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CORD’s Spring Conference June 8th, 2022
Don Watts, President & GM, Khure Health
Khure Health
Clinical Decision Support for Rare & Complex Conditions
Mission:
To help physicians save lives and end the suffering of rare
and complex disease patients through the use of advanced
AI for earlier diagnosis.
How:
• Putting the vast amounts of EMR data sitting idle to good
use
• Employing AI to help connect the clinical dots for complex
diseases
• Powerful clinical decision-support tool
* C.O.R.D – Canadian Organization for Rare Disease
Traditional investments in technology have done
little to help over-burdened physicians diagnose
complex patients
Major clinical leap:
AI-enabled Clinical Decision Support
1 in 12 Canadians
has a rare
disorder*
Every Physician Has a Rare Disease Patient—Whether They Know It or Not
Khure Health’s Clinical Intelligence Platform
Quickly Understand Complex, High-Risk Patients
…and get them on the right care pathway.
Stratify
risk and understand
complex patient details
Optimize
diagnosis and care
pathways
Identify
potential risk.
The Data is There … Sitting Idle
• EMR agnostic, cloud-based
• 100+ Rare Disease algorithms
• Educational Content
• Streamlined Workflows
• Instant In-Visit Screen: Screen a challenging patient against all
available pathologies
• Clinical Support available from Khure’s Clinical Specialists (MDs)
We help HCPs put it to Good Use
Artificial Intelligence – Advanced NLP
Natural Language Processing
• Instant EMR analysis of meds, labs, specialist
reports, clinical history/notes
• NLP is a form of Machine Learning (ML)
• Like speech recognition only using text
• Understand the context (minimize false
positives)
• Connect the dots over a lifetime of data
Algorithm Development
Integrating Multiple Sources and Expertise
Cryptic, structured, and unstructured data within EMR can be
extracted, feature-classified, and incorporated into logical
operators capable of identifying clinically meaningful cohorts
Pathology
specific
algorithms
Data structuring
and feature
extraction
Unstructured
EMR Data
Accelerated
linkage to care
Pathologies currently on the Khure Health platform
100 rare pathologies and counting
(with integration of chronic conditions now in development)
1. Aagenaes Syndrome
2. Acquired Hemophilia A
3. Adult Dermatomyositis
4. Adult ITP (Idiopathic Thrombocytopenic Purpura)
5. Adult Onset Still's Disease
6. Adult Polymyositis
7. Alpha Thalassemia
8. Ankylosing Spondylitis
9. Acquired Pure Red Cell Aplasia
10. Atypical Haemolytic Uremic Syndrome
11. Autosomal Dominant Polycystic Kidney Disease
12. Beta Thalassemia
13. Chronic Idiopathic Urticaria
14. Cushing's Syndrome
15. Diabetic Macular Edema
16. Essential Thrombocythemia
17. Fabry's Disease
18. Gaucher's Disease
19. Giant Cell Arteritis
20. hATTR Amyloidosis
21. Henoch Schoenlein Purpura
22. Hepatitis C Virus (HCV)
23. Hepatopulmonary Syndrome
24. Hereditary Angioedema (HAE)
25. Hereditary Elliptocytosis
26. Hereditary Spherocytosis
27. HHRH (Hereditary Hypophosphatemic Rickets with Hypercalciuria)
28. Hunter Syndrome
29. Hurlers Disease
30. Hypophosphatasia
31. Hypophosphatemia X-Linked
32. Juvenile Dermatomyositis
33. Juvenile ITP (Idiopathic Thrombocytopenic Purpura)
34. Juvenile Polymyositis
35. Kawasaki Disease
36. Loeyz-Dietz Syndrome
37. Multiple Myeloma
38. Multi-focal Motor Neuropathy
39. Myelofibrosis
40. Neuroblastoma
41. Neuromyelitis Optica Spectrum Disorder
