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NICE guidelines update 2013

This update provides guidelines for the assessment, identification, and management of depression in primary care settings. It includes information on psychological and pharmacological interventions, relapse prevention, and the role of general practitioners.

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NICE guidelines update 2013

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  1. NICE guidelines update 2013 Katie Simpson South Central SHA IAPT GP Clinical Lead Mental Health Lead Berks East PCT

  2. Primary Care Mental Health • 281 million consultations in Primary Care annually • 30% of all GP consultations have a Mental Health component • 90% Mental Health Problems managed by Primary Care

  3. CG90 NICE Depression guidance • Depression: review of assessment • Emphasis on psychological interventions • Pharmacological interventions new information efficacy and cost effectiveness augmenting • Relapse prevention • GP key role

  4. Principles for assessment The guidelines discourage over reliance on the number of symptoms. Instead: • Distress • Duration • Disability If the patient’s symptoms have been distressing and have been present for 2 weeks or more at a level where they have affected their ability to function normally then it is likely that they are significant

  5. Identification and assessment • Be alert to possible depression • Particularly in people with a past history of depression or a chronic physical health problem with associated functional impairment. • Consider asking people who may have depression two questions, specifically: • During the last month, have you often been bothered by feeling down, depressed or hopeless? • During the last month, have you often been bothered by having little interest or pleasure in doing things? (PHQ2) • “Is this something with which you would like help”?

  6. Role of the General Practitioner • GPs ideally placed to detect depression • “Watchful waiting” vs GP involvement in all steps of the model CG 90 not so explicit about boundaries primary care/ specialist care • But: dangers of false diagnosis and medicalisation of distress Some evidence of diagnosis and prescription in pts. not actually depressed

  7. Key points for intervention • Step 1 • Identification • Risk assessment • Active monitoring • Step 2 • Advice on sleep hygiene and activity • Low intensity psychological interventions • Step 3 • High intensity psychological interventions • Referral • Steps 2, 3, and 4 • Antidepressants • Steps 2, 3 and 4 • Provision of service delivery system

  8. The Characteristics of IAPT • Implements NICE Guidelines • Not only CBT • Stepped care • Outcome focused • Self referral

  9. Stepped Care

  10. Referral Criteria • Problems suitable for Talking Therapies • Depression • Generalised anxiety disorder • Psychological problems arising from long term medical conditions • Panic disorder • Social phobia • Specific phobias • OCD   Obsessive compulsive disorder • PTSD Post- traumatic stress disorder –moderate/single trauma e.g. RTA • Health anxiety • Medically Unexplained Physical Symptoms • Post natal depression (mild/moderate) • Employment stress, support required to stay in or obtain work.

  11. Not suitable: • Children • Psychosis • Actively suicidal • Complex problems eg PD, Severe PTSD, Moderate/Severe Eating disorders • Drug/Alcohol problems • Under Secondary Care Services

  12. NICE conclusions on antidepressant medication • When prescribing, should normally be SSRI (Selective Serotonin Receptor Inhibitors) in generic form • Avoid using routinely for subthreshold depressive symptoms • Discuss options, consider side effects, discontinuation, potential interactions, physical health, previous experience

  13. Starting antidepressant treatment Obtain patient’s agreement that they have a depressive illness, then: • Address patient concerns, views on tablets and antidepressants, and discuss common myths • Gradual effects and need to persevere • Side effects and drug interactions • Previous experience of efficacy/side effects • Discontinuation symptoms • Not addictive • Ask about St. John’s Wort • Review after 2 weeks, then at least monthly • If suicide risk or <30years review after 1 week, then frequently

  14. Mode of action: SSRI (Selective Serotonin Receptor Inhibitors)

  15. Common Side Effects of SSRIs • Nausea • Diarrhoea • Headache • Anxiety • Insomnia/drowsiness- adapt time of taking • Weight loss/gain • Sexual difficulties: lack of orgasm • Short term rx (<2 weeks) with a benzodiazepine • Care in people at risk of falls

  16. Generic SSRIs: Fluoxetine, Citalopram, Sertraline, Paroxetine • Sertraline & Citalopram are safer in patients with Long term conditions as less interactions with other medication • Paroxetine more discontinuation symptoms • Fluoxetine can increase anxiety in approx 10%

  17. Escitalopram • Isomer of citalopram • Cochrane report supported it BUT • Small no’s of patients, short term follow up, Pharmaceutically sponsored trials • Not enough information to recommend it above other treatments as much more expensive.

  18. SNRIs (Serotonin & Noradrenaline Reuptake Inhibitors) • Venlafaxine: can increase blood pressure, more toxic in overdose. • Duloxetine: Also used in diabetic neuropathy (& stress incontinence) • Side effects similar to SSRI

  19. MIRTAZEPINE

  20. Mirtazepine • Works by increasing noradrenaline and serotonin in unique way (blocking alpha adrenergic receptors) • Weight gain • Sedation- some times useful • Often used to augment other antidepressants

  21. TCADS (Tricylic Anti Depressants) e.g amitriptyline, clomipramine, dothiepin • Work on serotonin and noradrenaline • Side effects: dry mouth, constipation, blurred vision, palpitations, urinary retention • Very toxic in over dose (especially dothiepine) except lofepramine

  22. Starting Treatment • Response by 2-4 weeks • Switch or increase dose if: • Inadequate response • Side effects • Patient prefers

