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      Effective, polyvalent, affordable antivenom needed to treat snakebite in Nepal

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          Abstract

          Nepal has one of the highest snakebite fatality rates in south Asia. A study in the country in 2001 indicated an annual incidence, in the study area, of 162 snakebite-related deaths per 100 000 population. 1 Between 1987 and 2013, in other studies in Nepal, snakebite fatality rates ranging between 3% (2 deaths out of 71 envenomed people) and 58% (28 deaths out of 48 envenomed people) were reported. 2 An epidemiological survey of 15 hospitals indicated that, nationwide, approximately 20 000 snakebite cases and about 1000 snakebite-related deaths were occurring each year. 3 Many of the reported rates underestimate the true burden posed by venomous snakes in Nepal because data recording in Nepalese hospitals is generally poor 4 and many Nepalese depend on traditional healers and or do not seek hospital treatment because they consider themselves to be too poor to pay for treatment, or think there will be no benefit. 2 , 5 If the numbers of out-of-hospital deaths caused by snakebite are to be reduced in Nepal, there needs to be improvements in the public awareness of the benefits of snakebite treatment in hospital and in the pre-hospital care of snakebite – as seen, for example, in Sri Lanka. 6 The corresponding in-hospital mortality will only be reduced by increasing the availability of safe and effective antivenoms and improving critical care for people bitten by snakes. Even though at least 70 snake species are known to exist in Nepal, most of the serious envenoming and deaths from snakebite are caused by just seven species: the kraits Bungarus caeruleus, B. walli, B. lividus and B. niger, the cobras Naja naja and N. kaouthia and the viper Daboia russelii. 7 , 8 Although hospital data indicate that just 3% of snakebites (10 out of 349 recorded snakebites) in Nepal are caused by pit vipers, 7 many people bitten are never admitted to hospitals because the resultant envenoming is usually mild and or the bitten individuals prefer to seek care from traditional healers. However, some pit viper bites can cause severe coagulopathy. 9 In Nepal, antivenom for treating pit viper bites is currently unavailable, but two antivenoms, raised against pit vipers from other countries, were used successfully, in Australia, to treat a pit viper bite that occurred in Nepal. 9 Antivenom shortages Antivenom is generally in short supply in most parts of Africa and many parts of Asia. 10 As the safe production of efficacious antivenoms becomes generally more expensive and less profitable for the manufacturers and are either discontinuing the production of some antivenoms or only producing them in very limited amounts. In 2012, an Indian court order decreased the export of antivenom manufactured in India to Nepal until sufficient quantity of antivenom was available to meet the requirement needs of all Indian citizens. This order led to a reduction in the availability of antivenom in Nepal. 11 To address the shortfall, the Nepalese government aims to begin its own production of antivenom. However, the achievement of this goal is hampered by the lack of adequate relevant information on snakebite epidemiology, clinical studies and assessments of the economic costs of antivenom production. The treatment of snake envenoming in Nepal is mostly reliant on a single polyvalent antivenom produced, in Indian horses, against the venoms of Indian B. caeruleus, D. russelii, Echis carinatus and N. naja. Until Nepal is able to produce antivenom of high quality, antivenoms will need to be imported from other Asian countries or elsewhere. As a temporary measure, i.e. until local production is ready in terms of capacity and funding, antivenoms produced by competent non-profit institutions, e.g. in Brazil or Costa Rica, 12 could be imported. Even antivenoms produced in neighbouring India may be less efficacious against some snake species in Nepal than against the same species in India because of geographical intraspecific differences in venom composition. 13 Such differences may explain reports of the low efficacy or failure of Indian polyvalent antivenom in the neutralization of Sri Lankan snake venoms. 13 , 14 The efficacy of the Indian antivenom in neutralizing the venoms from all of the species of venomous snake in Nepal, not just those from B. caeruleus, D. russelii, E. carinatus and N. naja – needs to be assessed in both in vitro studies and comprehensive clinical trials. The results of such assessments may help in the Nepalese government’s attempts to design a new and improved polyvalent antivenom specifically for use in Nepal. Antivenom production in Nepal To develop a new and cost–effective antivenom, the Nepalese government will need to develop sufficient infrastructure, including snake farms for the provision of venom, horses or other appropriate animals that can be injected with the venoms and laboratory facilities for the preparation of safe antivenoms. In Nepal, as a single vial of imported antivenom costs the equivalent of US$ 19 (United States dollars) and about 40 000 such vials are used annually, 15 there is a considerable potential market for a new antivenom. The production of antivenom tailored specifically to the needs of Nepal would be expected to reduce snakebite-related morbidity and mortality in the country. However, the production of such antivenom is unlikely to be profitable and, without the support of humanitarian organizations, it is unlikely to be sustainable. Therefore, increased awareness, greater political will, adequate financial support and vested interest from the public health sector are needed. In addition, there will need to be collaboration with national and international experts in the field and quality research to determine the appropriate use, effectiveness and safety of any new antivenom in Nepal. Stakeholders will need to acquire certain information before developing and producing a new antivenom in Nepal. First, stakeholders should do a formal assessment of the impact of snake envenoming in the country, overall improvement of the treatment of snakebite and the relevant national guidelines. They should conduct epidemiological studies of snake envenoming across the country, both to identify the snake species of greatest medical importance and current reaction rates to any Indian antivenom being used. Also, improved data recording of snakebites in hospitals is needed. Second, stakeholders should make a comparison of the cost–effectiveness between the Indian antivenoms in current use with that of any new Nepalese antivenom, which is likely to be more expensive but may cause fewer adverse reactions. Stakeholders should consider that launching the production of a new antivenom in Nepal may be problematic and pose a substantial financial burden for the country.

