已发表论文

山东第一医科大学附属中心医院戊糖苷在三级医院应用的合理性分析

 

Authors Zheng Y, Yin Y, Liu H, Gao W, Wang Q

Received 21 February 2025

Accepted for publication 23 June 2025

Published 9 July 2025 Volume 2025:18 Pages 2335—2350

DOI https://doi.org/10.2147/RMHP.S517679

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 3

Editor who approved publication: Dr Jongwha Chang

Yuanyuan Zheng,1,2,* Yanhui Yin,1,* Hong Liu,3 Wenwen Gao,1 Qian Wang1 

1Department of Pharmacy, Central Hospital Affiliated to Shandong First Medical University, Jinan, 250013, People’s Republic of China; 2The First Affiliated Hospital of Shandong First Medical University, Jinan, 250014, People’s Republic of China; 3Department of Pharmacy, Laiwu District People’s Hospital, Jinan, 271100, People’s Republic of China

*These authors contributed equally to this work

Correspondence: Qian Wang, Department of Pharmacy, Central Hospital Affiliated to Shandong First Medical University, No. 105 Jiefang Road, Lixia District, Jinan City, Shandong Province, 252213, People’s Republic of China, Email 13165131021@163.com

Objective: This study aimed to evaluate the rational use, safety, and economic implications of pentoxifylline in a hospital setting and provide recommendations for its appropriate clinical application.
Methods: A retrospective analysis was conducted on 322 patients discharged from September to December 2020, who received pentoxifylline. Data were collected from the hospital information system, and the rationality of prescriptions was assessed based on drug instructions and guidelines. Adverse drug reactions (ADRs) were analyzed using CTCAE criteria. Economic evaluations included defined daily dose cost (DDDc) and incremental cost-effectiveness ratio (ICER) analyses.
Results: The rational prescription rate for pentoxifylline was 38.51%, with the main irrationalities observed in indications (31.82%), dosage and usage (21.21%), contraindications (47.98%), and drug combinations (40.40%). Adverse reactions were reported in 12 cases (3.73%), primarily involving the nervous (75.00%) and digestive systems (41.67%). Most ADRs were mild (58.33%) or moderate (41.67%), with no severe cases observed. The DDDc of pentoxifylline was 143.4 yuan. Cost-effectiveness analysis demonstrated strong economic viability, with ICER values of 55.7 yuan per percentage point improvement in ulcer healing rate and 9.0 yuan per additional meter of pain-free walking distance, significantly below the willingness-to-pay threshold.
Conclusion: Pentoxifylline demonstrates cost-effectiveness and manageable safety risks but has a low rational prescription rate, highlighting the need for improved clinical practices. Enhanced collaboration between pharmacists and medical staff, alongside stricter adherence to guidelines, is essential to optimizing its utilization.

Keywords: pentoxifylline, special evaluation, adverse drug reactions, defined daily dose consumption, rational use