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"Painkiller" redirects here. For other uses, see Painkiller (disambiguation). An analgesic (colloquially known as a painkiller) is any member of the diverse group of drugs used to relieve pain (achieve analgesia). The word analgesic derives from Greek an- ("without") and -algia ("pain"). Analgesic drugs act in various ways on the peripheral and central nervous systems; they include paracetamol (acetaminophen), the non-steroidal anti-inflammatory drugs (NSAIDs) such as the salicylates, narcotic drugs such as morphine, synthetic drugs with narcotic properties such as tramadol, and various others. In choosing analgesia, the severity and response to other medication determines the choice of agent; the WHO "pain ladder", originally developed in cancer-related pain, is widely applied to find suitable drugs in a stepwise manner. The choice of analgesia is also determined by the type of pain: for neuropathic pain, traditional analgesia is less effective, and there is often benefit from classes of drugs that are not normally considered analgesics, such as tricyclic antidepressants and anticonvulsants.
The major classes
Paracetamol and NSAIDsThe exact mechanism of action of paracetamol/acetaminophen is uncertain, but it appears to be acting centrally. Aspirin and the other NSAIDs inhibit cyclooxygenase, leading to a decrease in prostaglandin production; this reduces pain and also inflammation (in contrast to paracetamol and the opioids). Paracetamol has few side effects and is regarded as very safe; excessive doses lead to hepatotoxicity (liver damage). NSAIDs predispose to peptic ulcers, renal failure, allergic reactions, and occasionally hearing loss, and they can increase the risk of hemorrhage by affecting platelet function. The use of certain NSAIDs in children under 16 suffering from viral illness may contribute to Reye's syndrome.
COX-2 inhibitorsThese drugs have been derived from NSAIDs. The cyclooxygenase enzyme inhibited by NSAIDs was discovered to have at least 2 different versions: COX1 and COX2. Research suggested that most of the adverse effects of NSAIDs were mediated by blocking the COX1 (constitutive) enzyme, with the analgesic effects being mediated by the COX2 (inducible) enzyme. The COX2 inhibitors were thus developed to inhibit only the COX2 enzyme (traditional NSAIDs block both versions in general). These drugs (such as rofecoxib and celecoxib) are equally effective analgesics when compared with NSAIDs, but cause less gastrointestinal hemorrhage in particular. However, post-launch data indicated increased risk of cardiac and cerebrovascular events with these drugs due to an increased likelihood of clotting in the blood due to a decrease in the production of protoglandin around the platelets causing less clotting factor to be released, and rofecoxib was subsequently withdrawn from the market. The role for this class of drug is currently hotly debated.
Opiates and morphinomimeticsMorphine, the archetypal opioid, and various other substances (e.g. codeine, oxycodone, hydrocodone, diamorphine, pethidine) all exert a similar influence on the cerebral opioid receptor system. Tramadol and buprenorphine are thought to be partial agonists of the opioid receptors. Dosing of all opioids may be limited by opioid toxicity (confusion, respiratory depression, myoclonic jerks and pinpoint pupils), but there is no dose ceiling in patients who tolerate this. Opioids, while very effective analgesics, may have some unpleasant side-effects. Up to 1 in 3 patients starting morphine may experience nausea and vomiting (generally relieved by a short course of antiemetics). Pruritus (itching) may require switching to a different opioid. Constipation occurs in almost all patients on opioids, and laxatives (lactulose, macrogol-containing or co-danthramer) are typically co-prescribed. When used appropriately, opioids and similar narcotic analgesics are otherwise safe and effective, however risks such as addiction and the body becoming used to the drug can occur. Due to the body getting used to the drug often the dose must be increased if it is for a chronic disease this is where the no ceiling limit of the drug comes into play. However what must be remembered is although there is no upper limit there is a still a toxic dose even if the body has become used to lower doses.
