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Changing the Time of Blood Collection to Determine Vancomycin Concentrations in Intensive Care Unit Patients.
Hammond, Drayton A; James, Taylor B; Atkinson, Lexis N; Painter, Jacob T; Lusardi, Katherine.
Afiliação
  • Hammond DA; Drayton A. Hammond is a clinical pharmacy specialist at the Rush University Medical Center, Chicago, Illinois. dahammond@uams.edu.
  • James TB; Taylor B. James is a first-year pharmacy resident at the University of Arkansas for Medical Sciences Medical Center, Little Rock, Arkansas. dahammond@uams.edu.
  • Atkinson LN; Lexis N. Atkinson is a first-year pharmacy resident at the University of Arkansas for Medical Sciences Medical Center. dahammond@uams.edu.
  • Painter JT; Jacob T. Painter is an assistant professor of pharmacy practice within the Division of Pharmaceutical Evaluation and Policy at the University of Arkansas for Medical Sciences College of Pharmacy. dahammond@uams.edu.
  • Lusardi K; Katherine Lusardi is an antimicrobial stewardship pharmacist at the University of Arkansas for Medical Sciences College of Pharmacy. dahammond@uams.edu.
Crit Care Nurse ; 38(1): 24-28, 2018 Feb.
Article em En | MEDLINE | ID: mdl-29437075
ABSTRACT

BACKGROUND:

Clinical practice guidelines for initiation and therapeutic drug monitoring, but not timing, of vancomycin dosing exist at many institutions. Scheduling vancomycin trough measurements and doses around the morning blood sample collection could yield more interpretable troughs and increase patient safety.

OBJECTIVE:

To evaluate the appropriateness of blood sample collection times for vancomycin trough measurements before and after an initiative to change the timing of blood sampling to determine vancomycin doses and trough levels in a medical intensive care unit.

METHODS:

A retrospective cohort study was conducted of patients in a medical intensive care unit who received intravenous vancomycin at a scheduled interval. Differences in continuous and categorical data were compared between pre- and postintervention groups. The primary outcome was proportion of blood samples collected for vancomycin trough measurements within 30 minutes of the next scheduled vancomycin dose.

RESULTS:

Baseline characteristics were similar between the preintervention (n = 68) and postintervention (n = 176) groups except for the percentage of blood samples drawn for trough measurements and morning laboratory tests (6% vs 81%; P < .001). Frequency of loading doses was similar between patients in the pre- and postintervention groups, as was weight-based maintenance dosing. There was no significant difference in the percentage of blood samples collected to measure vancomycin trough levels appropriately at 30, 60, or 75 minutes from the next scheduled dose.

CONCLUSION:

Measuring vancomycin trough levels in morning blood samples did not affect the percentage of inappropriately collected blood samples used to measure vancomycin trough levels.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções Bacterianas / Vancomicina / Monitoramento de Medicamentos / Testes Hematológicos / Antibacterianos Tipo de estudo: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções Bacterianas / Vancomicina / Monitoramento de Medicamentos / Testes Hematológicos / Antibacterianos Tipo de estudo: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article