The first International Consortium for Health Outcomes Measurement (ICHOM) standard dataset for reporting outcomes in heart valve disease: moving from device- to patient- centered outcomes
European Heart Journal - Quality of Care and Clinical Outcomes

Abstract
Globally significant variation in treatment and course of heart valve disease (HVD) exists, and outcome measurement is procedure focused instead of patient focused. This article describes the development of a patient-related (International Consortium for Health Outcomes Measurement) standard set of outcomes and case mix to be measured in patients with HVD.
A multisociety working group was formed that included patient representatives and representatives from scientific cardiology and cardiothoracic surgery societies that publish current guidelines for HVD. The standard set was developed to monitor the patient's journey from diagnosis to treatment with either a surgical or transcatheter procedure. Candidate clinical and patient-reported outcome measures (PROMs) and case mix were identified through benchmark analyses and systematic reviews. Using an online modified Delphi process, the working group voted on final outcomes/case mix and corresponding definition.
Patients with aortic/mitral/tricuspid valve disease or root/ascending aorta >40 mm were included in the standard set. Patients entered the dataset when the diagnosis of HVD was established, allowing outcome measurement in the preprocedural, periprocedural, and postprocedural phases of patients’ lives. The working group defined 5 outcome domains: vital status, patient-reported outcomes, progression of disease, cardiac function and durability, and complications of treatment. Subsequently, 16 outcome measures, including 2 patient-reported outcomes, were selected to be tracked in patients with HVD. Case-mix variables included demographic factors, demographic variables, echocardiographic variables, heart catheterization variables, and specific details on aortic/mitral/tricuspid valves and their specific interventions.
Through a unique collaborative effort between patients and cardiology and cardiothoracic surgery societies, a standard set of measures for HVD was developed. This dataset focuses on outcome measurement regardless of treatment, moving from procedure- to patient-centered outcomes. Implementation of this dataset will facilitate global standardization of outcome measurement, allow meaningful comparison between health care systems and evaluation of clinical practice guidelines, and eventually improve patient care for those experiencing HVD worldwide.
Contributors

Emmanuel Lansac
Author

Kevin M Veen
Author

Andria Joseph
Author

Paula Blancarte Jaber
Author

Frieda Sossi
Author

Zofia Das-Gupta
Author

Suleman Aktaa
Author

J Rafael Sádaba
Author

Vinod H Thourani
Author

Gry Dahle
Author

Wilson Y Szeto
Author

Faisal Bakaeen
Author

Elena Aikawa
Author

Frederick J Schoen
Author

Evaldas Girdauskas
Author

Aubrey Almeida
Author

Andreas Zuckermann
Author

Bart Meuris
Author

John Stott
Author

Jolanda Kluin
Author

Ruchika Meel
Author

Wil Woan
Author

Daniel Colgan
Author

Hani Jneid
Author

Husam Balkhy
Author

Molly Szerlip
Author

Ourania Preventza
Author

Pinak Shah
Author

Vera H Rigolin
Author

Silvana Medica
Author

Philip Holmes
Author

Marta Sitges
Author

Philippe Pibarot
Author

Erwan Donal
Author

Rebecca T Hahn
Author

