Drug-Induced Liver Injury (DILI)

 
Drugs induced liver injury
DILI
 
Prepared by:
Dr. Muntadher Abdulkareem Abdullah
M.B.Ch.B,CABM,FIBMS,FIBMS(GE.&HEP.)
 
 
introduction :
 
Drug toxicity should always be considered in the differential  diagnosis of patients presenting with acute liver failure, jaundice  or
abnormal liver biochemistry.
 
Types of liver injury
 
Different histological patterns of liver injury may occur with  drug injury:
 
 
 
 
 
1.
Cholestasis:
 
 
Pure cholestasis :
 
 
(selective interference with bile flow in the  absence of liver injury) like estrogen , this mainly occur with high
concentration of estrogen , Both the current oral contraceptive  pill and hormone replacement therapy can be safely
used in  chronic liver disease
 
Drugs that cause cholestatic hepatitis:
 
 Like Chlorpromazine and antibiotics such as flucloxacillin
 
characterised by inflammation and canalicular injury
 
Co amoxiclav is the most common antibiotic to cause abnormal LFTs but,  unlike other antibiotics, it may not produce
symptoms until  10–42 days after it is stopped.
 
Anabolic glucocorticoids used  by body-builders may also cause a cholestatic hepatitis.
 
 
2.Hepatocyte necrosis :
 
 
Acute hepatocellular necrosis with high serum transaminase concentrations; paracetamol is the best
known.
 
In diclofenac (an NSAID) and isoniazid  (an anti-tuberculous drug), Inflammation is not always present but does
accompany  necrosis in liver injury .
 
Granulomas may be seen in liver injury  following the use of allopurinol
 
Acute hepatocellular necrosis has  also been described following the use of several herbal remedies,  including
germander, comfrey and jin bu huan. Recreational  drugs, including cocaine and ecstasy, can also cause severe  acute
hepatitis.
 
 
 
 
 
 
3. Steatosis:
tetracyclines  and sodium valproate can cause microvesicular hepatocyte fat deposition, due to direct effects on
mitochondrial beta-oxidation.
 
Tamoxifen, and amiodarone toxicity cause macrovesicular hepatocyte fat deposition a similar histological picture to
NASH.
 
 
 
 
4. Vascular/sinusoidal lesion:
 
alkylating agents used in oncology can  damage the vascular endothelium and lead to hepatic venous outflow
obstruction , Chronic overdose of vitamin A can damage  the sinusoids and trigger local fibrosis that can result in
portal  hypertension.
 
 
 
 
 
 
 
 
5. Hepatic fibrosis:
 
Methotrexate, however, as well as causing  acute liver injury when it is started, can lead to cirrhosis when  used in high
doses over a long period of time.
Risk factors for  drug-induced hepatic fibrosis include pre-existing liver disease  and a high alcohol intake.
 
Drug induced hepatic fibrosis is  very uncommon
 
Approach to a patient with drug induced liver injury :
 
Tabulate the drugs taken:
Prescribed and self-administered
• Establish whether hepatotoxicity is reported in the literature
• Relate the time the drugs were taken to the onset of illness: 4 days to 8 weeks (usual)
• Establish the effect of stopping the drugs on normalization of liver
 
 
Biochemistry:
Hepatitic liver function tests (2 months)
Cholestatic/mixed liver function tests (6 months)
N.B. Challenge tests with drugs should be avoided
 
 
Exclude other causes:
Viral hepatitis
Biliary disease
 
 
 
• Consider liver biopsy
 
 
 
Treatment :
 
 
Stop the offending medication , use of safe alternatives
 
Supportive and symptomatic treatment for nausea, vomiting , itching , etc
Short coarse of steroid can be beneficial in certain cases
 
Close monitoring of patient condition and follow up biochemical investigations
 
Liver transplantation in case of fulminant liver failure
 
Thanks
Slide Note
Embed
Share

Drug-induced liver injury (DILI) can present as cholestasis, hepatocyte necrosis, steatosis, vascular damage, and hepatic fibrosis. Various drugs like antibiotics, NSAIDs, recreational drugs, and herbal remedies can cause liver damage. Recognizing DILI is crucial in patients with liver dysfunction or abnormal liver tests. A detailed history of prescribed and self-administered drugs is essential for diagnosis and management.

