# When access ≠ acceptance: How clinical specialty demands shape mutual recognition on medical examination/test result reuse in Chinese hospitals: A study on a pilot province of China’s medical digital reform

**Authors:** Chao Song, Xinmian Huang, Shasha Qian, Chaoyun Yuan, Shuning Liu, Jun Zhou, Pengpeng Ye, Pengpeng Ye, Pengpeng Ye

PMC · DOI: 10.1371/journal.pone.0318899 · PLOS One · 2025-10-15

## TL;DR

A study in China finds that simply making medical test results accessible across hospitals doesn't ensure they are actually used, with significant differences across medical specialties.

## Contribution

The study identifies how clinical specialty-specific factors influence the recognition of shared medical test results, beyond mere accessibility.

## Key findings

- Blocking the 'Overlook Access' pathway increased access rates but decreased recognition rates in medical test result sharing.
- Orthopedics and traditional Chinese medicine showed higher recognition rates compared to hepatobiliary and endocrinology.
- Pediatrics had high access but very low recognition of shared medical records due to concerns about data applicability.

## Abstract

Despite widespread electronic health records adoption, interoperability for sharing examination/test results across healthcare institutions remains limited, leading to redundant testing, increased costs, and compromised care. China’s mutual recognition policy for medical examination/test results, implemented via the interoperable results sharing platform(IRSP), aims to address this. However, variations in adoption across clinical specialties and the impact of hospital-level pathway interventions are poorly understood.

Utilizing hospital-level administrative data from Zhejiang Province’s IRSP (Oct 2023 – Sep 2024), this quasi-experimental study compared three intervention hospitals (blocking the “Overlook Access” pathway) with three control hospitals. We analyzed core recognition metrics (Access Rate-AR, Total Recognition Rate-TRR, Cross-Hospital Access Rate-CHAR, Cross-Hospital Recognition Rate-CHRR) across 12 clinical specialties. Analyses employed magnitude-based inference for intervention effects, Spearman correlations for specialty variations, and descriptive statistics for hospital-type comparisons.

Blocking the “Overlook Access” pathway significantly increased access metrics (AR: Intervention median 98.9% vs. Control 44.6%, Cohen’s d = 2.02; CHAR: 99.5% vs. 57.6%, d = 2.85) but paradoxically decreased TRR (18.2% vs. 44.3%, d = −2.72), with minimal impact on CHRR. Substantial variations existed across specialties: Orthopedics and traditional Chinese medicine showed consistently higher access and recognition, while hepatobiliary and endocrinology faced significant challenges. Pediatrics exhibited high access but critically low recognition (e.g., Hospital H: TRR 2.05%, CHRR 2.82%), attributed to rapid physiological changes and data applicability concerns. Strong correlations existed within access metrics (AR-CHAR, ρ = 0.92, p < 0.001) and within recognition metrics (TRR-CHRR, ρ = 0.88, p < 0.001), but weak correlations between access and recognition.

This study reveals a critical distinction between access to external medical records and their actual clinical recognition, demonstrating that information interventions alone are insufficient to improve the recognition rates. Clinical specialty-specific factors significantly influence recognition behaviors, reflecting variations in data utility, stability, and diagnostic practices. Institutional success in promoting mutual recognition depends on comprehensive, multi-level strategies. The IRSP exemplifies China’s progress in health data interoperability, yet sustainable mutual recognition ultimately hinges on clinical relevance rather than mere accessibility.

## Full-text entities

- **Genes:** TRR [NCBI Gene 7870], CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, ZFTRAF1 (zinc finger TRAF-type and ring finger containing 1) [NCBI Gene 50626] {aka CHRP, CYHR1}
- **Diseases:** acute myocardial infarction (MESH:D009203), pain (MESH:D010146), fractures (MESH:D050723), CHAR (MESH:D003428), chronic obstructive pulmonary disease (MESH:D029424), Cancer (MESH:D009369), infections (MESH:D007239), cerebral infarction (MESH:D002544), MR (MESH:D020238)
- **Chemicals:** bilirubin (MESH:D001663), -D-25-02593 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12527183/full.md

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Source: https://tomesphere.com/paper/PMC12527183