- •Foreword
- •Preface
- •Contents
- •1.1 Introduction
- •1.2 Method
- •1.2.1 Databases
- •1.2.2 Dates
- •1.2.3 Keywords
- •1.2.4 Criteria for Inclusion
- •1.2.5 Criteria for Exclusion
- •1.2.6 Selection of Papers
- •1.3 Results
- •1.3.1 Subspecialty
- •1.3.2 Type of Telemedicine
- •1.3.3 Study Design
- •1.3.4 Final Conclusions of Papers
- •1.4 Discussion
- •References
- •2.1 Introduction
- •2.2 The Need for Diabetic Retinopathy Screening Programs
- •2.4 Guidelines for Referring Patients
- •2.7 Program Models for Diabetic Retinopathy Screening
- •2.9 Program Personnel and Operations
- •2.9.1 Primary Care Providers
- •2.9.2 Photographers
- •2.9.3 Clinical Consultants
- •2.9.4 Administrators
- •2.9.5 A Note to CEOs, Operations Directors, and Clinic Managers
- •2.10 Policies and Procedures
- •2.10.1 Sample Protocol 1
- •2.10.1.1 Diabetic Retinopathy Screening Services
- •Policy
- •Background
- •Procedure
- •2.10.2 Sample Protocol 2
- •2.10.2.1 Pupil Dilation Before Diabetic Retinopathy Photography
- •Policy
- •Background
- •Procedure
- •2.10.3 Sample Protocol 3
- •2.10.3.1 Diabetic Retinopathy Photography Review
- •Policy
- •Background
- •Procedure
- •2.11 Technical Requirements
- •2.11.1 Connectivity
- •2.11.2 Resolution
- •2.11.3 Color
- •2.11.4 Stereopsis
- •2.11.5 Compression
- •2.11.6 Enhancement
- •2.11.7 Pupil Dilation
- •2.11.8 Early California Telemedicine Initiatives Diabetic Retinopathy Screening
- •2.11.9 The American Indian Diabetes Teleophthalmology Grant Program
- •2.11.10 Central Valley EyePACS Diabetic Retinopathy Screening Project
- •2.12.1 Diabetic Retinopathy
- •2.12.1.1 ADA Guidelines Terms
- •2.12.1.2 Vitrectomy
- •References
- •3: Stereopsis and Teleophthalmology
- •3.1 Introduction
- •3.2 History of Stereopsis and Stereopsis in Ophthalmology
- •3.3 Technology and Photography
- •3.3.3 Imaging Fields
- •3.3.4 Image Viewing Techniques
- •3.3.5 Image Compression
- •3.4 Stereoscopic Teleophthalmology Systems
- •3.4.1 University of Alberta
- •3.4.4 Joslin Vision Network
- •3.5 Conclusion
- •References
- •4.1 Introduction
- •4.2 Methods
- •4.2.1 Main Outcome Measures
- •4.3 Results
- •4.3.1 Retinal Video Recording Versus Retinal Still Photography
- •4.3.2 Video Compression Analysis
- •4.4 Discussion
- •References
- •5.1 Introduction
- •5.1.1 Automated, Remote Image Analysis of Retinal Diseases
- •5.1.2 Telehealth
- •5.2 Design Requirements
- •5.2.1 Telehealth Network Architecture
- •5.2.2 Work Flow
- •5.2.3 Performance Evaluation of the Network
- •5.3 Automated Image Analysis Overview
- •5.3.1 Quality Assessment Module
- •5.3.2 Vascular Tree Segmentation
- •5.3.3 Quality Evaluation
- •5.4 Anatomic Structure Segmentation
- •5.4.1 Optic Nerve Detection
- •5.4.2 Macula
- •5.4.3 Lesion Segmentation
- •5.4.4 Lesion Population Description
- •5.4.5 Image Query
- •5.5 Summary
- •References
- •6.1 Introduction
- •6.3 Optical Coherence Tomography to Detect Leakage
- •References
- •7.1 Introduction
- •7.2 Patients and Methods
- •7.2.1 Participants
- •7.2.2 Methods
- •7.2.3 Statistics
- •7.3 Results
- •7.3.1 Reliability of Image Evaluation
