TY - JOUR
T1 - Neuropsychiatric Symptoms in Dementia
T2 - Considerations for Pharmacotherapy in the USA
AU - Phan, Stephanie V.
AU - Osae, Sharmon
AU - Morgan, John C.
AU - Inyang, Mfon
AU - Fagan, Susan C.
N1 - Funding Information:
Howard et al. [108]; Medical Research Council and the Alzheimer’s Society
Funding Information:
AD Alzheimer’s disease, AE adverse event, ALF assisted living facility, BADLS Bristol Activities of Daily Living Scale, CGI-C Clinical Global Impression of Change, CHL chlorpromazine, CIT citalopram, CMAI Cohen-Mansfield Agitation Inventory, CSDD Cornell Scale for Depression in Dementia, DB double blind, DSM-IV Diagnostic and Statistical Manual of Mental Disorders, Fourth edition, ESC escitalopram, HAL haloperidol, ICD-10 International Statistical Classification of Diseases – tenth revision, MC multicenter, MEM memantine, MMSE Mini-Mental State Examination, M-UPDRS Modified Unified Parkinson’s Disease Rating Scale, ND no difference(s), NIH National Institutes of Health, NINCDS-ADRDA National Institute of Neurological and Communication Disorders and Stroke-Alzheimer Disease and Related Disorders Association criteria, NPI neuropsychiatric inventory, NPI-Q neuropsychiatric inventory Questionnaire, NR not reported, OLA olanzapine, PAR paroxetine, PC placebo controlled, PG parallel group, PL placebo, RAN randomized, RIS risperidone, SAE serious adverse event, SER sertraline, SIB Severe Impairment Battery, SMMSE Standardized Mini-Mental State Examination, THI thioridazine, TRI trifluoperazine, UPDRS Unified Parkinson’s disease rating scale, wk week
Funding Information:
AD Alzheimer’s disease, ADCS-ADL Alzheimer Disease Cooperative Study-activities of daily living, ADCS-CGIC Alzheimer’s Disease Cooperative Study – Clinical Global Impression of Change, AE adverse effect, AES Apathy Evaluation Scale, AIMS Abnormal Involuntary Movement Scale, ALF assisted-living facilities, ARI aripiprazole, BARS Brief Agitation Rating Scale, BEHAVE-AD Behavioral Pathology in Alzheimer’s Disease Rating Scale, BEHAVE-AD-K Korean version of the Behavioral Pathology in Alzheimer’s Disease Rating Scale, BMI body mass index, BPRS Brief Psychiatric Rating Scale, CDR Clinical Dementia Rating Scale, CGI-C Clinical Global Impression of Change, CGI-I Clinical Global Impression – Improvement, CGI-S Clinical Global Impression – Severity, CIT citalopram, CMAI Cohen-Mansfield Agitation Inventory, CMAI-C Cohen-Mansfield Agitation Inventory-Community, CMAI-K Korean version of the Cohen-Mansfield Agitation Inventory, CO crossover, CSDD Cornell Scale for Depression in Dementia, DB double blind, DLB dementia with Lewy bodies, DON donepezil, DS divalproex sodium, DSM-IV Diagnostic and Statistical Manual of Mental Disorders, Fourth edition, DXQ dextromethorphan-quinidine, ECG electrocardiogram, EPS extrapyramidal symptoms, ESRS Extrapyramidal Symptoms Rating Scale, FAST Functional Assessment Staging Test, GAL galantamine, GI gastrointestinal, h hour(s), HAL haloperidol, HAMD Hamilton Depression Rating Scale, ICD-10 International Statistical Classification of Diseases – tenth revision, IR immediate release, LOCF last observation carried forward, LTC long-term care, mADCS-CGIC modified Alzheimer Disease Cooperative Study – Clinical Global Impression of Change, MC multicenter, MEM memantine, MET methylphenidate, MMSE Mini-Mental State Examination, NBRS Neu-robehavioral Rating Scale, NBRS-A Neurobehavioral Rating Scale, agitation subscale, ND no difference(s), NIA National Institute on Aging, NIH National Institutes of Health, NIMH National Institute of Mental Health, NINCDS National Institute of Neurological and Communication Disorders and Stroke-Alzheimer Disease and Related Disorders Association criteria, NINCDS-ADRDA National Institute of Neurological and Communication Disorders and Stroke-Alzheimer Disease and Related Disorders Association criteria, NINCDS-AIREN National Institute of Neurological Disorders and Stroke-Association Internationale pour la Recherche en l’Enseignement en Neurosciences, NPI neuropsychiatric inventory, NPI-NH neuropsychiatric inventory nursing
Publisher Copyright:
© 2019, The Author(s).
PY - 2019/6/1
Y1 - 2019/6/1
N2 - Dementia affects all domains of cognition. The relentless progression of the disease after diagnosis is associated with a 98% incidence of neuropsychiatric symptoms (NPS) at some point in the disease, including depression, psychosis, agitation, aggression, apathy, sleep disturbances, and disinhibition. These symptoms can be severe and lead to excess morbidity and mortality. The purpose of this article was to describe current literature on the medication management of NPS of dementia and highlight approaches to and concerns about the pharmacological treatment of NPS in the USA. Guidelines and expert opinion favor nonpharmacologic management of NPS as first-line management. Unfortunately, lack of adequate caregiver training and a high failure rate eventually result in the use of psychotropic agents in patients with dementia. Various psychotropic medications have been studied, although how they should be used in the management of NPS remains unclear. A systematic approach to evaluation, treatment, and monitoring, along with careful documentation and evidenced-based agent and dose selection, is likely to reduce risk and improve patient outcomes. Considerations should be given to the NPS presentation, including type, frequency, and severity, when weighing the risks and benefits of initiating, continuing, or discontinuing psychotropic management. Use of antidepressants, sedative/hypnotics, antipsychotics, and antiepileptic agents should include a clear and documented analysis of risk and benefit in a given patient with dementia.
AB - Dementia affects all domains of cognition. The relentless progression of the disease after diagnosis is associated with a 98% incidence of neuropsychiatric symptoms (NPS) at some point in the disease, including depression, psychosis, agitation, aggression, apathy, sleep disturbances, and disinhibition. These symptoms can be severe and lead to excess morbidity and mortality. The purpose of this article was to describe current literature on the medication management of NPS of dementia and highlight approaches to and concerns about the pharmacological treatment of NPS in the USA. Guidelines and expert opinion favor nonpharmacologic management of NPS as first-line management. Unfortunately, lack of adequate caregiver training and a high failure rate eventually result in the use of psychotropic agents in patients with dementia. Various psychotropic medications have been studied, although how they should be used in the management of NPS remains unclear. A systematic approach to evaluation, treatment, and monitoring, along with careful documentation and evidenced-based agent and dose selection, is likely to reduce risk and improve patient outcomes. Considerations should be given to the NPS presentation, including type, frequency, and severity, when weighing the risks and benefits of initiating, continuing, or discontinuing psychotropic management. Use of antidepressants, sedative/hypnotics, antipsychotics, and antiepileptic agents should include a clear and documented analysis of risk and benefit in a given patient with dementia.
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U2 - 10.1007/s40268-019-0272-1
DO - 10.1007/s40268-019-0272-1
M3 - Review article
C2 - 31098864
AN - SCOPUS:85066040186
SN - 1174-5886
VL - 19
SP - 93
EP - 115
JO - Drugs in R and D
JF - Drugs in R and D
IS - 2
ER -