People have the right to be involved in discussions and make informed decisions about their care, as described in NICE's information on making decisions about your care.
Making decisions using NICE guidelines explains how we use words to show the strength (or certainty) of our recommendations, and has information about prescribing medicines (including off-label use), professional guidelines, standards and laws (including on consent and mental capacity), and safeguarding.
Healthcare professionals should follow our general guidelines for people delivering care:
1.2 Stepped care for adults, young people and children with OCD or BDD
The stepped‑care model draws attention to the different needs of people with OCD and BDD, depending on the characteristics of their disorder, their personal and social circumstances, their age, and the responses that are required from services. It provides a framework in which to organise the provision of services in order to identify and access the most effective interventions (see figure 1).
1.3 Step 1: awareness and recognition
Although the more common forms of OCD are likely to be recognised when people report symptoms, less common forms of OCD and many cases of BDD may remain unrecognised, sometimes for many years. Relatively few mental health professionals or GPs have expertise in the recognition, assessment, diagnosis and treatment of the less common forms of OCD and BDD.
1.3.1.1
Each primary care trust, mental healthcare trust and children's trust that provides mental health services should have access to a specialist OCD/BDD multidisciplinary team offering age‑appropriate care. This team would perform the following functions: increase the skills of mental health professionals in the assessment and evidence‑based treatment of people with OCD or BDD, provide high‑quality advice, understand family and developmental needs, and, when appropriate, conduct expert assessment and specialist cognitive‑behavioural and pharmacological treatment.
1.3.1.2
Specialist mental healthcare professionals in OCD or BDD should collaborate with local and national voluntary organisations to increase awareness and understanding of the disorders and improve access to high‑quality information about them. Such information should also be made available to primary and secondary healthcare professionals, and to professionals from other public services who may come into contact with people of any age with OCD or BDD.
1.3.1.3
Specialist OCD/BDD teams should collaborate with people with OCD or BDD and their families or carers to provide training for all mental health professionals, cosmetic surgeons and dermatology professionals.
1.5 Steps 3 to 5: treatment options for people with OCD or BDD
Effective treatments for OCD and BDD should be offered at all levels of the healthcare system. The difference in the treatments at the higher levels will reflect increasing experience and expertise in the implementation of a limited range of therapeutic options. For many people, initial treatment may be best provided in primary care settings. However, people with more impaired functioning, higher levels of comorbidity, or poor response to initial treatment will require care from teams with greater levels of expertise and experience in the management of OCD/BDD.
Irrespective of the level of care, the following recommendations should be taken into account when selecting initial treatments for people with OCD or BDD. The specific recommendations on how to provide these treatments follow in the subsequent sections.
Regulatory authorities have identified that the use of selective serotonin reuptake inhibitors (SSRIs) to treat depression in children and young people may be associated with the appearance of suicidal behaviour, self‑harm or hostility, particularly at the beginning of treatment. There is no clear evidence of an increased risk of self‑harm and suicidal thoughts in young adults aged 18 years or older. But individuals mature at different rates and young adults are at a higher background risk of suicidal behaviour than older adults. Hence, young adults treated with SSRIs should be closely monitored as a precautionary measure. The Committee on Safety of Medicine's Expert Working Group on SSRIs, at a meeting in February 2005, advised that it could not be ruled out that the risk of suicidal behaviour, hostility and other adverse reactions seen in the paediatric depression trials applies to use in children or young people in all indications. Consequently, the recommendations about the use of SSRIs for people of any age with OCD or BDD have taken account of the position of regulatory authorities.
1.5.1 Initial treatment options
Adults
The intensity of psychological treatment has been defined as the hours of therapist input per patient. By this definition, most group treatments are defined as low intensity treatment (less than 10 hours of therapist input per patient), although each patient may receive a much greater number of hours of therapy.
1.5.1.1
In the initial treatment of adults with OCD, low intensity psychological treatments (including exposure and response prevention [ERP]; up to 10 therapist hours per patient) should be offered if the patient's degree of functional impairment is mild and/or the patient expresses a preference for a low intensity approach. Low intensity treatments include:
-
brief individual cognitive behavioural therapy (CBT; including ERP) using structured self‑help materials
-
brief individual CBT (including ERP) by telephone
-
group CBT (including ERP; note, the patient may be receiving more than 10 hours of therapy in this format).
1.5.1.2
Adults with OCD with mild functional impairment who are unable to engage in low intensity CBT (including ERP), or for whom low intensity treatment has proved to be inadequate, should be offered the choice of either a course of an SSRI or more intensive CBT (including ERP; more than 10 therapist hours per patient), because these treatments appear to be comparably efficacious.
