Opioid analgesic: Difference between revisions

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<ref name="pmid20504256">{{cite journal| author=Stamer UM, Zhang L, Stüber F| title=Personalized therapy in pain management: where do we stand? | journal=Pharmacogenomics | year= 2010 | volume= 11 | issue= 6 | pages= 843-64 | pmid=20504256 | doi=10.2217/pgs.10.47 | pmc= | url= }} </ref><ref>http://pubmed.gov/</ref>
<ref name="pmid20504256">{{cite journal| author=Stamer UM, Zhang L, Stüber F| title=Personalized therapy in pain management: where do we stand? | journal=Pharmacogenomics | year= 2010 | volume= 11 | issue= 6 | pages= 843-64 | pmid=20504256 | doi=10.2217/pgs.10.47 | pmc= | url= }} </ref><ref>http://pubmed.gov/</ref>


Ultrarapid metabolizers of [[codeine]]<ref name="pmid19692698">{{cite journal| author=Ciszkowski C, Madadi P, Phillips MS, Lauwers AE, Koren G| title=Codeine, ultrarapid-metabolism genotype, and postoperative death. | journal=N Engl J Med | year= 2009 | volume= 361 | issue= 8 | pages= 827-8 | pmid=19692698 | doi=10.1056/NEJMc0904266 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19692698  }} </ref><, [[oxycodone]], and [[hydrocodone]] may have increased [[drug toxicity]] due to increased conversion to morphine.ref name="pmid19059064">{{cite journal| author=Reynolds KK, Ramey-Hartung B, Jortani SA| title=The value of CYP2D6 and OPRM1 pharmacogenetic testing for opioid therapy. | journal=Clin Lab Med | year= 2008 | volume= 28 | issue= 4 | pages= 581-98 | pmid=19059064 | doi=10.1016/j.cll.2008.10.003 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19059064}}</ref>
Reduced metabolizers of codeine, tramadol, oxycodone, hydrocodone may have reduced effect due to decreased conversion to morphine.<ref name="pmid19059064">{{cite journal| author=Reynolds KK, Ramey-Hartung B, Jortani SA| title=The value of CYP2D6 and OPRM1 pharmacogenetic testing for opioid therapy. | journal=Clin Lab Med | year= 2008 | volume= 28 | issue= 4 | pages= 581-98 | pmid=19059064 | doi=10.1016/j.cll.2008.10.003 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19059064}}</ref>
 
Ultrarapid metabolizers of [[codeine]]<ref name="pmid19692698">{{cite journal| author=Ciszkowski C, Madadi P, Phillips MS, Lauwers AE, Koren G| title=Codeine, ultrarapid-metabolism genotype, and postoperative death. | journal=N Engl J Med | year= 2009 | volume= 361 | issue= 8 | pages= 827-8 | pmid=19692698 | doi=10.1056/NEJMc0904266 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19692698  }} </ref>, [[oxycodone]], and [[hydrocodone]] may have increased [[drug toxicity]] due to increased conversion to morphine.<ref name="pmid19059064">{{cite journal| author=Reynolds KK, Ramey-Hartung B, Jortani SA| title=The value of CYP2D6 and OPRM1 pharmacogenetic testing for opioid therapy. | journal=Clin Lab Med | year= 2008 | volume= 28 | issue= 4 | pages= 581-98 | pmid=19059064 | doi=10.1016/j.cll.2008.10.003 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19059064}}</ref>


==Available opioid analgesics==
==Available opioid analgesics==

Revision as of 13:25, 28 June 2011

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Opioid analgesics, also called narcotics, are drugs usually used for treating pain. Opioid analgesics are defined as "all of the natural and semisynthetic alkaloid derivatives from opium, their pharmacologically similar synthetic surrogates, as well as all other compounds whose opioid-like actions are blocked by the nonselective opioid receptor antagonist naloxone.[1]

Pharmacology

There a several opioid receptors. All are are G-protein-coupled cell surface receptors. Clinically useful analgesic families vary in their receptor effects; they range from pure agonists of all receptor types, to selective agonists, to agonist-antagonists.

