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Adrenergic agonists have diverse therapeutic uses across various medical conditions and emergencies.
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Mixed-action adrenergic agonists, like ephedrine and pseudoephedrine, directly and indirectly affect adrenergic receptors. These agents stimulate adrenoceptors and indirectly release stored neurotransmitters, amplifying the adrenergic response.
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The enteral drug administration involves three primary routes: oral, sublingual, and buccal. Oral ingestion is the most prevalent, safe, economical, and convenient method for drug administration. However, it has certain drawbacks, including limited absorption due to the drug's low water solubility or poor membrane permeability, possible emesis from GI mucosa irritation, destruction of drugs by digestive enzymes or low gastric pH, and irregular absorption along with food or other drugs.
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Food-induced anaphylaxis in educational settings: Data from the European anaphylaxis registry.

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Alternatives to Injectable Adrenaline for Treating Anaphylaxis.

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  • 1Service de Pédiatrie, Pavillon Médicochirurgical de Pédiatrie, Boulevard Lacordaire, Roubaix, France.

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PubMed
Summary

New adrenaline nasal sprays offer an alternative to auto-injectors for anaphylaxis treatment. These innovative devices may improve medication use and effectiveness, addressing limitations of current adrenaline auto-injectors (AAI).

Keywords:
adrenalineallergyanaphylaxisauto‐injectorsnasalsublingual

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Area of Science:

  • Allergy and Immunology
  • Pharmacology
  • Medical Devices

Background:

  • Anaphylaxis requires immediate adrenaline treatment.
  • Adrenaline auto-injectors (AAI) are standard but have limitations hindering use.
  • Alternative administration routes are being explored to improve anaphylaxis management.

Purpose of the Study:

  • To review limitations of AAIs in anaphylaxis treatment.
  • To summarize data on novel adrenaline delivery devices using alternative routes.
  • To discuss the potential of non-injectable adrenaline for anaphylaxis.

Main Methods:

  • Literature review of AAI limitations and barriers.
  • Summary of pharmacokinetic, pharmacodynamic, and safety data for alternative adrenaline devices.
  • Analysis of approved non-injectable adrenaline devices.

Main Results:

  • AAIs have significant limitations leading to underuse.
  • Novel devices for nasal, sublingual, and transcutaneous adrenaline delivery are in development.
  • The first non-injectable adrenaline device (nasal spray) is approved for specific patient groups.

Conclusions:

  • Non-injectable adrenaline devices show promise for improving anaphylaxis treatment.
  • These innovations may overcome some AAI limitations, potentially increasing adrenaline use.
  • Multiple alternatives to injectable adrenaline are expected soon, enhancing anaphylaxis care.