1.5.1.3
Adults with OCD with moderate functional impairment should be offered the choice of either a course of an SSRI or more intensive CBT (including ERP; more than 10 therapist hours per patient), because these treatments appear to be comparably efficacious.
1.5.1.4
Adults with OCD with severe functional impairment should be offered combined treatment with an SSRI and CBT (including ERP).
1.5.1.5
Adults with BDD with mild functional impairment should be offered a course of CBT (including ERP) that addresses key features of BDD in individual or group formats. The most appropriate format should be jointly decided by the patient and the healthcare professional.
1.5.1.6
Adults with BDD with moderate functional impairment should be offered the choice of either a course of an SSRI or more intensive individual CBT (including ERP) that addresses key features of BDD.
1.5.1.7
Adults with BDD with severe functional impairment should be offered combined treatment with an SSRI and CBT (including ERP) that addresses key features of BDD.
Children and young people
1.5.1.8
For children and young people with OCD with mild functional impairment, guided self‑help may be considered in conjunction with support and information for the family or carers.
1.5.1.9
Children and young people with OCD with moderate to severe functional impairment, and those with OCD with mild functional impairment for whom guided self‑help has been ineffective or refused, should be offered CBT (including ERP) that involves the family or carers and is adapted to suit the developmental age of the child as the treatment of choice. Group or individual formats should be offered depending upon the preference of the child or young person and their family or carers.
1.5.1.10
All children and young people with BDD should be offered CBT (including ERP) that involves the family or carers and is adapted to suit the developmental age of the child or young person as first‑line treatment.
1.5.1.11
If psychological treatment is declined by children or young people with OCD or BDD and their families or carers, or they are unable to engage in treatment, an SSRI may be considered with specific arrangements for careful monitoring for adverse events.
1.5.1.12
The co‑existence of comorbid conditions, learning disorders, persisting psychosocial risk factors such as family discord, or the presence of parental mental health problems, may be factors if the child or young person's OCD or BDD is not responding to any treatment. Additional or alternative interventions for these aspects should be considered. The child or young person will still require evidence‑based treatments for his or her OCD or BDD.
1.5.2 How to use psychological interventions
Adults
1.5.2.2
For adults with obsessive thoughts who do not have overt compulsions, CBT (including exposure to obsessive thoughts and response prevention of mental rituals and neutralising strategies) should be considered.
1.5.2.3
For adults with OCD, cognitive therapy adapted for OCD may be considered as an addition to ERP to enhance long‑term symptom reduction.
1.5.2.4
For adults with OCD living with their family or carers, involving a family member or carer as a co‑therapist in ERP should be considered where this is appropriate and acceptable to those involved.
1.5.2.5
For adults with OCD with more severe functional impairment who are housebound, unable or reluctant to attend a clinic, or have significant problems with hoarding, a period of home‑based treatment may be considered.
1.5.2.6
For adults with OCD with more severe functional impairment who are housebound and unable to undertake home‑based treatment because of the nature of their symptoms (such as contamination concerns or hoarding that prevents therapists' access to the patient's home), a period of CBT by telephone may be considered.
1.5.2.7
For adults with OCD who refuse or cannot engage with treatments that include ERP, individual cognitive therapy specifically adapted for OCD may be considered.
1.5.2.8
When adults with OCD request forms of psychological therapy other than cognitive and/or behavioural therapies as a specific treatment for OCD (such as psychoanalysis, transactional analysis, hypnosis, marital or couple therapy) they should be informed that there is as yet no convincing evidence for a clinically important effect of these treatments.
1.5.2.9
When family members or carers of people with OCD or BDD have become involved in compulsive behaviours, avoidance or reassurance seeking, treatment plans should help them reduce their involvement in these behaviours in a sensitive and supportive manner.
1.5.2.10
Adults with OCD or BDD with significant functional impairment may need access to appropriate support for travel and transport to allow them to attend for their treatment.
1.5.2.11
Towards the end of treatment, healthcare professionals should inform adults with OCD or BDD about how the principles learned can be applied to the same or other symptoms if they occur in the future.
Children and young people
Psychological treatments for children and young people should be collaborative and engage the family or carers. When using psychological treatments for children or young people, healthcare professionals should consider the wider context and other professionals involved with the individual. The recommendations on the use of psychological interventions for adults may also be considered, where appropriate.
