De-implementing Inhaled Steroids to Improve Care and Safety in COPD (DISCUSS COPD)

De-implementing Inhaled Steroids to Improve Care and Safety in COPD (DISCUSS COPD) (QUE 15-471)

This Quality Enhancement Research Initiative (QuERI) project is designed to determine efficacy and acceptance of an intervention method to provide primary care providers with patient-tailored electronic consults and corresponding unsigned orders for de-implementation of inhaled corticosteroids (ICS) for patients with COPD when ICS are not indicated by guidelines.

Study Overview

• Status: Completed
• Conditions: Treatment of Chronic Obstructive Pulmonary Disease
• Intervention / Treatment: Other: Guideline treatment recommendations

Detailed Description

Chronic obstructive pulmonary disease (COPD) is among the most common medical diagnoses among Veterans. Approximately half of those who carry a diagnosis of COPD are prescribed inhaled corticosteroids (ICS), despite ICS having no role among those patients without fixed airflow obstruction (AFO) and a limited role among those who do. Guidelines explicitly state that ICS for COPD patients should be limited to those with severe AFO and those with frequent exacerbations. Even this benefit comes at a cost, as ICS use has been shown in multiple randomized controlled trials to increase rates of pneumonia. After prolonged exposure, ICS is also associated with higher bone fracture risk, incidence of cataracts and poor diabetes control. Among patients without disease or with mild-moderate AFO and low risk of exacerbation, ICS have no demonstrated efficacy, but retain the risk of harm. For this reason, evidence-based guidelines specifically recommend against their use in mild-moderate AFO.

The goal of this project is to improve the delivery and safety of care by de-implementing the ineffective use of ICS among Veterans with a diagnosis of COPD who otherwise lack a clinical indication for the medication. The primary aim is to reduce ICS use among Veterans with limited clinical indication for the medication. Investigators will test an intervention to de-implement unnecessary use of inhaled corticosteroids in Veterans with chronic obstructive pulmonary disease (COPD) by having pulmonologists assume more responsibility for supporting COPD patients. The investigators will compare a substitution approach using proactive patient-tailored electronic consult (E-consult) compared to usual care with a single-session education outreach, which represents a non-intensive unlearning approach. The investigators are targeting the intervention to Patient Aligned Care Team (PACT) providers who are randomized to either receive the intervention or not receive the intervention. For patients within intervention PACTs, the project clinicians will leverage the VA's integrated healthcare informatics system using specialist support through proactive patient-tailored electronic consults (E-consult) and inputting unsigned orders on behalf of Primary Care Providers (PCPs) to recommend and facilitate de-implementation of ICS. Primary care providers will have final say in accepting (signing), modifying, or declining the recommendations.

• Study Type: Interventional
• Enrollment (Actual): 181
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Massachusetts
    • Bedford, Massachusetts, United States, 01730-1114
      • VA Bedford HealthCare System, Bedford, MA
  • Washington
    • Seattle, Washington, United States, 98108-1532
      • VA Puget Sound Health Care System Seattle Division, Seattle, WA

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Child; Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

Provider:

Primary care provider (medical doctor/osteopathic physician, nurse practitioner, physician assistant [MD/DO, NP, PA]) assigned to a PACT from VA Puget Sound Health Care System or Edith Nourse Rogers Memorial Veterans Hospital (Bedford VA).

Patient:

• Patient is a Veteran who is assigned a VA PCP and has received Rx for an inhaled corticosteroid within the past 180 days.
• Patient has an inpatient or outpatient diagnosis of COPD in the prior two years.
• Patient has undergone spirometry in the past 5 years that indicates either no airflow obstruction or mild to moderate airflow obstruction indicated by a forced expiratory volume 1 (FEV1)/[greater of forced vital capacity (FVC) or vital capacity (VC)] =< 0.7 & FEV1% predicted >= 30%.

