Beriberi: Difference between revisions

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==Background==
==Background==
*Dry Beriberi: neuro sx caused by thiamine deficiency
*Dry Beriberi: neuro symptoms caused by thiamine deficiency
*Wet Beriberi: cardiac sx caused by thiamine deficiency
*Wet Beriberi: cardiac symptoms caused by thiamine deficiency
*Infantile Beriberi: neuro/cardiac sx caused by thiamine deficiency in <1 year old infant
*Infantile Beriberi: neuro/cardiac symptoms caused by thiamine deficiency in <1 year old infant


===Causes===
===Causes===
*Anything that causes thiamine (vitamin B1) deficiency: poor dietary intake, malabsorption, increased metabolic requirement
*Anything that causes [[thiamine deficiency|thiamine (vitamin B1) deficiency]]: poor dietary intake, malabsorption, increased metabolic requirement
**Chronic alcoholism, dieting/fasting/starvation, anorexia, vomiting/diarrhea, unbalanced TPN, GI surgery, malignancy, dialysis, AIDS, IBD, pancreatitis, liver disease, thyrotoxicosis
**Chronic [[alcoholism]], dieting/fasting/starvation, [[anorexia nervosa|anorexia]], [[vomiting]]/[[diarrhea]], unbalanced TPN, GI surgery, malignancy, [[dialysis complications|dialysis]], [[AIDS]], [[IBD]], [[pancreatitis]], liver disease, [[thyrotoxicosis]]


===Pathophysiology===
===Pathophysiology===
*Thiamine is a cofactor for enzymes required in:
*Thiamine is a cofactor for enzymes required in:
**krebs cycle
**Krebs cycle
**Pentose phosphate pathway
**Pentose phosphate pathway
**Alpha-ketoglutarate dehydrogenase
**Alpha-ketoglutarate dehydrogenase
**pyruvate dehydrogenase.
**Pyruvate dehydrogenase.
*Because thiamine is an important cofactor in critical pathways for energy production, deficiency results in lactic acidosis and alteration of brain metabolism.
*Because thiamine is an important cofactor in critical pathways for energy production, deficiency results in lactic acidosis and alteration of brain metabolism.
*Thiamine is also important for lipid metabolism and may affect myelin sheath formation. This may explain peripheral neuropathy symptoms in dry beriberi.
*Thiamine is also important for lipid metabolism and may affect myelin sheath formation. This may explain peripheral neuropathy symptoms in dry beriberi.
{{Thiamine deficiency types}}


==Clinical Features==
==Clinical Features==
[[File:Beriberi USNLM.jpg|thumb|Dry Beriberi with symmetric peripheral neuropathy.]]
[[File:PMC3237207 JFCM-18-162-g001.png|thumb|Bariatric beriberi with bilateral wrist drop and peripheral neuropathy after bariatric surgery for morbid obesity.]]
===Dry Beriberi===
===Dry Beriberi===
*Symmetrical peripheral neuropathy (motor and sensory) mostly distal extremities
*Symmetrical peripheral neuropathy ([[weakness|motor]] and [[numbness|sensory]]) mostly distal extremities


===Wet Beriberi===
===Wet Beriberi===
*CHF, high output heart failure, cardiomegaly, peripheral edema, tachycardia, DOE/PND/orthopnea
*[[CHF]], [[high output heart failure]], cardiomegaly, peripheral edema, [[tachycardia]], [[SOB|DOE/PND/orthopnea]]
*Can include neuropathy seen in Dry Beriberi
*Can include neuropathy seen in Dry Beriberi


===Infantile Beriberi===
===Infantile Beriberi===
*CHF, cardiomegaly, tachycardia, cyanosis, dyspnea, weight loss, marasmus, vomiting, loud cry, nystagmus, seizure
*[[CHF]], cardiomegaly, [[tachycardia]], [[hypoxia|cyanosis]], [[shortness of breath (peds)|dyspnea]], [[failure to thrive (peds)|weight loss]], marasmus, [[nausea and vomiting (peds)|vomiting]], loud cry, [[nystagmus]], [[seizure (peds)|seizure]]


===Bariatric Beriberi===
===Bariatric Beriberi===
*Occurs 1-3 months post-op
*Occurs 1-3 months post-[[weight loss surgery complications|bariatric surgery]]
*Causes are multifactorial, including low nutritional intake, poor baseline nutrition, persistent vomiting, malabsorption
*Causes are multifactorial, including low nutritional intake, poor baseline [[malnutrition|nutrition]], persistent [[vomiting]], malabsorption


==Differential Diagnosis==
==Differential Diagnosis==
{{Vitamin deficiencies DDX}}
{{Vitamin deficiencies DDX}}


==Diagnosis==
==Evaluation==
[[File:PMC3772304 kcj-43-569-g002.png|thumb|Chest x-ray showing cardiomegaly with mild pulmonary congestion and pleural effusion in a patient with wet beriberi.]]
*Clinical diagnosis
*Clinical diagnosis