1.5.2.12
In the cognitive‑behavioural treatment of children and young people with OCD or BDD, particular attention should be given to:
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developing and maintaining a good therapeutic alliance with the child or young person, as well as their family or carers
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maintaining optimism in both the child or young person and their family or carers
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collaboratively identifying initial and subsequent treatment targets with the child or young person
-
actively engaging the family or carers in planning treatment and in the treatment process, especially in ERP where, if appropriate and acceptable, they may be asked to assist the child or young person
-
encouraging the use of ERP if new or different symptoms emerge after successful treatment
-
liaising with other professionals involved in the child or young person's life, including teachers, social workers and other healthcare professionals, especially when compulsive activity interferes with the ordinary functioning of the child or young person
-
offering 1 or more additional sessions if needed at review appointments after completion of CBT.
1.5.2.13
In the psychological treatment of children and young people with OCD or BDD, healthcare professionals should consider including rewards in order to enhance their motivation and reinforce desired behaviour changes.
1.5.3 How to use pharmacological interventions in adults
Current published evidence suggests that SSRIs are effective in treating adults with OCD or BDD, although evidence for the latter is limited and less certain. However, SSRIs may increase the risk of suicidal thoughts and self‑harm in people with depression and in younger people. It is currently unclear whether there is an increased risk for people with OCD or BDD. Regulatory authorities recommend caution in the use of SSRIs until evidence for differential safety has been demonstrated.
Starting the treatment
1.5.3.1
Common concerns about taking medication for OCD or BDD should be addressed. Patients should be advised, both verbally and with written material, that:
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craving and tolerance do not occur
-
there is a risk of discontinuation or withdrawal symptoms on stopping the drug, missing doses, or reducing the dose
-
there is a range of potential side effects, including worsening anxiety, suicidal thoughts and self‑harm, which need to be carefully monitored, especially in the first few weeks of treatment
-
there is commonly a delay in the onset of effect of up to 12 weeks, although depressive symptoms improve more quickly
-
taking medication should not be seen as a weakness.
Monitoring risk
1.5.3.2
Adults with OCD or BDD started on SSRIs who are not considered to be at increased risk of suicide or self‑harm should be monitored closely and seen on an appropriate and regular basis. The arrangements for monitoring should be agreed by the patient and the healthcare professional, and recorded in the notes.
1.5.3.3
Because of the potential increased risk of suicidal thoughts and self‑harm associated with the early stages of SSRI treatment, younger adults (younger than age 30 years) with OCD or BDD, or people with OCD or BDD with comorbid depression, or who are considered to be at an increased risk of suicide, should be carefully and frequently monitored by healthcare professionals. Where appropriate, other carers – as agreed by the patient and the healthcare professional – may also contribute to the monitoring until the risk is no longer considered significant. The arrangements for monitoring should be agreed by the patient and the healthcare professional, and recorded in the notes.
1.5.3.4
For adults with OCD or BDD at a high risk of suicide, a limited quantity of medication should be prescribed.
1.5.3.5
When adults with OCD or BDD, especially those with comorbid depression, are assessed to be at a high risk of suicide, the use of additional support such as more frequent direct contacts with primary care staff or telephone contacts should be considered, particularly during the first weeks of treatment.
1.5.3.6
For adults with OCD or BDD, particularly in the initial stages of SSRI treatment, healthcare professionals should actively seek out signs of akathisia or restlessness, suicidal ideation and increased anxiety and agitation. They should also advise patients to seek help promptly if symptoms are at all distressing.
1.5.3.7
Adults with OCD or BDD should be monitored around the time of dose changes for any new symptoms or worsening of their condition.
Choice of drug treatment
Selective serotonin reuptake inhibitors (SSRIs)
1.5.3.8
For adults with OCD, the initial pharmacological treatment should be 1 of the following SSRIs: fluoxetine, fluvoxamine, paroxetine, sertraline or citalopram.
Note that this is an off-label use of citalopram. See NICE's information on prescribing medicines.
1.5.3.9
For adults with BDD (including those with beliefs of delusional intensity), the initial pharmacological treatment should be fluoxetine because there is more evidence for its effectiveness in BDD than there is for other SSRIs.
Note that this is an off-label use of fluoxetine. See NICE's information on prescribing medicines.
1.5.3.10
In the event that an adult with OCD or BDD develops marked and/or prolonged akathisia, restlessness or agitation while taking an SSRI, the use of the drug should be reviewed. If the patient prefers, the drug should be changed to a different SSRI.
1.5.3.11
Healthcare professionals should be aware of the increased risk of drug interactions when prescribing an SSRI to adults with OCD or BDD who are taking other medications.
1.5.3.12
For adults with OCD or BDD, if there has been no response to a full course of treatment with an SSRI, healthcare professionals should check that the patient has taken the drug regularly and in the prescribed dose and that there is no interference from alcohol or substance use.
