Key result
Dallas-positive histopathology is linked to ~58% lower risk of death or transplant in LV dysfunction.
Why the study?
Parameters of prognostic relevance in patients with chronic left ventricular dysfunction undergoing endomyocardial biopsy were not well defined.
Cohort (n=351)
Hazard Ratio: 0.42 (95% CI 0.29–0.84)
p-value: p=0.031
In patients with chronic left ventricular dysfunction, Dallas-positive histopathology, higher ejection fraction, and beta-blocker therapy are independent predictors of improved survival free from heart transplantation.
May refine risk stratification in chronic LV dysfunction; supports observational associations but leaves causal effects open for trials.
BACKGROUND: The objective of this study was to identify parameters of prognostic relevance in patients presenting with chronic left ventricular dysfunction who underwent endomyocardial biopsy. MATERIALS AND METHODS: A total of 351 consecutive patients (age 47·7 ± 12·6 years, 281 male) with a chronic left ventricular dysfunction were enrolled. Endomyocardial biopsies were analysed by histopathology according to Dallas criteria and immunohistological WHO criteria. Virus genome was detected by polymerase chain reaction. The combined end point was time to death or heart transplantation. RESULTS: About 19% of patients (n = 67) showed positive Dallas criteria and 39% (n = 118) immunohistochemical signs of inflammation. Viral genome was present in 58% (n = 155). During follow-up, 25% (n = 89; 76 death, 13 HTx) reached the end point. Dallas-positive histopathology (hazard ratio: 0·42; 95% CI: 0·29-0·84, P = 0·031), ejection fraction (hazard ratio: 0·97; 95% CI: 0·94-0·99, P = 0·019) and β-blocker therapy (hazard ratio: 0·41; 95% CI: 0·23-0·69, P = 0·003) were independent outcome predictors. For patients under β-blocker therapy, Dallas-positive histopathology (hazard ratio: 0·37; 95% CI: 0·25-0·76, P = 0·009) and NYHA class III and class IV (hazard ratio: 2·11; 95% CI: 1·04-3·12, P = 0·006) were independent predictors. CONCLUSIONS: For patients with a chronic left ventricular dysfunction, Dallas-positive histopathology, β-blocker therapy and left ventricular ejection fraction are the most striking parameters for outcome prediction.
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Kuethe et al. (2017) conducted a cohort in chronic left ventricular dysfunction (n=351). Dallas-positive histopathology was evaluated on time to death or heart transplantation (HR 0.42, 95% CI 0.29-0.84, p=0.031). Dallas-positive histopathology independently predicted a lower risk of death or heart transplantation in patients with chronic left ventricular dysfunction (HR 0.42; 95% CI 0.29-0.84; P=0.031).
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