PMID- 22928861 OWN - NLM STAT- MEDLINE DCOM- 20130606 LR - 20130131 IS - 1364-6915 (Electronic) IS - 1360-7863 (Linking) VI - 17 IP - 1 DP - 2013 TI - The effects of abrupt antipsychotic discontinuation in cognitively impaired older persons: a pilot study. PG - 125-32 LID - 10.1080/13607863.2012.717255 [doi] AB - BACKGROUND: Antipsychotic use for behavioural and psychological symptoms of dementia (BPSD) is controversial. Guidelines advise to reduce antipsychotics given the adverse effects and limited efficacy, to limit dose and treatment duration as well as to undertake discontinuation. METHODS: A pilot study with 40 hospitalised geriatric cognitively impaired patients, in which the effects of abrupt antipsychotic discontinuation were investigated, using neuropsychiatric inventory (NPI) scores before and one month after discontinuation. Withdrawal symptoms were monitored thrice a day with a checklist during five consecutive days. RESULTS: Participants (n = 40) had a mean age of 84 years (range 67-95) and 53% were male. The total mean baseline NPI score was 21 (SD 12) with predominantly behavioural rather than psychological disturbances. After abrupt discontinuation, mild withdrawal symptoms were observed in 72% of the patients, with frequencies of symptoms peaking on day 2 (53%) and day 3 (48%). After one month, 31 patients (85%) were still off antipsychotics and improved on the majority of NPI domains, with a total mean NPI score decreasing from 18 (SD 13) to 12 (SD 8, p = 0.003). In the relapse group, there was no deterioration associated with the abrupt discontinuation and subsequent resumption of therapy with a total mean NPI score decreasing from 31 (SD 12) at baseline to 27 (SD 8) at one-month follow-up (p = 0.345). CONCLUSION: Abrupt antipsychotic discontinuation appears to be feasible in older individuals with BPSD. Systematically performed discontinuation efforts in clinical practice are needed to differentiate between patients where antipsychotics have no added value and patients where the benefits outweigh the risks. FAU - Azermai, M AU - Azermai M AD - Division of Clinical Pharmacology, Heymans Institute of Pharmacology, Ghent University, Ghent, Belgium. majda.azermai@ugent.be FAU - Petrovic, M AU - Petrovic M FAU - Engelborghs, S AU - Engelborghs S FAU - Elseviers, M M AU - Elseviers MM FAU - Van der Mussele, S AU - Van der Mussele S FAU - Debruyne, H AU - Debruyne H FAU - Van Bortel, L AU - Van Bortel L FAU - Vander Stichele, R H AU - Vander Stichele RH LA - eng PT - Journal Article DEP - 20120828 PL - England TA - Aging Ment Health JT - Aging & mental health JID - 9705773 RN - 0 (Antipsychotic Agents) SB - IM MH - Activities of Daily Living MH - Aged MH - Aged, 80 and over MH - Antipsychotic Agents/*adverse effects/therapeutic use MH - Dementia/*drug therapy/psychology MH - Dose-Response Relationship, Drug MH - Drug Administration Schedule MH - Feasibility Studies MH - Female MH - Follow-Up Studies MH - Humans MH - Kaplan-Meier Estimate MH - Length of Stay/statistics & numerical data MH - Male MH - Neuropsychological Tests MH - Pilot Projects MH - Severity of Illness Index MH - *Substance Withdrawal Syndrome MH - Time Factors MH - Treatment Outcome EDAT- 2012/08/30 06:00 MHDA- 2013/06/07 06:00 CRDT- 2012/08/30 06:00 PHST- 2012/08/30 06:00 [entrez] PHST- 2012/08/30 06:00 [pubmed] PHST- 2013/06/07 06:00 [medline] AID - 10.1080/13607863.2012.717255 [doi] PST - ppublish SO - Aging Ment Health. 2013;17(1):125-32. doi: 10.1080/13607863.2012.717255. Epub 2012 Aug 28.