The role of patiromer: Comparing OPAL-HK data with untreated real-world patients in the United Kingdom-A retrospective, propensity-matched analysis.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 26 04 2020
accepted: 27 07 2020
entrez: 28 8 2020
pubmed: 28 8 2020
medline: 9 10 2020
Statut: epublish

Résumé

The first phase of the published OPAL-HK study was a single-group treatment phase, which showed that patiromer normalised serum potassium at 4weeks in patients with chronic kidney disease stages 3-4 who were receiving renin-angiotensin-aldosterone inhibitors. We utilised real-world data to provide a control comparison to evaluate patiromer's efficacy in lowering serum potassium. The Salford Kidney Study (SKS) in the United Kingdom provided a matched cohort. After applying OPAL-HK inclusion and exclusion criteria, patients with an outpatient potassium level between 5.1mmol/L to <6.5mmol/L and whose next outpatient level was checked 24-42 days later were selected. Patients underwent 1:1 matching with the 243 OPAL-HK patients using propensity matching based on 6 variables: age, gender, estimated glomerular filtration rate, diabetes, heart failure and potassium level. The study outcomes aligned with the OPAL-HK treatment phase: mean change in baseline potassium, and the proportion of patients with a potassium of 3.8 to <5.1mmol/L at follow-up. The study comprised 87 precisely matched patients. The mean follow-up in the 87 SKS patients was 31±5 days. At baseline, matched patients had a mean potassium of 5.5±0.3mmol/L. At follow-up, the mean level was unchanged in SKS patients but was 4.5±0.5mmol/L in the OPAL-HK group (p<0.001), a mean (±SE) change of -1.00±0.06mmol/L. The target range of 3.8 to <5.1mmol/L was reached in 80% of OPAL-HK patients compared with 0% in the SKS cohort. There were very few interventions undertaken to reduce hyperkalaemia in SKS patients. Using real-world data as a matched control arm for the first phase of the OPAL-HK study, we highlight a potential role for patiromer in lowering potassium levels in patients with CKD 3-4 receiving renin-angiotensin-aldosterone inhibitors.

Identifiants

pubmed: 32853209
doi: 10.1371/journal.pone.0237467
pii: PONE-D-20-12120
pmc: PMC7451519
doi:

Substances chimiques

Angiotensin-Converting Enzyme Inhibitors 0
Mineralocorticoid Receptor Antagonists 0
Potassium RWP5GA015D

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0237467

Déclaration de conflit d'intérêts

PK received research grants and speaker/consultancy fees from Vifor Fresenius Medical Care Renal Pharma outside the submitted work. GC is an employee and holds shares of the Vifor Pharma Group. MI was an employee of the Vifor Pharma Group from September 2018 to May 2020. Vifor Pharma markets patiromer. These declarations do not alter our adherence to PLOS ONE policies on sharing data and materials.

Références

Kidney Int. 2018 Feb;93(2):325-334
pubmed: 29276100
J Am Soc Nephrol. 2007 Jun;18(6):1889-98
pubmed: 17494885
JAMA. 2015 Jul 14;314(2):151-61
pubmed: 26172895
Lancet. 2019 Oct 26;394(10208):1540-1550
pubmed: 31533906
Eur Heart J. 2011 Apr;32(7):820-8
pubmed: 21208974
Clin J Am Soc Nephrol. 2012 Aug;7(8):1234-41
pubmed: 22595825
Nat Rev Nephrol. 2014 Nov;10(11):653-62
pubmed: 25223988
N Engl J Med. 2015 Jan 15;372(3):211-21
pubmed: 25415805

Auteurs

Ibrahim Ali (I)

Department of Renal Medicine, Salford Royal NHS Foundation Trust, Salford, United Kingdom.

Rajkumar Chinnadurai (R)

Department of Renal Medicine, Salford Royal NHS Foundation Trust, Salford, United Kingdom.

Georgiana Cornea (G)

Vifor Pharma Group, Glattbrugg, Switzerland.

Michele Intorcia (M)

Vifor Pharma Group, Glattbrugg, Switzerland.

Philip A Kalra (PA)

Department of Renal Medicine, Salford Royal NHS Foundation Trust, Salford, United Kingdom.

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