Glyburide

Article Author:
Maiah Hardin
Article Editor:
Tibb Jacobs
Updated:
7/22/2019 10:08:10 AM
PubMed Link:
Glyburide

Indications

Glyburide also referred to as glibenclamide, is a second-generation sulfonylurea approved by the Food and Drug Administration (FDA) for the treatment of type 2 diabetes mellitus. The medication is available as a generic formulation. It is an adjunct therapy along with diet and exercise for the management of diabetes.[1] Treatment with glyburide has been and continues to be successful in sufficiently lowering blood glucose levels, but is also available in combination therapy with metformin. Typical doses for glyburide are relatively minute compared to first-generation sulfonylureas and dosing is usually as a once-daily morning dose.[1] According to the American Diabetes Association (ADA) Standards of Medical Care in Diabetes 2019 update,[2] sulfonylureas such as glyburide are considered as one of six options for adjunct therapy with metformin, the first-line anti-diabetic medication. The patient population that this recommendation focuses on is non-ASCVD, non-CKD Type 2 diabetic patients that have not reached their HbA1C target after three months.[2]

For many years, glyburide has been studied off-label for the treatment of neonatal syndromic hyperglycemia for patients with Kir6.2 or SUR1 mutations.[3] Although no dosage forms are yet available for children with these potassium channel defects, studies included a newly-designed suspension with orphan drug status to evaluate its efficacy with glyburide tablets.[4] Results from the research reflected significant decreases in HbA1C, further warranting its off-label uses.[4]

Due to its overlap in the mechanism of action, recent studies have even begun to highlight low doses of glyburide as a possible agent for reducing intracranial pressure and cerebral edema.[5]

Mechanism of Action

Glyburide, along with others in its class of sulfonylureas, exerts its mechanism of action based on increasing the secretion of insulin from beta cells in the pancreas.[6] Specifically, sulfonylureas bind to the SUR1 receptors in the membranes of the beta cells of potassium ATP-dependent channels.[6][7] These agents act by blocking these channels, and insulin is released after the cell becomes depolarized.[8] At times, sulfonylureas tend to bind to SUR2 receptors, located on cells in cardiac tissue and the endothelium.[7] After the initial insulin secretion, sulfonylureas can also decrease the clearance of insulin in the liver, furthermore contributing to increased insulin levels in the plasma.[9] Glyburide, along with glipizide, is classified as second-generation sulfonylureas due to their increased potency and difference in elimination, allowing their use in patients with renal and hepatic dysfunction.

Administration

Glyburide is orally administered in typical initial dosages of 2.5 mg to 5 mg, with a maximum of 40 mg daily – the maximum dosage is rarely used, as many type 2 diabetic patients do not require dosages greater than 10 mg per day.[1] Clinical effects are also not significant beyond 10 to 15 mg total daily doses.[1][9] Most sulfonylureas should be taken by mouth about 30 minutes before the intake of food, as both food intake and hyperglycemia may reduce sulfonylurea absorption and its associated antidiabetic effect.[1] Patients should take lower doses of glyburide (less than or equal to 10 mg) with breakfast, or as soon as the patient consumes the breakfast meal; with higher daily doses (greater than 10 mg) usually divided between breakfast and evening meals.[1]

Adverse Effects

Hypoglycemia and weight gain are the most frequently encountered side effects of glyburide. Although glyburide is one of the most popular sulfonylureas prescribed, a systematic review conducted by the ADA supports evidence that glyburide has correlations with a significantly higher risk of hypoglycemic episodes than other insulin secretagogues sulfonylureas by 80% and 44%, respectively.[10] However, these episodes are most often seen with higher initial glyburide dosing and in patients that have been recently diagnosed – especially in those 65 years of age and older.[1] For this reason, it is important to consider patient-specific factors and susceptibility to hypoglycemic episodes when considering prescribing glyburide for a sulfonylurea-naïve patient. 

