1 Mazugul

Confirmatory Assignment Meaning In Urdu

Chikungunya is an infection caused by the chikungunya virus (CHIKV).[3] Symptoms include fever and joint pain.[2] These typically occur two to twelve days after exposure.[3] Other symptoms may include headache, muscle pain, joint swelling, and a rash.[2] Most people are better within a week; however, occasionally the joint pain may last for months.[2] The risk of death is around 1 in 1,000.[4] The very young, old, and those with other health problems are at risk of more severe disease.[2]

The virus is spread between people by two types of mosquitos: Aedes albopictus and Aedes aegypti.[3] They mainly bite during the day.[5] The virus may circulate within a number of animals including birds and rodents.[3] Diagnosis is by either testing the blood for the virus's RNA or antibodies to the virus.[3] The symptoms can be mistaken for those of dengue fever and Zika fever.[3] After a single infection it is believed most people become immune.[2][2]

The best means of prevention is overall mosquito control and the avoidance of bites in areas where the disease is common.[4] This may be partly achieved by decreasing mosquitoes' access to water and with the use of insect repellent and mosquito nets.[3] There is no vaccine and no specific treatment as of 2016.[3] Recommendations include rest, fluids, and medications to help with fever and joint pain.[3][2]

While the disease typically occurs in Africa and Asia, outbreaks have been reported in Europe and the Americas since the 2000s.[3] In 2014 more than a million suspected cases occurred.[3] In 2014 it was occurring in Florida in the continental United States but as of 2016 there was no further locally acquired cases.[6][7] The disease was first identified in 1952 in Tanzania.[3] The term is from the Kimakonde language and means "to become contorted".[3]

Signs and symptoms[edit]

The incubation period of the chikungunya virus ranges from one to twelve days, and is most typically three to seven.[8] The disease may be asymptomatic, but generally is not, as 72% to 97% of those infected will develop symptoms.[8] Characteristic symptoms include sudden onset with high fever, joint pain, and rash. Other symptoms may occur, including headache, fatigue, digestive complaints, and conjunctivitis.[9]

Information gained during recent epidemics suggests that chikungunya fever may result in a chronic phase as well as the phase of acute illness.[10] Within the acute phase, two stages have been identified: a viral stage during the first five to seven days, during which viremia occurs,[11] followed by a convalescent stage lasting approximately ten days, during which symptoms improve and the virus cannot be detected in the blood.[8] Typically, the disease begins with a sudden high fever that lasts from a few days to a week, and sometimes up to ten days. The fever is usually above 39 °C (102 °F) and sometimes reaching 40 °C (104 °F) and may be biphasic—lasting several days, breaking, and then returning. Fever occurs with the onset of viremia, and the level of virus in the blood correlates with the intensity of symptoms in the acute phase.[11] When IgM, an antibody that is a response to the initial exposure to an antigen, appears in the blood, viremia begins to diminish. However, headache, insomnia and an extreme degree of exhaustion remain, usually about five to seven days.[12]

Following the fever, strong joint pain or stiffness occurs; it usually lasts weeks or months, but may last for years. The joint pain can be debilitating, often resulting in near immobility of the affected joints.[13] Joint pain is reported in 87–98% of cases, and nearly always occurs in more than one joint, though joint swelling is uncommon.[8] Typically the affected joints are located in both arms and legs, and are affected symmetrically. Joints are more likely to be affected if they have previously been damaged by disorders such as arthritis.[10] Pain most commonly occurs in peripheral joints, such as the wrists, ankles, and joints of the hands and feet as well as some of the larger joints, typically the shoulders, elbows and knees.[8][10] Pain may also occur in the muscles or ligaments.

Rash occurs in 40–50% of cases, generally as a maculopapular rash occurring two to five days after onset of symptoms.[8] Digestive symptoms, including abdominal pain, nausea, vomiting or diarrhea, may also occur.[8][9][14] In more than half of cases, normal activity is limited by significant fatigue and pain.[8] Infrequently, inflammation of the eyes may occur in the form of iridocyclitis, or uveitis, and retinal lesions may occur.[15]

Temporary damage to the liver may occur.[16]

Rarely, neurological disorders have been reported in association with chikungunya virus, including Guillain–Barré syndrome, palsies, meningoencephalitis, flaccid paralysis and neuropathy.[9] In contrast to dengue fever, Chikungunya fever very rarely causes hemorrhagic complications. Symptoms of bleeding should lead to consideration of alternative diagnoses or co-infection with dengue fever or coexisting congestive hepatopathy.[11]

