The goal of this clinical trial is to learn if artificial intelligence within digital wound monitoring of surgical wounds can prioritise non-healing wounds for urgent review in patients having first/redo CABG surgeries with or without additional cardiac procedures; could include any of the following: any gender, age ≥18. The main question it aims to answer is: Can investigators successfully develop artificial intelligence to prioritise images of patients' surgical wounds that are failing to heal or are infected, in order to facilitate early treatment? Researchers will compare the wound prioritisation module with standard care to determine safety and acceptability outcomes. Participants from the control group will: * Have standard post-operative wound care follow-up at day 30 (survey, interview and phone call) * Have standard post-operative wound care follow-up at day 60 (phone call) Participants from the intervention group will: * Use platform with new AI prioritisation module for 30 days after surgery * Be contacted via SMS text message seven days, fourteen days and twenty-one days after surgery with the link request remaining open for 6 days until the next request is sent out * Submit a photo of their wound and complete the UKHSA wound surveillance questionnaire * Have standard post-operative wound care follow-up at day 30 (survey, interview and phone call) * Have standard post-operative wound care follow-up at day 60 (phone call)
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Quality of images assessed by clinicians, in frequencies
Timeframe: 30 days
Quality of images assessed by clinicians, in percentages
Timeframe: 30 days
Clinician satisfaction using surveys
Timeframe: 30 days
Clinician satisfaction using interviews
Timeframe: 30 days
Patient satisfaction using surveys
Timeframe: 30 days
Patient satisfaction using interviews
Timeframe: 30 days
Recruitment rate (number and percentage of eligible patients recruited to the study). Patients who were consented but not randomised will not be included in the recruitment rate.
Timeframe: 30 days
Adherence with the module (intervention group only). Adherence will be reported as the number and percentage of adherent patients in the intervention group.
Timeframe: 30 days
Loss to follow-up (number and percentage of intervention patients complete the study)
Timeframe: 30 days
Number of wound problems/infections (in number and percentage)
Timeframe: 30 days
Severity of wound problems/infections
Timeframe: 30 days
Wound-related hospital admissions (in number and percentage)
Timeframe: 30 days
Prescribed antibiotics (in number and percentage)
Timeframe: 30 days
Time to review images in minutes (intervention only)
Timeframe: 30 days
Further surgery to treat wounds in number and percentage
Timeframe: 30 days
Prescribed wound treatments
Timeframe: 30 days
Number of clinic visits in number and percentage
Timeframe: 30 days
Number of General Practice visits in frequency and percentage
Timeframe: 30 days
Patient travel time in minutes
Timeframe: 30 days
Quality of life survey using SF-6D v2
Timeframe: At baseline, 30 days, and 60 days