Metronidazole induced liver injury: a rare immune mediated drug reaction

Dayakar Kancherla1, Mahesh Gajendran1, Priyanka Vallabhaneni2

  • 1Division of General Internal Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA.

Insights

This case report details a rare instance of metronidazole causing delayed, immune-allergic liver injury that mimicked autoimmune hepatitis. Prompt treatment with prednisone led to significant patient recovery and improved liver function tests.

Area of Science:

  • Hepatology
  • Clinical Case Reports
  • Pharmacology

Background:

  • Drug-induced liver injury (DILI) presents as direct hepatotoxicity or idiosyncratic reactions.
  • Idiosyncratic DILI occurs unpredictably, with an estimated incidence of 10-15 per 100,000 patient-years.

Purpose of the Study:

  • To report an extremely rare case of metronidazole-induced delayed immune-allergic hepatocellular liver injury.
  • To highlight its presentation mimicking autoimmune hepatitis.

Main Methods:

  • A case study of a 54-year-old male treated with metronidazole for Clostridium difficile infection.
  • Clinical presentation, laboratory findings (bilirubin, ALT, AST, AP, INR), and treatment response were documented.

Main Results:

  • The patient developed hepatocellular liver injury three months post-metronidazole treatment, with elevated liver enzymes and bilirubin.
  • A diagnosis of metronidazole-induced liver injury was made after excluding other causes.
  • Treatment with oral prednisone resulted in significant clinical improvement and normalization of liver function tests.

Conclusions:

  • Metronidazole can cause delayed immune-allergic hepatocellular liver injury, presenting atypically as autoimmune hepatitis.
  • Early recognition and corticosteroid treatment are crucial for managing this rare adverse drug reaction.

Related Concept Videos

Drug toxicity: Idiosyncratic Reactions01:16

Drug toxicity: Idiosyncratic Reactions

Idiosyncratic drug reactions represent abnormal chemical responses that vary significantly among individuals, ranging from extreme sensitivity to low doses to insensitivity to high doses. These reactions often occur due to the drug's covalent binding with serum proteins, forming a foreign hapten that triggers an immunotoxicological response. The variability in drug reactions has a strong pharmacogenetic foundation, with genetic differences crucial in how individuals metabolize drugs. For...
220
Drug Toxicity: Allergic Reactions01:30

Drug Toxicity: Allergic Reactions

Drug-related allergies are immune-mediated responses triggered by the administration of pharmacological agents. These hypersensitivity reactions are classified based on the immune mechanisms involved. The four primary types—Type I, II, III, and IV—are mediated by different immunological pathways and exhibit distinct clinical manifestations.Type I Hypersensitivity/ IgE-Mediated Reactions: Immunoglobulin E (IgE) immediately mediates Type I hypersensitivity reactions. Upon initial...
209
Drug toxicity: Drug–Drug Interaction01:30

Drug toxicity: Drug–Drug Interaction

Drug–drug interactions can precipitate toxicity through multiple mechanisms. Absorption interactions alter how drugs enter the body, exemplified when ranitidine increases the absorption of basic drugs, while cholestyramine decreases the levels of propranolol. Protein binding interactions occur when drugs share the same binding sites on plasma proteins. Drugs like aspirin and warfarin, when bound in excess, can lead to increased free drug concentrations, enhancing the potential for...
423
Drug Toxicity: Risk factors01:24

Drug Toxicity: Risk factors

Adverse Drug Reactions (ADRs) are potential complications that arise during pharmacotherapy, influenced by multiple risk factors. Age plays a significant role; both neonates and the elderly are at heightened risk due to their respective immature and diminished metabolic and elimination processes. Gender also impacts ADRs, with females experiencing a 1.5 to 1.7-fold greater risk than males, which may be linked to pharmacokinetic, pharmacodynamic, and hormonal differences. Notably, neonates, the...
229
Drug Toxicity: Dose-Dependent Reactions01:24

Drug Toxicity: Dose-Dependent Reactions

Drug toxicities can be stratified into pharmacological, pathological, or genotoxic based on their mechanisms. The incidence and severity of these toxicities generally increase with the drug's concentration in the body and exposure time.Pharmacological toxicity is evident when the therapeutic effects of drugs overshoot into adverse reactions in a predictable, dose-dependent manner. Central nervous system (CNS) depression from barbiturates is a classic example, with effects escalating from...
229
Allergic Drug Reactions01:27

Allergic Drug Reactions

Allergic reactions related to drugs are hypersensitivity responses driven by the immune system and bear no connection to the drug's therapeutic action. While drugs in isolation do not trigger an immune response, they can interact with endogenous proteins to form antigens. These antigens stimulate lymphocytes to produce antibodies. IgE-type antibodies attach themselves to mast cells. Upon subsequent exposure to the same stimulus, the antigen-antibody interaction is initiated, unleashing...
1.6K