Abstract
Background: Improved health-related quality of life (HRQOL) is an important outcome following durable left ventricular assist device (LVAD) implant. However, half of pre-implant HRQOL data are incomplete in The Society of Thoracic Surgeons’ Intermacs registry. Pre-implant HRQOL incompleteness may reflect patient status or hospital resources to capture HRQOL data. We hypothesized that pre-implant HRQOL incompleteness predicts 90 day outcomes and serves as a novel quality metric. Methods: Risk factors for pre-implant HRQOL (EQ-5D-5L visual analog scale; 12-item Kansas City Cardiomyopathy Questionnaire “KCCQ”) incompleteness were examined by stepwise logistic modeling. Direct standardization method was used to calculate adjusted incompleteness rates using a mixed effects logistic model. Hospitals were dichotomized as low or high based on median adjusted incompleteness rates. Andersen-Gill models were used to associate pre-implant HRQOL adjusted incompleteness rate with adverse events within 90 day post-implant. Results: The study cohort included 14,063 patients receiving a primary LVAD (4/2012-8/2017). HRQOL incompleteness at high-rate hospitals was more often due to administrative reasons (risk difference, EQ-5D: 10.1%; KCCQ-12: 11.6%) and less likely due to patient reasons (risk difference, EQ-5D: -8.9%; KCCQ-12: -11.4%). A 10% increase in the adjusted pre-implant EQ-5D incompleteness rate was significantly associated with higher risk of infection-related mortality (HR: 1.09), infection (HR: 1.05), and renal dysfunction (HR: 1.03). A 10% increase in the adjusted pre-implant KCCQ-12 incompleteness rate was significantly associated with higher risk of infection (HR: 1.04). Conclusions: Hospital adjusted pre-implant HRQOL incompleteness was predictive of 90-day post-implant outcomes and may serve as a novel quality metric.
Original language | English (US) |
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Pages (from-to) | 1520-1528 |
Number of pages | 9 |
Journal | Journal of Heart and Lung Transplantation |
Volume | 41 |
Issue number | 10 |
DOIs | |
State | Published - Oct 2022 |
Funding
This study was supported by a grant from the Agency for Healthcare Research and Quality (R01HS026003). The content is solely the responsibility of the authors and does not necessarily represent the official views of the Agency for Healthcare Research and Quality. Support for the Michigan Society of Thoracic and Cardiovascular Surgeons Quality Collaborative (MSTCVS-QC) is provided by Blue Cross and Blue Shield of Michigan and Blue Care Network as part of the BCBSM Value Partnerships program. The opinions, beliefs, and viewpoints expressed by the authors do not necessarily reflect the opinions, beliefs, and viewpoints of BCBSM, The Society of Thoracic Surgeons, National Heart, Lung, and Blood Institute, or any of its employees. Donald S. Likosky receives research funding from the Agency for Healthcare Research and Quality ( R01HS026003 ) and the National Institutes of Health ( R01HL146619 ) and serves as a consultant for the American Society of Extracorporeal Technology. Donald S. Likosky receives partial salary support from Blue Cross Blue Shield of Michigan to advance quality in Michigan in conjunction with the Michigan Society of Thoracic and Cardiovascular Surgeons Quality Collaborative. Francis D. Pagani is an ad hoc, non-compensated scientific advisor for Medtronic, Abbott, FineHeart, and CH Biomedical and a member of the Data Safety Monitoring Board for Carmat and the National Heart, Lung, and Blood Institute PumpKIN Study. Keith D. Aaronson has consulting relationships with Medtronic (honoraria) and Abbott (honoraria). James W. Stewart II is funded through the Veterans Affairs as a National Clinician Scholars Program (NCSP) research fellow at the University of Michigan. Donald S. Likosky receives research funding from the Agency for Healthcare Research and Quality (R01HS026003) and the National Institutes of Health (R01HL146619) and serves as a consultant for the American Society of Extracorporeal Technology. Donald S. Likosky receives partial salary support from Blue Cross Blue Shield of Michigan to advance quality in Michigan in conjunction with the Michigan Society of Thoracic and Cardiovascular Surgeons Quality Collaborative. Francis D. Pagani is an ad hoc, non-compensated scientific advisor for Medtronic, Abbott, FineHeart, and CH Biomedical and a member of the Data Safety Monitoring Board for Carmat and the National Heart, Lung, and Blood Institute PumpKIN Study. Keith D. Aaronson has consulting relationships with Medtronic (honoraria) and Abbott (honoraria). James W. Stewart II is funded through the Veterans Affairs as a National Clinician Scholars Program (NCSP) research fellow at the University of Michigan.
Keywords
- infection
- left ventricular assist device
- mortality
- outcomes
- quality metrics
- quality of life
- renal dysfunction
ASJC Scopus subject areas
- Cardiology and Cardiovascular Medicine
- Transplantation
- Pulmonary and Respiratory Medicine
- Surgery