Literature DB >> 21245913

Factors associated with the prevalence of circulating antigens to porcine cysticercosis in three villages of burkina faso.

Rasmané Ganaba1, Nicolas Praet, Hélène Carabin, Athanase Millogo, Zékiba Tarnagda, Pierre Dorny, Sennen Hounton, Adama Sow, Pascal Nitiéma, Linda D Cowan.   

Abstract

BACKGROUND: little is known about porcine cysticercosis in Burkina Faso. We conducted a pilot study to estimate the prevalence of antigens of Taenia solium cysticercosis and to identify associated factors in pigs of three villages in Burkina Faso, selected to represent different pig management practices: one village where pigs are allowed to roam freely (Batondo), one village where pigs are penned part of the time (Pabré) and one village with limited pig farming (Nyonyogo). METHODS/PRINCIPAL
FINDINGS: a clustered random sampling design was used. Data on socio-demographic characteristics (source of drinking water, presence of latrines in the household, type and number of breeding animals) and pig management practices were collected using a standardized questionnaire. Blood samples were collected from one pig per household to determine the presence of antigens of the larval stages of T. solium by the B158/B60 Ag-ELISA. The associations between seropositivity and socio-demographic and pig management practices were estimated using logistic regression. Proportions of 32.5% (95% CI 25.4-40.3), 39.6% (31.9-47.8), and 0% of pigs, were found positive for the presence of circulating antigens of T. solium in Batondo, Pabré, and Nyonyogo, respectively. The results of the logistic regression analyses suggested that people acquire knowledge on porcine cysticercosis following the contamination of their animals. The presence of antigens in the pigs' sera was not associated with the absence of latrines in the household, the source of drinking water or the status of infection in humans but was associated with pig rearing practices during the rainy season.
CONCLUSIONS/SIGNIFICANCE: the results suggest that education of pig farmers is urgently needed to reduce the prevalence of this infection.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21245913      PMCID: PMC3014946          DOI: 10.1371/journal.pntd.0000927

Source DB:  PubMed          Journal:  PLoS Negl Trop Dis        ISSN: 1935-2727


Introduction

Burkina Faso is one of the poorest countries in the world ranking 177th out of 182 according to the Human Development Index (HDI) [1]. Its economy relies predominantly on agriculture (40% of GDP), with cotton production being the most important, followed by livestock production, accounting for 12% of the GDP [2]. The main livestock species are cattle, small ruminants, poultry and pigs. The relative importance of each species varies across the thirteen regions of the country. The country's pig population is estimated at 2 million, and is more concentrated in the regions of Centre West, South West, and Boucle du Mouhoun (with 45% of the pig population) [3]. Pigs are kept mainly in a traditional way, with most being either tethered or allowed to roam freely for some time during the year (Figure 1).
Figure 1

Pigs kept roamed laying in a puddle of water from toilet behind a concession.

Porcine cysticercosis is a parasitic zoonosis caused by the larval stage of Taenia solium. While pigs are the intermediate host, man is the only natural definitive host. Human tapeworm carriers shed thousands of eggs daily through their feces. Pigs usually get infected by eating infected human feces or by consuming feed or water contaminated with human feces. Humans can also become accidental intermediate hosts upon ingestion of T. solium eggs. In both humans and pigs, the larval stage of T. solium can establish in the muscles and/or in the brain, the latter resulting in neurocysticercosis (NCC). Human NCC may lead to acute seizures, epilepsy and other neurological manifestations [4]. Ingestion of larvae (cysticerci) present in raw or under-cooked pork may result in human tapeworm infection. Porcine cysticercosis is common in developing countries where pigs are raised. Porcine cysticercosis is associated with poor sanitation and hygiene (absence of latrines, defecation in pigpens, poor handwashing practices), poor methods of pig husbandry (free-roaming), lack of meat inspection, and poor knowledge of the disease [5]–[11], all of which are associated with poverty. In order to avoid economic losses due to condemnation of infected pig carcasses in places where meat inspection is performed [10], farmers may sell contaminated pigs, either alive or for clandestine slaughtering. Information on porcine cysticercosis in Burkina Faso is very limited. Coulibaly and Yameogo (2000) [12] reported a prevalence of cysticercosis of 0.6% among pigs inspected at slaughter. Based on data from the main abattoir in Ouagadougou for 2005 to 2007, of 10,505, 12,651, and 11,887 pigs slaughtered during each of these three years, respectively, only 8 (0.08%), 13 (0.10%), and 10 (0.08%) were condemned because of cysticercosis; whereas 472, 186, and 133 carcasses, respectively, were reportedly condemned because of illegal slaughtering. These data clearly show that inspection of pork is very poor in Burkina, and reliable prevalence of porcine cysticercosis is lacking in the country. The aims of this study were therefore: 1) to estimate the prevalence of T. solium cysticercosis among pigs in three villages with distinct pigs raising techniques, and 2) to measure the association between potential risk factors and the prevalence of infection in pigs.

