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ADHERE Tree Model for Acute HF Mortality Calculator

  • Admission BUN (mg/dL)
  • Admission Systolic Blood Pressure (mmHg)
  • Admission Serum Creatinine (mg/dL)
  • ADHERE Classification and Regression Tree (CART) — explanation and clinical context
    The ADHERE CART is a simple bedside decision tree developed from the Acute Decompensated Heart Failure National Registry to estimate the risk of in-hospital mortality for patients hospitalized with acute decompensated heart failure. The CART analysis identified three sequential admission variables that provided the best discrimination: admission blood urea nitrogen (BUN), admission systolic blood pressure (SBP), and serum creatinine. Specifically, the published branch points are BUN ≥ 43 mg/dL, SBP < 115 mmHg, and serum creatinine ≥ 2.75 mg/dL; using these splits the original derivation produced five terminal risk groups with predicted in-hospital mortality that ranged from approximately 2.1% (low risk) to 21.9% (high risk). These thresholds permit rapid stratification at the bedside without calculator apps or complex scoring.

    Clinical interpretation: the ADHERE tree is intended as a pragmatic risk-stratification aid at hospital presentation. A patient with low BUN (<43 mg/dL) and SBP ≥115 mmHg is classified as low risk (predicted in-hospital mortality ≈ 2.1% in the original cohort), whereas the combination of high BUN (≥43), low SBP (<115) and markedly elevated creatinine (≥2.75) identifies the small high-risk subgroup with substantially higher observed mortality (≈21.9% in the derivation cohort). Intermediate groups (for example BUN ≥43 but SBP ≥115, or BUN <43 but SBP <115) have intermediate predicted mortality (originally reported ~5.6% and ~4.9% respectively, and one intermediate node ~13.2%). These node probabilities were reported in ADHERE and reproduced in multiple external validations and comparisons.

    Limitations & recommended use: the ADHERE tree was derived from a large US registry and provides quick prognostic insight, but calibration and absolute probabilities vary by population and time: several validation studies found differences between predicted and observed mortalities and advise local validation before using the exact percentages to make treatment-limiting decisions. Use clinical judgment—treat the ADHERE group as an adjunct (triage / escalation signal), not a replacement for bedside assessment or local prognostic models. For contemporary deployments, consider local recalibration (or use local registry estimates) if you require absolute probability precision.

    References:
    Fonarow GC, et al. Risk stratification for in-hospital mortality in acutely decompensated heart failure: classification and regression tree analysis. JAMA. 2005;293:572-580.
    Thakkar R, et al. Evaluation and external comparisons of the ADHERE CART in clinical trials and registries (discussion/validation literature). Crit Care / PubMed Central 2007.
    Marques I, et al. Predicted ADHERE risk versus observed mortality — external cohort comparisons and discussion on calibration. (PRECIC comparison / SSRN).

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