Peer-reviewed veterinary case report
Glucagon infusion used to treat low blood sugar in 9 dogs
By Datte, Kristen et al.·Published in Journal of veterinary emergency and critical care (San Antonio, Tex. : 2001)·2016·Department of Veterinary Clinical Sciences, United States·View original on PubMed →
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Original publication title: Retrospective evaluation of the use of glucagon infusion as adjunctive therapy for hypoglycemia in dogs: 9 cases (2005-2014).
- Species:
- dog
Plain-English summary
A group of 9 dogs with low blood sugar (hypoglycemia) were treated with glucagon, a hormone that helps raise blood sugar levels. Most of these dogs had a condition called insulinoma, which causes excessive insulin production. After receiving glucagon, all the dogs showed improvement in their blood sugar levels, and five of them were able to go home after treatment. The glucagon infusion was effective and safe, helping to stabilize their blood sugar without causing further issues.
People also search for: dog hypoglycemia treatment · insulinoma in dogs · glucagon for low blood sugar in dogs
Abstract
OBJECTIVE: To describe the use of glucagon infusion for adjunctive treatment of hypoglycemia in dogs. DESIGN: Multicenter retrospective case series. SETTING: One university and 1 private veterinary referral hospital. ANIMALS: Dogs were included if they were hospitalized and received glucagon therapy for hypoglycemia, defined as blood glucose concentration (BG) <60 mg/dL. A total of 9 dogs were included from September 2005 to May 2014. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: The medical record for each eligible case was reviewed. Data recorded included signalment, presenting complaint, underlying disease process, presenting BG, BG after dextrose supplementation, BG before glucagon administration, maximum BG while receiving glucagon, and BG after discontinuation of glucagon, if available. Adverse reactions to glucagon and outcome of case were recorded if available. The most common causative disease was insulinoma (n = 7). Median serum glucose concentration on presentation was 30 mg/dL (20-41 mg/dL). The median bolus of glucagon was 50 ng/kg followed by a median maximum dose of a glucagon CRI of 15 ng/kg/min. The mean time period on glucagon CRI until normoglycemia (defined as BG > 60 mg/dL) was 7 hours. All hypoglycemic patients had improvement of BGs when glucagon was added. Statistically significant differences (P < 0.05) were found between BG measurements on glucagon CRI compared to BG at presentation, BG after dextrose, and BG prior to glucagon with a Friedman statistic of 17.3. A CRI was found to effectively increase the BG without recurrence of hypoglycemia after weaning. The majority of patients (5/9) survived to discharge. CONCLUSION: Glucagon CRI was accompanied by an increase in BG in hypoglycemic dogs. Glucagon CRI appears to be a safe method and can be readily utilized in most practice settings.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/27541206/