Mem Inst Oswaldo Cruz, Rio de Janeiro, 99(7) November 2004
Epidemiology of Leishmaniasis in Ecuador: Current Status of Knowledge - A Review
Department of Parasitology, Kochi Medical School, Kochi University, Kochi 783-8505, Japan
IUnidad de Inmunologia y Medicina Tropical, Centro de Biomedicina, Universidad Central del Ecuador, Quito, Ecuador
IIHealth Sciences Program, College of Health Sciences, University of Texas at El Paso, El Paso, TX, US
Although leishmaniasis is regarded as a significant health problem in Ecuador by the Ministry of Health, and the incidence has increased over the last years, an official map on the geographic distribution of disease and sand fly vectors or a control strategy do not exist yet. This article reviews the current situation based on published information to improve our knowledge and understand the epidemiological situation of leishmaniasis in Ecuador in order to help future research and to develop a national control strategy. The disease is endemic in most provinces throughout Pacific coastal region, Amazonian lowlands, and some inter-Andean valleys with a total 21,805 cases reported during 1990-2003. Whereas cutaneous leishmaniasis (CL) is found throughout Ecuador, mucocutaneous leishmaniasis (MCL) appears to be restricted to the Amazon region; one, parasitologically unconfirmed case of visceral form was reported in 1949. Most human infections are caused byu00a0Leishmania (Viannia)u00a0spp., which is distributed in the subtropical and tropical lowlands; infections due tou00a0L. (Leishmania)u00a0spp. are found in the Andean highlands and in the Pacific lowlands as well. The proven vectors areu00a0Lutzomyia trapidoiandu00a0Lu. ayacuchensis. Canis familiaris, Sciurus vulgaris, Potos flavus,u00a0andu00a0Tamandua tetradactyla have been found infected withu00a0Leishmania spp. It is estimated that around 3000-4500 people may be infected every year, and that 3.1 to 4.5 millions people are estimated to be at risk of contracting leishmaniasis.
Ecuador is located in north-west South America and straddles both the line of the Equator and the Andes mountain range (Fig. 1). The Andes cross the country from North to South and divide it into three different natural regions: the Pacific coast with subtropical and tropical lowlands, the Andean region with high mountains and valleys where temperatures range from 15 to 22oC and, in the East, a region which encompasses a section of Amazon lowlands covered by humid tropical rain forest. Ecologically, Ecuador is an extremely diverse country with a total area of 283,560 km2, ranging from tropical to nival (permanent snow) and from the rainforest to desert brush. The total population is 12,156,600 inhabitants, of which 6,053,987 live in the Pacific coast, 5,458,313 in the Andean region and 547,047 in the Amazon region; the remaining in the Galapagos Islands (Census 2001).
Ancient representations of skin lesions and facial deformities have been found on pre-Inca pottery from Peru, Colombia, and Ecuador, estimated to date from AD 400 to AD 900. According Ecuadorian ceramics, cutaneous (CL) and mucocutaneous (MCL) leishmaniasis has existed for hundreds or perhaps thousands of years before the arrival of the Spanish conquerors. Historians at the time of the conquerors wrote of skin lesions seen among the Inca Indians which resulted in mutilations similar to those of some human figures (huacos) (Ala-Vedra 1952). The first human case of CL in Ecuador was reported in 1920 (Rodriguez 1974). Hashiguchi and Gomez (1991) have published a detailed description of chronological events associated with leishmaniasis up to 1987.
THE GEOGRAFICAL DISTRIBUTION AND INCIDENCE RATES OF HUMAN INFECTIONS
Human leishmanial infections have been reported from 20/22 of the country's provinces (Fig. 1). Cases are recorded from sea level up to approximately 2700 m elevation, mainly from rural areas. An endemic belt is formed along the western slopes of the Andes involving new settlements in Imbabura, Pichincha, Cotopaxi, Bolivar, and Cañar provinces. CL and MCL forms had been recorded from all 6 Amazonian provinces (Amunarriz 1991). Since 1986 Ecuadorian Andean leishmaniasis has been reported from valleys of Paute (2300-2500 m), Alausi (2300-2700 m), and Huigra (1200-1500 m).
