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A randomized trial of Plasma-Lyte A and 0.9 % sodium chloride in acute pediatric gastroenteritis

BACKGROUND: Compare the efficacy and safety of Plasma-Lyte A (PLA) versus 0.9 % sodium chloride (NaCl) intravenous (IV) fluid replacement in children with moderate to severe dehydration secondary to acute gastroenteritis (AGE). METHODS: Prospective, randomized, double-blind study conducted at eight...

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Autores principales: Allen, Coburn H., Goldman, Ran D., Bhatt, Seema, Simon, Harold K., Gorelick, Marc H., Spandorfer, Philip R., Spiro, David M., Mace, Sharon E., Johnson, David W., Higginbotham, Eric A., Du, Hongyan, Smyth, Brendan J., Schermer, Carol R., Goldstein, Stuart L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969635/
https://www.ncbi.nlm.nih.gov/pubmed/27480410
http://dx.doi.org/10.1186/s12887-016-0652-4
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author Allen, Coburn H.
Goldman, Ran D.
Bhatt, Seema
Simon, Harold K.
Gorelick, Marc H.
Spandorfer, Philip R.
Spiro, David M.
Mace, Sharon E.
Johnson, David W.
Higginbotham, Eric A.
Du, Hongyan
Smyth, Brendan J.
Schermer, Carol R.
Goldstein, Stuart L.
author_facet Allen, Coburn H.
Goldman, Ran D.
Bhatt, Seema
Simon, Harold K.
Gorelick, Marc H.
Spandorfer, Philip R.
Spiro, David M.
Mace, Sharon E.
Johnson, David W.
Higginbotham, Eric A.
Du, Hongyan
Smyth, Brendan J.
Schermer, Carol R.
Goldstein, Stuart L.
author_sort Allen, Coburn H.
collection PubMed
description BACKGROUND: Compare the efficacy and safety of Plasma-Lyte A (PLA) versus 0.9 % sodium chloride (NaCl) intravenous (IV) fluid replacement in children with moderate to severe dehydration secondary to acute gastroenteritis (AGE). METHODS: Prospective, randomized, double-blind study conducted at eight pediatric emergency departments (EDs) in the US and Canada (NCT#01234883). The primary outcome measure was serum bicarbonate level at 4 h. Secondary outcomes included safety and tolerability. The hypothesis was that PLA would be superior to 0.9 % NaCl in improvement of 4-h bicarbonate. Patients (n = 100) aged ≥6 months to <11 years with AGE-induced moderate-to-severe dehydration were enrolled. Patients with a baseline bicarbonate level ≤22 mEq/L formed the modified intent to treat (mITT) group. RESULTS: At baseline, the treatment groups were comparable except that the PLA group was older. At hour 4, the PLA group had greater increases in serum bicarbonate from baseline than did the 0.9 % NaCl group (mean ± SD at 4 h: 18 ± 3.74 vs 18.0 ± 3.67; change from baseline of 1.6 and 0.0, respectively; P = .004). Both treatment groups received similar fluid volumes. The PLA group had less abdominal pain and better dehydration scores at hour 2 (both P = .03) but not at hour 4 (P = 0.15 and 0.08, respectively). No patient experienced clinically relevant worsening of laboratory findings or physical examination, and hospital admission rates were similar. One patient in each treatment group developed hyponatremia. Four patients developed hyperkalemia (PLA:1, 0.9 % NaCl:3). CONCLUSION: In comparison with 0.9 % NaCl, PLA for rehydration in children with AGE was well tolerated and led to more rapid improvement in serum bicarbonate and dehydration score. TRIAL REGISTRATION: NCT#01234883 (Registration Date: November 3, 2010). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12887-016-0652-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-49696352016-08-03 A randomized trial of Plasma-Lyte A and 0.9 % sodium chloride in acute pediatric gastroenteritis Allen, Coburn H. Goldman, Ran D. Bhatt, Seema Simon, Harold K. Gorelick, Marc H. Spandorfer, Philip R. Spiro, David M. Mace, Sharon E. Johnson, David W. Higginbotham, Eric A. Du, Hongyan Smyth, Brendan J. Schermer, Carol R. Goldstein, Stuart L. BMC Pediatr Research Article BACKGROUND: Compare the efficacy and safety of Plasma-Lyte A (PLA) versus 0.9 % sodium chloride (NaCl) intravenous (IV) fluid replacement in children with moderate to severe dehydration secondary to acute gastroenteritis (AGE). METHODS: Prospective, randomized, double-blind study conducted at eight pediatric emergency departments (EDs) in the US and Canada (NCT#01234883). The primary outcome measure was serum bicarbonate level at 4 h. Secondary outcomes included safety and tolerability. The hypothesis was that PLA would be superior to 0.9 % NaCl in improvement of 4-h bicarbonate. Patients (n = 100) aged ≥6 months to <11 years with AGE-induced moderate-to-severe dehydration were enrolled. Patients with a baseline bicarbonate level ≤22 mEq/L formed the modified intent to treat (mITT) group. RESULTS: At baseline, the treatment groups were comparable except that the PLA group was older. At hour 4, the PLA group had greater increases in serum bicarbonate from baseline than did the 0.9 % NaCl group (mean ± SD at 4 h: 18 ± 3.74 vs 18.0 ± 3.67; change from baseline of 1.6 and 0.0, respectively; P = .004). Both treatment groups received similar fluid volumes. The PLA group had less abdominal pain and better dehydration scores at hour 2 (both P = .03) but not at hour 4 (P = 0.15 and 0.08, respectively). No patient experienced clinically relevant worsening of laboratory findings or physical examination, and hospital admission rates were similar. One patient in each treatment group developed hyponatremia. Four patients developed hyperkalemia (PLA:1, 0.9 % NaCl:3). CONCLUSION: In comparison with 0.9 % NaCl, PLA for rehydration in children with AGE was well tolerated and led to more rapid improvement in serum bicarbonate and dehydration score. TRIAL REGISTRATION: NCT#01234883 (Registration Date: November 3, 2010). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12887-016-0652-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-02 /pmc/articles/PMC4969635/ /pubmed/27480410 http://dx.doi.org/10.1186/s12887-016-0652-4 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Allen, Coburn H.
Goldman, Ran D.
Bhatt, Seema
Simon, Harold K.
Gorelick, Marc H.
Spandorfer, Philip R.
Spiro, David M.
Mace, Sharon E.
Johnson, David W.
Higginbotham, Eric A.
Du, Hongyan
Smyth, Brendan J.
Schermer, Carol R.
Goldstein, Stuart L.
A randomized trial of Plasma-Lyte A and 0.9 % sodium chloride in acute pediatric gastroenteritis
title A randomized trial of Plasma-Lyte A and 0.9 % sodium chloride in acute pediatric gastroenteritis
title_full A randomized trial of Plasma-Lyte A and 0.9 % sodium chloride in acute pediatric gastroenteritis
title_fullStr A randomized trial of Plasma-Lyte A and 0.9 % sodium chloride in acute pediatric gastroenteritis
title_full_unstemmed A randomized trial of Plasma-Lyte A and 0.9 % sodium chloride in acute pediatric gastroenteritis
title_short A randomized trial of Plasma-Lyte A and 0.9 % sodium chloride in acute pediatric gastroenteritis
title_sort randomized trial of plasma-lyte a and 0.9 % sodium chloride in acute pediatric gastroenteritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969635/
https://www.ncbi.nlm.nih.gov/pubmed/27480410
http://dx.doi.org/10.1186/s12887-016-0652-4
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