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Thrombotic thrombocytopenia purpura caused by piperacillin successfully treated with plasma infusion

Y Yata1, M Miyagiwa, S Inatsuchi

  • 1Department of Internal Medicine, Toyama Red Cross Hospital, Japan. yyata@duke.edu

Annals of Hematology
|December 2, 2000
PubMed

Insights

Piperacillin-induced thrombotic thrombocytopenic purpura (TTP) is rare, presenting with neurological issues, kidney dysfunction, and anemia. This case highlights TTP with unusual hemorrhagic colitis and skin eruption, successfully treated with plasma infusion.

Area of Science:

  • Internal Medicine
  • Pharmacology
  • Hematology

Background:

  • Antibiotic-associated adverse events can manifest with diverse clinical presentations.
  • Piperacillin sodium (PIPC) is a commonly used antibiotic with a known side effect profile.
  • Thrombotic thrombocytopenic purpura (TTP) is a rare but serious thrombotic microangiopathy.

Observation:

  • An 81-year-old male developed fever and loss of appetite, followed by thrombocytopenia, hemorrhagic colitis, and skin eruption after PIPC treatment.
  • The patient subsequently experienced neurological abnormalities, renal dysfunction, and microangiopathic hemolytic anemia (MAHA).
  • These clinical features led to a diagnosis of TTP.

Findings:

  • The patient's symptoms, including hemorrhagic colitis and skin eruption, were attributed to PIPC-induced TTP.
  • Treatment with fresh-frozen plasma infusion resulted in significant clinical improvement.
  • This case underscores the rare association of TTP with hemorrhagic colitis and skin eruption.

Implications:

  • Physicians should consider TTP in patients presenting with unexplained thrombocytopenia, MAHA, renal, and neurological dysfunction, especially after antibiotic administration.
  • Early recognition and prompt plasma infusion are crucial for managing TTP and improving patient outcomes.
  • The unusual presentation emphasizes the need for vigilance regarding rare drug-induced adverse events.

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