eMedicine Specialties > Endocrinology > Diabetes Mellitus

Diabetic Ketoacidosis: Follow-up

Author: Osama Hamdy, MD, MB, BCh, PhD, Medical Director, Obesity Clinical Program, Joslin Diabetes Center, Assistant Professor of Medicine, Harvard Medical School, Boston, MA
Contributor Information and Disclosures

Updated: Sep 1, 2009

Follow-up

Further Inpatient Care

  • Patients are not usually discharged from the hospital unless they have switched back to their daily insulin regimen without recurrence of ketosis. When the condition is stable, pH is greater than 7.3, and bicarbonate is greater than 18 mEq/L, the patient is allowed to eat a meal preceded by an SC dose of regular insulin. Insulin infusion can be discontinued 30 minutes later. If the patient is still nauseated and cannot eat, continue dextrose infusion and administer regular or ultra–short-acting insulin SC every 4 hours according to blood glucose level, while trying to maintain blood glucose values at 100-180 mg/dL.
  • In established patients with diabetes, SC long-acting insulin (eg, insulin glargine, Detemir, Ultralente) should be initiated back at the same dose that was used prior to diabetic ketoacidosis. However, if neutral protamine Hagedorn (NPH) insulin was previously used, start back at the usual dose only when the patient eats well and is able to retain meals without vomiting; otherwise, the dose should be reduced to avoid hypoglycemia during its peak efficacy period.
  • In newly diagnosed patients with type 1 DM, a careful estimate of the long-acting insulin dose should be considered. Starting with smaller doses generally is recommended to avoid unneeded hypoglycemia.

Further Outpatient Care

  • Psychological counseling of young children and adolescents usually is helpful.

Complications

  • Cerebral edema is a serious, major complication that may evolve during treatment of diabetic ketoacidosis (DKA). Be extremely cautious to avoid cerebral edema during initiation of therapy. Deterioration of the level of consciousness in spite of improved metabolic state usually indicates the occurrence of cerebral edema. MRI usually is used to confirm the diagnosis. If cerebral edema occurs at initiation of therapy, it usually worsens during the course of treatment. Clinical cerebral edema is rare and carries the highest mortality rate. Although mannitol (0.25-1 g/kg IV) and dexamethasone (2-4 mg q6-12h) frequently are used in this situation, no specific medication has proven to be useful in such instances.
  • Cardiac dysrhythmia may occur secondary to severe hypokalemia and/or acidosis either initially or as a result of therapy. Usually, correction of the cause is sufficient to treat cardiac dysrhythmia, but, if it persists, consultation with a cardiologist is mandatory. Performing cardiac monitoring on patients with DKA during correction of electrolytes always is advisable.
  • Pulmonary edema may occur for the same reasons as cerebral edema. Although it is rare, be cautious of possible overcorrection of fluid loss. Diuretics and oxygen therapy are often sufficient for the management of pulmonary edema.
  • Nonspecific myocardial injury may occur in severe DKA, which is associated with minute elevations of myocardial biomarkers (troponin T and CK-MB) and initial ECG changes compatible with myocardial infarction (MI). Acidosis and very high levels of free fatty acids could cause membrane instability and biomarker leakage. Coronary arteriography usually is normal, and patients usually recover fully without further evidence of ischemic heart disease. Regardless of the pathogenesis, the presence of minute biomarker elevations and ECG changes do not necessarily signify MI in DKA.
  • Microvascular changes consistent with diabetic retinopathy have been reported prior to and after treatment of DKA; however, the blood-retinal barrier does not experience the same degree of perturbation as the blood-brain barrier does.

Prognosis

  • The prognosis of properly treated patients with diabetic ketoacidosis is excellent, especially in younger patients if intercurrent infections are absent. The worst prognosis is usually observed in patients who are older with severe intercurrent illnesses, eg, myocardial infarction, sepsis, or pneumonia, especially when they are treated outside an ICU.
  • The presence of deep coma at the time of diagnosis, hypothermia, and oliguria are signs of poor prognosis.

Patient Education

  • Educate patients in the prevention of diabetic ketoacidosis so that a recurrent episode can be avoided.
  • Promotion of self-management and dealing with the stress of intercurrent illness always is part of the education process for adult patients with diabetes.9,10
  • For excellent patient education resources, visit eMedicine's Diabetes Center. Also, see eMedicine's patient education article, Diabetic Ketoacidosis.

