Treeprasertsuk Sombat, Krudsood Srivicha, Tosukhowong Thanawat, Maek-A-Nantawat Wirach, Vannaphan Suparp, Saengnetswang Tosaporn, Looareesuwan Sornchai, Kuhn Walter F, Brittenham Gary, Carroll James
Bangkok Hospital for Tropical Diseases, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Southeast Asian J Trop Med Public Health. 2003 Mar;34(1):37-42.
One hundred and eight patients with severe falciparum malaria underwent a placebo controlled trial with the antioxidant, N-acetylcysteine (NAC), as an adjunctive therapy along with standard intravenous artesunate therapy. Three NAC dosage regimens were used: an intravenous loading dose of 140 mg/kg followed by 70 mg/kg every four hours intravenously for up to 18 doses (Group 1); a single intravenous loading dose followed by oral NAC in the same amount as for Group 1 (Group 2); a regimen identical to Group 1 except that oral NAC was administered after the first 24 hours (Group 3). Fifty-four patients received placebo plus artesunate. Two critically ill patients died in Group 1. No patient sustained an adverse reaction to the NAC other than vomiting, and the deaths were attributed to severe disease with multiple organ involvement. The excellent results with NAC, the lack of adverse effects, and the rationale for NAC benefit supports the need for a large, double blind trial of NAC as an adjunctive therapy for severe malaria.
108例重症恶性疟患者接受了一项安慰剂对照试验,将抗氧化剂N-乙酰半胱氨酸(NAC)作为标准静脉注射青蒿琥酯治疗的辅助疗法。使用了三种NAC给药方案:静脉注射负荷剂量140mg/kg,随后每4小时静脉注射70mg/kg,最多注射18次(第1组);单次静脉注射负荷剂量,随后口服与第1组相同剂量的NAC(第2组);与第1组相同的方案,但在最初24小时后口服NAC(第3组)。54例患者接受了安慰剂加青蒿琥酯治疗。第1组有2例重症患者死亡。除呕吐外,没有患者对NAC产生不良反应,死亡归因于多器官受累的严重疾病。NAC的优异效果、缺乏不良反应以及NAC有益的理论依据支持有必要进行一项大型双盲试验,以评估NAC作为重症疟疾辅助疗法的效果。