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LOMR Portal Project Chris Marsh MD, FACS, Project Lead
Heather Neil, Research Project Leader UNOS Research Department Jamie Case, Research Scientist Scripps Ann M. Harper, MPH 15 March 2017
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LOMR Portal Project Purpose: advancement of usage of ECD/DCD levers in region 5 Who: region 5 liver programs What: TransQIP light for post op liver transplant outcomes Next steps ; Commitment of Centers-sign off on participation agreement IRB needed by center practice and future publications Build out of portal and testing: April Data entry: retrospective for 6 months: kick off May Go forward for 2 years ( and beyond?) Share best practices DMG data to improve donor selection
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Adult Recipients of Deceased Donor Liver Transplants, Potential Participants in Region 5 January 1, December 31, 2016 Txp Centers who indicated support ECD/DCD/SDC Total DCD ECD SCD N % AZMC: Mayo Clinic Hospital 40 33.1 26 21.5 55 45.5 121 CACS: Cedars-Sinai Medical Center 21 26.6 58 73.4 79 CAGH: Scripps Green Hospital 4 11.8 30 88.2 34 CAPM: California Pacific Medical Center 5 8.3 16 26.7 39 65.0 60 CASF: Univ of California San Francisco Medical Center 11.1 18.1 102 70.8 144 CASU-TX1: Stanford Health Care 3 5.0 11 18.3 46 76.7 CAUC: Univ of California at Los Angeles Medical Center 6 4.0 17 11.3 128 84.8 151 CAUH Keck Hospital of USC 17.7 82.3 96 67 9.8 127 18.5 491 71.7 685
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Adult Recipients of Deceased Donor Liver Transplants, Potential Participants in Region 5 January 1, December 31, 2016 Txp Centers who indicated support Macro Fat > 20% DRI > 1.8 N % AZMC: Mayo Clinic Hospital 23 19.0 59 48.8 CACS: Cedars-Sinai Medical Center 2 2.5 18 22.8 CAGH: Scripps Green Hospital 5.9 4 11.8 CAPM: California Pacific Medical Center 3 5.0 14 23.3 CASF: Univ of California San Francisco Medical Center 6 4.2 34 23.6 CASU-TX1: Stanford Health Care 5 8.3 10.0 CAUC: Univ of California at Los Angeles Medical Center 1.3 16 10.6 CAUH Keck Hospital of USC 3.1 16.7 Total 41 6.0 161 23.5
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Adult Recipients of Deceased Donor Liver Transplants, Select Programs in Region 5 (LOMR), January 1, December 31, 2016 Type Variable N Mean Median DCD Total Cold Ischemic Time (Hours) Length of Post-tx Hospitalization M/P Lab score DRI DDR (LI) Macro Fat (%) ECD Total Cold Ischemic Time (Hours) Length Of Post-tx Hospitalization M/P Lab score DRI DDR (LI) Macro Fat (%) SCD
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Adult Recipients of Deceased Donor Liver Transplants, Select Programs in Region 5 (LOMR), January 1, December 31, 2016 Macro Fat > 20% Variable N Mean Median No Total Cold Ischemic Time (Hours) Length Of Post-Tx Hospitalization M/P Lab score Yes DRI > 1.8 No Total Cold Ischemic Time (Hours) Length Of Post-Tx Hospitalization M/P Lab score Yes
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Adult Recipients of Deceased Donor Liver Transplants, Select Programs in Region 5 (LOMR), January 1, December 31, 2016 M/P Lab Score 35+ N Mean Median No Total Cold Ischemic Time (Hours) Length Of Post-Tx Hospitalization Yes
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Adult Recipients of Deceased Donor Liver Transplants, Select Programs in Region 5 (LOMR), January 1, December 31, 2016 Share Type DCD ECD SCD Total N % Local 23 6.9 78 23.4 233 69.8 334 47 11.4 60 14.6 304 74.0 411 70 9.4 138 18.5 537 72.1 745
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DRAFT Registry Variables – Populated from UNet℠
Transplant Hospital Code Recipient BMI at Transplant Date of Procedure Recipient Identification Number (UNOS PX ID) Recipient Diabetes Mellitus at Listing Cold Ischemia Time UNOS Donor ID Functional Health Status at TRR Multi-organ Transplant Donor Age Dialysis At Least Twice in the Prior Week Graft Type Allocation Type Recipient Blood Type Length of Initial Hospital Stay Donor Gender Serum Creatinine at Transplant Graft Loss at Discharge Donor Ethnicity Total Bilirubin at Transplant Death at Discharge Donor Height INR at Transplant Graft Loss at 90 Days Donor Weight Calculated MELD score at Transplant Death at 90 Days Donor Cause of Death Recipient Medical Condition at Transplant Death ( days) Donor Cause of Death, Other Specify Pathology Confirmed Diagnosis Reason(s) for Graft Loss % Macro Vesicular Fat Text of Pathology Confirmed Diagnosis Recipient Primary Cause of Death Was this donor recovered under DCD protocol Exception Case at Transplant Recipient Contributory Causes of Death Donor ABO Allocation MELD/PELD or Status at Transplant Recipient date of Birth Recipient Portal Vein Thrombosis at Transplant Recipient Primary Cause of Death - Other Specify Text Recipient Gender Recipient History of Malignancy at Listing Recipient Contributory Cause of Death 1 - Other Specify Text Recipient Ethnicity Recipient Ever Hepatocellular Carcinoma (HCC) Diagnosis? Recipient Contributory Cause of Death 2 - Other Specify Text Highest Education Level at Listing Recipient (TIPS) at Transplant Donor Length of Hospital Stay Employment Status at Transplant Recipient Prior Abdominal Surgery at Listing Warm Ischemia Time Recipient had a Prior Liver Transplant Procedure Recipient Prior Abdominal Surgery at Transplant Recipient Height (cm) at Transplant History of Spontaneous Bacterial Peritonitis (SBP) at Listing Recipient Weight (kg) at Transplant
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DRAFT Registry Variables – Entered by Centers
Recipient Hypertension Total number of Post-Procedural ICU days Current Smoker within One Year On Ventilator > 48 Hours Recipient Recent Infection Intraoperative or Postoperative Cardiac Arrest Requiring CPR Urinary Tract Portal Vein Thrombosis/Stenosis requiring Therapy Pneumonia Hepatic Artery Stenosis/Thrombosis requiring Therapy Bacteremia Biliary Stricture requiring Intervention Cholangitis Biliary Leak requiring Intervention SBP Hospital Readmission Within 30 Days Soft Tissue Return to the OR within 30 days Other Biliary Stricture requiring intervention within 90 Days Other Specify Text Initiation of postoperative dialysis within 90 days WBC at Transplant Reoperation within 90 Days AST at Transplant Re Intervention-performed IR, procedural room within 90 days ALT at Transplant Hospital Readmission within 90 Days Recipient intubated at time of transplant Biliary Stricture ( days) Biliary Stent Present at Transplant Graft Loss ( days) Biliary Anastomosis Hospital Readmission ( days) Portal Vein Reconstruction/Graft Type Reoperation ( days) Hepatic Artery Reconstruction/Bypass Return to the OR ( days) PRBC Units - Incision to 12 hours post-op Re Intervention-performed IR, procedural room ( days) PRBC Units - 12 to 72 hours post-op FFP Units - Incision to 12 hours post-op
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LOMR Registry Prototype – Registration Form
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LOMR Registry Prototype – 30 Day Post-Op Form
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LOMR Registry Prototype – 90 Day Follow-Up Form
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LOMR Registry Prototype – 1 Yr Follow-Up Form
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