This article reviews the most common and immediately life-threatening diabetes-related conditions seen in hospital emergency departments: diabetic ketoacidosis, hyperglycemic hyperosmolar state, and hypoglycemia. It also addresses the evaluation of patients with hyperglycemia and no previous diagnosis of diabetes.
Diabetes is a common condition, afflicting > 20% of the American population over the age of 60 years.1 Patients with diabetes, particularly those with lower socioeconomic status or limited access to primary care, frequently seek care in hospital emergency departments.2–6 This article will review the most common and immediately life-threatening diabetes-related complications seen in emergency departments: diabetic ketoacidosis (DKA), hyperglycemic hyperosmolar state (HHS), and hypoglycemia. It will also address the evaluation of patients with hyperglycemia and no previous diagnosis of diabetes.
Hyperglycemic Crisis: DKA and HHS
DKA is responsible for > 110,000 hospitalizations annually in the United States, with mortality ranging from 2 to 10%.7–9 HHS is much less common but confers a much greater mortality.10 In both diseases, mortality is largely related to underlying comorbidities such as sepsis.11
DKA and HHS are characterized by absolute or relative insulin deficiency, which prevents the body from metabolizing carbohydrates and results in severe hyperglycemia. As blood glucose levels rise, the renal glucose threshold is overwhelmed, and urine becomes more dilute, leading to polyuria, dehydration, and polydipsia.
Patients with DKA classically present with the triad of uncontrolled hyperglycemia, metabolic acidosis, and increased total body ketone concentration. On the other hand, HHS is defined by altered mental status caused by hyperosmolality, profound dehydration, and severe hyperglycemia without significant ketoacidosis (Table 1).9,12
Patients with severe hyperglycemia should immediately undergo assessment and stabilization of their airway and hemodynamic status. Naloxone, to reverse potential opiate overdose, should be considered for all patients with altered mentation. Thiamine, for acute treatment of Wernicke’s encephalopathy, should be considered in all patients with signs of malnutrition. In cases requiring intubation, the paralytic succinylcholine should not be used if hyperkalemia is suspected; it may acutely further elevate potassium.
Immediate assessment also includes placing patients on a cardiac monitor and oxygen as well as obtaining vital signs, a fingerstick glucose, intravenous (IV) access, and an electrocardiogram to evaluate for arrhythmias and signs of hyper- and hypokalemia.
The differential diagnosis for hyperglycemic crisis includes the “Five I’s”: infection, infarction, infant (pregnancy), indiscretion (including cocaine ingestion), and insulin lack (nonadherence or inappropriate dosing). In addition to clinical history and physical examination, diagnostic tests should include a venous blood gas,13–15 complete blood count, basic metabolic panel, and urinalysis; a urine pregnancy test must be sent for all women with childbearing potential.
Critically ill patients should undergo additional testing as clinically indicated, including a complete metabolic panel, serum osmolality, phosphate, lactate, and cardiac markers for older patients. A urine drug screen, blood alcohol level, and aspirin and acetaminophen levels should be sent for any patient with unexplained DKA and all patients with HHS. Evaluation for infection or injury should be guided by history and the physical examination. Effective serum osmolality should be calculated (Table 1). The corrected serum sodium is estimated by decreasing measured serum sodium by 1.6 mEq/L for every 100 mg/dl increase in blood glucose over a baseline of 100 mg/dl16,17; for every 100 mg/dl increment increase in blood glucose > 400 mg/dl, measured serum sodium is decreased by an additional 4 mEq/L.18
Although DKA and HHS share some similar features, they should be treated as distinct clinical entities with different etiologies and treatments. Patients with DKA require insulin to reverse their ketoacidosis. Patients with HHS require fluid resuscitation first and foremost; they may or may not require insulin, and those who do rarely require a continuous infusion. An algorithm for the initial evaluation and treatment of patients with DKA can be found in Figure 1.
