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CH Brown , MJ Bradshaw, EA Natelson, CP Alfrey and TW Williams
Platelet function and blood coagulation were studied in five human
volunteers receiving penicillin-G in incremental doses of 1.2--48 million
U/day, in six volunteers receiving ampicillin in incremental doses of
60--300 mg/kg/day (4--20 g/day), and in six volunteers receiving
methicillin in incremental doses of 60--300 mg/kg/day. Coagulation tests
remained normal in all 17 volunteers. However, ADP- induced platelet
aggregation became abnormal in every subject except one receiving
ampicillin and one receiving methicillin. Defective aggregation occurred
with predictability with the following doses: penicillin-G, 24 million
U/day; ampicillin, 300 mg/kg/day; methicillin, 300 mg/kg/day. All
volunteers given penicillin-G and all given ampicillin experienced
dose-related prolongation of bleeding time which did not occur with
methicillin. Striking prolongation of bleeding time occurred only with
penicillin-G in doses of 48 million U/day. Other tests of platelet function
including clot retraction, platelet factor 3 availability, and
collagen-induced or epinephrine-induced aggregation remained normal during
the administration of these drugs. Measurement of intracellular adenine
nucleotides revealed that the ADP and ATP content of platelets was
unaffected. It appears that at least one mechanism by which the penicillin
compounds alter platelet behavior is by interfering with activation of
these cells by ADP.
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| Copyright © 1976 by American Society of Hematology Online ISSN: 1528-0020 | |||||||||