Miscellaneous

Medicolegal Pitfalls

  • Failure to diagnose diabetic ketoacidosis (DKA) in the absence of a urinary test result that is positive for ketones
  • False belief that DKA is worsening based on positive results of a urine test for ketones, while, in fact, DKA is improving with return of predominate ketones from beta hydroxybutyrate to acetoacetate
  • Failure to recognize associated conditions, eg, myocardial infarction, UTI, pneumonia, perinephric abscess, or hidden sepsis
  • Failure to recognize signs and symptoms of cerebral edema
  • Rapid correction of hyperglycemia in the first 4-5 hours
  • Rapid correction of metabolic acidosis with sodium bicarbonate before correction of fluid loss
  • Stopping monitoring of serum potassium after it returns to the reference range
  • Infusing potassium chloride without continuous monitoring of serum potassium or ECG
 


More on Diabetic Ketoacidosis

Overview: Diabetic Ketoacidosis
Differential Diagnoses & Workup: Diabetic Ketoacidosis
Treatment & Medication: Diabetic Ketoacidosis
Follow-up: Diabetic Ketoacidosis
References
Further Reading

References

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Further Reading

Related eMedicine topics:
Diabetes Mellitus, Type 1 [Endocrinology]
Diabetes Mellitus, Type 1 [Pediatrics: General Medicine]
Diabetes Mellitus, Type 1 - A Review
Diabetes Mellitus, Type 2 [Endocrinology]
Diabetes Mellitus, Type 2 [Pediatrics: General Medicine]
Diabetes Mellitus, Type 2 - A Review
Diabetic Ketoacidosis [Emergency Medicine]
Diabetic Ketoacidosis [Pediatrics: Cardiac Disease and Critical Care Medicine]
Disorders of Carbohydrate Metabolism
Metabolic Acidosis [Emergency Medicine]
Metabolic Acidosis [Nephrology]
Pediatrics, Diabetic Ketoacidosis

Clinical guidelines:
Care of children and adolescents with type 1 diabetes: a statement of the American Diabetes Association. American Diabetes Association - Professional Association.  2005 Jan.  27 pages.  NGC:004193

Hyperglycemic crises in diabetes. American Diabetes Association - Professional Association.  2000 Oct (revised 2001; republished 2004 Jan).  9 pages.  NGC:003428

Clinical trials:
Cerebral Edema in Pediatric Diabetic Ketoacidosis

Ketosis Prone Diabetes in African-Americans

Use of Insulin Glargine to Treat Diabetic Ketoacidosis

Keywords

diabetic ketoacidosis, ketoacidosis, acidosis, DKA, metabolic acidosis, diabetes, hyperglycemia, ketonuria, diabetes mellitus, type 1 diabetes, diabetes type 1, type 2 diabetes, diabetes type 2, insulin, human insulin, type 1 DM, type 2 DM,  ketogenesis, ketones, ketoacids, acetone, beta hydroxybutyrate, acetoacetate, Kussmaul respirations, increased thirst, polydipsia, increased urination, polyuria

Contributor Information and Disclosures

Author

Osama Hamdy, MD, MB, BCh, PhD, Medical Director, Obesity Clinical Program, Joslin Diabetes Center, Assistant Professor of Medicine, Harvard Medical School, Boston, MA
Osama Hamdy, MD, MB, BCh, PhD is a member of the following medical societies: American Association of Clinical Endocrinologists and American Diabetes Association
Disclosure: Takeda phamaceutical North America Honoraria Speaking and teaching; Merck Inc Honoraria Speaking and teaching; Novo Nordisk Honoraria Speaking and teaching; Amylin Pharmaceutical Honoraria Speaking and teaching; Aventis Honoraria Speaking and teaching

Medical Editor

David S Schade, MD, Chief, Division of Endocrinology and Metabolism, Professor, Department of Internal Medicine, University of New Mexico School of Medicine and Health Sciences Center
David S Schade, MD is a member of the following medical societies: American College of Physicians, American Diabetes Association, American Federation for Medical Research, Endocrine Society, New Mexico Medical Society, New York Academy of Sciences, and Society for Experimental Biology and Medicine
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Don S Schalch, MD, Professor Emeritus, Department of Internal Medicine, Division of Endocrinology, University of Wisconsin Hospitals and Clinics
Don S Schalch, MD is a member of the following medical societies: American Diabetes Association, American Federation for Medical Research, Central Society for Clinical Research, and Endocrine Society
Disclosure: Nothing to disclose.

CME Editor

Mark Cooper, MBBS, PhD, FRACP, Head, Diabetes & Metabolism Division, Baker Heart Research Institute, Professor of Medicine, Monash University
Disclosure: Nothing to disclose.

Chief Editor

George T Griffing, MD, Professor of Medicine, St Louis University School of Medicine
George T Griffing, MD is a member of the following medical societies: American Association for the Advancement of Science, American College of Medical Practice Executives, American College of Physician Executives, American College of Physicians, American Diabetes Association, American Federation for Medical Research, American Heart Association, Central Society for Clinical Research, Endocrine Society, International Society for Clinical Densitometry, and Southern Society for Clinical Investigation
Disclosure: Nothing to disclose.

 
 
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