Central Nervous System Pain Management PDF

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GenerousReef

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pain management analgesic drugs opioid analgesics central nervous system

Summary

This document provides a comprehensive overview of pain management, focusing on analgesic drugs, classifications of pain, and the mechanism of action of opioid analgesics. It details various aspects including the gate theory and mentions conditions where opioid analgesics are indicated and contraindicated.

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Analgesic Drugs - Medications that relieve pain without causing loss of consciousness - “Pain Killers” - Opioids - Adjuvants - i.e. NSAIDs, Antidepressants, Anticonvulsants, Corticosteroids, etc. — example: adjuvant drugs for neuropathic pain ——- Amitriptyline (antidepressant) ——-Gabapentin or preg...

Analgesic Drugs - Medications that relieve pain without causing loss of consciousness - “Pain Killers” - Opioids - Adjuvants - i.e. NSAIDs, Antidepressants, Anticonvulsants, Corticosteroids, etc. — example: adjuvant drugs for neuropathic pain ——- Amitriptyline (antidepressant) ——-Gabapentin or pregabalin (anticonvulsants) Classification of Pain Vascular: Vascular or perivascular tissues. Thought to account for vast majority of migraine headaches Referred: Visceral nerve fibres synapse at the spinal cord close to fibres from tissues in the body Neuropathic: Damage to nerve fibres Phantom: Occurs in body part that has been removed Cancer: Caused from pressure of tumours against nerves, organs, or tissues Central: Tumours, trauma, inflammation or disease affecting CNS tissues Onset and Duration of Pain Acute: Sudden, usually subsides once treated or less then 3 months Persistent/Chronic: Persistent or recurring, lasts 3-6 months or longer, often difficult to treat • Acute examples: • Persistent/Chronic examples: Gate Theory Pain transmission Gate theory 1. Transduction • The transformation of stimuli into electrochemical energy • Nociceptors detect depth/impact of harmful stimulus. Release of pain-medicating chemicals 2. Transmission • Pain impulses move along pain fibres to activate pain receptors up the spinal cord to brain • If no impulses are transmitted to higher centre’s in the brain, there is no pain perception 3. Perception • Subjective phenomenon of pain ; “How it is felt” • Complex behavioural psychological, and emotional factors 4. Modulation • Neural activity that controls pain transmission to neurons, both in CNS and PNS • descending nerve fibres release endogenous neurotransmitters to fight pain Pain Interpreted Pain threshold: • Level of stimulus needed to produce the perception of pain • Measure. Of the physiological response of the nervous system Pain Tolerance Amount of Pain a patient can endure without its interfering with normal function • Varies with each individual • Subjective response • Point beyond which pain becomes unbearable Treatment of Pain in special Situations • Patient-controlled analgesia (PCA) • Patient comfort versus fear of drug addiction • Opioid tolerance • Use of placebos • Recognizing patients who are opioid tolerant • Breakthrough Pain • Synergistic effects Mechanism of action: Opioid Analgesics • Opioid analgesics act by depressing pain impulse transmission at the spinal cord level by interacting with opioid receptors • Three classifications based on their ‘actions’ 1. Agonist = binds to a pain receptor in brain & produces analgesia (a reduction of pain sensation) • mild agonist - i.e. codeine, hydrocodone (more commonly used as an antitussive) • Strong agonist - i.e. morphine, hydromorphone, fentanyl, methadone ———Hydromorphone: very potent opioid analgesic ————- 1mg of IV or IM = 7mg of morphine 2. Agonist-Antagonist = binds to receptor causing a weaker pain response that full agonist • also called partial agonists or mixed agonists • i.e. Suboxone - buprenorphine with naloxone to enhance antagonist effect 3. Antagonist = non-analgesics that bind to pain receptors but do not reduce pain signals • Reverses the effects of these drugs on pain receptors • Also known as competitive antagonists • I.e. Naloxone Equianalgesia • Ability to provide equivalent pain relief by calculating dosages of different drugs or routes of administration that provide comparable analgesia Examples: morphine, hydromorphone, oxycodone, hydrocodone, bitartrate, fentanyl • continuous release vs. Immediate release formulations Opioid Analgesics: Indications • Mainly used to alleviate moderate to severe pain • Often first line analgesic in immediate post operative setting • Often given with analgesic drugs to assist primary drugs with pain relief Opioids are also used for: • cough centre suppression - codeine • Treatment of diarrhea Contraindications • Known drug allergy ——Often patient had side effect not true allergy (e.g. nausea) • Severe asthma • Use with extreme caution in patients with the following: — Respiratory insufficiency — Elevated intracranial pressure —Morbid obesity or sleep apnea — Paralytic ileus — Pregnancy Adverse effects • GI symptoms (most common) — Nausea, vomiting, constipation, and cramps • CNS depression — Leads to respiratory depression = Most serious adverse effect — Sedation • • • • Urinary retention Hypotension Itching, rash Pinpoint pupils indicating a possible overdose Opiate Tolerance • Common physiological result of chronic opioid treatment • State of adaptation • Once tolerance occurs, larger dose of opioids is required to maintain same level of analgesia Dependence to opiates Physical • Adaption of the body to the presence of an opioid • This is expected with long-term opioid treatment Psychological • A pattern of compulsive drug use characterized by a continued craving for an opioid and the need to use the opioid for effect other than pain relief Opioid Ceiling Effect • Drug reaches a maximum analgesic effect • Analgesia does not improve, even with higher doses *Tolerance and physical dependence should not be confused with psychological dependence (addiction) Addiction: A pattern of compulsive drug use characterized by a continued craving for an opioid and the need to use the opioid for effects other than pain relief. Assess for • #1 Respiratory dysfunction - resp depr

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