Skip to main content

Response to Cocaine,TCA,Opiates overdose




Your response to Cocaine overdose:

Drug induced hypertensive emergencies are often short lived, and often aggressive therapy is not needed. Cocaine in particular is noted to be associated with hypertension, ventricular arryhthmias, and acute coronary syndromes.

The important key to the treatment of this toxicity is avoiding the use of beta blockers (Class III), especially nonselective agents such as propranolol, as this allows for unopposed alpha adrenergic stimulation and worsening of the hypertension.

Benzodiazepines (Class IIa) in addition to a short acting, titrateable antihypertensive such as nitrates (Class I) should be the first line of therapy. Should the hypertension be refractory, the use of alpha adrenergic blocking agents (Class IIb) may be considered, keeping in mind that tachycardia and hypotension may result .

Your response to tricyclic overdose

Tricyclic antidepressants (TCA) are sodium channel blockers that may result in prolongation of ventricular conduction (increases the PR and QT intervals) and ultimately monomorphic VT . The most common clinical features are dry mouth, blurred vision, dilated pupils, sinus tachycardia, pyramidal neurological signs, and drowsiness.

As these patient are often hypoxemic and acidotic, respiratory alkalosis can be induced as a temporizing measure, until the drug of choice sodium bicarbonate (Class IIa) can be used.

Convulsions should be treated with diazepam.

 Hypotension should be treated by fluid replacement and sympathomimetic agents (dopamine or dobutamine) if necessary.

Although physostigmine salicylate can reverse most of the features of TCA poisoning, its effects are short-lived in serious toxicity and it can produce significant side effects. As such, physostigmine should be reserved for those patients who have complications of coma or who have resistant cardiotoxicity or convulsions.

Your response to Opioids overdose

If a pulse exists in patients with respiratory insufficiency suspected of an opiate overdose, naloxone should be administered, either intramuscularly, subcutaneously, or intravenously.

IM and SC routes may provide less risk of severe withdrawal in patients addicted to IV narcotics.

The initial dose of naloxone in 0.4-0.8 mg IV or 0.8 mg IM or SC and should be given to the desired endpoint of adequte airway reflexes and ventilation .

The goal of complete arousal is not recommended, as the abrupt withdrawal from opiates may increase such complications as pulmonary edema, ventricular arrhythmias, and severe agitation .

Comments

Popular posts from this blog

The 100 essentials in icu and anesthesia

The most visual experience in anesthesia and critical care education  The 100 essentials of anesthesia and critical care  COMING VERY SOON  stay tuned 

Driving Pressure in ARDS: A new concept!

Driving Pressure and Survival in the Acute Respiratory Distress Syndrome Marcelo B.P. Amato, M.D., Maureen O. Meade, M.D., Arthur S. Slutsky, M.D., Laurent Brochard, M.D., Eduardo L.V. Costa, M.D., David A. Schoenfeld, Ph.D., Thomas E. Stewart, M.D., Matthias Briel, M.D., Daniel Talmor, M.D., M.P.H., Alain Mercat, M.D., Jean-Christophe M. Richard, M.D., Carlos R.R. Carvalho, M.D., and Roy G. Brower, M.D. N Engl J Med 2015; 372:747-755 February 19, 2015 DOI: 10.1056/NEJMsa1410639 BACKGROUND Mechanical-ventilation strategies that use lower end-inspiratory (plateau) airway pressures, lower tidal volumes (V T ), and higher positive end-expiratory pressures (PEEPs) can improve survival in patients with the acute respiratory distress syndrome (ARDS), but the relative importance of each of these components is uncertain. Because respiratory-system compliance (C RS ) is strongly related to the volume of aerated remaining functional lung during disease (termed functional lung size)...