Methods

We conducted a cross-sectional study in three villages including serological detection of active cysticercosis in pigs and a questionnaire survey for the identification of potential risk factors. In two villages, Batondo and Pabré, located 140 km west and 20 km north of Ouagadougou (the capital of Burkina Faso), respectively, pig breeding and pork consumption are very common. In a third village, Nyonyogo, located 30 km north of Ouagadougou, both pig breeding and pork consumption are rare. The sampling of pigs took place between 26 May and 29 October 2007, which corresponds to the rainy season and the very start of the dry season. The sampling was implemented by a research team composed of one physician, one veterinarian, two interviewers, and one translator (for Batondo only).

Sampling and measurement of potential risk factors

The first step in the sampling process was to determine the sampling frame. This was done by using information from the national population census conducted in 2006 during which all villages were divided into enumeration areas (EA), a geographical unit which is intended to include approximately 1,000 persons. In each of the three villages, the sampling process started by identifying the geographic limits of each EA. In each EA, each concession (a grouping of several households, usually members of the same family) was numbered. In Batondo (4 EAs) and Nyonyogo (3 EAs), all the concessions were included because of the small number of concessions present. In Pabré (5 EAs), 50% of all concessions were randomly selected. In each concession, all the households were invited to participate. The head of each household was asked to list all the members of the household and the mother or the oldest woman (in the case of polygamy) was asked questions regarding selected characteristics of the household, such as the source of drinking water, the presence of latrines, breeding livestock, and cooking pork. The person in charge of pig farming was asked about how pigs were managed and slaughtered. Knowledge of porcine cysticercosis was assessed through questions about seeing lesions in the meat on dead animals or cysts under the tongue of live animals. Before the data collection started, the questionnaires were validated during a pre-test conducted in Tenado, a village located eight km from Batondo. One pig was randomly sampled per household for blood sample collection. Blood samples were also collected in humans (one person randomly selected per household) (see [13] for more details on the human component of the study). All questionnaires are available on request. Blood samples were left to decant and the sera were transported to the Institut de Recherche en Sciences de la Santé (IRSS) in Bobo-Dioulasso where they were kept at −20°C until analysis.

Serological test

The serum samples were tested in duplicate with the enzyme-linked immunosorbent assay (ELISA) for the detection of circulating antigens of the metacestode of T. solium (Ag-ELISA) [14]. Sera showing a coefficient of variation of more than 50% between the duplicate results were considered as missing values (n = 10). The Ag-ELISA has been reported to have a sensitivity of 76.3% (95%CI: 60.9%–88.6%), 86.7% (95%CI: 62.0%–98.0%) and 85.8% (95%CI: 71.9%–99.7%) and a specificity of 84.1% (95%CI: 74.4%–93.3%), 94.7% (95%CI: 90.0%–99.7%) and 98.9% (95%CI: 97.3%–100%) in pigs in South Africa, Zambia and West Cameroon, respectively [6], [14], [15].

Statistical analysis

First, the relative frequencies of categorical variables and the mean and extreme values of quantitative variables were calculated. Wealth quintiles for households were derived from a score calculated based on the asset ownership of each household (e.g., source of drinking water, presence of toilet, radio, bicycle, presence, type and number of livestock, types of roof and walls) using factor analysis as described by Gwatkin et al. (2000) [16]. Secondly, bivariate analyses were conducted to assess the associations between pigs' serological status and location (village), human socio-demographic and health factors (source of drinking water, presence of latrine, presence of antigens to the larval stages of T. solium, wealth quintile), and pig management factors. Finally, a multiple logistic regression was used to estimate the adjusted associations between the factors mentioned above and the presence of antigens to T. solium in pigs. Data from Nyonyogo were excluded from the logistic regression because of the small number of pigs in the village (only 6 pigs were sampled there). All the analyses were performed using STATA9 software. The prevalence of infection and 95% Bayesian credible intervals (BCI), adjusted for measurement error in serology, were also estimated in Batondo and Pabré using a Bayesian approach suggested by Joseph et al. (1995) [17]. We used two sets of priors for the sensitivity and specificity of the AgELISA test based on two studies conducted in infected pigs, one in Zambia and one in South Africa [6], [14].

