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HAND DIAGNOSTIC ISSUES OHTN HIV End Game October 26, 2016 Reuben - PowerPoint PPT Presentation

HAND DIAGNOSTIC ISSUES OHTN HIV End Game October 26, 2016 Reuben N. Robbins, PhD New York State Psychiatric Institute and Columbia University Disclosures No financial conflicts of interest to disclose Funded by NIH: NIMH, NIAID, NINR,


  1. HAND DIAGNOSTIC ISSUES OHTN HIV End Game October 26, 2016 Reuben N. Robbins, PhD New York State Psychiatric Institute and Columbia University

  2. Disclosures • No financial conflicts of interest to disclose • Funded by NIH: NIMH, NIAID, NINR, NICHD

  3. Clinical Presentation  Memory problems  Slowed thinking  Concentration problems  Planning difficulties  Multitasking difficulties

  4. Consequences  Disrupt ADLs/IADLs  Work/employment difficulties  Mild symptoms can predict further decline  Lower quality of life  Greater need for social services  Neurocognitive deficits linked to greater HIV risk behaviors and poor decision making

  5. Clinical Assessment  Neuropsychological Assessment/Evaluation Detailed history: medical, psychiatric, psychosocial,  education, work/employment/functional status Series of tests to evaluate domains of cognitive  functioning (usually multiple tests per domain):  Verbal and visual learning and memory  Working memory/attention  Motor functioning  Speed of information processing  Executive functions (set-shifting, problem solving, abstract thinking)  And measures for psychological/emotional functioning

  6. HAND Nosology  Developed primarily for research to describe the cognitive effects of HIV  Where cognitive effects not better explained by factors/co-morbidities other than HIV  Asymptomatic Neurocognitive Impairment (ANI)  Mild Neurocognitive Disorder (MND)  HIV-Associated Dementia (HAD)

  7. HAND Criteria ANI Abnormality in two or more cognitive abilities MND (≥ 2 cognitive domains, each 1 SD below mean) Abnormality in two or HAD No functional more cognitive abilities Marked cognitive impairment (≥ 2 cognitive domains, impairment (2 each 1 SD below mean) cognitive domains, 2 SD below mean) With marked With mild functional functional impairment impairment

  8. Screening for HAND  In absence of a neuropsychological evaluation, screening tests can assist in detecting HAND  Recommended for routine and ongoing care/monitoring (e.g., at HIV diagnosis, at regular check-ups, and/or use algorithms to screen most at risk for HAND)  Commonly used tests in HIV, such HDS, MoCA, and MMSE, relatively brief and easier to administer than a neuropsychological battery  However, these tests often lack adequate sensitivity and/or specificity to detect mild HAND

  9. Screening for HAND  Computerized/tablet-based screening tests may be better at detecting milder forms of HAND  CogState  CAMCI Brain Baseline   NeuroScreen  Easy to administer by non-specialized personnel  Hold potential to be scale-able and more easily implementable than paper-and-pencil tests  ‘Connected’ technology can integrate into EMRs, databases/big data platforms

  10. Screening for HAND Ongoing research to evaluate screening tests sensitivity  and specificity to detect mild impairment in a variety of HIV populations  Older age  Co-morbidities  Different countries/languages  Resource limited settings, e.g., inner New York City and sub- Saharan Africa Still very important to know the normative sample used  to validate the test Computerized tests, at least currently, do not include  measures of mental health (e.g., depression) or daily functioning

  11. Screening for HAND  Important caveats for screening tests: Not definitive – trying to find patients most likely to  have HAND/impairment  Test subject to false positives and false negatives  In absence of definitive biomarker, must work with these short comings Often not done with a detailed history  Positive result on a screening test should trigger  follow-up evaluation

  12. Challenges  Is it normal aging?  How bad is it?  Do I have Alzheimer’s?  What can I expect?  Level if impairment in HIV can fluctuate over time  Pre-ART/post-ART  Is it due to HIV?  Is it ART toxicity?  What role are co-morbidities playing?  What do we do?

  13. Other Challenges  Research has identified numerous challenges to neurocognitive testing:  Education  Language  Cultural acceptance  Test exposure  Norms  Provider and patient awareness/concern

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