Vector Control Division, Ministry of Health, Kampala, Uganda.
Trans R Soc Trop Med Hyg. 2013 Jun;107(6):397-404. doi: 10.1093/trstmh/trt024. Epub 2013 Apr 17.
The current recommended control strategy for schistosomiasis is annual treatment using 40 mg/kg of praziquantel. However, praziquantel is only effective on adult worms and giving a second dose may increase its efficacy. We assessed the effect of one versus two doses of praziquantel on cure rate and re-infection with Schistosoma mansoni in a high endemic community along Lake Victoria, Uganda.
To investigate the effect of the two regimens, 395 infected people were randomised into two groups; one received a single standard dose of praziquantel (Distocide® 600 mg, Shin Poong Pharmaceuticals, Seoul, Republic of Korea), 40mg/kg body weight, while the other group received a second dose 2 weeks later. Cure rate and infection intensity were assessed 9 weeks after the first treatment using standard parasitological procedures. Re-infection levels were monitored 8 and 24 months after treatment.
Those who received two doses were more likely to be cured (69.7%) compared to those who received a single dose (47.9%) (χ(2) = 18.5, p < 0.001). Geometric mean intensity (GMI) of infection at 9 weeks (eggs per gram of faeces [epg]) was 12.0 epg (CI95: 8.9-16.1) for individuals who received 2 doses and 22.1 epg (CI95: 16.9-28.8) for those in the single dose arm. Eight months after treatment, prevalence of re-infection for individuals in the double dose arm (61.6%, CI95: 50.2-73.1) was not significantly different from that of those in a single dose arm (68.3%, CI95: 59.9-76.8). The difference in GMI of re-infection for individuals in the single dose arm (33.8 epg, CI95: 23.2-49.3) and those in the double dose arm (34.5 epg, CI95: 24.7-48.1) was not significant. Twenty four months after treatment, prevalence of re-infection was not significantly different. The difference in GMI of re-infection for those in the single dose arm (57.5 epg, CI95: 33.9-97.5) and those in the double dose arm (42.2 epg, CI95: 29.9-59.6) was also insignificant.
Our results suggest that a second dose of praziquantel given 2 weeks after the first dose improves cure rate and reduces S. mansoni infection intensity. However, there is no added advantage on reduction of S. mansoni re-infection by administering two doses of praziquantel. CLINICAL TRIALS.GOV IDENTIFIER: NCT00215267.
目前推荐的血吸虫病控制策略是每年使用 40mg/kg 的吡喹酮进行治疗。然而,吡喹酮仅对成虫有效,给予第二剂可能会提高其疗效。我们在乌干达维多利亚湖沿岸的一个高流行地区评估了一剂与两剂吡喹酮对曼氏血吸虫治愈率和再感染的影响。
为了研究两种方案的效果,将 395 名感染者随机分为两组;一组接受单标准剂量的吡喹酮(来自 Shin Poong 制药的 Distocide® 600mg,韩国首尔),40mg/kg 体重,而另一组在 2 周后接受第二剂。第一次治疗后 9 周,采用标准寄生虫学程序评估治愈率和感染强度。治疗后 8 个月和 24 个月监测再感染水平。
接受两剂治疗的患者比接受单剂治疗的患者更有可能治愈(69.7%对 47.9%)(χ(2) = 18.5,p < 0.001)。第 9 周时感染的几何平均强度(每克粪便中的虫卵数[epg])为接受 2 剂的个体为 12.0 epg(95%CI:8.9-16.1),接受单剂的个体为 22.1 epg(95%CI:16.9-28.8)。治疗 8 个月后,双剂量组个体的再感染率(61.6%,95%CI:50.2-73.1)与单剂量组个体的再感染率(68.3%,95%CI:59.9-76.8)无显著差异。单剂量组个体(33.8 epg,95%CI:23.2-49.3)和双剂量组个体(34.5 epg,95%CI:24.7-48.1)的再感染 GM 差异无统计学意义。治疗 24 个月后,再感染率无显著差异。单剂量组个体(57.5 epg,95%CI:33.9-97.5)和双剂量组个体(42.2 epg,95%CI:29.9-59.6)的再感染 GM 差异也无统计学意义。
我们的结果表明,在第一次治疗后 2 周给予第二剂吡喹酮可提高治愈率并降低曼氏血吸虫感染强度。然而,给予两剂吡喹酮并没有降低曼氏血吸虫再感染的优势。临床试验。注册号:NCT00215267。