Continuous infusion of vancomycin improved therapeutic levels in term and preterm infants.


Journal

Journal of perinatology : official journal of the California Perinatal Association
ISSN: 1476-5543
Titre abrégé: J Perinatol
Pays: United States
ID NLM: 8501884

Informations de publication

Date de publication:
06 2021
Historique:
received: 27 07 2020
accepted: 01 12 2020
revised: 26 10 2020
pubmed: 21 1 2021
medline: 9 10 2021
entrez: 20 1 2021
Statut: ppublish

Résumé

Growing evidence suggests that continuous infusion of vancomycin (CIV) is superior to intermittent infusion of vancomycin (IIV) in neonates. This quality improvement (QI) project aimed to transition from IIV to CIV with earlier and improved attainment of therapeutic vancomycin levels. The Model for Improvement framework with Plan Do Study Act cycles was used. Prospective data were collected during three phases: IIV, CIV-1 and CIV-2. A QI team developed a CIV drug monograph and a multidisciplinary education package. Using IIV, 36% (9/25) of first vancomycin levels were within target range. CIV achieved therapeutic levels twice as quickly as IIV (p < 0.05) with improved first vancomycin target levels (IIV 36%, 9/25; CIV-1 55%, 16/29; CIV-2 61%, 14/23) and total therapeutic levels (IIV 44%, 37/84; CIV-1 56%, 55/98; CIV-2 69%, 79/114). This QI project demonstrated a successful transition from IIV to CIV with reduced time to achieve target vancomycin and an increased proportion of therapeutic levels.

Sections du résumé

BACKGROUND
Growing evidence suggests that continuous infusion of vancomycin (CIV) is superior to intermittent infusion of vancomycin (IIV) in neonates. This quality improvement (QI) project aimed to transition from IIV to CIV with earlier and improved attainment of therapeutic vancomycin levels.
METHODS
The Model for Improvement framework with Plan Do Study Act cycles was used. Prospective data were collected during three phases: IIV, CIV-1 and CIV-2.
INTERVENTIONS
A QI team developed a CIV drug monograph and a multidisciplinary education package.
RESULTS
Using IIV, 36% (9/25) of first vancomycin levels were within target range. CIV achieved therapeutic levels twice as quickly as IIV (p < 0.05) with improved first vancomycin target levels (IIV 36%, 9/25; CIV-1 55%, 16/29; CIV-2 61%, 14/23) and total therapeutic levels (IIV 44%, 37/84; CIV-1 56%, 55/98; CIV-2 69%, 79/114).
CONCLUSIONS
This QI project demonstrated a successful transition from IIV to CIV with reduced time to achieve target vancomycin and an increased proportion of therapeutic levels.

Identifiants

pubmed: 33469164
doi: 10.1038/s41372-020-00909-3
pii: 10.1038/s41372-020-00909-3
doi:

Substances chimiques

Vancomycin 6Q205EH1VU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1459-1466

Références

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Auteurs

Antonia Round (A)

Leicester Medical School, George Davies Centre, Leicester, UK. antoniacharlotteround@gmail.com.

Emily Clifton (E)

Leicester Medical School, George Davies Centre, Leicester, UK.

Lucy Stachow (L)

Pharmacy Department, Leicester Royal Infirmary, Leicester, UK.

Sumit Mittal (S)

Neonatal Intensive Care Unit, Leicester Royal Infirmary, Leicester, UK.

Kamini Yadav (K)

Neonatal Intensive Care Unit, Leicester Royal Infirmary, Leicester, UK.

Hira Ashraf (H)

Paediatric Department, Leicester Royal Infirmary, Leicester, UK.

Ranveer Singh Sanghera (RS)

Neonatal Intensive Care Unit, Leicester Royal Infirmary, Leicester, UK.

Khuen Foong Ng (KF)

Paediatric Infectious Diseases and Immunology Department, Bristol Royal Hospital for Children, Bristol, UK.

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