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Efficacy of antibiotic therapy for peritoneal dialysis-associated peritonitis: a proportional meta-analysis

BACKGROUND: The choice of antimicrobials for initial treatment of peritoneal dialysis (PD)-related peritonitis is crucial for a favorable outcome. There is no consensus about the best therapy; few prospective controlled studies have been published, and the only published systematic reviews did not r...

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Autores principales: Barretti, Pasqual, Doles, João Vitor Pereira, Pinotti, Douglas Gonçalves, El Dib, Regina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4262222/
https://www.ncbi.nlm.nih.gov/pubmed/25135487
http://dx.doi.org/10.1186/1471-2334-14-445
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author Barretti, Pasqual
Doles, João Vitor Pereira
Pinotti, Douglas Gonçalves
El Dib, Regina
author_facet Barretti, Pasqual
Doles, João Vitor Pereira
Pinotti, Douglas Gonçalves
El Dib, Regina
author_sort Barretti, Pasqual
collection PubMed
description BACKGROUND: The choice of antimicrobials for initial treatment of peritoneal dialysis (PD)-related peritonitis is crucial for a favorable outcome. There is no consensus about the best therapy; few prospective controlled studies have been published, and the only published systematic reviews did not report superiority of any class of antimicrobials. The objective of this review was to analyze the results of PD peritonitis treatment in adult patients by employing a new methodology, the proportional meta-analysis. METHODS: A review of the literature was conducted. There was no language restriction. Studies were obtained from MEDLINE, EMBASE, and LILACS. The inclusion criteria were: (a) case series and RCTs with the number of reported patients in each study greater than five, (b) use of any antibiotic therapy for initial treatment (e.g., cefazolin plus gentamicin or vancomycin plus gentamicin), for Gram-positive (e.g., vancomycin or a first generation cephalosporin), or for Gram-negative rods (e.g., gentamicin, ceftazidime, and fluoroquinolone), (c) patients with PD-related peritonitis, and (d) studies specifying the rates of resolution. A proportional meta-analysis was performed on outcomes using a random-effects model, and the pooled resolution rates were calculated. RESULTS: A total of 64 studies (32 for initial treatment and negative culture, 28 reporting treatment for Gram-positive rods and 24 reporting treatment for Gram-negative rods) and 21 RCTs met all inclusion criteria (14 for initial treatment and negative culture, 8 reporting treatment for Gram-positive rods and 8 reporting treatment for Gram-negative rods). The pooled resolution rate of ceftazidime plus glycopeptide as initial treatment (pooled proportion = 86% [95% CI 0.82–0.89]) was significantly higher than first generation cephalosporin plus aminoglycosides (pooled proportion = 66% [95% CI 0.57–0.75]) and significantly higher than glycopeptides plus aminoglycosides (pooled proportion = 75% [95% CI 0.69–0.80]. Other comparisons of regimens used for either initial treatment, treatment for Gram-positive rods or Gram-negative rods did not show statistically significant differences. CONCLUSION: We showed that the association of a glycopeptide plus ceftazidime is superior to other regimens for initial treatment of PD peritonitis. This result should be carefully analyzed and does not exclude the necessity of monitoring the local microbiologic profile in each dialysis center to choice the initial therapeutic protocol. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2334-14-445) contains supplementary material, which is available to authorized users.
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spelling pubmed-42622222014-12-11 Efficacy of antibiotic therapy for peritoneal dialysis-associated peritonitis: a proportional meta-analysis Barretti, Pasqual Doles, João Vitor Pereira Pinotti, Douglas Gonçalves El Dib, Regina BMC Infect Dis Research Article BACKGROUND: The choice of antimicrobials for initial treatment of peritoneal dialysis (PD)-related peritonitis is crucial for a favorable outcome. There is no consensus about the best therapy; few prospective controlled studies have been published, and the only published systematic reviews did not report superiority of any class of antimicrobials. The objective of this review was to analyze the results of PD peritonitis treatment in adult patients by employing a new methodology, the proportional meta-analysis. METHODS: A review of the literature was conducted. There was no language restriction. Studies were obtained from MEDLINE, EMBASE, and LILACS. The inclusion criteria were: (a) case series and RCTs with the number of reported patients in each study greater than five, (b) use of any antibiotic therapy for initial treatment (e.g., cefazolin plus gentamicin or vancomycin plus gentamicin), for Gram-positive (e.g., vancomycin or a first generation cephalosporin), or for Gram-negative rods (e.g., gentamicin, ceftazidime, and fluoroquinolone), (c) patients with PD-related peritonitis, and (d) studies specifying the rates of resolution. A proportional meta-analysis was performed on outcomes using a random-effects model, and the pooled resolution rates were calculated. RESULTS: A total of 64 studies (32 for initial treatment and negative culture, 28 reporting treatment for Gram-positive rods and 24 reporting treatment for Gram-negative rods) and 21 RCTs met all inclusion criteria (14 for initial treatment and negative culture, 8 reporting treatment for Gram-positive rods and 8 reporting treatment for Gram-negative rods). The pooled resolution rate of ceftazidime plus glycopeptide as initial treatment (pooled proportion = 86% [95% CI 0.82–0.89]) was significantly higher than first generation cephalosporin plus aminoglycosides (pooled proportion = 66% [95% CI 0.57–0.75]) and significantly higher than glycopeptides plus aminoglycosides (pooled proportion = 75% [95% CI 0.69–0.80]. Other comparisons of regimens used for either initial treatment, treatment for Gram-positive rods or Gram-negative rods did not show statistically significant differences. CONCLUSION: We showed that the association of a glycopeptide plus ceftazidime is superior to other regimens for initial treatment of PD peritonitis. This result should be carefully analyzed and does not exclude the necessity of monitoring the local microbiologic profile in each dialysis center to choice the initial therapeutic protocol. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2334-14-445) contains supplementary material, which is available to authorized users. BioMed Central 2014-08-18 /pmc/articles/PMC4262222/ /pubmed/25135487 http://dx.doi.org/10.1186/1471-2334-14-445 Text en © Barretti et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Barretti, Pasqual
Doles, João Vitor Pereira
Pinotti, Douglas Gonçalves
El Dib, Regina
Efficacy of antibiotic therapy for peritoneal dialysis-associated peritonitis: a proportional meta-analysis
title Efficacy of antibiotic therapy for peritoneal dialysis-associated peritonitis: a proportional meta-analysis
title_full Efficacy of antibiotic therapy for peritoneal dialysis-associated peritonitis: a proportional meta-analysis
title_fullStr Efficacy of antibiotic therapy for peritoneal dialysis-associated peritonitis: a proportional meta-analysis
title_full_unstemmed Efficacy of antibiotic therapy for peritoneal dialysis-associated peritonitis: a proportional meta-analysis
title_short Efficacy of antibiotic therapy for peritoneal dialysis-associated peritonitis: a proportional meta-analysis
title_sort efficacy of antibiotic therapy for peritoneal dialysis-associated peritonitis: a proportional meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4262222/
https://www.ncbi.nlm.nih.gov/pubmed/25135487
http://dx.doi.org/10.1186/1471-2334-14-445
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