Metabolism

Some opioids are metabolized by cytochrome P-450 and cytochrome P-450 CYP2D6.[2] [3][4]

Reduced metabolizers of codeine, tramadol, oxycodone, hydrocodone may have reduced effect due to decreased conversion to morphine.[2]

Ultrarapid metabolizers of codeine[5], oxycodone, and hydrocodone may have increased drug toxicity due to increased conversion to morphine.[2]

Available opioid analgesics

Current opioid analgesics are below [6]

Tables of morphine equivalent daily dose and IV to PO conversion are available to help dosing, although direct conversion is unwise with opioids with complex pharmacodynamics, such as methadone.

A number of oral forms are combined with acetaminophen to reduce the possibility of diversion to injected abuse, although acetaminophen also has a distinct and potentially synergistic analgesic effect. Acetaminophen has been found to be more toxic, with or without opioids, than had been generally believed, and the FDA has recommended restrictions on its uses.[7][6] The American Pain Foundation is concerned that these recommendations consider the matter carefully, lest there be undertreatment with appropriate opioids. [8] Combination with aspirin and other non-narcotic agents was common before the widespread use of acetaminophen

Selected opioids[9]
Specific drug Potency relative to morphine[10] Chemical class Receptor action Metabolism[11][12] Comments
Naturally occurring opium alkaloids
Morphine 1 morphine mu, kappa (weak)
Codeine 0.15 morphine mu (partial agonist) Good oral absorption
Semi-synthetic opioids
Diacetylmorphine (heroin) morphine Faster blood-brain transfer than morphine but both produce the same primary active metabolite
Hydrocodone 1 morphine mu (partial)
Oxycodone 1.5 morphine mu (partial) Oxycodone may increase mortality relative to other opioids[13] and may cause more drug toxicity in geriatrics than other opioids.[13]
Hydromorphone (Dilaudid) 4 morphine mu Mostly hepatic Oral bioavailability is approximately 24%[14]
Buprenorphine Thebaine mu, antagonist of delta and kappa
Fully synthetic opioids
Meperidine 0.1 Meperidine mu Good oral absorption; toxic metabolite accumulates on prolonged use
Fentanyl 2.4 Meperidine mu Transdermal and transmucosal absorption
Methadone 3 methadone mu Good oral absorption. Bioavailability of methadone ranges between 36 to 100%.[15] Different half-lives for analgesia and for blocking withdrawal
Tramadol 0.1 codeine mu Also inhibits monoamine oxidase; can raise norepinephrine and serotonin, and cause serotonin syndrome
Propoxyphene 0.23 propoxyphene mu L-isomer is antitussive; analgesic D-isomer was removed from the U.S. market as too risky for its limited effectiveness.[16]

Effectiveness

Opioids are commonly prescribed for pain, and their usage may be increasing.[17] In emergency rooms, non-Hispanic white patients are more likely to receive narcotics than patients of other ethnicities.[17]

Opioids are effective for short term use (1-16 weeks)[18].

For chronic, non-cancer pain, opioids may give short term reduction in pain compared to placebo.[19][20][21] The role of long term treatment of chronic non-cancer pain is not clear and a systematic review by the Cochrane Collaboration found "weak evidence suggests that patients who are able to continue opioids long-term experience clinically significant pain relief. Whether quality of life or functioning improves is inconclusive."[22]

One systematic review found that trials of short term opioids did not improve functional status compared to placebo in chronic pain.[19] However, a second systematic review, found that opioids improved functional status compared to placebo, but not compared to other drugs.[21] As example randomized controlled trials, opioids reduced pain, but did not improve function in comparison to an cholinergic antagonist placebo[23] or tricyclic antidepressant.[24]

Most trials are funded by industry.[21]

Administration

Clinical practice guidelines are available.[25]

Tables of morphine equivalent daily dose and IV to PO conversion are available to help dosing, but must be used with caution. Some opioids, such as methadone, do not lend themselves to simple conversion due to greatly differing half-lives. While an antagonist or partial antagonist may have equianalgesic dosing in an opioid-naive patient, switching from, for example, long-term morphine to buprenorphine can cause withdrawal.

