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Alpha-2 Adrenergic and Imidazoline Receptor Agonists: Clonidine, Dexmedetomidine, and Related Antihypertensives, Decongestants, and Sedatives

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Abstract

Since the introduction of the imidazoline derivative clonidine, a topical nasal decongestant, in 1962, the number of agents in its class and the indications for their use have expanded greatly. Thousands of cases of clonidine exposure are reported to US poison centers annually (over 9700 exposures in 2014) with nearly 1 in 5 coded as resulting in moderate or major effect [1]. Exposures to guanfacine and other imidazolines increase the magnitude of the problem of alpha agonist exposures.

This is an update of a chapter written with Kevin L. Wallace in the first edition of this text.

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Correspondence to Anthony J. Tomassoni .

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Grading System for Levels of Evidence Supporting Recommendations in Critical Care Toxicology, 2nd Edition

  1. I

    Evidence obtained from at least one properly randomized controlled trial.

  2. II-1

    Evidence obtained from well-designed controlled trials without randomization.

  3. II-2

    Evidence obtained from well-designed cohort or case–control analytic studies, preferably from more than one center or research group.

  4. II-3

    Evidence obtained from multiple time series with or without the intervention. Dramatic results in uncontrolled experiments (such as the results of the introduction of penicillin treatment in the 1940s) could also be regarded as this type of evidence.

  5. III

    Opinions of respected authorities, based on clinical experience, descriptive studies and case reports, or reports of expert committees.

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Tomassoni, A.J. (2017). Alpha-2 Adrenergic and Imidazoline Receptor Agonists: Clonidine, Dexmedetomidine, and Related Antihypertensives, Decongestants, and Sedatives. In: Brent, J., et al. Critical Care Toxicology. Springer, Cham. https://doi.org/10.1007/978-3-319-17900-1_27

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