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在苏里南,预防复发方面,7天双倍剂量的伯氨喹不如14天单剂量治疗。

Primaquine double dose for 7 days is inferior to single-dose treatment for 14 days in preventing recurrent episodes in Suriname.

作者信息

Mac Donald-Ottevanger M Sigrid, Adhin Malti R, Jitan Jeetendra Kumar, Bretas Gustavo, Vreden Stephen Gs

机构信息

Foundation for Scientific Research Suriname (SWOS).

Department of Biochemistry, Anton de Kom University of Suriname.

出版信息

Infect Drug Resist. 2017 Dec 20;11:3-8. doi: 10.2147/IDR.S135897. eCollection 2018.

Abstract

BACKGROUND

Recurrent episodes of are caused by dormant liver stages of the parasite, which are not eradicated by choloroquine. Therefore, effective treatment also includes the use of primaquine (PQ). However, this secondary preventive therapy is often not effective, mostly due to poor adherence to the relatively long treatment course, justifying a comparative study of the efficacy of different durations of PQ treatment.

MATERIALS AND METHODS

We included patients presenting with an acute and documented infection from January 2006 to February 2008. All patients received chloroquine 25 mg/kg over a 3-day period. Subsequently, patients in group 7D received PQ 30 mg/day for 7 days, and patients in group 14D received standard PQ 15 mg/day for 14 days. All doses were given under supervision and patients were followed up for at least 6 months. The Kaplan-Meier method was used to estimate cumulative probability of recurrence up to 12 months after treatment initiation stratified by treatment group. Cox regression was used to assess possible determinants for recurrent parasitemia.

RESULTS

Forty-seven of the 79 included patients (59.5%) were allocated to group 7D and 32 patients (40.5%) were allocated to group 14D. Recurrent parasitemia was detected in 31.9% of the cases in group 7D compared to 12.5% of the cases in group 14D (hazard ratio [HR] =3.36, 95% CI 1.11-10.16). Cumulative probability for recurrent parasitemia at 3, 6, and 12 months was 0.201 (95% CI 0.106-0.362), 0.312 (95% CI 0.190-0.485), and 0.424 (95% CI 0.274-0.615) for group 7D and 0.100 (95% CI 0.033-0.279), 0.100 (95% CI 0.033-0.279), and 0.138 (95% CI 0.054-0.327) for group 14D, respectively. When adjusted for possible confounders, differences in recurrent parasitemia remained significant between the two regimens in Cox regression analysis.

CONCLUSION

More than 30% of the patients receiving shorter treatment course had recurrent parasitemia, suggesting that the standard dose of 15 mg/day PQ for 14 days is more efficacious than 30 mg for 7 days in preventing recurrent episodes. Furthermore, we suggest that treatment in Suriname should be changed to PQ 30 mg/day for 14 days, as per Center for Disease Control and Prevention recommendation, in light of a recurrence rate of over 10%, even in group 14D.

摘要

背景

疟疾病情复发是由寄生虫的肝脏休眠期引起的,氯喹无法根除这些休眠期。因此,有效的治疗还包括使用伯氨喹(PQ)。然而,这种二级预防疗法往往无效,主要原因是对相对较长的治疗疗程依从性差,这使得对不同疗程PQ治疗效果进行比较研究成为必要。

材料与方法

我们纳入了2006年1月至2008年2月期间出现急性且有记录的疟原虫感染的患者。所有患者在3天内接受25mg/kg的氯喹治疗。随后,7天组的患者接受30mg/天的PQ治疗,为期7天,14天组的患者接受标准剂量15mg/天的PQ治疗,为期14天。所有剂量均在监督下给予,患者至少随访6个月。采用Kaplan-Meier方法估计治疗开始后12个月内按治疗组分层的复发累积概率。使用Cox回归评估复发寄生虫血症的可能决定因素。

结果

79例纳入患者中,47例(59.5%)被分配到7天组,32例(40.5%)被分配到14天组。7天组31.9%的病例检测到复发寄生虫血症,而14天组为12.5%(风险比[HR]=3.36,95%可信区间1.11-10.16)。7天组在3、6和12个月时复发寄生虫血症的累积概率分别为0.201(95%可信区间0.106-0.362)、0.312(95%可信区间0.190-0.485)和0.424(95%可信区间0.274-0.615),14天组分别为0.100(95%可信区间0.033-0.279)、0.100(95%可信区间0.033-0.279)和0.138(95%可信区间0.054-0.327)。在对可能的混杂因素进行调整后,Cox回归分析显示两种治疗方案在复发寄生虫血症方面的差异仍然显著。

结论

接受较短疗程治疗的患者中超过30%出现了复发寄生虫血症,这表明在预防疟疾复发方面,标准剂量15mg/天的PQ治疗14天比30mg/天治疗7天更有效。此外,鉴于即使在14天组复发率仍超过10%,我们建议根据疾病控制与预防中心的建议,将苏里南的疟疾治疗方案改为30mg/天的PQ治疗14天。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ed9/5743107/31e9942af368/idr-11-003Fig1.jpg

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