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Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
Profound delayed thrombocytopenia presenting 16 days after Abciximab (Reopro®) administration
G J Webb1, J M A Swinburn, H Grech
1Royal Berkshire Hospital, London Road, Reading, RG1 5AN, UK.
Platelets
|April 30, 2011
Summary
Abciximab can cause severe thrombocytopenia, a dangerous drop in platelets. This case study details a rare instance of this side effect occurring 16 days after Abciximab administration, highlighting a significantly delayed reaction.
Area of Science:
- Cardiology
- Pharmacology
- Hematology
Background:
- Abciximab is a glycoprotein IIb/IIIa inhibitor used during percutaneous coronary interventions.
- Thrombocytopenia is a known, albeit infrequent, adverse effect of Abciximab therapy.
- The onset of Abciximab-induced thrombocytopenia is typically rapid, occurring within hours to days of administration.
Observation:
- This report details a unique case of severe, life-threatening thrombocytopenia.
- The patient experienced thrombocytopenia 16 days post-Abciximab administration.
- This represents the longest documented delay in the presentation of Abciximab-induced thrombocytopenia.
Findings:
- The patient required significant supportive care, including transfusions.
- Treatment with dexamethasone and intravenous immunoglobulin led to patient improvement.
- Delayed-onset Abciximab-induced thrombocytopenia can occur and may be severe.
Implications:
- Clinicians should maintain a high index of suspicion for delayed Abciximab-induced thrombocytopenia, even weeks after administration.
- Extended monitoring may be warranted in select patients.
- This case expands the known temporal spectrum of Abciximab-associated adverse events.
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