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Developing a practical Hospital Intravenous Therapy Quality Assessment Tool: Design, refinement, and feasibility
Huapeng Lu1, Qigui Xiao1, Fuhui Sui2
1Department of Hepatobiliary and Pancreas Surgery, The First Affiliated Hospital, Xi'an Jiaotong University, Xi'an, Shaanxi, P. R. China.
The Journal of Vascular Access
|July 13, 2026
Summary
A new electronic tool, the Hospital Intravenous Therapy Quality Assessment Tool (HIT-QAT), was developed to improve patient safety during intravenous therapy. This practical tool is feasible for hospital-wide audits, enhancing quality monitoring.
Area of Science:
- Healthcare Quality Improvement
- Patient Safety
- Clinical Auditing
Background:
- Intravenous therapy is a common but high-risk procedure associated with patient discomfort and potential complications.
- Optimal management and quality monitoring of intravenous therapy are crucial for patient safety.
- A gap exists in standardized, practical tools for hospital-wide intravenous therapy audits.
Purpose of the Study:
- To develop and refine a practical, electronic quality assessment tool for hospital-wide intravenous therapy surveillance.
- To evaluate the feasibility of this tool in clinical practice as Phase I of a larger project.
Main Methods:
- A multidisciplinary team developed the Hospital Intravenous Therapy Quality Assessment Tool (HIT-QAT) based on standards.
- The tool underwent 14 iterative refinement cycles involving pilot testing, auditor training, audits, and revisions.
- Feasibility was assessed through audit completion time, data completeness, and user acceptance.
Main Results:
- The finalized HIT-QAT is an electronic, mobile-accessible survey with seven sections and automated skip logic.
- Across 14 audits (2016-2023), 22,789 vascular access devices (VADs) were assessed.
- Auditor training was standardized, completed with zero resistance, and audits were efficient.
Conclusions:
- The HIT-QAT is a feasible, practical, and efficient electronic tool for hospital-wide intravenous therapy quality assessment.
- Phase I focused on tool design, refinement, and feasibility testing.
- Future studies (Phase II) will use the tool for deficiency identification, outcome tracking, and quality improvement.
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