scholarly journals Characterization of digestive disorders of patients with chronic Chagas disease in Cochabamba, Bolivia

Heliyon ◽  
2019 ◽  
Vol 5 (2) ◽  
pp. e01206 ◽  
Author(s):  
Jimy-Jose Pinto ◽  
Maria-Jesus Pinazo ◽  
Jaime Saravia ◽  
Ingrid Gainsborg ◽  
Helmut-Ramon Magne ◽  
...  
2000 ◽  
Vol 156 (5) ◽  
pp. 1805-1809 ◽  
Author(s):  
Annamaria R. Vago ◽  
Luciana O. Andrade ◽  
Adriana A. Leite ◽  
Débora d'Ávila Reis ◽  
Andrea M. Macedo ◽  
...  

2021 ◽  
Vol 15 (8) ◽  
pp. e0009680
Author(s):  
Erika Alessandra Pellison Nunes da Costa ◽  
Cassiano Victória ◽  
Carlos Magno Castelo Branco Fortaleza

American trypanosomiasis (Chagas disease, CD) affects circa 7 million persons worldwide. While of those persons present the asymptomatic, indeterminate chronic form (ICF), many will eventually progress to cardiac or digestive disorders. We studied a nonconcurrent (retrospective) cohort of patients attending an outpatient CD clinic in Southeastern Brazil, who were admitted while presenting the ICF in the period from 1998 through 2018 and followed until 2019. The outcomes of interest were the progression to cardiac or digestive CD forms. We were also interested in analyzing the impact of Benznidazole therapy on the progression of the disease. Extensive review of medical charts and laboratory files was conducted, collecting data up to year 2019. Demographics (upon inclusion), body mass index, comorbidities (including the Charlson index) and use of Benznidazole were recorded. The outcomes were defined by abnormalities in those test that could not be attributed to other causes. Statistical analysis included univariate and multivariable Cox regression models. Among 379 subjects included in the study, 87 (22.9%) and 100 (26.4%) progressed to cardiac and digestive forms, respectively. In the final multivariable model, cardiac disorders were positively associated with previous coronary syndrome (Hazzard Ratio [HR], 2.42; 95% Confidence Interval [CI], 1.53–3.81) and negatively associated with Benznidazole therapy (HR, 0.26; 95%CI, 0.11–0.60). On the other hand, female gender was the only independent predictor of progression to digestive forms (HR, 1.56; 95%CI, 1.03–2.38). Our results point to the impact of comorbidities on progression do cardiac CD, with possible benefit of the use of Benznidazole.


1997 ◽  
Vol 20 (10) ◽  
pp. 865-869 ◽  
Author(s):  
Hugo A. Carrasco G. ◽  
Leopoldo Olmos ◽  
Alberto Dipaolo ◽  
Marino Alarcon ◽  
José Burguera ◽  
...  

1996 ◽  
Vol 34 (8) ◽  
pp. 1957-1962 ◽  
Author(s):  
R S Corral ◽  
J Altcheh ◽  
S R Alexandre ◽  
S Grinstein ◽  
H Freilij ◽  
...  

Stress ◽  
2009 ◽  
Vol 12 (2) ◽  
pp. 144-151 ◽  
Author(s):  
Leony Cristina Caetano ◽  
Vânia Brazão ◽  
Marina Del Vecchio Filipin ◽  
Fabricia Helena Santello ◽  
Luana Naiara Caetano ◽  
...  

2021 ◽  
Author(s):  
Kárita Cláudia Freitas Lidani ◽  
Fabiana Antunes Andrade ◽  
Marcia Holsbach Beltrame ◽  
Indira Chakravarti ◽  
Maria Regina Tizzot ◽  
...  

2016 ◽  
Vol 54 (6) ◽  
pp. 1566-1572 ◽  
Author(s):  
Alba Abras ◽  
Montserrat Gállego ◽  
Teresa Llovet ◽  
Silvia Tebar ◽  
Mercedes Herrero ◽  
...  

Chagas disease has spread to areas that are nonendemic for the disease with human migration. Since no single reference standard test is available, serological diagnosis of chronic Chagas disease requires at least two tests. New-generation techniques have significantly improved the accuracy of Chagas disease diagnosis by the use of a large mixture of recombinant antigens with different detection systems, such as chemiluminescence. The aim of the present study was to assess the overall accuracy of a new-generation kit, the Architect Chagas (cutoff, ≥1 sample relative light units/cutoff value [S/CO]), as a single technique for the diagnosis of chronic Chagas disease. The Architect Chagas showed a sensitivity of 100% (95% confidence interval [CI], 99.5 to 100%) and a specificity of 97.6% (95% CI, 95.2 to 99.9%). Five out of six false-positive serum samples were a consequence of cross-reactivity withLeishmaniaspp., and all of them achieved results of <5 S/CO. We propose the Architect Chagas as a single technique for screening in blood banks and for routine diagnosis in clinical laboratories. Only gray-zone and positive sera with a result of ≤6 S/CO would need to be confirmed by a second serological assay, thus avoiding false-positive sera and the problem of cross-reactivity withLeishmaniaspecies. The application of this proposal would result in important savings in the cost of Chagas disease diagnosis and therefore in the management and control of the disease.


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