- •7.3.2 Prevalence of Glaucomatous Optic Nerve Atrophy
- •7.4 Discussion
- •7.5 Perspectives
- •References
- •8.1 Introduction
- •8.1.2 Homology Between Retinal and Systemic Microvasculature
- •8.1.3 Need for More Precise CVD Risk Prediction
- •8.2.1 Retinal Microvascular Signs
- •8.2.2 Retinal Vessel Biometry
- •8.2.3 Newer Retinal Imaging for Morphologic Features of Retinal Vasculature
- •8.3 Associations of Retinal Imaging and CVD Risk
- •8.3.1.1 Risk of Pre-clinical CVD
- •8.3.1.2 Risk of Stroke
- •8.3.1.3 Risk of Coronary Heart Disease
- •8.3.2.1 Risk of Hypertension
- •8.3.2.2 Risk of Stroke
- •8.3.2.3 Risk of Coronary Heart Disease
- •8.3.2.4 Risk of Peripheral Artery Disease
- •8.3.3 Newer Morphologic Features of Retinal Vasculature
- •8.4 Retinal Imaging and Its Potential as a Tool for CVD Risk Prediction
- •References
- •9.1 Alzheimer’s Disease
- •9.2 Treatments
- •9.3 Diagnosis
- •9.6 Conclusions
- •References
- •10.1 Introduction
- •10.1.1 Stroke
- •10.1.2 Heart Disease
- •10.1.3 Arteriovenous Ratio
- •10.2 Purpose
- •10.3 Method
- •10.3.1 Medical Approach
- •10.3.2 Technical Approach
- •10.3.3 Output of Medical Data
- •10.4 Patients
- •10.5 Results
- •10.5.1 Medical History
- •10.5.2 Telemedical Evaluation of Retinal Vessels
- •10.5.2.1 Prevalence of Retinal Microangiopathy
- •10.5.2.2 Arteriovenous Ratio
- •10.5.2.3 PROCAM-Index
- •10.6 Discussion and Perceptive
- •10.6.1 Estimation of “Stroke Risk” Estimated by the Stage of Retinal Microangiopathy
- •References
- •11.1 Introduction
- •11.2 System Requirements
- •11.3 Fundus Camera
- •11.4 Imaging Procedure
- •11.4.1 Reading Center Procedure
- •11.5 Detection of Macular Edema
- •11.6 Implementation
- •11.7 Unreadable Images
- •11.7.1 Impact on Overall Diabetic Retinopathy Assessment Rates
- •11.7.2 Compliance with Recommendations
- •11.7.3 Challenges
- •11.7.4 Summary
- •References
- •12.1 Screening
- •12.2 Background
- •12.3 Historical Perspective in England
- •12.4 Methodology
- •12.4.1 The Aim of the Programme
- •12.5 Systematic DR Screening
- •12.6 Cameras for Use in the English Screening Programme
- •12.7 Software for Use in the English Screening Programme
- •12.9 Implementation in England
- •12.11 Quality Assurance
- •12.12 The Development of External Quality Assurance in the English Screening Programme
- •12.13 Information Technology (IT) Developments for the English Screening Programme
- •12.14 Dataset Development
- •12.15 The Development of External Quality Assurance Test Set for the English Screening Programme
- •12.16 Failsafe
- •12.17 The Epidemic of Diabetes
- •References
- •13.1 Introduction
- •13.2 Burden of Diabetes and Diabetic Retinopathy in India
- •13.3 Diabetic Retinopathy Screening Models
- •13.4 Need for Telescreening
- •13.5 Guidelines for Telescreening
- •13.6 ATA Categories of DR Telescreening Validation
- •13.7 Yield of Diabetic Retinopathy in a Telescreening Model
- •13.8 How Are Images Transferred
- •13.10 How Many Fields Are Enough for Diabetic Retinopathy Screening
- •13.11 Is Mydriasis Needed While Using Nonmydriatic Camera?
