Hepatorenal syndrome: Difference between revisions

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==Background==
==Background==
*Acute renal failure in pt w/ nl kidneys in presence of acute/chronic hepatic failure  
 
*Often heralded by the presence of SBP
*[[Special:MyLanguage/Acute renal failure|Acute renal failure]] in patient with normal kidneys in presence of acute/chronic hepatic failure  
*Cause is unknown
*Often heralded by the presence of [[Special:MyLanguage/SBP|SBP]]
* Arterial vasodilatation in the splanchnic circulation, which is triggered by portal hypertension
*Diagnosis of exclusion
 
 


==Clinical Features==
==Clinical Features==
*Type 1
*Type 1
**Doubling of serum Cr over a 2-week period
**Doubling of serum creatinine over a 2-week period
**Progressive oliguria
**Progressive oliguria
*Type 2
*Type 2
**Gradual impairment in renal function (that may not advance beyond moderate)
**Gradual impairment in renal function (that may not advance beyond moderate)
Type 1 & 2 both require:
 
*Cr >1.5mg/dl
 
*Cr not reduced below 1.5 w/ albumin (1g/kg) and after minimum of 2 days off diuretics
*Absence of current or recent rx with potentially nephrotoxic drugs
*Absence of shock
*Absence of renal parenchymal disease:


==Differential Diagnosis==
==Differential Diagnosis==
*Hypovolemia-induced renal failure
*Hypovolemia-induced renal failure
**[[GI bleed]]
**[[Special:MyLanguage/GI bleed|GI bleed]]
**[[Diuretics]]
**[[Special:MyLanguage/Diuretics|Diuretics]]
**[[Diarrhea]]
**[[Special:MyLanguage/Diarrhea|Diarrhea]]
*Parenchymal renal disease
*Parenchymal renal disease
**Urinary excretion of >500mg protein/d, >50 RBC/hpf, abnl kidneys on U/S
**Urinary excretion of >500mg protein/d, >50 RBC/hpf, abnormal kidneys on U/S
*Drug-induced renal failure ([[NSAIDs]], [[aminoglycosides]])
*Drug-induced renal failure ([[Special:MyLanguage/NSAIDs|NSAIDs]], [[Special:MyLanguage/aminoglycosides|aminoglycosides]])
 
 
 
==Evaluation<ref>Deepika D et al. Hepatorenal Syndrome Workup. Dec 27, 2015. http://emedicine.medscape.com/article/178208-workup#showall</ref>==
 
*[[Ultrasound: Abdomen|Abdominal US]]
*Diagnostic [[Special:MyLanguage/paracentesis|paracentesis]]
*Ascites fluid cultures and analysis
*Labs:
**CBC with diff
**BMP
**[[Special:MyLanguage/LFTs|LFTs]]
**Blood cultures
**[[Special:MyLanguage/Urinalysis|Urinalysis]]
**Urine electrolytes and osmolality
**Consultants: alpha-fetoprotein, cryoglobulins
*All major criteria must be met for diagnosis for both HRS types 1 and 2:
**Serum creatinine >1.5mg/dL
**No improvement in renal function after halting diuretics AND admin of 1.5 L of plasma expander
**[[Special:MyLanguage/Proteinuria|Proteinuria]] <500mg/d
**No [[Special:MyLanguage/ultrasound|ultrasound]] evidence of obstructive uropathy or renal parenchymal disease
**Absence of shock, bacterial infection, hypovolemia, nephrotoxic meds
*Supporting criteria not required for diagnosis:
**Uop <500 cc/day
**Urine sodium <10 mEq/L
**Urine osmolality > plasma osmolality
**Urine RBC <50 cells/hpf
**Serum sodium <130 mEq/L


==Diagnosis==




==Treatment==
==Management==
*[[Vasoconstrictors]]
 
*[[Special:MyLanguage/Vasopressors|Vasopressors]]
**Terlipressin: 0.5-1mg q 4-6 IV us 5-15d
**Terlipressin: 0.5-1mg q 4-6 IV us 5-15d
**[[Norepinepherine]]: 0.5-3mg/hr to increase MAP by 10mmHg
**[[Special:MyLanguage/Norepinephrine|Norepinephrine]]: 0.5-3mg/hr to increase MAP by 10mmHg
**Midrodrine: 7.5mg PO tid with Octreotide 100mcg sq
**[[Special:MyLanguage/Midodrine|Midodrine]]: 7.5mg PO tid with Octreotide 100mcg sq
*Albumin: 1-1.5g/kg with one of above
*Albumin: 1-1.5g/kg with one of above
*Other:
*Other:
**TIPS, renal replacement therapy
**[[Special:MyLanguage/TIPS|TIPS]], [[Special:MyLanguage/hemodialysis|renal replacement therapy]]
**Avoid diuretics and benzodiazepines
**Discuss giving octreotide and/or midodrine with admitting physician
 
 


==Disposition==
==Disposition==
*1-month survival: 50%
*1-month survival: 50%
*6-month survival: 20%
*6-month survival: 20%
*Should be evaluated at liver transplant center
*May require TIPS, vasoconstrictors as bridge to transplant
==See Also==


==References==
==References==
*NEJM vol 361 no 13 P. Gines
*NEJM vol 361 no 13 P. Gines
<references/>
[[Category:GI]]
[[Category:Renal]]


[[Category:GI]]
</translate>

Latest revision as of 23:04, 4 January 2026


Background

  • Acute renal failure in patient with normal kidneys in presence of acute/chronic hepatic failure
  • Often heralded by the presence of SBP
  • Arterial vasodilatation in the splanchnic circulation, which is triggered by portal hypertension
  • Diagnosis of exclusion


Clinical Features

  • Type 1
    • Doubling of serum creatinine over a 2-week period
    • Progressive oliguria
  • Type 2
    • Gradual impairment in renal function (that may not advance beyond moderate)


Differential Diagnosis


Evaluation[1]

  • Abdominal US
  • Diagnostic paracentesis
  • Ascites fluid cultures and analysis
  • Labs:
    • CBC with diff
    • BMP
    • LFTs
    • Blood cultures
    • Urinalysis
    • Urine electrolytes and osmolality
    • Consultants: alpha-fetoprotein, cryoglobulins
  • All major criteria must be met for diagnosis for both HRS types 1 and 2:
    • Serum creatinine >1.5mg/dL
    • No improvement in renal function after halting diuretics AND admin of 1.5 L of plasma expander
    • Proteinuria <500mg/d
    • No ultrasound evidence of obstructive uropathy or renal parenchymal disease
    • Absence of shock, bacterial infection, hypovolemia, nephrotoxic meds
  • Supporting criteria not required for diagnosis:
    • Uop <500 cc/day
    • Urine sodium <10 mEq/L
    • Urine osmolality > plasma osmolality
    • Urine RBC <50 cells/hpf
    • Serum sodium <130 mEq/L


Management

  • Vasopressors
    • Terlipressin: 0.5-1mg q 4-6 IV us 5-15d
    • Norepinephrine: 0.5-3mg/hr to increase MAP by 10mmHg
    • Midodrine: 7.5mg PO tid with Octreotide 100mcg sq
  • Albumin: 1-1.5g/kg with one of above
  • Other:


Disposition

  • 1-month survival: 50%
  • 6-month survival: 20%
  • Should be evaluated at liver transplant center
  • May require TIPS, vasoconstrictors as bridge to transplant


See Also

References

  • NEJM vol 361 no 13 P. Gines
  1. Deepika D et al. Hepatorenal Syndrome Workup. Dec 27, 2015. http://emedicine.medscape.com/article/178208-workup#showall