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The management of heart failure cardiogenic shock: an international RAND appropriateness panel

  • Stefan Williams,
  • Antonis Kalakoutas,
  • Segun Olusanya,
  • Benedict Schrage,
  • Guido Tavazzi,
  • Anthony P. Carnicelli,
  • Santiago Montero,
  • Christophe Vandenbriele,
  • Adriana Luk,
  • Hoong Sern Lim,
  • Sai Bhagra,
  • Sascha C. Ott,
  • Marta Farrero,
  • Marc D. Samsky,
  • Jamie L. W. Kennedy,
  • Sounok Sen,
  • Richa Agrawal,
  • Penelope Rampersad,
  • Amanda Coniglio,
  • Federico Pappalardo,
  • Christopher Barnett,
  • Alastair G. Proudfoot

摘要

Background

Observational data suggest that the subset of patients with heart failure related CS (HF-CS) now predominate critical care admissions for CS. There are no dedicated HF-CS randomised control trials completed to date which reliably inform clinical practice or clinical guidelines. We sought to identify aspects of HF-CS care where both consensus and uncertainty may exist to guide clinical practice and future clinical trial design, with a specific focus on HF-CS due to acute decompensated chronic HF.

Methods

A 16-person multi-disciplinary panel comprising of international experts was assembled. A modified RAND/University of California, Los Angeles, appropriateness methodology was used. A survey comprising of 34 statements was completed. Participants anonymously rated the appropriateness of each statement on a scale of 1 to 9 (1–3 as inappropriate, 4–6 as uncertain and as 7–9 appropriate).

Results

Of the 34 statements, 20 were rated as appropriate and 14 were rated as inappropriate. Uncertainty existed across all three domains: the initial assessment and management of HF-CS; escalation to temporary Mechanical Circulatory Support (tMCS); and weaning from tMCS in HF-CS. Significant disagreement between experts (deemed present when the disagreement index exceeded 1) was only identified when deliberating the utility of thoracic ultrasound in the immediate management of HF-CS.

Conclusion

This study has highlighted several areas of practice where large-scale prospective registries and clinical trials in the HF-CS population are urgently needed to reliably inform clinical practice and the synthesis of future societal HF-CS guidelines.