Luxemburger C, ter Kuile F O, Nosten F, Dolan G, Bradol J H, Phaipun L, Chongsuphajaisiddhi T, White N J
Shoklo Malaria Research Unit, Mae Sod, Thailand.
Trans R Soc Trop Med Hyg. 1994 Mar-Apr;88(2):213-7. doi: 10.1016/0035-9203(94)90303-4.
The therapeutic efficacy and toxicity of a combination of low dose mefloquine (15 mg/kg) plus artesunate 10 mg/kg in one day (MA) was compared with the currently used regimen of high dose mefloquine (25 mg/kg) (MQ) in 552 patients with uncomplicated falciparum malaria in an area of multi-drug resistance on the Thai-Burmese border. MA gave faster clinical and parasitological responses and prevented early treatment failure; 15 patients in the MQ group (6%) were early failures (< 9 d) compared with none receiving MA (P = 0.0001). Overall failure rates by day 28 were 19% in the MA group and 24% in with MQ group (relative risk (RR) = 0.78, 95% confidence interval (CI) 0.54-1.12). In the subgroup of patients who required re-treatment, MA proved significantly more effective than MQ; failure rates were 25% and 52% respectively (RR = 0.49, 95% CI = 0.29-0.83). Treatment failures were associated with mefloquine treatment in the previous month (RR = 1.72, 95% CI = 1.09-2.70) and diarrhoea (RR = 1.55, 95% CI = 1.05-2.28). Gastrointestinal side-effects and dizziness were more likely in the MQ group. There was no evident adverse effect associated with artesunate. A single day's treatment with artesunate augments the antimalarial efficacy of mefloquine.
在泰缅边境多药耐药地区,对552例非复杂性恶性疟患者比较了低剂量甲氟喹(15毫克/千克)加青蒿琥酯10毫克/千克一天方案(MA)与目前使用的高剂量甲氟喹(25毫克/千克)方案(MQ)的治疗效果和毒性。MA组临床和寄生虫学反应更快,并预防了早期治疗失败;MQ组有15例患者(6%)为早期失败(<9天),而MA组无早期失败患者(P = 0.0001)。到第28天,MA组总体失败率为19%,MQ组为24%(相对危险度(RR)= 0.78,95%置信区间(CI)0.54 - 1.12)。在需要再次治疗的患者亚组中,MA组明显比MQ组更有效;失败率分别为25%和52%(RR = 0.49,95% CI = 0.29 - 0.83)。治疗失败与前一个月使用甲氟喹治疗(RR = 1.72,95% CI = 1.09 - 2.70)和腹泻(RR = 1.55,95% CI = 1.05 - 2.28)有关。MQ组胃肠道副作用和头晕更常见。青蒿琥酯未发现明显不良反应。青蒿琥酯单日治疗可增强甲氟喹的抗疟效果。