Fig. 2 shows the incidence of tegumentary leishmaniasis for the past 14 years as reported by the Ecuadorian Ministry of Public Health, based on passive case detection. However, this is probably an underestimate as patients consult private practitioners and non-governmental organizations (NGOs); also, CL can self-heal and, thus, these cases are not recorded. As noted in the Fig. 2, the average annual number of cases for the three geographical regions is 1558 (range: 531-3610). Given the differences in population size, the highest incidence rate is found in the Pacific region. The number of cases decreased steadily during the 1990s but suddenly increased in the last four years, with more than 75% of cases occurring in the Pacific region. As in other leishmaniasis-endemic areas throughout Latin America, this increase may be attributed to changes in land use, the construction of new dams and human activity patterns like internal migration, leading to increase exposure of humans to the zoonoticLeishmania life cycles (Desjeux 2001). The decline and the increase of numbers of cases could be due to the frequency of the El Niño Southern Oscillation in Ecuador, but there are no evidences (Davies et al. 2000). Despite, the official epidemiological data showing that the disease prevalence has been decreasing in the last decade, active case detection studies have shown an increase in case numbers in several provinces (Alava et al. 1992, Barrera et al. 1994, Garcia et al. 1997, Nonaka et al. 1997). In fact, Armijos et al. (1997) and Hashiguchi et al. (1987) have reported that 14% (65/466) and 7.5% (7/93) of subjects surveyed in a subtropical rainforest area and Andean slope of Ecuador had CL, respectively. The incidence of leishmaniasis is expected to remain stable or increase in the near future due to the large number of previously unexposed groups such as young children and persons who visit (e.g., tourists) or move from non-endemic areas (e.g., agriculturalist, lumberjacks, workers for petrol exploitation, and subsequent colonization).
ATTITUDES OF THE LOCAL POPULATIONS TO LEISHMANIASIS
Most adults from leishmaniasis-endemic areas of NW Ecuador are familiar with the disease and believe that it has a negative impact on the capacity to perform normal work duties and it needs some type of intervening treatment (Weigel et al. 1994, Weigel & Armijos 2001). However, few knew about the transmission, etiology, ulcer healing, and conventional treatment. Women appeared to be more aware of the disease and scars because of the associated stigmatization of people affected. In the Amazon foci, because of tissue destruction and mutilation in the mucocutaneous form, patients tend to be isolated by the family and friends causing psychosocial impact with social and economic consequences (Amunarriz 1991). These local perceptions should be considered when planning future control programs and would be helpful to establish the communication channels that would be most effective with respect to control activities (e.g., identification of target groups). However, studies on people's knowledge, attitudes, and practices towards leishmaniasis do not exist in the Andean and Amazon regions. Certainly, the popular ideas and cultural practices in other foci might be different because of clinical presentation, cultural background, level of education, and environment between Amerindians in the Amazon and mestizo in the Andes foci. Further, plants and ethnomedical inventory used for the Amerindians in the Amazon foci do not exist in other regions (Amunarriz 1991).
The popular name for leishmaniasis in Ecuador differs from region to region. In the Pacific it is called sarna brava (angry sore), charra brava (angry ulcer) or charra colombiana (Colombian ulcer). In the Amazon region asmilliai caracha or ulcera brava (angry ulcer) for CL and lepra de montaña (mountain leprosy) for MCL, whilst in the Andes people refer to it as nigua de raton (mice chigger) or grano malo (bad sore). In all regions manta blanca (white blanket) is the popular name for the vector.