- •13.12 Validation Studies on Telescreening
- •13.12.1 Accuracy of Telescreening
- •13.12.2 Patient Satisfaction in Telescreening
- •13.12.3 Cost Effectivity
- •13.12.4 Telescreening for Diabetic Retinopathy: Our Experience
- •13.13 Future of Diabetic Retinopathy Screening
- •References
- •14.1 Introduction
- •14.2 Methods
- •14.3 Discussion
- •14.4 Conclusion
- •References
- •15.1 Introduction
- •15.1.1 Description of the EADRSI
- •15.5 State Support of Screening in the Safety Net
- •15.7 Screening Economics for Providers
- •15.8 Patient Sensitivity to Fees
- •15.9 Conclusion
- •References
- •16.1 Introduction
- •16.2 Setting Up the New Screening Model
- •16.2.1 Phase 1: Training
- •16.2.2 Phase 2: Evaluation of Agreement
- •16.2.3 Phase 3: Implementation of the Screening Model
- •16.3 Technologic Requirements
- •16.3.1 Data Management
- •16.3.2 Data Models
- •16.3.2.1 Data Scheme for Patient-Related Information
- •16.3.2.2 Data Scheme for Images
- •Fundus Camera VISUCAM Pro NM
- •PACS Server
- •ClearCanvas DICOM Visualizer
- •16.4 Results
- •16.4.1 Phase 2: Agreement Evaluation
- •16.4.2 Phase 3: Implementation of the Screening Model
- •16.5 Discussion
- •16.5.1 Evaluation of the Screening Model
- •16.5.2 Prevalence of DR
- •16.5.3 Quality Evaluation
- •16.6 Conclusion
- •References
- •17.1.3 Examination and Treatment
- •17.1.4 Limitations of Current Care
- •17.2 Telemedicine and ROP
- •17.2.2 Accuracy and Reliability of Telemedicine for ROP Diagnosis
- •17.2.3 Operational ROP Telemedicine Systems
- •17.2.4 Potential Barriers
- •17.3 Closing Remarks
- •17.3.1 Future Directions
- •References
- •18.1 Introduction
- •18.2 Neonatal Stress and Pain
- •18.3 ROP Screening Technique
- •18.4 Effect of Different Examination Techniques on Stress
- •18.5 Future of Retinal Imaging in Babies
- •References
- •19.1 Introduction
- •19.2 History of the Program
- •19.3 Telehealth Technologies
- •19.4 Impact of the Program
- •Selected References
- •Preamble
- •Introduction
- •Background
- •The Diabetic Retinopathy Study (DRS)
- •Mission
- •Vision
- •Goals
- •Guiding Principles
- •Ethics
- •Clinical Validation
- •Category 1
- •Category 2
- •Category 3
- •Category 4
- •Communication
- •Medical Care Supervision
- •Patient Care Coordinator
- •Image Acquisition
- •Image Review and Evaluation
- •Information Systems
- •Interoperability
- •Image Acquisition
- •Compression
- •Data Communication and Transmission
- •Computer Display
- •Archiving and Retrieval
- •Security
- •Reliability and Redundancy
- •Documentation
- •Image Analysis
- •Legal Requirements
- •Facility Accreditation
- •Privileging and Credentialing
- •Stark Act and Self-referrals
- •State Medical Practice Acts/Licensure
- •Tort Liability
- •Duty
- •Standards of Care
- •Consent
- •Quality Control
- •Operations
- •Customer Support
- •Originating Site
- •Transmission
- •Distant Site
- •Financial Factors
- •Reimbursement
- •Grants
- •Federal Programs
- •Other Financial Factors
- •Equipment Cost
- •Summary
- •Abbreviations
- •Appendices
- •Appendix A: Interoperability
- •Appendix B: DICOM Metadata
- •Appendix C: Computer-Aided Detection
- •Appendix D: Health Insurance Portability and Accountability Act (HIPAA)
- •Appendix F: Quality Control
- •Appendix H: Customer Support
- •Level 1
- •Level 2
- •Level 3
- •Appendix I: Reimbursement
- •Medicare
- •Medicaid
- •Commercial Insurance Carrier Reimbursement
- •Other Financial Factors
- •Disease Prevention
- •Resource Utilization
- •American Telemedicine Association’s Telehealth Practice Recommendations for Diabetic Retinopathy
- •Conclusion
- •References
- •Contributors
- •Second Edition
- •First Edition
- •Index
112 |
G. Michelson and M. Laser |
|
|
Precalence of procam high risk as a function of retinal findings
6.00
5.00
4.00
Prevalence of Procam risk >5% in %
3.00
2.00
1.00
0.0 |
0.5 |
1.0 |
1.5 |
2.0 |
2.5 |
3.0 |
3.5 |
4.0 |
4.5 |
5.0 |
5.5 |
6.0 |
6.5 |
7.0 |
Stage of retinal microangiopathy
Fig. 10.8 Prevalence of patients with a PROCAM-index >5% in groups with increasing degree of retinal microangiopathy. Groups with relevant retinal alterations showed increased prevalence of high PROCAM-scores
evaluation of retinal vessels in a high number of cases. Interdisciplinary prevention of vascular diseases should be a worthwhile goal in modern societies to reduce the number of vascular impaired persons.
