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Pharm Pain
| Question | Answer |
|---|---|
| nociception | the process by which information about tissue damage is conveyed to the CNS |
| four processes in nociception | transduction, transmission, perception, modulation--CNS functioning properly |
| transduction | the process of converting a stimulus into a pain impulse--NSAIDS and local anesthetics |
| transmission | taken to the brain from the nerve impulses via neurotransmittors--opioids, GABA analogs |
| perception | how we perceive it--general anesthetics |
| modulation | attenuation of the pain sensation--Opioids, SSRI's, TCA's, gabapentin |
| neuropathic pain | CNS not functioning properly--poorly responsive to opioids and NSAIDS |
| Non-opioid | acetominophen, NSAIDS |
| quasi-opioid | ultram/tramadol--SE--drowsiness, GI, diaphoresis |
| opioids | synthetic--opiates, natural--MOA--bind to receptors in CNS, inhibit transmission from periphery to spinal cord, activating inhibitory pathways, alters limbic system pathways |
| opioids for cough supression | dextromethorphan, codeine, and hydrocodone--caution < 6yo |
| opioids for diarrhea | loperamide (immodium)OTC and diphenoxylate (lomotil) Rx only |
| opioid systemic effects | CNS, Cardiovascular, Gastrointestinal, renal, genitourinary |
| opioid SE | euphoria, sedation, respiratory depression, miosis, nausea and vomiting, consipation, pruritis |
| phenanthrenes | strong--morphine, heroin--moderate--oxycodone, codeine, hydro--agonist/antagonist--nalbuphine, buprenorphine |
| phenylheptylamines | strong--methadone--weak--propoxyphene (darvocet, darvon) |
| phenylpiperidines | strong--fentanyl (most potent)(combined with benzo's for procedural sedation), meperidine( demerol)--weak--diphenoxylate, loperamide |
| morphine-sulfate | schedule II--standard of comparison |
| opioid antagonists | naloxone, naltrexone, nalmefene |