Traditional treatments are frequently used, especially by rural populations who often lack access to conventional treatment. For example, the use of traditional methods is reported to be as high as 70% in NW Ecuador (Weigel et al. 1994), and 100% in the Amazon region (Amunarriz 1991), with up to 150 different anti-leishmanial therapies used. The therapies described included various indigenous plants, chemicals or petroleum-based products. Although widely used by the communities, their efficacy is largely anecdotal and has never been proven in a controlled study. Other treatments methods such as cauterization with hot metal objects, strong acids, tobacco ash, and heated wax are also frequently used. These often cause tissue burns and promote the development of secondary infections, lengthen the cure and leaving bigger and permanent scars worse than those caused by the leishmaniasis itself (Weigel et al. 1994, Weigel & Armijos 2001).
CLINICAL FORMS AND THEIR CAUSATIVE PARASITES
The diseases occur in Ecuador in most of its recognized American tegumentary forms: CL, MCL, and diffuse cutaneous (DCL) leishmaniasis. The reported ratio of MCL:CL is low (1:13) (Hashiguchi & Gomez 1991). The unique cases reported as visceral leishmaniasis (VL) and DCL came from Esmeraldas province. DCL case was caused by L. (L.) mexicana (Reyna et al. 1994). To date, no other case of VL has been recorded, since the only case reported by Leon in 1949 was not confirmed by parasite isolation; it probably was a misdiagnosis. This is supported by the apparent absence of L. chagasi/infantum parasites and their vectors in the country (Young & Rogers 1984, Alexander et al. 1992).
The clinical features of CL are different between highland and lowland cases. "Andean type" occurs usually as single lesion, measuring less than 5 mm in diameter; most of them are crusted papules with plenty parasites, and reported to be caused only by L. (L.) mexicana and L. (L.) major-like (Armijos et al. 1990, Hashiguchi et al. 1991). The lesions here are clinically similar to "uta" described in the highlands of Peru; however the parasite species and the vector are different (Lainson 1983). Whereas "lowland type" is larger, usually wet with secondary bacterial infection and multiple lesions.
Commonly, CL lesions are ulcerative, but non-ulcerated such as papules, plaques, nodules, and erysipeloid forms are also seen (Chico & Guderian 1989, Nonaka et al. 1990, Armijos et al. 1997).
In the lowlands, cases of sporotrichoid or "pian-bois" form and the chiclero's ulcer have also been diagnosed and to be caused by L. (V.) guyanensis and panamensis (Armijos RX unpublished data). Six cases of leishmaniasis recidiva cutis (LRC), a cutaneous variant characterized for reactivations in old scars, and two patients having dozens of cutaneous ulcers described as disseminated leishmaniasis are reported from the Pacific region, the causative agent was identified to be L. (V.) panamensis (Lazo & Hashiguchi 1994, Calvopina et al. 2004). Recently, in an active survey for MCL in the Amazonian provinces of Sucumbios, Orellana, and Napo we encountered 13 active cases of MCL caused by L. (V.) braziliensis (Calvopina et al. 2001a), suggesting that this form and parasite could be prevalent in this humid tropical forest. MCL originating from the Pacific or Andean regions has never been recorded (Hashiguchi et al. 1991, Barrera et al. 1994, Armijos et al. 1997). This is surprising, as Osorio et al. (1998) reported MCL among residents of the Colombian Pacific coast caused by the same species circulating in this Ecuadorian region.
