The algorithmic performance of J-Tpeak for drug safety clinical trial.

Introduction: The interval from J-point to T-wave peak (JTp) in ECG is a new biomarker able to identify drugs that prolong the QT interval but have different ion channel effects. If JTp is not prolonged, the prolonged QT may be associated with multi ion channel block that may have low torsade de poi...

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Publicado en:Journal of Electrocardiology Vol. 50; no. 6; pp. 762 - 769
Autores principales: Chien, Simon C., Gregg, Richard E.
Formato: research Journal Article
Publicado: W B Saunders Nov2017
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Nov2017
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      pub: W B Saunders
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        126251984
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        126251984
        10.1016/j.jelectrocard.2017.08.018
        NLM28942951
        126251984
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        atl: The algorithmic performance of J-Tpeak for drug safety clinical trial.
      aug:
        au:
          Chien, Simon C.
          Gregg, Richard E.
        affil: Advanced Algorithm Research Center, Philips Healthcare, Andover, MA, USA
      sug:
        subj:
          Algorithms
          Sodium Channel Blockers Pharmacodynamics
          Heart Conduction System Drug Effects
          Membrane Proteins Drug Effects
          Potassium Channel Blockers Pharmacodynamics
          Electrocardiography Methods
          Phenethylamines Pharmacodynamics
          Sulfonamides Pharmacodynamics
          Verapamil Pharmacodynamics
          Quinidine Pharmacodynamics
          Female
          Male
          Human
          Female
          Male
      ab: Introduction: The interval from J-point to T-wave peak (JTp) in ECG is a new biomarker able to identify drugs that prolong the QT interval but have different ion channel effects. If JTp is not prolonged, the prolonged QT may be associated with multi ion channel block that may have low torsade de pointes risk. From the automatic ECG measurement perspective, accurate and repeatable measurement of JTp involves different challenges than QT. We evaluated algorithm performance and JTp challenges using the Philips DXL diagnostic 12/16/18-lead algorithm. Measurement of JTp represents a different use model. Standard use of corrected QT interval is clinical risk assessment on patients with cardiac disease or suspicion of heart disease. Drug safety trials involve a very different population - young healthy subjects - who commonly have J-waves, notches and slurs. Drug effects include difficult and unusual morphology such as flat T-waves, gentle notches, and multiple T-wave peaks.Methods: The JTp initiative study provided ECGs collected from 22 young subjects (11 males and females) in randomized testing of dofetilide, quinidine, ranolazine, verapamil and placebo. We compare the JTp intervals between DXL algorithm and the FDA published measurements. The lead wise, vector-magnitude (VM), root-mean-square (RMS) and principal-component-analysis (PCA) representative beats were used to measure JTp and QT intervals. We also implemented four different methods for T peak detection for comparison.Results: We found that JTp measurements were closer to the reference for combined leads RMS and PCA than individual leads. Differences in J-point location led to part of the JTp measurement difference because of the high prevalence of J-waves, notches and slurs. Larger differences were noted for drug effect causing multiple distinct T-wave peaks (Tp). The automated algorithm chooses the later peak while the reference was the earlier peak. Choosing among different algorithmic strategies in T peak measurement results in the tradeoff between stability and the accurate detection of calcium or sodium channel block.Conclusion: Measurement of JTp has different challenges than QT measurement. JTp measurement accuracy improved with combined leads RMS and PCA over lead II or V5.
      pubtype: Academic Journal
      doctype:
        research
        Journal Article
      ougenre: Article
    language: English
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