Specific agentsIn patients with chronic or neuropathic pain, various other substances may have analgesic properties. Tricyclic antidepressants, especially amitriptyline, have been shown to improve pain in what appears to be a central manner. The exact mechanism of carbamazepine, gabapentin and pregabalin is similarly unclear, but these anticonvulsants are used to treat neuropathic pain with modest success.
Specific forms and uses
CombinationsAnalgesics are frequently used in combination, such as the paracetamol and codeine preparations found in many non-prescription pain relievers. They can also be found in combination with vasoconstrictor drugs such as pseudoephedrine for sinus-related preparations, or with antihistamine drugs for allergy sufferers. The use of paracetamol, as well as aspirin, ibuprofen, naproxen, and other NSAIDS concurrently with weak to mid-range opiates (up to about the hydrocodone level) has been shown to have beneficial synergistic effects by combatting pain at multiple sites of action—NSAIDs reduce inflammation which, in some cases, is the cause of the pain itself while opiates dull the perception of pain—thus, in cases of mild to moderate pain caused in part by inflammation, it is generally recommended that the two be prescribed together.
Topical or systemicTopical analgesia is generally recommended to avoid systemic side-effects. Painful joints, for example, may be treated with an ibuprofen- or diclofenac-containing gel; capsaicin also is used topically. Lidocaine, an anesthetic, and steroids may be injected into painful joints for longer-term pain relief. Lidocaine is also used for painful mouth sores and to numb areas for dental work and minor medical procedures.
Psychotropic agentsTetrahydrocannabinol (THC) and some other cannabinoids, either from the Cannabis sativa plant or synthetic, have analgesic properties, although the use of cannabis derivatives is illegal in many countries. Other psychotropic analgesic agents include ketamine (an NMDA receptor antagonist), clonidine and other α2-adrenoreceptor agonists, and mexiletine and other local anaesthetic analogues.
Atypical and/or adjuvant analgesicsOrphenadrine, cyclobenzaprine, scopolamine, atropine, gabapentin, first-generation antidepressants and other drugs possessing anticholinergic and/or antispasmodic properties are used in many cases along with analgesics to potentiate centrally acting analgesics such as opioids when used against pain especially of neuropathic origin and to modulate the effects of many other types of analgesics by action in the parasympathetic nervous system. Dextromethorphan has been noted to slow the development of tolerance to opioids and exert additional analgesia by acting upon the NMDA receptors; some analgesics such as methadone and ketobemidone and perhaps piritramide have intrinsic NMDA action. The use of adjuvant analgesics is an important and growing part of the pain-control field and new discoveries are made practically every year. Many of these drugs combat the side effects of opioid analgesics, an added bonus. For example, antihistamines including orphenadrine combat the release of histamine caused by many opioids, methylphenidate, caffeine, ephedrine, dextroamphetamine, and cocaine work against heavy sedation and may elevate mood in distressed patients as do the antidepressants. A well-accepted benefit of THC to chronic pain patients on opioids is its superior anti-nauseant action. However, it would make more sense to use the Marinol capsule, or oral, rectal, or vapour administration of hash oil, rather than smoking cannabis, for the same reasons most doctors advise against smoking tobacco.
AddictionIn the United States in recent years, there has been a wave of new addictions to prescription narcotics such as oxycodone (such as OxyContin, or with acetaminophen, as Percocet) and hydrocodone (commonly prescribed with acetaminophen, as in Vicodin, Lortab etc.) when available in pure formulations as opposed to combined with other medications (as in Percocet which contains both oxycodone and acetaminophen/paracetamol).
See also- Pain management
- Patient-controlled analgesia
- Co-proxamol
References- ^ Anonymous (1990). Cancer pain relief and palliative care; report of a WHO expert committee, World Health Organization Technical Report Series, 804 (in English). Geneva, Switzerland: World Health Organization, 1-75. ISBN 924120804X.