Currently, six Leishmania spp. have been identified from humans, sand flies and non-human mammals (Table). The map (Fig. 1) shows the distribution of identified species by regions and provinces. Findings are that the ratio of L. (Viannia) to L. (Leishmania) infections is about 6:1. Clearly, L. (V.) panamensis and guyanensis are predominant in the subtropical and tropical lowlands of the Pacific region (62.1% of all). Recently, Bañuls et al. (1997, 1999) doubted the separate taxonomic status of the latest two species. L. (L.) amazonensis has been only reported from subtropical Ecuador in human CL (Armijos et al. 1990, Furuya et al. 1997), but also infecting other mammals (Mimori et al. 1989). Notoriously, L. (V.) braziliensis is geographically the species most widespread in the country, having been isolated from CL and MCL patients in nine of 15 surveyed provinces (Armijos et al. 1990, 1997, Bañuls et al. 1999, Furuya et al. 1997, Calvopina et al. 2001a). In the Amazon region only L. (V.) braziliensis was identified, but hybrid genotypes between L. (V.) panamensis/guyanensis and L. (V.) braziliensishad also been reported (Bañuls et al. 1997). Furthermore, Pratlong et al. (2002) identified L. naiffi in a German patient with CL suspected to be infected in this region.
For Andean leishmaniasis the parasite is reported to belongs only to the subgenus Leishmania: L. mexicana for 82.4% (28/34) and L. major-like (Armijos et al. 1990, Hashiguchi et al. 1991), where lesions resembled to "uta" of Andean valleys of Peru; but the causative agent there is identified as L. (V.) peruviana (Lainson et al. 1983) hence, further studies with a standardized methodology have to be established in order to enable comparisons between both foci. L. major-like parasite had also been reported from Brazil, Paraguay, Venezuela, and Mexico (Cupolillo et al. 1994, Yamasaki et al. 1994) suggesting that some of these populations may have been imported into the Americas (Momen et al. 1993). The nucleotide sequences of cytochrome b of L. major-like isolated from the Ecuadorian Andes and the WHO reference strain L. major had a 99.9% homology (Luyo-Acero et al. 2004).
Parasite isolates from a sloth (Choloepus hoffmani) and a squirrel (Sciurus granatensis) caught in tropical forest of the Pacific region characterized before as L. (V.) equatorensis (Grimaldi et al. 1992), actually Uezato et al. (2001) and Katakura et al. (2003) using molecular methods identified that it belongs to the genus Endotrypanumspp.
Since a small proportion of all leishmaniasis cases are ever diagnosed to species level, with a total of 270 cases from nine surveys, further studies are needed in order to isolate and identified the parasites circulating in most provinces reporting the disease.
AGE, GENDER, AND BODY DISTRIBUTION OF LESIONS
The age groups affected differ from region to region. In the Andean foci the most affected are children under two years, suggesting indoor-transmission and probably dogs as reservoirs (Hashiguchi et al. 1991). In the lowlands are children under the age of ten in tropical and five years in subtropical Pacific region (Alava et al. 1992, Armijos et al. 1997). The increased disease prevalence in children could be associated with no previous exposure to the parasite, the role of cellular immune status and/or with malnutrition (Weigel et al. 1995). Nevertheless, for the Amazon region in a passive hospital-based report the mean age of leishmaniasis diagnosis was 33.4 and 19.7 years for MCL and CL respectively (Amunarriz 1991), suggesting unknown reasons for delays in the diagnosis in this wide and disperse region. However, it is also evident that exposure to transmission at any age as do immigrants or tourists they will develop the disease.
No gender difference in the incidence is observed among children at any endemic regions surveyed (Hashiguchi et al. 1991, Weigel et al. 1994). However, the sex difference regarding disease prevalence in the adult population appears to be important. Thus, in the Amazon region a passive hospital-based reported 81% (22/27) of MCL and 83% (67/81) of CL cases to be male (Amunarriz 1991); Calvopina et al. (2001a) also encountered 85% (11/13) of MCL in male. Hence, the excess risk observed in this region is for male older than 14 years suggesting that it could be associated with their occupational exposure (i.e., hunting and agricultural work) characteristic of sylvatic transmission cycle of Leishmania. In a community-based study in the subtropical of Pacific region adult male had a disease risk almost three times greater than of adult female (Weigel et al. 1994). But, several years after in the same study area, no differences were observed (Weigel & Armijos 2001) changes here appeared to be associated with change from sylvatic to domestic and peridomiciliary transmission.
