Background Large language models (LLMs) have shown promise in generating patient-friendly medical content, but their outputs often vary in accuracy, readability, and relevance. Prompt engineering—structuring inputs to guide LLM responses—may improve the quality of educational materials, yet its impact on patient education remains unclear.
Objectives To systematically review whether prompt engineering improves readability, accuracy, and usability of LLM-generated content for patient education.
Methods We conducted a systematic review in accordance with PRISMA guidelines. PubMed, Scopus, and Web of Science were searched for original studies evaluating prompt engineering techniques in patient education. Data were extracted on prompt types, LLM models used, and outcomes. Risk of bias was assessed using the QUADAS-2 tool, and a narrative synthesis was performed.
Results Our search identified five studies that met our criteria, focusing on answering patient questions and generating medical information. Prompt engineering techniques included instruction-based, elaborated, role-defining, scene-defining, and domain-specific prompts. Structured prompting improved accuracy and comprehensiveness in several cases, particularly when specific formats or custom instructions were used. Readability gains were notable when prompts explicitly requested simpler language and reading levels, though some strategies unintentionally increased complexity. Variability in effectiveness across LLMs and prompt types was observed.
Conclusion Prompt engineering can enhance the clarity and, in some cases, the accuracy of LLM-generated patient education materials. However, benefits vary by model and strategy. Standardized approaches and further research are needed to optimize prompts, minimize bias, and support reliable, accessible patient communication.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis study did not receive any funding
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
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I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
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I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityAll data produced in the present study are available upon reasonable request to the authors
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