Evidence map›Paper›PMID 37140706›Full record

ArticleAdvances in therapy2023

Real-World Modifications of Renin-Angiotensin-Aldosterone System Inhibitors in Patients with Hyperkalemia Initiating Sodium Zirconium Cyclosilicate Therapy: The OPTIMIZE I Study.

Abiy Agiro, Amin An, Erin E Cook, Fan Mu, Jingyi Chen, Pooja Desai, Yemmie Oluwatosin, Charles V Pollack

Open access · hybridAbstract read
In one paragraph

Article in Advances in therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
5.9field-weighted citation impact, top 3% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 2 countries.

Abiy AgiroAstraZeneca, US Medical Affairs, 1800 Concord Pike, Wilmington, DE, 19850, USA. abiy.agiro@astrazeneca.com.
Amin AnUniversity of California Irvine, Irvine, CA, 92697, USA.
Erin E CookAnalysis Group, Inc., 111 Huntington Ave, 14th Floor, Boston, MA, 02199, USA.
Fan MuAnalysis Group, Inc., 111 Huntington Ave, 14th Floor, Boston, MA, 02199, USA.
Jingyi ChenAnalysis Group, Inc., 111 Huntington Ave, 14th Floor, Boston, MA, 02199, USA.
Pooja DesaiAstraZeneca, US Medical Affairs, 1800 Concord Pike, Wilmington, DE, 19850, USA.
Yemmie OluwatosinAstraZeneca, US Medical Affairs, 1800 Concord Pike, Wilmington, DE, 19850, USA.
Charles V PollackUniversity of Mississippi, Jackson, MS, 38677, USA.
Analysis Group (United States) · USAstraZeneca (United States) · USAstraZeneca (France) · FRUniversity of California, Irvine · USUniversity of Mississippi · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionHyperkalemia (HK) may result in disruptions of guidelines-concordant renin-angiotensin-aldosterone system inhibitors (RAASi), a standard of care in persons with chronic kidney disease (CKD). Such disruptions-dose reduction or discontinuation-diminish the benefits of RAASi, placing patients at risk of serious events and renal dysfunction. This real-world study evaluated RAASi modifications among patients who initiated sodium zirconium cyclosilicate (SZC) for HK.

methodsAdults (≥ 18 years) initiating outpatient SZC (index date) while on RAASi were identified from a large US claims database (January 2018-June 2020). RAASi optimization (maintain same or up-titration of RAASi dosage), non-optimization (down-titration of RAASi dosage or discontinuation), and persistence were descriptively summarized following index. Predictors of RAASi optimization were assessed using multivariable logistic regression models. Analyses were conducted by subgroups, including patients without end-stage kidney disease (ESKD), with CKD, and with CKD + diabetes.

resultsA total of 589 patients initiated SZC during RAASi therapy (mean age 61.0 years, 65.2% male), and 82.7% patients (n = 487) kept RAASi after index (mean follow-up  = 8.1 months). Most patients (77.4%) optimized RAASi therapy after initiating SZC; 69.6% maintained the same dosage while 7.8% had up-titrations. A similar rate of RAASi optimization was observed among subgroups without ESKD (78.4%), with CKD (78.9%), and with CKD + diabetes (78.1%). At 1-year post-index, 73.9% of all patients who optimized RAASi were still on therapy, while only 17.9% of patients who did not optimize therapy were still on a RAASi. Among all patients, predictors of RAASi optimization included fewer prior hospitalizations (odds ratio = 0.79, 95% CI [0.63-1.00]; p < 0.05) and fewer prior emergency department (ED) visits (0.78 [0.63-0.96]; p < 0.05).

conclusionConsistent with clinical trial findings, nearly 80% of patients who initiated SZC for HK optimized their RAASi therapy. Patients may require long-term SZC therapy to encourage continuation of RAASi therapy especially after inpatient and ED visits.

Indexed as

HyperkalemiaKidney Failure, ChronicRenal Insufficiency, ChronicAdultAngiotensin-Converting Enzyme InhibitorsFemaleHumansMaleMiddle AgedRenin-Angiotensin SystemSilicatesAngiotensin-Converting Enzyme InhibitorsSilicatessodium zirconium cyclosilicateChronic kidney diseaseHyperkalemiaModificationOptimizationReal-world evidenceRenin-angiotensin-aldosterone system inhibitorsRetrospective cohort studySodium zirconium cyclosilicateTreatment persistence

Identifiers

PMID37140706
PMCPMC10220114
OpenAlexW4368356339

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.