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SGLT2i use linked to lower adherence and QOL in HF patients in cross-sectional MTAC studyTaking More Heart Pills May Actually Feel Better, Not Worse

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Key Takeaway
Consider that SGLT2i use in HF may correlate with lower adherence and QOL in observational data.

This cross-sectional study involved 78 heart failure patients enrolled in a medication therapy adherence clinic (MTAC) program at a secondary hospital in Shah Alam, Malaysia. It assessed therapeutic intensity, including full guideline-directed medical therapy (GDMT), SGLT2 inhibitor use, and medication load, compared to patients not on full GDMT or ARNI, with patient-reported outcomes (PROs) such as adherence, treatment burden, and quality of life as primary and secondary measures.

Main results showed SGLT2i users had significantly lower adherence (p = 0.037) and quality of life (p = 0.018) compared to others, while medication load had a positive correlation with quality of life (r = 0.295, p = 0.009). No associations were found between full GDMT and adherence, burden, or quality of life, or between medication load and adherence or burden. Patients on full GDMT or ARNI had similar scores to those not on these therapies across all outcomes.

Safety and tolerability data were not reported. Key limitations include the exploratory nature of the findings, which may reflect differences in disease severity or treatment complexity rather than a direct effect of therapy, and the need for confirmation in larger, longitudinal studies with appropriate adjustment for clinical variables. In practice, these observational insights highlight the importance of monitoring patient-reported outcomes in HF management, but avoid overstating causation due to the study's design and small sample size.

Why so many pills anyway

Heart failure happens when the heart cannot pump blood as well as it should. It leaves people tired, short of breath, and often struggling to walk short distances.

Modern treatment uses a combination of medicines, called guideline-directed medical therapy (GDMT). Each pill targets a different part of the problem. Together, they help people live longer and stay out of the hospital.

But here is the frustration. Taking four, six, or eight medicines every day sounds exhausting. Doctors and patients have long worried that more pills could mean more side effects, more confusion, and a worse daily life.

What doctors used to assume

For years, the common belief was simple: more medicines equal more burden. Patients on heavier drug regimens were thought to skip doses more often, feel weighed down, and enjoy life less.

But here is the twist. This new study found something different.

Patients taking the most medicines did not feel more burdened. In fact, they reported slightly better quality of life than those on fewer drugs.

The pit-crew approach to heart care

Think of heart failure treatment like a pit crew working on a race car. One person checks the tires, another the fuel, another the engine.

Each heart failure medicine has its own job. One relaxes blood vessels. Another slows the heart. A newer class, called SGLT2 inhibitors, helps the kidneys flush out extra salt and water.

When all these "crew members" work together, the car — your heart — runs smoother. Take away one, and the whole system struggles.

That teamwork may be why patients on full therapy did not feel worse. The pills were doing their jobs quietly in the background.

A closer look at the study

Researchers followed 78 heart failure patients at a pharmacist-led clinic in Shah Alam, Malaysia. This type of clinic, called a Medication Therapy Adherence Clinic (MTAC), gives patients extra coaching on how and when to take their medicines.

Patients filled out three surveys. One measured how well they stuck to their medicines. Another measured how heavy treatment felt. The third measured overall quality of life.

Most patients were men in their late 50s. About two-thirds were on the full four-drug heart failure plan, and more than 80% were taking an SGLT2 inhibitor.

Patients on full therapy and those on fewer drugs had similar scores for sticking to medicines and treatment burden. That was reassuring.

Then came the unexpected part. Patients taking more pills actually scored a little higher on quality of life. The link was modest but real.

This does not mean adding pills automatically makes anyone feel better.

There was also a puzzle. People taking SGLT2 inhibitors reported lower adherence and lower quality of life than those not on them. That sounds alarming — but the researchers caution against jumping to conclusions.

Here is where it gets interesting

Patients prescribed SGLT2 inhibitors may simply have more advanced heart failure to begin with. Sicker patients often feel worse no matter what medicine they take.

So the lower scores might reflect the disease, not the drug itself.

How this fits the bigger picture

Doctors around the world have been pushing for fuller heart failure treatment because trials show it saves lives. Some worried this would come at a cost to daily well-being.

This study gently pushes back on that worry. When patients get proper support — like a pharmacist who explains each medicine and checks in regularly — complex regimens can feel manageable.

The role of the pharmacist may be the quiet hero here.

If you or a loved one has heart failure, do not be afraid of a longer medication list on principle. The number of pills alone is not a reliable sign of how hard treatment will feel.

Talk with your doctor or pharmacist if your regimen feels overwhelming. Ask about clinics or coaching programs in your area that help people manage multiple medicines.

Never stop or skip a heart failure medicine on your own. These drugs work as a team.

What this study cannot tell us

This was a small study at one hospital, with only 78 patients. It looked at one moment in time rather than following people over months or years.

The researchers themselves call the SGLT2 findings "exploratory." That means the results point to questions worth asking, not final answers.

Bigger, longer studies are needed to confirm what this clinic observed. Future research will likely track patients over time and adjust for how sick they are at the start.

The hope is to learn which patients thrive on full therapy, which ones struggle, and what kind of support makes the biggest difference. Research like this takes years, but each study adds one more piece to the puzzle — and this one offers a quietly encouraging message for people living with heart failure today.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
Guideline-directed medical therapy (GDMT) and newer agents such as sodium-glucose cotransporter 2 inhibitors (SGLT2i) have significantly improved outcomes in heart failure (HF). However, their impact on patient experience—including medication adherence, treatment burden, and quality of life (QOL)—remains less understood in Malaysia, especially in structured outpatient settings such as Medication Therapy Adherence Clinic (MTAC). To evaluate associations between therapeutic intensity (full GDMT, SGLT2i use, and medication load) and patient-reported outcomes (PROs) in HF patients enrolled in an MTAC program. A cross-sectional study was conducted among 78 HF patients at a secondary hospital MTAC in Shah Alam, Malaysia. PROs were assessed using the Malaysia Medication Adherence Assessment Tool (MyMAAT-12), the Treatment Burden Questionnaire (TBQ), and WHOQOL-BREF. Full GDMT was defined as concurrent use of a RAAS inhibitor, beta blocker, MRA, and SGLT2i. Group comparisons were performed using Mann–Whitney U tests, and associations between medication load and PROs were assessed using Spearman correlation. The mean age of patients was 57.3 ± 11.5 years; 74.4% were male. Most were on polypharmacy (mean medication classes: 6.6 ± 1.2); 64.1% were on full GDMT and 82.1% were prescribed SGLT2i. Median adherence, burden, and QOL scores were 47.0 (IQR: 40.0–53.0), 39.0 (IQR: 24.0–58.0), and 88.0 (IQR: 77.0–98.0), respectively. Patients on full GDMT or ARNI had similar adherence, burden, and QOL scores compared to those not on these therapies. However, SGLT2i users reported significantly lower adherence (p = 0.037) and QOL (p = 0.018). Medication load was positively correlated with QOL (r = 0.295, p = 0.009), but not with adherence or burden. In this MTAC-supported cohort, polypharmacy and full GDMT were not associated with increased burden or reduced adherence. A modest positive association between medication count and QOL was observed. SGLT2i use was associated with lower adherence and QOL, although these findings are exploratory and may reflect differences in disease severity or treatment complexity rather than a direct effect of therapy. Overall, these results provide observational insights into the relationship between therapeutic intensity and PROs within a pharmacist-led care setting, and warrant confirmation in larger, longitudinal studies with appropriate adjustment for clinical variables.
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