Development of Screening Tools to Predict Medication-Related Problems Across the Continuum of Emergency Department Care: A Prospective, Multicenter Study

被引:4
作者
Taylor, Simone E. [1 ,2 ,3 ]
Mitri, Elise A. [1 ,2 ]
Harding, Andrew M. [1 ,2 ]
Taylor, David McD [2 ,3 ,4 ]
Weeks, Adrian [5 ,6 ]
Abbott, Leonie [6 ]
Lambros, Pani [7 ,8 ]
Lawrence, Dona [9 ,10 ]
Strumpman, Dana [11 ]
Senturk-Raif, Reyhan [12 ]
Louey, Stephen [13 ]
Crisp, Hamish [14 ]
Tomlinson, Emily [15 ]
Manias, Elizabeth [15 ]
机构
[1] Austin Hlth, Pharm Dept, Heidelberg, Vic, Australia
[2] Austin Hlth, Emergency Dept, Heidelberg, Vic, Australia
[3] Univ Melbourne, Melbourne Med Sch, Dept Crit Care, Parkville, Vic, Australia
[4] Univ Melbourne, Fac Med Dent & Hlth Sci, Parkville, Vic, Australia
[5] Western Hlth, Pharm Dept, Footscray, Vic, Australia
[6] Barwon Hlth, Pharm Dept, Geelong, Vic, Australia
[7] Northern Hlth, Pharm Dept, Epping, Vic, Australia
[8] Eastern Hlth, Box Hill Hosp, Pharm Dept, Box Hill, Vic, Australia
[9] Manly Hosp, Pharm Dept, Manly, NSW, Australia
[10] Northern Beaches Hosp, Pharm Dept, Frenchs Forest, NSW, Australia
[11] Prince Wales Hosp, Pharm Dept, Randwick, NSW, Australia
[12] Monash Hlth, Dandenong Hosp, Pharm Dept, Dandenong, Vic, Australia
[13] Monash Hlth, Casey Hosp, Pharm Dept, Berwick, Vic, Australia
[14] Launceston Gen Hosp, Pharm Dept, Launceston, Tas, Australia
[15] Deakin Univ, Inst Hlth Transformat, Fac Hlth, Ctr Qual & Patient Safety Res,Sch Nursing & Midwif, Burwood, Vic, Australia
关键词
emergency department; medication management; risk factors; patient transfer; workforce; RANDOMIZED CONTROLLED-TRIAL; CLINICAL PHARMACISTS; ERRORS; RISK; ADMISSION; MEDICINE; RECONCILIATION; VALIDATION; PEOPLE; IMPACT;
D O I
10.3389/fphar.2022.865769
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Medication-related problems (MRPs) occur across the continuum of emergency department (ED) care: they may contribute to ED presentation, occur in the ED/short-stay unit (SSU), at hospital admission, or shortly after discharge to the community. This project aimed to determine predictors for MRPs across the continuum of ED care and incorporate these into screening tools (one for use at ED presentation and one at ED/SSU discharge), to identify patients at greatest risk, who could be targeted by ED pharmacists.Methods: A prospective, observational, multicenter study was undertaken in nine EDs, between July 2016 and August 2017. Blocks of ten consecutive adult patients presenting at pre-specified times were identified. Within 1 week of ED discharge, a pharmacist interviewed patients and undertook a medical record review to determine a medication history, patient understanding of treatment, risk factors for MRPs and to manage the MRPs. Logistic regression was undertaken to determine predictor variables. Multivariable regression beta coefficients were used to develop a scoring system for the two screening tools.Results: Of 1,238 patients meeting all inclusion criteria, 904 were recruited. Characteristics predicting MRPs related to ED presentation were: patient self-administers regular medications (OR = 7.95, 95%CI = 3.79-16.65), carer assists with medication administration (OR = 15.46, 95%CI = 6.52-36.67), or health-professional administers (OR = 5.01, 95%CI = 1.77-14.19); medication-related ED presentation (OR = 9.95, 95%CI = 4.92-20.10); age >= 80 years (OR = 3.63, 95%CI = 1.96-6.71), or age 65-79 years (OR = 2.01, 95%CI = 1.17-3.46); potential medication adherence issue (OR = 2.27, 95%CI = 1.38-3.73); medical specialist seen in past 6-months (OR = 2.02, 95%CI = 1.42-2.85); pharmaceutical benefit/pension/concession cardholder (OR = 1.89, 95%CI = 1.28-2.78); inpatient in previous 4-weeks (OR = 1.60, 95%CI = 1.02-2.52); being male (OR = 1.48, 95%CI = 1.05-2.10); and difficulties reading labels (OR = 0.63, 95%CI = 0.40-0.99). Characteristics predicting MRPs related to ED discharge were: potential medication adherence issue (OR = 6.80, 95%CI = 3.97-11.64); stay in ED > 8 h (OR = 3.23, 95%CI = 1.47-7.78); difficulties reading labels (OR = 2.33, 95%CI = 1.30-4.16); and medication regimen changed in ED (OR = 3.91, 95%CI = 2.43-6.30). For ED presentation, the model had a C-statistic of 0.84 (95% CI 0.81-0.86) (sensitivity = 80%, specificity = 70%). For ED discharge, the model had a C-statistic of 0.78 (95% CI 0.73-0.83) (sensitivity = 82%, specificity = 57%).Conclusion: Predictors of MRPs are readily available at the bedside and may be used to screen for patients at greatest risk upon ED presentation and upon ED/SSU discharge to the community. These screening tools now require external validation and implementation studies to evaluate the impact of using such tools on patient care outcomes.
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页数:12
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