Bismuth toxicity: Difference between revisions
(Created page with "==Background== *Heavy Metal *Available in two forms **Elemental ***Nontoxic **Bismuth Salts ***Uses ****Oral preparations for traveler's diarrhea, nausea, and vomiting ***...") |
Elcatracho (talk | contribs) |
||
| (7 intermediate revisions by 3 users not shown) | |||
| Line 10: | Line 10: | ||
****Gastric ulcers | ****Gastric ulcers | ||
***Cause toxicity | ***Cause toxicity | ||
==Toxicokinetics== | |||
===Toxicokinetics=== | |||
*Poorly understood due to lack of data | *Poorly understood due to lack of data | ||
*Low absorption in the GI tract, approximately 0.2% is systemically absorbed <ref>Hundal O, Bergseth M, Gharehnia B, et al. Absorption of bismuth from two bismuth compounds before and after healing of peptic ulcers. Hepatogastroenterology. 1999;46:2882-2886.</ref> | *Low absorption in the GI tract, approximately 0.2% is systemically absorbed <ref>Hundal O, Bergseth M, Gharehnia B, et al. Absorption of bismuth from two bismuth compounds before and after healing of peptic ulcers. Hepatogastroenterology. 1999;46:2882-2886.</ref> | ||
| Line 16: | Line 17: | ||
*Levels may be increased in those taking PPI | *Levels may be increased in those taking PPI | ||
**Ranitidine does not alter the absorption of bismuth | **Ranitidine does not alter the absorption of bismuth | ||
==Clinical Features== | ==Clinical Features== | ||
===Acute=== | |||
* | *[[Abdominal pain]] | ||
*Oliguria | |||
*Acute tubular necrosis and renal failure | |||
===Chronic=== | |||
*Diffuse progressive encephalopathy | |||
*Neurobehavioral changes | |||
**Apathy | |||
**Irritability | |||
**Poor concentration | |||
**Worsened short term memory | |||
**Visual hallucinations | |||
*Movement disorders | |||
** | **Myoclonus | ||
**[[Ataxia]] | |||
**Tremors | |||
* | *Pigmentation of skin and oral mucosa | ||
* | *[[Seizure]] | ||
*[[Coma]] and [[death]] | |||
==Differential Diagnosis== | ==Differential Diagnosis== | ||
{{Heavy metals list}} | |||
===[[Encephalopathy]]=== | ===[[Encephalopathy]]=== | ||
*[[Viral encephalopathy]] | *[[Viral encephalopathy]] | ||
| Line 71: | Line 52: | ||
*[[Postanoxic encephalopathies]] | *[[Postanoxic encephalopathies]] | ||
*[[Progressive multifocal ataxia]] | *[[Progressive multifocal ataxia]] | ||
==Evaluation== | ==Evaluation== | ||
*Need to have high index of suspicion | *Need to have high index of suspicion | ||
*BMP | *BMP | ||
*CBC | *CBC | ||
* | *[[Urinalysis]] | ||
*CT head for cases of encephalopathy | *CT head for cases of encephalopathy | ||
**May show diffuse cortical hyperdensity of the grey matter | **May show diffuse cortical hyperdensity of the grey matter | ||
*Salicylate level | *[[Salicylate]] level | ||
**In the United States bismuth subsalicylate is the most common oral compound, and up to 90% of salicylate is absorbed <ref>Pickering LK, Feldman S, Ericsson CD, Cleary TG. Absorption of salicylate and bismuth from a bismuth subsalicylate containing compound (Pepto- Bismol). J Pediatr. 1981;99:654-656.</ref> | **In the United States [[bismuth subsalicylate]] is the most common oral compound, and up to 90% of salicylate is absorbed <ref>Pickering LK, Feldman S, Ericsson CD, Cleary TG. Absorption of salicylate and bismuth from a bismuth subsalicylate containing compound (Pepto- Bismol). J Pediatr. 1981;99:654-656.</ref> | ||
*EEG | *EEG | ||
==Management== | ==Management== | ||
*Supportive care | *Supportive care | ||
| Line 87: | Line 70: | ||
**Limited data to support its use | **Limited data to support its use | ||
**Exact timing and dosages are unknown | **Exact timing and dosages are unknown | ||
** | **[[Dimercaprol]] (BAL) | ||
***Undergoes biliary elimination which is useful in those with renal insufficiency | ***Undergoes biliary elimination which is useful in those with renal insufficiency | ||
***Benefits shown in experimental models | ***Benefits shown in experimental models | ||
| Line 93: | Line 76: | ||
