Upload
others
View
2
Download
0
Embed Size (px)
Citation preview
DISCLOSURES
None of the faculty, planners, speakers, providers
nor CME committee has any relevant financial
relationships with commercial interest
There is no commercial support for this CME
activity
Jaswinder K. Walia, M.D.
Assistant Clinical Professor
UCR SOM, Dept of Psychiatry and Neurosciences
Associate Medical Director
RUHS BH – Western Region
Depression
Outline
Epidemiology
DSM Criteria
Types
Pathophysiology
Treatment overview
Q & A
Case
DB is a 70y/o CF w/ MDD, Passive-Aggressive PD traits
and tx non-adherence.
Seen since 2012, most recent f/u 2/2019
Case
◦ H/o Depression since her 20s
◦ Sought tx at RCMHD '85-'90, self-d/c'd b/c felt better. Was sx
free until 3/2011 when dx'd w/ breast ca and underwent
mastectomy w/in a week of dx
◦ H/o depressive sxs c/w MDD episodes
◦ No h/o mania
◦ No h/o AH/VH/PI/IOR
◦ H/o self-sabotaging behavior and passive-aggressive traits
◦ H/o intermittent passive SI consisting of "day dreams of death",
none reported in last 1y
◦ Tends to focus on Psych issues w/ PCP and DM issues in psych
office
◦ H/o good response w/ Zoloft, but chronically tx non-adherent
Case
Past Psych hx:
Psych adm x1: ITF 3/26-3/31/14 for depression and passive SI.
ETS - 11/29/11 and 12/8/11 for passive SI (also had FSBS 600).
H/o passive SI off/on
Past tx:
Zoloft 50mg qd by ETS 12/2011 - helped remit sxs.
Vistaril - helped, self-d/c'd.
Elavil ?mg + Valium 5mg qd '85-'90.
Substance use hx: none x3
Social hx: Single, lives in an indep apt since 6/10/13. IHSS 5d/wk
by PCP.
Case
PMH: Hypothyroidism (dx 11/2018), poorly controlled IDDM,
Bladder ca stage I s/p tumor resection 6/2017 w/ new recent spots
x4, h/o breast ca, s/p Rt mastectomy 3/11/11, no chemo/rad. HA1C
10 (per pt).
breast mammogram +ve 5/2018, Lt breast lumpectomy/bx on
8/1/18 neg for ca per pt
No bladder ca, ruled out by Onc in 5/2018
PCP: Dr. Kenoye Uku ("Ookoo"), Endocrine Dr. Diaz
Case
ALL: NKDA
MEDS:
Zoloft 100mg po qd
Synthroid 25mcg qam
Benazepril 2.5mg QD
OTC Ca + Vit D
OTC B-complex
OTC Vit C 1000mg qd
ASA 81mg qd
Atorvastatin 20mg po qd
Metformin 500mg bid
Novolog 70/30 20U QAM + SS tid
Lantus 70U SQ qhs
Case
Labs:
4/3/18: Lipids: chol nl, HDL 40, TG 152 CMP: glu 227,
rest nl CBC nl A1C 8.9 TSH nl B12/Folate nl UTX neg
7/13/16: Lipids: chol 203, LDL 134, HDL nl, TG nl; CMP:
glu 128, rest nl; CBC nl, TSH nl, A1C 9.2 B12/folate nl,
UTX: unable to void, to return later
7/1/15: CBC nl, TSH nl, CMP nl, Lipid nl except TG 179,
HA1C 10, B12 nl 500, TSH 3.55
Case
MSE: remarkable for:
◦ Obese (BMI 35)
◦ Rt mastectomy scar
◦ Multiple lesions, mostly old - none new, no bleed or discharge
◦ Multi old well-healed hyperpigmented lesions on b/l LE and UE,
lower legs, chest, shoulders, abdomen.
◦ Appro g+h+a. Gait steady. No PM abnl. Good eye contact. Calm,
pleasant. Speech clear/fluent. Mood "good". Affect euthymic, FR. TP
linear/goal directed. No SI/HI, intent or plan. No AH/VH/PI/IOR. AAOx4,
memory grossly intact, attn/conc nl, est intelligence avg, fund of GK avg. I
poor, J fair, IC good. Future oriented.
Case
Most recent f/u: doing well, taking meds on most days
Skin picking (legs, chest, arms, back, abdomen) continues,
no new lesions at present.
