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Efficacy of pentoxifylline treatment for neonatal sepsis: a meta-analysis of randomized controlled studies

INTRODUCTION: Pentoxifylline may be an important approach to treat neonatal sepsis. However, its use has not been well established. We conduct a systematic review and meta-analysis to evaluate the efficacy of pentoxifylline treatment for neonatal sepsis. METHODS: PubMed, Embase, and the Cochrane Cen...

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Autores principales: Tian, Jun, Shen, Peifang, Pan, Kaiyu, Zhou, Qiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6704640/
https://www.ncbi.nlm.nih.gov/pubmed/31439016
http://dx.doi.org/10.1186/s13052-019-0697-8
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author Tian, Jun
Shen, Peifang
Pan, Kaiyu
Zhou, Qiong
author_facet Tian, Jun
Shen, Peifang
Pan, Kaiyu
Zhou, Qiong
author_sort Tian, Jun
collection PubMed
description INTRODUCTION: Pentoxifylline may be an important approach to treat neonatal sepsis. However, its use has not been well established. We conduct a systematic review and meta-analysis to evaluate the efficacy of pentoxifylline treatment for neonatal sepsis. METHODS: PubMed, Embase, and the Cochrane Central Register of Controlled Trials are searched. Randomized controlled trials (RCTs) assessing the influence of pentoxifylline treatment on neonatal sepsis are included. Two investigators independently have searched articles, extracted data, and assessed the quality of included studies. This meta-analysis is performed using the random-effect model. RESULTS: Seven RCTs involving 439 patients are included in the meta-analysis. Compared with control intervention for neonatal sepsis, pentoxifylline treatment is associated with reduced hospital stay (Std. MD = -0.61; 95% CI = -0.93 to − 0.29; P = 0.0002) and metabolic acidosis (RR = 0.38; 95% CI = 0.22 to 0.66; P = 0.0006), but has no remarkable impact on mortality (RR = 0.59; 95% CI = 0.30 to 1.16; P = 0.13), serum TNF-α (Std. MD = -0.38; 95% CI = -1.29 to 0.52; P = 0.41), serum CRP (Std. MD = -0.25; 95% CI = -0.92 to 0.42; P = 0.47), plasma IL-6 (Std. MD = -0.13; 95% CI = -0.41 to 0.15; P = 0.37), disseminated intravascular coagulopathy (RR = 0.55; 95% CI = 0.25 to 1.21; P = 0.14), and oliguria/anuria (RR = 0.77; 95% CI = 0.28 to 2.16; P = 0.62). In addition, pentoxifylline treatment can significantly reduce mortality (RR = 0.50; 95% CI = 0.29 to 0.88; P = 0.02) after excluding the study conducted by Akdag during the sensivity analysis. CONCLUSIONS: Pentoxifylline treatment may be associated with reduced mortality and hospital stay in neonatal sepsis.
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spelling pubmed-67046402019-08-22 Efficacy of pentoxifylline treatment for neonatal sepsis: a meta-analysis of randomized controlled studies Tian, Jun Shen, Peifang Pan, Kaiyu Zhou, Qiong Ital J Pediatr Review INTRODUCTION: Pentoxifylline may be an important approach to treat neonatal sepsis. However, its use has not been well established. We conduct a systematic review and meta-analysis to evaluate the efficacy of pentoxifylline treatment for neonatal sepsis. METHODS: PubMed, Embase, and the Cochrane Central Register of Controlled Trials are searched. Randomized controlled trials (RCTs) assessing the influence of pentoxifylline treatment on neonatal sepsis are included. Two investigators independently have searched articles, extracted data, and assessed the quality of included studies. This meta-analysis is performed using the random-effect model. RESULTS: Seven RCTs involving 439 patients are included in the meta-analysis. Compared with control intervention for neonatal sepsis, pentoxifylline treatment is associated with reduced hospital stay (Std. MD = -0.61; 95% CI = -0.93 to − 0.29; P = 0.0002) and metabolic acidosis (RR = 0.38; 95% CI = 0.22 to 0.66; P = 0.0006), but has no remarkable impact on mortality (RR = 0.59; 95% CI = 0.30 to 1.16; P = 0.13), serum TNF-α (Std. MD = -0.38; 95% CI = -1.29 to 0.52; P = 0.41), serum CRP (Std. MD = -0.25; 95% CI = -0.92 to 0.42; P = 0.47), plasma IL-6 (Std. MD = -0.13; 95% CI = -0.41 to 0.15; P = 0.37), disseminated intravascular coagulopathy (RR = 0.55; 95% CI = 0.25 to 1.21; P = 0.14), and oliguria/anuria (RR = 0.77; 95% CI = 0.28 to 2.16; P = 0.62). In addition, pentoxifylline treatment can significantly reduce mortality (RR = 0.50; 95% CI = 0.29 to 0.88; P = 0.02) after excluding the study conducted by Akdag during the sensivity analysis. CONCLUSIONS: Pentoxifylline treatment may be associated with reduced mortality and hospital stay in neonatal sepsis. BioMed Central 2019-08-22 /pmc/articles/PMC6704640/ /pubmed/31439016 http://dx.doi.org/10.1186/s13052-019-0697-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Tian, Jun
Shen, Peifang
Pan, Kaiyu
Zhou, Qiong
Efficacy of pentoxifylline treatment for neonatal sepsis: a meta-analysis of randomized controlled studies
title Efficacy of pentoxifylline treatment for neonatal sepsis: a meta-analysis of randomized controlled studies
title_full Efficacy of pentoxifylline treatment for neonatal sepsis: a meta-analysis of randomized controlled studies
title_fullStr Efficacy of pentoxifylline treatment for neonatal sepsis: a meta-analysis of randomized controlled studies
title_full_unstemmed Efficacy of pentoxifylline treatment for neonatal sepsis: a meta-analysis of randomized controlled studies
title_short Efficacy of pentoxifylline treatment for neonatal sepsis: a meta-analysis of randomized controlled studies
title_sort efficacy of pentoxifylline treatment for neonatal sepsis: a meta-analysis of randomized controlled studies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6704640/
https://www.ncbi.nlm.nih.gov/pubmed/31439016
http://dx.doi.org/10.1186/s13052-019-0697-8
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