42. Paroxysmal Nocturnal Hemoglobinuria
43. Pompe Disease
44. PPP (Palmoplantar Pustular Psoriasis)
45. Primary Biliary Cholangitis
46. Pulmonary Arterial Hypertension
47. Severe Allergic Asthma
48. Severe Eosinophilic Asthma
49. Sideroblastic Anemia
50. Thrombotic Thrombocytopenic Purpura
51. Typical Hemolytic Uremic Syndrome
52. Von Willebrand’s
53. AA Amyloidosis
54. Atrial Fibrillation
55. Bernard-Soulier Syndrome
56. Brugada Syndrome
57. Cold Agglutinin Disease
58. Ebstein anomaly
59. Eisenmenger syndrome
60. Fanconi Anemia
61. Glanzmann Thrombasthenia
62. Immune Thrombocytopenia Purpura (ITP)
63. Marfans Syndrome
64. Myelodysplastic Syndrome
65. Non-ischemic pediatric cardiomyopathy
66. Patent ductus arteriosus
67. Polycythemia Vera
68. Psoriatic Arthritis
69. Severe Plaque Psoriasis
70. Shprintzen-Goldberg syndrome
71. Sickle Cell Anemia
72. ALS
73. nmCRPC
74. Transthyretin Amyloid Cardiomyopathy
75. Recurrent Fever Syndromes
76. Castleman Disease
77. Neiman Pick
78. Primary Sclerosing Cholangitis
Pathologies on the Khure Health Platform
100 rare & specialty pathologies and counting
79. Rheumatoid Arthritis
80. Secondary hyperparathyroidism
81. Spinal Muscular Atrophy
82. Long-Chain Fatty Acid Oxidation Disorders
83. Anaplastic lymphoma kinase (ALK)-positive metastatic Non-small cell lung cancer
84. Best Vitelliform Macular Dystrophy
85. Budd-Chiari Syndrome
86. Cerebral Adrenoleukodystrophy
87. Cone Dystrophy
88. Cystic Fibrosis
89. Emphysema - severe hereditary deficiency of alpha1-PI alpha1-antitrypsin deficiency)
90. Endometriosis
91. Guillain-Barre Syndrome
92. Hemiplegic Migraines
93. Hepatopulmonary Syndrome
94. Juvenile idiopathic arthritis
95. Metastatic Colorectal Cancer
96. Morquio syndrome
97. Multiple Sclerosis (Remitting-Relapsing)
98. Myasthenia gravis
99. Narcolepsy
100. B-cell precursor acute lymphoblastic leukemia (relapsed or refractory)
By Specialty Total:100
1
1
1
2
2
3
3
4
5
5
6
6
10
13
14
24
Immunology
Obstetrics & Gynaecology
Urology
Dermatology
Gastroenterology
Nephrology
Ophthamology
Pulmonology
Endocrinology
Hepatology
Metabolic
Oncology
Neurology
Cardiology
Rheumatology
Hematology
Poster Presented at the Canadian Society of Nephrology Meeting May 12-14, 2022
Immense Opportunity to Support Improved Care

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Day 1: KHURE Health: Don Watts, KHURE

  • 1. CORD’s Spring Conference June 8th, 2022 Don Watts, President & GM, Khure Health
  • 2. Khure Health Clinical Decision Support for Rare & Complex Conditions Mission: To help physicians save lives and end the suffering of rare and complex disease patients through the use of advanced AI for earlier diagnosis. How: • Putting the vast amounts of EMR data sitting idle to good use • Employing AI to help connect the clinical dots for complex diseases • Powerful clinical decision-support tool
  • 3. * C.O.R.D – Canadian Organization for Rare Disease Traditional investments in technology have done little to help over-burdened physicians diagnose complex patients Major clinical leap: AI-enabled Clinical Decision Support 1 in 12 Canadians has a rare disorder* Every Physician Has a Rare Disease Patient—Whether They Know It or Not
  • 4. Khure Health’s Clinical Intelligence Platform Quickly Understand Complex, High-Risk Patients …and get them on the right care pathway. Stratify risk and understand complex patient details Optimize diagnosis and care pathways Identify potential risk.
