Risk stratification for hospital-acquired venous thromboembolism in medical patients (RISE): Protocol for a prospective cohort study.

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Version: Final published version
License: CC BY 4.0
Serval ID
serval:BIB_AE9B01203B0B
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Risk stratification for hospital-acquired venous thromboembolism in medical patients (RISE): Protocol for a prospective cohort study.
Journal
PloS one
Author(s)
Choffat D., Farhoumand P.D., Jaccard E., de la Harpe R., Kraege V., Benmachiche M., Gerber C., Leuzinger S., Podmore C., Truong M.K., Dumans-Louis C., Marti C., Reny J.L., Aujesky D., Rakovic D., Limacher A., Rossel J.B., Baumgartner C., Méan M.
ISSN
1932-6203 (Electronic)
ISSN-L
1932-6203
Publication state
Published
Issued date
2022
Peer-reviewed
Oui
Editor
Roza Chaireti
Volume
17
Number
5
Pages
e0268833
Language
english
Notes
Publication types: Clinical Trial Protocol ; Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: epublish
Abstract
Hospital-acquired venous thromboembolism (VTE) is one of the leading preventable causes of in-hospital mortality. However, its risk assessment in medically ill inpatients is complicated due to the patients' heterogeneity and complexity of currently available risk assessment models (RAMs). The simplified Geneva score provides simplicity but has not yet been prospectively validated. Immobility is an important predictor for VTE in RAMs, but its definition is inconsistent and based on subjective assessment by nurses or physicians. In this study, we aim to prospectively validate the simplified Geneva score and to examine the predictive performance of a novel and objective definition of in-hospital immobilization using accelerometry.
RISE is a multicenter prospective cohort study. The goal is to recruit 1350 adult inpatients admitted for medical illness in three Swiss tertiary care hospitals. We collect data on demographics, comorbidities, VTE risk and thromboprophylaxis. Mobility from admission to discharge is objectively measured using a wrist-worn accelerometer. Participants are followed for 90 days for the occurrence of symptomatic VTE (primary outcome). Secondary outcomes are the occurrence of clinically relevant bleeding, and mortality. The evolution of autonomy in the activities of daily living, the length of stay, and the occurrence of readmission are also recorded. Time-dependent area under the curve, sensitivity, specificity, and positive and negative predictive values are calculated for each RAM (i.e. the simplified and original Geneva score, Padua, and IMPROVE score) with and without the objective mobility measures to assess their accuracy in predicting hospital-acquired VTE at 90 days.
The ethics committee approved the protocol and the study was registered on ClinicalTrials.gov as NCT04439383. RISE has the potential to optimize VTE risk stratification, and thus to improve the quality of care of medically hospitalized patients.
Keywords
Activities of Daily Living, Anticoagulants/therapeutic use, Hospitals, Humans, Multicenter Studies as Topic, Prospective Studies, Retrospective Studies, Risk Assessment, Risk Factors, Venous Thromboembolism/prevention & control
Pubmed
Web of science
Open Access
Yes
Create date
22/07/2022 10:36
Last modification date
17/05/2023 6:56
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