Characterizing Persistent Disturbing Behavior Using Longitudinal and Multivariate Techniques Jan...
-
date post
20-Dec-2015 -
Category
Documents
-
view
220 -
download
0
Transcript of Characterizing Persistent Disturbing Behavior Using Longitudinal and Multivariate Techniques Jan...
Characterizing Persistent Disturbing Behavior Using Longitudinal and
Multivariate Techniques Jan Serroyen, UHasselt
Liesbeth Bruckers, UHasselt
Geert Rogiers, PZ Sancta Maria
Geert Molenberghs, UHasselt
QMSS - UHasselt - 2 -
Outline
Persistent Disturbing Behavior (PDB)
Research questions
Pilot study
Longitudinal analysis
Cluster analysis
Concluding remarks
QMSS - UHasselt - 3 -
Persistent Disturbing Behavior
Observation by mental health care professionals
Problematic group of patients:Disturbing behavior
Therapy resistant
Living together is extremely difficult
Intensive supervision over 24h
QMSS - UHasselt - 4 -
Where do they belong?
Psychiatric hospital (PH): Definition: non-residential institution for intensive
specialist care Problem: need for a prolonged stay
Psychiatric nursing home (PNH): Royal Decree: chronic and stabilized psychiatric
conditions Problem: instable disease status
QMSS - UHasselt - 5 -
Research Questions
Distinguish PDB from non-PDB
Size of PDB group
Homogeneous group or subgroups
QMSS - UHasselt - 6 -
Minimal Psychiatric Data (MPD)
Imposed by the Ministry of Public Health
Started in 1996
Goal : Transparency in care Diversity of patients Variability in care
Items Socio demographic Diagnostic items (DSM IV) Psycho-social problems Received treatment
QMSS - UHasselt - 7 -
Pilot study
Cross-sectional study in 1998 (N = 611)
Discriminant analysis: PDB screening by expert opinion
Discriminant function: based on MPD data
Sensitivity & Specificity: 72% - 85%
80% correctly classified
Conclusion: PDB is a substantial group
Focus on disturbance aspect
QMSS - UHasselt - 8 -
QMSS - UHasselt - 9 -
Longitudinal analysis
Aim: study persistence dimension
Discriminant analysis -> PDB-score
Calculate score at other registration occasions
-> PDB-score over time
QMSS - UHasselt - 10 -
QMSS - UHasselt - 11 -
QMSS - UHasselt - 12 -
Linear mixed-effects model
QMSS - UHasselt - 13 -
Linear mixed-effects model
Separate models for both types of institutions
Starting model:Mean structure: PDB group, time, time² and pairwise
interactions
Variance model: 3 group-specific random effects: intercept, time, time²
PH: group specific power-of-mean structure
PNH: group specific Gaussian serial correlation structure
QMSS - UHasselt - 14 -
Linear mixed-effects model
Final model:Mean structure:
Random-effects covariance matrix:
QMSS - UHasselt - 15 -
QMSS - UHasselt - 16 -
QMSS - UHasselt - 17 -
QMSS - UHasselt - 18 -
QMSS - UHasselt - 19 -
Cluster analysis
Identify subgroups within PDB group
Gower’s distance:
can handle all outcome types
Ward’s minimum variance method
Result: 2 clusters
QMSS - UHasselt - 20 -
QMSS - UHasselt - 21 -
Concluding remarks
Differences PDB & non-PDB:Mean profilesVarianceCorrelation structure
Numerous PDB patients
Need for specialized treatment facilities