# Effect of a WeChat-based medication reminder platform on Helicobacter pylori therapy

**Authors:** Bin-Chun Huang, Yu-Zhen Wang, Liu-Cheng Li, Lian-Di Kan

PMC · DOI: 10.3389/fmed.2026.1715027 · Frontiers in Medicine · 2026-02-09

## TL;DR

A WeChat-based medication reminder system improved H. pylori treatment success, compliance, and patient satisfaction without increasing side effects.

## Contribution

Integration of a WeChat platform with hospital systems to enhance H. pylori therapy outcomes through medication reminders.

## Key findings

- The intervention group had a significantly higher H. pylori eradication rate (97.0% vs. 86.6%).
- Medication compliance improved in the WeChat group (92.5% vs. 73.1%).
- Treatment satisfaction was higher in the intervention group (95.5% vs. 80.6%).

## Abstract

Helicobacter pylori (H. pylori) infection is a significant global health concern, and effective eradication therapy is crucial for preventing its associated complications. Poor medication compliance is a major barrier to successful eradication. This study aimed to evaluate the impact of a WeChat-based medication reminder platform integrated with the hospital information system (HIS) on improving eradication rates, medication compliance, and treatment satisfaction among patients undergoing H. pylori eradication therapy.

This was a non-randomized, prospective observational study. A total of 142 H. pylori-positive patients were enrolled at our hospital, and 134 eligible patients were finally included after exclusions. The patients were divided into an intervention group (receiving medication reminders via the WeChat platform) and a control group (receiving only standard medication instructions), with 67 patients in each group. Group allocation was based on accessibility to the WeChat platform. All patients received a 14-day quadruple regimen consisting of amoxicillin, furazolidone, rabeprazole, and bismuth potassium citrate. Medication compliance was assessed using a validated 5-item questionnaire on the second day after medication completion, and H. pylori eradication status was re-evaluated 4 weeks after treatment using the 13C-Urea Breath Test (13C-UBT) or 14C-UBT. Adverse reactions and treatment satisfaction were also recorded as outcome indicators.

The eradication rate in the intervention group was significantly higher than that in the control group (97.0% [95% confidence interval [CI]: 90.1–99.4%] vs. 86.6% [95% CI: 76.2–93.4%], p = 0.022). Medication compliance was also significantly improved in the intervention group (92.5% vs. 73.1%, p = 0.003). Treatment satisfaction was higher in the intervention group (95.5% vs. 80.6%, p = 0.011). No significant difference was observed in the incidence of adverse reactions between the two groups (14.9% vs. 11.9%, p = 0.596). A sensitivity analysis based on the intention-to-treat (ITT) principle confirmed the robustness of the results.

The WeChat-based medication reminder platform integrated with the HIS significantly improved medication compliance, H. pylori eradication rates, and treatment satisfaction without increasing adverse reactions. This digital intervention offers a promising strategy for enhancing the effectiveness of H. pylori eradication therapy and optimizing patient outcomes in clinical practice. Large-scale, multicenter randomized controlled trials (RCTs) are required to further confirm its effectiveness and popularize its application.

## Linked entities

- **Chemicals:** amoxicillin (PubChem CID 33613), furazolidone (PubChem CID 5323714), rabeprazole (PubChem CID 5029), bismuth potassium citrate (PubChem CID 10101269)
- **Species:** Helicobacter pylori (taxon 210)

## Full-text entities

- **Diseases:** nausea (MESH:D009325), gastric carcinoma (MESH:D013274), esophageal or gastric fundus varices (MESH:D004932), pyloric obstruction (MESH:D011707), cardiac, hepatic, pulmonary, or renal insufficiency (MESH:D011665), gastrinoma (MESH:D015408), headache (MESH:D006261), critical illness (MESH:D016638), H. pylori (MESH:D016481), dysplasia (MESH:D015792), drug or alcohol dependence (MESH:D019966), mental illness (MESH:D001523), malignancy (MESH:D009369), abdominal pain (MESH:D015746), dry mouth (MESH:D014987), constipation (MESH:D003248), allergy (MESH:D004342), chronic gastritis (MESH:D005756), gastrointestinal bleeding (MESH:D006471), cognitive impairment (MESH:D003072), L-CL (MESH:D002971), peptic ulcer disease (MESH:D010437), gastrointestinal adverse reactions (MESH:D005767), mucosa-associated lymphoid tissue lymphoma (MESH:D018442), dizziness (MESH:D004244), ulcers (MESH:D014456)
- **Chemicals:** amoxicillin (MESH:D000658), 13C (MESH:C000615229), bismuth potassium citrate (MESH:C002791), clarithromycin (MESH:D017291), 14C (MESH:C000615234), furazolidone (MESH:D005664), metronidazole (MESH:D008795), alcohol (MESH:D000438), Rabeprazole (MESH:D064750), 13C-UBT (-), bismuth (MESH:D001729), Urea (MESH:D014508)
- **Species:** Helicobacter pylori (species) [taxon 210], Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926105/full.md

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Source: https://tomesphere.com/paper/PMC12926105