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Availability, Coverage, and Scope of Health Information Systems for Kidney Care Across World Countries and Regions Publisher Pubmed



See EJ1, 2 ; Bello AK3 ; Levin A4 ; Lunney M5 ; Osman MA3 ; Ye F3 ; Ashuntantang GE6 ; Bellorinfont E7 ; Benghanem Gharbi M8 ; Davison S3 ; Ghnaimat M9 ; Harden P10 ; Htay H11 ; Jha V12, 13 Show All Authors
Authors
  1. See EJ1, 2
  2. Bello AK3
  3. Levin A4
  4. Lunney M5
  5. Osman MA3
  6. Ye F3
  7. Ashuntantang GE6
  8. Bellorinfont E7
  9. Benghanem Gharbi M8
  10. Davison S3
  11. Ghnaimat M9
  12. Harden P10
  13. Htay H11
  14. Jha V12, 13
  15. Kalantarzadeh K14
  16. Kerr PG15, 16
  17. Klarenbach S3
  18. Kovesdy CP17
  19. Luyckx V18, 19
  20. Neuen B20
  21. Odonoghue D21, 22
  22. Ossareh S23
  23. Perl J24, 25
  24. Rashid HU26
  25. Rondeau E27, 28
  26. Syed S3
  27. Sola L29
  28. Tchokhonelidze I30
  29. Tesar V31
  30. Tungsanga K32, 33
  31. Kazancioglu RT34
  32. Wang AYM35
  33. Yang CW36
  34. Zemchenkov A37, 38
  35. Zhao MH39, 40, 41, 42
  36. Jager KJ43
  37. Caskey F44, 45, 46
  38. Perkovic V47
  39. Jindal KK2
  40. Okpechi IG48, 49
  41. Tonelli M50, 51
  42. Feehally J52
  43. Harris DC53
  44. Johnson DW54, 55, 56

Source: Nephrology Dialysis Transplantation Published:2022


Abstract

Background: Health information systems (HIS) are fundamental tools for the surveillance of health services, estimation of disease burden and prioritization of health resources. Several gaps in the availability of HIS for kidney disease were highlighted by the first iteration of the Global Kidney Health Atlas. Methods: As part of its second iteration, the International Society of Nephrology conducted a cross-sectional global survey between July and October 2018 to explore the coverage and scope of HIS for kidney disease, with a focus on kidney replacement therapy (KRT). Results: Out of a total of 182 invited countries, 154 countries responded to questions on HIS (85% response rate). KRT registries were available in almost all high-income countries, but few low-income countries, while registries for non-dialysis chronic kidney disease (CKD) or acute kidney injury (AKI) were rare. Registries in high-income countries tended to be national, in contrast to registries in low-income countries, which often operated at local or regional levels. Although cause of end-stage kidney disease, modality of KRT and source of kidney transplant donors were frequently reported, few countries collected data on patient-reported outcome measures and only half of low-income countries recorded process-based measures. Almost no countries had programs to detect AKI and practices to identify CKD-targeted individuals with diabetes, hypertension and cardiovascular disease, rather than members of high-risk ethnic groups. Conclusions: These findings confirm significant heterogeneity in the global availability of HIS for kidney disease and highlight important gaps in their coverage and scope, especially in low-income countries and across the domains of AKI, non-dialysis CKD, patient-reported outcomes, process-based measures and quality indicators for KRT service delivery. © 2020 The Author(s) 2020. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved.
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