Lesions are most frequent on the exposed parts of the body. The children face is more frequently affected (92%) in the Andean foci (Hashiguchi et al. 1990), probably because mother's cultural behavior in taking care small children in this cool region and where probably indoor-transmission occur. Whilst, in the lowlands, lesions or scars are mostly in the extremities (53.8 to 92%), it is hypothesized because of difference of biting behaviors of sand flies or clothing habits of inhabitants in hot climate (Amunarriz 1991, Alava et al. 1992, Armijos et al. 1997). Chiclero's ulcer is not rare in lowlands foci. Other sites affected include the trunk and, less commonly the scalp, buttocks, eyelids, and genitalia. MCL affects the nasal mucosa, septum and turbinate, upper lip, pharynx and larynx producing dyspnoea, and face deformities (Calvopina et al. 2001a).
The Table lists the sand fly species incriminated as vectors of Leishmania in Ecuador. More than 60 species of phlebotomine sand flies, including 55 species belonging to the genus Lutzomyia have been described (Young & Rogers 1984, Alexander et al. 1992). At least 15 Lutzomyia spp. are known to be anthropophilic and are strongly suspected as vectors. Natural infection with promastigotes morphologically identical to Leishmania have been observed but not characterized in Lu. gomezi, hartmanni and panamensis. In the Pacific region, Lu. trapidoi, a proved vector here, is more abundant in the dry season whilst Lu. gomezi in the wet season (Le Pont et al. 1994a,b). Dujardin et al. (1996) demonstrated the presence of cryptic species in Lu. trapidoi. Studies carried out in 1982 (Hashiguchi et al. 1985) and in 1993 (Furuya et al. 1998) in this region, demonstrated that in 1982 the predominant species was Lu. trapidoi with 8.1% of flagellates in their hindgut, but 10 years later Lu. hartmannipredominate with 9.8% of infection. The latter species was recently confirmed to harbor Endotrypanum spp. (Uezato et al. 2001, Katakura et al. 2003), believed before to be L. (V.) equatorensis (Furuya et al. 1998).
For Andes foci, six anthropophilic Lutzomyia (aya-cuchensis, hartmanni, nevesi, gomezi, serrana, and osornoi) have been identified so far (Gomez et al. 1994), with, only ayacuchensis shown to be naturally infected with L. (L.) mexicana (Hashiguchi et al. 1991). Lu. ayacuchensis abounds in the wet season and its infection rate is found to be highest during the period from the early rainy season to the beginning of the dry season (Gomez & Hashiguchi 1991). It correlates with the appearance of new human cases. In these inter-Andean valleys, there is strong evidence that transmission of Leishmania occurs indoors and in urban settings (Hashiguchi et al. 1987, Armijos et al. 1990).
For the Amazon region, in the Zumba focus south wards of Ecuador bordering with Peru several man-biting species have been recorded, Lu. serrana abounds inside dwellings where it even bite during daytime (Alexander et al. 1992, Le Pont et al. 1994c), suggesting this species as a candidate vector in an indoor-transmission manner. In the inter-Andean Ecuadorian-Peruvian border Lu. robusta was also described (Galati et al. 1995). Both species are suspected vectors of human bartonellosis as well, since there is no probed vector for Bartonella bacilliformisendemic in those areas (Cooper et al. 1996). From Orellana province seven anthropophilic species captured in MCL focus were identified but all negatives for natural infection (Calvopina et al. 2001a). In the whole country there are no reports on Lu. longipalpus and evansi a confirmed vectors of L. chagasi/infantum in the neighboring countries.
