# Utility of inhaled β2-agonists in reducing serum potassium levels in adult patients with hyperkalemia: A scoping review

**Authors:** Leonardo Arzayus-Patiño, Ashley Y. Hinojosa-Angulo, Karen A. Rodríguez-Angulo, Michelle A. Sánchez-Caicedo, Vicente Benavides-Córdoba

PMC · DOI: 10.1371/journal.pone.0342309 · PLOS One · 2026-02-03

## TL;DR

This review explores how inhaled β2-agonists like salbutamol can quickly lower high potassium levels in adults, offering a useful option in emergency settings.

## Contribution

The study systematically evaluates the effectiveness and safety of inhaled β2-agonists for acute hyperkalemia management.

## Key findings

- Nebulized salbutamol reduced serum potassium by 0.62 to 1.636 mEq/L within 1-4 hours.
- Adverse effects like tachycardia and mild hyperglycemia were manageable and common.
- Effectiveness was observed in both patients with chronic kidney disease and those with normal renal function.

## Abstract

Hyperkalemia is a potentially life-threatening condition that requires prompt intervention to prevent cardiac complications. While insulin and glucose administration remains a cornerstone of treatment, inhaled β2-adrenergic agonists have been proposed as a complementary or alternative strategy, particularly in emergency settings. This scoping review aimed to describe the utility of inhaled β2-agonists in lowering serum potassium levels in adult patients.

A scoping review was conducted following the PRISMA-ScR guidelines and the Joanna Briggs Institute methodology. Experimental studies published within the past ten years evaluating the use of inhaled β2-agonists in adult patients with hyperkalemia were included. Five studies were analyzed (three randomized controlled trials and three quasi-experimental studies), assessing dosage, route of administration, magnitude of potassium reduction, and reported adverse events.

Most studies used nebulized salbutamol at a dose of 10 mg, with observed reductions in serum potassium ranging from 0.62 to 1.636 mEq/L, and a peak effect between 1 and 4 hours post-administration. One study also reported the use of levalbuterol. The most common adverse effects were tachycardia, dizziness, and mild hyperglycemia, all of which were clinically manageable. Efficacy was demonstrated in both patients with chronic kidney disease and in individuals with normal renal function.

Inhaled β2-agonists, particularly nebulized salbutamol, represent an effective and safe therapeutic option for the acute reduction of serum potassium in adults with hyperkalemia. Their rapid onset of action and applicability across various patient profiles make them a valuable tool in emergency settings, especially where immediate access to advanced therapies such as dialysis is limited. Further research is warranted to evaluate long-term outcomes, safety in patients with cardiovascular comorbidities, and optimal dosing strategies.

## Linked entities

- **Chemicals:** salbutamol (PubChem CID 2083), levalbuterol (PubChem CID 123600)
- **Diseases:** chronic kidney disease (MONDO:0005300)

## Full-text entities

- **Genes:** ADRB2 (adrenoceptor beta 2) [NCBI Gene 154] {aka ADRB2R, ADRBR, ARB2, B2AR, BAR, BETA2AR}, BDKRB1 (bradykinin receptor B1) [NCBI Gene 623] {aka B1BKR, B1R, BKB1R, BKR1, BRADYB1}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, IGKV5-2 (immunoglobulin kappa variable 5-2) [NCBI Gene 28907] {aka B2, IGKV52}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, BDKRB2 (bradykinin receptor B2) [NCBI Gene 624] {aka B2R, BK-2, BK2, BKR2, BRB2}
- **Diseases:** hyperglycemia (MESH:D006943), tachycardia (MESH:D013610), AKI (MESH:D058186), rhabdomyolysis (MESH:D012206), hypoglycemia (MESH:D007003), cardiac arrest (MESH:D006323), conditions (MESH:D020763), DeCS - MESH (MESH:C535675), fatigue (MESH:D005221), Hyperkalemia (MESH:D006947), acute respiratory failure (MESH:D012131), muscle cramps (MESH:D009120), cardiovascular adverse effects (MESH:D002318), acid-base disorders (MESH:D000137), abnormalities (MESH:D000014), COPD (MESH:D029424), hypokalemic (MESH:D020514), hypokalemia (MESH:D007008), metabolic disturbances (MESH:D024821), diabetes (MESH:D003920), cardiac electrical disturbances (MESH:D004556), crush injury (MESH:D000071576), Headache (MESH:D006261), muscle weakness (MESH:D018908), dizziness (MESH:D004244), bronchospasm (MESH:D001986), adrenal insufficiency (MESH:D000309), anxiety (MESH:D001007), cardiac complications (MESH:D006331), hyperglycemic (MESH:D006944), renal dysfunction (MESH:D007674), arrhythmia (MESH:D001145), muscle tremors (MESH:D014202), myocardial ischemia (MESH:D017202), unstable angina (MESH:D000789), CKD (MESH:D051436), acute myocardial infarction (MESH:D009203)
- **Chemicals:** dextrose (MESH:D005947), levalbuterol (MESH:D064412), sodium (MESH:D012964), beta2- (-), calcium gluconate (MESH:D002125), cAMP (MESH:D000242), ATP (MESH:D000255), oxygen (MESH:D010100), fenoterol (MESH:D005280), Potassium (MESH:D011188), Albuterol (MESH:D000420), sodium polystyrene sulfonate (MESH:C003321), terbutaline (MESH:D013726), blood glucose (MESH:D001786), aldosterone (MESH:D000450)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12867269/full.md

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Source: https://tomesphere.com/paper/PMC12867269