A Case of Piperacillin-Induced Immune Thrombocytopenia: Diagnostic Challenges and Management

Drug-induced immune thrombocytopenia (DITP) is a rare yet critical disorder that requires prompt recognition and discontinuation of the causative drug to prevent severe complications. In DITP, platelet-reactive antibodies lead to significant platelet destruction. Heparin-induced thrombocytopenia is the most well-studied; yet, antibiotics have also been described. Herein is a case of a 97-year-old woman with a history of hypertension and hyperlipidemia who was admitted with rhabdomyolysis and sepsis secondary to choledocholithiasis and gallstone pancreatitis. She was started on intravenous fluids and broad-spectrum antibiotics, including piperacillin-tazobactam and vancomycin. Within days, her platelet count dropped from 323,000/μL to 1,000/μL. Schistocytes and hemolysis were absent on a peripheral smear. The patient had normal coagulation studies, and she had a low 4T (thrombocytopenia, timing of platelet count fall, thrombosis or other sequelae, and other causes for thrombocytopenia) score, ruling out thrombotic microangiopathies, such as disseminated intravascular coagulation (DIC), thrombotic thrombocytopenic purpura (TTP), and heparin-induced thrombocytopenia (HIT), respectively. While immune thrombocytopenic purpura (ITP) was seriously considered, the temporal relationship between the drop in platelet count and the administration of broad-spectrum antibiotics led to greater suspicion of DITP. Piperacillin was suspected to be the cause and was promptly discontinued. The suspicion was subsequently confirmed, as supported by the detection of positive drug-dependent IgG antibodies. The patient's platelet count normalized within a week after stopping piperacillin and receiving IV immunoglobulin (1 g/kg). Hence, DITP needs to be considered among other causes in patients with acute severe thrombocytopenia, as early recognition and prompt cessation of the offending agent are important for preventing life-threatening hemorrhagic sequelae.

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Journal
Cureus
Published
2025-10-09
DOI
https://doi.org/10.7759/cureus.94174
Primary Topic
Platelet Disorders and Treatments
Type
article
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article

A Case of Piperacillin-Induced Immune Thrombocytopenia: Diagnostic Challenges and Management

Amish Patel, Niharika Kottapalli, Andrew Rettew, Pratap Tetali et al.
Cureus
Platelet Disorders and Treatments
article

A Case of Piperacillin-Induced Immune Thrombocytopenia: Diagnostic Challenges and Management

Amish Patel, Niharika Kottapalli, Andrew Rettew, Pratap Tetali, Kuldeepsinh Atodaria
article en

Abstract

Drug-induced immune thrombocytopenia (DITP) is a rare yet critical disorder that requires prompt recognition and discontinuation of the causative drug to prevent severe complications. In DITP, platelet-reactive antibodies lead to significant platelet destruction. Heparin-induced thrombocytopenia is the most well-studied; yet, antibiotics have also been described. Herein is a case of a 97-year-old woman with a history of hypertension and hyperlipidemia who was admitted with rhabdomyolysis and sepsis secondary to choledocholithiasis and gallstone pancreatitis. She was started on intravenous fluids and broad-spectrum antibiotics, including piperacillin-tazobactam and vancomycin. Within days, her platelet count dropped from 323,000/μL to 1,000/μL. Schistocytes and hemolysis were absent on a peripheral smear. The patient had normal coagulation studies, and she had a low 4T (thrombocytopenia, timing of platelet count fall, thrombosis or other sequelae, and other causes for thrombocytopenia) score, ruling out thrombotic microangiopathies, such as disseminated intravascular coagulation (DIC), thrombotic thrombocytopenic purpura (TTP), and heparin-induced thrombocytopenia (HIT), respectively. While immune thrombocytopenic purpura (ITP) was seriously considered, the temporal relationship between the drop in platelet count and the administration of broad-spectrum antibiotics led to greater suspicion of DITP. Piperacillin was suspected to be the cause and was promptly discontinued. The suspicion was subsequently confirmed, as supported by the detection of positive drug-dependent IgG antibodies. The patient's platelet count normalized within a week after stopping piperacillin and receiving IV immunoglobulin (1 g/kg). Hence, DITP needs to be considered among other causes in patients with acute severe thrombocytopenia, as early recognition and prompt cessation of the offending agent are important for preventing life-threatening hemorrhagic sequelae.

CureusVol. 17(10)
Reading Hospital (US), Drexel University (US)
Openalex Percentile: Top 64%
Platelet Disorders and Treatments
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