Key result
Herpes zoster linked to ~10 days earlier diuretic escalation in heart failure patients.
Why the study?
Immune-mediated inflammation from herpes zoster may destabilise underlying heart failure, but its clinical and healthcare resource impact among adults with HF remains poorly understood.
Does incident herpes zoster increase the need for diuretic modification and healthcare resource utilisation in adults aged ≥50 years with heart failure?
Cohort (n=7,131)
Yes
Does incident herpes zoster increase the need for diuretic modification and healthcare resource utilisation in adults aged ≥50 years with heart failure?
In older Japanese adults with heart failure, incident herpes zoster is associated with significantly earlier diuretic escalation and higher long-term healthcare resource utilization, highlighting a potential destabilizing impact of herpes zoster on heart failure management.
Background Herpes zoster (HZ) and its complications are associated with severe pain and reduced quality of life. In individuals with cardiovascular diseases, such as heart failure (HF), the immune-mediated inflammation caused by HZ may contribute to the destabilisation of their underlying condition.1 However, the clinical and healthcare impact of HZ among adults with HF remains poorly understood. Purpose To assess the impact of incident HZ on HF management and associated healthcare resource utilisation (HCRU) among adults aged ≥50 years with HF in Japan. Methods This is a retrospective cohort study based on the Medical Data Vision nationwide claims database of more than 600 acute-care hospitals in Japan (April 2008–December 2023). Patients with HZ were propensity score-matched 1:2 to patients without HZ based on key baseline characteristics, with exact matching on index year. The primary outcome was the time to first change in diuretics (defined as initiation of a diuretic class not used at baseline or dose increase during follow-up), up to 1 year after the HZ episode. The primary outcome was assessed using cumulative incidence probabilities (CIPs) and restricted mean survival time (RMST) differences (HZ−non-HZ), with 95% confidence intervals (CIs). Secondary outcomes evaluated the long-term impact of HZ and included the time to first change in diuretics at 3 and 5 years, as well as annualised all-cause HCRU (hospitalisations, length of stay, and outpatient visits) during follow-up, reported as median (quartile 1, quartile 3 [Q1, Q3]) with differences between cohorts measured with Wilcoxon rank sum test . Results The analyses included 2,378 HZ and 4,753 non-HZ patients with HF (median age [Q1, Q3]: 80.0 [72.0, 86.0] years for both cohorts; female: 60.9% [HZ] vs 59.4% [non-HZ]). Diuretic modification occurred earlier in the HZ cohort versus the non-HZ cohort at all timepoints (Figure 1). For the time to first change in diuretics at 1 year, CIP (95% CI) was 13.3% (11.9, 14.9) vs 9.8% (8.9, 10.8) with RMST difference (95% CI) of −9.6 days (−13.9, −5.2). For the time to first change in diuretics at 3 and 5 years, CIPs (95% CI) were 24.3% (22.3, 26.5) vs 19.3% (18.0, 20.8) and 31.8% (29.2, 34.6) vs 27.7% (25.8, 29.7) with RMST differences (95% CI) of −43.4 days (−61.6, −25.2) and −75.7 days (−111.3, −40.1), respectively. Annualised HCRU analyses showed higher all-cause hospitalisations (median [Q1, Q3]: 0.2 [0.0, 0.8] vs 0.0 [0.0, 0.4]; p<0.001) and outpatient visits (median [Q1, Q3]: 10.9 [6.1, 17.5] vs 7.3 [3.9, 13.0]; p<0.001), and substantially longer length of stay among those hospitalised (median [Q1, Q3]: 51.2 [4.7, 256.3] vs 16.7 [2.8, 153.6] days; p<0.001) in the HZ cohort compared with the non-HZ cohort. Conclusion Among patients with HF, HZ was associated with earlier diuretic modification and increased HCRU, suggesting a short- and long-term impact of HZ on HF management and overall healthcare burden.
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Yoshifuji et al. (2026) conducted a cohort in Heart failure (n=7,131). Incident herpes zoster vs. Patients with heart failure without herpes zoster was evaluated on Time to first change in diuretics (initiation of a new diuretic class or dose increase) up to 1 year (RMST difference -9.6 days, 95% CI -13.9 to -5.2). Incident herpes zoster in heart failure patients was associated with earlier diuretic change at 1 year vs non-HZ (13.3% vs 9.8%; RMST difference -9.6 days, 95% CI -13.9 to -5.2).
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