Background
It has been 15 years since the 16th Surgeon General’s landmark report on mental health, which conveyed a central message that mental health is fundamental to health and that mental disorders are real health conditions. Yet, patients and providers continue to struggle with stigma and systems of care that make addressing mental health a challenge and eliminating disparities an elusive aim. Routine screening for depression in primary care is recommended when staff-assisted supports are in place.1 Health care professionals are also advised to ask adults about their drinking habits and provide counselling to those who drink at a risky or hazardous level.2 Comorbid mental health conditions are also prevalent in primary care and concerning in settings with high rates of unmet mental health needs.
Assessment of mental health is challenging in part because providers have a limited amount of time with each patient to collect important clinical data and provide preventive medical services.3,4 Social history and behavioural health information are among commonly missed preventive screens.5 This may in part be due to the perceived extended time to assess these domains, and the fact that it may represent more sensitive data. Relying on existing staff to interview patients is time consuming, and research has shown that patients are more likely to disclose sensitive information to a computer.6 Freely available standardised, validated self-assessments exist that can accurately detect depression (Patient Health Questionnaire, PHQ-2 & PHQ-9), substance abuse (Drug Abuse Screening Test, DAST-10, Alcohol Use Disorders Identification Test, AUDIT- 10), risk for bipolar disorder (Mood Disorders Questionnaire, MDQ) and post-traumatic stress disorder (Posttraumatic Stress Disorder-Primary Care, PTSD-PC). Having self-service kiosks that patients can engage for ‘wellness assessment’ and screening for risky use of substances and highly prevalent mood disorders in primary care is both patient-centred and promotes efficiency in patient flow as patients spend valuable time waiting during the clinic visit. Patients’ wait time can be used to collect important clinical information that providers could use to aid their decision-making and prioritisation of issues.
Grady Health System is one of the nation’s largest public hospitals. The Asa G. Yancey, Sr. M.D. Health Center (Asa Yancey), was the first of six neighbourhood health centres with comprehensive primary care services in the greater Atlanta community.
Asa Yancey provides primary and preventive health care to adult and paediatric patients. Additional services on site include nutrition, pharmacy, radiology and laboratory, social services, and family planning. Physicians employed with Grady Health System provide medical care with nurse practitioners and midwives on site. The clinic is located approximately five miles from the main campus, and in 2012, it had over 20,000 patient encounters, of which almost 15,000 were for adult patients. Consistent with the mission of the health system, the clinic provides primary care services to individuals regardless of their ability to pay. Of the patient population, within the clinic, 45% is uninsured; Medicare covers 20%, and 15% of the population is covered by Medicaid. The clinic population is predominantly English speaking (99%), non-Hispanic (91%) and African-American (96%). Of the patients, 68% are women, and the mean age is 52 years. Most of the patients are unmarried (56%) or divorced (17%). The clinic is staffed by six adult providers who provide 4.6 full-time equivalent (FTE) staffing for adult primary care services. Providers were previously trained in the use of paper versions of these standardised, validated instruments and were also trained in the use of treatment algorithms to respond to assessment results. Providers also participated in SBIRT (screening, brief intervention, referral and treatment) training, which included exposure to motivational interviewing techniques.
A quality improvement project was designed to pilot the feasibility and acceptability of a self-service kiosk in a primary care waiting room, and later, in triage areas. Prior to this improvement project, only some behavioural health domains were assessed routinely. When these data were collected, paper forms were completed and then scanned into electronic health record (EHR), or written within the progress note. This prohibited tracking of progress or outcomes at the individual patient or system level. Although there were some clinician-administered surveys that could have been written into the health system’s EHR with significant cost investment, this would also require more provider/staff time, and the benefits were perceived as limited due to the length of assessment time within the context of patient visits. The current report describes the kiosk pilot implementation and presents results from screening efforts.