DM cont to be poorly controlled, in FBS 200-300 on
most days, in high 300s every 2-3wks and then drops to
70s x1-2/mo. Insulin and meds adjusted recently.
Case has a drawer full of multiples of all meds, including insulin. "I
have my method of numbering and how I take them."
multiples of most meds, including 4 bottles of Zoloft, all
partially full, all filled in 2016
Goes for daily walks or window shopping w/ IHSS. Goes to a
weekly Church gr. Enjoys crotchet, cross stitching and
reading. this helps her cope w/ anxiety. Feels supported by
her tx teams and church gr.
Epidemiology
Mood Disorders Prevalence : 9.5%, or 20.9 million
adults, in a given year
Median age of onset for mood disorders is 30 years.
Prevalence of all-cause depression: 6.9% in 2012 in the
U.S (NIMH)
◦ 16 million adults!
◦ Note: no exclusions were made for a major
depressive episode caused by medical illness,
bereavement, or substance use disorders.
M:F = 1:2
Depressive disorders often co-occur with anxiety
disorders and substance abuse.nimh.nih.gov
Epidemiology
Major depression one of the most common mental
disorders in the United States
Major Depressive Disorder is the leading cause of
disability in the U.S. for ages 15-44. (WHO; 2008)
MDD median age at onset is 32 years
Major depressive disorder is more prevalent in women
than in men
More than 90% of people who commit suicide have a
diagnosable mental disorder, most commonly a
depressive disorder or a substance abuse disorder.*
nimh.nih.gov
Depression - Types
Disruptive Mood Dysregulation Disorder
Major Depressive Disorder
Persistent Depressive Disorder (Dysthymia)
Premenstrual Dysphoric Disorder
Substance/Medication-Induced Depressive Disorder
Depressive Disorder Due to Another Medical Condition
Other Specified Depressive Disorder
Unspecified Depressive Disorder
Adjustment Disorder with Depressed Mood
Major Depressive Disorder
DSM -5 Diagnostic Criteria:
A) 5 or more symptoms lasting >2 wk, change from
previous functioning:
◦ Depressed mood and/or loss of interest
◦ Altered sleep, loss of energy, appetite or weight
change, feelings of worthlessness/guilt, psychomotor
changes, loss of concentration or indecisiveness,
recurrent thoughts of death/SI.
MDD
B) Symptoms cause clinically significant distress or
impairment in social, occupational, or other important
areas of function.
C) Episode not attributable to physiological effects of a
substance or medical condition.
D)Symptoms Not better explained by SAD,
Schizophreniform, Delusional D/o, or other
Schizophrenia spectrum or other psychotic disorders.
E) There has never been a manic or hypomanic episode.
MDD
Atypical presentation in the elderly:
Less sadness and feelings of guilt and more somatic
symptoms, impaired cognition and behavioral symptoms
Reversed-vegetative symptoms (e.g., hyperphagia,
hypersomnia), or leaden paralysis (heavy arms or legs)
Rejection sensitivity: a distinct, enduring pattern of
interpersonal rejection sensitivity not limited to mood
disturbances, resulting in significant social or
occupational impairment
◦ for ex: ‘my feelings are easily hurt’, ‘others do not understand
me or are unsympathetic’, and ‘others are unfriendly toward me’
MDD
Atypical presentation in the elderly:
mood reactivity (i.e., mood brightens in response to
actual or potential positive events)
Exaggerated physical symptoms – pain, GI (constipation),
insomnia
hypochondriac complaints, psychomotor
retardation/agitation
Dwelling on death themes, giving up, passive SI
At risk population
Who Tends to be Most Depressed?
