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Platelet-mediated bleeding caused by broad-spectrum penicillins.
The Journal of Infectious Diseases
|June 1, 1987
Summary
Ticarcillin and piperacillin significantly increased bleeding times and bleeding risk in hospitalized patients. Cefotaxime showed a lower risk, highlighting antibiotic-associated bleeding risks.
Area of Science:
- Pharmacology
- Hematology
Background:
- Antibiotics like ticarcillin, piperacillin, and mezlocillin are frequently used in hospitalized patients.
- Platelet dysfunction and bleeding are potential adverse effects of certain antibiotic therapies.
Purpose of the Study:
- To prospectively determine the frequencies of platelet dysfunction and bleeding in patients treated with ticarcillin, piperacillin, mezlocillin, or cefotaxime.
- To identify risk factors associated with antibiotic-induced bleeding.
Main Methods:
- Prospective observation of 156 hospitalized adult patients.
- Assessment of bleeding times and occurrence of significant bleeding.
- Statistical analysis of covariables including age, chemotherapy, and pre-existing conditions.
Main Results:
- Elevated bleeding times occurred in 73% of ticarcillin, 43% of piperacillin, 25% of mezlocillin, and 17% of cefotaxime recipients.
- Significant bleeding was observed in 34% of ticarcillin, 17% of piperacillin, 2% of mezlocillin, and 5% of cefotaxime recipients.
- Chemotherapy, thrombocytopenia, older age, higher dose, and longer treatment duration were significant risk factors for bleeding.
Conclusions:
- Ticarcillin and piperacillin are associated with a higher incidence of platelet dysfunction and bleeding compared to mezlocillin and cefotaxime.
- Bleeding risk is influenced by patient-specific factors and treatment parameters, necessitating careful monitoring.