
ADA 2026: Subcutaneous Furosemide May Reduce Heart Failure Hospitalizations in Patients With Diabetes
Key Takeaways
- Diabetes confers heightened heart failure hospitalization burden, prompting American Diabetes Association guidance to consider natriuretic peptide screening in asymptomatic adults with diabetes to detect preclinical heart failure risk.
- Subcutaneous Furoscix (80 mg/10 mL) achieves approximately 99.65% bioavailability, reaches therapeutic levels within 30 minutes, and sustains exposure up to 6 hours, approximating 80 mg intravenous (IV) diuresis.
A post hoc analysis of the AT HOME-HF trial found lower hospitalization rates and longer time to admission among patients with diabetes treated with subcutaneous furosemide compared with usual care.
Researchers presenting at the 2026 American Diabetes Association (ADA) Scientific Sessions in New Orleans, Louisiana, shared findings from a post hoc analysis suggesting that subcutaneous (SC) furosemide injection (Furoscix; scPharmaceuticals) may offer a meaningful advantage over usual oral diuretic therapy in reducing heart failure (HF) hospitalizations among persons living with diabetes.1
The Burden of HF: Why Furosemide Plays a Key Role
HF is one of the most serious and costly comorbidities associated with diabetes. The risk of developing HF is increased in individuals with obesity, diabetes, hypertension, and chronic kidney disease, and research has demonstrated that diabetes is associated with a higher rate and burden of hospitalization in people with HF, including elevated rates of decompensated HF events. Recognizing the scale of this risk, the ADA's 2025 Standards of Care recommend that clinicians consider screening asymptomatic adults with diabetes for HF using natriuretic peptide levels.1-3
Against this backdrop, the phase 2 AT HOME-HF trial (NCT04593823) evaluated the potential of SC furosemide as an outpatient alternative to intravenous (IV) diuresis. Furoscix is an 80-mg/10-mL buffered formulation of furosemide designed for self-administered SC delivery. SC infusion using a biphasic delivery profile resulted in complete bioavailability (99.65%) and equivalent diuresis when compared with 80 mg of IV furosemide, with therapeutic levels reached within 30 minutes and maintained for up to 6 hours.4,5
AT HOME-HF was an open-label, randomized pilot trial in which patients with HF and signs and symptoms of fluid overload were randomly assigned 2:1 to receive SC furosemide (once or twice daily) or usual care (UC), defined as oral diuretic augmentation guided by investigator clinical judgment. The post hoc analysis presented at the ADA sessions stratified 30-day hospitalization outcomes by diabetes status.1,6
Of 51 patients with HF enrolled, 28 had concomitant diabetes—19 in the SC furosemide group and 9 in the UC group. Among persons with diabetes, HF hospitalization occurred in 11% of those receiving SC furosemide compared with 22% of those receiving UC. Additionally, among patients with diabetes who were hospitalized, the mean time to admission was 17 days for SC furosemide vs 4 days for UC, a clinically meaningful difference suggesting that SC furosemide may delay disease deterioration requiring inpatient care. Ninety percent of SC furosemide doses were administered within the first 7 days, with 97% delivered once daily.1
Pharmacy Implications: Ambulatory, Primary, and Cardiology Care Settings
These findings build on prior evidence supporting the outpatient use of furosemide. An earlier trial (the phase 3 FREEDOM-HF; NCT03458325) comparing outpatient furosemide with hospital admission for IV diuresis found that no patients in the furosemide group required an initial HF hospital admission, and 96% of furosemide-treated patients remained out of the hospital for 30 days after treatment. Admitting patients to the hospital solely for the administration of IV furosemide is expensive and increases risks of hospital-associated morbidity and mortality, underscoring the need for treatment paradigms that shift HF management outside of the hospital.7-8
The poster's authors noted that the results were descriptive only and that larger studies are warranted to validate the findings in the diabetes population. Nevertheless, they emphasized the clinical relevance for pharmacists and other clinicians who manage patients with diabetes, who face elevated HF risk and may benefit from awareness of SC furosemide as a strategy to reduce hospitalizations.1
Pharmacists practicing in ambulatory care, primary care, and cardiology settings are well positioned to identify patients with diabetes who may be candidates for outpatient diuretic augmentation with SC furosemide. As the intersection of diabetes and HF continues to drive substantial health care utilization, tools that enable hospital avoidance—without sacrificing diuretic efficacy—represent an important addition to the outpatient management tool kit.1












































































































