Health status trajectories using Markov modeling in patients with heart failure with preserved ejection fraction.

Rev Esp Cardiol (Engl Ed)Feb 4, 2026 (epub)
Clinical ResearchCardiology

Wonse Kim, Minjae Yoon, Jin Joo Park et al.

✦ AI-curated · Sources linked

In 30 seconds

This post hoc multistate Markov analysis of the PARAGON-HF randomized trial examined serial Kansas City Cardiomyopathy Questionnaire scores and clinical outcomes in 4707 patients with heart failure with preserved ejection fraction. Patients moved in both directions among four health-status categories, with death as a fifth state. Annual mortality rose as health status worsened, from 3.1% in the excellent state to 15.6% in the poor state. Overall time spent in health states did not differ between sacubitril/valsartan and valsartan, although the poor-health subgroup showed more favorable transitions with sacubitril/valsartan.

Key findings

  • Annual mortality increased across worsening health states: 3.1% (excellent), 4.3% (good), 9.4% (fair), and 15.6% (poor).
  • The excellent state had the longest sojourn time at 1.57 years (95%CI, 1.51-1.63); transitions between health states occurred in both directions.
  • Among patients in the poor state, sacubitril/valsartan was associated with greater likelihood of improvement to fair than valsartan (93.1% vs 86.9%) and lower risk of death (6.9% vs 13.1%).
  • Overall sojourn times did not differ between sacubitril/valsartan and valsartan.

Why it matters

The findings show that health status in HFpEF can change over time and that serial patient-reported assessments may help characterize prognosis beyond a single baseline score. The graded association between poorer KCCQ state and higher mortality underscores the clinical relevance of tracking symptoms and functional impact, while the treatment subgroup result warrants interpretation in the context of a post hoc analysis.

What to keep in mind

This was a post hoc analysis using a multistate model; the reported treatment-associated findings in the poor-health subgroup do not establish a causal treatment effect.

Source

Published in Rev Esp Cardiol (Engl Ed). This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

ShareTelegramLinkedIn

AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

More in Cardiology

Clinical ResearchOncology (Medical)

Zamtocabtagene autoleucel, a tandem CD20-CD19-directed CAR T-cell therapy, for second line treatment of large B-cell lymphoma in patients ineligible for transplantation (DALY 2-EU): primary analysis of an open-label, multicentre, randomised phase 2 study.

DALY 2-EU was an open-label, multicentre, randomised phase 2 trial comparing tandem CD20-CD19-directed zamtocabtagene autoleucel (zamto-cel) with R-GemOx in adults with second-line relapsed or refractory large B-cell…

Lancet OncolOct 27, 2026Read summary
Clinical ResearchOncology (Medical)

Neoadjuvant short-course radiotherapy followed by camrelizumab and chemotherapy versus standard of care for locally advanced rectal cancer (UNION): a prespecified interim analysis of a multicentre, open-label, randomised, phase 3 trial.

UNION was a multicentre, open-label, randomised phase 3 trial at nine hospitals in China comparing neoadjuvant short-course radiotherapy followed by camrelizumab plus CAPOX with long-course chemoradiotherapy followed by…

Lancet OncolOct 25, 2026Read summary
Clinical ResearchHematology

Efficacy and safety of mitapivat in patients with sickle cell disease (RISE UP): a phase 3, double-blind, global, randomised, placebo-controlled trial.

RISE UP was a phase 3, double-blind, global, randomised, placebo-controlled trial conducted at 69 sites in 15 countries. It evaluated twice-daily mitapivat in patients older than 16 years with sickle cell disease…

LancetOct 24, 2026Read summary

Want this personalized?

Stop searching the literature. Choose what you follow and xxcode will build your personalized medical digest.

  • Your specialties
  • Your filters and thresholds
  • Clinical Research + Case Reports, tuned separately
  • Automatic weekly delivery
  • Audio and text

Prefer listening? Personalized audio digests are available with Pro.

Stay updated for free

Get the 3 most interesting publications in one specialty each week.

Weekly email. Unsubscribe anytime.