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Print version ISSN 0042-9686
Bull World Health Organ vol.83 n.5 Genebra May. 2005
Réévaluation de la charge que représente la rage en Afrique et en Asie
Reevaluación de la carga de rabia en África y Asia
Darryn L. KnobelI,1; Sarah CleavelandI; Paul G. ColemanII; Eric M. FèvreI; Martin I. MeltzerIII; M. Elizabeth G. MirandaIV; Alexandra ShawV; Jakob ZinsstagVI; François-Xavier MeslinVII
ICentre for Tropical Veterinary Medicine, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Roslin, Midlothian EH25 9RG, Scotland
IILondon School of Hygiene and Tropical Medicine, Keppel Street, London, England
IIICenters for Disease Control and Prevention, Atlanta, GA 30333, USA
IVCommunicable Disease, Surveillance and Response, World Health Organization, Regional Office for the Western Pacific, Manila, Philippines
VAP Consultants, Andover SP11 7BA, England
VISwiss Tropical Institute, Basel, Switzerland
VIIWorld Health Organization, Geneva, Switzerland
OBJECTIVE: To quantify the public health and economic burden of endemic canine rabies in Africa and Asia.
METHODS: Data from these regions were applied to a set of linked epidemiological and economic models. The human population at risk from endemic canine rabies was predicted using data on dog density, and human rabies deaths were estimated using a series of probability steps to determine the likelihood of clinical rabies developing in a person after being bitten by a dog suspected of having rabies. Model outputs on mortality and morbidity associated with rabies were used to calculate an improved disability-adjusted life year (DALY) score for the disease. The total societal cost incurred by the disease is presented.
FINDINGS: Human mortality from endemic canine rabies was estimated to be 55 000 deaths per year (90% confidence interval (CI) = 24 00093 000). Deaths due to rabies are responsible for 1.74 million DALYs lost each year (90% CI = 0.752.93). An additional 0.04 million DALYs are lost through morbidity and mortality following side-effects of nerve-tissue vaccines. The estimated annual cost of rabies is US$ 583.5 million (90% CI = US$ 540.1626.3 million). Patient-borne costs for post-exposure treatment form the bulk of expenditure, accounting for nearly half the total costs of rabies.
CONCLUSION: Rabies remains an important yet neglected disease in Africa and Asia. Disparities in the affordability and accessibility of post-exposure treatment and risks of exposure to rabid dogs result in a skewed distribution of the disease burden across society, with the major impact falling on those living in poor rural communities, in particular children.
Keywords: Rabies/mortality/economics; Dogs; Cost of illness; Disability evaluation; Health care costs; Probability; Models, Theoretical; Africa; Asia (source: MeSH, NLM).
OBJECTIF: Quantifier le fardeau économique et la charge pour la santé publique que représente la rage canine endémique en Afrique et en Asie.
MÉTHODES: Les données provenant de ces régions ont été appliquées à un ensemble de modèles épidémiologiques et économiques associés. On a estimé le nombre de personnes qui seraient exposées à la rage canine endémique à partir des données de la densité canine et le nombre des décès humains dus à la rage au moyen d'un modèle de probabilité pas à pas utilisé pour déterminer la probabilité qu'une personne mordue par un chien présumé enragé présente la maladie. La mortalité et la morbidité liées à la rage fournies par les modèles ont été utilisées pour affiner le calcul des années de vie ajustées sur l'incapacité (DALY) pour la maladie. Le coût social total de la maladie est présenté.
RÉSULTATS: On a estimé à 55 000 [intervalle de confiance (IC) à 90% = 24 000-93 000] le nombre annuel des décès humains dus à la rage canine endémique. Les décès dus à la rage sont responsables de 1,74 million d'années de vie ajustées sur l'incapacité perdues chaque année (IC à 90% = 0,75-2,93). Quelque 0,04 million d'années de vie ajustées sur l'incapacité supplémentaires sont en outre perdues du fait de la morbidité et de la mortalité dues aux effets secondaires des vaccins préparés sur tissu nerveux. Le coût annuel estimatif de la rage est de US$ 583,5 millions (IC à 90% = US$ 540,1 626,3 millions). Le coût des traitements post-exposition supporté par les malades constitue l'essentiel des dépenses, soit près de la moitié du coût total de la rage.
