Literature DB >> 35368791

From Theory to Reality: Establishing a Successful Kidney Genetics Clinic in the Outpatient Setting.

Andrew L Lundquist1, Renee C Pelletier2, Courtney E Leonard2, Winfred W Williams1, Katrina A Armstrong3, Heidi L Rehm2,4,5, Eugene P Rhee1.   

Abstract

Background: Genetic testing in nephrology is increasingly described in the literature and several groups have suggested significant clinical benefit. However, studies to date have described experience from established genetic testing centers or from externally funded research programs.
Methods: We established a de novo kidney genetics clinic within an academic adult general nephrology practice. Key features of this effort included a pipeline for internal referrals, flexible scheduling, close coordination between the nephrologist and a genetic counselor, and utilization of commercial panel-based testing. Over the first year, we examined the outcomes of genetic testing, the time to return of genetic testing, and out-of-pocket cost to patients.
Results: Thirty patients were referred and 23 were evaluated over the course of five clinic sessions. Nineteen patients underwent genetic testing with new diagnoses in nine patients (47%), inconclusive results in three patients (16%), and clearance for kidney donation in two patients (11%). On average, return of genetic results occurred 55 days (range 9-174 days) from the day of sample submission and the average out-of-pocket cost to patients was $155 (range $0-$1623). Conclusions: We established a kidney genetics clinic, without a pre-existing genetics infrastructure or dedicated research funding, that identified a new diagnosis in approximately 50% of patients tested. This study provides a clinical practice model for successfully incorporating genetic testing into ambulatory nephrology care with minimal capital investment and limited financial effect on patients.
Copyright © 2020 by the American Society of Nephrology.

Entities:  

Keywords:  ambulatory care facilities; familial nephropathy; genetic kidney disease; genetics; kidney dysfunction; outpatients

Mesh:

Year:  2020        PMID: 35368791      PMCID: PMC8815482          DOI: 10.34067/KID.0004262020

Source DB:  PubMed          Journal:  Kidney360        ISSN: 2641-7650


  36 in total

1.  Clinical and biochemical phenotypes of adults with monoallelic and biallelic CYP24A1 mutations: evidence of gene dose effect.

Authors:  D T O'Keeffe; P J Tebben; R Kumar; R J Singh; Y Wu; R A Wermers
Journal:  Osteoporos Int       Date:  2016-04-29       Impact factor: 4.507

2.  Genetic spectrum and clinical correlates of somatic mutations in aldosterone-producing adenoma.

Authors:  Fabio Luiz Fernandes-Rosa; Tracy Ann Williams; Anna Riester; Olivier Steichen; Felix Beuschlein; Sheerazed Boulkroun; Tim M Strom; Silvia Monticone; Laurence Amar; Tchao Meatchi; Franco Mantero; Maria-Verena Cicala; Marcus Quinkler; Francesco Fallo; Bruno Allolio; Giampaolo Bernini; Mauro Maccario; Gilberta Giacchetti; Xavier Jeunemaitre; Paolo Mulatero; Martin Reincke; Maria-Christina Zennaro
Journal:  Hypertension       Date:  2014-05-27       Impact factor: 10.190

3.  Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.

Authors:  Nina Mann; Daniela A Braun; Kassaundra Amann; Weizhen Tan; Shirlee Shril; Dervla M Connaughton; Makiko Nakayama; Ronen Schneider; Thomas M Kitzler; Amelie T van der Ven; Jing Chen; Hadas Ityel; Asaf Vivante; Amar J Majmundar; Ankana Daga; Jillian K Warejko; Svjetlana Lovric; Shazia Ashraf; Tilman Jobst-Schwan; Eugen Widmeier; Hannah Hugo; Shrikant M Mane; Leslie Spaneas; Michael J G Somers; Michael A Ferguson; Avram Z Traum; Deborah R Stein; Michelle A Baum; Ghaleb H Daouk; Richard P Lifton; Shannon Manzi; Khashayar Vakili; Heung Bae Kim; Nancy M Rodig; Friedhelm Hildebrandt
Journal:  J Am Soc Nephrol       Date:  2019-01-17       Impact factor: 10.121

4.  Kidney function and influence of sunlight exposure in patients with impaired 24-hydroxylation of vitamin D due to CYP24A1 mutations.

