Evidence map›Paper›PMID 30228150›Full record

ReviewJournal of the American Society of Nephrology : JASN2018

A Practical Guide for Treatment of Rapidly Progressive ADPKD with Tolvaptan.

Fouad T Chebib, Ronald D Perrone, Arlene B Chapman, Neera K Dahl, Peter C Harris, Michal Mrug, Reem A Mustafa, Anjay Rastogi, Terry Watnick, Alan S L Yu and 1 more

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Journal of the American Society of Nephrology : JASN, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07016282 (Simulated and Synthetic Health Data), which is not on this map. Cited by 151 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
151citing papers in PubMed, 1 pooled it
15.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07016282 active not recruitingnot on this mapstarted 2025, after this paper: background citation

Simulated and Synthetic Health Data: Improving Clinical Research on Rare Diseases. A Real-World Data Simulation of Autosomal Dominant Polycystic Kidney Disease (ADPKD) Trials. A Retrospective, Observational Study

TypeobservationalSponsorMario Negri Institute for Pharmacological ResearchRan2025 to 2027Enrolled100ConditionsAutosomal Dominant Polycystic Kidney Disease (ADPKD)
3 · Its place in the literature

Who cites it

151 citing papers in PubMed, 1 synthesis or guideline pooled it, 246 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Article
  8. Broadening horizons: Pathogenesis and therapeutics of renal ciliopathies.Journal of cell communication and signaling · 2026
    Review
  9. Review
  10. Review
  11. Polyphenols and ADPKD: A Further Aid from Nature?Life (Basel, Switzerland) · 2026
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. SAR-Guided Scaffold Innovation of Selective VACS medicinal chemistry letters · 2026
    Article
  18. Article
  19. Review
  20. Article

91 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 8 institutions in 1 country.

Fouad T ChebibDivision of Nephrology and Hypertension, Mayo Clinic College of Medicine, Rochester, Minnesota; torres.vicente@mayo.edu chebib.fouad@mayo.edu.
Ronald D PerroneDivision of Nephrology, Department of Medicine, Tufts Medical Center, Boston, Massachusetts.
Arlene B ChapmanSection of Nephrology, University of Chicago School of Medicine, Chicago, Illinois.
Neera K DahlSection of Nephrology, Yale University School of Medicine, New Haven, Connecticut.
Peter C HarrisDivision of Nephrology and Hypertension, Mayo Clinic College of Medicine, Rochester, Minnesota.ORCID 0000-0002-5304-6593
Michal MrugDivision of Nephrology, Department of Veterans Affairs Medical Center and University of Alabama, Birmingham, Alabama.
Reem A MustafaDivision of Nephrology and Hypertension and the Kidney Institute, University of Kansas Medical Center, Kansas City, Kansas.
Anjay RastogiDivision of Nephrology, Department of Medicine, University of California, Los Angeles, Los Angeles, California; and.
Terry WatnickDivision of Nephrology, University of Maryland School of Medicine, Baltimore, Maryland.
Alan S L YuDivision of Nephrology and Hypertension and the Kidney Institute, University of Kansas Medical Center, Kansas City, Kansas.
Vicente E TorresDivision of Nephrology and Hypertension, Mayo Clinic College of Medicine, Rochester, Minnesota; torres.vicente@mayo.edu chebib.fouad@mayo.edu.
Mayo Clinic · USUniversity of Kansas Medical Center · USTufts Medical Center · USUniversity of Alabama · USUniversity of California, Los Angeles · USUniversity of Chicago · USUniversity of Maryland, Baltimore · USYale University · US

Funding

Pilot and FeasibilityP30DK090728 · NIDDK · MAYO CLINIC ROCHESTER · PI TORRES, VICENTE E · 2010 to 2019
$11.8M
Research BaseP30DK090868 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI WATNICK, TERRY J · 2010 to 2019
$11.1M
RENIN ANGIOTENSIN SYSTEM IN THE PATHOGENESIS OF ADPKDR01DK044863 · NIDDK · MAYO CLINIC ROCHESTER · PI TORRES, VICENTE E · 1991 to 2019
$4.5M
NIDDK NIH HHS P30 DK090728NIDDK NIH HHS P30 DK090868NIDDK NIH HHS R01 DK044863
6 · The paper itself

Abstract

In the past, the treatment of autosomal dominant polycystic kidney disease (ADPKD) has been limited to the management of its symptoms and complications. Recently, the US Food and Drug Administration (FDA) approved tolvaptan as the first drug treatment to slow kidney function decline in adults at risk of rapidly progressing ADPKD. Full prescribing information approved by the FDA provides helpful guidelines but does not address practical questions that are being raised by nephrologists, internists, and general practitioners taking care of patients with ADPKD, and by the patients themselves. In this review, we provide practical guidance and discuss steps that require consideration before and after prescribing tolvaptan to patients with ADPKD to ensure that this treatment is implemented safely and effectively. These steps include confirmation of diagnosis; identification of rapidly progressive disease; implementation of basic renal protective measures; counseling of patients on potential benefits and harms; exclusions to use; education of patients on aquaresis and its expected consequences; initiation, titration, and optimization of tolvaptan treatment; prevention of aquaresis-related complications; evaluation and management of liver enzyme elevations; and monitoring of treatment efficacy. Our recommendations are made on the basis of published evidence and our collective experiences during the randomized, clinical trials and open-label extension studies of tolvaptan in ADPKD.

Indexed as

AlgorithmsAntidiuretic Hormone Receptor AntagonistsClinical ProtocolsDehydrationDisease ProgressionDiuresisFemaleGlomerular Filtration RateHumansLiverMagnetic Resonance ImagingMalePatient SelectionPolycystic Kidney, Autosomal DominantTime FactorsTolvaptanAntidiuretic Hormone Receptor AntagonistsTolvaptanADPKDhepatotoxicitypolycystic kidney diseaseTolvaptanV2 Receptor Antagonistvasopressin

Identifiers

PMID30228150
PMCPMC6171265
OpenAlexW2891820180

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.