Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 2012 Oct;27(5):447-53.
doi: 10.1016/j.jcrc.2011.10.009. Epub 2012 Jan 4.

Prehospital amiodarone may increase the incidence of acute respiratory distress syndrome among patients at risk

Collaborators, Affiliations
Clinical Trial

Prehospital amiodarone may increase the incidence of acute respiratory distress syndrome among patients at risk

Lioudmila V Karnatovskaia et al. J Crit Care. 2012 Oct.

Abstract

Purpose: Amiodarone has been implicated as a risk factor for acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) when used in the hospital. This study aims to estimate whether prehospital amiodarone also increases the risk of ALI/ARDS.

Materials: Adult patients admitted to 22 centers with at least 1 risk factor for developing ALI were recruited. In a secondary analysis of this cohort, the prehospital use of amiodarone was documented on admission, and the patients followed for the primary outcome of ALI and secondary outcomes of ARDS, the need for invasive ventilation, and mortality. Dose/duration of amiodarone therapy was not available. Propensity matching was performed to account for imbalances in being assigned to amiodarone. The adjusted risk for ALI/ARDS was then estimated from a conditional logistic regression model of this propensity-matched set.

Results: Forty of 5584 patients were on amiodarone at the time of hospitalization; of those, 6 developed ALI, with 5 progressing to ARDS. In comparison, 371 patients not on amiodarone developed ALI, with 224 having ARDS. After propensity score matching, the prehospital use of amiodarone was not statistically associated with an increased risk for all ALI (odds ratio [OR], 1.8; 95% confidence interval [CI], 0.7-5.0; P = .25), invasive ventilation (OR, 1.9; 95% CI, 1.0-3.6; P = .059), or in-hospital mortality (OR, 1.2; 95% CI, 0.5-2.9; P = .75); but its use appeared to significantly increase the risk for ARDS (OR 3.8; 95% CI, 1.1-13.1; P = .036).

Conclusions: Prehospital use of amiodarone may independently increase the risk for ARDS in patients who have at least 1 predisposing condition for ALI.

PubMed Disclaimer

Conflict of interest statement

Conflicts of interest: none of the authors have conflicts of interest to report.

Figures

Fig. 1
Fig. 1
Frequency of ALI/ARDS in patients on amiodarone and remaining cohort.
Fig. 2
Fig. 2
Amiodarone and the adjusted risk for respiratory complications after propensity matching. Prehospital use of amiodarone did not significantly increase the risk for all ALI or invasive ventilation but did suggest a significant increase in risk for ARDS. The risk of in-hospital mortality was not increased (see Table 2 for specific numeric figures).

References

    1. Papiris SA, Triantafillidou C, Kolilekas L, et al. Amiodarone: review of pulmonary effects and toxicity. Drug Saf. 2010;33(7):539–558. - PubMed
    1. Ashrafian H, Davey P. Is amiodarone an underrecognized cause of acute respiratory failure in the ICU? Chest. 2001;120(1):275–282. - PubMed
    1. Rotmensch HH, Liron M, Tupilski M, et al. Possible association of pneumonitis with amiodarone therapy. Am Heart J. 1980;100(3):412–413. - PubMed
    1. Darmanata JI, van Zandwijk N, Düren DR, et al. Amiodarone pneumonitis: three further cases with a review of published reports. Thorax. 1984;39(1):57–64. - PMC - PubMed
    1. Ott MC, Khoor A, Leventhal JP, et al. Pulmonary toxicity in patients receiving low-dose amiodarone. Chest. 2003;123(2):646–651. - PubMed

Publication types