Impact of Continuous Pharmaceutical Care by a Collaborative Pharmacy Team on Reducing Drug-Related Problems in Coronary Heart Disease Patients: A Randomized Controlled Trial in an Integrated Healthcare System
Abstract Aims Building upon continuous pharmaceutical care (CPC) models led solely by clinical pharmacists, this study evaluated a collaborative pharmacy team model for reducing drug-related problems (DRPs) in coronary heart disease (CHD) patients during care transitions. Methods and results In a randomized controlled trial, 60 hospitalized CHD patients were allocated equally to a CPC group or a usual-care control group. The CPC group received structured pharmaceutical interventions in which clinical pharmacists led hospital care and community pharmacists led post-discharge care during key care transition periods: within 24 hours of admission (T0), 24 hour pre-discharge (T1), 24-72 hour post-discharge (T2), and at 1-month follow-up (T3). DRPs were identified using the Pharmaceutical Care Network Europe (PCNE) classification. Mean DRPs per patient were comparable at T0 (Control: 3.03 ± 1.16 vs. CPC: 3.10 ± 1.24; p = 0.827). Subsequently, the CPC group showed significantly fewer DRPs than the control group at T1 (0.17 ± 0.59 vs. 2.13 ± 1.04), T2 (0.03 ± 0.18 vs. 1.97 ± 1.03), and T3 (0.67 ± 0.76 vs. 2.63 ± 1.13) (all p < 0.001). Pharmacist interventions in the CPC group had a high DRP acceptance rate 91.4% (181/198) and a resolution rate 89.1% (106/119). At 1-month follow-up, the CPC group demonstrated superior outcomes compared to the control group: LDL-C goal attainment (63.3% vs. 30.0%, p = 0.010), medication adherence (90.0% vs. 66.7%, p = 0.028), patient satisfaction (Numeric Rating Scale: 9.27 ± 0.52 vs. 8.59 ± 0.52, p < 0.001), and willingness to pay for pharmaceutical services (86.7% vs. 50.0%, p = 0.002). Conclusion This collaborative pharmacy team model effectively reduced DRPs and improved lipid control and patient-reported outcomes in CHD patients, offering a scalable approach for integrated healthcare systems. Registered at the Chinese Clinical Trial Registry on July 1, 2024 (Registration number: ChiCTR2400086416; URL: https://www.chictr.org.cn/bin/project/edit?pid=235446).
Authors
- Lingyan Gao (ORCID: https://orcid.org/0000-0003-4475-8668)
- Lihua Gao (ORCID: https://orcid.org/0000-0002-4955-3250)
- Meijing Zhang (ORCID: https://orcid.org/0000-0002-8429-4565)
- Dawei Zhu (ORCID: https://orcid.org/0000-0003-0167-6603)
- Dongxiao Wang (ORCID: https://orcid.org/0000-0001-5358-196X)
- Lichaoyue Sun
- Stephen Nicholas
- Elizabeth Maitland
- Na Guo
- Lina Zhang (ORCID: https://orcid.org/0009-0002-1801-2344)
- Zimeng Li (ORCID: https://orcid.org/0009-0009-9519-4277)
- Hua Liu
Institutions
- University of Liverpool (GB)
- Peking University (CN)
- Australian Institute of Business (AU)
- Aerospace Center Hospital (CN)
- Peking University International Hospital (CN)
- China Population and Development Research Center (CN)
- University of Newcastle Australia (AU)
Publication Details
- Journal
- European Journal of Cardiovascular Nursing
- Published
- 2026-06-18
- DOI
- https://doi.org/10.1093/eurjcn/zvag151
- Primary Topic
- Pharmaceutical Practices and Patient Outcomes
- Type
- article
- Field-Weighted Citation Impact
- 0.00