L-精氨酸可改善疟疾患者的内皮功能,但其安全性尚未得到详细描述。我们评估了中度严重疟疾成年患者单次输注L-精氨酸前后的临床症状、血流动力学状态和生化参数。
在一项剂量递增研究中,除标准奎宁治疗外,将辅助静脉注射盐酸L-精氨酸以3g、6g和12g的剂量在30分钟内分别输注给三组,每组10名因恶性疟原虫引起的中度严重疟疾住院的成年患者。在输注前、输注期间和输注后24小时评估症状、生命体征和选定的生化指标。除两名患者静脉插管部位出现轻度不适外,未出现新的或加重的症状。mg/kg剂量增加与收缩压最大降幅(rho = 0.463;Spearman检验,p = 0.02)和舒张压最大降幅(r = 0.42;Pearson检验,p = 0.02)之间存在剂量反应关系,与血钾最大增幅(r = 0.70,p<0.001)、碳酸氢盐浓度最大降幅(r = 0.53,p = 0.003)和pH值最大降幅(r = 0.48,p = 0.007)也存在剂量反应关系。在最高剂量(12g)时,血压和电解质变化在临床上无显著意义,平均动脉血压最大降幅为6mmHg(范围:0 - 11;p<0.001),血钾平均最大增幅为0.5mmol/L(范围0.2 - 0.7mmol/L;p<0.001),碳酸氢盐平均最大降幅为3mEq/L(范围1 - 7;p<0.01),pH值无显著变化。与血磷、乳酸、阴离子间隙和血糖浓度无显著剂量反应关系。所有患者临床恢复均顺利。
结论/意义:在中度严重疟疾成年患者中,30分钟内静脉输注高达12g盐酸L-精氨酸耐受性良好,血流动力学或生化状态无临床重要变化。辅助L-精氨酸的试验可扩展至重症疟疾的2期研究。
ClinicalTrials.gov NCT00147368