CONCLUSION: La rage reste une maladie importante mais négligée en Afrique et en Asie. Les écarts aux plans de l'accessibilité financière et physique du traitement post-exposition et du risque d'exposition aux chiens enragés rendent inégale la distribution de la charge de morbidité dans la société, les personnes les plus touchées étant les habitants des communautés rurales défavorisées, et en particulier les enfants.
Mots clés: Rage (Maladie)/mortalité/économie; Chien; Coût maladie; Evaluation incapacité; Coût soins médicaux; Probabilité; Modèle théorique; Afrique; Asie (source: MeSH, INSERM).
OBJETIVO: Cuantificar la carga que supone la rabia canina endémica en África y Asia en términos económicos y de salud pública.
MÉTODOS: Se aplicaron datos de esas regiones a un conjunto de modelos epidemiológicos y económicos relacionados. La población humana expuesta al riesgo de sufrir rabia canina endémica se predijo a partir de los datos disponibles sobre la densidad de perros, y las defunciones por rabia humana se estimaron usando una serie de pasos probabilísticos para determinar el riesgo de aparición de rabia clínica en una persona que hubiera sido mordida por un perro sospechoso de albergar rabia. Los resultados modelizados sobre la mortalidad y la morbilidad asociadas a la rabia se usaron para obtener un valor mejorado de los años de vida ajustados en función de la discapacidad (AVAD) para la enfermedad. Se presenta el costo social total asociado a esta dolencia.
RESULTADOS: La mortalidad humana por rabia canina endémica se estimó en 55 000 defunciones anuales (intervalo de confianza (IC) del 90% = 24 000-93 000). Las defunciones por rabia causan unas pérdidas de 1,74 millones de AVAD cada año (IC90% = 0,75-2,93). Otros 40 000 AVAD se pierden como consecuencia de la morbilidad y mortalidad asociadas a los efectos colaterales de las vacunas obtenidas con tejido nervioso. El costo anual estimado de la rabia asciende a US$ 583,5 millones (IC90% = US$ 540,1 - 626,3 millones). Los costos del tratamiento postexposición asumidos por los pacientes constituyen el grueso del gasto correspondiente, pues suponen casi la mitad del costo total de la rabia.
CONCLUSIÓN: La rabia sigue siendo una importante y sin embargo descuidada enfermedad en África y Asia. Las disparidades en la asequibilidad y accesibilidad del tratamiento postexposición y en el riesgo de exposición a perros rabiosos se traducen en una distribución asimétrica de la carga de morbilidad en la sociedad, de tal manera que el impacto principal de la enfermedad recae en los habitantes de las comunidades rurales pobres, sobre todo en los niños.
Palabras clave: Rabia/mortalidad/economía; Perros; Costo de la enfermedad; Evaluación de la incapacidad; Costos de la atención en salud; Probabilidad; Modelos teóricos; África; Asia (fuente: DeCS, BIREME).
More than 99% of all human deaths from rabies occur in the developing world (1), and although effective and economical control measures are available (2, 3) , rabies remains a neglected disease throughout most of these countries (4, 5). A major factor in the low level of political commitment to rabies control is a lack of accurate data on the true public health impact of the disease. It is widely recognized that the number of deaths officially reported greatly underestimates the true incidence of disease. Patients may not present to medical facilities for treatment of clinical disease; few cases receive laboratory confirmation; and clinical cases are often not reported by local authorities to central authorities (1, 6, 7).
These problems are not unique to rabies, and the recognized poor quality of much public health information from developing countries has prompted several investigations into the distribution of major infectious diseases and the mortality and morbidity attributable to them. Such studies are based on estimates of occurrence extrapolated from more readily quantifiable determinants of disease, such as vector distribution or host immunity (810). For rabies, a similar predictive approach has been used to estimate human deaths from rabies in the United Republic of Tanzania using a probability decision tree method to determine the likelihood of clinical rabies developing in a person bitten by a dog suspected to be rabid (6). Dog bites are reported proportionately more frequently than human cases of rabies and may provide an accessible data source from which human deaths from rabies can be inferred.
