Tools for Practice Outils pour la pratique


#213 Smell This: Isopropyl alcohol for nausea/vomiting in the emergency department


CLINICAL QUESTION
QUESTION CLINIQUE
Can inhaled isopropyl alcohol be used to treat nausea/vomiting in the emergency department?


BOTTOM LINE
RÉSULTAT FINAL
Two trials with ~200 non-pregnant adults presenting to emergency found inhaled (smelling) isopropyl alcohol improved mild-moderate nausea/vomiting. For example, after 30 minutes nausea improved from 50 out of 100 down to 20 with inhaled isopropyl alcohol versus 40 with oral ondansetronOnly one study reported adverse events and found none



CFPCLearn Logo

Reading Tools for Practice Article can earn you MainPro+ Credits

La lecture d'articles d'outils de pratique peut vous permettre de gagner des crédits MainPro+

Join Now S’inscrire maintenant

Already a CFPCLearn Member? Log in

Déjà abonné à CMFCApprendre? Ouvrir une session



EVIDENCE
DONNÉES PROBANTES
Two blinded, emergency department, Randomized Controlled Trials (RCTs).  
  • 122 non-pregnant adults with mild-moderate nausea/vomiting (majority infectious gastroenteritis), randomize(with matching placebos) to inhaled isopropyl alcohol, ondansetron, or both.1   
    • At 30 minutes, statistically significant reduction in nausea score: From a baseline of ~50 on a 100-point scale, nausea decreased to 40 with ondansetron versus 20 with inhaled isopropyl alcohol.   
    • Other outcomes:  
      • Patient satisfaction scores on 100-point scale (lower score=more satisfied): ~20 for inhaled isopropyl alcohol versus 44 for ondansetron. 
      • Trend to fewer rescue antiemetics with inhaled isopropyl alcohol (~26% versus 45%). If real, Number Needed to Treat (NNT)=6. 
      • No difference: ED length of stay, vomiting rates. 
    • There were no adverse effects.  
    • Limitations: Possible selection bias, single centre military hospital, up to 60% of patients on inhaled isopropyl alcohol able to identify their treatment group. 
  • 84 patients randomized to inhaled isopropyl alcohol or saline-soaked pads (placebo).  Baseline nausea score=6/10. At 10 minutes:2 
    • Lower median nausea score: 6 (placebo) versus 3, statistically different. 
    • Improved patient satisfaction (out of 5, higher more satisfied): 2 (placebo) versus 4. 
    • No difference in number receiving antiemetic or serious adverse effects.   
Context: 
  • Patients inhaled deeply as frequently as required to achieve nausea relief from commercially available isopropyl alcohol pad held 1-2 cm below nares.1 
  • Recent systematic review found no evidence to support any one pharmacologic treatment over another in ED for nausea.3 
  • Ondansetron costs ~$4 per tablet.4 
  • Systematic review of four RCTs (215 patients)5 of inhaled isopropyl alcohol for post-operative nausea found fewer patients required rescue antiemetics versus standard therapy (26% versus 39% placebo), NNT=8. Other outcomes inconsistent and adverse effects not reported. 


Latest Tools for Practice
Derniers outils pour la pratique

#378 Tony Romo-sozumab: Winning touchdown in osteoporosis or interception for the loss?

What is the efficacy and safety of romosozumab in postmenopausal women with osteoporosis?
Read Lire 0.25 credits available Crédits disponibles

#377 How to slow the flow IV: Combined oral contraceptives

In premenopausal heavy menstrual bleeding due to benign etiology, do combined oral contraceptives (COC) improve patient outcomes?
Read Lire 0.25 credits available Crédits disponibles

#376 Testosterone supplementation for cis-gender men: Let’s (andro-)pause for a moment (Update)

What are the benefits and harms of testosterone supplementation in healthy cis-gender men or those with age-related low testosterone?
Read Lire 0.25 credits available Crédits disponibles

This content is certified for MainPro+ Credits, log in to access

Ce contenu est certifié pour les crédits MainPro+, Ouvrir une session


Author(s)
Auteur(s)
  • Adrienne J Lindblad BSP ACPR PharmD
  • Kevin Harris MD CCFP(EM)

1. April MD, Oliver JJ, Davis WT, et al. Ann Emerg Med. 2018 Feb 17. pii: S0196-0644(18)30029-5. [Epub ahead of print].

2. Beadle KL, Helbling AR, Love SL, et al. Ann Emerg Med. 2016 Jul; 68(1):1-9.e1. [Epub 2015 Dec 8].

3. Furyk JS, Meek RA, Egerton-Warburton D. Cochrane Database Syst Rev. 2015 Sep 28; (9):CD010106.

4. Nickonchuk T, Lee J, Kolber MR, et al. Available from: https://www.acfp.ca/wp-content/uploads/2018/03/ACFPPricingDoc2018.pdf. Last Accessed: May 15, 2018.

5. Hines S, Steels E, Chang A, et al. Cochrane Database Syst Rev. 2018; (3):CD007598.

Authors do not have any conflicts of interest to declare.

Les auteurs n’ont aucun conflit d’intérêts à déclarer.