Ultrasound assessment of bowel motility & vascularity as predictors of necrotising enterocolitis Caron Parsons What is NEC? Necrosis of wall of any part of the GI tract Most common acquired disorder of premature infant 7 – 10% infants < 1500g No change in mortality in last 30 years Serious long term sequelae Pathophysiology Gut immaturity Feeding NEC Hypoxic Ischaemic Injury Abnormal Bacterial Colonization Data from NDAU Mortality Data From NDAU Clinical Presentation NEC Vomiting Abdominal distension PR bleeding Temp instability Bilious aspirates Lethargy SEPSIS Jaundice Seizures How Do We Diagnose NEC? How do we diagnose NEC? X-ray Bowel wall thickening/loop separation Pneumatosis – gas in bowel wall Portal venous gas Free gas Non-specific Necessary to repeat X-rays ?NEC Definitive NEC Are there other diagnostic methods? Ultrasound of NEC • • • • • Bowel wall thickening Focal fluid collections Pneumatosis/ Portal venous gas Changes in Doppler signal Bowel motility What have other groups done? Motility • Definite diagnosis of NEC • Aperistalsis • Counted number of contractions • 30 secs – 1 min • No data presented on reliability of data acquisition • Reliability of analysis performed in one study • No longitudinal studies & no evaluation of infants prior to the development of NEC Muchantef, K., et al., Sonographic and radiographic imaging features of the neonate with necrotizing enterocolitis: correlating findings with outcomes. Pediatr Radiol, 2013 What have other groups done? Vascularity • Square regions of interest • Counted number of dots of colour Doppler signal/cm2 • No data on reliability of data acquisition or analysis. Faingold, R., et al., Necrotizing enterocolitis: assessment of bowel viability with color doppler US. Radiology, 2005. 235(2): p. 587-94. Faingold R et al. Radiology 2005;235:587-594 ©2005 by Radiological Society of North America Faingold R et al. Radiology 2005;235:587-594 ©2005 by Radiological Society of North America Feasibility Study – Aims • To study appearances of bowel in healthy infants on NICU/SCBU • To evaluate bowel motility on ultrasound • To evaluate reliability of acquiring and analysing 3D power Doppler datasets • Overall to explore possible methods of quantification Feasibility Study – Longer Term Aims • Establish normal parameters of motility and vascularity • Enable sample size calculation for longitudinal study Feasibility Study – Methodology • • • • Recruit 30 healthy infants (GA <40/40) Perform single ultrasound Motility – 2D cine loops Vascularity – 3D volumes with Doppler Inclusion Criteria • All infants admitted to NICU or SCBU at UHCW with gestation of 40+0 weeks or less. Exclusion Criteria • Gestation more than 40+0 weeks • Current diagnosis/ treatment of NEC • Too unstable to tolerate ultrasound as dictated by the clinical team • Undergoing high-frequency oscillation ventilation • Known diagnosis of congenital bowel disorder • Previous bowel surgery/abdominal wall defect Recruitment 15 Approached 13 Yes 4 Discharged 2 No 9 Scanned Break There was a change to the protocol during recruitment Therefore Evaluate the protocol and set-up of the study Start evaluating the image analysis methodology Motility – Original Methodology • Acquire cine-loops in a four quadrant approach • Two observers • Analyse as per previous groups • Presence/absence of contractions • Number of contractions/minute • Computerised vectorial analysis - ShIRT Motility Methodology This part of the study did not change 2D cine loops (10 secs) Evaluation Basic ShIRT – by colleagues in Sheffield 2D Cine-Loop Initial ShIRT Evaluation Vascularity – Original Methodology • • • • • • Acquire 3D power Doppler volumes 2 observers 2 sets of data per observer Off-line analysis in VOCAL software Select ROI Software calculates vascularity indices Vascularity – Changes To Methodology Suggestion of 2D acquisition over time rather than 3D volume This was then trialed on the latter 6 of the recruited patients Availability of proprietary software for 2D Doppler data However….. Issues with proprietary software Cost Understanding of physics/ mathematics behind calculations Difficulty with obtaining trial versions 2D Doppler Cine-Loop Baby with NEC Initial Evaluation with Q-Flow Vascularity – Where next? We designed our own. Using MatLab software and a very clever physicist Data Analysis The idea is to use random ROI placement within the Power Doppler data clips to sample the bowel and calculate a global measure of vascularity for each subject Two measures %Colour – proportion of colour pixels to grey-scale pixels in ROI Luminance – intensity of each colour pixel Summated for ROI MatLab Software Luminance: Total v Sampled Why sample? In the future we will be acquiring repeated samples on a daily basis Bowel is mobile The width of the Doppler box cannot be standardised What Next? Motility – Waiting for results from Sheffield Vascularity Statistician looking at random circle ROI data Intraclass correlations for reliability of Data acquisition Data analysis Design software for 3D Doppler volumes Next stage of feasibility study Pre and post feeding in healthy premature infants Summary • NEC is difficult to diagnose in the early stages • The role of ultrasound is increasing in NEC • Motility and vascularity have postulated roles in the pathophysiology of NEC • There is potential to characterize motility and measure vascularity with novel software Study Group • • • • • • • Dr. E. Helm, Consultant Radiologist, UHCW Prof. C. Hutchinson, Prof of Imaging, University of Warwick Dr. V. Sherwood, Clinical Scientist, UHCW Dr. P. Satodia, Consultant Neonatologist, UHCW Dr. R. DeBoer, Consultant Neonatologist, UHCW Dr. H.Parsons, Research Fellow in Statistics, University of Warwick Dr. J. Fenner, Medical Physics Group, University of Sheffield