The objective of our study was to estimate the burden of rabies in Africa and Asia by applying data derived from these regions to this model and to thereby present a data-driven assessment of the human and economic costs of rabies in the developing world. We define Africa as all mainland countries on the continent plus Madagascar; Asia is defined as those countries falling under the WHO-defined South-East Asia Region and Western Pacific Region, including Pakistan. Only countries considered by WHO and the Office International des Epizooties as having endemic canine rabies were considered in this analysis. The list of all countries included in the study available from http://www.vet.ed.ac.uk/ctvm/Research/Appendices/appendices.html.
Human rabies deaths
Full details of the methods used in the dog-bite probability model have been published elsewhere (6). Briefly, the model recognizes that not all bites from rabid dogs result in infection and that not every infection leads to clinical signs and death. One of the principal factors influencing the outcome of a bite from a rabid dog is the location of the bite on the body (11, 12). The model uses the distribution of injuries on the body together with the likelihood of the patient receiving successful treatment to predict the outcomes of bites from rabid dogs. The model thus allows the incidence of bites from suspected rabid dogs among the human population considered to be at risk to be used as a determinant of the number of human deaths from rabies.
The human population at risk from canine rabies was taken as the number of people living in areas affected by canine rabies where the density of the dog population exceeds the threshold density at which canine rabies is capable of being maintained endemically. Dog-population densities were inferred from human densities derived from two regional population density datasets (13, 14) with adjustments made to account for population growth (15). Associated dog-population numbers were calculated by dividing human figures by the regional average ratio of humans to dogs, based on values given in Table 1. The threshold density for rabies persistence was taken as 4.5 dogs/km², based on predictions produced from data on rabies transmission in rural Kenya (16); these data are consistent with empirical observations from elsewhere in Africa (1720). This density falls within the range of estimates of rural dog-population densities (2123), so the human population considered to be at risk was calculated using the regional rural ratios for humans to dogs. Implicit in this approach is the assumption that all human urban populations are at risk in rabies-affected areas.
Four basic scenarios were considered (Africa and Asia, both rural and urban); these reflect broad differences in factors that influence rabies epidemiology and the treatment of people exposed to the disease. Initial parameter estimates were derived following a review of the relevant literature, including publications from peer-reviewed journals and grey literature sources. Parameter estimates and confidence distributions were then fixed using a three-stage consensus approach (as described in reference 9) within the WHO Burden of Rabies Working Group. First, a workshop was held during which parameter estimates were presented and discussed and preliminary predictions made using the model. Second, a comprehensive analysis using agreed upon estimates was conducted, and the model was validated against known data. Third, each participant was sent the results of this analysis, along with the data and assumptions. These were reviewed and adjusted as appropriate before final agreement was reached. The final model parameter estimates and distributions are presented in Table 2 (web version only, available at: http://www.who.int/bulletin).
For the analysis, Asia was subdivided into three units: China, India and Other Asia. Initial data sources and model validation indicated that parameter estimates for India and Other Asia were similar. However, preliminary model predictions for China overestimated the number of deaths by one order of magnitude when these same estimates were used compared with the 1000 deaths suggested by expert opinion. The discrepancy is possibly explained by the use of post-exposure treatment in China: the country accounts for two-thirds (5 million cases) of total post-exposure treatment (PET) used in Asia (24), and the locally-produced tissue-culture vaccine is safe and relatively inexpensive (25). These factors suggest that PET for rabies is more accessible and utilized more frequently in China than in the rest of Asia. To account for this in the model, the probability of a person bitten by a suspected rabid dog and receiving PET was assumed to be equally high in both urban and rural settings in China (minimum = 95%; most likely = 97%; maximum = 100%). In light of the paucity of data for China, the model's predictions for this country should be treated with caution.