Chronic disease[edit]

Observations during recent epidemics have suggested chikungunya may cause long-term symptoms following acute infection.[17][18][19] This condition has been termed chronic chikungunya virus-induced arthralgia.[4] Long-term symptoms are not an entirely new observation; long-term arthritis was observed following an outbreak in 1979.[20] Common predictors of prolonged symptoms are advanced age and prior rheumatological disease.[21][22][23][24]

During the La Reunion outbreak in 2006, more than 50% of subjects over the age of 45 reported long-term musculoskeletal pain[22] with up to 60% of people reporting prolonged painful joints three years following initial infection.[21] A study of imported cases in France reported that 59% of people still suffered from arthralgia two years after acute infection.[25] Following a local epidemic of chikungunya in Italy, 66% of people reported muscle pains, joint pains, or asthenia at one year after acute infection.[23]

Currently, the cause of these chronic symptoms is not fully known. Markers of autoimmune or rheumatoid disease have not been found in people reporting chronic symptoms.[21][26] However, some evidence from humans and animal models suggests chikungunya may be able to establish chronic infections within the host. Viral antigen was detected in a muscle biopsy of a person suffering a recurrent episode of disease three months after initial onset.[27] Additionally, viral antigen and viral RNA were found in macrophages in the synovial joint of a person experiencing a relapse of musculoskeletal disease 18 months after initial infection.[28] Several animal models have also suggested chikungunya virus may establish persistent infections. In a mouse model, viral RNA was detected specifically in joint-associated tissue for at least 16 weeks after inoculation, and was associated with chronic synovitis.[29] Similarly, another study reported detection of a viral reporter gene in joint tissue of mice for weeks after inoculation.[30] In a nonhuman primate model, chikungunya virus was found to persist in the spleen for at least six weeks.[31]

Cause[edit]

Virology[edit]

Chikungunya virus (CHIKV), is a member of the alphavirus genus, and Togaviridae family. It was first isolated in 1953 in Tanzania and is an RNA virus with a positive-sense single-stranded genome of about 11.6kb.[33] It is a member of the Semliki Forest virus complex and is closely related to Ross River virus, O'nyong'nyong virus, and Semliki Forest virus.[34] Because it is transmitted by arthropods, namely mosquitoes, it can also be referred to as an arbovirus (arthropod-borne virus). In the United States, it is classified as a category C priority pathogen,[35] and work requires biosafety level III precautions.[36]

Transmission[edit]

Chikungunya is generally transmitted from mosquitoes to humans. Less common modes of transmission include vertical transmission, which is transmission from mother to child during pregnancy or at birth. Transmission via infected blood products and through organ donation is also theoretically possible during times of outbreak, though no cases have yet been documented.[10]

Chikungunya is related to mosquitoes, their environments, and human behavior. The adaptation of mosquitoes to the changing climate of North Africa around 5,000 years ago made them seek out environments where humans stored water. Human habitation and the mosquitoes’ environments were then very closely connected. During periods of epidemics humans are the reservoir of the virus. Because high amounts of virus are present in the blood in the beginning of acute infection, the virus can be spread from a viremic human to a mosquito, and back to a human.[37] During other times, monkeys, birds and other vertebrates have served as reservoirs.[38] Three genotypes of this virus have been described, each with a distinct genotype and antigenic character: West African, East/Central/South African, and Asian genotypes.[39] The Asian lineage originated in 1952 and has subsequently split into two lineages – India (Indian Ocean Lineage) and South East Asian clades. This virus was first reported in the Americas in 2014. Phylogenetic investigations have shown that there are two strains in Brazil – the Asian and East/Central/South African types – and that the Asian strain arrived in the Caribbean (most likely from Oceania) in about March 2013.[40] The rate of molecular evolution was estimated to have a mean rate of 5 × 10−4 substitutions per site per year (95% higher probability density 2.9–7.9 × 10−4) typical of RNA viruses.

