Real-time pharmacy surveillance and clinical decision support to reduce adverse drug events in acute kidney injury

被引:33
作者
McCoy, A. B. [1 ]
Cox, Z. L. [2 ,3 ]
Neal, E. B. [2 ]
Waitman, L. R. [4 ]
Peterson, N. B. [5 ]
Bhave, G. [6 ]
Siew, E. D. [6 ]
Danciu, I. [1 ]
Lewis, J. B. [6 ]
Peterson, J. F. [1 ,5 ,7 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Biomed Informat, Nashville, TN 37212 USA
[2] Vanderbilt Univ, Med Ctr, Dept Biomed Informat, Nashville, TN USA
[3] Lipscomb Univ, Coll Pharm, Nashville, TN USA
[4] Univ Kansas, Med Ctr, Dept Biostat, Kansas City, KS 66103 USA
[5] Vanderbilt Univ, Med Ctr, Dept Med, Div Gen Internal Med & Publ Hlth, Nashville, TN USA
[6] Vanderbilt Univ, Med Ctr, Dept Med, Div Nephrol, Nashville, TN USA
[7] VA Tennessee Valley Healthcare Syst, Geriatr Res Educ Clin Ctr, Nashville, TN USA
来源
APPLIED CLINICAL INFORMATICS | 2012年 / 3卷 / 02期
关键词
Clinical decision support systems; electronic health records; randomized controlled trial; medication errors; medication error prevention and control; adverse drug reaction reporting systems; PHYSICIAN ORDER ENTRY; COMPUTERIZED SURVEILLANCE; MEDICATION SAFETY; ALERTS; PREVENTABILITY; IMPACT; ERRORS; INTERVENTION; PREVENTION;
D O I
10.4338/ACI-2012-03-RA-0009
中图分类号
R-058 [];
学科分类号
摘要
Objectives: Clinical decision support (CDS), such as computerized alerts, improves prescribing in the setting of acute kidney injury (AKI), but considerable opportunity remains to improve patient safety. The authors sought to determine whether pharmacy surveillance of AKI patients could detect and prevent medication errors that are not corrected by automated interventions. Methods: The authors conducted a randomized clinical trial among 396 patients admitted to an academic, tertiary care hospital between June 1, 2010 and August 31, 2010 with an acute 0.5 mg/dl change in serum creatinine over 48 hours and a nephrotoxic or renally cleared medication order. Patients randomly assigned to the intervention group received surveillance from a clinical pharmacist using a web-based surveillance tool to monitor drug prescribing and kidney function trends. CDS alerting and standard pharmacy services were active in both study arms. Outcome measures included blinded adjudication of potential adverse drug events (pADEs), adverse drug events (ADEs) and time to provider modification or discontinuation of targeted nephrotoxic or renally cleared medications. Results: Potential ADEs or ADEs occurred for 104 (8.0%) of control and 99 (7.1%) of intervention patient-medication pairs (p=0.4). Additionally, the time to provider modification or discontinuation of targeted nephrotoxic or renally cleared medications did not differ between control and intervention patients (33.4 hrs vs. 30.3hrs, p=0.3). Conclusions: Pharmacy surveillance had no incremental benefit over previously implemented CDS alerts
引用
收藏
页码:221 / 238
页数:18
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