Related Experiment Video
Updated: Jun 18, 2025

09:47
A Rat Model of Ventricular Fibrillation and Resuscitation by Conventional Closed-chest Technique
Published on: April 26, 2015
15.9K
Reevaluating the epinephrine myth: A comprehensive review.
Sreeganesh Krishnaprabhu1, Joe M Das2
1Department of Orthopedic Surgery, Fatima Hospital, Kochi, Kerala, India.
Indian Journal of Pharmacology
|July 30, 2024
Summary
Local anesthesia with epinephrine is generally safe for acral areas, despite past concerns. A review found few necrosis cases, highlighting the need for careful patient selection and adherence to guidelines.
Area of Science:
- Anesthesiology
- Plastic Surgery
- Dermatology
Background:
- Historically, epinephrine in local anesthesia was contraindicated in acral regions due to necrosis risk.
- Recent studies since 2001 challenge this contraindication, suggesting safety and efficacy.
Purpose of the Study:
- To review and analyze reported cases of acral necrosis after local anesthesia with epinephrine since 2001.
- To assess the current understanding of risks and benefits associated with epinephrine use in acral local anesthesia.
Main Methods:
- Systematic literature search on PubMed and Google Scholar.
- Inclusion of articles reporting acral necrosis following local anesthesia with epinephrine.
Main Results:
- Eight publications identified 13 cases of ischemic events in acral areas.
- Cases included finger (5), scrotal (2), and eyelid (6) necrosis after lignocaine with epinephrine.
- Most affected patients were female undergoing surgical reconstruction.
Conclusions:
- Epinephrine in local anesthesia offers benefits and is generally safe for acral areas.
- Necrosis risk, though low, persists, especially in patients with vascular compromise.
- Proper patient selection, adherence to guidelines, and phentolamine as a rescue agent can mitigate risks.
Related Concept Videos
Adrenergic Agonists: Therapeutic Uses
759
Adrenergic agonists have diverse therapeutic uses across various medical conditions and emergencies.
Emergency and Intensive Care Unit (ICU) applications: Pressor agents increase blood pressure, heart rate, and contractility in shock and organ failure situations. Dopamine can induce vasodilation and stimulate adrenoceptors. Endogenous catecholamines are effective in treating cardiogenic shock. α2-agonists like clonidine can reverse anesthesia-induced hypertension.
Allergies and...
Emergency and Intensive Care Unit (ICU) applications: Pressor agents increase blood pressure, heart rate, and contractility in shock and organ failure situations. Dopamine can induce vasodilation and stimulate adrenoceptors. Endogenous catecholamines are effective in treating cardiogenic shock. α2-agonists like clonidine can reverse anesthesia-induced hypertension.
Allergies and...
759
Adrenergic Neurons: Neurotransmission
3.5K
Postganglionic sympathetic fibers (except those supplying the sweat glands) releasing noradrenaline or norepinephrine are called noradrenergic or adrenergic neurons. Noradrenaline, dopamine, adrenaline, or epinephrine are collectively called "catecholamines" as they contain a catechol moiety and an amine side chain. The five stages of neurotransmitter release involve their synthesis, storage, release, reuptake and metabolism.
Synthesis: Catecholamine synthesis requires tyrosine, which...
Synthesis: Catecholamine synthesis requires tyrosine, which...
3.5K
Adrenergic Agonists: Mixed-Action Agents
698
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.
Ephedrine and pseudoephedrine lack a catecholamine group, making them less susceptible to degradation by metabolic enzymes. They have increased oral bioavailability and lipophilicity, resulting in a longer duration of action. Their response is reduced by...
Ephedrine and pseudoephedrine lack a catecholamine group, making them less susceptible to degradation by metabolic enzymes. They have increased oral bioavailability and lipophilicity, resulting in a longer duration of action. Their response is reduced by...
698
Allergic Reactions
27.3K
Overview
27.3K
Adrenergic Receptors: β Subtype
1.6K
β-adrenoceptors have varied sensitivities towards adrenaline, noradrenaline, and isoprenaline. The order of agonist potency is as follows:
Isoprenaline > Adrenaline > Noradrenaline
Neurotransmitter binding to these receptors causes activation of adenylyl cyclase resulting in increased concentrations of cAMP and modulation of calcium ion channels within the cell. They are further classified into β1, β2, and β3 subtypes.
β1-adrenoceptors: β1-adrenoceptors...
Isoprenaline > Adrenaline > Noradrenaline
Neurotransmitter binding to these receptors causes activation of adenylyl cyclase resulting in increased concentrations of cAMP and modulation of calcium ion channels within the cell. They are further classified into β1, β2, and β3 subtypes.
β1-adrenoceptors: β1-adrenoceptors...
1.6K
Anatomy of the Adrenal Glands
2.1K
The adrenal or supra-renal glands, situated above the kidneys and aligned with the twelfth rib, are paired pyramid-shaped structures crucial for the body's stress response. During stress, these glands secrete hormones vital for adaptive physiological reactions.
These glands possess a distinctive yellow tinge due to the stored cholesterol and fatty acids required for hormone synthesis. They are encased in a fibrous capsule and cushioned by fat.
The adrenal gland comprises two distinct...
These glands possess a distinctive yellow tinge due to the stored cholesterol and fatty acids required for hormone synthesis. They are encased in a fibrous capsule and cushioned by fat.
The adrenal gland comprises two distinct...
2.1K