Possible weight gain can also be a distressing side effect for patients taking glyburide, as with all sulfonylureas. Although the ADA’s systematic review states that weight gain was not a major outcome for glyburide when compared with other insulin secretagogues, if weight gain does occur, co-administration with metformin, which is a weight-neutral biguanide agent, can aid with the issue.[1][10]

A cohort study on Type 2 diabetic patients compared all-cause and cardiovascular mortality for patients on either glyburide or metformin for blood glucose management.[11] The study found that glyburide monotherapy, when compared to metformin, was associated with higher percentages of all-cause (6.3% and 1.6%, respectively) and cardiovascular (4.1% and 0.4%, respectively) deaths, in addition to increases in plasma creatinine.[11] Other nationwide studies, retrospective cohort studies, and other recent studies have confirmed metformin as having lower all-cause mortality rates and higher survival rates compared to glyburide and other drugs of its class as well.[11] This data helps to establish metformin, rather than glyburide, as the first-line antidiabetic agent for newly diagnosed Type 2 diabetic patients; this is in addition to its additive effects on HbA1C and its weight neutrality.[2]

Adverse effects that are less likely to occur with glyburide and other sulfonylureas include skin rashes, nausea, and sensitivity to light on rare occasions.[9]

Contraindications

There have been multiple studies concerning glyburide use in pregnant patients with gestational diabetes mellitus. Although glyburide is considered a Category C drug by the FDA, expert bodies have begun to introduce glyburide as a possible alternative to insulin for antidiabetic therapy.[7] Glyburide does cross the placenta in utero and gets metabolized by placental microsomes, so the fetus has exposure to the medication.[7] Concerning lactation, glyburide, along with its second-generation counterpart glipizide, is very compatible with breastfeeding, and does not cross into breastmilk to affect breastfed children.[7]

Glyburide therapy should not be re-initiated if the patient has a history of allergic reactions to the medication. However, patients who have had previous allergic reactions to drugs of the same class may not necessarily react glyburide.[1]

Also, it is essential to use caution with glyburide in patients who are in the hospital, are malnourished, abuse alcohol, have renal and cardiac dysfunctions, or gastrointestinal disease.[9]

Monitoring

As rates for hypoglycemia can be higher with glyburide than other oral antidiabetic agents, close monitoring for signs and symptoms of declining blood glucose levels is required. Hypoglycemia can be life-threatening, and it is crucial to ensure taking proper measures if it occurs in any patient. It is also necessary to monitor glyburide patients even further if they are in circumstances that provoke the onset of hypoglycemia: this includes exercise, lack of eating, and accidental overdosages.[9] Knowledge of the signs and symptoms of hypoglycemia is vital when starting a patient on glyburide, as well as self-monitoring of blood glucose and regularly scheduled testing of blood glucose and HbA1C as recommended by the ADA.

Glyburide and other sulfonylureas may also cause liver dysfunction that could result in cholestatic jaundice, hepatitis, and liver failure, although this is rare.[9] In patients with liver dysfunction, monitoring of liver function tests may be necessary.

Toxicity

Glyburide toxicity is most likely to result from severe hypoglycemia from an excessive dosage, whether accidentally or intentionally.[9][11] Drug-drug interactions with glyburide and other sulfonylureas, due to duplicate metabolism through the CYP2C9 enzyme, can also potentiate hypoglycemia.[11] It is essential to monitor for potentially harmful drug-drug interactions with concurrent therapy with salicylates, sulfonamides, drugs containing fibric acid, and warfarin.[9] Additional drugs that may inhibit or induce CYP2C9 includes azole antifungals, carbamazepine, phenobarbital, rifampin, St. Johns wort, and dexamethasone.[11] In terms of mitigating sulfonylurea and glyburide toxicity, the most beneficial way is to treat the patient to elevate the blood glucose back to its normalized range, depending on the setting.[11]

Enhancing Healthcare Team Outcomes

Members of the interprofessional healthcare team, such as physicians, pharmacists, nurses, and nurse practitioners must work together to ensure that the best possible treatment outcomes occur in type 2 diabetes patients. Consistent monitoring of blood glucose and HbA1C are vital in determining treatment success with glyburide. It is also crucial for all interprofessional healthcare providers to recognize the signs, symptoms, and frequency of hypoglycemia if it occurs while the patient is on glyburide and report back to the senior clinician managing the patient. The best clinician judgment should be practiced upon notice of hypoglycemia to determine if therapy should continue or not. If type 2 diabetic patients are not at their goal HbA1C or blood glucose targets, glyburide dosages may be increased every 2 to 4 weeks until meeting the desired objective.[9] Upon initiating glyburide, starting at a low dosage would be considered the safest precautionary measure in regards to hypoglycemia and possible weight gain.