- ^ Dworkin RH, Backonja M, Rowbotham MC, et al (2003). "Advances in neuropathic pain: diagnosis, mechanisms, and treatment recommendations". Arch. Neurol. 60 (11): 1524-34. doi:10.1001/archneur.60.11.1524. PMID 14623723.
- ^ Mehlisch DR (2002). "The efficacy of combination analgesic therapy in relieving dental pain". J Am Dent Assoc 133 (7): 861-71. PMID 12148679.
External links- Bandolier pain site (Oxford pain group)
| Analgesic products (N02A, N02B) |
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| Opioids
See also: Opioids template | Alphaprodine · Anileridine · Buprenorphine · Butorphanol · Codeine · Dextromoramide · Dextropropoxyphene · Dezocine · Desomorphine · Diamorphine · Dihydrocodeine · Dihydromorphine · Fentanyl · Hydrocodone · Hydromorphone · Ketobemidone · Levorphanol · Meptazinol · Methadone · Morphine · Nalbuphine · Nicomorphine · Opium · Oxycodone · Oxymorphone · Pethidine · Pentazocine · Pethidine · Piminodine · Piritramide · Tilidine · Tramadol · Tapentadol | | | Salicylic acid and derivatives | Aspirin (Acetylsalicylic Acid) · Benorylate · Diflunisal · Ethenzamide · Magnesium Salicylate · Salicin · Salicylamide · Salsalate · See also: NSAIDs | | | Pyrazolones | Ampyrone/Aminophenazone · Metamizole · Phenazone | | | Cannabinoids | Cannabis · Tetrahydrocannabinol · AM404 | | | Anilides | Paracetamol (acetaminophen) · Phenacetin · Propacetamol | | Non-Salicylate Non-Steroidal
Anti-Inflammatories
See also: NSAIDs template | Propionic Acid NSAIDs | Fenoprofen · Flurbiprofen · Ibuprofen · Ketoprofen · Naproxen · Oxaprozin | | Oxicam NSAIDs | Meloxicam · Piroxicam · | | Acetic Acid NSAIDs | Diclofenac · Indometacin · Ketorolac · Sulindac · Tolmetin | | COX-2 NSAIDs | | | Anthranilic Acid
(Fenamate) NSAIDS | Meclofenamate · Mefenamic acid | | Other NSAIDS | |
| | Atypical, Adjunct
& Miscellaneous | Bicifadine · Clonidine · Cyclobenzaprine · Duloxetine · Flupirtine · Gabapentin · Nefopam · Orphenadrine · Trazadone · Ziconotide |
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| Major drug groups |
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| | Gastrointestinal tract (A) | Antacids • Antiemetics • H2 antagonists • Proton pump inhibitors • Laxatives • Antidiarrhoeals | | | Blood and blood forming organs (B) | Anticoagulants • Antiplatelets • Thrombolytics | | | Cardiovascular system (C) | Antiarrhythmics • Antihypertensives • Diuretics • Vasodilators • Antianginals • Beta blockers • Angiotensin converting enzyme inhibitors • Antihyperlipidemics | | | Skin (D) | Emollients - Antipruritics | | | Reproductive system (G) | Hormonal contraception • Fertility agents • Selective estrogen receptor modulators • Sex hormones | | | Endocrine system (H) | Anti-diabetics • Corticosteroids • Sex hormones • Thyroid hormones | | | Infections and infestations (J, P) | Antibiotics • Antivirals • Vaccines • Antifungals • Antiprotozoals • Anthelmintics | | | Malignant and immune disease (L) | Anticancer agents • Immunostimulators • Immunosuppressants | | | Muscles, bones, and joints (M) | Anabolic steroids • Anti-inflammatories • Antirheumatics • Corticosteroids • Muscle relaxants | | | Brain and nervous system (N) | Anesthetics • Analgesics • Anticonvulsants • Mood stabilizers • Anxiolytics • Antipsychotics • Antidepressants • Nervous system stimulants • Sedatives | | | Respiratory system (R) | Bronchodilators • Decongestants • H1 antagonists |
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