==Disposition== | ==Disposition== | ||
*Admission if evidence of renal failure or encephalopathy manifestations | *Admission if evidence of renal failure or encephalopathy manifestations | ||
*Consult Toxicology or | *Consult Toxicology or [[poison control]] | ||
==See Also== | |||
*[[Toxicology (main)]] | |||
==References== | ==References== | ||
<references/> | <references/> | ||
Rao, R. Bismuth. In: Goldfrank's Toxicologic Emergencies. 9th Ed. New York: McGraw-Hill; 2011: 1233-1236 | Rao, R. Bismuth. In: Goldfrank's Toxicologic Emergencies. 9th Ed. New York: McGraw-Hill; 2011: 1233-1236 | ||
[[Category:Toxicology]] | |||
Latest revision as of 21:51, 8 March 2021
Background
- Heavy Metal
- Available in two forms
- Elemental
- Nontoxic
- Bismuth Salts
- Uses
- Oral preparations for traveler's diarrhea, nausea, and vomiting
- Bismuth-impregnated surgical packing pastes for ileostomies and colostomies
- Gastric ulcers
- Cause toxicity
- Uses
- Elemental
Toxicokinetics
- Poorly understood due to lack of data
- Low absorption in the GI tract, approximately 0.2% is systemically absorbed [1]
- 90% excreted from kidneys
- Levels may be increased in those taking PPI
- Ranitidine does not alter the absorption of bismuth
Clinical Features
Acute
- Abdominal pain
- Oliguria
- Acute tubular necrosis and renal failure
Chronic
- Diffuse progressive encephalopathy
- Neurobehavioral changes
- Apathy
- Irritability
- Poor concentration
- Worsened short term memory
- Visual hallucinations
- Movement disorders
- Myoclonus
- Ataxia
- Tremors
- Pigmentation of skin and oral mucosa
- Seizure
- Coma and death
Differential Diagnosis
- Aluminum toxicity
- Antimony toxicity
- Arsenic toxicity
- Barium toxicity
- Beryllium toxicity
- Bismuth toxicity
- Boron toxicity
- Cadmium toxicity
- Cesium toxicity
- Chromium toxicity
- Cobalt toxicity
- Copper toxicity
- Gold toxicity
- Iron toxicity
- Lead toxicity
- Lithium toxicity
- Manganese toxicity
- Mercury toxicity
- Nickel toxicity
- Phosphorus toxicity
- Platinum toxicity
- Selenium toxicity
- Silver toxicity
- Thallium toxicity
- Tin toxicity
- Vanadium toxicity
- Zinc toxicity
Encephalopathy
- Viral encephalopathy
- Ethanol withdrawal
- Creutzfeld-Jacob disease
- Lithium toxicity
- Neurodegenerative leukoencephalopathies
- Nonketotic hyperosmolar coma
- Postanoxic encephalopathies
- Progressive multifocal ataxia
Evaluation
- Need to have high index of suspicion
- BMP
- CBC
- Urinalysis
- CT head for cases of encephalopathy
- May show diffuse cortical hyperdensity of the grey matter
- Salicylate level
- In the United States bismuth subsalicylate is the most common oral compound, and up to 90% of salicylate is absorbed [2]
- EEG
Management
- Supportive care
- Consider whole bowel irrigation
- Chelation
- Limited data to support its use
- Exact timing and dosages are unknown
- Dimercaprol (BAL)
- Undergoes biliary elimination which is useful in those with renal insufficiency
- Benefits shown in experimental models
Disposition
- Admission if evidence of renal failure or encephalopathy manifestations
- Consult Toxicology or poison control
See Also
References
- ↑ Hundal O, Bergseth M, Gharehnia B, et al. Absorption of bismuth from two bismuth compounds before and after healing of peptic ulcers. Hepatogastroenterology. 1999;46:2882-2886.
- ↑ Pickering LK, Feldman S, Ericsson CD, Cleary TG. Absorption of salicylate and bismuth from a bismuth subsalicylate containing compound (Pepto- Bismol). J Pediatr. 1981;99:654-656.
Rao, R. Bismuth. In: Goldfrank's Toxicologic Emergencies. 9th Ed. New York: McGraw-Hill; 2011: 1233-1236
