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B-lines Lung Ultrasound Guided ED Management of Acute Heart Failure Pilot Trial (BLUSHED-AHF)

Primary Purpose

Heart Failure, Heart Failure Acute, Acute Cardiac Pulmonary Edema

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
LUS-guided strategy-of-care
Usual Care
Intravenous Loop Diuretic
Vasodilator
Non invasive Ventilation (NIV)
Sponsored by
Indiana University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure focused on measuring Heart Failure, Acute Heart Failure, Pulmonary Edema, Lung ultrasound, Extra vascular lung water, B-lines

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 21 years
  • Presents with shortness of breath at rest or with minimal exertion
  • Clinical diagnosis of AHF and presence of > 15 total bilateral B-lines distributed in at least 4 zones on initial LUS
  • Hx of chronic HF and any one of the following:

    • Chest radiograph consistent with AHF
    • Jugular venous distension
    • Pulmonary rales on auscultation
    • Lower extremity edema

Exclusion Criteria:

  • Chronic renal dysfunction, including end-stage renal disease (ESRD) or estimated glomerular filtration rate (eGFR) < 45ml//min/1.73m2.
  • Shock of any kind. Any requirement for vasopressors or inotropes.
  • Systolic blood pressure (SBP) < 100 or >175 mmHg
  • Need for immediate intubation
  • Acute Coronary Syndrome- Presentation consistent with myocardial ischemia AND either new ST-segment elevation/depression
  • Fever >101.5 ºF or chest radiograph or clinical picture of pneumonia
  • End stage HF: transplant list, ventricular assist device
  • Anemia requiring transfusion
  • Known interstitial lung disease
  • Suspected acute lung injury or acute respiratory distress syndrome (ARDS)
  • Pregnant or recently pregnant within the last 6 months

Sites / Locations

  • Eskenazi Health
  • IU Health Methodist Hospital
  • Detroit Receiving Hospital
  • Case Western Reserve University
  • Vanderbilt University
  • INOVA Health System

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

LUS-guided strategy-of-care

Usual care

Arm Description

Patients randomized to the LUS strategy of care arm will be treated according to protocol. This protocol only involves therapies used in everyday AHF clinical practice.

Patients randomized to the usual care arm will also undergo lung ultrasound assessments. However, these results will not be revealed to the care team. Patients will receive treatment per usual, standard care.

Outcomes

Primary Outcome Measures

Number of Participants With B-lines ≤ 15 at the Conclusion of ED AHF Management
B-lines ≤ 15 at the conclusion of ED AHF management or maximum of 6 hours after enrollment, whichever comes first.

Secondary Outcome Measures

Full Information

First Posted
April 19, 2017
Last Updated
May 19, 2020
Sponsor
Indiana University
Collaborators
Inova Fairfax Hospital, Vanderbilt University, Case Western Reserve University, Wayne State University
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1. Study Identification

