everything you need to know about mental health in 60 minutes… dr tom tasker gp with special...
TRANSCRIPT
Everything you need to Everything you need to know about Mental Health know about Mental Health
in 60 minutes…in 60 minutes…
Dr Tom Tasker
GP with Special Interest in Mental Health NHS Salford
OverviewOverviewAntidepressantsNew NICE guidanceImproving Access To Psychological
Therapies (IAPT)Stepped Care ModelPhysical health in SMICase Studies
When – DepressionWhen – Depression Mild (PHQ-9: < 10)
– Avoid – Unless:
– Past h/o severe depression– Not responding to other interventions
Moderate (PHQ-9: 10 – 19)– Consider – Discuss with patient
Severe (PHQ-9: 20+)– Encourage to take– Evidence best for comb’n of AD + Psychological therapy
When – Anxiety DisordersWhen – Anxiety Disorders
Mild/moderate– Avoid– Psychological Therapy 1st line (NICE)
Moderate/severe– Consider if loss of function– Should be an adjunct to Psychological therapies
When – Depression/anxietyWhen – Depression/anxiety
If depression is accompanied by marked anxiety….
TREAT DEPRESSION FIRST
Consider AD as appropriate
Draft NICE guidance re ADsDraft NICE guidance re ADs
Generic SSRI 1st line– Efficacy– Better tolerated– Favourable risk-benefit ratio– Less likely to be discontinued because of side
effects– Low acquisition-cost
– (Paroxetine: higher rate of discontinuation symptoms)
Draft NICE Guidance for ADsDraft NICE Guidance for ADs
2nd line:– Different SSRI– Better tolerated newer generation AD
Combining ADs– Remit of GPSI/psychiatrist– SSRI plus mirtazapine
Do not initiate dosulepin– Increased cardiac risk – Toxicity in OD
Draft NICE guidance for ADSDraft NICE guidance for ADS
What is the best strategy following 6-8 weeks of adequate treatment?
– Suggest RCT to assess: Continuing same/increasing dose of SSRI Switch to another SSRI Switch to AD of different class
Which – Depression (Salford)Which – Depression (Salford)
1st line:– Sertraline
2nd line– Change class
Mirtazapine Venlafaxine Duloxetine
Which – Anxiety (Salford)Which – Anxiety (Salford)
1st Line– Citalopram
2nd line– Escitalopram– Venlafaxine
Cost per monthly prescriptionsCost per monthly prescriptions
Fluoxetine 20mg 69p Citalopram 20mg £1.24 Sertraline 50mg £1.37 Escitalopram 10/20mg £15/£25 Mirtazapine 30/45mg £3.28 - £19 Duloxetine 60mg £27.72 Venaxx/venlalic 75–225mg £10 - £30
Good prescribing tipsGood prescribing tips
Considerations– Length of initial prescription– Toxicity in overdose– When to review– Careful in < 30 years old
Good prescribing tipsGood prescribing tips
How often to review?– (1) week– 2 weeks– 4 or 5 weeks– 8 weeks– 12 weeks– 1 – 2 monthly thereafter
Good prescribing tipsGood prescribing tips
When to consider increasing dose?– No response – 2-3 weeks– Partial response – 4 – 6 weeks– Switch after 4-6w if unsatisfactory
response
Good prescribing tipsGood prescribing tips
How long to treat for?– At least 6 months after remission– If recurrent consider 1 – 2 years
Consider acute v repeat prescriptions
Try to avoid ADs in bereavement (except in past h/o depression)
Good prescribing tipsGood prescribing tips
Tricyclics– Avoid subtherapeutic doses– Helps anxiety symptoms but not depression
Avoid dosulepin altogether– No new initiations– Consider switching
How much is being invested in the Improving How much is being invested in the Improving Access to Psychological Therapies programme Access to Psychological Therapies programme
in the next 3 years?in the next 3 years?
A £173,000
C £ 17.3million
B £1.73 million
D £173 million
How much is being invested in the Improving How much is being invested in the Improving Access to Psychological Therapies programme Access to Psychological Therapies programme
in the next 3 years?in the next 3 years?
