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Role of hypertonic saline and mannitol in the management of raised intracranial pressure in children: A randomized comparative study

OBJECTIVE: To compare the efficacy and side effects of 3% hypertonic saline and mannitol in the management of raised intracranial pressure in children. DESIGN: Prospective randomized study. SETTING: Pediatric intensive care unit (PICU) in a tertiary care hospital. SUBJECT: 200 patients with raised i...

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Autores principales: Upadhyay, Piyush, Tripathi, V. N., Singh, R. P., Sachan, D.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2964805/
https://www.ncbi.nlm.nih.gov/pubmed/21042500
http://dx.doi.org/10.4103/1817-1745.66673
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author Upadhyay, Piyush
Tripathi, V. N.
Singh, R. P.
Sachan, D.
author_facet Upadhyay, Piyush
Tripathi, V. N.
Singh, R. P.
Sachan, D.
author_sort Upadhyay, Piyush
collection PubMed
description OBJECTIVE: To compare the efficacy and side effects of 3% hypertonic saline and mannitol in the management of raised intracranial pressure in children. DESIGN: Prospective randomized study. SETTING: Pediatric intensive care unit (PICU) in a tertiary care hospital. SUBJECT: 200 patients with raised intracranial pressure. MATERIALS AND METHODS: Patients were randomized into two statistically comparable groups; Group A (n = 98) was treated with mannitol while Group B (n = 100) was treated with 3% hypertonic saline. Group C (n = 2) included those members of Group A in whom serum osmolality ≥320 mosmol/kg and were then treated with 3% hypertonic saline. Both Drugs were given at a loading dose of 5 ml/kg stat followed by 2 ml/kg in every 6 h(both have same osmolarity) for two days in their respective groups. Besides monitoring, blood pressure (NIBP), mean arterial pressure (pre and post 30 min of drug), serum sodium, chloride and osmolality were measured. Intracranial pressure was assessed indirectly by measuring mean arterial ressure “MAP”. Student paired ‘t’ test was applied. RESULTS: Decrease in MAP was highly significant (P<0.001) at 0 h in males 0,6 h in females, and moderately significant at 12,36 h in females and significant(P<0.05) at 6,24,42 h in males of Group B. Decrease in coma hours was a highly significant finding (P<0.001) in Group B. In Group B, serum sodium and chloride increased significantly but remained within acceptable limits. There was no difference in osmolality and mortality (fisher Z). CONCLUSION: Mannitol has several side effects, 3% hypertonic saline is a safe and effective alternative in managing cerebral edema.
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spelling pubmed-29648052010-11-01 Role of hypertonic saline and mannitol in the management of raised intracranial pressure in children: A randomized comparative study Upadhyay, Piyush Tripathi, V. N. Singh, R. P. Sachan, D. J Pediatr Neurosci Original Article OBJECTIVE: To compare the efficacy and side effects of 3% hypertonic saline and mannitol in the management of raised intracranial pressure in children. DESIGN: Prospective randomized study. SETTING: Pediatric intensive care unit (PICU) in a tertiary care hospital. SUBJECT: 200 patients with raised intracranial pressure. MATERIALS AND METHODS: Patients were randomized into two statistically comparable groups; Group A (n = 98) was treated with mannitol while Group B (n = 100) was treated with 3% hypertonic saline. Group C (n = 2) included those members of Group A in whom serum osmolality ≥320 mosmol/kg and were then treated with 3% hypertonic saline. Both Drugs were given at a loading dose of 5 ml/kg stat followed by 2 ml/kg in every 6 h(both have same osmolarity) for two days in their respective groups. Besides monitoring, blood pressure (NIBP), mean arterial pressure (pre and post 30 min of drug), serum sodium, chloride and osmolality were measured. Intracranial pressure was assessed indirectly by measuring mean arterial ressure “MAP”. Student paired ‘t’ test was applied. RESULTS: Decrease in MAP was highly significant (P<0.001) at 0 h in males 0,6 h in females, and moderately significant at 12,36 h in females and significant(P<0.05) at 6,24,42 h in males of Group B. Decrease in coma hours was a highly significant finding (P<0.001) in Group B. In Group B, serum sodium and chloride increased significantly but remained within acceptable limits. There was no difference in osmolality and mortality (fisher Z). CONCLUSION: Mannitol has several side effects, 3% hypertonic saline is a safe and effective alternative in managing cerebral edema. Medknow Publications 2010 /pmc/articles/PMC2964805/ /pubmed/21042500 http://dx.doi.org/10.4103/1817-1745.66673 Text en © Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Upadhyay, Piyush
Tripathi, V. N.
Singh, R. P.
Sachan, D.
Role of hypertonic saline and mannitol in the management of raised intracranial pressure in children: A randomized comparative study
title Role of hypertonic saline and mannitol in the management of raised intracranial pressure in children: A randomized comparative study
title_full Role of hypertonic saline and mannitol in the management of raised intracranial pressure in children: A randomized comparative study
title_fullStr Role of hypertonic saline and mannitol in the management of raised intracranial pressure in children: A randomized comparative study
title_full_unstemmed Role of hypertonic saline and mannitol in the management of raised intracranial pressure in children: A randomized comparative study
title_short Role of hypertonic saline and mannitol in the management of raised intracranial pressure in children: A randomized comparative study
title_sort role of hypertonic saline and mannitol in the management of raised intracranial pressure in children: a randomized comparative study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2964805/
https://www.ncbi.nlm.nih.gov/pubmed/21042500
http://dx.doi.org/10.4103/1817-1745.66673
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