References
1. Wong TY, Klein R, Klein BE, Tielsch JM, Hubbard L, Nieto FJ (2001) Retinal microvascular abnormalities and their relationship with hypertension, cardiovascular disease, and mortality. Surv Ophthalmol 46:59–80
2. Tso MO, Jampol LM (1982) Pathophysiology of hypertensive retinopathy. Ophthalmology 89:1132–1145
3. Patton N, Aslam T, Macgillivray T, Pattie A, Deary IJ, Dhillon B (2005) Retinal vascular image analysis as a potential screening tool for cerebrovascular disease: a rationale based on homology between cerebral and retinal microvasculatures. J Anat 206:319–348
4. Wong TY, Klein R, Couper DJ et al (2001) Retinal microvascular abnormalities and incident stroke: the Atherosclerosis Risk in Communities study. Lancet 358:1134–1140
5. Wong TY, Klein R, Nieto FJ et al (2003) Retinal microvascular abnormalities and 10-year cardiovascular mortality: a population-based case-control study. Ophthalmology 110:933–940
6. Mitchell P, Wang JJ, Wong TY, Smith W, Klein R, Leeder SR (2005) Retinal microvascular signs and risk of stroke and stroke mortality. Neurology 65: 1005–1009
7.Michelson EL, Morganroth J, Nichols CW, MacVaugh H 3rd (1979) Retinal arteriolar changes as an indica-
tor of coronary artery disease. Arch Intern Med 139: 1139–1141
8. Duncan BB, Wong TY, Tyroler HA, Davis CE, Fuchs FD (2002) Hypertensive retinopathy and incident coronary heart disease in high risk men. Br J Ophthalmol 86:1002–1006
9. Wong TY, Klein R, Sharrett AR et al (2002) Retinal arteriolar narrowing and risk of coronary heart disease in men and women. The Atherosclerosis Risk in Communities study. JAMA 287:1153–1159
10. Wong TY, Rosamond W, Chang PP et al (2005) Retinopathy and risk of congestive heart failure. JAMA 293:63–69
11. Wong TY, Coresh J, Klein R et al (2004) Retinal microvascular abnormalities and renal dysfunction: the atherosclerosis risk in communities study. J Am Soc Nephrol 15:2469–2476
10 Screening the Retina for Heart Disease/Stroke (talkingeyes®) |
113 |
|
|
12. Cuspidi C, Meani S, Salerno M et al (2004) Retinal microvascular changes and target organ damage in untreated essential hypertensives. J Hypertens 22: 2095–2102
13. Saitoh M, Matsuo K, Nomoto S et al (1998) Relationship between left ventricular hypertrophy and renal and retinal damage in untreated patients with essential hypertension. Intern Med 37:576–580
14. McGeechan K, Liew G, Macaskill P, Irwig L, Klein R, Klein BE, Wang JJ, Mitchell P, Vingerling JR, Dejong PT, Witteman JC, Breteler MM, Shaw J, Zimmet P, Wong TY (2009) Meta-analysis: retinal vessel caliber and risk for coronary heart disease. Ann Intern Med 151(6):404–413
15. McGeechan K, Liew G, Macaskill P, Irwig L, Klein R, Klein BE, Wang JJ, Mitchell P, Vingerling JR, de Jong PT, Witteman JC, Breteler MM, Shaw J, Zimmet P, Wong TY (2009) Prediction of incident stroke events based on retinal vessel caliber: a systematic review and individual-participant meta-analysis. Am J Epidemiol 170(11):1323–1332
16. Williams B, Poulter NR, Brown MJ et al (2004) British Hypertension Society guidelines for hypertension management 2004 (BHS-IV): summary. BMJ 328:634–640
17.Chobanian AV, Bakris GL, Black HR et al (2003) The seventh report of the Joint National Committee on prevention, detection, evaluation, and treatment of high blood pressure: the JNC 7 report. JAMA 289:2560–2572
18. Assmann G, Cullen P, Schulte H (2002) A simple scoring scheme for calculating the risk of acute
coronary events based on the 10-year follow-up of the prospective cardiovascular Münster (PROCAM) study. Circulation 105(3):310–315
19. Adler W, Wärntges S, Lausen B, Michelson G (2010) Prevalence of glaucomatous optic nerve atrophy among a working population in Germany diagnosed by a telemedical approach. Klin Monbl Augenheilkd 227(11):905–911
20. Michelson G, Laser M, Müller S, Weber F, Wärntges S (2011) Validation of telemedical fundus images from patients with retinopathy. Klin Monbl Augenheilkd 228(3):234–238
