Ultrasound Prediction of Successful Balloon Assisted AVF Maturation

The study will be a prospective, longitudinal cohort study assessing maturation success following BAM procedures in immature AVFs. The primary outcome measure is successful AVF maturation at time of routine clinic appointment at 6 weeks post BAM procedure. Successful maturation is defined using a hybrid radiographic and clinical approach, namely a volume flow rate of ≥600ml/min, fistula vein diameter of ≥6mm combined with suitability for haemodialysis use as determined by clinician review. Failure to meet either criteria will be defined as failure to mature. The primary objectives of the study will be met by comparing preoperative, postoperative and 6 week DUS values with maturation outcome. By comparing values obtained at these timepoints the investigators aim to identify factors predictive of maturation failure post BAM procedure. Neutrophil, platelet and lymphocyte values will be obtained from routine blood tests preoperatively and 2 week (+/- 1 week), and used to calculate both the neutrophil-lymphocyte (NLR) and platelet-lymphocyte ratios (PLR). Both ratios provide an indication of inflammatory status and will be compared with successful maturation post BAM procedure. DUS scans will be performed pre- and post-BAM procedure in interventional radiology. Follow-up DUS scan will be performed when the participant is attending their 6 week routine clinical follow-up outpatient appointment. All scans will be performed by highly experienced clinical scientists using a single Philips Epiq 7 DUS scanner and L12-3 linear array transducer in accordance with a specified study scan protocol. A study preset will be used to standardise ultrasound settings. The DUS scan protocol will assess arterial inflow, arterio-venous anastomosis and venous outflow. Scan protocol and required measurements is the same for all DUS scans performed. Arterial Inflow Peak systolic velocity (PSV), end diastolic velocity (EDV) and time averaged mean velocity (TAMV) will be measured in the brachial artery at each scan timepoint. TAMV will be measured across three cardiac cycles and combined with internal luminal diameter to calculate volume flow rate (Qa). Three measurements will be taken 10cm cranial to the antecubital fossa with a mean calculated. Sample volume gate for PSV measurements will be standardised at 1mm. Sample volume gate will be expanded to encompass the full vessel lumen for TAMV. TAMV sample volume gate will be recorded and remain consistent for subsequent scans for the same participant. Resistive (RI) and pulsatility indices (PI) will be calculated from the PSV and EDV values. All DUS-derived measurements will be recorded as absolute values and percentage change across DUS scans. Access Anastomosis Anatomical location of the artery-vein anastomotic site will be recorded. PSV and EDV will be measured 5cm proximal to the anastomosis. Juxta-anastomotic PSV and EDV will also be measured. Stenoses present at the anastomosis will be graded using a ratio between PSV in the stenotic segment and the reference value 5cm proximally. Severity of stenoses will be recorded as a percentage. Minimal lumen diameter (MLD), defined as the narrowest luminal segment at the anastomosis will be recorded. Diameter of the arterial segment 2cm cranial to the anastomosis will be compared with the MLD to calculate the artery/fistula vein diameter ratio (A/V ratio). Venous Outflow Venous outflow diameter and TAMV will be measured 10cm cranial to the arterial anastomosis, with venous Qa measured in the same way as for the brachial artery. Stenotic venous segments will be graded in the same way as the arterial inflow. Treatment of lesions as part of the BAM procedure will be noted from operative notes, and the treated lesions subsequently assessed. Residual stenosis, the presence of intimal hyperplasia and vein diameter will be measured at treatment site. Neutrophil, lymphocyte and plasma values will be obtained from routine full blood count (FBC) results in the patient's electronic records. Neutrophil, lymphocyte and plasma values will be used to calculate neutrophil-to-lymphocyte (NLR) and plasma-to-lymphocyte ratios (PLR). Blood tests will be performed in accordance with standard of care. Patient age, sex, relevant medical history, current medication, and AVF configuration will be obtained from electronic patient records.