Skip to main content
. Author manuscript; available in PMC: 2020 May 1.
Published in final edited form as: Heart Rhythm. 2018 Nov 24;16(5):743–753. doi: 10.1016/j.hrthm.2018.11.026

Figure 5.

Figure 5.

(A) Distribution of Biomarker CRT Score as a function of a composite MADITCRT Score.5 With higher MADIT-CRT Scores (>5), a subset of patients could still be identified with a high probability of a favorable response to CRT using the Biomarker CRT Score (bracket indicates p<0.05). Thus, despite classifying patients using a previously established CRT clinical scoring algorithm, a subset of patients could be identified over and above this clinical scoring algorithm. (B) Using an adaptive design and recursive partitioning (Supplemental Methods) demonstrated that the Biomarker CRT Score identified a subset of patients with a low likelihood of response to CRT, which would not have been realized by a clinical scoring algorithm alone.