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Therapeutic alternatives in painful diabetic neuropathy: a meta-analysis of randomized controlled trials

BACKGROUND: One of the most frequent problems caused by diabetes is the so called painful diabetic neuropathy. This condition can be treated through numerous types of therapy. The purpose of this study was to analyze, as a meta-analysis, different treatments used to alleviate painful diabetic neurop...

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Autores principales: Vilar, Samuel, Castillo, Jose Manuel, Munuera Martínez, Pedro V., Reina, María, Pabón, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pain Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177536/
https://www.ncbi.nlm.nih.gov/pubmed/30310550
http://dx.doi.org/10.3344/kjp.2018.31.4.253
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author Vilar, Samuel
Castillo, Jose Manuel
Munuera Martínez, Pedro V.
Reina, María
Pabón, Manuel
author_facet Vilar, Samuel
Castillo, Jose Manuel
Munuera Martínez, Pedro V.
Reina, María
Pabón, Manuel
author_sort Vilar, Samuel
collection PubMed
description BACKGROUND: One of the most frequent problems caused by diabetes is the so called painful diabetic neuropathy. This condition can be treated through numerous types of therapy. The purpose of this study was to analyze, as a meta-analysis, different treatments used to alleviate painful diabetic neuropathy, with the aim of generating results that help making decisions when applying such treatments to tackle this pathology. METHODS: A search was conducted in the main databases for Health Sciences, such as PUBMED, Web of Science (WOS), and IME biomedicina (Spanish Medical Reports in Biomedicine), to gather randomized controlled trials about treatments used for painful diabetic neuropathy. The analyzed studies were required to meet the inclusion criteria selected, especially those results related to pain intensity. RESULTS: Nine randomized controlled trials were chosen. The meta-analysis shows significant positive effects for those treatments based on tapentadol [g: −1.333, 95% CI (−1.594; −1.072), P < 0.05], duloxetine [g: −1.622, 95 % CI (−1.650; −1.594), P < 0.05], pregabalin [g: −0.607, 95% CI (−0.980; −0.325), P < 0.05], and clonidine [g: −0.242, 95 % CI (−0.543; −0.058), P < 0.05]. CONCLUSIONS: This meta-analysis indicates the effectiveness of the treatments based on duloxetine, gabapentin and pregabalin, as well as other drugs, such as tapentadol and topic clonidine, whose use is better prescribed in more specific situations. The results provided can help increase the knowledge about the treatment of painful diabetic neuropathy and also in the making of clinical practice guidelines for healthcare professionals.
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spelling pubmed-61775362018-10-11 Therapeutic alternatives in painful diabetic neuropathy: a meta-analysis of randomized controlled trials Vilar, Samuel Castillo, Jose Manuel Munuera Martínez, Pedro V. Reina, María Pabón, Manuel Korean J Pain Review Article BACKGROUND: One of the most frequent problems caused by diabetes is the so called painful diabetic neuropathy. This condition can be treated through numerous types of therapy. The purpose of this study was to analyze, as a meta-analysis, different treatments used to alleviate painful diabetic neuropathy, with the aim of generating results that help making decisions when applying such treatments to tackle this pathology. METHODS: A search was conducted in the main databases for Health Sciences, such as PUBMED, Web of Science (WOS), and IME biomedicina (Spanish Medical Reports in Biomedicine), to gather randomized controlled trials about treatments used for painful diabetic neuropathy. The analyzed studies were required to meet the inclusion criteria selected, especially those results related to pain intensity. RESULTS: Nine randomized controlled trials were chosen. The meta-analysis shows significant positive effects for those treatments based on tapentadol [g: −1.333, 95% CI (−1.594; −1.072), P < 0.05], duloxetine [g: −1.622, 95 % CI (−1.650; −1.594), P < 0.05], pregabalin [g: −0.607, 95% CI (−0.980; −0.325), P < 0.05], and clonidine [g: −0.242, 95 % CI (−0.543; −0.058), P < 0.05]. CONCLUSIONS: This meta-analysis indicates the effectiveness of the treatments based on duloxetine, gabapentin and pregabalin, as well as other drugs, such as tapentadol and topic clonidine, whose use is better prescribed in more specific situations. The results provided can help increase the knowledge about the treatment of painful diabetic neuropathy and also in the making of clinical practice guidelines for healthcare professionals. The Korean Pain Society 2018-10 2018-10-01 /pmc/articles/PMC6177536/ /pubmed/30310550 http://dx.doi.org/10.3344/kjp.2018.31.4.253 Text en Copyright © The Korean Pain Society, 2018 http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Vilar, Samuel
Castillo, Jose Manuel
Munuera Martínez, Pedro V.
Reina, María
Pabón, Manuel
Therapeutic alternatives in painful diabetic neuropathy: a meta-analysis of randomized controlled trials
title Therapeutic alternatives in painful diabetic neuropathy: a meta-analysis of randomized controlled trials
title_full Therapeutic alternatives in painful diabetic neuropathy: a meta-analysis of randomized controlled trials
title_fullStr Therapeutic alternatives in painful diabetic neuropathy: a meta-analysis of randomized controlled trials
title_full_unstemmed Therapeutic alternatives in painful diabetic neuropathy: a meta-analysis of randomized controlled trials
title_short Therapeutic alternatives in painful diabetic neuropathy: a meta-analysis of randomized controlled trials
title_sort therapeutic alternatives in painful diabetic neuropathy: a meta-analysis of randomized controlled trials
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177536/
https://www.ncbi.nlm.nih.gov/pubmed/30310550
http://dx.doi.org/10.3344/kjp.2018.31.4.253
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