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A randomised comparison of the effect of haemodynamic monitoring with CardioMEMS in addition to standard care on quality of life and hospitalisations in patients with chronic heart failure : Design and rationale of the MONITOR HF multicentre randomised clinical trial.
Brugts, J J; Veenis, J F; Radhoe, S P; Linssen, G C M; van Gent, M; Borleffs, C J W; van Ramshorst, J; van Pol, P; Tukkie, R; Spee, R F; Emans, M E; Kok, W; van Halm, V; Handoko, L; Beeres, S L M A; Post, M C; Boersma, E; Lenzen, M J; Manintveld, O C; Koffijberg, H; van Baal, P; Versteegh, M; Smilde, T D; van Heerebeek, L; Rienstra, M; Mosterd, A; Delnoy, P P H; Asselbergs, F W; Brunner-La Rocca, H P; de Boer, R A.
Affiliation
  • Brugts JJ; Erasmus MC, University Medical Centre, Thorax Centre, Rotterdam, The Netherlands. j.brugts@erasmusmc.nl.
  • Veenis JF; Erasmus MC, University Medical Centre, Thorax Centre, Rotterdam, The Netherlands.
  • Radhoe SP; Erasmus MC, University Medical Centre, Thorax Centre, Rotterdam, The Netherlands.
  • Linssen GCM; Hospital Group Twente, Almelo and Hengelo, The Netherlands.
  • van Gent M; Albert Schweitzer Hospital, Dordrecht, The Netherlands.
  • Borleffs CJW; HAGA, The Hague, The Netherlands.
  • van Ramshorst J; Noordwest Ziekenhuisgroep, Alkmaar, The Netherlands.
  • van Pol P; Alrijne Ziekenhuis, Leiderdorp, The Netherlands.
  • Tukkie R; Spaarne Gasthuis, Haarlem, The Netherlands.
  • Spee RF; Maxima Medisch Centrum, Veldhoven, The Netherlands.
  • Emans ME; Ikazia, Rotterdam, The Netherlands.
  • Kok W; Amsterdam UMC, locatie AMC, Amsterdam, The Netherlands.
  • van Halm V; Amsterdam UMC, locatie VUMC, Amsterdam, The Netherlands.
  • Handoko L; Amsterdam UMC, locatie VUMC, Amsterdam, The Netherlands.
  • Beeres SLMA; Leiden Universitair Medisch Centrum, Leiden, The Netherlands.
  • Post MC; St. Antonius Ziekenhuis, Nieuwegein, The Netherlands.
  • Boersma E; Erasmus MC, University Medical Centre, Thorax Centre, Rotterdam, The Netherlands.
  • Lenzen MJ; Erasmus MC, University Medical Centre, Thorax Centre, Rotterdam, The Netherlands.
  • Manintveld OC; Erasmus MC, University Medical Centre, Thorax Centre, Rotterdam, The Netherlands.
  • Koffijberg H; Health Technology and Services Research Department, University of Twente, Enschede, The Netherlands.
  • van Baal P; Erasmus School of Health Policy and Management, Erasmus University, Rotterdam, The Netherlands.
  • Versteegh M; Institute for Medical Technology Assessment, Erasmus University, Rotterdam, The Netherlands.
  • Smilde TD; TREANT zorggroep, Emmen, The Netherlands.
  • van Heerebeek L; Onze Lieve Vrouwe Gasthuis, Amsterdam, The Netherlands.
  • Rienstra M; Universitair Medisch Centrum Groningen (UMCG), Groningen, The Netherlands.
  • Mosterd A; Meander Medisch Centrum, Amersfoort, The Netherlands.
  • Delnoy PPH; ISALA Klinieken, Zwolle, The Netherlands.
  • Asselbergs FW; Division Heart and Lungs, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.
  • Brunner-La Rocca HP; Institute of Cardiovascular Science, Faculty of Population Health Sciences, and Health Data Research and Institute of Health Informatics, University College London, London, UK.
  • de Boer RA; Maastricht University Medical Centre MUMC, Maastricht, The Netherlands.
Neth Heart J ; 28(1): 16-26, 2020 Jan.
Article in En | MEDLINE | ID: mdl-31776915
ABSTRACT

BACKGROUND:

Assessing haemodynamic congestion based on filling pressures instead of clinical congestion can be a way to further improve quality of life (QoL) and clinical outcome by intervening before symptoms or weight gain occur in heart failure (HF) patients. The clinical efficacy of remote monitoring of pulmonary artery (PA) pressures (CardioMEMS; Abbott Inc., Atlanta, GA, USA) has been demonstrated in the USA. Currently, the PA sensor is not reimbursed in the European Union as its benefit when applied in addition to standard HF care is unknown in Western European countries, including the Netherlands.

AIMS:

To demonstrate the efficacy and cost-effectiveness of haemodynamic PA monitoring in addition to contemporary standard HF care in a high-quality Western European health care system.

METHODS:

The current study is a prospective, multi-centre, randomised clinical trial in 340 patients with chronic HF (New York Heart Association functional class III) randomised to HF care including remote monitoring with the CardioMEMS PA sensor or standard HF care alone. Eligible patients have at least one hospitalisation for HF in 12 months before enrolment and will be randomised in a 11 ratio. Minimum follow-up will be 1 year. The primary endpoint is the change in QoL as measured by the Kansas City Cardiomyopathy Questionnaire (KCCQ). Secondary endpoints are the number of HF hospital admissions and changes in health status assessed by EQ-5D-5L questionnaire including health care utilisation and formal cost-effectiveness analysis.

CONCLUSION:

The MONITOR HF trial will evaluate the efficacy and cost-effectiveness of haemodynamic monitoring by CardioMEMS in addition to standard HF care in patients with chronic HF. Clinical Trial Registration number NTR7672.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Aspects: Patient_preference Language: En Journal: Neth Heart J Year: 2020 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Aspects: Patient_preference Language: En Journal: Neth Heart J Year: 2020 Document type: Article Affiliation country:
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