Evidence map›Paper›PMID 37810894›Full record

SynthesisFrontiers in endocrinology2023

Should we suspect primary aldosteronism in patients with hypokalaemic rhabdomyolysis? A systematic review.

Everardo Josué Díaz-López, Rocio Villar-Taibo, Gemma Rodriguez-Carnero, Antia Fernandez-Pombo, Roberto Garcia-Peino, Manuel Narciso Blanco-Freire, Alberto Pena-Dubra, Teresa Prado-Moraña, Irea- Fernández-Xove, Edurne Pérez-Béliz and 3 more

Open access · goldAbstract readCase ReportsSystematic Review
In one paragraph

Synthesis in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. 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

13 authors at 2 institutions in 1 country.

Everardo Josué Díaz-LópezDivision of Endocrinology and Nutrition, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Rocio Villar-TaiboDivision of Endocrinology and Nutrition, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Gemma Rodriguez-CarneroDivision of Endocrinology and Nutrition, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Antia Fernandez-PomboDivision of Endocrinology and Nutrition, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Roberto Garcia-PeinoDivision of Endocrinology and Nutrition, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Manuel Narciso Blanco-FreireDivision of Surgery, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Alberto Pena-DubraDivision of Endocrinology and Nutrition, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Teresa Prado-MorañaDivision of Endocrinology and Nutrition, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Irea- Fernández-XoveDivision of Endocrinology and Nutrition, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Edurne Pérez-BélizDivision of Pathology, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Jose Manuel Cameselle-TeijeiroDivision of Pathology, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Alvaro Hermida-AmeijeirasDivision of Internal Medicine, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Miguel Angel Martinez-OlmosDivision of Endocrinology and Nutrition, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Universidade de Santiago de Compostela · ESCenter for Research in Molecular Medicine and Chronic Diseases · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe hypokalaemia causing rhabdomyolysis (RML) in primary aldosteronism (PA) is a rare entity, and only a few cases have been reported over the last four decades. This systematic review and case report aims to gather all published data regarding a hypokalaemic RML as presentation of PA in order to contribute to the early diagnosis of this extremely rare presentation. With the use of PubMed Central, EMBASE, and Google Scholar, a thorough internet-based search of the literature was conducted to identify articles and cases with RML secondary to hypokalaemia due to PA between June 1976 and July 2023. The case study concerns a 68-year-old male patient with hypokalaemic RML at presentation of PA. In the systematic review of the literature, 37 cases of RML secondary to hypokalaemia due to PA have been reported to date. In summary, the median age was 47.5 years, the male/female ratio was 17/21, all patients presented symptoms (weakness and/or myalgia), all the patients were hypertensive, and only four patients had complications with acute kidney injury (AKI). Although PA rarely presents with RML, it should be suspected when marked hypokalaemia and hypertension are also present. Early detection and management are essential to reduce the frequency of manifestations such as AKI.

Indexed as

Acute Kidney InjuryHyperaldosteronismHypertensionHypokalemiaRhabdomyolysisAgedFemaleHumansMaleMiddle Agedacute kidney injuryhypokalaemiahypokalaemic rhabdomyolysisprimary aldosteronismrhabdomyolysis

Identifiers

PMID37810894
PMCPMC10558179
OpenAlexW4386967923

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.