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.
Обработка статьи · этапы, ошибки и управление
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Lansac Emmanuel, Veen Kevin M, Joseph Andria, Blancarte Jaber Paula, Sossi Frieda, Das-Gupta Zofia, Aktaa Suleman, Sádaba J Rafael, Thourani Vinod H, Dahle Gry, Szeto Wilson Y, Bakaeen Faisal, Aikawa Elena, Schoen Frederick J, Girdauskas Evaldas, Almeida Aubrey, Zuckermann Andreas, Meuris Bart, Stott John, Kluin Jolanda, Meel Ruchika, Woan Wil, Colgan Daniel, Jneid Hani, Balkhy Husam, Szerlip Molly, Preventza Ourania, Shah Pinak, Rigolin Vera H, Medica Silvana, Holmes Philip, Sitges Marta, Pibarot Philippe, Donal Erwan, Hahn Rebecca T, Takkenberg Johanna J M
Аннотация
METHODS: 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.
RESULTS: 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.
CONCLUSIONS: 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.