Critically ill patients with severe hyperglycemia resulting from DKA or HHS should be treated immediately with a bolus of normal saline.11,19 The average fluid deficit for patients with DKA is 3–5 liters; fluid resuscitation in young, otherwise healthy patients should begin with a rapid bolus of 1 liter of normal saline followed by an infusion of normal saline at 500 ml/hour for several hours.11,19–21
Patients with HHS are often severely dehydrated, with cumulative fluid deficits of 10 liters or more. However, because they tend to be older and sicker, they require careful resuscitation. Expert opinion advocates for a rapid bolus of 250 ml of normal saline repeated as needed until the patient is well perfused.19,22,23 Fluid therapy is then continued at a rate of 150–250 ml/hour based on cardiopulmonary status and serum osmolality.23–25
The choice and rate of IV fluid for patients with DKA who are not critically ill should be based on their corrected serum sodium and overall fluid status. While awaiting laboratory study results, most of these patients may be given a bolus of 500 ml of normal saline.11,19 Patients with mild to moderate DKA should be given normal saline at 250 ml/hour; those with an elevated corrected serum sodium should be given half-normal saline at 250 ml/hour.26
Critically ill patients with DKA should be given a loading dose of regular insulin at 0.1 units/kg body weight to a maximum of 10 units followed by an infusion of regular insulin at 0.1 units/kg body weight/hour, to a maximum of 10 units/hour.11,19 Other doses and routes of insulin administration have been studied,27–29 but these have not been evaluated outside of the research setting or in critically ill patients.11
Less seriously ill patients with DKA should be given an infusion of regular insulin at 0.1 units/kg body weight/hour without a loading dose to minimize the risk of hypoglycemia. Insulin should not be started until hypovolemia has been addressed and serum potassium has been confirmed to be > 3.5 mEq/L. Giving insulin to patients with a serum potassium level < 3.5 mEq/L may precipitate life-threatening arrhythmias.
Expert opinion regarding the use of insulin for patients with HHS is mixed.11,19,22 Because some patients with HHS achieve euglycemia with fluid resuscitation alone,30 and given the theoretical risks of precipitating oliguric renal failure or cerebral edema in inadequately fluid-resuscitated patients,22 insulin should not be given as part of initial therapy.31–33 However, if the patient’s serum glucose does not decrease by 50–70 mg/dl per hour despite appropriate fluid management, a bolus of IV regular insulin at 0.1 units/kg body weight to a maximum of 10 units may be given.
Patients with DKA or HHS experience rapid shifts in potassium during resuscitation that may trigger life-threatening arrhythmias. Death during initial resuscitation of patients with DKA is usually caused by hyperkalemia, whereas hypokalemia is the most common cause of death after treatment has been initiated. Therefore, serum potassium should be checked every 2 hours until it has stabilized in all patients with hyperglycemic crisis, and these patients should remain on a cardiac monitor. Guidelines for the treatment of hyperkalemia and hypokalemia in patients with hyperglycemic crisis based on expert opinion and our clinical experience are found in Table 2.
Many critically ill patients with DKA manifest hypophosphatemia during resuscitation. To avoid potential cardiac and skeletal muscle weakness and respiratory depression from hypophosphatemia, a serum phosphate of < 1.5 mg/dl should be repleted with K2PO4 at 0.5 ml/hour.34 No studies have evaluated replacement of phosphate in HHS, but critically ill patients with HHS should have their phosphate monitored and replaced appropriately.
Bicarbonate should not be used routinely in the treatment of DKA or HSS.19 Expert opinion suggests that it may be used in patients with DKA and severe acidosis (pH < 6.9) or in patients with severe hyperglycemia who present with a wide-complex or disorganized cardiac rhythm thought to be caused by hyperkalemia. Several small studies have shown no improvement in mortality when bicarbonate is used in patients with a pH > 6.9.35 Additionally, bicarbonate may prolong hypokalemia,36 has been associated with longer hospitalizations,37 and is thought to cause paradoxical acidosis of the cerebral spinal fluid and decrease oxygen tissue delivery.22 In children, its use has been associated with increased risk of cerebral edema.38
Continued evaluation and treatment
All patients with hyperglycemic crisis require fingerstick glucose measurements hourly until they have stabilized. In patients with DKA, an additional bolus of regular insulin at 0.14 units/kg body weight by IV administration should be given if the blood glucose level does not decrease by 10% in the first hour; the continuous infusion of regular insulin should then resume at the original dose.