D £173 million
Improving Access to Psychological Improving Access to Psychological Therapies (IAPT)Therapies (IAPT)
Comprehensive Spending Review 2007
– £30 million in 2008/9– £70 million in 2009/10– £70 million in 2010/11
11stst wave - IAPT 2008/9 wave - IAPT 2008/9
35 pilot sites in 2008/9
5 sites in NW SHA
Salford – 26 new trainees– 11 Low Intensity (Graduate Workers)– 15 High intensity (CBT workers)
IAPTIAPT
NICE-compliant (Stepped care model) Step up/down as necessary Step 2
– Low Intensity Interventions Step 3
– High Intensity Interventions (CBT, IPT) Step 4
– Non-IAPT (Psychology Services)
Low Intensity WorkersLow Intensity Workers
Low intensity interventions- Medication management– Behavioural activation– Problem-solving– Guided self-management– Brief CBT– Signposting
4 – 6 sessions x 30 minutes
Condition requiring Condition requiring treatmenttreatment
Who’s responsible for care?Who’s responsible for care? What do they do?What do they do?
Step 4Step 4
Complex DisordersComplex Disorders
Significant TraumaSignificant Trauma
Abnormal Grief ReactionsAbnormal Grief Reactions
Non-IAPTNon-IAPT
(Psychologists,counsellors)(Psychologists,counsellors)
Medication
Complex psychological interventions
Combined treatments
Step 3Step 3
Moderate/severe depression/anxiety disorders not responding to LI
PTSD/Severe OCD
High Intensity IAPTHigh Intensity IAPT
CBT
IPT
Step 2Step 2 Mild depression/anxietyMild depression/anxiety
Moderate/severe anxiety Moderate/severe anxiety disordersdisorders
Low Intensity IAPT workers (PCMHS)Low Intensity IAPT workers (PCMHS)
Watchful waiting
Medication Management
Behavioural Activation
Problem-solving
Brief CBT
Signposting
Step 1Step 1 RecognitionRecognition GP and practice teamGP and practice team Assessment
Stepped Care ModelStepped Care Model
Framework in which to organise services
Aim is to provide the least intrusive, most effective intervention first
Patients should enter at the step that is appropriate to them but generally the least intensive
Patients can be stepped up or down as necessary
Condition requiring Condition requiring treatmenttreatment
Who’s responsible for care?Who’s responsible for care? What do they do?What do they do?
Step 5Step 5
Risk to lifeRisk to life
Severe Self- NeglectSevere Self- Neglect
Acute inpatient serviceAcute inpatient service Assessment, Medication, observation, therapies,
24hr in-patient care
Step 4Step 4
Treatment-resistantTreatment-resistant
Atypical & Psychotic Atypical & Psychotic Depression & those at Depression & those at significant risksignificant risk
Clinical psychology (non-IAPT)Clinical psychology (non-IAPT)
CMHT input if appropriateCMHT input if appropriate
Medication
Complex psychological interventions
Combined treatments
Step 3Step 3
Moderate/severe depression
GPwSIGPwSI
Honorary Consultant PsychiatristHonorary Consultant Psychiatrist
High Intensity IAPT (PCPS)High Intensity IAPT (PCPS)
Gateway WorkersGateway Workers
Case Management (PCMHS)Case Management (PCMHS)
Medication
Liaison
CBT & Counselling
Case Management
Step 2Step 2 Mild/moderate disordersMild/moderate disorders Low Intensity IAPT workers (PCMHS)Low Intensity IAPT workers (PCMHS)
Social Prescribing Social Prescribing
Third SectorThird Sector
Watchful waiting
Behavioural Activation
Problem-solving
Brief CBT
Signposting
Arts on Prescription
Comm Health Trainers
Computerised CBT
Step 1Step 1 RecognitionRecognition GP and practice teamGP and practice team Assessment
Physical Health & SMIPhysical Health & SMI
Life expectancy– Reduced by 10 – 15 years– Younger patients at very high risk compared with general
population
Cardiovascular Disease– Mortality in excess of 2x that of general population
Diabetes– Up to 5x that of general population
Other health related issuesOther health related issues
Health inequalities Lifestyle Smoking
– 61% schizophrenia, 46% BPD(Social Exclusion Unit Report - Mental health and social exclusion) 2004
Alcohol & Drug Misuse Obesity Metabolic Syndrome Hyperprolactinaemia
Cardiovascular Risk Factors Cardiovascular Risk Factors and Schizophreniaand Schizophrenia
Non-modifiable risk factors
Modifiable risk factors
Prevalence inschizophrenia
Gender Obesity1 30–40% (1.5–2 ×)
Family history Smoking2 50–80% (2–3 ×)
Personal history Diabetes3 11–15% (2 ×)
Age Hypertension4 58%
Ethnicity Dyslipidaemia4 45%
1Davidson et al. Aust NZ J Psychiatry. 2001;35:196–202;; 2Herran et al. Schizophr Res. 2000;4:373–381; ; 3Dixon et al. Schizophr Bull. 2000;26:903–912; 4Kato et al. Prim Care Companion J Clin Psychiatry. 2005;7:115–118
Metabolic Syndrome Metabolic Syndrome (IDF Definition 2005)(IDF Definition 2005)
• Metabolic syndrome defined as criterion one plus
any two of next four criteria:1. Central obesity Men 94 cm (37inches)
Women 80 cm (31.5 inches)
Blood pressure ≥130/85 mmHg
Triglycerides ≥1.7 mmol/L
HDL cholesterol Men <1.03 mmol/L
Women <1.29mmol/L
Fasting blood glucose
≥5.6 mmol/L
IDF = International Diabetes Federation; HDL = High-density Lipoprotein; Available at www.idf.org
The core problem...?The core problem...?
