Subcutaneous Furosemide in Acute Decompensated Heart Failure: The SUBQ-HF Study

SUBQ-HF is a multicenter clinical trial of selected AHF patients with persistent congestion.
This study will evaluate a strategy of early discharge (pathway 1) or admission avoidance
(pathway 2) with daily SQ furosemide compared to usual care in a population who have
objective evidence of persistent congestion requiring ongoing parenteral diuretics. This will
be an unblinded, randomized, controlled study of approximately 300 evaluable patients.
Eligible patients will be randomized (1:1) to either:

Usual care strategy, during which patients will have continued inpatient treatment and
discharge follow-up as per usual standard of care plus a Day 7 phone call and Day 30 study
visit.

or

Subcutaneous strategy, in which patients will be discharged home within 24 hours of
randomization (pathway 1) or sent home from clinic or ED to receive furosemide with the SQ
pump for 1-7 days (based on clinical response) plus a Day 7 and Day 30 visit.

Subcutaneous furosemide/early discharge strategy:

Subjects will receive device training and study materials (SQ pump device and up to a 7 day
supply of SQ furosemide vials) on the day of randomization (study day 0) and discharged
within 24 hours. Training will include instruction on daily weights and dyspnea numerical
rating for symptoms. Scales will be provided to subjects. Subjects will be discharged with
planned treatment of 80 mg SQ furosemide injection over 5-hours either QD or BID, depending
on anticipated diuretic requirements. If there are unanticipated delays in discharge after
randomization, subjects will continue with their assigned therapy and assessments in the
hospital. Discharged subjects will receive a phone contact from study team on D1, D3, and D5
in order to assess adequacy of diuresis, persistence of congestion, and planned duration,
dose of ongoing SQ therapy (see Appendix for guidelines on adjusting therapy) and adverse
events. Additional clinical contact (additional phone contacts or clinical visits) may be
performed if felt clinically indicated by the study team or clinical provider. All subjects
will have assessment of electrolytes and renal function by protocol 2 days post discharge.
More frequent electrolyte monitoring can be performed at the discretion of the study team or
clinical provider as clinically indicated. Patients receiving the SQ pump for outpatient use
should be prescribed a supplementation regimen based on electrolyte supplementation needs in
the hospital with IV diuretic therapy. The duration of subcutaneous therapy will be planned
for 1-7 days depending on clinical response. Dose and frequency of oral diuretics once SQ
therapy is completed will be per the discretion of the treating physician.

Usual care strategy:

Subjects randomized to usual care will continue to receive inpatient therapy, eventual
transition to oral diuretics, and discharge and post discharge care as per the discretion of
the treating clinician and standard treatment guidelines. In addition, they will have a Day 7
study phone call and a Day 30 study visit.

Inclusion Criteria for Pathway 1 (patients hospitalized with acute heart failure)

1. Age >18 years

2. Willingness and ability to provide informed consent

3. Hospitalization for AHF with at least 1 symptom (dyspnea, orthopnea, or edema) AND 1
sign (rales on auscultation, peripheral edema, ascites, pulmonary vascular congestion
on chest radiography, BNP > 250 ng/mL or NTproBNP > 1000 ng/mL) of congestion

4. Persistent congestion defined by the presence of at least 2 or more of the following
at the time of consent:

1. Peripheral edema

2. Rales

3. Elevated JVP

4. Ascites

5. BNP > 250 ng/mL or NTproBNP > 1000 ng/mL during index hospitalization

6. Orthopnea

5. Total anticipated daily IV furosemide dose (at time of screening) >80-240 mg (or
equivalent)/day

6. Anticipated need for at least 24 more hours of parenteral diuretic therapy

Exclusion Criteria for Pathway 1

1. Severe renal dysfunction (eGFR< 20 ml/min/1.73m2) within 24 hours of enrollment

2. Requirement for inotropes (other than digoxin) or mechanical support during
hospitalization

3. Clinically significant electrical instability during hospitalization

4. Anticipated need for ongoing intravenous therapies beyond diuretics (electrolyte
repletion, vasodilators, antibiotics, etc.)

5. Planned discharge to location other than home (e.g., hospice, skilled nursing
facility, etc.)

6. Anticipated cardiac transplantation or left ventricular assist device within the next
30 days

7. Primary hypertrophic cardiomyopathy, infiltrative cardiomyopathy, acute myocarditis,
constrictive pericarditis or tamponade

8. Known or anticipated pregnancy in the next 30 days

9. Prior use of a subcutaneous furosemide pump or current use of any subcutaneous pump,
on-body infusion devices or patients who give regimented injections at the intended
site of the furosemide infusion device.

10. Other psychosocial or physical barriers to following the protocol and using SQ pump
device outside the hospital setting

11. Known allergy to furosemide

12. Known sensitivity or allergy to medical adhesive tape

13. Enrollment or planned enrollment in another therapeutic clinical trial in next 3
months

14. Presentation is for indication other than CHF

Inclusion Criteria for Pathway 2 (Outpatients with heart failure presenting with volume
overload necessitating treatment with parenteral loop diuretics)

1. Age >18 years

2. Willingness and ability to provide informed consent

3. HF now presenting with volume overload defined by the presence of at least 2 or more
of the following at the time of consent:

1. Peripheral edema

2. Rales

3. Elevated JVP

4. Ascites

5. BNP > 250 ng/mL or NTproBNP > 1000 ng/mL during this episode of decompensation

6. Orthopnea

4. Need for parenteral furosemide with an estimated SQ furosemide requirement between
80-240 mg/day

5. Anticipated need for at least 24 hours of parenteral diuretic therapy

Exclusion Criteria for Pathway 2

1. Severe renal dysfunction (eGFR< 20 ml/min/1.73m2) within 24 hours of enrollment

2. Anticipated need for inotropes (other than digoxin) or mechanical support to treat
current episode of decompensation

3. Clinically significant electrical instability requiring hospitalization

4. Anticipated need for ongoing intravenous therapies beyond diuretics (electrolyte
repletion, vasodilators, antibiotics, etc.)

5. Residence at location other than home (e.g., hospice, skilled nursing facility, etc.)

6. Anticipated cardiac transplantation or left ventricular assist device within the next
30 days

7. Primary hypertrophic cardiomyopathy, infiltrative cardiomyopathy, acute myocarditis,
constrictive pericarditis or tamponade

8. Known or anticipated pregnancy in the next 30 days

9. Prior use of a subcutaneous furosemide pump or current use of any subcutaneous pump,
on-body infusion devices or patients who give regimented injections at the intended
site of the furosemide infusion device.

10. Other psychosocial or physical barriers to following the protocol and using SQ pump
device outside the hospital setting

11. Known allergy to furosemide

12. Known sensitivity or allergy to medical adhesive tape

13. Enrollment or planned enrollment in another therapeutic clinical trial in next 3
months.

14. Presentation is for indication other than CHF.