Predictive models for the diagnostic of human visceral leishmaniasis in Brazil.
<h4>Background and objectives</h4>In Brazil, as in many other affected countries, a large proportion of visceral leishmaniasis (VL) occurs in remote locations and treatment is often performed on basis of clinical suspicion. This study aimed at developing predictive models to help with th...
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doaj-ff6f4a54d2c7435da1caff1611c62e5e2021-03-03T08:06:57ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352012-01-0162e154210.1371/journal.pntd.0001542Predictive models for the diagnostic of human visceral leishmaniasis in Brazil.Tália S Machado de AssisAna RabelloGuilherme L Werneck<h4>Background and objectives</h4>In Brazil, as in many other affected countries, a large proportion of visceral leishmaniasis (VL) occurs in remote locations and treatment is often performed on basis of clinical suspicion. This study aimed at developing predictive models to help with the clinical management of VL in patients with suggestive clinical of disease.<h4>Methods</h4>Cases of VL (n = 213) had the diagnosis confirmed by parasitological method, non-cases (n = 119) presented suggestive clinical presentation of VL but a negative parasitological diagnosis and a firm diagnosis of another disease. The original data set was divided into two samples for generation and validation of the prediction models. Prediction models based on clinical signs and symptoms, results of laboratory exams and results of five different serological tests, were developed by means of logistic regression and classification and regression trees (CART). From these models, clinical-laboratory and diagnostic prediction scores were generated. The area under the receiver operator characteristic curve, sensitivity, specificity, and positive predictive value were used to evaluate the models' performance.<h4>Results</h4>Based on the variables splenomegaly, presence of cough and leukopenia and on the results of five serological tests it was possible to generate six predictive models using logistic regression, showing sensitivity ranging from 90.1 to 99.0% and specificity ranging from 53.0 to 97.2%. Based on the variables splenomegaly, leukopenia, cough, age and weight loss and on the results of five serological tests six predictive models were generated using CART with sensitivity ranging from 90.1 to 97.2% and specificity ranging from 68.4 to 97.4%. The models composed of clinical-laboratory variables and the rk39 rapid test showed the best performance.<h4>Conclusion</h4>The predictive models showed to be a potential useful tool to assist healthcare systems and control programs in their strategical choices, contributing to more efficient and more rational allocation of healthcare resources.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22389742/pdf/?tool=EBI |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tália S Machado de Assis Ana Rabello Guilherme L Werneck |
spellingShingle |
Tália S Machado de Assis Ana Rabello Guilherme L Werneck Predictive models for the diagnostic of human visceral leishmaniasis in Brazil. PLoS Neglected Tropical Diseases |
author_facet |
Tália S Machado de Assis Ana Rabello Guilherme L Werneck |
author_sort |
Tália S Machado de Assis |
title |
Predictive models for the diagnostic of human visceral leishmaniasis in Brazil. |
title_short |
Predictive models for the diagnostic of human visceral leishmaniasis in Brazil. |
title_full |
Predictive models for the diagnostic of human visceral leishmaniasis in Brazil. |
title_fullStr |
Predictive models for the diagnostic of human visceral leishmaniasis in Brazil. |
title_full_unstemmed |
Predictive models for the diagnostic of human visceral leishmaniasis in Brazil. |
title_sort |
predictive models for the diagnostic of human visceral leishmaniasis in brazil. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Neglected Tropical Diseases |
issn |
1935-2727 1935-2735 |
publishDate |
2012-01-01 |
description |
<h4>Background and objectives</h4>In Brazil, as in many other affected countries, a large proportion of visceral leishmaniasis (VL) occurs in remote locations and treatment is often performed on basis of clinical suspicion. This study aimed at developing predictive models to help with the clinical management of VL in patients with suggestive clinical of disease.<h4>Methods</h4>Cases of VL (n = 213) had the diagnosis confirmed by parasitological method, non-cases (n = 119) presented suggestive clinical presentation of VL but a negative parasitological diagnosis and a firm diagnosis of another disease. The original data set was divided into two samples for generation and validation of the prediction models. Prediction models based on clinical signs and symptoms, results of laboratory exams and results of five different serological tests, were developed by means of logistic regression and classification and regression trees (CART). From these models, clinical-laboratory and diagnostic prediction scores were generated. The area under the receiver operator characteristic curve, sensitivity, specificity, and positive predictive value were used to evaluate the models' performance.<h4>Results</h4>Based on the variables splenomegaly, presence of cough and leukopenia and on the results of five serological tests it was possible to generate six predictive models using logistic regression, showing sensitivity ranging from 90.1 to 99.0% and specificity ranging from 53.0 to 97.2%. Based on the variables splenomegaly, leukopenia, cough, age and weight loss and on the results of five serological tests six predictive models were generated using CART with sensitivity ranging from 90.1 to 97.2% and specificity ranging from 68.4 to 97.4%. The models composed of clinical-laboratory variables and the rk39 rapid test showed the best performance.<h4>Conclusion</h4>The predictive models showed to be a potential useful tool to assist healthcare systems and control programs in their strategical choices, contributing to more efficient and more rational allocation of healthcare resources. |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22389742/pdf/?tool=EBI |
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