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Protocols - Hemorio

Protocols - Hemorio

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AVOID IN CHRONIC SUBJECTS:<br />

Meperidine: the chronic use leads to an accumulation of metabolic that is neurotoxic, and causes delirium<br />

and convulsion.<br />

Partial agonist (e.g.: buprenorphine): has lesser effect at the opioid receptor than the pure agonist and has<br />

a maximum effect.<br />

Agonist-antagonist (nalbufine, pentazocina), they block or are neutral in one kind of opioid receptor while<br />

they activate another receptor; it has a high incidence of psychomimetic effects and may cause abstinence<br />

syndrome.<br />

SPECIFICITIES OF EACH OPIATE:<br />

CODEINE When in association to acetaminophen, the maximum dose is 360 mg/day (6<br />

takes of 60 mg), in order not to overtake the maximum dose of acetaminophen,<br />

TRAMADOL<br />

HYDROCHLORIDE<br />

capsule (50mg)<br />

drops (100mg/ml)<br />

suppository and (100<br />

mg)<br />

ampule (50 and<br />

100mg)<br />

NALBUFINE<br />

HYDROCHLORIDE<br />

ampule 1 and 2ml<br />

(1 ml = 10mg of<br />

nalbufine<br />

hydrochloride)<br />

BUPRENORPHINE<br />

HYDROCHLORIDE<br />

ampule 1ml<br />

(0.3mg of<br />

buprenorphine<br />

hydrochloride)<br />

Sublingual tablet (0.2<br />

mg)<br />

that may be harmful to the renal function.<br />

- It presents an analgesic effect for about 6 to 8 h. By parenteral path, 100 mg<br />

are injected via IM or 100 mg IV, slowly, diluted in a saline solution or<br />

glycolated serum.<br />

- For the maintenance of the effect, dilute 2 ampules of 100 mg of Tramadol<br />

Hydrochloride in 500 ml of glycolated or physiological serum, keeping the<br />

dripping at 10 to 20 drops / minute or at an infusion pump 30 to 60 ml/h.<br />

- It is not a pure agonist, it also presents an analogous antagonist effect to<br />

naloxone. It is not recommended for subjects with oncologic pain that have<br />

used another opioid previously, because it can cause abstinence syndrome.<br />

- It must be prescribed the dosage of 10 mg every 3 or 4 h, by parenteral path.<br />

In children, the dose of 0.1mg/kg, by parenteral path, every 3 or 4 h.<br />

- It presents an agonist and antagonist effect. It is a partial agonist.<br />

- It has a maximum effect above 1.2 mg. It may precipitate the abstinence<br />

syndrome in subjects who use another opioid chronically.<br />

- Usually, the opioid agonists are preferred, such as codeine, morphine,<br />

methadone, fentanil, oxycodone, hydromorphine (not yet AVAILABLE in<br />

Brazil). Its effectiveness is not limited by the maximum effect when we increase<br />

the dosage. In addition, the agonists do not antagonize or reverse the effect of<br />

other agonists if we need to use both drugs, what the partial agonists or the<br />

agonists-antagonists do.<br />

203

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