Authors:  Marie-Lucile Figueres; Agnès Linglart; Frank Bienaime; Emma Allain-Launay; Gwenaelle Roussey-Kessler; Amélie Ryckewaert; Marie-Laure Kottler; Maryvonne Hourmant
Journal:  Am J Kidney Dis       Date:  2014-11-04       Impact factor: 8.860

5.  Genetic Counseling Assistants: an Integral Piece of the Evolving Genetic Counseling Service Delivery Model.

Authors:  Sara Pirzadeh-Miller; Linda S Robinson; Parker Read; Theodora S Ross
Journal:  J Genet Couns       Date:  2016-11-10       Impact factor: 2.537

6.  CYP24A1 Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive Trait.

Authors:  A Molin; R Baudoin; M Kaufmann; J C Souberbielle; A Ryckewaert; M C Vantyghem; P Eckart; J Bacchetta; G Deschenes; G Kesler-Roussey; N Coudray; N Richard; M Wraich; Q Bonafiglia; A Tiulpakov; G Jones; M-L Kottler
Journal:  J Clin Endocrinol Metab       Date:  2015-07-27       Impact factor: 5.958

Review 7.  Unanswered Questions in the Genetic Basis of Primary Aldosteronism.

Authors:  Ute I Scholl
Journal:  Horm Metab Res       Date:  2017-10-24       Impact factor: 2.936

8.  The Exome Clinic and the role of medical genetics expertise in the interpretation of exome sequencing results.

Authors:  Dustin Baldridge; Jennifer Heeley; Marisa Vineyard; Linda Manwaring; Tomi L Toler; Emily Fassi; Elise Fiala; Sarah Brown; Charles W Goss; Marcia Willing; Dorothy K Grange; Beth A Kozel; Marwan Shinawi
Journal:  Genet Med       Date:  2017-03-02       Impact factor: 8.822

9.  Randomized dose-escalation trial of elamipretide in adults with primary mitochondrial myopathy.

Authors:  Amel Karaa; Richard Haas; Amy Goldstein; Jerry Vockley; W Douglas Weaver; Bruce H Cohen
Journal:  Neurology       Date:  2018-03-02       Impact factor: 11.800

10.  Chromosome 17q12 microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorder.

Authors:  Rhian L Clissold; Charles Shaw-Smith; Peter Turnpenny; Benjamin Bunce; Detlef Bockenhauer; Larissa Kerecuk; Simon Waller; Pamela Bowman; Tamsin Ford; Sian Ellard; Andrew T Hattersley; Coralie Bingham
Journal:  Kidney Int       Date:  2016-05-24       Impact factor: 10.612

View more
  2 in total

1.  Establishing an Ehlers-Danlos Syndrome Clinic: Lessons Learned.

Authors:  Dacre R T Knight; Sunnie M Confiado; Katelyn A Bruno; DeLisa Fairweather; Andrea M Seymour-Sonnier; Angita Jain; Jessica M Gehin; Emily R Whelan; Joshua H Culberson; Bala Munipalli; Nancy L Dawson; Todd D Rozen; Joseph J Wick; Archana Kotha
Journal:  SN Compr Clin Med       Date:  2022-07-05

Review 2.  The Evolving Role of Diagnostic Genomics in Kidney Transplantation.

Authors:  Jacqueline Soraru; Aron Chakera; Nikky Isbel; Amali Mallawaarachichi; Natasha Rogers; Peter Trnka; Chirag Patel; Andrew J Mallett
Journal:  Kidney Int Rep       Date:  2022-05-25
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.