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Treatment for Post-hemorrhagic Ventricular Dilatation: A Multiple-Treatment Meta-Analysis

Objective: To perform a systematic review and multiple-treatment meta-analysis for the treatment of premature infants with post-hemorrhagic ventricular dilatation (PHVD), to prevent death or long-term neuro-disability. Design/Method: A systematic review was performed using PubMed, EMBASE, and the Co...

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Autores principales: Mahoney, Liam, Luyt, Karen, Harding, David, Odd, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7324764/
https://www.ncbi.nlm.nih.gov/pubmed/32656162
http://dx.doi.org/10.3389/fped.2020.00238
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author Mahoney, Liam
Luyt, Karen
Harding, David
Odd, David
author_facet Mahoney, Liam
Luyt, Karen
Harding, David
Odd, David
author_sort Mahoney, Liam
collection PubMed
description Objective: To perform a systematic review and multiple-treatment meta-analysis for the treatment of premature infants with post-hemorrhagic ventricular dilatation (PHVD), to prevent death or long-term neuro-disability. Design/Method: A systematic review was performed using PubMed, EMBASE, and the Cochrane Library. A free-word search was performed to identify likely relevant literature intervention trials of PHVD in preterm infants. Initially, network mapping was performed followed by performing a Bayesian random-effects model using the Markov chain Monte Carlo method. Areas under the cumulative ranking curve (SUCRA) were calculated as a measure of the probability that each intervention was likely to be the 1st, 2nd, 3rd, etc. best therapy. Primary outcome measure was death or moderate or severe neurodevelopmental outcome at or beyond 12 months of corrected age. Results: Ten different trials were identified, enrolling 700 individuals (449 for the primary outcome). Seven intervention categories were identified, and of the 15 possible pair comparisons, 6 have been studied directly. In the multiple-treatment meta-analysis, no comparison reached conventional levels of statistical significance. Drainage Irrigation and Fibrinolytic Therapy (DRIFT) had the highest probability of being the best treatment for the primary outcome (82.1%), followed by CSF removal (10.8%), conservative management (6.7%), and then diuretic therapy (0.4%). Conclusions: PHVD is a significant cause of death and disability in developed countries, yet few therapeutic options have so far been trialed. While new therapies are urgently needed for these infants, at present, NMA shows that DRIFT appears to be the most likely candidate to improve outcomes after sIVH.
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spelling pubmed-73247642020-07-10 Treatment for Post-hemorrhagic Ventricular Dilatation: A Multiple-Treatment Meta-Analysis Mahoney, Liam Luyt, Karen Harding, David Odd, David Front Pediatr Pediatrics Objective: To perform a systematic review and multiple-treatment meta-analysis for the treatment of premature infants with post-hemorrhagic ventricular dilatation (PHVD), to prevent death or long-term neuro-disability. Design/Method: A systematic review was performed using PubMed, EMBASE, and the Cochrane Library. A free-word search was performed to identify likely relevant literature intervention trials of PHVD in preterm infants. Initially, network mapping was performed followed by performing a Bayesian random-effects model using the Markov chain Monte Carlo method. Areas under the cumulative ranking curve (SUCRA) were calculated as a measure of the probability that each intervention was likely to be the 1st, 2nd, 3rd, etc. best therapy. Primary outcome measure was death or moderate or severe neurodevelopmental outcome at or beyond 12 months of corrected age. Results: Ten different trials were identified, enrolling 700 individuals (449 for the primary outcome). Seven intervention categories were identified, and of the 15 possible pair comparisons, 6 have been studied directly. In the multiple-treatment meta-analysis, no comparison reached conventional levels of statistical significance. Drainage Irrigation and Fibrinolytic Therapy (DRIFT) had the highest probability of being the best treatment for the primary outcome (82.1%), followed by CSF removal (10.8%), conservative management (6.7%), and then diuretic therapy (0.4%). Conclusions: PHVD is a significant cause of death and disability in developed countries, yet few therapeutic options have so far been trialed. While new therapies are urgently needed for these infants, at present, NMA shows that DRIFT appears to be the most likely candidate to improve outcomes after sIVH. Frontiers Media S.A. 2020-06-23 /pmc/articles/PMC7324764/ /pubmed/32656162 http://dx.doi.org/10.3389/fped.2020.00238 Text en Copyright © 2020 Mahoney, Luyt, Harding and Odd. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Mahoney, Liam
Luyt, Karen
Harding, David
Odd, David
Treatment for Post-hemorrhagic Ventricular Dilatation: A Multiple-Treatment Meta-Analysis
title Treatment for Post-hemorrhagic Ventricular Dilatation: A Multiple-Treatment Meta-Analysis
title_full Treatment for Post-hemorrhagic Ventricular Dilatation: A Multiple-Treatment Meta-Analysis
title_fullStr Treatment for Post-hemorrhagic Ventricular Dilatation: A Multiple-Treatment Meta-Analysis
title_full_unstemmed Treatment for Post-hemorrhagic Ventricular Dilatation: A Multiple-Treatment Meta-Analysis
title_short Treatment for Post-hemorrhagic Ventricular Dilatation: A Multiple-Treatment Meta-Analysis
title_sort treatment for post-hemorrhagic ventricular dilatation: a multiple-treatment meta-analysis
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7324764/
https://www.ncbi.nlm.nih.gov/pubmed/32656162
http://dx.doi.org/10.3389/fped.2020.00238
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