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Lispro insulin and electrolyte supplementation for treatment of diabetic ketoacidosis in cats
BACKGROUND: Intravenous continuous rate infusion (IVCRI) of lispro at a starting dose of 0.09 U/kg/h and the use of 0.9% sodium chloride (NaCl) for fluid resuscitation in cats with diabetic ketoacidosis (DKA) have not been reported. Protocols for correction of electrolyte deficiencies in cats with D...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639468/ https://www.ncbi.nlm.nih.gov/pubmed/31134702 http://dx.doi.org/10.1111/jvim.15518 |
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author | Anderson, Jodie D. Rondeau, Danielle A. Hess, Rebecka S. |
author_facet | Anderson, Jodie D. Rondeau, Danielle A. Hess, Rebecka S. |
author_sort | Anderson, Jodie D. |
collection | PubMed |
description | BACKGROUND: Intravenous continuous rate infusion (IVCRI) of lispro at a starting dose of 0.09 U/kg/h and the use of 0.9% sodium chloride (NaCl) for fluid resuscitation in cats with diabetic ketoacidosis (DKA) have not been reported. Protocols for correction of electrolyte deficiencies in cats with DKA are lacking. OBJECTIVES: To characterize the use of IVCRI lispro at an initial dose of 0.09 U/kg/h and the use of NaCl for resuscitation. Explore protocols for electrolyte supplementation in cats with DKA. ANIMALS: Twelve cats with DKA enrolled from the cat population of a university hospital. METHODS: Randomized, controlled, blinded study. Six cats were randomized into each group, the lispro insulin treatment group (LITG) and regular insulin treatment group (RITG). All cats received IVCRI fluid resuscitation with NaCl. Solutions with higher than previously published electrolyte concentrations were used to treat electrolyte deficiencies. RESULTS: The median time to blood glucose (BG) concentration <250 mg/dL was significantly shorter in the LITG (median 7 hours, 2‐10 hours) than the RITG (median 12.5 hours, 8‐20 hours; P = .02). Two cats had nonclinical hypoglycemia (BG = 40 mg/dL). The most rapid change in 157 measurements of corrected sodium concentrations was 0.7 mmol/L/h. Low concentrations of serum sodium, potassium, phosphate, and magnesium were over 3 times more common than above normal electrolyte concentrations, despite supplementation with fluids of high electrolyte concentrations. CONCLUSIONS AND CLINICAL IMPORTANCE: Lispro at a starting dose of 0.09 U/kg/h and NaCl administered for fluid resuscitation are safe and effective for treatment of DKA in cats. |
format | Online Article Text |
id | pubmed-6639468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66394682019-07-29 Lispro insulin and electrolyte supplementation for treatment of diabetic ketoacidosis in cats Anderson, Jodie D. Rondeau, Danielle A. Hess, Rebecka S. J Vet Intern Med SMALL ANIMAL BACKGROUND: Intravenous continuous rate infusion (IVCRI) of lispro at a starting dose of 0.09 U/kg/h and the use of 0.9% sodium chloride (NaCl) for fluid resuscitation in cats with diabetic ketoacidosis (DKA) have not been reported. Protocols for correction of electrolyte deficiencies in cats with DKA are lacking. OBJECTIVES: To characterize the use of IVCRI lispro at an initial dose of 0.09 U/kg/h and the use of NaCl for resuscitation. Explore protocols for electrolyte supplementation in cats with DKA. ANIMALS: Twelve cats with DKA enrolled from the cat population of a university hospital. METHODS: Randomized, controlled, blinded study. Six cats were randomized into each group, the lispro insulin treatment group (LITG) and regular insulin treatment group (RITG). All cats received IVCRI fluid resuscitation with NaCl. Solutions with higher than previously published electrolyte concentrations were used to treat electrolyte deficiencies. RESULTS: The median time to blood glucose (BG) concentration <250 mg/dL was significantly shorter in the LITG (median 7 hours, 2‐10 hours) than the RITG (median 12.5 hours, 8‐20 hours; P = .02). Two cats had nonclinical hypoglycemia (BG = 40 mg/dL). The most rapid change in 157 measurements of corrected sodium concentrations was 0.7 mmol/L/h. Low concentrations of serum sodium, potassium, phosphate, and magnesium were over 3 times more common than above normal electrolyte concentrations, despite supplementation with fluids of high electrolyte concentrations. CONCLUSIONS AND CLINICAL IMPORTANCE: Lispro at a starting dose of 0.09 U/kg/h and NaCl administered for fluid resuscitation are safe and effective for treatment of DKA in cats. John Wiley & Sons, Inc. 2019-05-27 2019 /pmc/articles/PMC6639468/ /pubmed/31134702 http://dx.doi.org/10.1111/jvim.15518 Text en © 2019 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | SMALL ANIMAL Anderson, Jodie D. Rondeau, Danielle A. Hess, Rebecka S. Lispro insulin and electrolyte supplementation for treatment of diabetic ketoacidosis in cats |
title | Lispro insulin and electrolyte supplementation for treatment of diabetic ketoacidosis in cats |
title_full | Lispro insulin and electrolyte supplementation for treatment of diabetic ketoacidosis in cats |
title_fullStr | Lispro insulin and electrolyte supplementation for treatment of diabetic ketoacidosis in cats |
title_full_unstemmed | Lispro insulin and electrolyte supplementation for treatment of diabetic ketoacidosis in cats |
title_short | Lispro insulin and electrolyte supplementation for treatment of diabetic ketoacidosis in cats |
title_sort | lispro insulin and electrolyte supplementation for treatment of diabetic ketoacidosis in cats |
topic | SMALL ANIMAL |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639468/ https://www.ncbi.nlm.nih.gov/pubmed/31134702 http://dx.doi.org/10.1111/jvim.15518 |
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