For patients with DKA, dextrose should be added to the continuous IV fluids once blood glucose has decreased to < 250 mg/dl. Patients with HHS whose blood glucose level decreases to < 300 mg/dl should be observed closely for signs of oliguric renal failure and cardiovascular collapse; these patients may require the addition of dextrose to IV fluids, even without administration of insulin.
In the treatment of DKA, expert opinion recommends continuing an insulin infusion until acidosis has resolved and an anion gap is no longer present, but there are no formally endorsed criteria for discontinuing insulin. When converting to subcutaneous insulin, a subcutaneous dose should be given 1 hour before stopping the IV infusion to prevent rebound hyperglycemia.11,19 Each institution should devise a standard protocol to provide consistent care for its patients.39
Patients with DKA or HHS rarely meet criteria to be safely discharged from emergency departments.1 These patients typically require admission to the hospital with hourly blood glucose and neurological checks until they have stabilized.
A definitive diagnosis of hypoglycemia requires Whipple’s triad: symptoms consistent with hypoglycemia, low blood glucose, and resolution of symptoms once blood glucose levels normalize.40 In practice, hypoglycemia is generally defined as a blood glucose level < 60 mg/dl.31,41 Severe hypoglycemia, requiring the assistance of another person to regain euglycemia, can cause significant morbidity, particularly in the chronically ill or elderly; it is the cause of death in ~ 3% of insulin-dependent diabetic patients.42
Iatrogenic hypoglycemia is often the limiting factor in glycemic management of diabetes.43–46 In the landmark Diabetes Control and Complications Trial,42 27% of patients with type 1 diabetes on intensive insulin regimens developed severe hypoglycemia annually.
Hypoglycemia is one of the most frequent diabetes-related chief complaints seen in emergency departments.47 Because of the high frequency of hypoglycemia as a cause of altered mental status, all patients who present to an emergency department with altered mentation should undergo immediate bedside blood glucose measurement.
Oral hypoglycemic agents and insulin as a cause of hypoglycemia
Although the differential diagnosis for hypoglycemia includes liver failure, severe sepsis, and renal disease, this article will focus on the most common cause of hypoglycemia in patients with diabetes: the use of insulin and oral antidiabetes medications for glycemic control.
The type and dose of medication used for glycemic control is crucially important in determining the risk for recurrent hypoglycemia. Biguanides such as metformin decrease hepatic production and intestinal absorption of glucose and decrease the oxidation of fatty acids. Alpha-glucosidase inhibitors decrease postprandial absorption of carbohydrates, and thiazolidinediones enhance the effects of insulin without increasing its secretion. These anti-hyperglycemic medications do not cause hypoglycemia when used in isolation.
In contrast, sulfonylureas and meglitinides increase insulin secretion and activity and therefore can cause hypoglycemia.48 The half-life for most sulfonylurea medications is 14–16 hours; they can cause severe, prolonged hypoglycemia. Although meglitinides have a shorter half-life, the risk of recurrent hypoglycemia from these medications is unknown; experts urge caution and recommend assuming that these patients have a high risk of recurrent hypoglycemia.49
Treatment of hypoglycemia
As with patients who present in hyperglycemic crisis, the initial evaluation of patients with suspected hypoglycemia includes securing the airway and assessing hemodynamic status. Altered mentation and signs of malnutrition should prompt administration of naloxone and thiamine, respectively. Naloxone and dextrose may completely reverse coma and eliminate the need for intubation; whenever possible, they should be given before proceeding to intubation.
Once bedside glucose measurement confirms hypoglycemia, treatment should be accomplished immediately with either oral intake of food, IV dextrose, or intramuscular glucagon. When decreased mentation precludes oral intake of food, IV dextrose is the first-line therapy. One amp of dextrose provides ~ 100 calories, raising blood glucose levels for 30–60 minutes (Figure 2). The treatment for hypoglycemia may have a shorter duration of action than many of the precipitating drugs, and patients who are successfully treated initially may require repeat doses of glucose. Additionally, depending on the cause of hypoglycemia (e.g., sulfonylurea ingestion), administration of dextrose may precipitate rebound hypoglycemia.
Dextrose is the treatment of choice for hypoglycemia. Glucagon, 1 mg, may be administered subcutaneously or intramuscularly if IV access is not available, but it requires 15 minutes or more for onset of action and is associated with vomiting.