Chikungunya is spread through bites from Aedes mosquitoes, and the species A. aegypti was identified as the most common vector, though the virus has recently been associated with many other species, including A. albopictus.[10] Research by the Pasteur Institute in Paris has suggested chikungunya virus strains in the 2005-2006 Reunion Island outbreak incurred a mutation that facilitated transmission by the Asian tiger mosquito (A. albopictus).[41] Other species potentially able to transmit the chikungunya virus include Ae. furcifer-taylori, Ae. africanus, and Ae. luteocephalus.[10]

Mechanism[edit]

The chikungunya virus is passed to humans when a bite from an infected mosquito breaks the skin and introduces the virus into the body. The pathogenesis of chikungunya infection in humans is still poorly understood, despite recent outbreaks. It appears that in vitro, chikungunya virus is able to replicate in human epithelial and endothelial cells, primary fibroblasts, and monocyte-derived macrophages. Viral replication is highly cytopathic, but susceptible to type-I and -II interferon.[42]In vivo, in studies using living cells, chikungunya virus appears to replicate in fibroblasts, skeletal muscle progenitor cells, and myofibers.[27][43][44]

The type-1 interferon response seems to play an important role in the host's response to chikungunya infection. Upon infection with chikungunya, the host's fibroblasts produce type-1 alpha and beta interferon (IFN-α and IFN-β).[45] In mouse studies, deficiencies in INF-1 in mice exposed to the virus cause increased morbidity and mortality.[45][46][47] The chikungunya-specific upstream components of the type-1 interferon pathway involved in the host's response to chikungunya infection are still unknown.[48] Nonetheless, mouse studies suggest that IPS-1 is an important factor,[48] and that IRF3 and IRF7 are important in an age-dependent manner.[49][50] Mouse studies also suggest that chikungunya evades host defenses and counters the type-I interferon response by producing NS2, a nonstructural protein that degrades RBP1 and turns off the host cell's ability to transcribe DNA.[51] NS2 interferes with the JAK-STAT signaling pathway and prevents STAT from becoming phosphorylated.[52]

In the acute phase of chikungunya, the virus is typically present in the areas where symptoms present, specifically skeletal muscles, and joints. In the chronic phase, it is suggested that viral persistence (the inability of the body to entirely rid itself of the virus), lack of clearance of the antigen, or both, contribute to joint pain. The inflammation response during both the acute and chronic phase of the disease results in part from interactions between the virus and monocytes and macrophages.[11] Chikungunya virus disease in humans is associated with elevated serum levels of specific cytokines and chemokines. High levels of specific cytokines have been linked to more severe acute disease: interleukin-6 (IL-6), IL-1β, RANTES, monocyte chemoattractant protein 1 (MCP-1), monokine induced by gamma interferon (MIG), and interferon gamma-induced protein 10 (IP-10). Cytokines may also contribute to chronic chikungunya virus disease, as persistent joint pain has been associated with elevated levels of IL-6 and granulocyte-macrophage colony-stimulating factor (GM-CSF).[37] In those with chronic symptoms, a mild elevation of C-reactive protein (CRP) has been observed, suggesting ongoing chronic inflammation. However, there is little evidence linking chronic chikungunya virus disease and the development of autoimmunity.

Viral replication[edit]

The virus consists of four nonstructural proteins and three structural proteins.[11] The structural proteins are the capsid and two envelope glycoproteins: E1 and E2, which form heterodimeric spikes on the viron surface. E2 binds to cellular receptors in order to enter the host cell through receptor-mediated endocytosis. E1 contains a fusion peptide which, when exposed to the acidity of the endosome in eukaryotic cells, dissociates from E2 and initiates membrane fusion that allows the release of nucleocapsids into the host cytoplasm, promoting infection.[53] The mature virion contains 240 heterodimeric spikes of E2/E1, which after release, bud on the surface of the infected cell, where they are released by exocytosis to infect other cells.[33]

Diagnosis[edit]

Chikungunya is diagnosed on the basis of clinical, epidemiological, and laboratory criteria. Clinically, acute onset of high fever and severe joint pain would lead to suspicion of chikungunya. Epidemiological criteria consist of whether the individual has traveled to or spent time in an area in which chikungunya is present within the last twelve days (i.e.) the potential incubation period). Laboratory criteria include a decreased lymphocyte count consistent with viremia. However a definitive laboratory diagnosis can be accomplished through viral isolation, RT-PCR, or serological diagnosis.[54]

The differential diagnosis may include infection with other mosquito-borne viruses, such as dengue or malaria, and infection with influenza. Chronic recurrent polyarthralgia occurs in at least 20% of chikungunya patients one year after infection, whereas such symptoms are uncommon in dengue.[55]

