Evidence map›Paper›PMID 34183459›Full record

ArticleEuropean journal of hospital pharmacy : science and practice2023

Effects of angiotensin II receptor blockers on serum potassium level and hyperkalemia risk: retrospective single-centre analysis.

Sakae Fukushima, Manami Oishi, Hiroya Aso, Kifumi Arai, Yuuki Sasaki, Naohiro Tochikura, Susumu Ootsuka, Noriyasu Fukuoka, Nobuhiro Ooba, Norikazu Kikuchi

Open access · hybridAbstract read
In one paragraph

Article in European journal of hospital pharmacy : science and practice, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
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

10 authors at 2 institutions in 1 country.

Sakae FukushimaPharmacy, Nihon University Itabashi Hospital, Itabashi-ku, Tokyo, Japan fukushima.sakae@nihon-u.ac.jp.
Manami OishiNihon University School of Pharmacy, Funabashi, Chiba, Japan.
Hiroya AsoNihon University School of Pharmacy, Funabashi, Chiba, Japan.
Kifumi AraiPharmacy, Nihon University Hospital, Chiyoda-ku, Tokyo, Japan.
Yuuki SasakiPharmacy, Nihon University Hospital, Chiyoda-ku, Tokyo, Japan.
Naohiro TochikuraPharmacy, Nihon University Itabashi Hospital, Itabashi-ku, Tokyo, Japan.
Susumu OotsukaPharmacy, Nihon University Itabashi Hospital, Itabashi-ku, Tokyo, Japan.
Noriyasu FukuokaNihon University School of Pharmacy, Funabashi, Chiba, Japan.
Nobuhiro OobaNihon University School of Pharmacy, Funabashi, Chiba, Japan.
Norikazu KikuchiPharmacy, Nihon University Hospital, Chiyoda-ku, Tokyo, Japan.
Nihon University · JPNihon University Itabashi Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo examine the effect of angiotensin II receptor blocker (ARB) treatment on serum potassium level and hyperkalaemia risk in a clinical setting with inpatients and outpatients using calcium channel blockers (CCBs) as a reference standard.

methodsThe increased risk of hyperkalaemia associated with ARB treatment is known, however only a few studies have used an active comparator to examine this risk. In this retrospective study at a 320-bed general hospital in Japan, the hospital information system was used to identify patients with at least one prescription for an ARB (819 patients) or a CCB (1015 patients) who were naive to these drugs before study initiation. Serum potassium levels before and after ARB treatment were compared. Additionally, the unadjusted and adjusted hazard ratios for the risk of hyperkalaemia in the ARB and CCB users were estimated.

resultsThe serum potassium level was higher in patients receiving ARB treatment (0.05 mEq/L, p=0.02) compared with those on CCB treatment. However, there was no significant association between ARB use and hyperkalaemia (adjusted HR 0.91, 95% CI 0.42 to 1.99, p=0.82).

conclusionThe increase in serum potassium level after ARB initiation makes it necessary to monitor serum potassium levels continuously during ARB treatment; however, the risk of hyperkalaemia appeared to be similar for ARB and CCB treatments.

Indexed as

HyperkalemiaAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsHumansPotassiumRetrospective StudiesAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsPotassiumclinical medicinedrug monitoringdrug-related side effects and adverse reactionshospitalpharmacy administrationpharmacy service

Identifiers

PMID34183459
PMCPMC10359795
OpenAlexW3174639079

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.