Ethical issues

The animal component of this protocol was approved by the Institutional Animal Care and Use Committee (IACUC) of the University of Oklahoma Health Sciences Center. No IACUC exists in Burkina Faso. The human component of this protocol was reviewed and approved by the ethical committee of the Center MURAZ (Ref. 02-2006/CE-CM) and by the Institutional Review Board of the University of Oklahoma Health Sciences Center (IRB# 12694) for both human and porcine participants. Informed consents for the interviews of participants and the provision of blood samples were obtained separately. The consent process was done orally because a very large proportion of the population had never been to school (62.5%). Oral consent was documented on the individual consent forms by the research staff (fingerprints were collected in place of signatures). Both IRBs approved the use of oral consents.

Results

Socio-demographic characteristics of the three villages are described in Table 1. The majority of people in Batondo and Pabré drank water from traditional or open wells, whereas in Nyonyogo, most used water from bore wells. There were a few households in Batondo (1.2%) and Pabré (0.3%) in which people drank water from the river, marsh or spring. More than one-third of households in Pabré had latrines in contrast to Batonto and Nyonyogo where latrines were very rare. Wealth quintiles classified approximately one-half (50.9%) of households in Batondo among the poorest compared to around 1% in Pabré and Nyonyogo. In contrast, nearly 30% of households in Pabré and Nyonyogo were classified among the wealthiest compared to only 4.4% in Batondo.
Table 1

Households' socio-demographic characteristics and human seropositivity to Taenia solium antigens by village, Burkina Faso, 2007.

VariableCategoryVillage
BatondoPabréNyonyogo
Number of households sampled 343358187
Source of household drinking water Bore well/Tap water102 (29.9)149 (41.6)177 (94.7)
Cemented well19 (5.6)4 (1.1)
Traditional well/open well216 (63.3)204 (57.0)10 (5.3)
River/Marsh/Spring4 (1.2)1 (0.3)
Missing200
Presence of latrines in the household Yes27 (7.8)137 (38.4)27 (14.4)
Missing010
Result of the AgELISA test in one human selected at random in the household Positive31 (10.3)4 (1.4)0 (0.0)
Borderline4 (1.3)1 (0.3)8 (4.5)
Missing437111
Wealth quintiles Mean ± std−0.83±0.780.53±0.790.49±0.65
1st quintile (poorest)(50.9)(0.6)(1.1)
5th quintile (wealthiest)(4.4)(29.8)(29.0)
Missing311
Presence of livestock Cattle60 (17.4)42 (11.7)99 (52.9)
Sheep45 (13.0)45 (12.6)58 (31.0)
Goats195 (56.8)187 (52.2)153 (81.8)
Donkey31 (9.0)236 (65.9)152 (81.3)
Poultry260 (75.9)247 (69.0)139 (74.3)
Pigs228 (66.4)189 (52.8)5 (2.7)
Missing000
Characteristics related to pigs and pig management are reported in Table 2. Pigs were raised in two-thirds (66.4%) of the surveyed households in Batondo and in more than half (52.8%) of the surveyed households in Pabré. In Nyonyogo, most surveyed households owned ruminants and only 3% owned pigs. In Batondo, pigs were almost exclusively cared for by women (98.8%) whereas in Pabré, pigs were taken care of by men in nearly two-thirds of cases (63.1%). Similarly, the mother or eldest woman of the family was in charge of pigs in 71.7% of surveyed households in Batondo, but in only 25.0% of surveyed households in Pabré. Children were more often in charge of pigs in Pabré (10.5%) than in Batondo (1.8%). More than one-half of the surveyed households owning pigs in Pabré kept them penned during the rainy season. This was in contrast to Batondo where only 10.4% were kept penned, although over 90% were tethered. During the dry season, pigs were left to roam in all three villages to scavenge around cropped fields.
Table 2

Number(%) of pig management characteristics and pig serological results by village, Burkina Faso, 2007.