Routes of administration

Most opioids can be administered parenterally. Recent developments have provided alternate formulation that improve oral effectiveness of drugs historically injected, such as morphine.

Novel routes are being found effective, such as transdermal skin patches that provide a constant low-rate dose, and transmucosal and intranasal routes for quick action.

Chronic use

Fear of addiction had long interfered with the extended use of opioids even in terminal patients. Current practice, however, includes the indefinite use of opioids in nonterminal patients with pain that can only be controlled by opioids. The World Health Organization, for example, has a "pain pyramid" for rheumatic disease, which begins with acetaminophen or equivalents, and moves to increasingly powerful opioids. Long-term opioid therapy is prescribed both for analgesia, and also the treatment of opioid dependence.

Mortality may be increased upon both starting and topic opioid maintenance.[26]

Advice for using administering chronic narcotics[25] and for treating acute pain among patients on chronic methadone is available[27]. Special technique may also be needed for patients receiving buprenorphine for chronic pain.

There are challenges in prescribing opioids with specialized actions, such as partial agonists and mixed agonist/antagonists. These may interfere with the effectiveness of breakthrough medications for additional acute pain. Such drugs also may be ineffective or produce withdrawal in patients receiving other long-term opioids.

Monitoring chronic use

Appropriate use may be improved with prescription-drug monitoring programs in which prescribers can track all opioid prescriptions for a patient. In the United States, the U.S. Department of Justice's Drug Enforcement Administration coordinates the State Prescription Drug Monitoring Programs. Prescription-drug monitoring programs have been studied for the Ohio Automated Rx Reporting System (OARRS).[28] Two additional systems under development are bu the United States Department of Health and Human Services and one by the Department of Justice.[29]

Opioid treatment agreements and urine drug testing may reduce opioid misuse by patients with chronic pain. [30] Urine drug testing is of two types:[31]

Adverse effects

Opioid analgesics may cause more drug toxicity, at least in geriatrics, than non-selective inhibitors of cyclooxygenase (non-steroidal anti-inflammatory agents) or cyclooxygenase 2 inhibitors.[32]

Opioid analgesics, with long-term use, 80% of patients may have drug toxicity, most commonly gastrointestinal. In addition, substance abuse and "aberrant medication-taking behaviors" may occur.[20]

Serious drug toxicity from long-term use may be low according to one systematic review.[22]

Constipation

Constipation may be reduced by methylnaltrexone, a mu-opioid receptor antagonist. In a randomized controlled trial, 48% of patients receiving methylnaltrexone had a bowel movement compared to 15% of patients received placebo (number needed to treat = 3.0. Click here to adjust these results for patients at higher or lower risk.)[33] Although mu-receptors provide analgesia, methylnaltrexone is a charged quaternary amine so that it does not well cross the blood-brain barrier.

Dietary agents and inert physical agents may help. A high-fiber diet is desirable, possibly with fiber supplements such as psyllium and metacellulose. The stool softener docusate is often prescribed. Stronger laxatives are not desirable.

Male hypogonadism

Chronic opioids may cause male hypogonadism.[34][35]

Impaired judgment

Opioids may increase risk of traffic accidents[36] and accidental falls[37].

Dependency

For more information, see: Opiate dependence.

Opioid agonist therapy includes buprenorphine and methadone. Although buprenorphine–naloxone may be less effective than methadone[38], it has more predictable dosing[39], and can be prescribed by qualifying office-based physicians.[40]

Overdose

Number of Poisoning Deaths Involving Opioid Analgesics and Other Drugs or Substances --- United States, 1999--2007.

