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在罗阿丝虫病流行地区使用美迪善(Mectizan®)治疗盘尾丝虫病后严重不良事件科学工作组报告

Report of a Scientific Working Group on Serious Adverse Events following Mectizan(R) treatment of onchocerciasis in Loa loa endemic areas.

机构信息

Mectizan(R) Donation Program, 750 Commerce Drive, Suite 400, Decatur, Georgia 30030, USA.

出版信息

Filaria J. 2003 Oct 24;2 Suppl 1(Suppl 1):S2. doi: 10.1186/1475-2883-2-S1-S2.

Abstract

The occurrence of Serious Adverse Experiences (SAEs) following Mectizan(R) treatment of onchocerciasis in Loa loa endemic areas has been increasingly reported over the past decade. These SAEs include a severely disabling, and potentially fatal, encephalopathy, which appears to correlate with a high load of L. loa microfilariae (> 30,000 mf/ml).Previous consultations organized by the Mectizan(R) Donation Program (MDP) in 1995 and 1999 have developed useful "case" definitions of encephalopathic SAEs following Mectizan(R) treatment and have summarized available evidence on its pathogenesis and optimal clinical management. At both meetings, the need for better understanding of the pathogenesis of the encephalopathy was emphasized, including the need for biological and autopsy specimens from the affected cases.Following a recommendation at the Joint Action Forum of the African Programme for Onchocerciasis Control in December 2001, the MDP, on behalf of the Mectizan(R) Expert Committee, organized a Scientific Working Group on L. loa associated SAEs following Mectizan(R) treatment in May 2002. The present report includes the background, new evidence, conclusions and recommendations from that Scientific Working Group. The following points represent a summary of the present status:1. Although there are more and better quality clinical and epidemiological data on L. loa, the pathogenesis of the Mectizan(R)-related L. loa encephalopathy remains obscure.2. Very limited progress has been made in research on the pathogenesis of encephalopathy, because of the lack of specimens from cases, and the lack of animal models.3. There has been no particular breakthrough in terms of the medical management of patients with L. loa encephalopathy; however, a favorable outcome usually results from prompt general nursing and nutritional care which remain the major interventions.The main recommendations for future actions are as follows:1. Validate and update the mapping of L. loa with a combination of remote sensing and RAPLOA techniques.2. Conduct an expert analysis of the apparent clustering of encephalopathic SAEs reported so far.3. Investigate a possible "pre-treatment" scheme with high-dose albendazole in L. loa endemic communities at high risk of encephalopathic SAEs if treated with Mectizan(R); this study will be conducted in collaboration with WHO/TDR.4. Establish a post of Loiasis Technical Advisor for research and operational support in Cameroon, to conduct population surveys and to facilitate better data collection from SAE cases, including postmortem studies as appropriate.5. Investigate the possibility of developing an animal model of L. loa encephalopathy; this activity would be linked to the above-mentioned research agenda in Cameroon.6. Investigate the best care model for encephalopathic SAEs, including identification of early warning signs and therapeutic interventions.7. Develop further models for health education messages needed for community compliance with Mectizan(R) treatment, and family support for SAE cases.8. Conduct research studies on the safety of combination therapy of Mectizan(R) and albendazole in areas co-endemic for L. loa and lymphatic filariasis (LF) with coordination from the relevant technical bodies that oversee these issues.The above recommendations will be implemented through a continuing collaboration between the interested parties represented at the Scientific Working Group, involved in onchocerciasis control and/or the Global Programme to Eliminate Lymphatic Filariasis.

摘要

在过去十年间,在罗阿丝虫病流行地区使用美迪善(Mectizan®)治疗盘尾丝虫病后出现严重不良事件(SAE)的报告日益增多。这些严重不良事件包括一种严重致残且可能致命的脑病,其似乎与高负荷的罗阿丝虫微丝蚴(> 30,000条微丝蚴/毫升)相关。1995年和1999年由美迪善捐赠计划(MDP)组织的前期磋商制定了美迪善治疗后脑病性严重不良事件的有用“病例”定义,并总结了关于其发病机制和最佳临床管理的现有证据。在这两次会议上,都强调了更好地了解脑病发病机制的必要性,包括需要从受影响病例获取生物标本和尸检标本。根据2001年12月非洲盘尾丝虫病控制计划联合行动论坛的一项建议,美迪善捐赠计划于2002年5月代表美迪善专家委员会组织了一个关于美迪善治疗后与罗阿丝虫相关的严重不良事件的科学工作组。本报告包括该科学工作组的背景、新证据、结论和建议。以下要点概述了当前状况:1. 尽管关于罗阿丝虫有更多且质量更好的临床和流行病学数据,但与美迪善相关的罗阿丝虫脑病的发病机制仍不清楚。2. 由于缺乏病例标本和动物模型,脑病发病机制的研究进展非常有限。3. 在罗阿丝虫脑病患者的医疗管理方面没有特别的突破;然而,及时的一般护理和营养护理通常会带来良好的结果,这些仍然是主要的干预措施。未来行动的主要建议如下:1. 结合遥感和RAPLOA技术验证并更新罗阿丝虫的分布图。2. 对迄今报告的脑病性严重不良事件的明显聚集情况进行专家分析。3. 对如果使用美迪善治疗有发生脑病性严重不良事件高风险的罗阿丝虫病流行社区,研究使用高剂量阿苯达唑的可能“预处理”方案;本研究将与世卫组织/热带病研究和培训特别规划合作进行。4. 在喀麦隆设立一个罗阿丝虫病技术顾问职位,以提供研究和业务支持,开展人群调查,并促进从严重不良事件病例收集更好的数据,包括酌情进行尸检研究。5. 研究开发罗阿丝虫脑病动物模型的可能性;这项活动将与喀麦隆上述研究议程相关联。6. 研究脑病性严重不良事件的最佳护理模式,包括识别早期预警信号和治疗干预措施。7. 进一步制定社区遵守美迪善治疗所需的健康教育信息模型以及对严重不良事件病例的家庭支持模型。8. 在监督这些问题的相关技术机构的协调下,对美迪善和阿苯达唑联合治疗在罗阿丝虫病和淋巴丝虫病(LF)共流行地区的安全性进行研究。上述建议将通过科学工作组中有兴趣的各方之间的持续合作来实施,这些各方参与盘尾丝虫病控制和/或全球消除淋巴丝虫病计划。

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