  • 5. The Data is There … Sitting Idle • EMR agnostic, cloud-based • 100+ Rare Disease algorithms • Educational Content • Streamlined Workflows • Instant In-Visit Screen: Screen a challenging patient against all available pathologies • Clinical Support available from Khure’s Clinical Specialists (MDs) We help HCPs put it to Good Use
  • 6. Artificial Intelligence – Advanced NLP Natural Language Processing • Instant EMR analysis of meds, labs, specialist reports, clinical history/notes • NLP is a form of Machine Learning (ML) • Like speech recognition only using text • Understand the context (minimize false positives) • Connect the dots over a lifetime of data
  • 7. Algorithm Development Integrating Multiple Sources and Expertise Cryptic, structured, and unstructured data within EMR can be extracted, feature-classified, and incorporated into logical operators capable of identifying clinically meaningful cohorts Pathology specific algorithms Data structuring and feature extraction Unstructured EMR Data Accelerated linkage to care
  • 8. Pathologies currently on the Khure Health platform 100 rare pathologies and counting (with integration of chronic conditions now in development) 1. Aagenaes Syndrome 2. Acquired Hemophilia A 3. Adult Dermatomyositis 4. Adult ITP (Idiopathic Thrombocytopenic Purpura) 5. Adult Onset Still's Disease 6. Adult Polymyositis 7. Alpha Thalassemia 8. Ankylosing Spondylitis 9. Acquired Pure Red Cell Aplasia 10. Atypical Haemolytic Uremic Syndrome 11. Autosomal Dominant Polycystic Kidney Disease 12. Beta Thalassemia 13. Chronic Idiopathic Urticaria 14. Cushing's Syndrome 15. Diabetic Macular Edema 16. Essential Thrombocythemia 17. Fabry's Disease 18. Gaucher's Disease 19. Giant Cell Arteritis 20. hATTR Amyloidosis 21. Henoch Schoenlein Purpura 22. Hepatitis C Virus (HCV) 23. Hepatopulmonary Syndrome 24. Hereditary Angioedema (HAE) 25. Hereditary Elliptocytosis 26. Hereditary Spherocytosis 27. HHRH (Hereditary Hypophosphatemic Rickets with Hypercalciuria) 28. Hunter Syndrome 29. Hurlers Disease 30. Hypophosphatasia 31. Hypophosphatemia X-Linked 32. Juvenile Dermatomyositis 33. Juvenile ITP (Idiopathic Thrombocytopenic Purpura) 34. Juvenile Polymyositis 35. Kawasaki Disease 36. Loeyz-Dietz Syndrome 37. Multiple Myeloma 38. Multi-focal Motor Neuropathy 39. Myelofibrosis 40. Neuroblastoma 41. Neuromyelitis Optica Spectrum Disorder 42. Paroxysmal Nocturnal Hemoglobinuria 43. Pompe Disease 44. PPP (Palmoplantar Pustular Psoriasis) 45. Primary Biliary Cholangitis 46. Pulmonary Arterial Hypertension 47. Severe Allergic Asthma 48. Severe Eosinophilic Asthma 49. Sideroblastic Anemia 50. Thrombotic Thrombocytopenic Purpura 51. Typical Hemolytic Uremic Syndrome 52. Von Willebrand’s 53. AA Amyloidosis 54. Atrial Fibrillation 55. Bernard-Soulier Syndrome 56. Brugada Syndrome 57. Cold Agglutinin Disease 58. Ebstein anomaly 59. Eisenmenger syndrome 60. Fanconi Anemia 61. Glanzmann Thrombasthenia 62. Immune Thrombocytopenia Purpura (ITP) 63. Marfans Syndrome 64. Myelodysplastic Syndrome 65. Non-ischemic pediatric cardiomyopathy 66. Patent ductus arteriosus 67. Polycythemia Vera 68. Psoriatic Arthritis 69. Severe Plaque Psoriasis 70. Shprintzen-Goldberg syndrome 71. Sickle Cell Anemia 72. ALS 73. nmCRPC 74. Transthyretin Amyloid Cardiomyopathy 75. Recurrent Fever Syndromes 76. Castleman Disease 77. Neiman Pick 78. Primary Sclerosing Cholangitis
  • 9. Pathologies on the Khure Health Platform 100 rare & specialty pathologies and counting 79. Rheumatoid Arthritis 80. Secondary hyperparathyroidism 81. Spinal Muscular Atrophy 82. Long-Chain Fatty Acid Oxidation Disorders 83. Anaplastic lymphoma kinase (ALK)-positive metastatic Non-small cell lung cancer 84. Best Vitelliform Macular Dystrophy 85. Budd-Chiari Syndrome 86. Cerebral Adrenoleukodystrophy 87. Cone Dystrophy 88. Cystic Fibrosis 89. Emphysema - severe hereditary deficiency of alpha1-PI alpha1-antitrypsin deficiency) 90. Endometriosis 91. Guillain-Barre Syndrome 92. Hemiplegic Migraines 93. Hepatopulmonary Syndrome 94. Juvenile idiopathic arthritis 95. Metastatic Colorectal Cancer 96. Morquio syndrome 97. Multiple Sclerosis (Remitting-Relapsing) 98. Myasthenia gravis 99. Narcolepsy 100. B-cell precursor acute lymphoblastic leukemia (relapsed or refractory) By Specialty Total:100 1 1 1 2 2 3 3 4 5 5 6 6 10 13 14 24 Immunology Obstetrics & Gynaecology Urology Dermatology Gastroenterology Nephrology Ophthamology Pulmonology Endocrinology Hepatology Metabolic Oncology Neurology Cardiology Rheumatology Hematology
  • 10. Poster Presented at the Canadian Society of Nephrology Meeting May 12-14, 2022 Immense Opportunity to Support Improved Care