Chronic use of the equivalent of more than 20 mg/day of morphine may lead to unintentional or intentional overdose.[41]

Overdose may be more common with with doses equivalent to more than 100 mg/day of morphine.[42] Overdose may[43] or may not[42] be increased with long acting opioids. Nevertheless, when the dose is managed by experts, the dose of most opioids can be raised indefinitely when needed to relieve pain. [44]

In veterinary medicine, there is a maximum effective analgesic dose of buprenorphine, although the frequency of administration may usefully be increased.[45]

Substance abuse

With chronic use for treatment of pain, dependency may lead to substance abuse and "aberrant medication-taking behaviors" may occur.[20] From 2000-2005, the abuse of prescribed opiods, especially oxycodone extended release (OxyContin) and hydrocodone, has increased.[46] From Contracts may reduce abuse, but comparative studies provide conflicting results.[47] Most agreements stated, "patients agreed not to abuse illicit drugs or alcohol, obtain opioids from more than 1 provider or pharmacy, or request a refill before the previous prescription should have been completed."

Withdrawal

Adding narcotic antagonists combined with alpha-adrenergic agonists may reduce withdrawal symptoms.[48]

Tolerance

N-methyl-d-aspartate receptor (NMDA) activation may lead to neuropathic pain and tolerance.[49][50] Methadone, which is a NMDA antagonist, may reduce tolerance.

Pruritis

Pruritis from histamine release may occur.[51] Anecdotally, one of the reason for using antihistamines as adjuvants, such as hydroxyzine and promethazine, are to alleviate some of these side effects, as well as nausea. The less sedating hydroxyzine also may potentiate analgesia and have a better antipruritic effect although promethazine may be stronger against nausea.

