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Chikungunya Confused With Dengue In Malaysia :Clinical, Serological And Molecular Perspective

机译:基孔肯雅热与马来西亚的登革热相混淆:临床,血清学和分子学的角度

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This study was to observe clinical, serolgical and molecular diagnosis of chikungunya viral fever patients and its comparison with dengue viral fever. For that 49 serologically negative dengue patients but clinically dengue like symptomms were included. Clinical investigation was carried out recording different profiles of hospitalized patients. Serology was performed using the Onsite? Chikungunya IgM Combo rapid test and molecular test RT-PCR was performed to detect the virus in the patients sera. It was observed that out of them 19 (38.7 %) were serologically confirmed chikungunya infection. Interestingly molecular detection of the patients sera did not show the presence chikungunya virus but detected dengue virus from 9 patients’s sera. Classical clinical features of chikungunya virus infected patients were recorded to differentiate chikungunya from dengue, which were fever, arthralgia, myalgia and rash. Detection of chikungunya IgM in these cohort means that this virus is circulating throughout the year although not as many as dengue. Laboratory confirmation is important to differentiate chikungunya fever from dengue fever. This study adds some information in local data and hopefully can help the clinicians to clinically and laboratory diagnosis and management of chikungunya infection in outbreak and non-outbreak setting. Serology was proven to be useful in confirming chikungunya infection. Introduction Chikungunya virus (CHIKV) infection has attracted so much attention since 2005. During that time it caused chikungunya fever with epidemics reported in Asia and Africa.Chikungunya is a crippling disease caused by the virus belong to the family Togaviridae(Chakkaravarthy et al, 2011). It is an arbovirus that shares the same vector with dengue virus. Thus, in dengue-endemic region, chikungunya is also a significant cause of viral fever causing outbreaks associted with severe morbidity. Clinically the virus causes high grade fever, chills and rigors associated with severe arthralgia and myalgia(Venkatesan et al, 2010) In Asia, urban mosquito sp, Aedes aegypti are primary vectors(El-Badry and Al-Ali, 2010)in comparison to forest-dwelling Aedes spp. seen in Africa. These spp are urban and peridomestic, anthropophilic mosquitoes that maintain close associations with humans and thus, are likely responsible for regional large outbreaks (Powers and Logue 2007).Since April 2008, nationwide outbreak has affected Malaysia with 4165 cases in 2008. In 2009, the Ministry of Health in Malaysia reported over 5430 cases of chikungunya fever. The most affected areas were the northern provinces of Sarawak, Kedah, followed by Kelantan, Selangor, and Perak. Chikungunya viral activity continued in the year 2010, with an additional 325 cases reported in the first 5 weeks (MOH, 2010). The symptoms of CHIKV infection are quite similar to those caused by many other infectious agents in the endemic areas. One particular difficulty in identifying CHIKV infection is its overlapping distribution with dengue viruses. It has been postulated that many cases of dengue virus infection are misdiagnosed and that the incidence of CHIKV infection is much higher than reported (Carey 1971). As a result management of patients with CHIKV infection has not been taken care of focusing appropriate causal agent. Through study has not been undertaken to determine the clear picture of CHIKV infection and its comparison with dengue in respect of clinical and serological and molecular investigation. Though, clinical and laboratory diagnosis are important for overall management and control of the disease.Therefore, the present study was undertaken to diagnose chikungunya infection by clinical, serological and molecular method in clinically suspected dengue patients presented to University Kebangsaan Malaysia Medical Centre (UKMMC). Material and Methods Study area: This study was conducted during January 2009 to January 2010 at Universiti Kebangsaan Malaysia Medical Centre (UK
机译:本研究旨在观察基孔肯雅病毒热患者的临床,血清学和分子诊断,并与登革热进行比较。对于该49名血清学阴性的登革热患者,但临床上有类似症状的登革热患者。进行临床研究以记录住院患者的不同情况。使用现场进行血清学检查?进行了基孔肯雅IgM Combo快速测试和分子测试RT-PCR,以检测患者血清中的病毒。观察到其中有19名(38.7%)在血清学上被确认为基孔肯雅病感染。有趣的是,对患者血清的分子检测未显示基孔肯雅病毒的存在,但从9例患者血清中检测到了登革热病毒。记录了基孔肯雅病毒感染患者的经典临床特征,以区分基孔肯雅与登革热,包括发烧,关节痛,肌痛和皮疹。在这些队列中检测到基孔肯雅IgM意味着该病毒全年都在传播,尽管没有登革热那么多。实验室确认对于区分基孔肯雅热和登革热很重要。这项研究在本地数据中增加了一些信息,希望可以帮助临床医生在暴发和非暴发环境中对基孔肯雅感染进行临床和实验室诊断与管理。血清学被证明对确认基孔肯雅感染有用。简介基孔肯雅病毒(CHIKV)感染自2005年以来受到了广泛关注。在此期间,它引起了基孔肯雅热并在亚洲和非洲引起了流行病。基孔肯雅热是由该病毒引起的致残性疾病,属于Togaviridae家族(Chakkaravarthy等,2011 )。它是一种与登革热病毒共享相同载体的虫媒病毒。因此,在登革热流行地区,基孔肯雅热也是病毒热的重要原因,引起与严重发病率有关的暴发。在临床上,这种病毒会引起严重的关节痛和肌痛,引起高烧,发冷和严酷(Venkatesan等,2010)。在亚洲,城市蚊子,埃及伊蚊是主要媒介(El-Badry和Al-Ali,2010)。森林住宅伊蚊属。在非洲见过。这些spp是城市和家庭中的嗜人性蚊子,与人类保持着密切的联系,因此很可能是造成区域性大爆发的原因(Powers and Logue 2007)。自2008年4月以来,全国性暴发已影响到马来西亚,2008年有4165例。2009年,马来西亚卫生部报告了5430例基孔肯雅热病例。受灾最严重的地区是吉打州的砂拉越北部省,其次是吉兰丹州,雪兰莪州和霹雳州。基孔肯雅热病毒活动在2010年继续进行,在头5周内又报告了325例病例(卫生部,2010年)。 CHIKV感染的症状与流行地区许多其他传染原引起的症状非常相似。识别CHIKV感染的一个特别困难是其与登革热病毒的重叠分布。据推测,许多登革热病毒感染病例被误诊,CHIKV感染的发生率比报道的要高得多(Carey 1971)。结果,对于CHIKV感染患者的治疗尚未得到关注,即集中适当的病因。还没有通过研究来确定CHIKV感染的清晰图片,以及在临床,血清学和分子研究方面与登革热的比较。虽然,临床和实验室诊断对于疾病的整体控制和控制很重要,因此,本研究旨在通过临床,血清学和分子方法对提交给马来西亚Kebangsaan马来西亚医学中心(UKMMC)的临床疑似登革热患者进行基孔肯雅病诊断。材料和方法研究区域:本研究于2009年1月至2010年1月在马来西亚大学医疗中心(英国)进行

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