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          Impact of snake bites and determinants of fatal outcomes in southeastern Nepal.

          Current available data on snake bites in Nepal are based solely on hospital statistics. This community-based study aimed at evaluating the impact of snake bites and determining the risk factors associated with a fatal outcome in southeastern Nepal. A total of 1,817 households, selected by a random proportionate sampling method, were visited by trained field workers in five villages. Extensive data from snake bite victims during the 14 previous months were recorded and analyzed. One hundred forty-three snake bites including 75 bites with signs of envenoming were reported (annual incidence = 1,162/100,000 and 604/100,000, respectively), resulting in 20 deaths (annual mortality rate = 162/100,000). Characteristics of krait bites such as bites occurring inside the house, while resting, and between midnight and 6:00 am were all factors associated with an increased risk of death, as were an initial consultation with a traditional healer, a long delay before transport, and a lack of available transport. An initial transfer to a specialized treatment center and transport by motorcycle were strong protective factors. Among the 123 survivors, wounds required dressing and surgery in 30 (24%) and 10 (8%) victims, respectively, the mean working incapacity period was 15 days, and the mean out-of-pocket expense was 69 U.S. dollars. Snake bite is a major but neglected public health problem in southeastern Nepal. Public health interventions should focus on improving victims' rapid access to anti-snake venom serum by promoting immediate and fast transport to adequate treatment centers, particularly for bites occurring at night.
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            Public perceptions of snakes and snakebite management: implications for conservation and human health in southern Nepal