PUTATIVE RESERVOIRS HOSTS
The Table lists the non-human mammals where Leishmania has been characterized. One Canis familiaris was found infected with L. (V.) panamensis or panamensis/guyanensis and one with L. (L.) mexicana in the Pacific and in the Andes region, respectively (Dereure et al. 1994, Bañuls et al. 1999, Hashiguchi et al. 1991). Both reports are congruent with the human strains isolated in the respective regions. Sciurus vulgaris, Potos flavus, andTamandua tetradactyla were found infected in the Pacific region with L. amazonensis (Mimori et al. 1989). Positive flagellate cultures from additional eight different mammalian species from the Pacific region have been grown, but were not characterized (Hashiguchi et al. 1985). No positive parasite isolation or detection has been done from putative reservoir hosts in the Amazon region.
Serological studies to examine the role of dogs in the leishmaniasis transmission cycle carried out in the inter-Andean valley of Alausi found 19/58 (32.8%) of surveyed dogs positive for ELISA; no dog had positive liver-puncture aspirates (Mimori et al. 1992). Another study also showed high ELISA-rate positivity using antigens ofL. (V.) panamensis and guyanensis in 12/17 dogs from Alausi and 12/20 from the Pacific region (Mori et al. 1994). These results showed high reactivity for ELISA but careful attention must be paid on the cross-reactivity (false-positives) where Trypanosoma cruzi is endemic as is in lowlands of Ecuador (Aguilar et al. 1999). The positive samples should be confirmed parasitologically and characterized, even that, it does not distinguish whether dogs are accidental or reservoir hosts, dogs seems to be a victim-host as humans are. Due to low specificity and sensitivity of the methods employed, the PCR-based method could show better results if it is carried out properly (Reithinger et al. 2000).
In endemic areas of Ecuador the diagnosis of leishmaniasis is generally based on clinical criteria, because few laboratories have the capacity of confirming and most of them are far from rural endemic areas. Specialized laboratories doing cultures, Montenegro skin test and/or PCR are rare and are restricted to research purposes. Microscopic examination of Giemsa-stained smears is the recommended method by the public health authorities. The examination, however, has shown to have a lower sensitivity than culture and PCR (Aviles et al. 1999, Matsumoto et al. 1999, Calvopina et al. 2001b). The sensitivity of smears and cultures decreased if lesions were chronic and due to microbial contamination. The rate of parasite isolation in MCL patients was low as 23%, probably due to chronicity and scarcity of parasites in mucosal lesions (Calvopina et al. 2001a). Parasitological diagnosis is the "gold standard" in leishmaniasis, as it is highly specific (Davies et al. 2000). However, in laboratories from endemic areas of Ecuador there are many false positives on the microscopic examination of Giemsa-stained smears that might due to untrained staff. The direct immunofluorescent antibody (DIFMA) test showed higher sensitivity and rapidity superior to scraping, culture and histology (Chico et al. 1995). The histology staining showed the lowest sensitivities (Aviles et al. 1999, Calvopina et al. 2001b); given the limited utility and dear of histology, this method should be reserved for selected patients.
Recently, several studies in Ecuador have found PCR-based method to be more sensitive (85.4% on average) than classical diagnostic techniques, named slit smears (45.4%), culture (57.2%), and histopathology (34.7%). In some way the sensitivity of PCR depended on the sample taken, from skin biopsies and exudates using cotton swabs it reached to 92% and 93.8%, respectively (Aviles et al. 1999, Calvopina et al. 2001b, Mimori et al. 2002), but using scrape/exudates or syringe-sucked fluid the sensitivities decrease to 70% (Matsumoto et al. 1999). The before collection procedures should be validated on large samples. However, still a concern the false-negative rate showed by PCR that could be as high as 15.4% (Mat-sumoto et al. 1999). The employment of PCR allowed the identification of Leishmania at subgenus or complex level, but recently a study using polymorphism-specific primers yielded to identify species from clinical samples (Mimori et al. 1998). Other advantage of PCR is that diagnosis could be obtained on biopsy samples which are either in formalin or ethanol fixed and paraffin-embedded histological sections (Uezato et al. 1998, Mimori et al. 2002). Finding on PCR amplification of theLeishmania mini-exon gene and karyotype characterization suggest that it would be used for diagnosis and for molecular epidemiology in Ecuador (Katakura et al. 1993, 1998). Nevertheless, in Ecuador, PCR system still expensive, personnel well trained and a reference center to process the samples are still needed.