VariableCategoryVillage
BatondoPabréNyonyogo
Number of households raising pigs interviewed 1731576
Number of pigs per household Minimum number111
Median number231
Maximum number24187
Mean ± std3.2±3.03.6±2.73.0±2.8
Missing310
Gender of the person in charge of pig management Female171 (98.8)56 (36.9)-
Male2 (1.2)96 (63.1)6 (100)
Missing050
Household role of the person in charge of pig management Father of the family2 (1.2)85 (55.9)6 (100)
Mother/eldest woman of the family119 (71.7)38 (25.0)ND*
One of the children3 (1.8)16 (10.5)ND
Other woman in the family42 (25.3)13 (8.6)ND
Missing750
Pigs are slaughtered at home (among household) Yes8 (4.6)108 (69.4)2 (33.3)
Missing000
Have you ever heard of white nodules that look like rice grains in pig meat? Yes143 (82.7)145 (92.9)6 (100)
Missing010
Purpose of pig raising To sell meat1 (0.6)7 (4.5)(0.0)
To sell live pigs138 (79.8)120 (76.9)5 (83.3)
Keep for reproduction142 (82.1)150 (96.1)5 (83.3)
Missing010
Pig management Keep in pen during rainy season18 (10.4)86 (55.1)0 (0.0)
Left roaming during rainy season2 (1.2)0 (0.0)0 (0.0)
Keep tethered during rainy season163 (94.2)74 (47.4)6 (100)
Keep in pen during dry season1 (0.6)15 (9.6)0 (0.0)
Left roaming during dry season172 (99.4)141 (90.4)6 (100)
Keep tethered during dry season1 (0.6)1 (0.6)0 (0.0)
Missing010
Result of the AgELISA for the detection of the larval stage of T. solium in pigs Borderline3 (1.9)5 (3.2)0 (0.0)
Positive52 (32.5)61 (39.6)0 (0.0)
Missing1331
A total of 336 pigs were sampled: 173 in Batondo, 157 in Pabré, and 6 in Nyonyogo. Four sera in Batondo, 3 in Pabré, and 1 in Nyonyogo were not tested because of insufficient volume. Using prior information on the sensitivity and specificity of the AgELISA from South Africa, the adjusted estimates of the seroprevalence of infection in Batondo and Pabré were 32.7% (95% BCI: 12.1%–54.3%) and 48.3% (95% BCI: 27.9%–74.8%), respectively. Using the priors from Zambia, the adjusted estimates of the seroprevalence of infection in Batondo and Pabré were 32.7% (95% BCI: 25.4%–68.3%) and 48.2% (95% BCI: 35.4%–82.6%), respectively. A total of 1.9% and 3.4% were found to be borderline positive in Batondo and Pabré, respectively. Neither serologically positive nor borderline animals were found in Nyonyogo. The results of the multivariable logistic regression are reported in Table 3. Allowing pigs to roam during the rainy season was associated with an increased prevalence odds of infection when compared to keeping pigs penned (POR = 6.48, 95%CI: 1.23–34.17). Being aware of pig cysticercosis was also associated with an increased prevalence odds of infection (POR = 4.70, 95%CI: 1.76–12.52). The village, while not statistically significant, was retained in the model because it was a confounding factor for most of the other variables explored, including those retained in the final model. Once the model is adjusted for pig management during the rainy season and awareness of the infection, the prevalence odds of infection tended to be higher in Pabré than in Batondo (OR = 1.63, 95%CI: 0.94–2.83).
Table 3

Adjusted prevalence odds ratios (95% CIs) for pigs' seropositivity to Taenia solium, Burkina Faso, 2007.

VariableFactorReferencePOR95% CI
Pig rearing during the rainy season Tethered all the timePenned all the time1.470.80 – 2.69
Roam some of the timePenned all the time6.481.23 – 34.17
Has heard of porcine cysticercosis YesNo4.701.76–12.52
Village PabréBatondo1.630.94–2.83

POR: Prevalence odds ratio.

CI: Confidence interval.

