COPD Exacerbation Follow Up
Investigating the Impact of AI Tools on COPD Follow-Up
Study Overview
The goal of this study is to evaluate the impact of implementing an AI-enabled clinical workflow tool (Viz COPD) on respiratory specialist follow up and clinical outcomes after an acute exacerbation.
Study Details
Time perspective: This study will collect data prospectively for the Experimental cohort and retrospectively for the Control cohort. There is also an Exploratory cohort which will collect retrospective and prospective data.
Eligibility Criteria
You may be eligible for this study if you meet the following criteria:
- Conditions: COPD (Chronic Obstructive Pulmonary Disease)
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Age: 40 years or above
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Gender: All
Inclusion Criteria:
- Patients aged 40 years or older at the time of arrival to the emergency department.
- Patients with a clinical diagnosis of COPD who present to the emergency department for a moderate or severe COPD exacerbation.
- A moderate exacerbation is defined as an acute exacerbation requiring either systemic corticosteroids (such as intramuscular, intravenous or oral) and/or antibiotics.
- A severe exacerbation is defined as an acute exacerbation requiring hospitalization, or observation for >24 hours in emergency department/urgent care facility or resulting in death.
- Patients on dual (LABA/LAMA, LABA/ICS, LAMA/ICS) or triple (LABA/LAMA/ICS) long-acting bronchodilator inhalers.
Exclusion Criteria:
- Patients on bronchodilator inhaler monotherapy.
- Patients leaving against medical advice or expiring during hospitalization.
- Patients with tracheostomy.
- Patients with advanced cancer.
- Patients who have received a lung transplant.
- Discharge to hospice care.
- Transfer to another hospital.
This study investigates COPD exacerbation. It looks into how an AI-enabled clinical workflow tool might affect follow-up care by respiratory specialists.
The study focuses on evaluating the impact of this tool on clinical outcomes. It examines how the tool might help in managing care after an acute exacerbation.
- Who can participate: Participants must be 40 years or older and have a clinical diagnosis of COPD. They should have visited the emergency department for a moderate or severe COPD exacerbation and be on dual or triple long-acting bronchodilator inhalers.
- Study details: Participants will be involved in using a tool to manage their care. The study will look at outcomes after an acute exacerbation.
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