In Ecuador, the differential diagnosis of leishmaniasis includes a range of skin conditions, which depend on the prevailing disease pattern in the different leishmaniasis-endemic regions. Similar to other endemic countries in Latin America, clinical diagnosis of leishmaniasis can be over-estimated in rural areas where appropriate tests to confirm lesion etiology are absent (Lopez et al. 1993, De Brujin et al. 1993, Calvopina et al. 2001b). In a hospital-based survey Hosokawa et al. (2001) showed that 5/16 (31.2%) were misdiagnosed as having CL and MCL and had been receiving anti-leishmanial drugs. The five misdiagnosed patients had basal cell carcinoma, chro-momycosis and ulcus cruris varicosum. Other skin conditions commonly misdiagnosed as leishmaniasis were furuncle, Bazin's disease, liquen vulgaris, mycetoma, sporotrichosis, myasis, leprosy, and bacterial ulcers. MCL should be differentiated from paracoccidioidomycosis which is prevalent in the tropical lowlands of Ecuador (Fernandez 1990). Leprosy still endemic in rural Ecuador and because is overlapping leishmaniasis-endemic areas could make clinical confusions.
In Ecuador, pentavalent antimonials are the first-line drugs recommended by the Ministry of Health, and indeed WHO; Glucantime® (meglumine antimoniate) is the only available drug and is delivered free of charge by the Ministry of Health, but it can be bought in pharmacies without medical prescription. There is shortage, however, every time principally in rural Ecuador where the disease is prevalent as was noted by Weigel et al. (1994). Some NGOs are also distributing the drug at a subsidized price. The recommended dose is 10-20 mg Sb/kg/d for 10-15 days for CL and 28 days for MCL, by intramuscular injection. However, a significant proportion of patients fail to complete their full course of treatment because of the drug's side-effects and the lengthy painful course of treatment; a full treatment course is also expensive, i.e. US$ 5 to 6 per ampoule. Thus, in an endemic CL subtropical area, where most of the adults are familiar with the disease, only 12% received a full course of Glucantime, while 7.5% got an incomplete course (Weigel et al. 1994). A follow-up 7 years after, the proportions of subjects who had used Glucantime remained low (20%) while the premature drug discontinuance appeared to have doubled (Weigel & Armijos 2001). Therefore, in order to monitor drug side-effects and responsiveness, it is not unusual for MCL patients to be hospitalized for two or three times (Amunarriz 1991). There is no available data on unresponsiveness to Glucantime but is frequently observed mainly in MCL cases and CL acquired in Amazonian lowlands, no study has been done on parasite resistance. The intralesional infiltration with Glucantime alone or combined with intramuscular injection is also popular in endemic areas and recommended for whom systemic chemotherapy is contraindicated. But, this method should not be applied in patients acquiring the infection in the Amazon region where L. (V.) braziliensis has the propensity to evolve into MCL. Second-line drugs (i.e. pentamidine and amphotericin B) are not available in the country.
Several clinical studies to test the efficacy of alternative anti-leishmanial drugs have been carried out in Ecuador. Guderian et al. (1991) tested allopurinol plus pro-benecid against CL, but only 9 (41%) were healed, compared with 96% of Pentostam® group and 75% healing rate for the placebo group. Nonaka et al. (1992) applied paromomycin (PM) ointment as a monotherapy showing to be rather ineffective against CL in the Pacific region with clinical cure in 10-54% of patients. Krause and Kroeger (1994) using PM plus methylbenzethonium (MBCL) for CL in the Pacific region cured 85% with 9% healed spontaneously in the placebo control group, but their follow-up was only 50 days. Armijos et al. (2004) using topical PM-MBCL and PM-urea reach clinical cure in 79.3% and 70% respectively, by 12 weeks of follow-up. Looking for an oral treatment Gomez et al. (1997) administered me-floquine (Mephaquin®) and artesunate (Plasmotrim®) to patients infected in the Pacific region, reporting cure rates of 100%. However, studies in the Pacific of Colombia (Hendrickx et al. 1998) and in the state of Bahia of Brazil (Laguna-Torres et al. 1999) showed that cure rates with mefloquine were similar than for the placebo controls and less than half observed in the Sb(v) group. Itraconazole (Sporanox®) was given orally at high dosage and for 90 days in 13 patients with MCL in the Amazon region, three patients were cured clinically and parasitologically, concluding that itraconazole is not longer effective in this clinical form (Calvopina et al. 2004). Nifurtimox (Lampit®) were administered in the Amazon region with apparently good results (Amunarriz 1991). Despite an uncontrolled study reporting cure rates of 100% using S-nitroso-N-acetylpenicillamine (SNAP), a compound that generates nitric-oxide (Lopez-Jaramillo et al. 1998), a subsequent study showed disappointing results in murine CL and in a clinical trial, showing low cure rate and a high rate of local reactions (Davidson et al. 2000).
The spontaneous healing of CL is common in patients infected in the Andean region, as well as in the subtropical Pacific region that can be as high as 75% (Hashiguchi et al. 1991, Guderian et al. 1991). Hence, patients been infected in the Andes foci usually should not be treated systemically because the lesions are small and self-heal within months leaving a small and imperceptible scar (Hashiguchi et al. 1991) and because there is no risk of metastasis. However, recently leishmaniasis recidivans has been reported in the subtropical Pacific region, such patients should be treated adequately. Patients with severe, sporotrichoid type, multiple lesions (> 3), diabetics and with lesions on the eyelid, the auricle of ear, face and nose which may cause disfiguring scars should also be treated promptly.
PREVENTION AND CONTROL MEASURES
Passive case finding and treatment is the only control measure followed in Ecuador with afore-mentioned limitations in sampling, diagnosis, drug availability, and training of medical staff. A vaccination trial with killed cocktail of promastigotes was conducted in the subtropical-Ecuador (Armijos et al. 1998) showing significant protection during the first 12 months (72.9%). Protection declined until month 60 of follow-up, with no difference in protection rate between the vaccinated and placebo groups (Armijos et al. 2003). Another study was conducted in a similar endemic area using Leishvaccin® plus BCG adjuvant, although two doses of the vaccine resulted in a significant increase in Montenegro skin test conversion, it did not appear to offer any significant protection against development of CL compared to the placebo group (Armijos et al. 2004). As outlined here, further region-specific studies are required on the geographic distribution of disease, sandfly vectors, reservoirs hosts and risk factors in order to identify and develop a leishmaniasis intervention strategy that is cost-effective.
Though the knowledge on the geographical distribution and burden of leishmaniasis in Ecuador has increased over the last years, it is still incomplete and patchy. The situation on the structure of vector and reservoir system is limited. The national recording and reporting system even that is compulsory since 1985, is limited by gaps in information, usually quantitative, sometimes qualitative. As there is little accurate data on country specific prevalence, estimates for the number of people infected and number at risk of infection must still be made based on extrapolations of passive case detection prevalence. Glucantime is still not reaching the majority of those who most need it; delivery of drug should be supported in a comprehensive reporting and actualized data. Most of the studies had been done by private initiatives. Health authorities must be able to translate the actual knowledge into better information, education, and research in accordance with the endemic level, principally in their peripheral health system. In the future, would be important to design trials in order to clarify aspects like El Niño and its impact in annual fluctuation of the vector population as well as the impact of the global warming phenomenon.Imaginative research studies, adequate funds and infrastructure are urgently needed to define the disease epidemiology and to develop a national prevention and control strategy.
To Richard Reithinger for his valuable comments.
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