The model was arrayed as a spreadsheet template (using Microsoft Excel 2000, Microsoft Inc., Redmond, WA). Uncertainty in parameter estimates, and inherent parameter variability due to between-country differences, were incorporated into the model by assigning confidence distributions to input parameters. Parameter distributions were sampled iteratively (until convergence at < 1.5%) using a Monte Carlo simulation procedure (@Risk Pro 4.5, Palisade Corp., Newfield, NY). Model predictions are reported using the means of the resulting probability distributions, with the 5th and 95th percentiles (90% confidence intervals) as the lower and upper bounds, respectively. A full account of the technical details of the model, including results of the sensitivity analysis, is available from: http://www.vet.ed.ac.uk/ctvm/Research/Appendices/appendices.html 3.
Disability-adjusted life year score
The disability-adjusted life year (DALY) score is a standardized, comparative measure of the burden of disease. The DALY score for a particular condition is a composite score of the years of life lost (YLL) due to premature mortality and the years of life lived with a disability (YLD) caused by the condition (26). To calculate a DALY score for rabies the following components were considered: a direct DALY score derived from mortality due to the disease and an indirect DALY score, taking into account morbidity and mortality following side-effects of nerve-tissue vaccines.
Direct DALY score
The output of the predictive model provided the estimated annual number of deaths due to rabies. Age-structures and sex-structures of rabies cases were obtained from seven reported studies (2733). All parameter estimates and data sources related to the calculation of the rabies DALY score are given in Table 3 (web version only, available at: http://www.who.int/bulletin). Using these parameter estimates, a DALY score for rabies was determined using previously described methods (26, 34). Parameter variability was again incorporated by assigning confidence distributions and using simulation software as described above. The 5th and 95th percentiles were used as the lower and upper bounds for the predicted scores.
Indirect DALY burden
Evidence suggests that non-rabies induced morbidity and mortality may constitute a sizeable proportion of the rabies burden in developing countries. Approximately one-third of all human rabies post-exposure treatments are carried out using crude nerve-tissue vaccines (35), despite the occurrence of severe and sometimes fatal allergic encephalomyelitic reactions (3638). Nerve-tissue vaccines were classified into two groups based on differing incidence rates and clinicopathological signs of adverse reactions (37, 38). These were the Semple type (made from phenol-treated sheep-brain or goat-brain tissue) and vaccines derived from suckling-mouse brain. For the purpose of this preliminary analysis, disability weights for post-vaccination neurological reactions, used in the calculation of the YLDs, were taken as those reported for similar conditions by Murray & Lopez (39) (Table 3). The use of equivalent disability weights represents an admittedly crude first attempt to determine a YLD component of the DALY score for rabies; future attempts would benefit from a formal disability weighting procedure.
The economic burden of rabies
The mortality rate and DALY score provide estimates of the burden of disease on human health. A second component of the impact of disease is the economic cost incurred by society as a result of the disease. The costs due to rabies were considered under the following categories:
- direct (medical) human costs from post-exposure treatment
- indirect (patient) costs from post-exposure treatment
- costs to control rabies among dogs
- livestock losses
- surveillance costs.
For this analysis, direct medical costs included the cost of biologicals (rabies vaccines and immunoglobulin) and the cost of their administration, including materials and staff salaries. Indirect costs included out-of-pocket expenses for patients, such as transport costs to and from rabies-treatment centres, and loss of income while receiving treatment (40). Costs associated with the treatment of dog bites and the administration of antibiotics and tetanus immunizations were not included. Due to the erratic frequency of reporting, national numbers of patients receiving post-exposure treatment annually were averaged over a period of 5 years (19962000). Countries for which no reports could be found for this period were considered not to have treated any patients. Post-exposure treatment was categorized by administration route (intramuscular or intradermal) on the basis that intradermal vaccination reduces costs by 6080% compared to the standard intramuscular regimen (41, 42). The total number of vaccine doses (i.e. injections) administered and the total number of visits made to rabies-treatment centres were derived from national estimates of the proportion of patients receiving treatment who were vaccinated with each schedule, after adjustment to account for patient drop-out during the course of treatment. Few published accounts dealing with treatment-seeking behaviour and compliance could be found so conservative estimates were made on the average number of visits per schedule: 3 instead of 5 for the Essen and Thai Red Cross regimens and 7 instead of 1021 for the nerve-tissue vaccine schedules. The proportion of patients receiving the Zagreb schedule, based on available data, was negligible at the scale of this study. It was assumed that all children aged < 16 years were accompanied by an adult. Assessment of transport costs and income loss include costs to both patients and those accompanying them.
