Lithium toxicity: Difference between revisions

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==Background==
==Background==
*Toxicity most often involves a drug-drug interaction or decreased renal excretion
*Lithium remains the most effective treatment for [[bipolar disorder]] despite availability of newer agents
*Pts most frequently die of respiratory failure or CV collapse
*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)<ref>Mowry JB, et al. 2012 annual report of the AAPCC NPDS. ''Clin Toxicol (Phila)''. 2013;51:949-1229. PMID 24359283</ref>


==Precipitants==
===Common Precipitants===
#Overdose
*Volume depletion: vomiting, diarrhea, diaphoresis, decreased PO intake
#Renal failure
*Medications that decrease lithium excretion:
#Volume depletion
**[[NSAIDs]], [[ACE inhibitors]]/ARBs, [[thiazide diuretics]]
##Diuretic use, vomiting, diarrhea, diaphoresis, decreased oral intake
*[[Acute kidney injury]] or chronic kidney disease
#Hyperthermia
*Intentional overdose
#Infection
*[[Hyperthermia]], [[CHF]], [[sepsis]]
#CHF
*Nephrogenic [[diabetes insipidus]] (caused by chronic lithium use) → dehydration → ↑ lithium levels
#Surgery
#Cirrhosis


==Clinical Features==
==Clinical Features==
#GI
Three recognized patterns of toxicity<ref>Waring WS, et al. Pattern of lithium exposure predicts poisoning severity. ''QJM''. 2007;100(5):271-6. PMID 17410291</ref>:
##Usually first to develop
##N/V
##Diarrhea
##Generalized abd pain
#CNS
##Usually develops as GI symptoms are abating; more common in chronic toxicity
##Tremor
##Muscle weakness
##Ataxia
##Stupor
##Seizure
##Coma
#Cardiac
##Hypotension
##Conduction Abnormalities
##Ventricular dysrhythmias
##Prolonged QT, transient ST depression, TWI
#Endocrine
##Hyper/Hypothyroidism or hyperparathyroidism
##Hypothyroidism most common
# Renal
##Nephrogenic Diabetes Insipidus
###Can be seen mildly at therapeutic levels
###Causes polyuria and polydipsia


==Diagnosis==
===Acute Ingestion===
*Lithium level
*Patient not previously on lithium (no body stores)
**Correlates better with chronic than acute toxicity
*GI symptoms predominate: nausea, vomiting, diarrhea, abdominal pain (earliest/most common)
**''level may be falsely elevated if placed in a green top tube due to the heparin lithium interaction''
*Cardiac: [[bradycardia]], QT prolongation, T-wave flattening/inversion, Brugada-like pattern<ref>Canan F, et al. Lithium intoxication related multiple temporary ECG changes. ''Cases Journal''. 2008;1:156. PMID 18801176</ref>
*Chemistry
*CNS depression is a late finding (takes time for lithium to redistribute to brain)
**Low or negative ion gap
*Serum levels may be very high but '''do not correlate with clinical toxicity'''
**Elevated osmolar gap
*TSH
*ECG
**QT prolongation
**Diffuse TWI


==Treatment==
===Acute-on-Chronic===
#GI decontamination
*Patient on chronic lithium who takes supra-therapeutic dose
##Consider lavage for massive ingestions (>4gm) if can be performed w/in 1hr
*Mixed GI and CNS symptoms
##Activated charcoal is ineffective
 
#Fluid resuscitation
===Chronic Toxicity===
##Average pt has Na/volume deficit; giving fluid helps reestablish normal Li excretion
*Insidious onset in patients on chronic therapy
###Give 2L NS bolus; then give 200mL/hr
*Due to increased absorption or decreased elimination
#Seizure
*CNS symptoms predominate (generally more severe than acute):
##Benzos are 1st line
**Mild: fine tremor, drowsiness, muscle weakness
##Phenobarbital is 2nd line
**Moderate: hyperreflexia, confusion, coarse tremor, ataxia, slurred speech
##Phenytoin is ineffective
**Severe: [[seizures]], myoclonus, coma, extrapyramidal symptoms
#Dialysis
*Hypothyroidism (lithium inhibits thyroid hormone release)
##Indications:
 
###Li level >4 (acute overdose)
===SILENT Syndrome<ref>Adityanjee, et al. The syndrome of irreversible lithium-effectuated neurotoxicity. ''Clin Neuropharmacol''. 2005;28(1):38-49. PMID 15681811</ref>===
###Li level >3.5 (chronic toxicity)
*Syndrome of Irreversible Lithium-Effectuated Neurotoxicity
###Little change in Li level after 6hr IVF
*Neurologic dysfunction persisting >2 months after cessation of lithium
###Sustained Li level >1.0 after 36hr
*Cerebellar dysfunction (dysarthria, ataxia, gait instability), peripheral neuropathy, dementia
###Baseline renal failure
 
###Ingestion of sustained-release preparations
==Differential Diagnosis==
##Goal:
*[[Serotonin syndrome]]
###Li level <1
*[[Neuroleptic malignant syndrome]]
####Must monitor for up to 8hr following dialysis to ensure levels stay <1
*[[Thyroid storm]] / [[hypothyroidism]]
*[[Alcohol]] or sedative-hypnotic intoxication
*Structural CNS lesion
*Other [[heavy metals]] toxicity
*[[Uremia]]
 
{{Heavy metals DDX}}
 
==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<ref>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</ref>:
**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==
==Disposition==
*Consider discharge for pts asymptomatic after 4-6hr obs with 2 downtrending levels
*Discharge considerations (acute ingestion):
*Admit all pts w/ Li level >1.5
**Asymptomatic after 4-6 hours observation
*Admit all pts w/ ingestion of sustained-release preparation (regardless of Li level)
**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==
==See Also==
*[[Toxicology (Main)]]
*[[Toxicology]]
*[[Heavy metals]]
*[[Bipolar disorder]]
*[[Serotonin syndrome]]
*[[Neuroleptic malignant syndrome]]


==References==
==References==
<references/>
<references/>
*Tintinalli
*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


[[Category:Tox]]
[[Category:Toxicology]]

Latest revision as of 09:30, 22 March 2026

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

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

Template:Heavy metals DDX

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

  1. Mowry JB, et al. 2012 annual report of the AAPCC NPDS. Clin Toxicol (Phila). 2013;51:949-1229. PMID 24359283
  2. Waring WS, et al. Pattern of lithium exposure predicts poisoning severity. QJM. 2007;100(5):271-6. PMID 17410291
  3. Canan F, et al. Lithium intoxication related multiple temporary ECG changes. Cases Journal. 2008;1:156. PMID 18801176
  4. Adityanjee, et al. The syndrome of irreversible lithium-effectuated neurotoxicity. Clin Neuropharmacol. 2005;28(1):38-49. PMID 15681811
  5. 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