Unique Protocol Identification Number
NCT03136198
Brief Title
B-lines Lung Ultrasound Guided ED Management of Acute Heart Failure Pilot Trial
Acronym
BLUSHED-AHF
Official Title
B-lines Lung Ultrasound Guided ED Management of Acute Heart Failure Pilot Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
July 10, 2017 (Actual)
Primary Completion Date
March 20, 2019 (Actual)
Study Completion Date
June 20, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indiana University
Collaborators
Inova Fairfax Hospital, Vanderbilt University, Case Western Reserve University, Wayne State University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Nearly 80% of acute heart failure (AHF) patients admitted to the hospital are initially treated in the emergency department (ED). Once admitted, within 30 days post-discharge, 27% of patients are re-hospitalized or die. Attempts to improve outcomes with novel therapies have all failed. The evidence for existing AHF therapies are poor: No currently used AHF treatment is known to improve outcomes. ED treatment is largely the same today as 40 years ago. Congestion, such as difficulty breathing, weight gain, and leg swelling, is the primary reason why patients present to the hospital for AHF. Treating congestion is the cornerstone of AHF management. Yet half of all AHF patients leave the hospital inadequately decongested. The investigators propose a novel approach to aggressively decongest patients in the ED setting: lung ultrasound guided, protocol driven, AHF management. LUS B-lines are a measure of extra-vascular lung water (EVLW). In the setting of AHF, LUS B-lines are a measure of congestion. This simple, easily learned technique has excellent reliability and reproducibility. The investigators hypothesize that a strategy-of-care will outperform usual care. At the present time, usual care is largely empirical. This study will improve the evidence base for ED AHF management. This proposed pilot study, if successful, will lead to an outcome trial examining whether an ED AHF strategy-of-care increases days alive and out of the hospital for patients.
Detailed Description
The primary goal of the BLUSHED AHF pilot trial is to determine whether an early lung ultrasound (LUS) guided, protocol-driven ED AHF strategy-of-care leads to more rapid and sustained resolution of congestion, as measured by LUS B-lines. If the investigators are able to demonstrate this necessary and sufficient information - targeted strategy-of-care is more effective than usual care - they will apply for a follow on study to achieve the following aim. Aim 1: To demonstrate the effectiveness of a targeted decongestion strategy - LUS guided, protocol-driven ED AHF management - will result in improved 30-day outcomes vs. usual care. This aim will be tested using a randomized, controlled, unblinded, pragmatic, multi-center, simple trial design. The pilot trial may determine that ED management alone is insufficient to impact the outcome. Thus, the investigators may need to modify their subsequent trial design to include targeted therapy throughout hospitalization. However, the pilot study will demonstrate whether targeted therapy effectively reduces B-lines. PUBLIC HEALTH IMPACT Over one million hospitalizations for AHF occur every year in the US. Within 30 days after hospitalization, over 25% of AHF patients will be dead or re-hospitalized.4 Up to 67% of patients will be re-hospitalized and 36% will be dead by one year. For patients aged 65 years and older, AHF is the most common and most expensive reason for hospitalization. Despite major reductions in morbidity and mortality for chronic HF, considerably less progress has been seen in AHF. Congestion is the primary reason why AHF patients present to the ED seeking medical care. Congestion is manifest by signs and symptoms of heart failure (HF); dyspnea, orthopnea, edema, and weight gain. Yet, how to best assess, grade, and manage congestion is not well established. Freedom from congestion is associated with improved outcomes; Yet many patients leave the hospital inadequately decongested. The absence of robust, reliable methods to assess congestion is a primary reason why it is not well-assessed. A recent consensus statement published in 2010 highlights this fact: "…no method to assess congestion…has been validated." The investigators would argue many ED AHF patients are poorly assessed prior to treatment. In addition, they are poorly re-assessed prior to hospitalization to gauge the success or failure of initial management. While physical exam is currently the cornerstone of congestion assessment, it lacks sensitivity and inter-rater reliability. The investigators challenge the current paradigm of relying on insensitive methods of congestion to guide therapy. Furthermore, they argue the lack of a robust evidence base for ED management of congestion contributes to poor outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Heart Failure Acute, Acute Cardiac Pulmonary Edema, Acute Cardiac Failure
Keywords
Heart Failure, Acute Heart Failure, Pulmonary Edema, Lung ultrasound, Extra vascular lung water, B-lines

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Care ProviderInvestigator
Masking Description
A central, independent, Core Lab will review all images.
Allocation
Randomized
Enrollment
130 (Actual)