Annual dog vaccination figures could not be found for all countries so the average vaccination coverage of the estimated national dog population was calculated for those countries that submitted reports between 1996 and 2000 (10.3% in Africa and 9.7% in Asia); this figure was then applied to all countries in the region to predict the total number of dogs vaccinated. Cost predictions were based on the use of a central-point vaccination system. Vaccination costs per dog include all components of campaign organization, public awareness efforts, and biological and material costs. Indirect costs borne by dog owners were not included in the analysis.
Livestock losses to rabies can be significant; however, there are few published estimates of rabies incidence in livestock. Submission of cattle specimens to central veterinary laboratories reveals an annual incidence of 0.52 deaths/100 000 head of cattle; this is certain to be a gross underestimate. Assuming a rate of underreporting of 10, and using the lower end of the range of incidence rates to exclude transmission from wildlife reservoirs, an estimated incidence of 5 deaths/100 000 cattle is obtained.
Insufficient data were available to enable parameter variability to be explicitly incorporated into the economic analysis. An attempt was made to model the uncertainty surrounding parameter estimates by inputting estimates as triangular distributions (43), with the maxima and minima set as ± 10% of each parameter's values.
The results of the predicted human mortality, disability-adjusted life year score and economic burden of rabies are presented in Table 6, Table 7 and Table 8, respectively. The predicted number of human deaths remained within the reported confidence limits when the threshold dog density was doubled to 9 dogs/km² (46 000; 90% confidence interval (CI) = 19 00079 000). Setting the threshold density to 0 (i.e. assuming that all people are at risk within areas where canine rabies is endemic) also had little effect on the model: in such a scenario the predicted number of deaths was 67 000 (90% CI = 30 000110 000).
This paper provides the results of the first attempt at a quantitative prediction of the burden of rabies in Africa and Asia. Although we attempted to incorporate the entire range of parameter variability, the final result is still likely to be an underestimate of total mortality and morbidity caused by rabies in these regions. Only deaths due to canine rabies were assessed, omitting that fraction of human cases resulting from exposure to rabid wild animals (35). In determining the number of humans at risk, only populations in areas where canine rabies is endemic were included. This ignores the possibility of sporadic outbreaks in areas of low dog density or the introduction of the virus into a previously rabies-free population, as happened on the Indonesian island of Flores in 1997 (44).
The results of the modelling are consistent with those of other studies that have estimated the true incidence of rabies at a national level. The recent national survey by the Association for the Prevention and Control of Rabies in India (45) estimated a total of 18 500 human deaths from rabies in the country each year, which is close to the predicted figure of 19 700 in this report. The model also estimated the annual number of patients receiving post-exposure treatment in India as 1.07 million, which again is in good agreement with the reported national estimate of 1.1 million (46). The model's predictions for China are less consistent: the predicted number of patients receiving post-exposure treatment is 1.25 million which is four times lower than national estimates of 5 million; the predicted number of deaths remains more than double that estimated by expert opinion. However, recent figures communicated by the Chinese authorities are more in line with the model’s predictions (Personal communication, 2004): more than 2000 cases of rabies in humans were reported in 2003, with an 80% increase in the first quarter of 2004 (compared to the same period in 2003). Given the gross underreporting associated with rabies deaths, this suggests that the model may in fact be an underestimate of the true number, and the original prediction of approximately 10 000 deaths may prove more realistic. Detailed studies on dog ecology and rabies epidemiology and treatment in China are necessary to resolve this.
WHO's 1999 World survey of rabies (35) reported 1722 human rabies deaths from the study regions: 147 in Africa and 1575 in Asia. The predicted figure of 55 000 deaths suggests that only 3% of human rabies deaths are recorded by central health authorities, a rate of underreporting of between 20 times (Asia) and 160 times (Africa). This is in agreement with findings from other studies using active surveillance methods that found the incidence of human rabies is up to 100 times greater than what is officially recorded (6, 47).
