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Blood filtration in children with severe sepsis: Safe adjunctive therapy

OBJECTIVE: To review the safety and efficacy of haemofiltration and plasmafiltration in children with severe sepsis. DESIGN: Retrospective case notes analysis. SETTING: University Paediatric Intensive Care Unit. PATIENTS: All children admitted to the intensive care unit between November 1985 and May...

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Detalles Bibliográficos
Autores principales: Reeves, J. H., Butt, W. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 1995
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7095059/
https://www.ncbi.nlm.nih.gov/pubmed/7560493
http://dx.doi.org/10.1007/BF01706203
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author Reeves, J. H.
Butt, W. W.
author_facet Reeves, J. H.
Butt, W. W.
author_sort Reeves, J. H.
collection PubMed
description OBJECTIVE: To review the safety and efficacy of haemofiltration and plasmafiltration in children with severe sepsis. DESIGN: Retrospective case notes analysis. SETTING: University Paediatric Intensive Care Unit. PATIENTS: All children admitted to the intensive care unit between November 1985 and May 1992 with a primary diagnosis of severe sepsis who also received blood filtration therapy. INTERVENTIONS: Continuous haemofiltration (HF) 18 patients; continuous haemofiltration and plasmafiltration (PF) 9 patients. MEASUREMENTS AND RESULTS: 27 children with sepsis-induced MOSF, median age 26.6 months (range 0.33–185), median weight 12 kg (range 2.5–58), mean PRISM score 19.4 (SD 8.6), mean number of organs failing 2.78 (SD 0.9) received filtration for a median duration of 36 hours (range 2–145). Eight (30%) survived (HF5/18, PF3/9). There was no significant difference in the demographic features between the HF group and the PF group and no difference in mortality. The two groups were pooled to assess the effect of commencement of filtration on clinical wellbeing. Arterial blood gases, electrolytes, full blood examination, ventilator settings and doses of inotropes were recorded immediately prior to commencement of filtration and 18 h after commencement. Serum anion gap and osmolality were calculated using conventional formulae. There were no significant changes in the level of cardiorespiratory support, or biochemical markers of severity following commencement of filtration. Platelet count fell 32% (p=0.029) but no bleeding was encountered. No severe complications were observed during 1222 h of filtration. No bleeding or infection was observed at the site of cannulation. One child developed haemodynamic instability following commencement of plasmafiltration necessitating abandonment of the procedure. CONCLUSION: Haemofiltration or plasmafiltration can be performed safely in children with severe sepsis but their effect on outcome remains unknown.
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spelling pubmed-70950592020-03-26 Blood filtration in children with severe sepsis: Safe adjunctive therapy Reeves, J. H. Butt, W. W. Intensive Care Med Neonatal and Pediatric Intensive Care OBJECTIVE: To review the safety and efficacy of haemofiltration and plasmafiltration in children with severe sepsis. DESIGN: Retrospective case notes analysis. SETTING: University Paediatric Intensive Care Unit. PATIENTS: All children admitted to the intensive care unit between November 1985 and May 1992 with a primary diagnosis of severe sepsis who also received blood filtration therapy. INTERVENTIONS: Continuous haemofiltration (HF) 18 patients; continuous haemofiltration and plasmafiltration (PF) 9 patients. MEASUREMENTS AND RESULTS: 27 children with sepsis-induced MOSF, median age 26.6 months (range 0.33–185), median weight 12 kg (range 2.5–58), mean PRISM score 19.4 (SD 8.6), mean number of organs failing 2.78 (SD 0.9) received filtration for a median duration of 36 hours (range 2–145). Eight (30%) survived (HF5/18, PF3/9). There was no significant difference in the demographic features between the HF group and the PF group and no difference in mortality. The two groups were pooled to assess the effect of commencement of filtration on clinical wellbeing. Arterial blood gases, electrolytes, full blood examination, ventilator settings and doses of inotropes were recorded immediately prior to commencement of filtration and 18 h after commencement. Serum anion gap and osmolality were calculated using conventional formulae. There were no significant changes in the level of cardiorespiratory support, or biochemical markers of severity following commencement of filtration. Platelet count fell 32% (p=0.029) but no bleeding was encountered. No severe complications were observed during 1222 h of filtration. No bleeding or infection was observed at the site of cannulation. One child developed haemodynamic instability following commencement of plasmafiltration necessitating abandonment of the procedure. CONCLUSION: Haemofiltration or plasmafiltration can be performed safely in children with severe sepsis but their effect on outcome remains unknown. Springer-Verlag 1995 /pmc/articles/PMC7095059/ /pubmed/7560493 http://dx.doi.org/10.1007/BF01706203 Text en © Springer-Verlag 1995 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Neonatal and Pediatric Intensive Care
Reeves, J. H.
Butt, W. W.
Blood filtration in children with severe sepsis: Safe adjunctive therapy
title Blood filtration in children with severe sepsis: Safe adjunctive therapy
title_full Blood filtration in children with severe sepsis: Safe adjunctive therapy
title_fullStr Blood filtration in children with severe sepsis: Safe adjunctive therapy
title_full_unstemmed Blood filtration in children with severe sepsis: Safe adjunctive therapy
title_short Blood filtration in children with severe sepsis: Safe adjunctive therapy
title_sort blood filtration in children with severe sepsis: safe adjunctive therapy
topic Neonatal and Pediatric Intensive Care
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7095059/
https://www.ncbi.nlm.nih.gov/pubmed/7560493
http://dx.doi.org/10.1007/BF01706203
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