Patients undergoing elective surgery Surgery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Male or female patients aged 18-65 years 2. Patient able to give informed consent 3. Patient undergoing elective open abdominal wall reconstruction surgery
Exclusion criteria
Exclusion criteria: 1. Under the age of 18 years and over the age of 65 years 2. A known malignancy 3. Pregnancy 4. The operation is contaminated (e.g. there is a bowel resection +/- anastomosis, iatrogenic bowel injury or presence of a stoma) 5. Minimally invasive (laparoscopic or robotic) surgery 6. Significant anaesthetic complication (such as anaphylaxis, malignant hyperthermia, negative pressure pulmonary oedema)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The metabolic activity of neutrophils and monocytes isolated from blood samples obtained from elective surgery patients will be measured by flow cytometry, enzyme-linked immunosorbent assays and metabolic tracing before and after their operation | — |
Secondary
| Measure | Time frame |
|---|---|
| The following secondary outcome measures will be assessed in blood samples obtained from elective surgery patients before and after their operations: 1. Anti-microbial activities and surface phenotype of isolated neutrophils, monocytes and/or peripheral blood mononuclear cells (in the absence and/or presence of ex vivo stimulation) will be measured using flow cytometry 2. Circulating markers of inflammation (e.g. pro-inflammatory cytokines, acute phase proteins, cell-free DNA, Damage-associated molecular patterns, whole blood cell counts) will be measured using enzyme-linked immunosorbent assays, whole blood cell haematological analysers and fluorometric-based assays 3. DNA and RNA epigenetic profiles of neutrophils and peripheral blood mononuclear cells RNA sequencing, DNA methylation assays and real-time polymerase chain reaction (RT-PCR) experiments | — |
Countries
England, United Kingdom