What's the difference????

  1. 0
    Can anyone please tell me the difference between dopamine, dobutamine, levophed, epinephrine, and neosynephrine? Know that dopamine has renal action up to 2mcg's; above that stimulates beta-1 and alpha-adrenergic receptors (positive inotropic and chronotropic effects); dobutamine is a pure beta-1 agonist (inotrope with mild chronotropic effects); levophed (norepinephrine) is a potent alpha-receptor agonist causing peripheral vasoconstriction, with minimal effect on beta receptors, and a positive inotrope (dilates coronary arteries), while at the same time increases myocardial oxygen demand and may therefore decrease cardiac output; epinephrine has both alpha and beta adrenergic activity (increases systemic vascular resistance, B/P, and heart rate); and neosynephrine is an alpha agonist, useful in septic shock. Please, please, please, all you experienced critical care nurses, relate your own perceptions and experiences with these drugs. Differences that just aren't found in the drug book. THANKS!!!!!
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  4. 2 Comments so far...

  5. 0
    Healingtouch
    We don't use levophed very much but see a lot of dopamine and dobutamine. The 2mcg renal dose of dopa dosen't seem to really have any effects on renal output and perfusion. Most often it's a small blood preassure increase that I've noticed...if anything at all. My main concern with dopa is that it not go in a peripheral line. Dobutamine patients seem to show more PVC's the longer they're on it. Epi is mainly used in emergent situations on our unit but is used as a bronchodilator at times. Some patients can get panicky and shaky when taking it. The more frail patients are prone to SVT. Hope some of this helps.
  6. 0
    i'm not really sure if you are asking the therapeutic uses of these drugs, but as you already know what receptors they hit, that is where i will focus.

    dopamine: for shock can increase cardiac output thereby increasing tissue perfusion, dilates the renal blood vessels improving renal perfusion and decreases the risk of renal failure.
    for heart failure, it increases cardiac output by increasing myocardial contractility. indicated for the management of cardiogenic and circulatory shock.

    dobutamine: in heart failure increases myocardial contractility and improves cardiac performance. since it does not activate alpha 1 receptor, it doesn't increase vascular resistance. it is generally preferred over dopamine in the short-term treatment of chf.

    epinephrine: this is used to delay the absorption of local anesthetics, control superficial bleeding, decrease nasal congestion and elevate bp, overcome a-v block (unknown what degree), and restore cardiac function in patients who have arrested. it is also the treatment of choice for anaphylactic shock. this drug is much more potent than dopamine, so the effective dosing range is less than that of dopamine.

    levophed (norepinephrine): although similar to epinephrine, it has limited clinical applications: hypotensive states and cardiac arrest
    cardiac output is increased only at low doses. with high doses, the cardiac output decreases in response to the vasoconstriction and increased afterload ( stress or tension placed on the ventricular wall during systole).

    i'm sorry that i wasn't able to find information about neo...i have seen it used in a hypovolemic shock situation where we weren't able to raise the blood pressure with volume via iv. in this particular person, the bp raised for maybe 5 minutes before it dropped off again. i think that the doctor's really expected that he would be dry (he had a perforated gallbladder that was necrotic, and they removed 2+ liters of bile from the peritineum).

    my sources for this information was the icu book, second edition by paul marino (i refer to this all the time, it is very helpful if you are a new ccu rn). i also used the second edition of pharmacology for nursing care by richard lehne, linda moore, leena crosby, and diane hamilton. i hope that this helps.
    teri.

    p.s. the gentlemen that i took care of with the gallbladder did live, was sent to another hospital for more invasive monitoring than my hospital is able to do and walked back in to see us.
    Last edit by tlmagraw2 on Jan 30, '02


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