The burden of rabies is not evenly distributed across all sectors of society but is influenced by age-related and socioeconomic factors. The total cost (direct medical costs and indirect patient costs, excluding those of any accompanying people) of an average post-exposure treatment course as determined in this study is US$ 39.57 in Africa and US$ 49.41 in Asia. This amounts to a substantial fraction of annual per capita gross national income (GNI): 5.80% for the average person living in Africa and 3.87% for someone living in Asia. Even if medical costs are fully subsidized by the government, out-of-pocket patient expenses still comprise 1.52% of per capita GNI. Often government subsidies extend only to the provision of cheaper nerve-tissue vaccines, with tissue-culture vaccines being provided only to those patients able to pay for them. There is therefore an income-related risk factor in exposure to the side-effects of nerve-tissue vaccines. This is compounded by occupational and socioeconomic risk factors in the initial exposure to infection, further skewing the burden of rabies towards those sectors of society least able to bear it (45, 48). The results of our study predict that there will be five times more rabies deaths in rural areas than in urban areas. Children in particular are at a higher risk of exposure to rabid dogs. Typically, 3050% of those receiving post-exposure treatment are children aged < 16 years (6, 49). Children are also more likely to suffer multiple bites and bites to the face and head, both of which carry a higher risk of contracting rabies (31, 50).
Rabies continues to impact human health despite the existence of proven cost-effective control measures. Vaccinating domestic dogs against rabies results in a significant reduction in the incidence of bites among the human population from dogs suspected to be rabid, and this control strategy has been shown to be the most cost-effective in the mediumlong term (4); costs are typically recouped within 510 years, mainly through decreased expenditure on human post-exposure treatment.
The authors thank Dr Alex Wandeler and Dr Ursula Kayali for their comments on an earlier draft of this manuscript and Dr Deborah Briggs for useful discussions.
Funding: DK and SC are supported by a grant from the Wellcome Trust. JZ is supported by NCCR "North-South" IP-4, which is funded by the Swiss National Science Foundation and the Swiss Development Cooperation.
Competing interests: none declared.
1. World Health Organization. World Survey of Rabies No. 32 for the year 1996. Geneva: WHO; 1998. WHO document EMC/ZDI/98.4. [ Links ]
2. Bögel K, Meslin F-X. Economics of human and canine rabies elimination: guidelines for programme orientation. Bulletin of the World Health Organization 1990;68:281-91. [ Links ]
3. Cleaveland S, Kaare M, Tiringa P, Mlengeya T, Barrat J. A dog rabies vaccination campaign in rural Africa: impact on the incidence of dog rabies and human dog-bite injuries. Vaccine 2003;21:1965-73. [ Links ]
4. Meslin F-X, Fishbein DB, Matter HC. Rationale and prospects for rabies elimination in developing countries. In: Rupprecht CE, Dietzschold B, Koprowski H, editors. Lyssaviruses. Berlin: Springer Verlag; 1994. p. 1-26. [ Links ]
5. Warrell DA, Warrell MJ. Human rabies: a continuing challenge in the tropical world. Schweizerische Medizinische Wochenschrift 1995;125:879-85. [ Links ]
6. Cleaveland S, Fèvre EM, Kaare M, Coleman PG. Estimating human rabies mortality in the United Republic of Tanzania from dog bite injuries. Bulletin of the World Health Organization 2002;80:304-10. [ Links ]
7. Fekadu M. Human rabies surveillance and control in Ethiopia. In: Kitala P, Perry B, Barrat J, King AA, editors. Proceedings of the Fourth International Conference of the Southern and East African Rabies Group, Nairobi, Kenya, 4-6 March, 7-8. Lyon : Editions Fondation Mérieux ; 1997. p. 78-9. [ Links ]