References

  1. ↑ Katzung, Bertram G. (2006). Basic and clinical pharmacology. New York: McGraw-Hill Medical Publishing Division, 512. ISBN 0-07-145153-6. 
  2. ↑ 2.0 2.1 2.2 Reynolds KK, Ramey-Hartung B, Jortani SA (2008). "The value of CYP2D6 and OPRM1 pharmacogenetic testing for opioid therapy.". Clin Lab Med 28 (4): 581-98. DOI:10.1016/j.cll.2008.10.003. PMID 19059064. Research Blogging.
  3. ↑ Stamer UM, Zhang L, Stüber F (2010). "Personalized therapy in pain management: where do we stand?". Pharmacogenomics 11 (6): 843-64. DOI:10.2217/pgs.10.47. PMID 20504256. Research Blogging.
  4. ↑ http://pubmed.gov/
  5. ↑ Ciszkowski C, Madadi P, Phillips MS, Lauwers AE, Koren G (2009). "Codeine, ultrarapid-metabolism genotype, and postoperative death.". N Engl J Med 361 (8): 827-8. DOI:10.1056/NEJMc0904266. PMID 19692698. Research Blogging.
  6. ↑ 6.0 6.1 (2003) “78. Management of Cancer Pain”, Cancer medicine 6. Hamilton, Ont.: BC Decker. ISBN 1-55009-213-8. 
  7. ↑ Joint Meeting of the Drug Safety and Risk Management Advisory Committee, Nonprescription Drugs Advisory Committee, and the Anesthetic and Life Support Drugs Advisory Committee, Center for Drug Evaluation and Research (CDER), Food and Drug Administration (FDA), June 29-30, 2009
  8. ↑ American Pain Foundation shares Acetaminophen Task Force's Concerns over Recent FDA Advisory Committee Recommendations Regarding Prescription Acetaminophen/Opioid Combination, American Pain Foundation
  9. ↑ Masters, Susan B.; Katzung, Bertram G.; Trevor, Anthony J. (2009). “Basic Pharmacology of the Opioid Analgesics”, Basic and Clinical Pharmacology, 11th. New York: McGraw-Hill Medical. ISBN 0-07-160405-7.  (Condensed from Table 31-2
  10. ↑ Korff MV, Saunders K, Thomas Ray G, Boudreau D, Campbell C, Merrill J et al. (2008). "De facto long-term opioid therapy for noncancer pain.". Clin J Pain 24 (6): 521-7. DOI:10.1097/AJP.0b013e318169d03b. PMID 18574361. Research Blogging.
  11. ↑ Davies G, Kingswood C, Street M (1996). "Pharmacokinetics of opioids in renal dysfunction.". Clin Pharmacokinet 31 (6): 410-22. PMID 8968655.
  12. ↑ Conway BR, Fogarty DG, Nelson WE, Doherty CC (2006). "Opiate toxicity in patients with renal failure.". BMJ 332 (7537): 345-6. DOI:10.1136/bmj.332.7537.345. PMID 16470057. PMC PMC1363915. Research Blogging.
  13. ↑ 13.0 13.1 Solomon DH, Rassen JA, Glynn RJ, Garneau K, Levin R, Lee J et al. (2010). "The comparative safety of opioids for nonmalignant pain in older adults.". Arch Intern Med 170 (22): 1979-86. DOI:10.1001/archinternmed.2010.450. PMID 21149754. Research Blogging.
  14. ↑ Hydromorphone - FDA approved drug information (drug label) from DailyMed (U.S. National Library of Medicine).
  15. ↑ Methadone - FDA approved drug information (drug label) from DailyMed (U.S. National Library of Medicine).
  16. ↑ Allison Gandey (19 November 2010), "Propoxyphene Withdrawn From US Market", Medscape Medical News
  17. ↑ 17.0 17.1 Pletcher MJ, Kertesz SG, Kohn MA, Gonzales R (2008). "Trends in opioid prescribing by race/ethnicity for patients seeking care in US emergency departments". JAMA 299 (1): 70–8. DOI:10.1001/jama.2007.64. PMID 18167408. Research Blogging.
  18. ↑ Chou R, Huffman LH, American Pain Society. American College of Physicians (2007). "Medications for acute and chronic low back pain: a review of the evidence for an American Pain Society/American College of Physicians clinical practice guideline.". Ann Intern Med 147 (7): 505-14. PMID 17909211. [e] Review in: Evid Based Nurs. 2008 Apr;11(2):50
  19. ↑ 19.0 19.1 Kalso E, Edwards JE, Moore RA, McQuay HJ (2004). "Opioids in chronic non-cancer pain: systematic review of efficacy and safety". Pain 112 (3): 372–80. DOI:10.1016/j.pain.2004.09.019. PMID 15561393. Research Blogging.