Virus isolation provides the most definitive diagnosis, but takes one to two weeks for completion and must be carried out in biosafety level III laboratories.[56] The technique involves exposing specific cell lines to samples from whole blood and identifying chikungunya virus-specific responses. RT-PCR using nested primer pairs is used to amplify several chikungunya-specific genes from whole blood, generating thousands to millions of copies of the genes in order to identify them. RT-PCR can also be used to quantify the viral load in the blood. Using RT-PCR, diagnostic results can be available in one to two days.[56] Serological diagnosis requires a larger amount of blood than the other methods, and uses an ELISA assay to measure chikungunya-specific IgM levels in the blood serum. One advantage offered by serological diagnosis is that serum IgM is detectable from 5 days to months after the onset of symptoms, but drawbacks are that results may require two to three days, and false positives can occur with infection due to other related viruses, such as o'nyong'nyong virus and Semliki Forest virus.[56]

Presently, there is no specific way to test for chronic signs and symptoms associated with Chikungunya fever although nonspecific laboratory findings such as C reactive protein and elevated cytokines can correlate with disease activity.[57]

Prevention[edit]

Because no approved vaccine exists, the most effective means of prevention are protection against contact with the disease-carrying mosquitoes and controlling mosquito populations by limiting their habitat.[4]Mosquito control focuses on eliminating the standing water where mosquitos lay eggs and develop as larva; if elimination of the standing water is not possible, insecticides or biological control agents can be added.[11] Methods of protection against contact with mosquitos include using insect repellents with substances such as DEET, icaridin, PMD (p-menthane-3,8-diol, a substance derived from the lemon eucalyptus tree), or IR3535. However, increasing insecticide resistance presents a challenge to chemical control methods.

Wearing bite-proof long sleeves and trousers also offers protection, and garments can be treated with pyrethroids, a class of insecticides that often has repellent properties. Vaporized pyrethroids (for example in mosquito coils) are also insect repellents. As infected mosquitos often feed and rest inside homes, securing screens on windows and doors will help to keep mosquitoes out of the house. In the case of the day-active A. aegypti and A. albopictus, however, this will have only a limited effect, since many contacts between the mosquitoes and humans occur outdoors.

Vaccine[edit]

As of 2017[update], no approved vaccines are available. A phase-IIvaccine trial used a live, attenuated virus, to develop viral resistance in 98% of those tested after 28 days and 85% still showed resistance after one year.[58] However, 8% of people reported transient joint pain, and attenuation was found to be due to only two mutations in the E2 glycoprotein.[59] Alternative vaccine strategies have been developed, and show efficacy in mouse models.[60][61] In August 2014 researchers at the National Institute of Allergy and Infectious Diseases in the USA were testing an experimental vaccine which uses virus-like particles (VLPs) instead of attenuated virus. All the 25 people participated in this phase 1 trial developed strong immune responses.[62] As of 2015, a phase 2 trial was planned, using 400 adults aged 18 to 60 and to take place at 6 locations in the Caribbean.[63] Even with a vaccine, mosquito population control and bite prevention will be necessary to control chikungunya disease.[64]

Treatment[edit]

Currently, no specific treatment for chikungunya is available.[4]Supportive care is recommended, and symptomatic treatment of fever and joint swelling includes the use of nonsteroidal anti-inflammatory drugs such as naproxen, non-aspirin analgesics such as paracetamol (acetaminophen) and fluids.[4]Aspirin is not recommended due to the increased risk of bleeding.[65] Despite anti-inflammatory effects, corticosteroids are not recommended during the acute phase of disease, as they may cause immunosuppression and worsen infection.[10]

Passive immunotherapy has potential benefit in treatment of chikungunya. Studies in animals using passive immunotherapy have been effective, and clinical studies using passive immunotherapy in those particularly vulnerable to severe infection are currently in progress.[66] Passive immunotherapy involves administration of anti-CHIKV hyperimmune human intravenous antibodies (immunoglobulins) to those exposed to a high risk of chikungunya infection. No antiviral treatment for chikungunya virus is currently available, though testing has shown several medications to be effective in vitro.[8]

Chronic arthritis[edit]

In those who have more than two weeks of arthritis, ribavirin may be useful.[4] The effect of chloroquine is not clear.[4] It does not appear to help acute disease, but tentative evidence indicates it might help those with chronic arthritis.[4]Steroids do not appear to be an effective treatment.[4]NSAIDs and simple analgesics can be used to provide partial symptom relief in most cases. Methotrexate, a drug used in the treatment of rheumatoid arthritis, has been shown to have benefit in treating inflammatory polyarthritis resulting from chikungunya, though the drug mechanism for improving viral arthritis is unclear.[18]