POR: Prevalence odds ratio. CI: Confidence interval.

Discussion

This is the first community-based study conducted in Burkina Faso to report seroprevalence of porcine cysticercosis. Our results show that cysticercosis is highly prevalent in the two villages where pigs are commonly raised. These estimates are nearly 100 times higher than the previous estimate of 0.57% based on reports from meat inspection services [12]. This finding supports the opinion of Zoli et al. (2003) [10] that data from meat inspection are not representative of the real situation, mainly because the method is insensitive [14] and depends on the technical skills and the motivation of the examiner. Pigs infected with cysticercosis may also never be sold in the official market. One-third (32.5%) of the pigs in Batondo and more than one-third (39.6%) in Pabré were infected, but none of the five sampled pigs in Nyonyogo was found to be positive. The latter is not surprising since pig breeding and pork consumption are very rare in this village. Similarly, Carabin et al. (2009) [13] reported very few cysticercosis seropositive inhabitants in Nyonyogo, and the few positives had all borderline reactions to the Ag ELISA. Using priors from either South Africa or Zambia to adjust for measurement error resulted in the same median prevalence, but 95% BCI were shifted towards higher values when using the Zambia priors. This is because both the prior values for sensitivity and specificity from the Zambian study were higher than the South Africa values. The B158/B60 AgELISA test used here was recently shown to have the highest sensitivity and specificity for detection of cysticercosis-infected pigs when compared to tongue examination, EITB, and HP10 Ag-ELISA [6], [14]. The seroprevalences in Batondo and Pabré were comparable to that reported in pigs in Mozambique [5] but were higher than that reported in several other African countries [9], [15], [18], [19] and lower than the seroprevalence reported in pigs slaughtered on the clandestine market in Lusaka, Zambia [14] and in the Eastern Cape province in South Africa [6]. Pigs allowed to roam some of the time during the rainy season were more likely to be seropositive than pigs penned during all of the rainy season. This association was statistically significant even though the proportion of pigs allowed to roam during the rainy season was small because the association was so strong (POR = 6.48, 95% CI 1.23–34.17). Given the imprecision of this estimate, however, the association will need to be further explored. This observation agrees with the findings of Pondja et al. (2010) [5] who identified the free-range pig husbandry system as an important risk factor for porcine cysticercosis. Conducting this pilot study lead to an appreciation that the pig management systems in Batondo and Pabré were different from what had been reported to us when the study was being planned. Indeed, in both of the two villages with pigs, animals were left roaming during dry seasons but restrained to one degree or another during crop production period (rainy season). The main difference in restraints was that pigs were confined in pens in Pabré and tethered to pillars in Batondo. The difference in pig management, mainly during the rainy season, between Batondo and Pabré might reflect the difference in who owns and is responsible for raising the pigs. In Batondo, almost all pigs were owned by women whereas they were kept by men in two-third of the cases in Pabré. This result suggests that the target for intervention when planning future cysticercosis control strategies depends on who is responsible for pig raising in any given village. Pigs owned by people who had heard of porcine cysticercosis were more likely to be seropositive than owners who were unaware of this infection. If pigs raised by the same farmers tend to become re-infected, this would suggest that people become aware of porcine cysticercosis when their pig is found to be infected. Despite the high frequency of households with latrines in Pabré and the low prevalence of active infections in humans [13], the seroprevalence in pigs in this village tended to be higher than that in Batondo. This result is counter-intuitive but could be explained by the following. First, the presence of latrines does not certify their use because of foul odors, flies, flooding, etc. Second, latrines may be inappropriately built (closing door, septic tank) allowing access of pigs to human feces [20]. More research is needed to explain this observation. It was anticipated that there would be an association of pig seropositivity and variables such as presence of a toilet in the household, household source of drinking water, and human serological status, but this was not confirmed by the statistical analysis. Indeed, the structure of community life in these villages means that any risk associated with lifestyle in a family is shared by other families nearby. For example, if a given family does not have access to latrines and thus defecates in nature, this will also affect the members of families equipped with latrines through environmental contamination. People with taeniasis may also infect a large number of pigs if they do not use latrines. Lescano et al. (2007) [21] demonstrated that a T. solium carrier can infect pigs within an area of 500 meters or more. In conclusion, a high prevalence of porcine cysticercosis was observed in pig populations in Burkina Faso in villages with traditional pig-rearing practices. The co-occurrence of knowledge about cysticercosis and owning seropositive pigs suggests that information about this disease may not be available to livestock managers until the disease is already present. If so, this emphasizes the clear need for improving education in order to control this zoonosis.
  16 in total

1.  Investigation of risk factors for porcine Taenia solium cysticercosis: a multiple regression analysis of a cross-sectional study in the Yucatan Peninsula, Mexico.

