•  
  •  
FEDERG
  • Donate
  • Menu Canvas
    • HOME
    • ABOUT FEDERG
      • WHAT WE DO
      • MEMBERS
      • GOVERNANCE
      • COLLABORATIONS
    • RARE/GENETIC KIDNEY CONDITIONS
    • NEWS & EVENTS
      • NEWS
      • EVENTS
      • FEDERG REPRESENTATIONS NEWSLETTERS
      • MEMBERS ACTIVITIES NEWSLETTERS
      • USEFUL LINKS
    • CONTACT
    • Sidebar

      Tags

      CKD Congress COVID-19 empowering patients ERN-Erknet EURORDIS HIPOFAM kidney diseases Patients Day Rare Disease trasplantation
FEDERG
Send us
an email
  • HOME
  • ABOUT FEDERG
    • WHAT WE DO
    • MEMBERS
    • GOVERNANCE
    • COLLABORATIONS
  • RARE/GENETIC KIDNEY CONDITIONS
  • NEWS & EVENTS
    • NEWS
    • EVENTS
    • FEDERG REPRESENTATIONS NEWSLETTERS
    • MEMBERS ACTIVITIES NEWSLETTERS
    • USEFUL LINKS
  • CONTACT
  • NEWS
  • SEARCH

Call to action to improve care of chronic kidney disease patients post COVID-19

Homepage COVID-19 Call to action to improve care of chronic kidney disease patients post COVID-19

Call to action to improve care of chronic kidney disease patients post COVID-19

Tess Harris
3 July 2020
COVID-19
CKD

Recent data show that people with chronic kidney disease (CKD) are at higher risk from COVID-19 than those with other known risk factors, including chronic heart and lung disease. Mortality rates are worryingly high amongst those on kidney replacement therapy: 20% in kidney transplant recipients and 21% in patients on dialysis.

The European Kidney Health Alliance (EKHA) has issued a ‘call to action’ of  sustainable and cost-effective recommendations to address the pressing and long-term challenges surrounding CKD in Europe in light of the COVID-19 pandemic to:
‣ Augment efforts on CKD prevention
‣ Collect and share data on CKD at EU level
‣ Promote home therapies, transplantation and the uptake of digital tools
‣ Make research and innovation in kidney replacement therapy an EU priority.

Tags: CKD COVID-19
Next Story
Patient partnerships in rare disease research

Related Articles

Representation of FEDERG at the ERA Congress, Stockholm from May 23 to 26.

From May 23 to 27, the ERA European Renal Association...

FEDERG at the 47th Congress of the AENP Spanish Association of Pediatric Nephrology, May 2024.

Susana Carvajal Arjona (FEDERG, hipofam) Mireya Carratalá (FEDERG ASHUA)

Recent Posts

  • Alport Syndrome Patient Information Day on September 6th, 2026! Wednesday, 14, Jan
  • AIRG, 21st Annual Meeting in Madrid, January 17, 2026 Sunday, 11, Jan
  • Members activities Newsletter, volume 2. Tuesday, 16, Sep
  • FEDERG support the adoption of the WHA Resolution on Rare Diseases. Tuesday, 16, Sep
  • FEDERG strongly support the WHA Resolution on rare Diseases Monday, 9, Jun

Categories

  • Charity (1)
  • COVID-19 (1)
  • Education (5)
  • Enviroment (1)
  • News (4)
  • Rare Disease (10)
  • Uncategorized (6)

Tags

CKD Congress COVID-19 empowering patients ERN-Erknet EURORDIS HIPOFAM kidney diseases Patients Day Rare Disease trasplantation

About Us

FEDERG is the non-profit federation of European associations of patients affected by rare and/or genetic kidney diseases.

FEDERG Homepage

Latest News

  • Alport Syndrome Patient Information Day on September 6th, 2026! Wednesday, 14, Jan
  • AIRG, 21st Annual Meeting in Madrid, January 17, 2026 Sunday, 11, Jan
  • Members activities Newsletter, volume 2. Tuesday, 16, Sep

Tags

CKD Congress COVID-19 empowering patients ERN-Erknet EURORDIS HIPOFAM kidney diseases Patients Day Rare Disease trasplantation
Copyright ©2021-2025 FEDERG. All Rights Reserved
SearchPosts
Wednesday, 14, Jan
Alport Syndrome Patient Information Day on September 6th, 2026!
Sunday, 11, Jan
AIRG, 21st Annual Meeting in Madrid, January 17, 2026
Tuesday, 16, Sep
Members activities Newsletter, volume 2.
Tuesday, 16, Sep
FEDERG support the adoption of the WHA Resolution on Rare Diseases.
Monday, 9, Jun
FEDERG strongly support the WHA Resolution on rare Diseases
Thursday, 19, Sep
Fighting for our federation Federg f2f Members meeting September 14 Martorell