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Предстои набиране Не е приложимо NCT07337577

Large Language Model-Generated Messages to Improve Guideline-Directed Medical Therapy in Heart Failure

Не е приложима фаза (напр. обсервационно)
Заболявания: Heart Failure

Спонсор: Brigham and Women's Hospital

Налично на: БГ
Обобщение
This study is an investigator-initiated, cluster-randomized implementation trial evaluating a large language model (LLM)-based clinical decision support (CDS) tool designed to improve guideline-directed medical therapy (GDMT) for adult patients with heart failure seen in outpatient cardiology clinics at Mass General Brigham. For eligible heart failure encounters, the CDS tool reviews existing electronic health record (EHR) data, including diagnoses, medications, vital signs, laboratory results, and recent notes, and generates brief, clinician-facing messages suggesting opportunities to initiate or optimize GDMT and highlighting relevant safety considerations. Messages are delivered to cardiology providers via Epic InBasket and/or institutional email prior to scheduled visits. The tool is advisory only and cannot place orders or change medications automatically; all treatment decisions remain at the discretion of the treating clinician and patient. Cardiology providers are assigned at the provider/clinic level to early implementation of the CDS tool versus usual care (no messages) during the initial phase. The primary outcome is GDMT optimization within 30 days of an index visit. Secondary outcomes include feasibility of CDS generation and delivery and a 30-day safety composite (e.g., heart failure hospitalization, acute kidney injury, hyperkalemia, hypotension or bradyarrhythmia plausibly related to GDMT).
Описание
Overview and Rationale Guideline-directed medical therapy (GDMT) for heart failure reduces hospitalizations and mortality, yet substantial underuse and suboptimal titration persist in routine practice, even in specialty cardiology clinics. Barriers include limited visit time, complex comorbidities, fragmented information across notes and structured data, and uncertainty about contraindications or prior intolerance. Electronic clinical decision support (CDS) tools that synthesize key patient information and highlight GDMT opportunities at the point of care may help close these gaps. Large language models (LLMs) can read both structured EHR data (e.g., diagnoses, medications, vital signs, laboratory results) and unstructured narrative notes to generate nuanced, patient-specific recommendations. We developed an LLM-based CDS tool that reviews an adult heart failure patient's EHR and produces a brief, free-text message to the treating cardiology provider summarizing heart failure status, suggesting potential GDMT changes consistent with contemporary guidelines, and flagging relevant safety issues (e.g., low blood pressure, bradycardia, renal dysfunction, hyperkalemia, prior documented intolerance). In retrospective testing, the tool's recommendations were generally concordant with expert clinician judgment. Study Design This is an interventional, cluster-randomized, provider-level trial conducted in adult outpatient cardiology clinics at Mass General Brigham. The intervention is a software-only, investigational clinical decision support device ("LLM-GDMT Clinical Decision Support Tool"). Eligible cardiology attendings and advanced practice providers are assigned at the provider/clinic level to one of two parallel arms during the initial phase: Early Implementation - LLM-GDMT CDS: Providers in this arm receive LLM-generated, clinician-facing messages for eligible heart failure encounters. For scheduled visits that meet predefined inclusion criteria, the tool reviews existing EHR data and generates a brief advisory message that is delivered via Epic InBasket and/or institutional email within the week prior to the visit. Usual Care (Delayed Implementation): Providers in this arm continue usual care and do not receive LLM-generated messages during the initial evaluation phase. EHR data are used to compute quality metrics for comparison. After the initial evaluation, the CDS tool may be expanded to these providers as part of routine care. Patients are not contacted for the study. All clinical decisions, including whether to start, stop, or adjust any medication, remain entirely at the discretion of the treating clinician in partnership with the patient. The CDS messages are advisory only and cannot place orders or directly change medications or monitoring plans. Population and Eligibility The study includes adult patients (age ≥18 years) with a documented heart failure diagnosis who are scheduled for outpatient visits with participating cardiology
Кой може да участва
Inclusion Criteria: * Age ≥18 years * Scheduled outpatient visit with a participating cardiology provider in an MGB outpatient cardiology clinic * At least one prior cardiology clinic visit in the MGB system within the past 2 years * Diagnosis of heart failure by ICD code within the past 2 years * Heart failure diagnosis supported by at least one of the following: * Current or recent use of a loop diuretic * Left ventricular ejection fraction ≤40% on the most recent echocardiogram * Explicit documentation of heart failure diagnosis or heart failure signs/symptoms in a prior cardiology note Exclusion Criteria: * Systolic blood pressure \<90 mmHg on the most recent recorded measurement * Heart rate \<50 beats per minute on the most recent recorded measurement * eGFR \<20 mL/min/1.73 m² on the most recent laboratory assessment * Known cardiac amyloidosis or hypertrophic cardiomyopathy * History of heart transplant or presence of a left ventricular assist device * Severe aortic stenosis, severe aortic insufficiency, or severe mitral stenosis on the most recent echocardiogram * Encounter occurs in an adult congenital heart disease clinic
Интервенции
LLM-GDMT Clinical Decision Support Tool
DEVICE
Места на провеждане 1
САЩ (1)
Mass General Brigham
Boston , Massachusetts
Jonathan W Cunningham, MD, MPH
Технически детайли
Статус
Предстои набиране
Фаза
Не е приложимо
Вид изследване
INTERVENTIONAL
Пол
Мъже и жени
Минимална възраст
18 Years
Максимална възраст
85 Years
Здрави доброволци
Не
Начална дата
01.06.2026
Крайна дата
01.12.2027
Регистрационен номер
NCT07337577
Източник
clinicaltrials.gov
Запитване за медицински туризъм

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