            Background Venomous snakebite and its effects are a source of fear for people living in southern Nepal. As a result, people have developed a negative attitude towards snakes, which can lead to human-snake conflicts that result in killing of snakes. Attempting to kill snakes increases the risk of snakebite, and actual killing of snakes contributes to loss of biodiversity. Currently, snake populations in southern Nepal are thought to be declining, but more research is needed to evaluate the conservation status of snakes. Therefore, we assessed attitudes, knowledge, and awareness of snakes and snakebite by Chitwan National Park’s (CNP) buffer zone (BZ) inhabitants in an effort to better understand challenges to snake conservation and snakebite management. The results of this study have the potential to promote biodiversity conservation and increase human health in southern Nepal and beyond. Methods We carried out face-to-face interviews of 150 randomly selected CNP BZ inhabitants, adopting a cross-sectional mixed research design and structured and semi-structured questionnaires from January–February 2013. Results Results indicated that 43 % of respondents disliked snakes, 49 % would exterminate all venomous snakes, and 86 % feared snakes. Farmers were the most negative and teachers were the most ambivalent towards snakes. Respondents were generally unable to identify different snake species, and were almost completely unaware of the need of conserve snakes and how to prevent snakebites. Belief in a snake god, and the ability of snakes to absorb poisonous gases from the atmosphere were among many superstitions that appeared to predispose negativity towards snakes of BZ residents. Conclusion People with predisposed negativity towards snakes were not proponents of snake conservation. Fear, negativity, ambivalence towards, and ignorance about, snakes and the need for snake conservation were strong indicators of the propensity to harm or kill snakes. It seems that if wanton killing of snakes continues, local snake populations will decline, and rare and endangered snake species may even become locally extirpated. Moreover, inappropriate perception and knowledge about snakes and snakebites may put BZ people at increased risk of venomous snakebite. Therefore, intensive, pragmatic educational efforts focused on natural history and ecology of snakes and prevention of snakebite should be undertaken in communities and at schools and universities.
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              A comparative study of venomics of Naja naja from India and Sri Lanka, clinical manifestations and antivenomics of an Indian polyspecific antivenom.

              Naja naja (Indian cobra) from Sri Lanka and India is the WHO Category 1 medically important snakes in both countries. Some antivenom produced against Indian N. naja (NNi) were less effective against Sri Lankan N. naja (NNsl). Proteomes of NNi and NNsl venoms were studied by RP-HPLC, SDS-PAGE and LC/MS/MS. Six protein families were identified in both venoms with the most abundant were the 3 finger toxins (3FTs) where cytotoxins (CTX) subtype predominated, followed by phospholipase A2, cysteine-rich venom protein, snake venom metalloproteases, venom growth factors, and protease inhibitors. Qualitative and quantitative differences in the venomics profiles were observed. Some proteins were isolated from either NNi or NNsl venom. Postsynaptic neurotoxins (NTX) were identified for the first time in NNsl venom. Thus, there are geographic intra-specific variations of venom composition of the two N. naja. The relative abundance of CTX and NTX explained well the clinical manifestations of these venoms. Antivenomics study of an Indian antivenom (Vins) showed the antibodies effectively bound all venom toxins from both snakes but more avidly to the Indian venom proteins. The lower antibody affinity towards the 'heterologous' venom was the likely cause of poor efficacy of the Indian antivenom used to treat NNsl envenoming.
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                Author and article information

                Journal
                Bull World Health Organ
                Bull. World Health Organ
                BLT
                Bulletin of the World Health Organization
                World Health Organization
                0042-9686
                1564-0604
                01 October 2017
                01 August 2017
                : 95
                : 10
                : 718-719
                Affiliations
                [a ]Curative Service Division, Ministry of Health and Population, Kathmandu, Nepal.
                [b ]South Asian Clinical Toxicology Research Collaboration, Faculty of Medicine, University of Peradeniya, Peradeniya, Sri Lanka.
                [c ]Bheri Zonal Hospital, Nepalgunj, Nepal.
                [d ]Kaligandaki Health Foundation, Kawasoti, Nepal.
                [e ]Clinical Toxicology Research Group, University of Newcastle, Newcastle, Australia.
                Author notes
                Correspondence to Deb P Pandey (email: debpandey@ 123456gmail.com ).
                Article
                BLT.17.195453
                10.2471/BLT.17.195453
                5689198
                924a48c4-1a43-40a2-bca8-c6bd4b018c9e
                (c) 2017 The authors; licensee World Health Organization.

                This is an open access article distributed under the terms of the Creative Commons Attribution IGO License ( http://creativecommons.org/licenses/by/3.0/igo/legalcode), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. In any reproduction of this article there should not be any suggestion that WHO or this article endorse any specific organization or products. The use of the WHO logo is not permitted. This notice should be preserved along with the article's original URL.

                History
                : 10 April 2017
                : 03 July 2017
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