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Published on: May 7, 2011
Thrombotic thrombocytopenic purpura after cephalosporin administration: a possible relationship
Beverly W Baron1, Koen van Besien, Philip C Hoffman
1Department of Pathology, Blood Bank, The University of Chicago, Chicago, Illinois, USA. bbaron@uchospitals.edu
Background:
Acquired thrombotic thrombocytopenic purpura (TTP) is an autoimmune disorder. The pathogenesis is believed to be mediated by an autoantibody directed against the metalloproteinase responsible for the degradation of the very-high-molecular-weight multimers of the vWF. The syndrome can be precipitated by a variety of conditions, and certain medications also have been implicated.
Case Reports:
The cases of two patients who took a cephalosporin antibiotic, cephalexin (Keflex, Eli Lilly), and then developed TTP are reported. One patient subsequently received a third-generation cephalosporin, ceftriaxone (Rocephin, Roche), without adverse reaction. Of interest, one patient had taken cefaclor (Ceclor, Eli Lilly) 8 years before and had also developed TTP at that time. The other patient also took cefaclor for approximately 3 weeks before taking cephalexin. In addition, she had had a dose of clarithromycin (Biaxin, Abbott Laboratories) the day before the onset of the TTP symptoms.
Conclusions:
To our knowledge, TTP has not been reported previously after administration of cephalosporin antibiotics. Attention is called to the possibility that this syndrome may occur after exposure to some of these drugs, although the incidence is very rare or, alternatively, underdiagnosed.
Insights
Acquired thrombotic thrombocytopenic purpura (TTP) can rarely be triggered by cephalosporin antibiotics like cephalexin. This rare autoimmune disorder highlights the need for vigilance when prescribing these drugs.
Area of Science:
- Hematology
- Immunology
- Pharmacology
Background:
- Acquired thrombotic thrombocytopenic purpura (TTP) is an autoimmune condition.
- Pathogenesis involves autoantibodies against vWF-cleaving metalloproteinase.
- Various conditions and medications can precipitate TTP.
Observation:
- Two patients developed TTP after cephalexin administration.
- One patient had a prior TTP episode after cefaclor.
- Another patient received ceftriaxone without adverse effects.
Findings:
- TTP following cephalosporin antibiotic use is reported.
- This association may be rare or underdiagnosed.
Implications:
- Clinicians should consider cephalosporins as a potential trigger for TTP.
- Further investigation into drug-induced TTP is warranted.
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