Exclusion Criteria:

Patients:

• Very severe airflow obstruction (<30% FEV1 % predicted)
• Severe disease as indicated by 1 inpatient COPD exacerbation in the year prior
• Severe disease as indicated by 2 outpatient COPD exacerbations in the year prior
• International Classification of Diseases (ICD) 9 and/or 10 diagnosed or clinically indicated asthmatics
• Significant bronchodilator response on spirometry (>12% increase in FEV1 post bronchodilator; >375 mL post-bronchodilator improvement)

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Other
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Other: Proactive patient-tailored electronic consult (E-consult); Primary care clinicians receive patient-tailored guideline concordant treatment recommendations, including orders and rationale to discontinue inhaled corticosteroids.	Other: Guideline treatment recommendations; Patient-tailored E-consult, orders and rationale to discontinue inhaled corticosteroids and discontinue or receive other COPD related care.
No Intervention: Usual care; Standard practice (usual care). Primary care providers treat their patients as usual.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Percentage of Patients With Discontinued or Expired and Not Renewed Inhaled Corticosteroids That Remain Off at 6 Months.	Percentage of patients with discontinued or expired and not renewed inhaled corticosteroids that remain off at 6 months from index date.	Assessed at 6 months post primary care visit defined as (index date + 180 days)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Rate of COPD Exacerbation	Rate of COPD exacerbation within 6 months starting the day after index date.	Within 6 months defined as (index date +1 day) to (index date + 180 days)
Rate of Pneumonia	Rate of pneumonia within 6 months starting the day after index date.	Within 6 months defined as (index date +1 day) to (index date + 180 days)
Mortality	Mortality determined by the presence of date of death occurring between (index date + 1 day) to (index date + 180 days)	Assessed during 6 months following primary care visit defined as (index date + 1 day) to (index date + 180 days)
Number of Patients Recommended to Stop Inhaled Corticosteroids	Among patients of intervention PCPs, number of patients recommended to stop inhaled corticosteroids	Collected at time of recommendation/order entry
Percentage of Recommendations to Discontinue Inhaled Corticosteroids Accepted by Primary Care Providers	Among patients assigned to intervention PCPs, percentage of recommendations to discontinue inhaled corticosteroids accepted by primary care providers	Assessed during 6 months following index date
Percentage of Patients Where ICS Discontinuation Recommendations Are Accepted But Restarted by 6 Months Following Index Date	Percentage of patients where ICS discontinuation recommendations are accepted but restarted by 6 months following index date	Assessed at 6 months post index date
Number of Patients for Whom Recommendations Are Made	Among patients assigned to intervention providers, number of patients for whom recommendations are made.	Collected at time or recommendation order entry

Collaborators and Investigators

• Sponsor: VA Office of Research and Development
• Investigators: Principal Investigator: David H. Au, MD MS, VA Puget Sound Health Care System Seattle Division, Seattle, WA; Principal Investigator: Christian D. Helfrich, PhD MPH BA, VA Puget Sound Health Care System Seattle Division, Seattle, WA

Study record dates

Study Major Dates

• Study Start (Actual): September 6, 2016
• Primary Completion (Actual): July 29, 2019
• Study Completion (Actual): June 30, 2021

Study Registration Dates

• First Submitted: August 12, 2016
• First Submitted That Met QC Criteria: September 6, 2016
• First Posted (Estimated): September 12, 2016

Study Record Updates

• Last Update Posted (Actual): July 27, 2023
• Last Update Submitted That Met QC Criteria: July 19, 2023
• Last Verified: July 1, 2023

More Information

Terms related to this study

• Keywords: Safety; Respiratory Tract Diseases; Lung Diseases, Obstructive; Pneumonia; Lung Diseases; Interventional; Inhaled corticosteroids; Multicenter; Quality Improvement; De-implementation; Quality Enhancement Research Initiatives; QuERI; Pulmonary Diseases, Chronic Obstructive COPD
• Additional Relevant MeSH Terms: Pathologic Processes; Respiratory Tract Diseases; Disease Attributes; Chronic Disease; Lung Diseases; Lung Diseases, Obstructive; Pulmonary Disease, Chronic Obstructive
• Other Study ID Numbers: QUX 16-009; QUE 15-271 (Other Grant/Funding Number: Department of Veterans Affairs)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No