8. Snow RW, Craig M, Deichmann U, Marsh K. Estimating mortality, morbidity and disability due to malaria among Africa's non-pregnant population. Bulletin of the World Health Organization 1999;77:624-40. [ Links ]
9. Dye C, Scheele S, Dolin P, Pathania V, Raviglione MC. Global burden of tuberculosis estimated incidence, prevalence, and mortality by country. JAMA 1999;282:677-86. [ Links ]
10. Roth F, Zinsstag J, Orkhon D, Chimed-Ochir G, Hutton G, Cosivi O, et al. Human health benefits from livestock vaccination for brucellosis: a case study. Bulletin of the World Health Organization 2003;81:867-76. [ Links ]
11. Baltazard M, Ghodssi M. Prevention of human rabies: treatment of persons bitten by rabid wolves in Iran. Bulletin of the World Health Organization 1954;10:797-802. [ Links ]
12. Shah U, Jaswal GS. Victims of a rabid wolf in India: effect of severity and location of bites on development of rabies. Journal of Infectious Diseases 1976;134:25-9. [ Links ]
16. Kitala PM, McDermott JJ, Coleman PG, Dye C. Comparison of vaccination strategies for the control of dog rabies in Machakos District, Kenya. Epidemiology and Infection 2002;129:215-22. [ Links ]
17. Bishop GC. Canine rabies in South Africa. In: Bingham J, Bishop GC, King AA, editors. Proceedings of the Third International Conference of the Southern and East African Rabies Group. Harare: Veterinary Research Laboratory; 1995. p. 104-11. [ Links ]
18. Brooks R. Survey of the dog population of Zimbabwe and its level of rabies vaccination. Veterinary Record 1990;127:592-6. [ Links ]
19. Cleaveland S, Dye C. Maintenance of a microparasite infecting several host species: rabies in the Serengeti. Parasitology 1995;111 Suppl:S33-47. [ Links ]
20. Foggin CM. Rabies and rabies-related viruses in Zimbabwe: historical, virological and ecological aspects. Harare: University of Zimbabwe; 1988. [ Links ]
21. Childs JE, Robinson LE, Sadek R, Madden A, Miranda ME, Miranda NL. Density estimates of rural dog populations and an assessment of marking methods during a rabies vaccination campaign in the Philippines. Preventive Veterinary Medicine 1998;33:207-18. [ Links ]
22. Perry BD, Brooks R, Foggin CM, Bleakley J, Johnston DH, Hill FW. A baiting system suitable for the delivery of oral rabies vaccine to dog populations in Zimbabwe. Veterinary Record 1988;123:76-9. [ Links ]
23. Pal SK. Population ecology of free-ranging urban dogs in West Bengal, India. Acta Theriologica 2001;46:69-78. [ Links ]
24. World Health Organization. World survey of rabies No. 34 for the year 1998. Geneva: WHO; 1999. WHO document CSR/APH/99.6. [ Links ]
25. Lin FT, Lina N. Developments in the production and application of rabies vaccine for human use in China. Tropical Doctor 2000;30:14-6. [ Links ]
26. Murray CJL. Quantifying the burden of disease: the technical basis for disability-adjusted life years. Bulletin of the World Health Organization 1994;72:429-45. [ Links ]
27. Yimer E, Newayeselassie B, Teferra G, Mekonnen Y, Bogale Y, Zewde B, et al. Situation of rabies in Ethiopia: a retrospective study 1990-2000. Ethiopian Journal of Health Development 2002;16:105-12. [ Links ]
28. Fekadu M. Rabies in Ethiopia. American Journal of Epidemiology 1982;115:266-73. [ Links ]
29. Ayalew Y. Analysis of 159 human rabies cases in Ethiopia. In: Kuwert E, Mérieux C, Koprowski H, Bögel K, editors. Rabies in the tropics. Berlin: Springer-Verlag; 1985. p. 481-4. [ Links ]
30. Belcher DW, Wurapa FK, Atuora DO. Endemic rabies in Ghana: epidemiology and control measures. American Journal of Tropical Medicine and Hygiene 1976;25:724-9. [ Links ]
31. Kureishi A, Xu LZ, Wu H, Stiver HG. Rabies in China: recommendations for control. Bulletin of the World Health Organization 1992;70:443-50. [ Links ]