n=12,363BMI = Body Mass IndexPark et al. Arch Intern Med. 2003;163:427–436
Prevalence of Metabolic Syndrome Prevalence of Metabolic Syndrome According to BMIAccording to BMI
Men Women
BMI ≥30
4.6 6.2
22.428.1
59.6
50
0
10
20
30
40
50
60
70
Pre
vale
nce
(%
)
Healthy
BMI <25
Overweight
BMI 25–29.9
Obese Overweight
BMI 25–29.9
Healthy
BMI <25 BMI ≥30
Obese
BMI = Body Mass IndexAllison et al. J Clin Psychiatry. 1999;60:215–220
Prevalence of Obesity is Increased in Prevalence of Obesity is Increased in SchizophreniaSchizophrenia
Normal weight Overweight Obese
0
5
10
15
20
25
30
BMI category
Schizophrenia
No schizophrenia
<2020–22
>22–25
>24–26
>26–28
>28–30
>30–33
>33–35>35
Per
cen
tag
e
Isomaa et al. Diabetes Care. 2001;24:683–689
4.6
2.2
12.0
18.0
0
2
4
6
8
10
12
14
16
18
20
Total mortality CV mortality
Mo
rtal
ity
(%)
Metabolic syndrome absent
Metabolic syndrome present
***p<0.001 vs. patients without metabolic syndromeCV = Cardiovascular
Median follow-up: 6.9 years
Metabolic Syndrome Increases Total Metabolic Syndrome Increases Total and Cardiovascular Mortalityand Cardiovascular Mortality
***
***
Prevalence of Diabetes in Prevalence of Diabetes in Schizophrenia vs. General Schizophrenia vs. General
PopulationPopulation
0
5
10
15
20
25
30
General population
People with schizophrenia
Pre
vale
nce
(%
)
25–3515–35 35–45 45–55 55–65
Age range (years)
De Hert et al. Clin Pract Epidemiol Mental Health. 2006;2:14n=415 patients with schizophrenia
Osborn et al, Arch Gen Psychiatry Vol Osborn et al, Arch Gen Psychiatry Vol 64 Feb 200764 Feb 2007
46 136 people with SMI 300 426 without SMI were selected for the study
Hazard ratios (HRs) in people with SMI compared with controls were:
for CHD mortality 3.22 (95% CI, 1.99-5.21) for people 18 - 49 yrs 1.86 (95% CI, 1.63-2.12) for those 50 - 75 yrs 1.05 (95% CI, 0.92-1.19) for those > 75 yrs
Osborn et al, Arch Gen Psychiatry Feb Osborn et al, Arch Gen Psychiatry Feb 20072007
For stroke deaths, the HRs were:
2.53 (95% CI, 0.99-6.47) for those < 50 yrs 1.89 (95% CI, 1.50-2.38) for 50 - 75 yrs 1.34 (95% CI, 1.17-1.54) for > 75 yrs
Increased HRs for CHD mortality occurred irrespective of:
sex SMI diagnosis Or prescription of antipsychotic medication
However a higher prescribed dose of antipsychotics predicted greater risk of mortality from CHD and stroke
Further Findings from Osborn et al, 2007
Other Common Physical Other Common Physical Health ProblemsHealth Problems
People with schizophrenia are also at increased risk for:– Hyperprolactinaemia
Particularly associated with conventional antipsychotics, risperidone, amisulpride
– Sexual dysfunction May also be a consequence of conventional
antipsychotic therapy; the causal link with atypical antipsychotics is less clear
Mental Health Indicator 9 -Mental Health Indicator 9 -Annual Physical Health CheckAnnual Physical Health Check
Alcohol & drug misuse Smoking BMI/waist circumference BP Diabetes screening Lipid profiles in patients
– > 40 years– Those on atypical antipsychotics
Mental Health Indicator 9 -Mental Health Indicator 9 -Other issues to considerOther issues to consider
Cervical ScreeningDental & Eye CareImms & VaccsMedication compliance & side effects
Mental Health Indicator 6 -Mental Health Indicator 6 - Psychiatry Care Plan Psychiatry Care Plan
Check contact details for:– Main Carer– Care Co-coordinator & all key people involved in care
Check follow up arrangements with specialist mental health services
Check patient awareness of early signs of relapse Check patient’s preferred course of action in event of
relapse Social situation
– CAB, Welfare, Benefits
Salford InitiativesSalford Initiatives
