Impact of Pharmacist-Led Multidisciplinary Team to Attain Targeted Vancomycin Area under the Curved Monitoring in a Tertiary Care Center in Thailand

Author:

Jantarathaneewat Kittiya12,Phodha Tuangrat1,Singhasenee Kankanit3,Katawethiwong Panipak4,Suwantarat Nuntra56,Camins Bernard7,Wongphan Thanawat18,Rutjanawech Sasinuch25,Apisarnthanarak Anucha25

Affiliation:

1. Center of Excellence in Pharmacy Practice and Management Research, Faculty of Pharmacy, Thammasat University, Pathum Thani 12120, Thailand

2. Research Group in Infectious Diseases Epidemiology and Prevention, Faculty of Medicine, Thammasat University, Pathum Thani 12120, Thailand

3. Pharmacy Unit, Thammasat University Hospital, Pathum Thani 12120, Thailand

4. Paholpolpayuhasena Hospital, Kanchanaburi 71000, Thailand

5. Division of Infectious Diseases, Faculty of Medicine, Thammasat University, Pathum Thani 12120, Thailand

6. Chulabhorn International College of Medicine, Thammasat University, Pathum Thani 12120, Thailand

7. Division of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029-6574, USA

8. Trat Provincial Public Health Office, Trat 23000, Thailand

Abstract

Vancomycin Area Under the Curve (AUC) monitoring has been recommended to ensure successful clinical outcomes and minimize the risk of nephrotoxicity, rather than traditional trough concentration. However, vancomycin AUC monitoring by a pharmacist-led multidisciplinary team (PMT) has not been well established in Southeast Asia. This study was conducted at Thammasat University Hospital. Adult patients aged ≥ 18 years who were admitted and received intravenous vancomycin ≥48 h were included. The pre-PMT period (April 2020–September 2020) was defined as a period using traditional trough concentration, while the post-PMT period (October 2020–March 2021) was defined as a period using PMT to monitor vancomycin AUC. The primary outcome was the rate of achievement of the therapeutic target of an AUC/MIC ratio of 400–600. There was a significantly higher rate of achievement of therapeutic target vancomycin AUC during post-PMT period (66.7% vs. 34.3%, p < 0.001). Furthermore, there was a significant improvement in the clinical cure rate (92.4% vs. 69.5%, p < 0.001) and reduction in 30-day ID mortality (2.9% vs. 12.4%, p = 0.017) during the post-PMT period. Our study demonstrates that PMT was effective to help attain a targeted vancomycin AUC, improve the clinical cure rate, and reduce 30-day ID mortality. This intervention should be encouraged to be implemented in Southeast Asia.

Funder

Faculty of Pharmacy, Thammasat University under the Specialized Research Grant, Research Unit: Pharmacy Practice and Management Research Unit

Thailand Science Research and Innovation Fundamental Fund

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Microbiology (medical),General Pharmacology, Toxicology and Pharmaceutics,Biochemistry,Microbiology

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