Meperidine, available as hydrochloride salt, is a narcotic analgesic, a classification term used to describe medications capable of producing a reversible depression of the central nervous system for pain control. Because of its potential for physical and psychological dependence, meperidine is a carefully controlled substance. It is commonly referred to by one of its brand names, Demerol.
There are several possible indications for the administration of meperidine. It is commonly used for the relief of moderate to severe pain, particularly in obstetrics. Meperidine is also widely used preoperatively, and as an adjunct to anesthesia during surgery. Meperidine is not recommended for long-term management of chronic pain, such as pain caused by cancer, because of its potential for psychological and physical dependence.
Meperidine is a synthetic compound that acts as an agonist—meaning it attaches to opioid receptors in the central nervous system and stimulates physiologic activity normally stimulated by naturally occurring substances such as endorphins (short for endogenous morphine). Meperidine acts much like morphine, although constipation, suppression of the cough reflex, and smooth muscle spasm are all reduced with meperidine.
Meperidine is available in a banana-flavored syrup, in a tablet, and in a liquid form for injection. Oral meperidine tends to be less effective than the injectable form. When taking the syrup, patients should dilute it with approximately one half glass of water to reduce temporary anesthesia to the mouth and tongue.
The recommended dosage of meperidine depends on the purpose for which it is prescribed, as well as the population in whom it is administered. For example, elderly patients, or patients with underlying medical problems that increase side effects or decrease drug metabolism, should generally be given reduced dosages. Meperidine can be taken orally, in tablet or syrup form, intravenously (directly into a vein), or by injection into the muscle (intramuscularly) or connective tissue (subcutaneously).
Generally, repeated doses administered to manage pain should be given by injection intramuscularly. The subcutaneous route is acceptable for occasional administration. When given intravenously, meperidine should be diluted and administered very slowly. When taken in conjunction with phenothiazine or other tranquilizers, the dose should be decreased by as much as a half. Specific dosages are as follows.
The recommended dosage for adults for pain relief is 50-150 mg every three to four hours by oral or intramuscular route. When given intravenously through a patient-controlled analgesia (PCA) device, an initial dose of 10 mg should be administered. The PCA should be programmed to administer between 1-5 mg every 6-10 minutes. If meperidine is given continuously through an intravenous line, the dose should be adjusted based on patient response to a range of 15-35 mg an hour. Children should be given 1-1.8 mg per kg (2.2 pounds) intramuscularly or subcutaneously.
Adults may be given 50-100 mg of meperidine intramuscularly, or subcutaneously 30-90 minutes prior to surgery. Children's dosages should be reduced to 1-2 mg per kg through the same routes.
For obstetric pain control. The recommended dosage for control of regular (not sporadic) pain in this setting is 50-100 mg every 1-3 hours intramuscularly or subcutaneously.
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Author Info: Tamara Brown R.N., The Gale Group Inc., Gale, Detroit, Gale Encyclopedia of Cancer, 2002 |