32. Lakhanpal U, Sharma RC. An epidemiological study of 177 cases of human rabies. International Journal of Epidemiology 1985;14:614-7. [ Links ]
33. Singh J, Jain DC, Bhatia R, Ichhpujani RL, Harit AK, Panda RC, et al. Epidemiological characteristics of rabies in Delhi and surrounding areas, 1998. Indian Pediatrics 2001;38:1354-60. [ Links ]
34. Mathers CD, Vos T, Lopez AD, Salomon J, Ezatti M. National burden of disease studies: a practical guide. 2nd edition. Geneva: World Health Organization; 2001 (Global Programme on Evidence for Health Policy). [ Links ]
35. World Health Organization. World survey of rabies No. 35 for the year 1999. Geneva: WHO; 2002. WHO document CDS/CSR/EPH/2002.10. [ Links ]
36. Bahri F, Letaief A, Ernez M, Elouni J, Chekir T, Ben Ammou S, et al. Neurological complications in adults following rabies vaccine prepared from animal brains. Presse Medicale 1996;25:491-3. [ Links ]
37. Held JR, Adaros HL. Neurological disease in man following administration of suckling mouse brain antirabies vaccine. Bulletin of the World Health Organization 1972;46:321-7. [ Links ]
38. Swaddiwuthipong W, Weniger BG, Wattanasri S, Warrell MJ. A high rate of neurological complications following Semple anti-rabies vaccine. Transactions of the Royal Society of Tropical Medicine and Hygiene 1988;82:472-5. [ Links ]
39. Murray CJL, Lopez AD. Global health statistics: a compendium of incidence, prevalence, and mortality estimates for over 200 conditions. Vol. 2. Boston (MA): Harvard School of Public Health; 1996. [ Links ]
40. Meltzer MI, Rupprecht CE. A review of the economics of the prevention and control of rabies. Part 1: Global impact and rabies in humans. Pharmacoeconomics 1998;14:365-83. [ Links ]
41. Pradhan S, Satapathy DM, Das BC. Pharmacoeconomics of antirabies vaccine treatment the case for intradermal administration of cell culture vaccines. Indian Journal of Internal Medicine 2001;11: 5 Suppl 1-12. [ Links ]
42. Kamoltham T, Khawplod P, Wilde H. Rabies intradermal post-exposure vaccination of humans using reconstituted and stored vaccine. Vaccine 2002;20:3272-6. [ Links ]
43. Vose D. Risk analysis: a quantitative guide. 2nd ed. New York: John Wiley Sons; 2000. [ Links ]
44. Bingham, J. Rabies on Flores Island, Indonesia: is eradication possible in the near future? In: Dodet B, Meslin F-X, Heseltine E, editors. Proceedings of the Fourth International Symposium of Rabies Control in Asia. Paris: John Libbey Eurotext; 2001. p.148-55. [ Links ]
45. Association for the Prevention and Control of Rabies in India. Assessing the burden of rabies in India: a national multicentric survey. Progress report. Bhubaneswar, India: Association for the Prevention and Control of Rabies; 2003. [ Links ]
46. Ichhpujani RL, Bhardwaj M, Chhabra M, Datta KK. Rabies in humans in India. In: Dodet B, Meslin F-X, Heseltine E. Proceedings of the Fourth International Symposium of Rabies Control in Asia. Montrouge: John Libbey Eurotext; 2001. p. 212-3. [ Links ]
47. Kitala PM, McDermott JJ, Kyule MN, Gathuma JM. Community-based active surveillance for rabies in Machakos District, Kenya. Preventive Veterinary Medicine 2000;44:73-85. [ Links ]
48. Tang Q, Xiuqin Z, Zhi D. Human epidemiology and risk factors for rabies. In: Dodet B, Meslin F-X, editors. Proceedings of the Third International Conference on Rabies Control in Asia. Paris: Elsevier; 1997. p. 130-6. [ Links ]
49. Dutta JK. Safety and tolerance of purified Vero rabies vaccine (Verorab): an Indian experience. Journal of the Association for Prevention and Control of Rabies in India 1999;1:26-30. [ Links ]
50. Pancharoen C, Thisyakorn U, Lawtongkum W, Wilde H. Rabies exposures in Thai children. Wilderness and Environmental Medicine 2001;12:239-43. [ Links ]
(Submitted: 16 February 2004 Final revised version received: 3 July 2004 Accepted: 5 July 2004)