Data Collection

 

CQI+ data is collected at three points in time during a patient's episode of care.  Data is collected at admission to, and discharge from the program by the program staff, and at post-discharge follow-up by MHO staff.  Data may be collected in either hardcopy or electronic form.

 


A wide range of clinical data is consistently collected at each of the three time-points allowing for an assessment of key clinical variables over time.  The depth of data collected depends on the specific CQI+ System purchased.

Medical History

■ Psychiatric and Physical
■ Medication Usage
  Co-morbid Illness
Demographics

Baseline Clinical Information
■ Level of Depression
■ Cognitive Functioning
■ Functioning
■ Symptomatology

Data collected at admission becomes the baseline measurement for each patient and the program as a whole.

 

■ Level of Depression
■ Cognitive Functioning
■ Functioning
■ Symptomatology
■ Medication Usage
■ Patient Satisfaction
■ Discharge Diagnosis Axis I-V
 
Data collected at program discharge allows each program to measure its immediate clinical impact on patients.

 

■ Level of Depression
■ Symptomatology
■ Medication Usage
■ Medical History Since Discharge
■ Living Arrangements

Data collected by MHO staff at post-discharge follow-up allows programs to assess whether clinical impact was sustained.

 

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