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| ID | Type | Description | Link |
|---|---|---|---|
| 14/EM/1136 | Other Identifier | East Midlands - Nottingham 1 Research Ethics Committee |
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| Name | Class |
|---|---|
| University Hospitals, Leicester | OTHER |
| Heart Link Children's Charity | OTHER |
| British Heart Foundation | OTHER |
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Acute kidney injury (AKI) complicates over 50% of cardiac surgical procedures in children where it increases morbidity and the use of healthcare resources. The pathogenesis of AKI is poorly understood, current diagnostic tests lack specificity and sensitivity, and there is no effective treatment. Improving outcomes in patients at risk of AKI has recently been defined as a National Health Service priority. The investigators are currently undertaking a program of work that is evaluating the role of plasma-derived microvesicles (MV) and MV associated microRNAs (miRNA) as diagnostic biomarkers or therapeutic targets in cardiac surgery patients at risk of developing AKI. Preliminary results indicate that these biomarkers may have clinical utility in adults. An important consideration is whether these biomarkers also have utility in children undergoing cardiac surgery. Measurement of MV at serial time points in children presents ethical challenges related to conducting clinical research in critically ill subjects. It also presents technical challenges related to the very small volumes of blood that may be sampled safely from babies and infants undergoing surgery. The aim of the study is to provide estimates of the perioperative variance of MV concentrations in 24 children undergoing cardiac surgery, as well as the frequency of AKI and other adverse events, protocol adherence and recruitment rates. This will assist with the design of a subsequent prospective observational study that will consider the role of MV/miRNA in children undergoing cardiac surgery.
This is a prospective, single-centre observational feasibility study that will measure changes in MV signalling and their relationship to inflammatory responses after cardiac surgery in children.
The investigators primary hypothesis is that inflammatory renal injury following paediatric cardiac surgery is regulated by circulating MV and more specifically MV associated miRNA.
The investigators secondary hypotheses are:
To assist with the design of a prospective observational study that will test these hypotheses the investigators propose to undertake a feasibility study in 24 children. The objectives of this feasibility study are:
A.To establish the numbers of patients that are eligible for enrolment in the study, the number recruited to the study, and their clinical and demographic characteristics.
B.To determine the proportion of consented patients who develop AKI following cardiac surgery.
C.To measure perioperative changes in MV subgroups and MV associated miRNA, as well as platelet and monocyte activation, and the variance of these measures.
D.To establish protocol adherence, with respect to the adequacy and timing of the blood samples that are taken and the calculation of creatinine clearance perioperatively.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Children undergoing cardiac surgery | Paediatric patients (<17 years with a body weight >2000g) undergoing cardiac surgery for congenital heart disease with extracorporeal circulation |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| cardiac surgery | Procedure | cardiac surgery with extracorporeal circulation for congenital heart disease |
|
| Measure | Description | Time Frame |
|---|---|---|
| change from baseline in annexin V positive microvesicles | Mean plasma concentration of Annexin V positive MV and the concentration variance in plasma from arterial blood samples collected prior to anaesthetic induction, and at 6-12 and 24 hours postoperatively. | Pre-operatively, 6-12 hrs post-op and 24 hrs post-op |
| change from baseline in microvesicles derived miRNA | Mean plasma concentration of MV derived miRNA and the concentration variance in plasma from arterial blood samples collected prior to anaesthetic induction, and at 6-12 and 24 hours postoperatively. | Pre-operatively, 6-12 hrs post-op and 24 hrs post-op |
| Measure | Description | Time Frame |
|---|---|---|
| Eligibility | Since this is a feasibility study, the investigators will evaluate the rate of patients who are eligible among the whole population of screened patients | pre-operatively |
| Recruitment |
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Inclusion Criteria:
Exclusion Criteria:
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Children undergoing cardiac surgery in a tertiary academic cardiac surgery unit
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| Name | Affiliation | Role |
|---|---|---|
| Gavin J Murphy, Prof | University of Leicester | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Glenfield Hospital | Leicester | Leicestershire | LE3 9QP | United Kingdom |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 29912813 | Derived | Sullo N, Mariani S, JnTala M, Kumar T, Wozniak MJ, Smallwood D, Pais P, Westrope C, Lotto A, Murphy GJ. An Observational Cohort Feasibility Study to Identify Microvesicle and Micro-RNA Biomarkers of Acute Kidney Injury Following Pediatric Cardiac Surgery. Pediatr Crit Care Med. 2018 Sep;19(9):816-830. doi: 10.1097/PCC.0000000000001604. |
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| ID | Term |
|---|---|
| D058186 | Acute Kidney Injury |
| ID | Term |
|---|---|
| D051437 | Renal Insufficiency |
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
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| ID | Term |
|---|---|
| D006348 | Cardiac Surgical Procedures |
| ID | Term |
|---|---|
| D013504 | Cardiovascular Surgical Procedures |
| D013514 | Surgical Procedures, Operative |
| D019616 | Thoracic Surgical Procedures |
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Since this is a feasibility study, the investigators will evaluate the rate of patients who will be recruited among the whole population of approached patients
| preoperatively |
| Protocol non-adherence | Since this is a feasibility study, the investigators will evaluate protocol non-adherence defined as the failure to obtain the specified blood volume or urine sample required for analysis at the required time. | Pre-operatively, 6-12 hrs post-op and 24 hrs post-op |
| Acute Kidney Injury | Acute kidney injury defined according to the Kidney Disease: Improving Global Outcomes (KDIGO) criteria | preoperatively, postoperatively every day until day 7 |
| Variation in Renal inflammation | Variation in Renal inflammation will be determined by variation in values of urine Neutrophil Gelatinase-Associated Lipocalin (NGAL) and Liver type- Fatty Acid Binding Protein (L-FABP) and urinary nitric oxide bioavailability . | Pre-operatively, 6-12 hrs post-op and 24 hrs post-op |
| Incidence of Acute Lung Injury - Low Cardiac Output | Acute Lung Injury (PaO2/FiO2<300mmHg) | preoperatively, postoperatively every day until day 7 |
| Incidence of Low Cardiac Output | Low Cardiac Output (the use of two or more inotropes) | preoperatively, postoperatively every day until day 7 |
| Variation in pro-coagulant potential of microvesicles | This is a measure of MV tissue factor expression and indicates the likely pro-inflammatory effect of the MV. | Pre-operatively, 6-12 hrs post-op and 24 hrs post-op |
| Variations in sources of microvesicles | Sources of MV: platelet, endothelial and monocyte activation will be determined by flow cytometry. | Pre-operatively, 6 - 12 hrs post-op and 24 hrs post-op |
| Variations in systemic inflammatory cytokine response | The systemic inflammatory cytokine response will be quantified by measurement of serum interleukin-8, interleukin-6, tumor necrosis factor -α, monocyte chemotactic protein -1, monocyte chemotactic protein -3, intercellular adhesion molecule, E-selectin. | Pre-operatively, 6 - 12 hrs post-op and 24 hrs post-op |
| D005261 |
| Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |