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Clinical and Laboratory Features Associated with Acute Kidney Injury in Severe Malaria
INTRODUCTION: Critically ill severe malaria constitutes one of the major hospital admissions in Indian setting. Clinical studies identifying the factors associated with acute kidney injury (AKI) in malaria are lacking. This study aimed to identify these factors. METHODS: This prospective observation...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6201649/ https://www.ncbi.nlm.nih.gov/pubmed/30405282 http://dx.doi.org/10.4103/ijccm.IJCCM_468_17 |
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author | Anghan, Hiren Sethi, Prayas Soneja, Manish Mahajan, Sandeep Wig, Naveet |
author_facet | Anghan, Hiren Sethi, Prayas Soneja, Manish Mahajan, Sandeep Wig, Naveet |
author_sort | Anghan, Hiren |
collection | PubMed |
description | INTRODUCTION: Critically ill severe malaria constitutes one of the major hospital admissions in Indian setting. Clinical studies identifying the factors associated with acute kidney injury (AKI) in malaria are lacking. This study aimed to identify these factors. METHODS: This prospective observational study was conducted in a tertiary care center of North India. All adult patients with severe malaria were studied during 2012–2014. RESULTS: The study included 79 patients and AKI was observed in 36 patients. Of these 79 patients, 52.7% were Plasmodium falciparum positive and 47.2% were Plasmodium vivax positive. In AKI patients, thrombocytopenia and jaundice were the most common other complications seen. Among P. vivax malarial patients, 17 (36%) patients had AKI. Features associated with AKI among patients admitted with P. vivax malaria were as follows: tachycardia (adjusted relative risk [RR]: 3.9; 95% confidence interval [CI]: 1.1–13.7), direct hyperbilirubinemia (adjusted RR: 4.7; 95% CI: 1.4–15.2), anemia (adjusted RR: 6; 95% CI: 1.7–22.4), and sepsis (adjusted RR: 3.3; 95% CI: 1.1–13.7). The presence of tachycardia, acidosis, cerebral malaria, acute respiratory distress syndrome/acute lung injury, hypotensive shock, and poor Glasgow Coma Scale were associated with higher mortality in patients with AKI. Patients who required mechanical ventilation and/or vasopressor support had higher mortality. CONCLUSION: P. vivax is an important cause of severe malaria with AKI in our setting. Various other clinical features are associated with AKI and related mortality. |
format | Online Article Text |
id | pubmed-6201649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-62016492018-11-07 Clinical and Laboratory Features Associated with Acute Kidney Injury in Severe Malaria Anghan, Hiren Sethi, Prayas Soneja, Manish Mahajan, Sandeep Wig, Naveet Indian J Crit Care Med Research Article INTRODUCTION: Critically ill severe malaria constitutes one of the major hospital admissions in Indian setting. Clinical studies identifying the factors associated with acute kidney injury (AKI) in malaria are lacking. This study aimed to identify these factors. METHODS: This prospective observational study was conducted in a tertiary care center of North India. All adult patients with severe malaria were studied during 2012–2014. RESULTS: The study included 79 patients and AKI was observed in 36 patients. Of these 79 patients, 52.7% were Plasmodium falciparum positive and 47.2% were Plasmodium vivax positive. In AKI patients, thrombocytopenia and jaundice were the most common other complications seen. Among P. vivax malarial patients, 17 (36%) patients had AKI. Features associated with AKI among patients admitted with P. vivax malaria were as follows: tachycardia (adjusted relative risk [RR]: 3.9; 95% confidence interval [CI]: 1.1–13.7), direct hyperbilirubinemia (adjusted RR: 4.7; 95% CI: 1.4–15.2), anemia (adjusted RR: 6; 95% CI: 1.7–22.4), and sepsis (adjusted RR: 3.3; 95% CI: 1.1–13.7). The presence of tachycardia, acidosis, cerebral malaria, acute respiratory distress syndrome/acute lung injury, hypotensive shock, and poor Glasgow Coma Scale were associated with higher mortality in patients with AKI. Patients who required mechanical ventilation and/or vasopressor support had higher mortality. CONCLUSION: P. vivax is an important cause of severe malaria with AKI in our setting. Various other clinical features are associated with AKI and related mortality. Medknow Publications & Media Pvt Ltd 2018-10 /pmc/articles/PMC6201649/ /pubmed/30405282 http://dx.doi.org/10.4103/ijccm.IJCCM_468_17 Text en Copyright: © 2018 Indian Journal of Critical Care Medicine http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Research Article Anghan, Hiren Sethi, Prayas Soneja, Manish Mahajan, Sandeep Wig, Naveet Clinical and Laboratory Features Associated with Acute Kidney Injury in Severe Malaria |
title | Clinical and Laboratory Features Associated with Acute Kidney Injury in Severe Malaria |
title_full | Clinical and Laboratory Features Associated with Acute Kidney Injury in Severe Malaria |
title_fullStr | Clinical and Laboratory Features Associated with Acute Kidney Injury in Severe Malaria |
title_full_unstemmed | Clinical and Laboratory Features Associated with Acute Kidney Injury in Severe Malaria |
title_short | Clinical and Laboratory Features Associated with Acute Kidney Injury in Severe Malaria |
title_sort | clinical and laboratory features associated with acute kidney injury in severe malaria |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6201649/ https://www.ncbi.nlm.nih.gov/pubmed/30405282 http://dx.doi.org/10.4103/ijccm.IJCCM_468_17 |
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