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1.
Am J Health Syst Pharm ; 81(12): 488-493, 2024 Jun 11.
Article in English | MEDLINE | ID: mdl-38365265

ABSTRACT

PURPOSE: This article discusses key considerations regarding ticagrelor's reported effect on heparin-induced thrombocytopenia functional assays, such as literature gaps and possible management strategies. SUMMARY: Limited data indicate that ticagrelor may induce false-negative results in functional assays used in the diagnosis of heparin-induced thrombocytopenia. False-negative functional assays for heparin-induced thrombocytopenia could have catastrophic consequences. The manufacturer labeling of ticagrelor now includes a warning for this potential drug-laboratory interaction. This article suggests areas that would benefit from further research and strategies in navigating this possible interaction. CONCLUSION: Clinicians should exercise caution when evaluating functional assays for heparin-induced thrombocytopenia in patients receiving ticagrelor. This article offers suggestions for future areas of research and potential management strategies.


Subject(s)
Heparin , Thrombocytopenia , Ticagrelor , Ticagrelor/adverse effects , Heparin/adverse effects , Humans , Thrombocytopenia/chemically induced , Thrombocytopenia/diagnosis , Anticoagulants/adverse effects , False Negative Reactions , Platelet Function Tests/methods , Platelet Aggregation Inhibitors/adverse effects , Purinergic P2Y Receptor Antagonists/adverse effects , Adenosine/analogs & derivatives , Adenosine/adverse effects , Adenosine/administration & dosage
2.
J Oncol Pharm Pract ; 25(3): 535-543, 2019 Apr.
Article in English | MEDLINE | ID: mdl-29207937

ABSTRACT

OBJECTIVE: The primary objective of this study was to identify factors that have predictive value in determining total hospital length of stay in patients with febrile neutropenia, particularly time to first antibiotic dose. METHODS: This study was a retrospective chart review analyzing patients admitted to a 443 bed tertiary county teaching hospital from 1 November 2010 through 1 November 2015. Patients were eligible for enrollment into the study if they met Infectious Diseases Society of America accepted criteria for febrile neutropenia. RESULTS: Ninety-three patients were included for analysis. Time to first antibiotic dose, first empirically appropriate antibiotic dose, and time to first isolate-appropriate antibiotic did not show a significant correlation to total hospital length of stay (p = 0.71, p = 0.342, and p = 0.77, respectively). Subject's Multinational Association for Supportive Care in Cancer and Simplified Acute Physiology II scores were significantly correlated with hospital lengths of stay (p = 0.0052, rs = -0.243 and p = 0.0001, rs = 0.344, respectively). Higher median (interquartile ranges) Simplified Acute Physiology II scores were also associated with hospital mortality [dead = 46 (34.8-51.7) vs. alive = 34 (28-43.3), p = 0.0173]. CONCLUSIONS: Measures of patient acuity, such as the Multinational Association for Supportive Care in Cancer and Simplified Acute Physiology II scores, did show a correlation to clinical outcomes in patients with febrile neutropenia. Timing of initial antibiotics between 2.32 and 6.27 hours after presentation in patients with febrile neutropenia did not correlate with clinical outcomes.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Febrile Neutropenia/drug therapy , Neoplasms/drug therapy , Adult , Aged , Anti-Bacterial Agents/therapeutic use , Female , Hospital Mortality , Hospitalization , Humans , Length of Stay , Male , Middle Aged , Retrospective Studies , Tertiary Care Centers
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