Systematic Comparison of Hospital-Wide Standard and Model-Based Therapeutic Drug Monitoring of Vancomycin in Adults

被引:4
|
作者
Gastmans, Heleen [1 ]
Dreesen, Erwin [2 ]
Wicha, Sebastian G. [3 ]
Dia, Nada [2 ]
Spreuwers, Ellen [1 ]
Dompas, Annabel [4 ]
Allegaert, Karel [2 ,5 ,6 ]
Desmet, Stefanie [7 ,8 ]
Lagrou, Katrien [7 ,8 ]
Peetermans, Willy E. [9 ,10 ]
Debaveye, Yves [11 ]
Spriet, Isabel [1 ,2 ]
Gijsen, Matthias [1 ,2 ]
机构
[1] UZ Leuven, Pharm Dept, B-3000 Leuven, Belgium
[2] Katholieke Univ Leuven, Dept Pharmaceut & Pharmacol Sci, Clin Pharmacol & Pharmacotherapy, B-3000 Leuven, Belgium
[3] Univ Hamburg, Inst Pharm, Dept Clin Pharm, D-20146 Hamburg, Germany
[4] Univ Hosp Leuven, Dept Informat Technol, B-3000 Leuven, Belgium
[5] Katholieke Univ Leuven, Dept Dev & Regenerat, B-3000 Leuven, Belgium
[6] Erasmus MC Univ Med Ctr, Dept Hosp Pharm, NL-3015 GD Rotterdam, Netherlands
[7] Katholieke Univ Leuven, Lab Clin Bacteriol & Mycol, Dept Microbiol Immunol & Transplantat, B-3000 Leuven, Belgium
[8] UZ Leuven, Dept Lab Med, B-3000 Leuven, Belgium
[9] Katholieke Univ Leuven, Lab Clin Infect & Inflammatory Dis, Dept Microbiol Immunol & Transplantat, B-3000 Leuven, Belgium
[10] Dept Gen Internal Med, UZ Leuven, B-3000 Leuven, Belgium
[11] Katholieke Univ Leuven, Lab Intens Care Med, Dept Cellular & Mol Med, B-3000 Leuven, Belgium
关键词
vancomycin; therapeutic drug monitoring; population pharmacokinetics; precision dosing; predictive performance; model averaging; model selection; Bayesian forecasting; CRITICALLY-ILL PATIENTS; PHARMACOKINETICS; GUIDELINE; CARE;
D O I
10.3390/pharmaceutics14071459
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We aimed to evaluate the predictive performance and predicted doses of a single-model approach or several multi-model approaches compared with the standard therapeutic drug monitoring (TDM)-based vancomycin dosing. We performed a hospital-wide monocentric retrospective study in adult patients treated with either intermittent or continuous vancomycin infusions. Each patient provided two randomly selected pairs of two consecutive vancomycin concentrations. A web-based precision dosing software, TDMx, was used to evaluate the model-based approaches. In total, 154 patients contributed 308 pairs. With standard TDM-based dosing, only 48.1% (148/308) of all of the second concentrations were within the therapeutic range. Across the model-based approaches we investigated, the mean relative bias and relative root mean square error varied from -5.36% to 3.18% and from 24.8% to 28.1%, respectively. The model averaging approach according to the squared prediction errors showed an acceptable bias and was the most precise. According to this approach, the median (interquartile range) differences between the model-predicted and prescribed doses, expressed as mg every 12 h, were 113 [-69; 427] mg, -70 [-208; 120], mg and 40 [-84; 197] mg in the case of subtherapeutic, supratherapeutic, and therapeutic exposure at the second concentration, respectively. These dose differences, along with poor target attainment, suggest a large window of opportunity for the model-based TDM compared with the standard TDM-based vancomycin dosing. Implementation studies of model-based TDM in routine care are warranted.
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页数:13
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