eMedicine Specialties > Endocrinology > Metabolic Disorders
Vitamin E Toxicity: Follow-up
Updated: Aug 12, 2008
Follow-up
Further Inpatient Care
- Patients with vitamin E toxicity require hospitalization only if bleeding complications, including intracranial hemorrhage, occur.
- If an intracranial hemorrhage is suggested or the patient has focal neurologic findings on examination, order a head CT scan without contrast to rule out an existing hemorrhage.
- If hemorrhage is present, the patient should receive inpatient medical management, with a neurosurgeon consulted for possible drainage of the fluid collection.
- Patients who present with other forms of bleeding should receive vitamin K and should be observed until they are stable, with follow-up evaluation provided on an outpatient basis.
Further Outpatient Care
- Patients with vitamin E toxicity who are stable can be treated in an outpatient setting, with periodic monitoring of the PT to ensure its return to normal levels if bleeding develops.
Deterrence/Prevention
- Individuals can avoid vitamin E toxicity by adhering to the daily recommended dosages of the vitamin and through monitoring of PT when anticoagulants are being taken.
- Patients with nutritional deficiency should increase their intake of vitamin K to prevent bleeding complications.
Prognosis
- In most patients with vitamin E toxicity, the prognosis is excellent once the supplements are discontinued.
- Patients with mild bleeding episodes are likely to fully recover once vitamin K is administered and the vitamin E supplements are discontinued.
- Patients with intracranial hemorrhage have an increased mortality rate; however, with proper diagnosis and management, many patients with this condition survive and recover some or all of their previous functions.
Miscellaneous
Medicolegal Pitfalls
- A medical and/or legal problem could arise if a patient develops a significant bleeding complication as a result of a physician-prescribed combination of oral anticoagulants and vitamin E without warning the patient of the increased risk of bleeding and elevated INR.
- If a patient is taking vitamin E while on oral anticoagulants, warn the patient of the possible adverse bleeding effects and recommend limiting vitamin E intake to the RDA (15 mg/d).
- Warn patients taking high doses of vitamin E (400 IU or more) that no compelling evidence exists that vitamin E reduces cardiovascular risk or cancer and that it may increase heart failure and mortality, especially in patients with chronic diseases.
- Warn patients taking lipid-lowering agents that vitamin E may blunt the beneficial effect on HDL.
We wish to thank Christy L Henry, MD, and Don S Schalch, MD, for their previous contributions to this article.
More on Vitamin E Toxicity |
| Overview: Vitamin E Toxicity |
| Differential Diagnoses & Workup: Vitamin E Toxicity |
| Treatment & Medication: Vitamin E Toxicity |
Follow-up: Vitamin E Toxicity |
| References |
| Further Reading |
| « Previous Page |
References
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Further Reading
Related eMedicine topics:
Toxicity, Vitamin
Vitamin E Deficiency
Vitamin K Deficiency
Keywords
vitamin E toxicity, hypervitaminosis E, vitamin poisoning, vitamin toxicity, vitamin E, alpha tocopherol, alpha-tocopherol, all-rac-alpha-tocopherol acetate, RRR–alpha tocopherol, RRR-alpha-tocopherol, antioxidant, free radical scavenger, fat-soluble vitamin, Alpha-Tocopherol, Beta Carotene Cancer Prevention Study, fatal subarachnoid hemorrhage, increased risk of bleeding, increased prothrombin time, necrotizing enterocolitis, intracranial hemorrhage, vitamin K
Follow-up: Vitamin E Toxicity