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Use of intravenous N-acetylcysteine in acute severe hepatitis due to severe dengue infection: a case series
BACKGROUND: Dengue fever is a common mosquito borne viral infection. Severe dengue fever associated severe hepatitis carries high mortality. Based on the beneficial effect of N-acetylcysteine (NAC) in paracetamol poisoning and non-acetaminophen induced liver failure, it is used in dengue fever assoc...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8454086/ https://www.ncbi.nlm.nih.gov/pubmed/34544380 http://dx.doi.org/10.1186/s12879-021-06681-9 |
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author | Dissanayake, D. M. D. I. B. Gunaratne, W. M. S. N. Kumarihamy, K. W. M. P. P. Kularatne, S. A. M. Kumarasiri, P. V. R. |
author_facet | Dissanayake, D. M. D. I. B. Gunaratne, W. M. S. N. Kumarihamy, K. W. M. P. P. Kularatne, S. A. M. Kumarasiri, P. V. R. |
author_sort | Dissanayake, D. M. D. I. B. |
collection | PubMed |
description | BACKGROUND: Dengue fever is a common mosquito borne viral infection. Severe dengue fever associated severe hepatitis carries high mortality. Based on the beneficial effect of N-acetylcysteine (NAC) in paracetamol poisoning and non-acetaminophen induced liver failure, it is used in dengue fever associated hepatitis in clinical practice. We aim to study the reversal of liver enzymes with NAC in the setting of severe hepatitis due to severe dengue infection. METHODS: A retrospective analysis was conducted on hospitalized 30 adults with severe dengue fever with severe hepatitis. These 30 patients had aspartate transaminase (AST) and alanine transaminases (ALT) more than 500 U/L and/or PT INR (prothrombin time and international normalized ratio) more than 1.5. They were treated with NAC infusion of 100 mg/h for 3 to 5 days. RESULTS: The mean age of the group was 49.9 ± 11.46 years and 18 (60%) patients were males. Nineteen patients (63%) developed dengue shock. Of them 12 patients (40%) developed hepatic encephalopathy. Median AST on the day of administration of NAC was 1125 U/L interquartile range (IQR) 1653.25 while median ALT was 752 (IQR 459.25). There was a statistically significant reduction of both ALT (p = 0.034) and AST (p = 0.049) from day 1 to 4 after NAC infusion. Rise of platelet count between day 1 and day 4 also showed statistically significant difference (p = 0.011) but the reduction of prothrombin time and international normalized ratio (PT/INR) from 1 to day 4 did not show statistical significance difference. Mean duration of treatment with NAC was 3.61 ± 0.75 days while mean length of hospital stay was 6.2 ± 1.27 days. Only one patient died (3.3%). None of the patients reported adverse drug reaction due to NAC. CONCLUSION: Majority of patients demonstrated marked clinical and biochemical improvements and they recovered fully. We observed faster and significant recovery of liver enzymes following administration of NAC. Based on the above findings, this study provides preliminary evidence for the beneficial effect of NAC in severe hepatitis in dengue infection with greater survival benefits. |
format | Online Article Text |
id | pubmed-8454086 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84540862021-09-21 Use of intravenous N-acetylcysteine in acute severe hepatitis due to severe dengue infection: a case series Dissanayake, D. M. D. I. B. Gunaratne, W. M. S. N. Kumarihamy, K. W. M. P. P. Kularatne, S. A. M. Kumarasiri, P. V. R. BMC Infect Dis Research BACKGROUND: Dengue fever is a common mosquito borne viral infection. Severe dengue fever associated severe hepatitis carries high mortality. Based on the beneficial effect of N-acetylcysteine (NAC) in paracetamol poisoning and non-acetaminophen induced liver failure, it is used in dengue fever associated hepatitis in clinical practice. We aim to study the reversal of liver enzymes with NAC in the setting of severe hepatitis due to severe dengue infection. METHODS: A retrospective analysis was conducted on hospitalized 30 adults with severe dengue fever with severe hepatitis. These 30 patients had aspartate transaminase (AST) and alanine transaminases (ALT) more than 500 U/L and/or PT INR (prothrombin time and international normalized ratio) more than 1.5. They were treated with NAC infusion of 100 mg/h for 3 to 5 days. RESULTS: The mean age of the group was 49.9 ± 11.46 years and 18 (60%) patients were males. Nineteen patients (63%) developed dengue shock. Of them 12 patients (40%) developed hepatic encephalopathy. Median AST on the day of administration of NAC was 1125 U/L interquartile range (IQR) 1653.25 while median ALT was 752 (IQR 459.25). There was a statistically significant reduction of both ALT (p = 0.034) and AST (p = 0.049) from day 1 to 4 after NAC infusion. Rise of platelet count between day 1 and day 4 also showed statistically significant difference (p = 0.011) but the reduction of prothrombin time and international normalized ratio (PT/INR) from 1 to day 4 did not show statistical significance difference. Mean duration of treatment with NAC was 3.61 ± 0.75 days while mean length of hospital stay was 6.2 ± 1.27 days. Only one patient died (3.3%). None of the patients reported adverse drug reaction due to NAC. CONCLUSION: Majority of patients demonstrated marked clinical and biochemical improvements and they recovered fully. We observed faster and significant recovery of liver enzymes following administration of NAC. Based on the above findings, this study provides preliminary evidence for the beneficial effect of NAC in severe hepatitis in dengue infection with greater survival benefits. BioMed Central 2021-09-20 /pmc/articles/PMC8454086/ /pubmed/34544380 http://dx.doi.org/10.1186/s12879-021-06681-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Dissanayake, D. M. D. I. B. Gunaratne, W. M. S. N. Kumarihamy, K. W. M. P. P. Kularatne, S. A. M. Kumarasiri, P. V. R. Use of intravenous N-acetylcysteine in acute severe hepatitis due to severe dengue infection: a case series |
title | Use of intravenous N-acetylcysteine in acute severe hepatitis due to severe dengue infection: a case series |
title_full | Use of intravenous N-acetylcysteine in acute severe hepatitis due to severe dengue infection: a case series |
title_fullStr | Use of intravenous N-acetylcysteine in acute severe hepatitis due to severe dengue infection: a case series |
title_full_unstemmed | Use of intravenous N-acetylcysteine in acute severe hepatitis due to severe dengue infection: a case series |
title_short | Use of intravenous N-acetylcysteine in acute severe hepatitis due to severe dengue infection: a case series |
title_sort | use of intravenous n-acetylcysteine in acute severe hepatitis due to severe dengue infection: a case series |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8454086/ https://www.ncbi.nlm.nih.gov/pubmed/34544380 http://dx.doi.org/10.1186/s12879-021-06681-9 |
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