How Institutional Guidelines for Urgent Inpatient Surgeries Affect Intensity of Perioperative Cardiovascular Testing

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorJohns Hopkins University

About this trial

This study will evaluate the impact of implementing an educational clinical decision support (CDS) tool designed to guide perioperative cardiovascular evaluation for adults undergoing urgent inpatient surgery. The CDS tool, integrated within the Epic electronic health record via AgileMD, provides evidence-informed recommendations regarding perioperative cardiac testing and specialty consultation based on American Heart Association guidance and multidisciplinary institutional consensus. The investigators will conduct a retrospective and prospective pre-post observational cohort study comparing perioperative cardiovascular testing intensity, consultation patterns, time to operating room, and clinical outcomes before and after implementation of the tool among adult patients admitted through the emergency department at Johns Hopkins Hospital and Johns Hopkins Bayview Medical Center who undergo urgent surgery. Data will be obtained from the Core for Clinical Research Data Acquisition (CCDA) and Epic electronic health record, with case-level chart review performed as needed to validate rare outcomes such as major adverse cardiac events.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults age 18 years or older

Admitted through the Emergency Department at Johns Hopkins Hospital or Johns Hopkins Bayview Medical Center Undergoing urgent inpatient surgery during the index hospitalization

Disqualifiers

Elective surgeries,

Outpatient procedures,

Procedures followed only by observation or extended-stay recovery rather than inpatient admission,

Patients younger than 18 years old

Trial population

Adults admitted through the Emergency Department to Johns Hopkins Hospital (JHH) Downtown or JHH Bayview Medical center above the age of 18 who require surgery during the stay.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

3,000 Participants
are grouped into 2 trial groups
Group A: Cohort 2: Perioperative Cardiovascular Clinical Decision Support
Group B: Cohort 1: Usual Care

Trial outcomes

Primary outcomes

1

Rate of preoperative tests and consult orders

Cardiovascular Testing and Consultative Intensity. Rate of preoperative tests and consult orders per patient per admission.

Time frame
From Presentation to the ED to 6 months post presentation

Secondary outcomes

1

Major Adverse Cardiac Events (MACE)

Major Adverse Cardiac Events (MI, Cerebrovascular Accident, Unstable Arrhythmia, Myocardial Injury after Non-cardiac Surgery (MINS), Sudden Cardiac Death)

Time frame
From presentation at the ED to 6 months post presentation
2

Time to OR

Time from Presentation at the ED to start of Surgery

Time frame
0 hours to 5 days

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Johns Hopkins University

Lead sponsor

Agency For Healthcare Research & Quality

Collaborator

Patient-Centered Outcomes Research Institute

Collaborator

This trial is not recruiting at the moment. You can still explore other options: