Clinical Pharmacist Impact on Care, Length of Stay, and Cost in Pediatric Cystic Fibrosis (CF) Patients

被引:23
作者
Cies, Jeffrey J. [1 ,2 ]
Varlotta, Laurie [1 ,2 ]
机构
[1] St Christophers Hosp Children, Philadelphia, PA 19134 USA
[2] Drexel Univ, Coll Med, Philadelphia, PA 19104 USA
关键词
cystic fibrosis; pharmacokinetics; therapeutic drug monitoring; aminoglycosides; pediatric; AMINOGLYCOSIDE PLASMA-LEVELS; ADVERSE DRUG EVENTS; PSEUDOMONAS-AERUGINOSA; MEDICATION ERRORS; INTENSIVE-CARE; DAILY GENTAMICIN; SERVICES; THERAPY; RESISTANCE; PHARMACOKINETICS;
D O I
10.1002/ppul.22745
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BackgroundCystic fibrosis (CF) patients are often treated with aminoglycoside (AG) antibiotics during infective pulmonary exacerbations. Achieving pharmacokinetic and pharmacodynamic (PK/PD) targets to improve outcomes and counteract resistance is paramount. PurposeThe primary objective was to compare the number of pediatric CF patients achieving AG PK/PD targets when a clinical pharmacist (CP) managed therapeutic drug monitoring (TDM) compared with usual care (UC). MethodsA retrospective cohort study was conducted on the records of 40 CF patients that received AGs and 2 serum samples between 1/2007 and 5/2009. Chi-square and Student's t-test were used to analyze nominal and continuous variables, respectively. ResultsTwenty-nine patients with 52 courses of AGs were included the CP group, and 22 patients with 42 courses were included the UC group. Ninety-eight percent of patients in the CP group reached AG PK/PD targets compared with 71% in the UC group, P<0.001. Patients in the CP group reached the AG PK/PD target in a mean of 1.90.8 days compared with 4.8 +/- 3.4 days in the UC group, P<0.0001. The average LOS in the CP group was 9 +/- 5 days compared with 12 +/- 7.5 days in the UC group, P=0.033. The mean number of levels per patient was 2.7 in the CP group compared with 5.2 (range of 2-20) in the UC group, P<0.001. Resource utilization associated with drug levels, dosing adjustments and LOS were $26,549, $14,069, and $1,680,000 in the CP group as compared with $40,683, $27,812, and $1,940,000, respectively, in the UC group. ConclusionCP managed TDM resulted in a significantly higher percentage of pediatric CF patients achieving AG PK/PD targets 3 days sooner with an average LOS that was 3 days shorter. CP managed TDM resulted in significantly fewer dosage adjustments, drug levels, and cost associated with serum sampling, drug wastage, and LOS. Pediatr Pulmonol. 2013; 48:1190-1194. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:1190 / 1194
页数:5
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