# Statin prescribing patterns in cardiovascular risk management among outpatients with type 2 diabetes: Real-world practices at a Vietnamese general hospital

**Authors:** Long Bui, Thu Thi Le, Nhung Hong Dao, Hoa Thi Nguyen, Thao Thi Nguyen, Van Thi Thuy Pham, Thao Thi Bich Cao, Phuong Thanh Nguyen, Phuong T. Xuan Dong

PMC · DOI: 10.1371/journal.pone.0343313 · PLOS One · 2026-02-27

## TL;DR

This study examines how statins are prescribed to diabetic outpatients in Vietnam, finding that prescriptions often don't match recommended guidelines for cardiovascular risk.

## Contribution

The study provides real-world insights into statin prescribing practices in a Vietnamese hospital for patients with type 2 diabetes.

## Key findings

- Most patients were eligible for high-intensity statins but none received them.
- Statin prescriptions were influenced by department, ASCVD status, and dyslipidemia.
- Over half of patients had changes in statin intensity during follow-up.

## Abstract

This study aimed to evaluate the current prescribing patterns of statin therapy among outpatients with type 2 diabetes at Friendship Hospital, with a focus on alignment between treatment intensity with cardiovascular risk factors.

A retrospective cohort study was conducted at Friendship Hospital from December 2022 to December 2023. Patient aged 40–75 years with type 2 diabetes mellitus who attended follow-up visits were included using stratified random sampling by treatment department. Clinical data were extracted from medical records to assess cardiovascular risk based on the 2023 American Diabetes Association guideline and to document statin use, intensity, treatment continuity and related factors. Multivariate logistic regression was performed to identify factors associated with whether or not patients were prescribed statins.

Among 407 patients, 30.5% were classified as having established ASCVD, 55.6% as having high cardiovascular risk, and 99.8% of patients were eligible for indication of high intensity statin. Despite this, none received high-intensity statin. Most patients (77.4%) were prescribed moderate-intensity statins, 8.6% received low-intensity statins, and 14.0% were not prescribed any statin. A total of 58.5% of patients received uninterrupted statin prescriptions over one year, whereas 54.3% underwent changes in statin intensity during the follow-up period. Statin prescription (versus non-prescription) was significantly influenced by the treatment department, ASCVD status, and the presence of dyslipidemia (p < 0.05).

Although statin use was common, the intensity and continuity of treatment were often inconsistent with cardiovascular risks. The absence of high-intensity statin prescriptions in a population largely at very high risk may limit the potential benefits of lipid-lowering therapy. These findings highlight the need to strengthen adherence to guideline-directed statin therapy in the management of type 2 diabetes mellitus.

## Linked entities

- **Diseases:** type 2 diabetes mellitus (MONDO:0005148), dyslipidemia (MONDO:0002525)

## Full-text entities

- **Genes:** CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}
- **Diseases:** TIA (MESH:D002546), T2DM (MESH:D003924), PAD (MESH:D058729), Coronary Artery Disease (MESH:D003324), albuminuria (MESH:D000419), hypertension (MESH:D006973), Atherosclerotic cardiovascular disease (MESH:D050197), CKD (MESH:D012080), CVD (MESH:D002318), MI (MESH:D009203), obese (MESH:D009765), stroke (MESH:D020521), overweight (MESH:D050177), arterimeal disease (MESH:D004194), hyperglycemia (MESH:D006943), Dyslipidemia (MESH:D050171), ACS (MESH:D054058), Diabetes (MESH:D003920), Chronic Kidney Disease (MESH:D051436)
- **Chemicals:** lipid (MESH:D008055), simvastatin (MESH:D019821), rosuvastatin (MESH:D000068718), ADA (-), atorvastatin (MESH:D000069059), Prav (MESH:D017035), ezetimibe (MESH:D000069438), -C (MESH:D002244)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12948102/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC12948102/full.md

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Source: https://tomesphere.com/paper/PMC12948102