Authors:  M A Widdowson; A J Cook; J J Williams; F Argaes; I Rodriguez; J L Dominguez; R Rodriguez
Journal:  Trans R Soc Trop Med Hyg       Date:  2000 Nov-Dec       Impact factor: 2.184

2.  Epidemiological survey of swine cysticercosis in two rural communities of West-Cameroon.

Authors:  M S R Pouedet; A P Zoli; L Vondou; E Assana; N Speybroeck; D Berkvens; P Dorny; J Brandt; S Geerts
Journal:  Vet Parasitol       Date:  2002-05-30       Impact factor: 2.738

3.  Prevalence and control of zoonotic diseases: collaboration between public health workers and veterinarians in Burkina Faso.

Authors:  N D Coulibaly; K R Yameogo
Journal:  Acta Trop       Date:  2000-07-21       Impact factor: 3.112

4.  Swine cysticercosis hotspots surrounding Taenia solium tapeworm carriers.

Authors:  Andres G Lescano; Hector H Garcia; Robert H Gilman; M Claudia Guezala; Victor C W Tsang; Cesar M Gavidia; Silvia Rodriguez; Lawrence H Moulton; Justin A Green; Armando E Gonzalez
Journal:  Am J Trop Med Hyg       Date:  2007-02       Impact factor: 2.345

5.  Prevalence and risk factors of porcine cysticercosis in Angónia District, Mozambique.

Authors:  Alberto Pondja; Luís Neves; James Mlangwa; Sónia Afonso; José Fafetine; Arve Lee Willingham; Stig Milan Thamsborg; Maria Vang Johansen
Journal:  PLoS Negl Trop Dis       Date:  2010-02-02

Review 6.  Regional status, epidemiology and impact of Taenia solium cysticercosis in Western and Central Africa.

Authors:  André Zoli; Oliver Shey-Njila; Emmanuel Assana; Jean-Pierre Nguekam; Pierre Dorny; Jef Brandt; Stanny Geerts
Journal:  Acta Trop       Date:  2003-06       Impact factor: 3.112

7.  Prevalence of Taenia solium cysticercosis in swine from a community-based study in 21 villages of the Eastern Cape Province, South Africa.

Authors:  R C Krecek; L M Michael; P M Schantz; L Ntanjana; M F Smith; P Dorny; L J S Harrison; F Grimm; N Praet; A L Willingham
Journal:  Vet Parasitol       Date:  2008-03-14       Impact factor: 2.738

8.  The prevalence of porcine cysticercosis in Eastern and Southern provinces of Zambia.

Authors:  I K Phiri; P Dorny; S Gabriel; A L Willingham; N Speybroeck; J Vercruysse
Journal:  Vet Parasitol       Date:  2002-08-30       Impact factor: 2.738

9.  Porcine cysticercosis in village pigs of North-West Cameroon.

Authors:  O Shey-Njila; P A Zoli; J Awah-Ndukum; E Assana; P Byambas; P Dorny; J Brandt; S Geerts
Journal:  J Helminthol       Date:  2003-12       Impact factor: 2.170

10.  Seroprevalence to the antigens of Taenia solium cysticercosis among residents of three villages in Burkina Faso: a cross-sectional study.

