Evidence map›Paper›PMID 42699677›Full record

ArticleRisk management and healthcare policy2026

Impact of Laboratory Data Integration into Outpatient Prescriptions on Community Pharmacist Feedback and Physician Responses: A Single-Center Retrospective Study.

Takahiro Motoki, Hiroaki Tanaka, Tatsuya Tai, Kazunori Yamaguchi, Shinji Kosaka, Yasuaki Mino

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Article in Risk management and healthcare policy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Takahiro MotokiDepartment of Pharmacy, Kagawa University Hospital, Miki, Kagawa, Japan.ORCID 0009-0006-2603-1915
Hiroaki TanakaDepartment of Pharmacy, Kagawa University Hospital, Miki, Kagawa, Japan.ORCID 0000-0002-2324-0248
Tatsuya TaiDepartment of Pharmacy, Kagawa University Hospital, Miki, Kagawa, Japan.ORCID 0000-0002-6252-4366
Kazunori YamaguchiDepartment of Pharmacy, Kagawa University Hospital, Miki, Kagawa, Japan.ORCID 0009-0007-0523-7225
Shinji KosakaDrug Information Center, Kagawa Pharmaceutical Association, Takamatsu, Kagawa, Japan.
Yasuaki MinoDepartment of Pharmacy, Kagawa University Hospital, Miki, Kagawa, Japan.ORCID 0000-0002-5706-1117

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Laboratory data with outpatient prescriptions have expanded, and their usefulness has been reported. However, the effect of a modification in laboratory data provision on the content of tracing reports (TRs) submitted by community pharmacists to provide clinical feedback to physicians and on physician responses remains unclear. This study aimed to evaluate the impact of a system-level modification in laboratory data provision on the inclusion of laboratory data-related descriptions in TRs and to assess the association between TR characteristics and physician responses. Patients and Methods: We used TRs submitted by community pharmacies to a university hospital in Japan. An integrated prescription format (IPF), containing laboratory data automatically printed on prescriptions, was introduced in addition to the existing separate sheet format (SSF). Laboratory data-related descriptions in the TRs were compared pre- and post-implementation. Physician responses were evaluated, and associated factors were analyzed using logistic regression. Results: Laboratory data provision using SSF remained approximately 4% pre- and post-implementation, whereas IPF printed laboratory data fields on all prescriptions post-implementation. A total of 761 TRs were analyzed (pre-implementation, 389; post-implementation, 372). Laboratory data-related descriptions were identified in 16 TRs (2.1%), with a significant increase post-implementation (1.0% vs 3.2%; odds ratio [OR] 3.21, 95% confidence interval [CI] 1.03-10.04). Physician responses were recorded for 210 TRs (27.6%), with no significant difference pre- and post-implementation (27.8% vs 27.4%; OR 0.98, 95% CI 0.71-1.35). Multivariable analysis showed a strong association between pharmacists' proposals or concerns and physician responses (adjusted OR 10.39, 95% CI 5.39-20.03). Conclusion: The IPF-based laboratory data provision system increased inclusion of laboratory data-related descriptions in TRs but not physician responses. The findings suggest that providing information that includes clinically relevant proposals or concerns, rather than simply increasing the amount of information available, may be more important for promoting physician responses.

Indexed as

clinical information sharingdrug-related problemsinterprofessional collaborationlaboratory data provisionpatient safetytracing reports

Identifiers

PMID42699677
PMCPMC13544119

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.