  • DILI
  • Liver Injury
  • Drug Toxicity
  • Hepatotoxicity
  • Medication Side Effects

Uploaded on Sep 29, 2024 | 0 Views


Download Presentation

Please find below an Image/Link to download the presentation.

The content on the website is provided AS IS for your information and personal use only. It may not be sold, licensed, or shared on other websites without obtaining consent from the author. Download presentation by click this link. If you encounter any issues during the download, it is possible that the publisher has removed the file from their server.

E N D

Presentation Transcript


  1. Drugs induced liver injury DILI Prepared by: Dr. Muntadher Abdulkareem Abdullah M.B.Ch.B,CABM,FIBMS,FIBMS(GE.&HEP.)

  2. introduction : Drug toxicity should always be considered in the differential diagnosis of patients presenting with acute liver failure, jaundice or abnormal liver biochemistry. Types of liver injury Different histological patterns of liver injury may occur with drug injury: 1. Cholestasis: Pure cholestasis : (selective interference with bile flow in the absence of liver injury) like estrogen , this mainly occur with high concentration of estrogen , Both the current oral contraceptive pill and hormone replacement therapy can be safely used in chronic liver disease

  3. Drugs that cause cholestatic hepatitis: Like Chlorpromazine and antibiotics such as flucloxacillin characterised by inflammation and canalicular injury Co amoxiclav is the most common antibiotic to cause abnormal LFTs but, unlike other antibiotics, it may not produce symptoms until 10 42 days after it is stopped. Anabolic glucocorticoids used by body-builders may also cause a cholestatic hepatitis. 2.Hepatocyte necrosis : Acute hepatocellular necrosis with high serum transaminase concentrations; paracetamol is the best known. In diclofenac (an NSAID) and isoniazid (an anti-tuberculous drug), Inflammation is not always present but does accompany necrosis in liver injury . Granulomas may be seen in liver injury following the use of allopurinol Acute hepatocellular necrosis has also been described following the use of several herbal remedies, including germander, comfrey and jin bu huan. Recreational drugs, including cocaine and ecstasy, can also cause severe acute hepatitis.

  4. 3. Steatosis: tetracyclines and sodium valproate can cause microvesicular hepatocyte fat deposition, due to direct effects on mitochondrial beta-oxidation. Tamoxifen, and amiodarone toxicity cause macrovesicular hepatocyte fat deposition a similar histological picture to NASH. 4. Vascular/sinusoidal lesion: alkylating agents used in oncology can damage the vascular endothelium and lead to hepatic venous outflow obstruction , Chronic overdose of vitamin A can damage the sinusoids and trigger local fibrosis that can result in portal hypertension.

  5. 5. Hepatic fibrosis: Methotrexate, however, as well as causing acute liver injury when it is started, can lead to cirrhosis when used in high doses over a long period of time. Risk factors for drug-induced hepatic fibrosis include pre-existing liver disease and a high alcohol intake. Drug induced hepatic fibrosis is very uncommon

  6. Approach to a patient with drug induced liver injury : Tabulate the drugs taken: Prescribed and self-administered Establish whether hepatotoxicity is reported in the literature Relate the time the drugs were taken to the onset of illness: 4 days to 8 weeks (usual) Establish the effect of stopping the drugs on normalization of liver Biochemistry: Hepatitic liver function tests (2 months) Cholestatic/mixed liver function tests (6 months) N.B. Challenge tests with drugs should be avoided Exclude other causes: Viral hepatitis Biliary disease Consider liver biopsy

  7. Treatment : Stop the offending medication , use of safe alternatives Supportive and symptomatic treatment for nausea, vomiting , itching , etc Short coarse of steroid can be beneficial in certain cases Close monitoring of patient condition and follow up biochemical investigations Liver transplantation in case of fulminant liver failure

  8. Thanks

Related


More Related Content

giItT1WQy@!-/#giItT1WQy@!-/#giItT1WQy@!-/#