Blood glucose levels should be checked hourly at a minimum. Patients who develop recurrent hypoglycemia or whose blood glucose levels decrease despite administration of dextrose should be started on continuous IV dextrose. These patients require more frequent blood glucose checks—as often as every 15 minutes—and admission to the hospital’s intensive care unit.
To prevent and treat undiagnosed Wernicke’s encephalopathy, thiamine at 100 mg IV should be administered to all patients who present with altered mentation and any signs of malnutrition.50 Despite traditional teaching to the contrary, there is no evidence that a dextrose load to reverse hypoglycemia without thiamine replacement acutely precipitates Wernicke’s encephalopathy. Therefore, when treating a patient with altered mental status and confirmed hypoglycemia, or possible hypoglycemia without access to a bedside glucose meter, dextrose should be given immediately; thiamine should be administered as soon thereafter as possible. Treatment with dextrose should not be delayed if thiamine is not immediately available.51
Patients without seizure should return to their baseline mental status immediately once euglycemia is achieved. In the case of a seizure caused by hypoglycemia, phenytoin is should not be considered first-line therapy because it is known to affect insulin secretion and action.52–54 Instead, benzodiazepines, phenobarbital, or levetiracetam may be used.55 Altered mental status that lasts > 15 minutes despite return to euglycemia should prompt reassessment of the patient and broadening of the differential diagnosis to include traumatic or anoxic brain injury, stroke, alcohol intoxication or withdrawal, opioid ingestion, central nervous system infection, liver failure,56 and renal failure. If lumbar puncture is performed, clinicians should be aware that glucose levels in cerebral spinal fluid remain low for several hours after the serum blood glucose level has been corrected.56
Disposition of patients
Patients who meet all of the following criteria may be considered for discharge from the emergency department after an episode of hypoglycemia.31
The episode of hypoglycemia was:
Isolated (a single episode of hypoglycemia without recurrence)
Completely and rapidly reversed without the need for a continuous dextrose infusion
The result of an identified cause that is unlikely to cause recurrence
Not caused by an oral hypoglycemic medication or long-acting insulin
And the patient:
Completed an uneventful 4-hour observation period with serial blood glucose measurements in the normal range and not trending downward
Ate a full meal during the observation period
Has no comorbidities that would interfere with proper administration of medications and intake of food
Understands how to prevent future episodes of hypoglycemia
Can accurately monitor blood glucose at home
Will be with a responsible adult who will monitor the patient
Has close, reliable follow-up with a primary care provider
Patients who meet these criteria and are discharged from the emergency department should reduce their insulin dose by 25% for at least the next 24 hours to reduce the risk of recurrent hypoglycemia.
Many states require that patients with symptomatic hypoglycemia refrain from driving for 6–12 months and obtain clearance from a physician before resuming driving. Research has shown that this issue is rarely addressed in the emergency department;57 for public health and the safety of patients, it must be included in discharge instructions.
Patients who do not meet all of the above discharge criteria warrant hospital admission. Oral hypoglycemic agents and intermediate- or long-acting forms of insulin (lente, NPH, glargine, and ultralente) are likely to cause recurrent hypoglycemia, and patients taking these medications generally should be admitted.
Patients with hypoglycemia that cannot be completely reversed, was caused by massive ingestion or overdose, or is associated with sepsis, starvation, liver failure, or adrenal insufficiency should be admitted to the hospital’s intensive care unit. Suicide attempts, factious disorder, or other psychiatric illnesses should be addressed with a psychiatric consultation.
