To review the safety, efficacy, and administration of intranasal (IN) glucagon for the management of hypoglycemia. A literature search of PubMed/MEDLINE (1995 to November 2019) using the terms , and was completed. English-language studies evaluating IN glucagon were evaluated. IN glucagon is a newly approved product for the treatment of hypoglycemia in patients with diabetes, 4 years and older. Administered as a 3-mg dose, it was shown to be noninferior to intramuscular (IM) glucagon. In comparison trials, more than 98% of hypoglycemic events were treated successfully with IN glucagon in both pediatric and adult patients. In simulated and real-world studies, IN glucagon was administered in less than a minute for the majority of scenarios. IM glucagon took longer to administer, ranging from 1 to 4 minutes, and often, patients did not receive the intended full dose. Nausea and vomiting, known adverse events for glucagon, as well as local adverse events were most commonly reported with IN glucagon. IN glucagon is safe, effective, easy to use, and does not require reconstitution prior to use, which can lead to faster delivery in a severe hypoglycemic event. It does not require age- or weight-based dosing. This delivery method offers an option for someone who fears needles or is uncomfortable with injections. IN glucagon is a safe, effective, easy to use, needle-free treatment option for severe hypoglycemia.
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http://dx.doi.org/10.1177/1060028020905846 | DOI Listing |
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