Uncategorized

Large language models in simplifying radiological reports: systematic review



Abstract

Objectives
Simplifying medical information to make it understandable for patients, specifically in the case of radiology reports, is challenging. It requires time and effort from medical personnel. This systematic review focuses on the application of large language models (LLMs) in generating simplified radiological imaging reports, as well as answering patient inquiries regarding radiological procedures.
Materials and Methods
The authors searched for studies published up to January 2024. Search terms focused on LLMs generated simplified radiological reports and answers to patient inquiries regarding radiological procedures. MEDLINE was used as a search database.
Results
Overall, eight studies published between May 2023 and November 2023 were included. All studies showed that LLMs can produce simplified medical information for patients. Four studies (50%) used GPT-3.5, Two studies (25%) conducted a comparative analysis between GPT-3.5 and GPT-4. One study (12.5%) examined Microsoft Bing. One study (12.5%) utilized GPT-4. Four studies (50%) used LLMs to simplify radiological reports. Four studies (50%) used LLMs to answer patient questions regarding radiological procedures. Only two studies (25%) used patients to evaluate the LLMs output. One study (12.5%) compared their initial prompt with optimized prompt. Five studies (62.5%) showed missing, inaccurate and potentially harmful AI outputs.
Conclusion
LLMs can be used to simplify medical imaging reports and procedures, for improved patient comprehension. However, their limitations cannot be ignored. Further study in this field is essential and more conclusive evidence is needed.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study did not receive any funding

Author Declarations

I 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I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the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.

Yes

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).

Yes

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



Source link

Leave a Reply

Your email address will not be published. Required fields are marked *