Literature DB >> 20213238

The dosing frequency of sustained-release opioids and the prevalence of end-of-dose failure in cancer pain control: a Korean multicenter study.

Do-Yeun Kim1, Hong-Suk Song, Jin-Seok Ahn, Baek-Yeol Ryoo, Dong-Bok Shin, Chang-Yeol Yim, Si-Young Kim.   

Abstract

BACKGROUND: End-of-dose failure is commonly observed as therapeutic levels of sustained-release opioids fall. However, little is known about using these medications for cancer pain control. To determine the dosing frequency of sustained-release opioids (morphine, oxycodone, and transdermal fentanyl) and the prevalence of end-of-dose failure in clinical practice, a patient-reported survey was performed.
METHODS: A multicenter survey was conducted in 56 hospitals in Korea between June and November 2008.
RESULTS: The study enrolled 1,097 cancer outpatients who were prescribed oral sustained-release opioids (morphine or oxycodone) or transdermal fentanyl. Of the oral sustained-release opioid patients, 67.0% took oral sustained-release oral opioids twice daily, while 26.2% took them more than twice daily. Of the transdermal fentanyl patients, 88.8% wore the patch for 72 h. Of the enrolled patients, 48.3% experienced worsening pain just before the next sustained-release opioid dose, and 36.8% of these patients took medication earlier than the prescribed dosing schedule. Patients felt that oral sustained-release opioids gave adequate pain control lasting an average of 9.6 h, versus an average of 62.9 h for transdermal fentanyl.
CONCLUSION: This survey demonstrated that sustained-release opioids are used by patients in a manner that is inconsistent with standard recommendations. End-of-dose failure is suggested to explain increased dosing frequency, and patients reported that adequate pain relief lasted for less time than was stated in the manufacturers' prescription recommendation.

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Year:  2010        PMID: 20213238     DOI: 10.1007/s00520-010-0825-x

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  10 in total

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Journal:  Cancer       Date:  2002-02-01       Impact factor: 6.860

2.  Pharmacokinetics and pharmacodynamics of controlled-release opioids.

Authors:  R F Kaiko
Journal:  Acta Anaesthesiol Scand       Date:  1997-01       Impact factor: 2.105

Review 3.  Treatment of cancer pain with transdermal fentanyl.

Authors:  G K Gourlay
Journal:  Lancet Oncol       Date:  2001-03       Impact factor: 41.316

4.  Assessment of dosing frequency of sustained-release opioid preparations in patients with chronic nonmalignant pain.

Authors:  Rollin M Gallagher; Maripat Welz-Bosna; Arnold Gammaitoni
Journal:  Pain Med       Date:  2007 Jan-Feb       Impact factor: 3.750

Review 5.  Oxycodone.

Authors:  Eija Kalso
Journal:  J Pain Symptom Manage       Date:  2005-05       Impact factor: 3.612

Review 6.  Clinical pharmacokinetics of morphine.

Authors:  Ralph A Lugo; Steven E Kern
Journal:  J Pain Palliat Care Pharmacother       Date:  2002

7.  Controlled-release oral morphine sulfate in the treatment of cancer pain with pharmacokinetic correlation.

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Review 8.  Oxycodone: new 'old' drug.

Authors:  Klaus T Olkkola; Nora M Hagelberg
Journal:  Curr Opin Anaesthesiol       Date:  2009-08       Impact factor: 2.706

9.  Control of cancer-related pain with MS Contin: a comparison between 12-hourly and 8-hourly administration.

Authors:  G G Mignault; J Latreille; F Viguié; P Richer; F Lemire; Z Harsanyi; J H Stewart
Journal:  J Pain Symptom Manage       Date:  1995-08       Impact factor: 3.612

10.  Morphine and alternative opioids in cancer pain: the EAPC recommendations.

Authors:  G W Hanks; F Conno; N Cherny; M Hanna; E Kalso; H J McQuay; S Mercadante; J Meynadier; P Poulain; C Ripamonti; L Radbruch; J R Casas; J Sawe; R G Twycross; V Ventafridda
Journal:  Br J Cancer       Date:  2001-03-02       Impact factor: 7.640

  10 in total
  6 in total

1.  Effect of dose escalation with single opioid, fentanyl matrix in patients not controlling cancer pain: a multicenter, prospective, observational study in Korea.

Authors:  Sung Ae Koh; Kyung Hee Lee; Mi Jung Kim; Kyu Taek Lee; Seung Woo Park; Seung Hyun Nam; Hun Mo Ryoo
Journal:  Cancer Res Treat       Date:  2013-12-31       Impact factor: 4.679

2.  Clinical efficacy of OROS® hydromorphone in patients suffering from severe chronic pain: A Study undertaken in routine clinical practice.

Authors:  Aleksander Stepanović; Jelka Pirc; Slavica Lahajnar Čavlović
Journal:  Wien Klin Wochenschr       Date:  2011-06-28       Impact factor: 1.704

3.  A new once-a-day fentanyl citrate patch (Fentos Tape) could be a new treatment option in patients with end-of-dose failure using a 72-h transdermal fentanyl matrix patch.

Authors:  Kazuhiko Koike; Takeshi Terui; Tomokazu Nagasako; Iori Horiuchi; Takayuki Machino; Toshiro Kusakabe; Yasuo Hirayama; Hiroyoshi Mihara; Michiaki Yamakage; Junji Kato; Takuji Nishisato; Kunihiko Ishitani
Journal:  Support Care Cancer       Date:  2015-08-07       Impact factor: 3.603

4.  Poor adhesion of fentanyl transdermal patches may mimic end-of-dosage failure after 48 hours and prompt early patch replacement in hospitalized cancer pain patients.

Authors:  Isabelle Arnet; Sabrina Schacher; Eva Balmer; Dieter Koeberle; Kurt E Hersberger
Journal:  J Pain Res       Date:  2016-11-09       Impact factor: 3.133

5.  OxyContin was submitted and justifiably approved by the agency as a 12-hour dosage form.

Authors:  Jeffrey Fudin; Mena Raouf; Erica L Wegrzyn
Journal:  J Pain Res       Date:  2016-09-07       Impact factor: 3.133

6.  Treatment with subcutaneous and transdermal fentanyl: results from a population pharmacokinetic study in cancer patients.

Authors:  Astrid W Oosten; João A Abrantes; Siv Jönsson; Peter de Bruijn; Evelien J M Kuip; Amílcar Falcão; Carin C D van der Rijt; Ron H J Mathijssen
Journal:  Eur J Clin Pharmacol       Date:  2016-01-14       Impact factor: 2.953

  6 in total

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