Nursing is also integral to glyburide therapy management for reporting possible hypoglycemia, as well as educating patients of the signs of hypoglycemia, which should be reported to the rest of the team immediately if present. At the same time, the pharmacist, nurse practitioner, and primary care provider should inform the patient regarding a positive lifestyle; this means the discontinuation of smoking, eating a healthy diet, joining an exercise program, and maintaining healthy body weight. There is ample evidence indicating that a lower body weight leads to better control of diabetes.[12] [Level V] Pharmacists should verify appropriate dosing and perform medication reconciliation, as glyburide does have several significant drug-drug interactions, which require informing the rest of the healthcare team if present.

In summary, while glyburide therapy can be useful for glycemic control in type 2 diabetes patients, it requires an interprofessional team approach, including physicians, specialists, specialty-trained nurses, and pharmacists, all collaborating across disciplines to achieve optimal patient results. [Level V]


References

[1] Glibenclamide: a review. Drugs. 1971;     [PubMed PMID: 5004340]
[2] 9. Pharmacologic Approaches to Glycemic Treatment: {i}Standards of Medical Care in Diabetes-2019{/i}. Diabetes care. 2019 Jan;     [PubMed PMID: 30559235]
[3] Bouazza N,Djerada Z,Gozalo C,Busiah K,Beltrand J,Berdugo M,Urien S,Treluyer JM,Polak M, Evaluation of the pharmacokinetics of glibenclamide tablet given, off label, orally to children suffering from neonatal syndromic hyperglycemia. European journal of clinical pharmacology. 2016 Nov;     [PubMed PMID: 27561267]
[4] Beltrand J,Baptiste A,Busiah K,Bouazza N,Godot C,Boucheron A,Djerada Z,Gozalo C,Berdugo M,Tréluyer JM,Elie C,Polak M, Glibenclamide oral suspension: Suitable and effective in patients with neonatal diabetes. Pediatric diabetes. 2019 May;     [PubMed PMID: 30684309]
[5] Tsarenko SV,Dzyadz'ko AM,Rybalko SS, [Glibenclamide as a promising agent for prevention and treatment of cerebral edema]. Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko. 2017;     [PubMed PMID: 28665392]
[6] Qureshi M,Gammoh E,Shakil J,Robbins R, Update on Management of Type 2 Diabetes for Cardiologists. Methodist DeBakey cardiovascular journal. 2018 Oct-Dec;     [PubMed PMID: 30788013]
[7] Kimber-Trojnar Ż,Marciniak B,Patro-Malysza J,Skorzynska-Dziduszko K,Poniedzialek-Czajkowska E,Mierzynski R,Galczynski K,Trojnar M,Leszczynska-Gorzelak B,Oleszczuk J, Is glyburide safe in pregnancy? Current pharmaceutical biotechnology. 2014;     [PubMed PMID: 24720590]
[8] Quianzon CC,Cheikh IE, History of current non-insulin medications for diabetes mellitus. Journal of community hospital internal medicine perspectives. 2012;     [PubMed PMID: 23882374]
[9] Sola D,Rossi L,Schianca GP,Maffioli P,Bigliocca M,Mella R,Corlianò F,Fra GP,Bartoli E,Derosa G, Sulfonylureas and their use in clinical practice. Archives of medical science : AMS. 2015 Aug 12;     [PubMed PMID: 26322096]
[10] Gangji AS,Cukierman T,Gerstein HC,Goldsmith CH,Clase CM, A systematic review and meta-analysis of hypoglycemia and cardiovascular events: a comparison of glyburide with other secretagogues and with insulin. Diabetes care. 2007 Feb;     [PubMed PMID: 17259518]
[11] Raee MR,Nargesi AA,Heidari B,Mansournia MA,Larry M,Rabizadeh S,Zarifkar M,Esteghamati A,Nakhjavani M, All-Cause and Cardiovascular Mortality following Treatment with Metformin or Glyburide in Patients with Type 2 Diabetes Mellitus. Archives of Iranian medicine. 2017 Mar;     [PubMed PMID: 28287807]
[12] Magkos F, Metabolically healthy obesity: what's in a name? The American journal of clinical nutrition. 2019 Jun 26     [PubMed PMID: 31240297]