PMID- 24683205 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20140331 LR - 20211021 IS - 0011-393X (Print) IS - 0011-393X (Linking) VI - 68 IP - 3 DP - 2007 May TI - Effectiveness of polymer-coated extended-release morphine sulfate capsules in older patients with persistent moderate-to-severe pain: A subgroup analysis of a large, open-label, community-based trial. PG - 137-50 LID - 10.1016/j.curtheres.2007.05.002 [doi] AB - Abstract. BACKGROUND: Opioid analgesics may offer benefits over nonopioids in some older patients, especially those with moderate-to-severe pain. Polymer-coated extended-release morphine sulfate (P-ERMS) has been found to be efficacious and well tolerated in patients with chronic, moderate-to-severe, nonmalignant pain when used QD or BID. OBJECTIVE: The purpose of this analysis was to determine the effectiveness of P-ERMS in older patients (aged >65 years) with persistent, moderate-to-severe, inadequately controlled, nonmalignant pain. METHODS: This was a subgroup analysis of the older population from an openlabel trial in community-based pain clinics in which patients underwent treatment with P-ERMS for persistent, moderate-to-severe, inadequately controlled, nonmalignant pain (>/=4 on a scale of 0-10). Patients received P-ERMS at a dose determined by the investigator based on their previous analgesic regimen, QD (morning or evening) for a 4-week treatment period. Dose increases were permitted after weeks 1 and 2; switching to BID was allowed after week 2, if needed. Measurements included changes in pain and sleep scores (0-10 scale), quality of life (QOL) scores (physical and mental component summaries [PCS and MCS, respectively] of the 36-Item Short-Form Health Survey instrument), and patient and clinician assessments of current treatment based on a 9-point scale ranging from -4 to +4. RESULTS: One hundred forty-eight older patients (mean [SD]age, 73.4 [5.5] years) began treatment with P-ERMS; 86 (58.1%) of those patients completed the study. Pain and sleep scores significantly improved (decreased) from baseline to week 4 (7.4 vs 5.0 and 5.0 vs 3.2, respectively; both, P < 0.001). PCS and MCS scores significantly improved (increased) from baseline (27.7 vs 31.6 and 37.6 vs 40.8, respectively; both, P < 0.05), as did patient and clinician global assessments (-1.2 vs 1.1 and -1.5 vs 1.4; both, P < 0.001). Results found in these older patients were similar to those observed in the younger patients (aged 70% remained on a QD administration regimen for the duration of the study. FAU - Sasaki, John AU - Sasaki J AD - Casa Colina Centers for Rehabilitation, Pomona, California, USA. FAU - Weil, Arnold J AU - Weil AJ AD - Non-Surgical Orthopedic & Spine Center, PC, Atlanta, Georgia, USA. FAU - Ross, Edgar L AU - Ross EL AD - Pain Management Center, Brigham and Women's Hospital, Boston, Massachusetts, USA. FAU - Nicholson, Bruce D AU - Nicholson BD AD - Division of Pain Medicine, Lehigh Valley Hospital & Health Network, Allentown, Pennsylvania, USA. LA - eng PT - Journal Article PL - United States TA - Curr Ther Res Clin Exp JT - Current therapeutic research, clinical and experimental JID - 0372621 PMC - PMC3967290 OTO - NOTNLM OT - KADIAN OT - analgesia OT - morphine OT - nonmalignant pain OT - persistent pain EDAT- 2007/05/01 00:00 MHDA- 2007/05/01 00:01 PMCR- 2007/05/01 CRDT- 2014/04/01 06:00 PHST- 2007/02/08 00:00 [accepted] PHST- 2014/04/01 06:00 [entrez] PHST- 2007/05/01 00:00 [pubmed] PHST- 2007/05/01 00:01 [medline] PHST- 2007/05/01 00:00 [pmc-release] AID - S0011-393X(07)00047-1 [pii] AID - 10.1016/j.curtheres.2007.05.002 [doi] PST - ppublish SO - Curr Ther Res Clin Exp. 2007 May;68(3):137-50. doi: 10.1016/j.curtheres.2007.05.002.