Prognosis[edit]

The mortality rate of chikungunya is slightly less than 1 in 1000.[67] Those over the age of 65, neonates, and those with underlying chronic medical problems are most likely to have severe complications.[37] Neonates are vulnerable as it is possible to vertically transmit chikungunya from mother to infant during delivery, which results in high rates of morbidity, as infants lack fully developed immune systems.[37] The likelihood of prolonged symptoms or chronic joint pain is increased with increased age and prior rheumatological disease.[21][22]

Epidemiology[edit]

Main article: Epidemiology of chikungunya

Historically, chikungunya has been present mostly in the developing world. The disease causes an estimated 3 million infections each year.[68] Epidemics in the Indian Ocean, Pacific Islands, and in the Americas, continue to change the distribution of the disease.[69] In Africa, chikungunya is spread by a sylvatic cycle in which the virus largely cycles between other non-human primates, small mammals, and mosquitos between human outbreaks.[9] During outbreaks, due to the high concentration of virus in the blood of those in the acute phase of infection, the virus can circulate from humans to mosquitoes and back to humans.[9] The transmission of the pathogen between humans and mosquitoes that exist in urban environments was established on multiple occasions from strains occurring on the eastern half of Africa in non-human primate hosts.[11] This emergence and spread beyond Africa may have started as early as the 18th century.[11] Currently, available data does not indicate whether the introduction of chikungunya into Asia occurred in the 19th century or more recently, but this epidemic Asian strain causes outbreaks in India and continues to circulate in Southeast Asia.[11] In Africa, outbreaks were typically tied to heavy rainfall causing increased mosquito population. In recent outbreaks in urban centers, the virus has spread by circulating between humans and mosquitoes.[10]

Global rates of chikungunya infection are variable, depending on outbreaks. When chikungunya was first identified in 1952, it had a low-level circulation in West Africa, with infection rates linked to rainfall. Beginning in the 1960s, periodic outbreaks were documented in Asia and Africa. However, since 2005, following several decades of relative inactivity, chikungunya has re-emerged and caused large outbreaks in Africa, Asia, and the Americas. In India, for instance, chikungunya re-appeared following 32 years of absence of viral activity.[70] Outbreaks have occurred in Europe, the Caribbean, and South America, areas in which chikungunya was not previously transmitted. Local transmission has also occurred in the United States and Australia, countries in which the virus was previously unknown.[10] In 2005, an outbreak on the island of Réunion was the largest then documented, with an estimated 266,000 cases on an island with a population of approximately 770,000.[71] In a 2006 outbreak, India reported 1.25 million suspected cases.[72] Chikungunya was recently introduced to the Americas, and from 2013-14 in the Americas, 1,118,763 suspected cases and 24,682 confirmed cases were reported by the PAHO.[73]

An analysis of the chikungunya virus's genetic code suggests that the increased severity of the 2005–present outbreak may be due to a change in the genetic sequence which altered the E1 segment of the virus' viral coat protein, a variant called E1-A226V. This mutation potentially allows the virus to multiply more easily in mosquito cells.[74] The change allows the virus to use the Asian tiger mosquito (an invasive species) as a vector in addition to the more strictly tropical main vector, Aedes aegypti.[75] Enhanced transmission of chikungunya virus by A. albopictus could mean an increased risk for outbreaks in other areas where the Asian tiger mosquito is present.[76]A albopictus is an invasive species which has spread through Europe, the Americas, the Caribbean, Africa and the Middle East.

After the detection of zika virus in Brazil in April 2015, the first ever in the Western Hemisphere,[77][78] it is now thought some chikungunya and dengue cases could in fact be zika virus cases or coinfections.

History[edit]

The word 'chikungunya' is believed to have been derived from a description in the Makonde language, meaning "that which bends up", of the contorted posture of people affected with the severe joint pain and arthritic symptoms associated with this disease.[79] The disease was first described by Marion Robinson[80] and W.H.R. Lumsden[81] in 1955, following an outbreak in 1952 on the Makonde Plateau, along the border between Mozambique and Tanganyika (the mainland part of modern-day Tanzania).

