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Appropriateness of tacrolimus therapeutic drug monitoring timing in the emergency department.
Chee-How, Emma L; Acquisto, Nicole M; Zhang, Y Victoria.
Affiliation
  • Chee-How EL; Emergency Medicine Pharmacy Resident, Department of Pharmacy, University of Rochester Medical Center, 601 Elmwood Ave., Box 638, Rochester, NY 14642, United States of America.
  • Acquisto NM; Emergency Medicine Clinical Pharmacy Specialist, Department of Pharmacy and Associate Professor, Department of Emergency Medicine, 601 Elmwood Ave., Box 638, Rochester, NY 14642, United States of America. Electronic address: nicole_acquisto@urmc.rochester.edu.
  • Zhang YV; Vice Chair for Clinical Enterprise Strategy, Department of Pathology and Laboratory Medicine, Medical Director of Ambulatory Lab Services, Department of Pathology and Laboratory Medicine, Director of Regional Toxicology and Mass Spectrometry Laboratory, Department of Pathology and Laboratory Medicine, Department of Pathology and Laboratory Medicine, University of Rochester Medical Center, 601 Elmwood Ave., Box 608, Rochester, NY 14642, United States of America. Electronic address: victoria_zhang
Am J Emerg Med ; 45: 233-236, 2021 07.
Article in En | MEDLINE | ID: mdl-33046300
PURPOSE: Evaluate the appropriateness of the timing of serum samples collected in the emergency department (ED) for tacrolimus (TAC) measurement. METHODS: Single-center, retrospective review of TAC samples collected in the ED from September 1 to October 31, 2017. The primary evaluation was incidence of inappropriate sample collection for TAC measurement, defined as samples not collected 12 h (±2 h; 10-14 h) after the last dose, or within 2 h of the next dose if last known dose time was not documented. Incidence of repeat TAC measurements obtained within 24 h of ED presentation (if initial sample collection inappropriate), inappropriate TAC regimen adjustments, and healthcare costs of inappropriate TAC measurements was evaluated. Data collection included patient demographics, ED visit information, TAC measurement and timing related to last or next dose, changes to TAC regimen, and ED disposition. Descriptive data are reported. RESULTS: Sixty-two patients were included. Forty-one (66%) initial TAC measurements were collected inappropriately in the ED. No patients had a regimen adjustment as a result of inappropriate concentration collection, but 32 patients (78%) did require a repeat measurement within 24 h of ED presentation due to initial inappropriate collection. Costs associated with incorrectly collected TAC measurements were $2,647.78 for the two-month time period and this is extrapolated to an estimated $15,886.68 annual expense for patients. CONCLUSIONS: Inappropriate sample collection for TAC measurements was common in the ED, resulting in frequent repeat laboratory draws and increased healthcare costs.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tacrolimus / Drug Monitoring / Emergency Service, Hospital / Transplant Recipients / Immunosuppressive Agents Type of study: Observational_studies Limits: Female / Humans / Male / Middle aged Language: En Journal: Am J Emerg Med Year: 2021 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tacrolimus / Drug Monitoring / Emergency Service, Hospital / Transplant Recipients / Immunosuppressive Agents Type of study: Observational_studies Limits: Female / Humans / Male / Middle aged Language: En Journal: Am J Emerg Med Year: 2021 Document type: Article Affiliation country: United States Country of publication: United States