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Vasoactive Inotropic Score in Adult Cardiac Surgery Outcomes

Serial Vasoactive Inotropic Score as a Predictor of Postoperative Outcomes in Adult Patients Undergoing Cardiac Surgery With Cardiopulmonary Bypass: A Prospective Observational Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07745283
Enrollment
617
Registered
2026-08-04
Start date
2018-10-01
Completion date
2022-06-30
Last updated
2026-08-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Surgical Procedures, Cardiac Surgical Procedures (Postoperative Population)

Keywords

Vasoactive Inotropic Score, Cardiac Surgery, Cardiopulmonary bypass, postoperative outcomes, risk stratification

Brief summary

This study looked at whether a bedside score called the Vasoactive Inotropic Score (VIS) could help doctors predict which adult patients are at higher risk of complications after heart surgery that uses a heart-lung machine (cardiopulmonary bypass). VIS is calculated from the doses of heart-support medications a patient is already receiving after surgery, so it does not require any extra tests or procedures. Researchers measured VIS at five points in the first two days after surgery in 232 adults undergoing a range of heart operations, including valve surgery and coronary artery bypass. The study found that VIS measured soon after surgery, and again at 24 hours, gave useful early warning of which patients were more likely to experience serious complications such as kidney injury, stroke, or the need for additional circulatory support. This information could help hospital teams identify at-risk patients earlier and monitor them more closely.

Detailed description

Serial Vasoactive Inotropic Score (VIS) was recorded prospectively at 5 postoperative timepoints (on shifting to the cardiac recovery unit, and at 6, 12, 24, and 48 hours) in 232 adults undergoing elective or semi-elective cardiac surgery with cardiopulmonary bypass at a single tertiary centre. The primary outcome was a composite of death, cardiac arrest, mechanical circulatory support, acute kidney injury (RIFLE criteria), or central nervous system injury. Secondary outcomes were ICU length of stay, hospital length of stay, and time to first extubation. Receiver operating characteristic (ROC) analysis, multivariate logistic regression, and Spearman rank correlation were used to evaluate the predictive performance of VIS at each timepoint, both independently and adjusted for EuroSCORE II, cardiopulmonary bypass time, aortic cross-clamp time, age, and pre-operative ejection fraction. A pre-specified sensitivity analysis incorporating low cardiac output syndrome into the primary composite outcome was also performed. This study is the first to evaluate serial (multi-timepoint) VIS measurement, rather than a single measurement, as a predictor of postoperative outcome in a heterogeneous adult cardiac surgical population.

Interventions

None listed

Sponsors

Sir Ganga Ram Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 18 years or older * Undergoing elective or semi-elective cardiac surgery with cardiopulmonary bypass (CPB)

Exclusion criteria

* Required CPB solely for extracorporeal membrane oxygenation (ECMO) * Pre-operative left ventricular assist device (LVAD) in situ * Pre-operative intra-aortic balloon pump (IABP) support * Declined to provide consent

Design outcomes

Primary

MeasureTime frameDescription
Composite poor outcomeFrom surgery until hospital discharge, or up to 30 days post-discharge for deathdeath, cardiac arrest, mechanical circulatory support, acute kidney injury, or central nervous system injury

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 5, 2026