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Predicting microbiologically defined infection in febrile neutropenic episodes in children: global individual participant data multivariable meta-analysis

BACKGROUND: Risk-stratified management of fever with neutropenia (FN), allows intensive management of high-risk cases and early discharge of low-risk cases. No single, internationally validated, prediction model of the risk of adverse outcomes exists for children and young people. An individual pati...

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Autores principales: Phillips, Robert S, Sung, Lillian, Amman, Roland A, Riley, Richard D, Castagnola, Elio, Haeusler, Gabrielle M, Klaassen, Robert, Tissing, Wim J E, Lehrnbecher, Thomas, Chisholm, Julia, Hakim, Hana, Ranasinghe, Neil, Paesmans, Marianne, Hann, Ian M, Stewart, Lesley A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800297/
https://www.ncbi.nlm.nih.gov/pubmed/26954719
http://dx.doi.org/10.1038/bjc.2016.28
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author Phillips, Robert S
Sung, Lillian
Amman, Roland A
Riley, Richard D
Castagnola, Elio
Haeusler, Gabrielle M
Klaassen, Robert
Tissing, Wim J E
Lehrnbecher, Thomas
Chisholm, Julia
Hakim, Hana
Ranasinghe, Neil
Paesmans, Marianne
Hann, Ian M
Stewart, Lesley A
author_facet Phillips, Robert S
Sung, Lillian
Amman, Roland A
Riley, Richard D
Castagnola, Elio
Haeusler, Gabrielle M
Klaassen, Robert
Tissing, Wim J E
Lehrnbecher, Thomas
Chisholm, Julia
Hakim, Hana
Ranasinghe, Neil
Paesmans, Marianne
Hann, Ian M
Stewart, Lesley A
author_sort Phillips, Robert S
collection PubMed
description BACKGROUND: Risk-stratified management of fever with neutropenia (FN), allows intensive management of high-risk cases and early discharge of low-risk cases. No single, internationally validated, prediction model of the risk of adverse outcomes exists for children and young people. An individual patient data (IPD) meta-analysis was undertaken to devise one. METHODS: The ‘Predicting Infectious Complications in Children with Cancer' (PICNICC) collaboration was formed by parent representatives, international clinical and methodological experts. Univariable and multivariable analyses, using random effects logistic regression, were undertaken to derive and internally validate a risk-prediction model for outcomes of episodes of FN based on clinical and laboratory data at presentation. RESULTS: Data came from 22 different study groups from 15 countries, of 5127 episodes of FN in 3504 patients. There were 1070 episodes in 616 patients from seven studies available for multivariable analysis. Univariable analyses showed associations with microbiologically defined infection (MDI) in many items, including higher temperature, lower white cell counts and acute myeloid leukaemia, but not age. Patients with osteosarcoma/Ewings sarcoma and those with more severe mucositis were associated with a decreased risk of MDI. The predictive model included: malignancy type, temperature, clinically ‘severely unwell', haemoglobin, white cell count and absolute monocyte count. It showed moderate discrimination (AUROC 0.723, 95% confidence interval 0.711–0.759) and good calibration (calibration slope 0.95). The model was robust to bootstrap and cross-validation sensitivity analyses. CONCLUSIONS: This new prediction model for risk of MDI appears accurate. It requires prospective studies assessing implementation to assist clinicians and parents/patients in individualised decision making.
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spelling pubmed-48002972017-03-15 Predicting microbiologically defined infection in febrile neutropenic episodes in children: global individual participant data multivariable meta-analysis Phillips, Robert S Sung, Lillian Amman, Roland A Riley, Richard D Castagnola, Elio Haeusler, Gabrielle M Klaassen, Robert Tissing, Wim J E Lehrnbecher, Thomas Chisholm, Julia Hakim, Hana Ranasinghe, Neil Paesmans, Marianne Hann, Ian M Stewart, Lesley A Br J Cancer Clinical Study BACKGROUND: Risk-stratified management of fever with neutropenia (FN), allows intensive management of high-risk cases and early discharge of low-risk cases. No single, internationally validated, prediction model of the risk of adverse outcomes exists for children and young people. An individual patient data (IPD) meta-analysis was undertaken to devise one. METHODS: The ‘Predicting Infectious Complications in Children with Cancer' (PICNICC) collaboration was formed by parent representatives, international clinical and methodological experts. Univariable and multivariable analyses, using random effects logistic regression, were undertaken to derive and internally validate a risk-prediction model for outcomes of episodes of FN based on clinical and laboratory data at presentation. RESULTS: Data came from 22 different study groups from 15 countries, of 5127 episodes of FN in 3504 patients. There were 1070 episodes in 616 patients from seven studies available for multivariable analysis. Univariable analyses showed associations with microbiologically defined infection (MDI) in many items, including higher temperature, lower white cell counts and acute myeloid leukaemia, but not age. Patients with osteosarcoma/Ewings sarcoma and those with more severe mucositis were associated with a decreased risk of MDI. The predictive model included: malignancy type, temperature, clinically ‘severely unwell', haemoglobin, white cell count and absolute monocyte count. It showed moderate discrimination (AUROC 0.723, 95% confidence interval 0.711–0.759) and good calibration (calibration slope 0.95). The model was robust to bootstrap and cross-validation sensitivity analyses. CONCLUSIONS: This new prediction model for risk of MDI appears accurate. It requires prospective studies assessing implementation to assist clinicians and parents/patients in individualised decision making. Nature Publishing Group 2016-03-15 2016-03-08 /pmc/articles/PMC4800297/ /pubmed/26954719 http://dx.doi.org/10.1038/bjc.2016.28 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Clinical Study
Phillips, Robert S
Sung, Lillian
Amman, Roland A
Riley, Richard D
Castagnola, Elio
Haeusler, Gabrielle M
Klaassen, Robert
Tissing, Wim J E
Lehrnbecher, Thomas
Chisholm, Julia
Hakim, Hana
Ranasinghe, Neil
Paesmans, Marianne
Hann, Ian M
Stewart, Lesley A
Predicting microbiologically defined infection in febrile neutropenic episodes in children: global individual participant data multivariable meta-analysis
title Predicting microbiologically defined infection in febrile neutropenic episodes in children: global individual participant data multivariable meta-analysis
title_full Predicting microbiologically defined infection in febrile neutropenic episodes in children: global individual participant data multivariable meta-analysis
title_fullStr Predicting microbiologically defined infection in febrile neutropenic episodes in children: global individual participant data multivariable meta-analysis
title_full_unstemmed Predicting microbiologically defined infection in febrile neutropenic episodes in children: global individual participant data multivariable meta-analysis
title_short Predicting microbiologically defined infection in febrile neutropenic episodes in children: global individual participant data multivariable meta-analysis
title_sort predicting microbiologically defined infection in febrile neutropenic episodes in children: global individual participant data multivariable meta-analysis
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800297/
https://www.ncbi.nlm.nih.gov/pubmed/26954719
http://dx.doi.org/10.1038/bjc.2016.28
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