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*Lithium is effective in acute mania management and bipolar prophylaxis. | *Lithium is effective in acute mania management and bipolar prophylaxis. | ||
*Lithium has psychoactive properties only as a positively-charged ion, Li+; to this end, it is manufactured as a salt, i.e. lithium carbonate or lithium chloride. '''Lithium carbonate''' causes less GI irritation and, thus, preferred to LiCl. Lithium citrate is available in a syrup form. | *Lithium has psychoactive properties only as a positively-charged ion, Li+; to this end, it is manufactured as a salt, i.e. lithium carbonate or lithium chloride. '''Lithium carbonate''' causes less GI irritation and, thus, preferred to LiCl. Lithium citrate is available in a syrup form. | ||
| − | *There is no "lithium receptor." It acts on many receptors, channels, and intracellular proteins. Among other effects it inhibits intracellular adenylyl cyclase, an enzyme in the second-messenger cascade of TSH, vasopressin (ADH), and many other cell processes. A serious side effect of lithium are hypothyroidism and failure to concentrate urine. | + | *There is no "lithium receptor." It acts on many receptors, channels, and intracellular proteins. Among other effects it inhibits intracellular adenylyl cyclase, an enzyme in the second-messenger cascade of '''TSH''', '''vasopressin (ADH)''', and many other cell processes. A serious side effect of lithium are hypothyroidism and failure to concentrate urine. |
| − | * Lithium has low therapeutic index (ratio of toxic level to therapeutic level, 1.5''mM''/1.0''mM'' = 1.5) or a narrow therapeutic range (0.8 to 1.2''mM''). | + | * Lithium has low therapeutic index (ratio of toxic level to therapeutic level, 1.5''mM''/1.0''mM'' = 1.5) or a narrow therapeutic range (0.8 to 1.2''mM''). Levels are drawn 12hrs after last dose, 4-5 days after dose change (half-life ~ 24hrs). |
| + | * Li+ is excreted by the kidney; as a tiny cation, it is freely filtered at the glomerulus and reabsorbed at the proximal tubule. Therefore, its excretion is directly related to GFR; reduce lithium dose in the elderly | ||
| + | * Since reabsorption of Li+ and Na+ is competitive at the proximal tubule, any '''hyponatremia'''(low Na+ diet, thiazides, dehydration) can lead to increase in Li+ rebasorption and toxicity, as it is returned to circulation. | ||
| + | * '''Loop diuretics''' (furosemide), caffeine? facilitate lithium excretion. | ||
===How to Start and Monitor=== | ===How to Start and Monitor=== | ||
| + | * Starting dose is 300mg BID or '''qPM'''(maybe easier on the kidney) and titrate to 1500mg +/-300mg, to plasma levels of 1.0''mM''. | ||
==Considerations in Children and Adolescents== | ==Considerations in Children and Adolescents== | ||
Revision as of 03:21, 15 October 2010
Medscape 2010 article
Contents
Introduction
Lithium, the lightest solid element on the periodic table, has a central role in managing pediatric bipolar disorder. This article describes the properties of lithium as a medication. For its role in the overall treatment guidelines, see the article on bipolar disorder.
Adult Psychiatry Review
- Lithium is effective in acute mania management and bipolar prophylaxis.
- Lithium has psychoactive properties only as a positively-charged ion, Li+; to this end, it is manufactured as a salt, i.e. lithium carbonate or lithium chloride. Lithium carbonate causes less GI irritation and, thus, preferred to LiCl. Lithium citrate is available in a syrup form.
- There is no "lithium receptor." It acts on many receptors, channels, and intracellular proteins. Among other effects it inhibits intracellular adenylyl cyclase, an enzyme in the second-messenger cascade of TSH, vasopressin (ADH), and many other cell processes. A serious side effect of lithium are hypothyroidism and failure to concentrate urine.
- Lithium has low therapeutic index (ratio of toxic level to therapeutic level, 1.5mM/1.0mM = 1.5) or a narrow therapeutic range (0.8 to 1.2mM). Levels are drawn 12hrs after last dose, 4-5 days after dose change (half-life ~ 24hrs).
- Li+ is excreted by the kidney; as a tiny cation, it is freely filtered at the glomerulus and reabsorbed at the proximal tubule. Therefore, its excretion is directly related to GFR; reduce lithium dose in the elderly
- Since reabsorption of Li+ and Na+ is competitive at the proximal tubule, any hyponatremia(low Na+ diet, thiazides, dehydration) can lead to increase in Li+ rebasorption and toxicity, as it is returned to circulation.
- Loop diuretics (furosemide), caffeine? facilitate lithium excretion.
How to Start and Monitor
- Starting dose is 300mg BID or qPM(maybe easier on the kidney) and titrate to 1500mg +/-300mg, to plasma levels of 1.0mM.
Considerations in Children and Adolescents
High-Yield Facts
References
Based on the research findings, modest improvement can be anticipated in youths with acute-phase bipolar disorder. Adjunctive medications for symptom management of bipolar and comorbid diagnoses may be warranted. While lithium is an US FDA-approved medication for 12–18-year-olds with bipolar disorder, it requires diligent monitoring. Lithium's small therapeutic window (0.8 to 1.2 mEq/l) can precipitate significant adverse effects, particularly at toxic levels. To achieve an accurate lithium level, blood should be drawn 12 h after a dose. A physical examination should be completed before the start of lithium treatment, and the patient should not have any renal problems. Baseline blood work should include a lithium level, blood urea nitrogen, creatinine concentration, thyroid function tests, electrolytes and a complete blood count, and should be repeated every 6 months once steady state is achieved (usually reached after 1 week in children). Pregnancy tests should be obtained for adolescents of childbearing age and education on appropriate measures to prevent pregnancy should be discussed. The starting dose is usually 300 mg per day titrated up every 3–5 days until the level is within a therapeutic range. Patients should be educated regarding adequate fluid intake and the use of a reliable contraception method due to lithium's potential to cause birth defects. Lithium has demonstrated significant weight gain, and weight should be monitored. Adverse effects of lithium include nausea, vomiting, diarrhea, hypothyroidism, renal function abnormalities, polyuria, polydipsia, leukocytosis, tremors and acne. The dose should be either discontinued or lowered if lithium toxicity occurs. Lithium toxicity symptoms include loss of balance, increased diarrhea, vomiting, anorexia, weakness, ataxia, blurred vision, tinnitus, polyuria, coarse tremor, muscle twitching, irritability and agitation. Several drugs have been found to increase lithium levels including carbamazapine, nonsteriodal anti-inflammatory drugs, tetracyclines and thiazide diuretics.[37]Theophylline and caffeine promote lithium excretion, resulting in lower serum levels of lithium at the same oral dose. Clinicians should discuss these potential interactions with patients and families.