Authors:  Hélène Carabin; Athanase Millogo; Nicolas Praet; Sennen Hounton; Zékiba Tarnagda; Rasmané Ganaba; Pierre Dorny; Pascal Nitiéma; Linda D Cowan
Journal:  PLoS Negl Trop Dis       Date:  2009-11-24
View more
  14 in total

1.  Risk factors associated with taeniosis-cysticercosis in rural farming communities in Gauteng Province, South Africa.

Authors:  A M Tsotetsi-Khambule; S Njiro; T C Katsande; L J S Harrison
Journal:  Trop Anim Health Prod       Date:  2018-05-30       Impact factor: 1.559

2.  Knowledge, attitudes, and practices related to epilepsy in rural Burkina Faso.

Authors:  Athanase Millogo; A Helena Ngowi; Hélène Carabin; Rasmané Ganaba; Alida Da; Pierre-Marie Preux
Journal:  Epilepsy Behav       Date:  2019-04-24       Impact factor: 2.937

3.  Taenia hydatigena in pigs in Burkina Faso: A cross-sectional abattoir study.

Authors:  Hélène Carabin; Pierre Dorny; Veronique Dermauw; Rasmané Ganaba; Assana Cissé; Boubacar Ouedraogo; Athanase Millogo; Zékiba Tarnagda; Anke Van Hul; Sarah Gabriël
Journal:  Vet Parasitol       Date:  2016-10-24       Impact factor: 2.738

4.  Prevalence of neurocysticercosis among people with epilepsy in rural areas of Burkina Faso.

Authors:  Athanase Millogo; Pascal Nitiéma; Hélène Carabin; Marie Paule Boncoeur-Martel; Vedantam Rajshekhar; Zékiba Tarnagda; Nicolas Praet; Pierre Dorny; Linda Cowan; Rasmané Ganaba; Sennen Hounton; Pierre-Marie Preux; Rabiou Cissé
Journal:  Epilepsia       Date:  2012-11-13       Impact factor: 5.864

5.  Spatio-temporal prevalence of porcine cysticercosis in Madagascar based on meat inspection.

Authors:  Vincent Porphyre; Harentsoaniaina Rasamoelina-Andriamanivo; Andriatsilavina Rakotoarimanana; Ony Rasamoelina; Claire Bernard; Ronan Jambou; Eric Cardinale
Journal:  Parasit Vectors       Date:  2015-07-25       Impact factor: 3.876

6.  Taenia solium taeniosis/cysticercosis and the co-distribution with schistosomiasis in Africa.

Authors:  Uffe Christian Braae; Christopher F L Saarnak; Samson Mukaratirwa; Brecht Devleesschauwer; Pascal Magnussen; Maria Vang Johansen
Journal:  Parasit Vectors       Date:  2015-06-12       Impact factor: 3.876

7.  Effectiveness of a community-based educational programme in reducing the cumulative incidence and prevalence of human Taenia solium cysticercosis in Burkina Faso in 2011-14 (EFECAB): a cluster-randomised controlled trial.

Authors:  Hélène Carabin; Athanase Millogo; Helena A Ngowi; Cici Bauer; Veronique Dermauw; Assana Cissé Koné; Ida Sahlu; Alicia L Salvator; Pierre-Marie Preux; Télesphore Somé; Zékiba Tarnagda; Sarah Gabriël; Rabiou Cissé; Jean-Bosco Ouédraogo; Linda D Cowan; Marie-Paule Boncoeur-Martel; Pierre Dorny; Rasmané Ganaba
Journal:  Lancet Glob Health       Date:  2018-04       Impact factor: 26.763

8.  Prevalence of and Factors Associated with Human Cysticercosis in 60 Villages in Three Provinces of Burkina Faso.

Authors:  Hélène Carabin; Athanase Millogo; Assana Cissé; Sarah Gabriël; Ida Sahlu; Pierre Dorny; Cici Bauer; Zekiba Tarnagda; Linda D Cowan; Rasmané Ganaba
Journal:  PLoS Negl Trop Dis       Date:  2015-11-20

9.  Development of a health education intervention strategy using an implementation research method to control taeniasis and cysticercosis in Burkina Faso.

Authors:  Helena Ngowi; Ivan Ozbolt; Athanase Millogo; Veronique Dermauw; Télesphore Somé; Paul Spicer; Lori L Jervis; Rasmané Ganaba; Sarah Gabriel; Pierre Dorny; Hélène Carabin
Journal:  Infect Dis Poverty       Date:  2017-06-01       Impact factor: 4.520

Review 10.  Animal influence on water, sanitation and hygiene measures for zoonosis control at the household level: A systematic literature review.

Authors:  Francisco Matilla; Yael Velleman; Wendy Harrison; Mandy Nevel
Journal:  PLoS Negl Trop Dis       Date:  2018-07-12
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.