  20. ↑ 20.0 20.1 20.2 Martell BA, O'Connor PG, Kerns RD, Becker WC, Morales KH, Kosten TR et al. (2007). "Systematic review: opioid treatment for chronic back pain: prevalence, efficacy, and association with addiction.". Ann Intern Med 146 (2): 116-27. PMID 17227935. Cite error: Invalid <ref> tag; name "pmid17227935" defined multiple times with different content Cite error: Invalid <ref> tag; name "pmid17227935" defined multiple times with different content
  21. ↑ 21.0 21.1 21.2 Furlan AD, Sandoval JA, Mailis-Gagnon A, Tunks E (2006). "Opioids for chronic noncancer pain: a meta-analysis of effectiveness and side effects". CMAJ 174 (11): 1589–94. DOI:10.1503/cmaj.051528. PMID 16717269. Research Blogging.
  22. ↑ 22.0 22.1 Noble M, Treadwell JR, Tregear SJ, Coates VH, Wiffen PJ, Akafomo C et al. (2010). "Long-term opioid management for chronic noncancer pain.". Cochrane Database Syst Rev (1): CD006605. DOI:10.1002/14651858.CD006605.pub2. PMID 20091598. Research Blogging. Cite error: Invalid <ref> tag; name "pmid20091598" defined multiple times with different content
  23. ↑ Moulin DE, Iezzi A, Amireh R, Sharpe WK, Boyd D, Merskey H (1996). "Randomised trial of oral morphine for chronic non-cancer pain.". Lancet 347 (8995): 143-7. PMID 8544547.
  24. ↑ Raja SN, Haythornthwaite JA, Pappagallo M, Clark MR, Travison TG, Sabeen S et al. (2002). "Opioids versus antidepressants in postherpetic neuralgia: a randomized, placebo-controlled trial.". Neurology 59 (7): 1015-21. PMID 12370455. [e] Review in: J Fam Pract. 2003 Jul;52(7):517-8
  25. ↑ 25.0 25.1 Chou R, Fanciullo GJ, Fine PG, Adler JA, Ballantyne JC, Davies P et al. (2009). "Clinical guidelines for the use of chronic opioid therapy in chronic noncancer pain.". J Pain 10 (2): 113-30. DOI:10.1016/j.jpain.2008.10.008. PMID 19187889. Research Blogging.
  26. ↑ Cornish R et al. (2010) Risk of death during and after opiate substitution treatment in primary care: prospective observational study in UK General Practice Research Database. BMJ 2010; 341:c5475 DOI:10.1136/bmj.c5475
  27. ↑ Alford DP, Compton P, Samet JH (2006). "Acute pain management for patients receiving maintenance methadone or buprenorphine therapy". Ann. Intern. Med. 144 (2): 127–34. PMID 16418412. [e]
  28. ↑ Baehren DF, Marco CA, Droz DE, Sinha S, Callan EM, Akpunonu P (2010). "A statewide prescription monitoring program affects emergency department prescribing behaviors.". Ann Emerg Med 56 (1): 19-23.e1-3. DOI:10.1016/j.annemergmed.2009.12.011. PMID 20045578. Research Blogging.
  29. ↑ McLellan AT, Turner BJ (2010). "Chronic noncancer pain management and opioid overdose: time to change prescribing practices.". Ann Intern Med 152 (2): 123-4. DOI:10.1059/0003-4819-152-2-201001190-00012. PMID 20083830. Research Blogging.
  30. ↑ Starrels JL, Becker WC, Alford DP, Kapoor A, Williams AR, Turner BJ (2010). "Systematic review: treatment agreements and urine drug testing to reduce opioid misuse in patients with chronic pain.". Ann Intern Med 152 (11): 712-20. DOI:10.1059/0003-4819-152-11-201006010-00004. PMID 20513829. Research Blogging.
  31. ↑ Tenore PL (October 2010). "Advanced urine toxicology testing". J Addict Dis 29 (4): 436–48. DOI:10.1080/10550887.2010.509277. PMID 20924879. Research Blogging.
  32. ↑ Solomon DH, Rassen JA, Glynn RJ, Lee J, Levin R, Schneeweiss S (2010). "The comparative safety of analgesics in older adults with arthritis.". Arch Intern Med 170 (22): 1968-76. DOI:10.1001/archinternmed.2010.391. PMID 21149752. Research Blogging.
  33. ↑ Thomas J, Karver S, Cooney GA, Chamberlain BH, Watt CK, Slatkin NE, Stambler N, Kremer AB, Israel RJ. Methylnaltrexone for opioid-induced constipation in advanced illness. N Engl J Med. 2008 May 29;358(22):2332-43. PMID 18509120
  34. ↑ Finch PM, Roberts LJ, Price L, Hadlow NC, Pullan PT (2000). "Hypogonadism in patients treated with intrathecal morphine.". Clin J Pain 16 (3): 251-4. PMID 11014399. [e]