21. Paulus J, Meier J, Bock R, Hornegger J, Michelson G (2010) Automated quality assessment of retinal fundus photos. Int J Comput Assist Radiol Surg 5(6): 557–564
22. Bock R, Meier J, Nyúl LG, Hornegger J, Michelson G (2010) Glaucoma risk index: automated glaucoma detection from color fundus images. Med Image Anal 14(3):471–481
23.Michelson G (2005) TalkingEyes-and-more. Biomed Tech (Berl) 50(7–8):218–226
24. Chrástek R, Wolf M, Donath K, Niemann H, Paulus D, Hothorn T, Lausen B, Lämmer R, Mardin CY, Michelson G (2005) Automated segmentation of the optic nerve head for diagnosis of glaucoma. Med Image Anal 9(4):297–314
25.Michelson G, Groh M, Groh MJ, Baleanu D, Harazny J, Horstmann R, Kolominsky-Rabas P (2005) Telemedicalsupported screening of retinal vessels (“talking eyes”). Klin Monbl Augenheilkd 222(4):319–325
Part II
The Telemedicine Applications and Global
Experience: Teleretinal Imaging in Adults
Diabetic Retinopathy Assessment |
11 |
in the Primary Care Environment: |
Lessons Learned from 100,000
Patient Encounters
Ingrid E. Zimmer-Galler
11.1Introduction
A major unresolved challenge in clinical ophthalmology is the elimination of avoidable vision loss due to diabetic retinopathy. Despite wellestablished guidelines for periodic retinal examinations in patients with diabetes, poor compliance with these recommendations still results in missed opportunities for management of treatable disease in a timely manner. In the past decade, numerous telemedicine diabetic retinopathy assessment programs have been established as a potential alternative strategy to assess patients who would not otherwise undergo a periodic dilated retinal examination. With increasing frequency, these telemedicine diabetic retinopathy surveillance programs are occurring outside of the traditional eye care setting in the primary care or general health arena. Because most patients with diabetes visit their primary care physicians with some regularity, this has been postulated as an ideal environment in which to assess for retinopathy [1]. This chapter describes the approach used by a primary care–based telemedicine diabetic retinopathy assessment program which has
I.E. Zimmer-Galler, M.D.
Department of Ophthalmology, Wilmer Eye Institute, Johns Hopkins University Medical Institutions, Maumenee 738, 600 N Wolfe Street, Baltimore,
MD 21287, USA
e-mail: izimmerg@jhmi.edu
been successfully implemented on a wide-scale and long-term basis.
11.2System Requirements
Practical implementation of a diabetic retinopathy assessment system in the primary care setting requires special considerations. Although the incidence of diabetes is rising at an alarming rate, the typical primary care medical practice still may see only a few patients with diabetes on any given day. Since it is estimated that at least half of these patients are already under the care of an ophthalmologist, the volume of patients requiring a screening retinal imaging procedure is likely to be relatively small in individual primary care practices. This implies that the cost of instrumentation for diabetic retinopathy assessment in this setting also needs to be low in order to remain cost-effec- tive. Additionally, the imaging procedure must be easy to administer by any non-eye care office personnel including physician’s assistants or technicians. The images obtained must be of adequate resolution to detect the small microvascular abnormalities seen in diabetic retinopathy. Another system requirement is the capability to transfer the data to a remote reading center in a secure manner as mandated by the Health Insurance Portability and Accountability Act (HIPAA). Finally, the remote reading center must have qualified personnel to analyze and grade the images as well as software for image analysis and a robust reporting and archiving platform.
K. Yogesan et al. (eds.), Digital Teleretinal Screening, |
117 |
DOI 10.1007/978-3-642-25810-7_11, © Springer-Verlag Berlin Heidelberg 2012 |
|