According to the initial 1955 report about the epidemiology of the disease, the term 'chikungunya' is derived from the Makonde root verb kungunyala, meaning to dry up or become contorted. In concurrent research, Robinson glossed the Makonde term more specifically as "that which bends up". Subsequent authors apparently overlooked the references to the Makonde language and assumed the term to have been derived from Swahili, the lingua franca of the region. The erroneous attribution to Swahili has been repeated in numerous print sources.[82] Many erroneous spellings of the name of the disease are also in common use.

Since its discovery in Tanganyika, Africa, in 1952, chikungunya virus outbreaks have occurred occasionally in Africa, South Asia, and Southeast Asia, but recent outbreaks have spread the disease over a wider range.

The first recorded outbreak of this disease may have been in 1779.[83] This is in agreement with the molecular genetics evidence that suggests it evolved around the year 1700.[84]

Biological weapon[edit]

Chikungunya was one of more than a dozen agents researched as potential biological weapons.[85]

Research[edit]

Infection was reduced in mosquitoes with the wMel strain of Wolbachia.[86][87]

It is part of the group of neglected tropical diseases.[88]

References[edit]

Transmission electron micrograph of Chikungunya virus particles
A. aegypti mosquito biting a person
Dark green denotes countries with current or previous local transmission of CHIKV, per CDC as of July 2015.
A. albopictus distribution as of December 2007
Dark blue: Native range
Teal: introduced
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  13. ^Capeding, MR; Chua, MN; Hadinegoro, SR; Hussain, II; Nallusamy, R; Pitisuttithum, P; Rusmil, K; Thisyakorn, U; Thomas, SJ; Huu Tran, N; Wirawan, DN; Yoon, IK; Bouckenooghe, A; Hutagalung, Y; Laot, T; Wartel, TA (2013). "Dengue and other common causes of acute febrile illness in Asia: an active surveillance study in children". PLoS neglected tropical diseases. 7 (7): e2331. doi:10.1371/journal.pntd.0002331. PMC 3723539. PMID 23936565. 
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Validation of the Urdu Version of Olweus Bully/Victim Questionnaire (OBVQ)

Rabia Khawar

Corresponding Author:

Rabia Khawar

                                    Department of Psychology, GC University, Katchehry Road,, 54000 Lahore, Pakistan.

                                    Department of Applied Psychology, GC University Allama Iqbal Road, 38000  Faisalabad, Pakistan.

E-mail - khawarthisend@gmail.com phone: 0923216996017

 

Abstract

Objective:       The study intended to validate the Urdu version of Revised Olweus Bully Victim Questionnaire (OBVQ) in our local settings.

Design:           Exploratory study

Place and Duration of Study: The study was conducted in different public and private schools of Lahore during 2012 to 2014.

Participants and Methods:               Participants were 817 students from grades four to six of 12 public and private schools of Lahore. Additionally, 106 teachers participated in bullying nomination of students. Purposive convenient sampling technique was used.

Results:           Confirmatory factor analysis resulted in a good model fit with acceptable values on indices and parameter estimates supporting the construct validity of the instrument. The reliability coefficients for bullying and victimization were comparable to international studies. Significant relationship between the OBVQ 8 types of victimization and bullying and two corresponding global items demonstrated concurrent validity. Children were involved in bullying roles with larger proportion in bully-victim group. OBVQ-Urdu version demonstrated concordance with the teacher nominations of bullying.

Conclusion:    The Urdu version of OBVQ has good psychometric properties and is appropriate for measuring the involvement of Pakistani school students in a variety of bullying behaviors.

 

 

Introduction

During the last two decades, bullying has been emerged as serious problem affecting many students in schools throughout the world1, 2. Researchers have distinguished bullying from ordinary fight or quarrelling between two parties of equal strength by emphasizing the notion of power imbalance. It’s a combination of certain direct and indirect negative actions performed by one or more students repeatedly over time with an intention to harm weaker students. Victims’ inability to defend him or her is another important feature of Olweus definition3, 4. Bullying can take several forms such as physical (e.g. hitting, punching, kicking, and beating up, pushing, spitting, property damage, and/or theft), verbal (e.g. teasing, mocking, name-calling, nasty comment and humiliation, threats and noxious remarks, extortion, and/or racist, sexist or homophobic insults), social (e.g. gossip, rumor spreading, embarrassment, alienation or exclusion from the group) or cyber (e.g. using the cell phone or internet i.e. email, text messaging, social media)5. All types of bullying causes some sort of psychological damage. Researchers have asserted that bullying may result in academic failure, health issues, loss of social relations and a variety of cognitive, affective and behavioral problems6, 7. Perpetrators of bullying are exposed to disrupted academic and social life at school that may result in delinquency and conduct problems in later life8