Patients With Undiagnosed Prediabetes or Diabetes
Of the 23.6 million Americans with diabetes in 2007, 5.7 million were unaware they had the disease. Additionally, 54 million Americans had prediabetes (impaired fasting glucose and impaired glucose tolerance).1 Patients who present to the emergency department are at high risk for undiagnosed diabetes;58 in one study, nearly four out of five patients in an urban emergency department met American Diabetes Association (ADA) criteria for diabetes screening.59
Currently, the diagnosis of diabetes requires testing performed on two separate occasions unless “unequivocal hyperglycemia” is present.60–62 Patients with unequivocal signs of hyperglycemia such as polyuria, polydipsia, nocturia, or acidosis are likely to need hospital admission, where further testing may be performed. Using an insulin protocol, treatment of hyperglycemia should ideally begin before admission and should not be delayed by confirmatory testing.63
Although hospital emergency departments cannot offer confirmatory testing, patients who are at high risk for prediabetes or diabetes can be identified, and these patients should be counseled regarding their likely diagnosis and lifestyle interventions. A prospective cohort study conducted in an urban emergency department found that all patients with risk factors for diabetes (age > 45 years, polyuria, and polydipsia) and a random blood glucose > 155 mg/dl were later diagnosed with prediabetes or diabetes.63 The use of A1C as a screening tool in emergency departments is being studied59 but is not currently recommended.60
Because most lifestyle interventions are initially unsuccessful,64 certain patients with extremely high risk for undiagnosed diabetes may be considered candidates for initiating the anti-hyperglycemic medication metformin in the emergency department. These patients include those with obesity, family history of diabetes, and polyuria who also have a blood glucose level > 200 mg/dl with no other obvious cause such as trauma or infection. Patients started on metformin in the emergency department should be otherwise healthy, with normal renal function, and should have reliable, close follow-up with a primary care physician.
Recommendations from ADA and the European Association for the Study of Diabetes for initiating therapy in patients with newly diagnosed diabetes are as follows:65
Begin low-dose metformin (500 mg) once or twice daily with meals (breakfast and/or dinner).
After 5–7 days, if gastrointestinal side effects have not occurred, advance the dose to 850–1,000 mg before breakfast and dinner.
If gastrointestinal side effects appear as doses advance, decrease dose to the previous lower dose and try to advance at a later time.
The typical therapeutic dose is 850 mg twice daily. Higher doses, up to 2,550 mg daily, can be used but tend to be associated with more significant side effects and are not recommended as starting doses.
The most common side effects of metformin are gastrointestinal, including nausea, vomiting, diarrhea, and abdominal pain. Lactic acidosis occurs in 3 per 100,000 patient-years, which is no higher than in the general diabetic patient population.64
Data from a before-after pilot study66 conducted in an urban emergency department suggest that starting metformin in the emergency department may be safe and effective. In this study, emergency physicians treating patients with hyperglycemia but no prior diagnosis of diabetes used an algorithm that provided guidelines for starting and titrating metformin and/or insulin. The majority of the patients with severe hyperglycemia experienced rapid and safe decreases in their blood glucose and A1C levels. Emergency department visits for patients in the intervention group also decreased by 78% from baseline.
At a minimum, it is imperative that patients with suspected prediabetes or diabetes be made aware of their abnormal test results and the need for urgent follow-up with a primary care provider. They should be counseled about lifestyle changes. For select patients, starting metformin in the emergency department may be a safe and effective initial medical therapy. However, this area of diabetes care needs further research and should only be considered as part of a multidisciplinary approach that includes a protocol for initiating diabetes medications that was developed in conjunction with a diabetologist.
Hypo- and hyperglycemia caused by diabetes are commonly treated in hospital emergency departments. Physicians must be skilled in diagnosing and stabilizing patients with these conditions.
Hypoglycemia related to oral hypoglycemic medications or intermediate- and long-acting insulin requires admission to the hospital. DKA and HHS are best treated with standardized protocols that specifically address electrolyte repletion, insulin dosing, and fluid management. Mortality in both DKA and HHS is often related to underlying comorbidities and the precipitating insult.
Patients with prediabetes and diabetes are frequently encountered in emergency departments. A random blood glucose level > 155 mg/dl in the setting of risk factors for diabetes should prompt a referral for a formal evaluation for diabetes.
This work was supported by the Office of Academic Affiliations, Department of Veterans Affairs, VA National Quality Scholars Program, with resources and the use of facilities at the VA Tennessee Valley Healthcare System in Nashville, Tenn. (McNaughton and Self).
Candace D. McNaughton, MD, is a clinical instructor in Emergency Medicine; Wesley H. Self, MD, is an assistant professor in Emergency Medicine; and Corey Slovis, MD, is a professor and chairman of the Department of Emergency Medicine at Vanderbilt University in Nashville, Tenn.
- American Diabetes Association(R) Inc., 2011