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解决卢旺达癫痫治疗缺口及社会影响——2005年开展的一项调查结果及后续行动

Addressing the treatment gap and societal impact of epilepsy in Rwanda--Results of a survey conducted in 2005 and subsequent actions.

作者信息

Sebera Fidèle, Munyandamutsa Naasson, Teuwen Dirk E, Ndiaye Ibrahim Pierre, Diop Amadou Gallo, Tofighy Azita, Boon Paul, Dedeken Peter

机构信息

Hôpital Neuro-Psychiatrique, Fracarita Ndera, Kigali, Rwanda.

Hôpital Neuro-Psychiatrique, Fracarita Ndera, Kigali, Rwanda.

出版信息

Epilepsy Behav. 2015 May;46:126-32. doi: 10.1016/j.yebeh.2015.03.028. Epub 2015 Apr 30.

Abstract

This study, supported by the Rwandan Ministry of Health and the World Health Organization, was conducted in 2005 to determine the prevalence of epilepsy and its sociocultural perception in Rwanda, as well as epilepsy-related knowledge and practices of health-care professionals (HCPs). A cross-sectional, nationally representative survey was conducted throughout Rwanda by trained investigators. Participants were recruited by random cluster sampling based on the organization of administrative units in the country. Overall, 1137 individuals (62% from rural areas) were interviewed. The prevalence of epilepsy was estimated to be 49 per 1000 people or 41 per 1000 for active epilepsy. Onset of epilepsy before the age of 2years was reported in 32% of the cases. Family history of epilepsy, head trauma, and premature delivery were reported in 53%, 50%, and 68% of the cases, respectively. Most (68%) patients did not receive any medical treatment for epilepsy; 21.5% had received some form of traditional treatment. According to responses from the general population, people with epilepsy should not be entitled to schooling (according to 66%), to work (according to 72%), to the use of public places (according to 69%), or to marriage (according to 66%). Furthermore, 50% believed that epilepsy was untreatable, and 40% thought that it was transmissible. Of the 29 HCPs interviewed, the majority knew the definition of epilepsy and status epilepticus, as well as basic treatment options and side effects. However, 90% believed that treatment was only necessary in the first week after a seizure. Living with epilepsy was associated heavily with stigma, and a significant treatment gap (68%) was identified. Following this study, numerous actions have been taken by the Rwandan government, the Rwandan League Against Epilepsy, and several nongovernmental organizations to increase awareness about epilepsy and to close the treatment gap. An overview of these activities is provided.

摘要

这项由卢旺达卫生部和世界卫生组织支持的研究于2005年开展,旨在确定卢旺达癫痫的患病率及其社会文化认知,以及医疗保健专业人员(HCPs)与癫痫相关的知识和做法。训练有素的调查人员在卢旺达全国范围内进行了一项具有全国代表性的横断面调查。参与者是根据该国行政单位的组织通过随机整群抽样招募的。总体而言,共采访了1137人(62%来自农村地区)。据估计,癫痫的患病率为每1000人中有49人,活动性癫痫的患病率为每1000人中有41人。32%的病例报告癫痫发作始于2岁之前。分别有53%、50%和68%的病例报告有癫痫家族史、头部外伤和早产。大多数(68%)患者未接受任何癫痫治疗;21.5%接受过某种形式的传统治疗。根据普通民众的回答,癫痫患者不应享有上学权利(66%的人这样认为)、工作权利(72%)、使用公共场所的权利(69%)或结婚权利(66%)。此外,50%的人认为癫痫无法治疗,40%的人认为它会传染。在接受采访的29名医疗保健专业人员中,大多数人知道癫痫和癫痫持续状态的定义,以及基本的治疗选择和副作用。然而,90%的人认为仅在癫痫发作后的第一周需要治疗。癫痫患者的生活与耻辱感紧密相关,并且发现了显著的治疗差距(68%)。这项研究之后,卢旺达政府、卢旺达癫痫防治联盟和几个非政府组织采取了许多行动来提高对癫痫的认识并缩小治疗差距。本文提供了这些活动的概述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d00/4464509/997d05ccb4a3/gr1.jpg

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