SANDER-KIESILING, A., P. LEYENDECKER, M. HOPP, L. TARAU, J. LEJCKO, Pavel ŠEVČÍK, Marek HAKL, Radovan HŘIB, R. UHL, H. DUERR, K. REIMER a W. MEISSNER. Long term efficacy and safety of combined prolonged-release oxycodone and naloxone in the management of non-cancer pain. International Journal of Clinical Practice. 2010, roč. 64, č. 6, s. 763-774. ISSN 1368-5031. Dostupné z: https://dx.doi.org/10.1111/j.1742-1241.2010.02360.x.
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Základní údaje
Originální název Long term efficacy and safety of combined prolonged-release oxycodone and naloxone in the management of non-cancer pain
Autoři SANDER-KIESILING, A. (40 Rakousko, garant), P. LEYENDECKER (276 Německo), M. HOPP (276 Německo), L. TARAU (276 Německo), J. LEJCKO (203 Česká republika), Pavel ŠEVČÍK (203 Česká republika, domácí), Marek HAKL (203 Česká republika, domácí), Radovan HŘIB (203 Česká republika, domácí), R. UHL (276 Německo), H. DUERR (276 Německo), K. REIMER (276 Německo) a W. MEISSNER (276 Německo).
Vydání International Journal of Clinical Practice, 2010, 1368-5031.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30104 Pharmacology and pharmacy
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 2.309
Kód RIV RIV/00216224:14110/10:00051722
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1111/j.1742-1241.2010.02360.x
UT WoS 000276490600016
Klíčová slova anglicky RANDOMIZED CONTROLLED-TRIAL; OPIOID-INDUCED CONSTIPATION; DIABETIC-NEUROPATHY; BOWEL DYSFUNCTION; CANCER PAIN; COMBINATION; MODERATE; PREVALENCE
Příznaky Mezinárodní význam
Změnil Změnil: Mgr. Michal Petr, učo 65024. Změněno: 20. 4. 2012 11:35.
Anotace
The aim of this study was to assess safety and efficacy of fixed combination oxycodone prolonged release (PR)/naloxone PR in terms of both analgesia and improving opioid-induced bowel dysfunction (OIBD) and associated symptoms, such as opioid-induced constipation (OIC), in adults with chronic non-cancer pain. Study design: These were open-label extension studies in which patients who had previously completed a 12-week, double-blind study received oxycodone PR /naloxone PR for up to 52 weeks. The analgesia study assessed pain using the modified Brief Pain Inventory-Short Form (BPI-SF). The bowel function study assessed improvements in constipation using the Bowel Function Index (BFI). Results: At open-label baseline in the analgesia study (n = 379), mean score [+/- standard deviation (SD)] for the BPI-SF item 'average pain over the last 24 h' was 3.9 +/- 1.52, and this remained low at 6 months (3.7 +/- 1.59) and 12 months (3.8 +/- 1.72). Mean scores for BPI-SF item 'sleep interference', and the BPI-SF 'pain' and 'interference with activities' subscales also remained low throughout the 52-week study. In the bowel function study (n = 258), mean BFI score (+/- SD) decreased from 35.6 +/- 27.74 at the start of the extension study to 20.6 +/- 24.01 after 12 months of treatment with oxycodone PR/naloxone PR. Pain scores also remained low and stable during this study. Adverse events in both extension phases were consistent with those associated with opioid therapy; no additional safety concerns were observed. Conclusion: Results from these two open-label extension studies demonstrate the long-term efficacy and tolerability of fixed combination oxycodone PR/naloxone PR in the treatment of chronic pain. Patients experienced clinically relevant improvements in OIBD while receiving effective analgesic therapy.
VytisknoutZobrazeno: 18. 7. 2024 14:17