  35. ↑ Bliesener N, Albrecht S, Schwager A, Weckbecker K, Lichtermann D, Klingmüller D (2005). "Plasma testosterone and sexual function in men receiving buprenorphine maintenance for opioid dependence.". J Clin Endocrinol Metab 90 (1): 203-6. DOI:10.1210/jc.2004-0929. PMID 15483091. Research Blogging.
  36. ↑ Orriols L, Delorme B, Gadegbeku B, Tricotel A, Contrand B, et al. 2010 Prescription Medicines and the Risk of Road Traffic Crashes: A French Registry-Based Study. PLoS Med 7(11): e1000366. DOI:10.1371/journal.pmed.1000366
  37. ↑ Miller M, Stürmer T, Azrael D, Levin R, Solomon DH (2011). "Opioid analgesics and the risk of fractures in older adults with arthritis.". J Am Geriatr Soc 59 (3): 430-8. DOI:10.1111/j.1532-5415.2011.03318.x. PMID 21391934. Research Blogging.
  38. ↑ Schottenfeld RS, Chawarski MC, Pakes JR, Pantalon MV, Carroll KM, Kosten TR (2005). "Methadone versus buprenorphine with contingency management or performance feedback for cocaine and opioid dependence.". Am J Psychiatry 162 (2): 340-9. DOI:10.1176/appi.ajp.162.2.340. PMID 15677600. Research Blogging. Review in: Evid Based Ment Health. 2005 Nov;8(4):112>
  39. ↑ Simoens S, Matheson C, Bond C, Inkster K, Ludbrook A (2005). "The effectiveness of community maintenance with methadone or buprenorphine for treating opiate dependence.". Br J Gen Pract 55 (511): 139-46. PMID 15720937. PMC PMC1463190.
  40. ↑ Sullivan LE, Fiellin DA (2008). "Narrative review: buprenorphine for opioid-dependent patients in office practice.". Ann Intern Med 148 (9): 662-70. PMID 18458279.
  41. ↑ Dunn KM, Saunders KW, Rutter CM, Banta-Green CJ, Merrill JO, Sullivan MD et al. (2010). "Opioid prescriptions for chronic pain and overdose: a cohort study.". Ann Intern Med 152 (2): 85-92. DOI:10.1059/0003-4819-152-2-201001190-00006. PMID 20083827. Research Blogging.
  42. ↑ 42.0 42.1 Bohnert AS, Valenstein M, Bair MJ, Ganoczy D, McCarthy JF, Ilgen MA et al. (2011). "Association between opioid prescribing patterns and opioid overdose-related deaths.". JAMA 305 (13): 1315-21. DOI:10.1001/jama.2011.370. PMID 21467284. Research Blogging. Cite error: Invalid <ref> tag; name "pmid21467284" defined multiple times with different content
  43. ↑ Braden JB, Russo J, Fan MY, Edlund MJ, Martin BC, DeVries A et al. (2010). "Emergency department visits among recipients of chronic opioid therapy.". Arch Intern Med 170 (16): 1425-32. DOI:10.1001/archinternmed.2010.273. PMID 20837827. Research Blogging.
  44. ↑ Melzack & Wall, Textbook of Pain
  45. ↑ need to dig up the Cornell handbook
  46. ↑ Cicero TJ, Inciardi JA, Muñoz A (2005). "Trends in abuse of Oxycontin and other opioid analgesics in the United States: 2002-2004.". J Pain 6 (10): 662-72. DOI:10.1016/j.jpain.2005.05.004. PMID 16202959. Research Blogging.
  47. ↑ Starrels, Joanna L.; William C. Becker, Daniel P. Alford, Alok Kapoor, Arthur Robinson Williams, Barbara J. Turner (2010-06-01). "Systematic Review: Treatment Agreements and Urine Drug Testing to Reduce Opioid Misuse in Patients With Chronic Pain". Annals of Internal Medicine 152 (11 pages = 712-720). DOI:10.1059/0003-4819-152-11-201006010-00004. Retrieved on 2010-06-01. Research Blogging.
  48. ↑ Gowing L, Ali R, White JM (2009). "Opioid antagonists with minimal sedation for opioid withdrawal.". Cochrane Database Syst Rev (4): CD002021. DOI:10.1002/14651858.CD002021.pub3. PMID 19821290. Research Blogging.
  49. ↑ Trujillo KA, Akil H (1991). "Inhibition of morphine tolerance and dependence by the NMDA receptor antagonist MK-801.". Science 251 (4989): 85-7. PMID 1824728.
  50. ↑ Prommer E (2006). "Rotating methadone to other opioids: a lesson in the mechanisms of opioid tolerance and opioid-induced pain.". J Palliat Med 9 (2): 488-93. DOI:10.1089/jpm.2006.9.488. PMID 16629581. Research Blogging.
  51. ↑ Cherny N, Ripamonti C, Pereira J, Davis C, Fallon M, McQuay H et al. (2001). "Strategies to manage the adverse effects of oral morphine: an evidence-based report.". J Clin Oncol 19 (9): 2542-54. PMID 11331334.
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