CDC study found the following groups to be more likely to meet criteria for major depression:
Persons 45-64 years of age
Women
Blacks, Hispanics, non-Hispanic persons of other races or multiple races
< high school education
those previously married, recently widowed
individuals unable to work or unemployed
persons without health insurance coverage
Of note: similar patterns were found among persons with "other depression" with the two following exceptions:
=> adults aged 18-24 yrs most likely to report "other depression" as were Hispanics (instead of other non-Hispanics)
At risk population
Other factors:
Presence of physical illness, esp chronic pain
Use of multiple drugs
Existence of psychosocial stressors
Presence of brain white matter changes
Variables Late onset
depression
Early onset
depression
Rate of
cardiovascular
diseases
High Low
Familial depression Low High
Comorbid
psychiatric disease
Low High
White matter
abnormality
High Low
Executive
dysfunction
High Low
Suicide High Low
Apathy and
psychomotor
changes
High Low
late onset depression and early onset depression
Anatomic Changes
Structural neuroimaging in patients with
longstanding or untreated depression shows
Increased ventricular-brain ratio
Smaller frontal lobe volumes
Smaller hippocampal volume
Brain Activity
Neuroimaging shows altered function during depression and
changes that occur after treatment
A review of functional imaging studies (regional cerebral
blood flow, glucose metabolism, positron emission
tomography, single photon emission computed tomography,
and functional magnetic resonance imaging) found evidence
suggesting several brain regions are involved in the
pathophysiology of depression, including…
frontal and temporal lobes along with parts of the striatum,
pallidum, and thalamus
The anterior cingulate cortex and the subgenual prefrontal
cortex
altered activity in the amygdala
Neurobiological Changes in MDD
Other Changes
Sleep and circadian rhythms
Changes in sleep architecture during depression include decreased
=> REM latency
=> Slow-wave sleep
Diurnal variation in symptoms
Blunted circadian rhythms may involve body temperature, blood pressure, pulse, plasma cortisol, norepinephrine, thyroid stimulating hormone, and melatonin
Hypothalamic-pituitary-adrenal axis
It is thought that overproduction of corticotropin
releasing hormone causes excess activity of the
hypothalamic-pituitary-adrenal cortex axis in many
depressed patients
Prolonged or excessive secretion of glucocorticoids
may lead to suppression of neurogenesis and
hippocampal atrophy
Neurotransmitters
Monoamines (serotonin, norepinephrine, and
dopamine)
Gamma-aminobutyric acid (GABA)
Glutamate
Some Medical causes of Depression
Textbook of
Psychiatry, Fifth
Edition. The
American
Psychiatric
Publishing.
Substances as causes of Depression
Textbook of
Psychiatry, Fifth
Edition. The American
Psychiatric Publishing.
Interventions
Coordinate medical care with PCP and other Specialists
Identify and treat underlying medical causes
Involve family and caretakers
Groups, Therapy: role transitions, grief, dependency,
support
Medications / ECT
Depression – Med Treatment
Textbook of Psychiatry, Fifth Edition. The American Psychiatric Publishing.
Depression Tx Cont’d
Textbook of Psychiatry, Fifth Edition. The American Psychiatric Publishing.
Recovery Model Challenges the idea that severe mental illness is chronic
and that stability is the best one could hope for.
Recovery = reclaiming a meaningful life, going BEYOND
stability.
SAMHSA (Substance Abuse and Mental Health Services
Administration): “A process of change through which
individuals improve their health and wellness, live a self-
directed life, and strive to reach their full potential”.
-adaa.org Anxiety and Depression Association of America
-samhsa.gov
Recovery Model
The American Association of Community Psychiatrists
(AACP): recovery is “a personal process of growth and
change, which typically embraces hope, autonomy, and
affiliation as elements of establishing satisfying and
productive lives in spite of disabling conditions or
experiences”
Guidelines: replace paternalistic, illness-oriented
perspectives with collaborative, autonomy-enhancing
approaches
Recovery Model – Basic Principles
Per SAMHSA, Recovery:
Based on HOPE
Person-driven: Self-determination and self-direction
Occurs via many pathways: Individuals/lives are unique
Holistic: it encompasses an individual’s whole life,
including mind, body, spirit, and community.
Supported by peers and allies: Mutual support
Supported through relationship and social
networks: the presence and involvement of people who
believe in the person’s ability to recover; who offer
hope, support, and encouragement; and who also
suggest strategies and resources for change.
samhsa.gov
Recovery Model Principles
Culturally-based and influenced: values, traditions, and
beliefs are keys in determining a person’s journey and
unique pathway to recovery.
Supported by addressing trauma: foster safety (physical
and emotional) and trust, as well as promote choice,
empowerment, and collaboration.
Involves individual, family, and community strengths and
responsibility: serve as a foundation for recovery.
Based on respect: Community, systems, and societal
acceptance and appreciation for people affected by
mental health and substance use problems – including
protecting their rights and eliminating discrimination –
are crucial in achieving recovery.
adaa.org Anxiety and Depression
Association of America
Please feel free to contact Socorro with an question you may have
Socorro Guerrero
Program Coordinator
Geriatric Medicine Division
(951) 486-5623