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Diagnostic-driven antifungal therapy in neutropenic patients using the D-index and serial serum galactomannan testing()

INTRODUCTION: Invasive mold disease is an important complication of patients with hematologic malignancies, and is associated with high mortality. A diagnostic-driven approach has been an alternative to the classical empiric antifungal therapy. In the present study we tested an algorithm that incorp...

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Autores principales: Garnica, Marcia, Sinhorelo, Aline, Madeira, Laura, Portugal, Rodrigo, Nucci, Marcio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427580/
https://www.ncbi.nlm.nih.gov/pubmed/27280789
http://dx.doi.org/10.1016/j.bjid.2016.04.007
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author Garnica, Marcia
Sinhorelo, Aline
Madeira, Laura
Portugal, Rodrigo
Nucci, Marcio
author_facet Garnica, Marcia
Sinhorelo, Aline
Madeira, Laura
Portugal, Rodrigo
Nucci, Marcio
author_sort Garnica, Marcia
collection PubMed
description INTRODUCTION: Invasive mold disease is an important complication of patients with hematologic malignancies, and is associated with high mortality. A diagnostic-driven approach has been an alternative to the classical empiric antifungal therapy. In the present study we tested an algorithm that incorporated risk stratification using the D-index, serial serum galactomannan and computed tomographic-scan to guide the decision to start antifungal therapy in neutropenic patients. PATIENTS AND METHODS: Between May 2010 and August 2012, patients with acute leukemia in induction remission were prospectively monitored from day 1 of chemotherapy until discharge or death with the D-index and galactomannan. Patients were stratified in low, intermediate and high risk according to the D-index and an extensive workup for invasive mold disease was performed in case of positive galactomannan (≥0.5), persistent fever, or the appearance of clinical manifestations suggestive of invasive mold disease. RESULTS: Among 29 patients, 6 (21%), 11 (38%), and 12 (41%) were classified as high, intermediate, and low risk, respectively. Workup for invasive mold disease was undertaken in 67%, 73% and 58% (p = 0.77) of patients in each risk category, respectively, and antifungal therapy was given to 67%, 54.5%, and 17% (p = 0.07). Proven or probable invasive mold disease was diagnosed in 67%, 45.5%, and in none (p = 0.007) of high, intermediate, and low risk patients, respectively. All patients survived. CONCLUSION: A risk stratification using D-index was a useful instrument to be incorporated in invasive mold disease diagnostic approach, resulting in a more comprehensive antifungal treatment strategy, and to guide an earlier start of treatment in afebrile patients under very high risk.
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spelling pubmed-94275802022-09-01 Diagnostic-driven antifungal therapy in neutropenic patients using the D-index and serial serum galactomannan testing() Garnica, Marcia Sinhorelo, Aline Madeira, Laura Portugal, Rodrigo Nucci, Marcio Braz J Infect Dis Original Article INTRODUCTION: Invasive mold disease is an important complication of patients with hematologic malignancies, and is associated with high mortality. A diagnostic-driven approach has been an alternative to the classical empiric antifungal therapy. In the present study we tested an algorithm that incorporated risk stratification using the D-index, serial serum galactomannan and computed tomographic-scan to guide the decision to start antifungal therapy in neutropenic patients. PATIENTS AND METHODS: Between May 2010 and August 2012, patients with acute leukemia in induction remission were prospectively monitored from day 1 of chemotherapy until discharge or death with the D-index and galactomannan. Patients were stratified in low, intermediate and high risk according to the D-index and an extensive workup for invasive mold disease was performed in case of positive galactomannan (≥0.5), persistent fever, or the appearance of clinical manifestations suggestive of invasive mold disease. RESULTS: Among 29 patients, 6 (21%), 11 (38%), and 12 (41%) were classified as high, intermediate, and low risk, respectively. Workup for invasive mold disease was undertaken in 67%, 73% and 58% (p = 0.77) of patients in each risk category, respectively, and antifungal therapy was given to 67%, 54.5%, and 17% (p = 0.07). Proven or probable invasive mold disease was diagnosed in 67%, 45.5%, and in none (p = 0.007) of high, intermediate, and low risk patients, respectively. All patients survived. CONCLUSION: A risk stratification using D-index was a useful instrument to be incorporated in invasive mold disease diagnostic approach, resulting in a more comprehensive antifungal treatment strategy, and to guide an earlier start of treatment in afebrile patients under very high risk. Elsevier 2016-06-06 /pmc/articles/PMC9427580/ /pubmed/27280789 http://dx.doi.org/10.1016/j.bjid.2016.04.007 Text en © 2016 Elsevier Editora Ltda. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Garnica, Marcia
Sinhorelo, Aline
Madeira, Laura
Portugal, Rodrigo
Nucci, Marcio
Diagnostic-driven antifungal therapy in neutropenic patients using the D-index and serial serum galactomannan testing()
title Diagnostic-driven antifungal therapy in neutropenic patients using the D-index and serial serum galactomannan testing()
title_full Diagnostic-driven antifungal therapy in neutropenic patients using the D-index and serial serum galactomannan testing()
title_fullStr Diagnostic-driven antifungal therapy in neutropenic patients using the D-index and serial serum galactomannan testing()
title_full_unstemmed Diagnostic-driven antifungal therapy in neutropenic patients using the D-index and serial serum galactomannan testing()
title_short Diagnostic-driven antifungal therapy in neutropenic patients using the D-index and serial serum galactomannan testing()
title_sort diagnostic-driven antifungal therapy in neutropenic patients using the d-index and serial serum galactomannan testing()
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427580/
https://www.ncbi.nlm.nih.gov/pubmed/27280789
http://dx.doi.org/10.1016/j.bjid.2016.04.007
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