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Treatment of Ventilator-associated Pneumonia with High-dose Colistin Under Continuous Veno-venous Hemofiltration
BACKGROUND AND OBJECTIVES: High-dose colistin (COL) ensures adequate treatment of pneumonia caused by multidrug resistant gram-negative bacteria (MDR-GNB) but must be weighed against a higher risk of nephrotoxicity. Continuous veno-venous hemofiltration (CVVH) clears COL by filtering and membrane ad...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sciendo
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795054/ https://www.ncbi.nlm.nih.gov/pubmed/31637180 http://dx.doi.org/10.2478/jtim-2019-0022 |
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author | Spapen, Herbert van Laethem, Johan Hites, Maya Verdoodt, An Diltoer, Marc Honoré, Patrick M. |
author_facet | Spapen, Herbert van Laethem, Johan Hites, Maya Verdoodt, An Diltoer, Marc Honoré, Patrick M. |
author_sort | Spapen, Herbert |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: High-dose colistin (COL) ensures adequate treatment of pneumonia caused by multidrug resistant gram-negative bacteria (MDR-GNB) but must be weighed against a higher risk of nephrotoxicity. Continuous veno-venous hemofiltration (CVVH) clears COL by filtering and membrane adsorption that permits to avoid dose accumulation and excessively high peak concentrations. We evaluated clinical/microbiological efficacy of the high-dose COL treatment under CVVH in patients with newly diagnosed MDR-GNB ventilator-associated pneumonia (VAP). METHODS: Observational cohort study in critically ill adult patients with MDR-GNB VAP. Colistimethate sodium (CMS) was administered as a 9 million international units (MIU) of loading dose followed by 3 × 4.5 MIU daily. CVVH was performed over a highly adsorptive membrane. Clinical and microbiological efficacies were assessed at the end of therapy. In survivors, serum creatinine level was evaluated before and at the end of therapy. RESULTS: Fourteen patients (8 male patients, aged 57 ± 14 years) were consecutively included. Isolated pathogens were Pseudomonas aeruginosa in 7, Klebsiella pneumoniae in 5, and other Enterobacteriaceae in 2 patients. A favorable clinical response was observed in 9 patients (64%). Full and presumed microbiological eradication was observed in 12 patients (86%). Two patients were diagnosed with Stage 1 acute kidney injury. CONCLUSIONS: In patients with MDR-GNB VAP, CVVH may represent an interesting option to enable effective high-dose COL treatment. |
format | Online Article Text |
id | pubmed-6795054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Sciendo |
record_format | MEDLINE/PubMed |
spelling | pubmed-67950542019-10-21 Treatment of Ventilator-associated Pneumonia with High-dose Colistin Under Continuous Veno-venous Hemofiltration Spapen, Herbert van Laethem, Johan Hites, Maya Verdoodt, An Diltoer, Marc Honoré, Patrick M. J Transl Int Med Original Article BACKGROUND AND OBJECTIVES: High-dose colistin (COL) ensures adequate treatment of pneumonia caused by multidrug resistant gram-negative bacteria (MDR-GNB) but must be weighed against a higher risk of nephrotoxicity. Continuous veno-venous hemofiltration (CVVH) clears COL by filtering and membrane adsorption that permits to avoid dose accumulation and excessively high peak concentrations. We evaluated clinical/microbiological efficacy of the high-dose COL treatment under CVVH in patients with newly diagnosed MDR-GNB ventilator-associated pneumonia (VAP). METHODS: Observational cohort study in critically ill adult patients with MDR-GNB VAP. Colistimethate sodium (CMS) was administered as a 9 million international units (MIU) of loading dose followed by 3 × 4.5 MIU daily. CVVH was performed over a highly adsorptive membrane. Clinical and microbiological efficacies were assessed at the end of therapy. In survivors, serum creatinine level was evaluated before and at the end of therapy. RESULTS: Fourteen patients (8 male patients, aged 57 ± 14 years) were consecutively included. Isolated pathogens were Pseudomonas aeruginosa in 7, Klebsiella pneumoniae in 5, and other Enterobacteriaceae in 2 patients. A favorable clinical response was observed in 9 patients (64%). Full and presumed microbiological eradication was observed in 12 patients (86%). Two patients were diagnosed with Stage 1 acute kidney injury. CONCLUSIONS: In patients with MDR-GNB VAP, CVVH may represent an interesting option to enable effective high-dose COL treatment. Sciendo 2019-10-12 /pmc/articles/PMC6795054/ /pubmed/31637180 http://dx.doi.org/10.2478/jtim-2019-0022 Text en © 2019 Herbert Spapen, Johan van Laethem, Maya Hites, An Verdoodt, Marc Diltoer, Patrick M. Honoré, published by Sciendo http://creativecommons.org/licenses/by-nc-nd/3.0 This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License. |
spellingShingle | Original Article Spapen, Herbert van Laethem, Johan Hites, Maya Verdoodt, An Diltoer, Marc Honoré, Patrick M. Treatment of Ventilator-associated Pneumonia with High-dose Colistin Under Continuous Veno-venous Hemofiltration |
title | Treatment of Ventilator-associated Pneumonia with High-dose Colistin Under Continuous Veno-venous Hemofiltration |
title_full | Treatment of Ventilator-associated Pneumonia with High-dose Colistin Under Continuous Veno-venous Hemofiltration |
title_fullStr | Treatment of Ventilator-associated Pneumonia with High-dose Colistin Under Continuous Veno-venous Hemofiltration |
title_full_unstemmed | Treatment of Ventilator-associated Pneumonia with High-dose Colistin Under Continuous Veno-venous Hemofiltration |
title_short | Treatment of Ventilator-associated Pneumonia with High-dose Colistin Under Continuous Veno-venous Hemofiltration |
title_sort | treatment of ventilator-associated pneumonia with high-dose colistin under continuous veno-venous hemofiltration |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795054/ https://www.ncbi.nlm.nih.gov/pubmed/31637180 http://dx.doi.org/10.2478/jtim-2019-0022 |
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