An update on the use of tolvaptan for autosomal dominant polycystic kidney disease: consensus statement on behalf of the ERA Working Group on Inherited Kidney Disorders, the European Rare Kidney Disease Reference Network and Polycystic Kidney Disease International. Issue 5 (19th November 2021)
- Record Type:
- Journal Article
- Title:
- An update on the use of tolvaptan for autosomal dominant polycystic kidney disease: consensus statement on behalf of the ERA Working Group on Inherited Kidney Disorders, the European Rare Kidney Disease Reference Network and Polycystic Kidney Disease International. Issue 5 (19th November 2021)
- Main Title:
- An update on the use of tolvaptan for autosomal dominant polycystic kidney disease: consensus statement on behalf of the ERA Working Group on Inherited Kidney Disorders, the European Rare Kidney Disease Reference Network and Polycystic Kidney Disease International
- Authors:
- Müller, Roman-Ulrich
Messchendorp, A Lianne
Birn, Henrik
Capasso, Giovambattista
Cornec-Le Gall, Emilie
Devuyst, Olivier
van Eerde, Albertien
Guirchoun, Patrick
Harris, Tess
Hoorn, Ewout J
Knoers, Nine V A M
Korst, Uwe
Mekahli, Djalila
Le Meur, Yannick
Nijenhuis, Tom
Ong, Albert C M
Sayer, John A
Schaefer, Franz
Servais, Aude
Tesar, Vladimir
Torra, Roser
Walsh, Stephen B
Gansevoort, Ron T - Abstract:
- ABSTRACT: Approval of the vasopressin V2 receptor antagonist tolvaptan—based on the landmark TEMPO 3:4 trial—marked a transformation in the management of autosomal dominant polycystic kidney disease (ADPKD). This development has advanced patient care in ADPKD from general measures to prevent progression of chronic kidney disease to targeting disease-specific mechanisms. However, considering the long-term nature of this treatment, as well as potential side effects, evidence-based approaches to initiate treatment only in patients with rapidly progressing disease are crucial. In 2016, the position statement issued by the European Renal Association (ERA) was the first society-based recommendation on the use of tolvaptan and has served as a widely used decision-making tool for nephrologists. Since then, considerable practical experience regarding the use of tolvaptan in ADPKD has accumulated. More importantly, additional data from REPRISE, a second randomized clinical trial (RCT) examining the use of tolvaptan in later-stage disease, have added important evidence to the field, as have post hoc studies of these RCTs. To incorporate this new knowledge, we provide an updated algorithm to guide patient selection for treatment with tolvaptan and add practical advice for its use.
- Is Part Of:
- Nephrology dialysis transplantation. Volume 37:Issue 5(2022)
- Journal:
- Nephrology dialysis transplantation
- Issue:
- Volume 37:Issue 5(2022)
- Issue Display:
- Volume 37, Issue 5 (2022)
- Year:
- 2022
- Volume:
- 37
- Issue:
- 5
- Issue Sort Value:
- 2022-0037-0005-0000
- Page Start:
- 825
- Page End:
- 839
- Publication Date:
- 2021-11-19
- Subjects:
- ADPKD -- polycystic kidney disease -- position statement -- tolvaptan -- vasopressin V2 receptor antagonist
Nephrology -- Periodicals
Hemodialysis -- Periodicals
Kidneys -- Transplantation -- Periodicals
Hemodialysis
Kidneys -- Transplantation
Nephrology
Periodicals
616.61 - Journal URLs:
- http://ndt.oxfordjournals.org/ ↗
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http://ukcatalogue.oup.com/ ↗
http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=0931-0509;screen=info;ECOIP ↗ - DOI:
- 10.1093/ndt/gfab312 ↗
- Languages:
- English
- ISSNs:
- 0931-0509
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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