The role of patiromer: Comparing OPAL-HK data with untreated real-world patients in the United Kingdom-A retrospective, propensity-matched analysis.
Adult
Aged
Aged, 80 and over
Angiotensin-Converting Enzyme Inhibitors
/ therapeutic use
Databases, Factual
Female
Glomerular Filtration Rate
Humans
Male
Middle Aged
Mineralocorticoid Receptor Antagonists
/ therapeutic use
Potassium
/ blood
Propensity Score
Renal Insufficiency, Chronic
/ drug therapy
Retrospective Studies
Severity of Illness Index
United Kingdom
Young Adult
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2020
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
e0237467Déclaration 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.
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