. Depending on the nature and design of the study, the participants’ age and the region, the proportion of school children repeatedly victimized ranges from 7.1 to 70.2%.9

The most commonly used measure to assess bully/victim status conflicts is the Revised Olweus Bully/Victim Questionnaire10. Though used widely by researchers and educators in different countries, information about the psychometric properties of OBVQ is not well documented11.  The measure provides two main dimensions (being bullied and bullying others) for classifying students as bullies, victims, bully/victims or uninvolved. Studies have provided evidence for the construct validity of these two dimensions 12,13.One of the most comprehensive analysis using Rasch model supported the conceptual design of both dimensions with acceptable psychometric elements for each scale14. Some recent researches have also shown adequate reliability and validity for the instrument when translated into another language (e.g. Greek) 15,16.

This the first attempt to validate the construct validity of Revised Olweus Bully Victim Questionnaire-Urdu version by using confirmatory factor analysis for the two dimensions, examining the classification of children as bullies, victims, or bully/victims and to determine its convergent validity with teacher nominations of children’s role in bullying.

Method

 Participants

The sample consisted of 817 students studying in 4th, 5th and 6th grades of both public and private sector schools of Lahore. Girls (n = 440) and boys (n = 377) with age range between 9 to12 years (M = 10.86, SD = 1.08) were selected from 12 schools that agreed to participate in the study. A total of 106 teachers participated in the nomination procedure (Mage = 29.79, SD age = 4.8). All the teachers had been teaching the same class for at least last four months.

Measures

Revised Olweus Bully-Victim Questionnaire-Urdu Version

Revised Olweus Bully Victim Questionnaire distinguishes among students for their involvement bullying roles with the help of two global questions i.e. item No. 4 (being bullied) and 24 (bullying others) along with 8 types, each answered on a 5 point scale with ‘‘I haven’t been bullied/bullied other students at school in the past couple of months,’’ coded as 1 and “several times a week” coded as 5. The questionnaire had shown good internal consistency (Cronbach’s α = .80 to .90) and can be easily administered in a group setting17. The present study utilized an Urdu version of the OBVQ developed using standardized translation procedures. Initial empirical investigation of the Urdu version had resulted in acceptable psychometric properties with being bullied and bullying others dimensions yielding Chronbach Alpha of .79 and .82 respectively. The current study further evaluated the reliability and validity of the two sets of items measuring bullying and victimization with a larger sample.

 

Teacher Nominations of Students’ Bullying Roles

A brief measure was developed using definition of bullying from Revised Olweus Bully Victim Questionnaire. Teachers were instructed to read the definition of bullying carefully followed by the description of all the bullying roles: bully, victim, bully/victim and uninvolved. They were then presented with the list of randomly selected students from their classes and were asked to assign them to one of the four bullying roles based on their past three months observation of student’s behavior and complaints reported by peers.

Results

Confirmatory Factor Analysis

To determine the construct validity of the set of items assessing being bullied and bullying others status and types in Revised OBVQ -Urdu, we performed a confirmatory factor analysis (CFA) using Analysis of Moment Structures (AMOS), Version 20.0. A poor fit was suggested by the chi square value being significant, χ2 (103) = 334.57, p < .05. Yet the CMIN/df value (CMIN/DF = 3.24) was found approximately acceptable.  Rest of the indices that have been considered for assessing the degree of fit between the hypothesized two factor model and the sample resulted in a good model fit.

Tucker Lewis Index and the Comparative Fit Index were found to be acceptable having values .93 and .94 respectively (TLI & CFI: >.90 acceptable, >.95 excellent18. Root Mean Square Error of Approximation yielded a score of .05 that had been considered excellent 19.

 

Factor loadings for victimization scale range from .59 to .71, and items on bullying scale also showed high loadings ranging between .54 and .65.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Figure 1

Confirmatory Factor Analysis for OBVQ-Urdu Version

 

 

 

Reliability Analysis

Internal consistency reliability of OBVQ-Urdu version, based on Cronbach’s Alpha, was also uniformly high across gender and grade level.