Shared Care Protocol for Atypical Antipsychotics
Tackling DNA rates for physical health checks
SCP for Atypical AntipsychoticsSCP for Atypical Antipsychotics
Incentivised scheme 3 visits: – baseline to be done by specialist MHS
– 3m & 6m checks to be done in Primary Care– Annually thereafter as part of QOF
At each visit:– BMI/waist– BP– Fasting BS– Fasting lipids (not at 3m visit)
Salford CMHT InitiativesSalford CMHT Initiatives
Care Programme Approach– Current CPA amended– Physical Illness Domain to be extended to include
physical health check
Care coordinator role– Pivotal– Responsibility to ensure health check has been done
Follow up of DNA’sFollow up of DNA’s
If patient DNAs their annual physical health check:
– Requirement under QuOF (MH 7)
– GP to cc DNA letter to care coordinator
– Care coordinator to follow up
““Hard to reach” SMI patientsHard to reach” SMI patients
CHUG (Cromwell House User group meeting):– No previous dialogue re physical health– Interested in physical health
Education, awareness
– Prefer to undergo check in CMHT– Don’t like attending GP surgeries
Don’t like environment Stigmatised Physical symptoms attributed to SMI Not listened to
SurveySurvey
Service User Representative:– Wider report to looked at:
How to deliver promotional campaign:– raise awareness– education
Check out why they won’t attend GP How to facilitate attendance at GP surgeries Types of interventions they want to see at
CMHT level
Results of SurveyResults of Survey
48 responses:– Education – want to talk to Care co-ordinator
(rather than leaflets/posters)– 70% had a physical health check in past 15m– >90% of checks done at GP surgery– Reassured – GP knows about physical health– Barriers:
Getting appointment GP running late
Case Study 1Case Study 1
AF: 28y, male– 1st episode of depression x 6w– Lost job, financial difficulties– Losing contact with friends– Stopped going to the gym– Putting on weight– PHQ score 11
Case Study 1 – Management PlanCase Study 1 – Management Plan
Mild depression Referred to Low Intensity Therapist
– Behavioural activation– Problem-solving approach– Signposted to CAB
Referred for cCBT for relapse prevention Liaison with JCP PHQ score 4 on discharge
Case Study 2Case Study 2
MS, 42y, female Chronic depression
– On maintenance dose of fluoxetine 20mg¹ x 5y Relapse Oct 08
– Relationship breakdown 2008– Miscarriage 2007– Sexually abused by her father 3y ago
PHQ 23 – fleeting suicidal ideation but no plans
Case Study 2 – what happened next?Case Study 2 – what happened next?
Severe depression Increased fluoxetine 40mg¹
– Agitated, not sleeping– Increasing thoughts of self-harm
Referred Psychology (non-IAPT - Step 4) PHQ 22 (Nov 2008)
Case Study 2Case Study 2
Switched to mirtazapine 30mg nocte– Much calmer– Sleeping better– Appetite improved– No longer having thoughts of self-harm
Started psychology PHQ 14 (Jan 2009)
Case Study 3Case Study 3
TF, 58y, male Depressive episode x 1y Past h/o 2 episodes of depression T2DM Controlled Hypertension BMI 33 PHQ 18 – no suicidal ideation
Case Study 3 – what happened next?Case Study 3 – what happened next?
Recurrent depression Started citalopram 20mg¹ After 3w, no subjective improvement (PHQ 19) Citalopram increased to 40mg¹ Referred to Low Intensity Therapist
– Medication Management– Behavioural activation– 6 sessions x 30 mins
6w after presentation - PHQ score 20
Case Study 3Case Study 3
Switched to duloxetine 60mg¹
Stepped up from Low Intensity to High Intensity i.e. step 2 step 3
10w later PHQ 8
Maintenance therapy – 2y according to NICE
Referred to Arts on Prescription
Thanks for your attentionThanks for your attentionAny questions?Any questions?