8. Arms, Groups, and Interventions

Arm Title
LUS-guided strategy-of-care
Arm Type
Experimental
Arm Description
Patients randomized to the LUS strategy of care arm will be treated according to protocol. This protocol only involves therapies used in everyday AHF clinical practice.
Arm Title
Usual care
Arm Type
Placebo Comparator
Arm Description
Patients randomized to the usual care arm will also undergo lung ultrasound assessments. However, these results will not be revealed to the care team. Patients will receive treatment per usual, standard care.
Intervention Type
Other
Intervention Name(s)
LUS-guided strategy-of-care
Intervention Description
For patients randomized to the strategy-of-care arm, the LUS guided protocol will be initiated and continued until there is a decrease in B-lines to ≤ 15 or 6 hours of care has been delivered, whichever comes first. Treatment protocol: IV furosemide (unless already given): 2x single oral dose if on chronic therapy or 20-40 mg if diuretic naive. Optional therapies: non-invasive ventilation, vasodilators (SL, topical, or IV) Reassessment every 2 hours
Intervention Type
Other
Intervention Name(s)
Usual Care
Intervention Description
Patients will receive usual AHF care
Intervention Type
Drug
Intervention Name(s)
Intravenous Loop Diuretic
Intervention Description
IV loop diuretic
Intervention Type
Drug
Intervention Name(s)
Vasodilator
Intervention Description
IV, topical, or SL Vasodilator
Intervention Type
Device
Intervention Name(s)
Non invasive Ventilation (NIV)
Intervention Description
Face, mouth, or nasal mask applied to provide positive pressure ventilation
Primary Outcome Measure Information:
Title
Number of Participants With B-lines ≤ 15 at the Conclusion of ED AHF Management
Description
B-lines ≤ 15 at the conclusion of ED AHF management or maximum of 6 hours after enrollment, whichever comes first.
Time Frame
During the ED phase of management, usually no more than 6 hours
Other Pre-specified Outcome Measures:
Title
Total Days Alive and Out Of Hospital (DAOOH)
Description
Total days alive and out of hospital through 30 and 90 days post-discharge
Time Frame
Up through 90 days, with specific reporting of events through 30 and 90 days
Title
Association of B-lines at Discharge and 30-day / 90-day Outcomes
Time Frame
Up through 90 days, with specific reporting of events through 30 and 90 days
Title
Change in Biomarkers From Presentation to Pre-discharge
Time Frame
From admission to pre-discharge from the hospital, on average 5 to 7 days.
Title
Time to Reach B-lines <15
Time Frame
Throughout hospitalization, on average 5-7 days
Title
B Lines < 15 at 24 Hours and at Discharge
Time Frame
Through the first 24 hours and then prior to discharge, on average 5-7 days after admission
Title
Composite of 30-day and 90-day All-cause Mortality, Cardiovascular (CV) Re-hospitalizations, and CV Emergency Department (ED) Revisits.
Description
CV endpoints are defined according to the 2014 American College of Cardiology/American Heart Association (ACC/AHA) Key Data Elements and Definitions for Cardiovascular Endpoint Events.
Time Frame
Up through 90 days, with specific reporting of events through 30 and 90 days
Title
All Cause Readmissions, All Cause ED Re-visits
Description
30- day and 90-day
Time Frame
Up through 90 days, with specific reporting of events through 30 and 90 days
Title
Number of Participants With Physical Exam Findings of Heart Failure When Discharge is Compared to Baseline
Description
Physical exam includes body weight, peripheral edema, jugular venous distention, pulmonary and cardiac auscultation
Time Frame
From admission throughout hospitalization, usually 5-7 days.
Title
Count of Pharmacologic Therapies the Patient Received in the ED
Description
This is a description of which pharmacologic therapies the patient has received.
Time Frame
From admission throughout hospitalization, usually 5-7 days.
Title
Count of Pharmacologic and Device Therapies the Patient Received During Hospitalization
Description
This is a description of which pharmacologic and device therapies the patient has received.
Time Frame
From admission throughout hospitalization, usually 5-7 days.
Title
Comparison of LUS Interpretation Within and Between Trained Investigators as Well as the Core Lab
Description
Calculation of intra and inter-agreement between investigators and also the Core Lab to determine the reproducibility of LUS
Time Frame
From admission throughout hospitalization, usually 5-7 days.
Title
Association of Baseline, Discharge, and Change With 30 and 90 Day Outcomes
Time Frame
Up through 90 days, with specific reporting of events through 30 and 90 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 21 years Presents with shortness of breath at rest or with minimal exertion Clinical diagnosis of AHF and presence of > 15 total bilateral B-lines distributed in at least 4 zones on initial LUS Hx of chronic HF and any one of the following: Chest radiograph consistent with AHF Jugular venous distension Pulmonary rales on auscultation Lower extremity edema Exclusion Criteria: Chronic renal dysfunction, including end-stage renal disease (ESRD) or estimated glomerular filtration rate (eGFR) < 45ml//min/1.73m2. Shock of any kind. Any requirement for vasopressors or inotropes. Systolic blood pressure (SBP) < 100 or >175 mmHg Need for immediate intubation Acute Coronary Syndrome- Presentation consistent with myocardial ischemia AND either new ST-segment elevation/depression Fever >101.5 ºF or chest radiograph or clinical picture of pneumonia End stage HF: transplant list, ventricular assist device Anemia requiring transfusion Known interstitial lung disease Suspected acute lung injury or acute respiratory distress syndrome (ARDS) Pregnant or recently pregnant within the last 6 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter S Pang, MD
Organizational Affiliation
Indiana University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Eskenazi Health
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States
Facility Name
IU Health Methodist Hospital
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States
Facility Name
Detroit Receiving Hospital
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States
Facility Name
Case Western Reserve University
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Facility Name
Vanderbilt University
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37235
Country
United States
Facility Name
INOVA Health System
City
Fairfax
State/Province
Virginia
ZIP/Postal Code
22042
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34246609
Citation
Pang PS, Russell FM, Ehrman R, Ferre R, Gargani L, Levy PD, Noble V, Lane KA, Li X, Collins SP. Lung Ultrasound-Guided Emergency Department Management of Acute Heart Failure (BLUSHED-AHF): A Randomized Controlled Pilot Trial. JACC Heart Fail. 2021 Sep;9(9):638-648. doi: 10.1016/j.jchf.2021.05.008. Epub 2021 Jul 7.
Results Reference
derived
PubMed Identifier
30448355
Citation
Russell FM, Ehrman RR, Ferre R, Gargani L, Noble V, Rupp J, Collins SP, Hunter B, Lane KA, Levy P, Li X, O'Connor C, Pang PS. Design and rationale of the B-lines lung ultrasound guided emergency department management of acute heart failure (BLUSHED-AHF) pilot trial. Heart Lung. 2019 May-Jun;48(3):186-192. doi: 10.1016/j.hrtlng.2018.10.027. Epub 2018 Nov 15.
Results Reference
derived

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B-lines Lung Ultrasound Guided ED Management of Acute Heart Failure Pilot Trial

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