  23. Risk • Assess, not just using a symptom count • Assess social support • Arrange appropriate help • Advise how to seek help • GP’s are used to living in a very risky world • We can each expect a suicide every 5 years

  24. Suicide risk • Review after 1 week • Consider other forms of support e.g. More frequent direct or telephone contact • Consider referral to crisis team • Advise and monitor potential for increased agitation, anxiety and suicidal ideation • Take into account toxicity in overdose • Venlafaxine associated with increased risk • TCAs increased risk (except lofepramine)

  25. Augmenting antidepressants If person is informed and prepared to accept additional side effects, consider augmenting with: • Lithium • An antipsychotic such as aripiprazole, olanzapine, quetiapine, risperidone • Another antidepressant, such as mirtazapine or venlafaxine

  26. Relapse prevention Need to continue treatment for at least 6/12 from recovery • Continue medication for at least 2 years (If 2+ recent episodes, other risk factors, relapse consequences severe e.g occupation) • Psychological interventions: For recurrent depression Individual CBT (16-20 sessions over 3-4 months) OR Mindfulness based cognitive therapy (8 week group)

  27. Discontinuation When stopping antidepressants, gradually reduce dosage over a 4 week period • Some people may require longer, esp. With e.g. paroxetine, venlafaxine • Exception is fluoxetine • Warn about discontinuation symptoms – usually settle within a week • If symptoms mild: reassure and monitor • If symptoms severe: reintroduce original dose or another with longer half life and reduce gradually

  28. Subthreshold and mild depression • Do not routinely use drugs • Consider them for: • Those with a PMH of moderate/severe depression • H/O 2y + subthreshold symptoms • Subthreshold / mild depression persisting after other interventions

  29. Key points • GPs should be alert to possible signs of depression in patients, but should not medicalise distress • Assessment and management should be carried out according to the stepped-care model • Patients should be supported by the GP throughout the management process • GPs should use active monitoring for patients as appropriate • GPs should have knowledge of: • low-intensity psychological interventions • locally available services • Pharmacological treatment choices should be tailored to the individual patient • The use of St John’s wort is not recommended • High-intensity psychological interventions should be offered to patients with moderate to severe depression

  30. How to manage anxiety disorders in general practice Katie Simpson South Central SHA IAPT GP Clinical Lead Mental Health Lead Berks East PCT

  31. Subtypes of anxiety disorders • GAD • Panic disorder • PTSD • OCD • Social phobia • Specific phobias (e.g. spiders) • Acute stress disorder

  32. Generalised anxiety disorder • GAD (5% of GP patients) • DSM IV: ‘excessive worry and heightened tension majority of days’ ‘difficulty controlling the worry’ ‘plus additional symptoms’ ‘should cause clinically significant distress or impairment of function’ ‘6 months’

  33. Who has GAD? chronic physical health problems OR people seeking reassurance about somatic symptoms (particularly the elderly and those from minority ethnic groups) OR repeatedly worrying about a range of issues

  34. Stepped care in GAD • Step 1 – identification and assessment, education and active monitoring • Step 2 – individual pure self help, individual guided self help or psycho-educational groups. Books: ‘Living with fear’ by Marks IM, ‘Mastery of your anxiety and panic’ by Barlow DH ‘Overcoming anxiety’ by Kennerley H. • Step 3 – high-intensity psychological interventions (CBT or applied relaxation) OR drug treatment (Sertraline). See them within 1 week of starting rx • Full anxiolytic effect takes 1 week or more. • Important to cont rx after remission to prevent relapse (at least 1 year). • Step 4 – consider referral to secondary care

  35. SSRI/SNRI at step 3 • Sertraline 1st line • If ineffective/ not tolerated then another SSRI or SNRI • Consider: withdrawal syndrome/ side effect profile/ risk of suicide/self harm-toxicity in OD/previous experience of drug rx

  36. Pregabalin • If pt cannot tolerate SSRIs then offer pregabalin or SNRI • Also used in neuropathic pain & epilepsy • Side effects : dizziness, drowsiness, dry mouth, ankle swelling , blurred vision, poor concentration, weight gain

  37. Benzodiazepines • Do not offer BDZs for Rx of GAD apart from short-term measures during a crisis. Advice in BNF - not be used as sole rx for chronic anxiety. • Avoid driving- even the next morning • Can become habit forming after 2 weeks • In long term can cause rebound insomnia and anxiety

  38. Beta Blockers • B blockers help with palpitations and tremor NOT psychological symptoms/muscle tension • Side effects: cold extremities, tiredness • NOT with asthma

  39. Anti- psychotics • Do not use antipsychotics for rx of GAD in primary care e.g chlorpromazine, haloperidol, risperidone, aripiprazole • Risks out weigh benefits • Weight gain, increased risk of Diabetes, Cardio vascular disease including stroke

  40. Principles of care in GAD • Provide contact numbers and info about what to do and who to contact in a crisis • Comorbid anxiety or physical disorder? Treat the primary disorder first (the one that is more severe) • Non-harmful alcohol misuse not a contraindication to rx of GAD. However with harmful and dependent alcohol misuse rx this first as alone it may lead to a significant improvement in GAD

  41. Thank you Dr Katie Simpson South Central SHA IAPT GP Clinical Lead Mental Health Lead Berks East PCT katiesimpson2@nhs.net

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