Lithium toxicity
Background
- Lithium remains the most effective treatment for bipolar disorder despite availability of newer agents
- Mechanism of action poorly understood; modulates neurotransmitter signaling
- Narrow therapeutic index (therapeutic level: 0.6-1.2 mEq/L)
- Pharmacokinetics:
- Rapidly absorbed (peak 1-2h for immediate release; 4-12h for sustained release)
- Initially distributes in extracellular fluid → gradually redistributes to CNS (up to 24 hours)
- 95% renally excreted; handled like sodium by proximal tubule
- Lithium toxicity rarely fatal (only 11 deaths out of 6815 reported toxic exposures in 2012)[1]
Common Precipitants
- Volume depletion: vomiting, diarrhea, diaphoresis, decreased PO intake
- Medications that decrease lithium excretion:
- Acute kidney injury or chronic kidney disease
- Intentional overdose
- Hyperthermia, CHF, sepsis
- Nephrogenic diabetes insipidus (caused by chronic lithium use) → dehydration → ↑ lithium levels
Clinical Features
Three recognized patterns of toxicity[2]:
Acute Ingestion
- Patient not previously on lithium (no body stores)
- GI symptoms predominate: nausea, vomiting, diarrhea, abdominal pain (earliest/most common)
- Cardiac: bradycardia, QT prolongation, T-wave flattening/inversion, Brugada-like pattern[3]
- CNS depression is a late finding (takes time for lithium to redistribute to brain)
- Serum levels may be very high but do not correlate with clinical toxicity
Acute-on-Chronic
- Patient on chronic lithium who takes supra-therapeutic dose
- Mixed GI and CNS symptoms
Chronic Toxicity
- Insidious onset in patients on chronic therapy
- Due to increased absorption or decreased elimination
- CNS symptoms predominate (generally more severe than acute):
- Mild: fine tremor, drowsiness, muscle weakness
- Moderate: hyperreflexia, confusion, coarse tremor, ataxia, slurred speech
- Severe: seizures, myoclonus, coma, extrapyramidal symptoms
- Hypothyroidism (lithium inhibits thyroid hormone release)
SILENT Syndrome[4]
- Syndrome of Irreversible Lithium-Effectuated Neurotoxicity
- Neurologic dysfunction persisting >2 months after cessation of lithium
- Cerebellar dysfunction (dysarthria, ataxia, gait instability), peripheral neuropathy, dementia
Differential Diagnosis
- Serotonin syndrome
- Neuroleptic malignant syndrome
- Thyroid storm / hypothyroidism
- Alcohol or sedative-hypnotic intoxication
- Structural CNS lesion
- Other heavy metals toxicity
- Uremia
Evaluation
- Lithium level:
- Therapeutic: 0.6-1.2 mEq/L
- Levels >1.5 mEq/L may be associated with toxicity (chronic > acute for same level)
- Do NOT use green top (lithium heparin) tube — falsely elevates level
- Serum levels do not predict CNS levels and only roughly correlate with clinical symptoms
- Serial levels every 2-4 hours (especially after overdose or post-HD)
- BMP: creatinine, sodium (often hyponatremic or hypernatremic), calcium
- TSH (chronic use → hypothyroidism)
- ECG: QT prolongation, T-wave changes, bradycardia, Brugada pattern
- Acetaminophen and salicylate levels (possible coingestants)
- Urinalysis (urine specific gravity to evaluate concentrating ability)
Management
GI Decontamination
- Whole bowel irrigation (WBI): only for sustained-release tablet ingestion
- PEG solution via NG at 1-2 L/hr (adults)
- Activated charcoal is NOT effective (lithium is not adsorbed)
- Gastric lavage generally not effective and potentially harmful
Fluid Resuscitation
- Most important initial intervention — most patients have volume/sodium deficit
- NS is preferred (restores sodium, promotes renal lithium excretion)
- Give 2L NS bolus, then 200 mL/hr (or 2× maintenance)
- Target UOP 1-2 mL/kg/hr
- Avoid forced diuresis with loop diuretics (may worsen lithium toxicity)
Hemodialysis
- Most effective method of lithium removal
- Must follow serial lithium levels post-HD — levels will rebound due to tissue redistribution
- May require multiple sessions
- EXTRIP Workgroup Indications[5]:
- Recommended (1D): impaired kidney function AND Li >4.0 mEq/L
- Recommended (1D): clinical deterioration (decreased LOC, seizures, life-threatening dysrhythmias) regardless of level
- Suggested (2D): Li >5.0 mEq/L
- Suggested (2D): expected time to Li <1.0 mEq/L with optimal management >36 hours
- Contraindication to aggressive fluids (CHF) lowers threshold for HD
- Consult toxicology and nephrology — complex decision
Endpoint of Dialysis
- Continue HD until lithium level <1.0 mEq/L
- Recheck level 6-8 hours post-HD for rebound
Disposition
- Discharge considerations (acute ingestion):
- Asymptomatic after 4-6 hours observation
- Two downtrending lithium levels
- No worsening renal function
- Admit:
- All patients with Li level >1.5 mEq/L
- All sustained-release preparation ingestions (regardless of Li level)
- Any patient with neurologic symptoms
- Any patient requiring hemodialysis
- Poison control: 1-800-222-1222
See Also
References
- ↑ Mowry JB, et al. 2012 annual report of the AAPCC NPDS. Clin Toxicol (Phila). 2013;51:949-1229. PMID 24359283
- ↑ Waring WS, et al. Pattern of lithium exposure predicts poisoning severity. QJM. 2007;100(5):271-6. PMID 17410291
- ↑ Canan F, et al. Lithium intoxication related multiple temporary ECG changes. Cases Journal. 2008;1:156. PMID 18801176
- ↑ Adityanjee, et al. The syndrome of irreversible lithium-effectuated neurotoxicity. Clin Neuropharmacol. 2005;28(1):38-49. PMID 15681811
- ↑ Decker BS, et al. Extracorporeal treatment for lithium poisoning: systematic review and recommendations from the EXTRIP Workgroup. Clin J Am Soc Nephrol. 2015;10(5):875-887. PMID 25583293
- Baird-Gunning J, et al. Lithium poisoning. J Intensive Care Med. 2017;32(4):249-263. PMID 27055773
- Ott M, et al. Lithium intoxication: incidence, clinical course and renal function — a population-based retrospective cohort study. J Psychopharmacol. 2016;30(10):1008-1019. PMID 27530173