==Treatment==
==Management==
''If you suspect Beriberi then treat it! Diagnosis is clinical and difficult to confirm, treatment is simple/inexpensive/effective, there is little risk to treatment, and the risk of morbidity/mortality from not treating is high''
''If you suspect Beriberi then treat it! Diagnosis is clinical and difficult to confirm, treatment is simple/inexpensive/effective, there is little risk to treatment, and the risk of morbidity/mortality from not treating is high''
#Thiamine 50-100 mg IV/IM q day x 7-14 days, then 10 mg PO q day until complete recovery
#[[Thiamine]] 50-100mg IV/IM q day x 7-14 days, then 10mg PO q day until complete recovery
#Magnesium; hypomagnesemic state may be resistant to thiamine administration
#[[Magnesium]]; hypomagnesemic state may be resistant to thiamine administration
#Multivitamin (at risk for other vitamin deficiencies)
#Multivitamin (at risk for other vitamin deficiencies)
*For chronic alcoholics consider banana bag: thiamine 100 mg + magnesium 2-4 g + folate 1 mg + multivitamin; all in 1L NS or D5W
*Give thiamine BEFORE glucose in patients requiring glucose who are at risk for thiamine deficiency; glucose without thiamine can precipitate/worsen WE by driving thiamine intracellularly
*Give thiamine BEFORE glucose in patients requiring glucose who are at risk for thiamine deficiency; glucose without thiamine can precipitate/worsen WE by driving thiamine intracellularly


==Disposition==
==Disposition==
==Prevention==
{{Vitamin prophylaxis for ETOH}}


==See Also==
==See Also==
 
*[[Thiamine]]
*[[Thiamine]
*[[Thiamine deficiency]]
*[[Thiamine deficiency]]


==References==
==References==
# Donnino, Michael, et al. “Myths and misconceptions of wernicke’s encephalopathy: what every emergency physician should know.” Annals of emergency medicine.  2007. Vol 50, no 6. Pages 715-721.
#Donnino, Michael, et al. “Myths and misconceptions of wernicke’s encephalopathy: what every emergency physician should know.” Annals of emergency medicine.  2007. Vol 50, no 6. Pages 715-721.
# Sechi, GianPietro; Serra, Alessandro.  “Wernicke’s encephalopathy: new clnical settings and recent advances in diagnosis and management.” Neurology. Vol 6, May 2007.  Pages 442-455
#Sechi, GianPietro; Serra, Alessandro.  “Wernicke’s encephalopathy: new clnical settings and recent advances in diagnosis and management.” Neurology. Vol 6, May 2007.  Pages 442-455
<references/>
[[Category:Neurology]]
[[Category:Neurology]]
[[Category:Cardiology]]
[[Category:Cardiology]]

Revision as of 21:25, 27 October 2020

Background

  • Dry Beriberi: neuro symptoms caused by thiamine deficiency
  • Wet Beriberi: cardiac symptoms caused by thiamine deficiency
  • Infantile Beriberi: neuro/cardiac symptoms caused by thiamine deficiency in <1 year old infant

Causes

Pathophysiology

  • Thiamine is a cofactor for enzymes required in:
    • Krebs cycle
    • Pentose phosphate pathway
    • Alpha-ketoglutarate dehydrogenase
    • Pyruvate dehydrogenase.
  • Because thiamine is an important cofactor in critical pathways for energy production, deficiency results in lactic acidosis and alteration of brain metabolism.
  • Thiamine is also important for lipid metabolism and may affect myelin sheath formation. This may explain peripheral neuropathy symptoms in dry beriberi.

Thiamine deficiency types

Clinical Features

Dry Beriberi with symmetric peripheral neuropathy.
Bariatric beriberi with bilateral wrist drop and peripheral neuropathy after bariatric surgery for morbid obesity.

Dry Beriberi

  • Symmetrical peripheral neuropathy (motor and sensory) mostly distal extremities

Wet Beriberi

Infantile Beriberi

Bariatric Beriberi

Differential Diagnosis

Vitamin deficiencies

Evaluation

Chest x-ray showing cardiomegaly with mild pulmonary congestion and pleural effusion in a patient with wet beriberi.
  • Clinical diagnosis

Management

If you suspect Beriberi then treat it! Diagnosis is clinical and difficult to confirm, treatment is simple/inexpensive/effective, there is little risk to treatment, and the risk of morbidity/mortality from not treating is high

  1. Thiamine 50-100mg IV/IM q day x 7-14 days, then 10mg PO q day until complete recovery
  2. Magnesium; hypomagnesemic state may be resistant to thiamine administration
  3. Multivitamin (at risk for other vitamin deficiencies)
  • Give thiamine BEFORE glucose in patients requiring glucose who are at risk for thiamine deficiency; glucose without thiamine can precipitate/worsen WE by driving thiamine intracellularly

Disposition

Prevention

Vitamin Prophylaxis for Chronic alcoholics

  • At risk for thiamine deficiency, but no symptoms: thiamine 100mg PO q day
  • Give multivitamin PO; patient at risk for other vitamin deficiencies

Banana bag

The majority of chronic alcoholics do NOT require a banana bag[1][2]

See Also

References

  1. Donnino, Michael, et al. “Myths and misconceptions of wernicke’s encephalopathy: what every emergency physician should know.” Annals of emergency medicine. 2007. Vol 50, no 6. Pages 715-721.
  2. Sechi, GianPietro; Serra, Alessandro. “Wernicke’s encephalopathy: new clnical settings and recent advances in diagnosis and management.” Neurology. Vol 6, May 2007. Pages 442-455
  1. Krishel, S, et al. Intravenous Vitamins for Alcoholics in the Emergency Department: A Review. The Journal of Emergency Medicine. 1998; 16(3):419–424.
  2. Li, SF, et al. Vitamin deficiencies in acutely intoxicated patients in the ED. The American Journal of Emergency Medicine. 2008; 26(7):792–795.