eMedicine Specialties > Emergency Medicine > Neurology
Lambert-Eaton Myasthenic Syndrome: Follow-up
Updated: Sep 2, 2009
Follow-up
Further Inpatient Care
- In patients in whom LEMS is suspected and history suggests acute worsening, admission for observation and testing is warranted.
- Patients experiencing acute exacerbations of weakness should be admitted for further testing and therapy that is best completed on an in-patient basis.
- Medical therapy, as previously mentioned, to include immunosuppression and plasmapheresis, may be indicated.
Further Outpatient Care
- Ideally, the patient's neurologist or primary care physician should coordinate all tests and procedures ordered on an outpatient basis.
- Physical therapy and exercise are important parts of the outpatient regimen to help maintain muscle tone and strength.
Deterrence/Prevention
- The ED physician should be aware of medications that can cause deterioration in the patient's condition. These include neuromuscular blocking agents, aminoglycosides, magnesium, iodinated intravenous contrast, and calcium channel blockers.
Complications
- The most significant complication, and the only one that applies to emergency medicine, is acute respiratory compromise. This is rare and usually is due to iatrogenic reasons (as already discussed).
- Increased temperatures from fever or the environment also may worsen the weakness.
- Patients may experience transient worsening following hot baths and showers or during systemic illnesses.
Prognosis
- The prognosis is difficult to determine since it often is linked with the progression of the underlying cancer.
- In most cases, therapy with agents such as DAP may help to relieve symptoms partially, but usually symptoms progress over time.
More on Lambert-Eaton Myasthenic Syndrome |
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| Treatment & Medication: Lambert-Eaton Myasthenic Syndrome |
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| Multimedia: Lambert-Eaton Myasthenic Syndrome |
| References |
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References
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Titulaer MJ, Wirtz PW, Willems LN, van Kralingen KW, Smitt PA, Verschuuren JJ. Screening for small-cell lung cancer: a follow-up study of patients with Lambert-Eaton myasthenic syndrome. J Clin Oncol. Sep 10 2008;26(26):4276-81. [Medline].
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Lee JH, Shin JH, Kim DS, et al. A case of Lambert-Eaton myasthenic syndrome associated with atypical bronchopulmonary carcinoid tumor. J Korean Med Sci. Oct 2004;19(5):753-5. [Medline].
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Sanders DB. Lambert-Eaton myasthenic syndrome: clinical diagnosis, immune-mediated mechanisms, and update on therapies. Ann Neurol. May 1995;37 Suppl 1:S63-73. [Medline].
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Verschuuren JJ, Wirtz PW, Titulaer MJ, et al. Available treatment options for the management of Lambert-Eaton myasthenic syndrome. Expert Opin Pharmacother. Jul 2006;7(10):1323-36. [Medline].
Further Reading
Keywords
LEMS, neuromuscular transmission, voltage-gated calcium channels, presynaptic motor nerve terminal, Lambert-Eaton myasthenic syndrome, muscle weakness, acetylcholine, ACh, myasthenia gravis
Follow-up: Lambert-Eaton Myasthenic Syndrome