Table 1

Reliability Coefficients for OBVQ-Urdu by Gender and Grade

 

Victimization

Bullying

Total

 

Boys

 

 

.83

 

.82

 

.85

Girls

.84

.83

 

.87

4th

.83

 

.83

 

.85

5th

.86

 

.81

 

.85

6th

.82

 

.82

 

.86

Total

.84

.82

 

.86

 

Furthermore, strong relationships between the 8 types of victimization and bullying, and OBVQ global items for being bullied (r = .40 to r =.65) and bullying others (r = .35 to r =.70) demonstrated adequate concurrent validity respectively with alpha significance at p < .001.

Bully-Victim Status Types

Being bullied

With regard to victims of bullying, about one third of the students (28%) reported not being bullied by others in the past couple of months, 25% reported being bullied “once or twice,” 25.5% reported being bullied “two or three times a month,” 9.9% reported being bullied “about once a week,” and 11.6% reported being bullied once a week “several times a week.” A large number of students (71.9%) reported being bullied; using milder criterion of “only once or twice”, and the standard Olweus cut-off classified nearly 47% students as victims of perpetration.

Bullying others

On the OBVQ, the majority of students (45.9%) reported not bullying others in the past couple of months, about 30% reported bullying others “once or twice,” 17% reported bullying others “two or three times a month,” and 9.1% reported bullying others “about once a week”, while 4.2 % bullied others “several times a week.”  Following the “at least once” criterion. More than half students in the sample (54.1%) were found involved in bullying others, and the Olweus standard criterion identified only 34.23% students reporting bullying others.

Finally, we identified children that were uniquely bullies (n = 141), uniquely victims (n = 158), and bully-victims (n = 235). The rest were grouped together as uninvolved (n = 283). To serve this purpose, we considered (1) the cases of the children that were involved in bullying others for “two to three times a month or more” on global item of bullying and at least one of the 8 subsequent forms of bullying, but had not been victims of bullying (2) the cases of the children that were bullied two to three times a month as measured by global item of victimization along with at least one of the 8 ways, but had not been involved in bullying others, and (3) the cases of the children that had been bullying others and been bullied two to three times a month or more on both global items and at least one of the 8 corresponding items for bullying and victimization. The results of these calculations show that only 35% of the students remain uninvolved, 17.3% of the students were uniquely bullies, 19.3% of the children were uniquely victims, and 28.8% were bully-victims. In total, 65.4% of the Pakistani school students have been found to be involved in bullying and victimization.

Relationship between OBVQ Results and Teacher Nominations

Data from the teacher estimates of students’ involvement in bullying served as a check on the accuracy of the self-report. The estimated number of class bullies (and victims) was compared to the total number of students who reported being bullies (and victims).

Table 2

Bullying Role Classification Following OBVQ and Teacher Nomination Criteria

Teacher Nominations

OBVQ Bullying Status

 

 

Bully

Victim

Bully-Victim

Uninvolved

Total

Bully

132

11

26

18

187

Victim

1

136

7

11

155

Bully-Victim

5

6

198

13

222

Uninvolved

3

5

4

241

253

Total

141

158

235

283

817

 

Total of 87 % of the original grouped cases as a result of self-report (OBVQ-Urdu) has been correctly classified as evidenced by teacher nominations. Cohen’s κ was conducted to determine the level of agreement between teacher nominations and self-reported bullying classification for 817 students. Kappa showed high correspondence between the two classification, κ = .82, p < .001.

The majority of the students (95.3%) labeled as uninvolved as a result of OBVQ received the same status in teacher nominations. High level of agreement (89.1%) was found between teacher nominations of students as bully-victim and self-reports. Most of the self-reported victims were accurately classified (87.7%) by teachers into the same role. Although, substantial number of students nominated as bullies by teachers acknowledged their role in self-report (70.6%), some of them were identified as bully-victims (13.9%), and victims (5.9%). A few (9.6%) reported them as uninvolved.

Subsequently, we performed multinomial logistic regression that can be used to observe the effects of independent variables on a nominal dependent variable, such as the teacher nominated groups of bullies, victims, bully/victims, and uninvolved children in our case. Two global items of OBVQ assessing bullying and victimization were added as covariates.

Table 3

Multinomial Logistic Regression Predicting Accuracy of Self-reported Bullying and Victimization

TN                     OBVQ

 

      B           SE

Wald

OR

    95% CI

L

U

Bully

 



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