1.5.3.13
For adults with OCD or BDD, if there has not been an adequate response to a standard dose of an SSRI, and there are no significant side effects after 4 to 6 weeks, a gradual increase in dose should be considered in line with the schedule suggested by the summary of product characteristics.
1.5.3.14
For adults with OCD or BDD, the rate at which the dose of an SSRI should be increased should take into account therapeutic response, adverse effects and patient preference. Patients should be warned about, and monitored for, the emergence of side effects during dose increases.
1.5.3.15
If treatment for OCD or BDD with an SSRI is effective, it should be continued for at least 12 months to prevent relapse and allow for further improvements.
1.5.3.16
When an adult with OCD or BDD has taken an SSRI for 12 months after remission (symptoms are not clinically significant and the person is fully functioning for at least 12 weeks), healthcare professionals should review with the patient the need for continued treatment. This review should consider the severity and duration of the initial illness, the number of previous episodes, the presence of residual symptoms, and concurrent psychosocial difficulties.
1.5.3.17
If treatment for OCD or BDD with an SSRI is continued for an extended period beyond 12 months after remission (symptoms are not clinically significant and the person is fully functioning for at least 12 weeks), the need for continuation should be reviewed at regular intervals, agreed between the patient and the prescriber, and written in the notes.
1.5.3.18
For adults with OCD or BDD, to minimise discontinuation or withdrawal symptoms when reducing or stopping SSRIs, the dose should be tapered gradually over several weeks according to the person's need. The rate of reduction should take into account the starting dose, the drug half‑life and particular profiles of adverse effects.
1.5.3.19
Healthcare professionals should encourage adults with OCD or BDD who are discontinuing SSRI treatment to seek advice if they experience significant discontinuation or withdrawal symptoms.
Other drugs
1.5.3.20
The following drugs should not normally be used to treat OCD or BDD without comorbidity:
-
tricyclic antidepressants other than clomipramine
-
tricyclic‑related antidepressants
-
serotonin and noradrenaline reuptake inhibitors (SNRIs), including venlafaxine
-
monoamine oxidase inhibitors (MAOIs)
-
anxiolytics (except cautiously for short periods to counter the early activation of SSRIs).
1.5.3.21
Antipsychotics as a monotherapy should not normally be used for treating OCD.
1.5.3.22
Antipsychotics as a monotherapy should not normally be used for treating BDD (including beliefs of delusional intensity).
1.5.4 Poor response to initial treatment in adults
If initial treatment does not result in a clinically significant improvement in both symptoms and functioning, other treatment options should be considered. When additional treatment options also fail to produce an adequate response, multidisciplinary teams with specific expertise in OCD/BDD should become involved. Their role should include supporting and collaborating with those professionals already involved in an individual's care.
1.5.4.1
For adults with OCD or BDD, if there has not been an adequate response to treatment with an SSRI alone (within 12 weeks) or CBT (including ERP) alone (more than 10 therapist hours per patient), a multidisciplinary review should be carried out.
1.5.4.2
Following multidisciplinary review, for adults with OCD or BDD, if there has not been an adequate response to treatment with an SSRI alone (within 12 weeks) or CBT (including ERP) alone (more than 10 therapist hours per patient), combined treatment with CBT (including ERP) and an SSRI should be offered.
1.5.4.3
For adults with OCD or BDD, if there has not been an adequate response after 12 weeks of combined treatment with CBT (including ERP) and an SSRI, or there has been no response to an SSRI alone, or the patient has not engaged with CBT, a different SSRI or clomipramine should be offered.
1.5.4.4
Clomipramine should be considered in the treatment of adults with OCD or BDD after an adequate trial of at least 1 SSRI has been ineffective or poorly tolerated, if the patient prefers clomipramine or has had a previous good response to it.
1.5.4.5
For adults with OCD or BDD, if there has been no response to a full trial of at least 1 SSRI alone, a full trial of combined treatment with CBT (including ERP) and an SSRI, and a full trial of clomipramine alone, the patient should be referred to a multidisciplinary team with specific expertise in the treatment of OCD/BDD for assessment and further treatment planning.
1.5.4.6
The assessment of adults with OCD or BDD referred to multidisciplinary teams with specific expertise in OCD/BDD should include a comprehensive assessment of their symptom profile, previous pharmacological and psychological treatment history, adherence to prescribed medication, history of side effects, comorbid conditions such as depression, suicide risk, psychosocial stressors, relationship with family and/or carers and personality factors.
1.5.4.7
Following multidisciplinary review, for adults with OCD if there has been no response to a full trial of at least 1 SSRI alone, a full trial of combined treatment with CBT (including ERP) and an SSRI, and a full trial of clomipramine alone, the following treatment options should also be considered (note, there is no evidence of the optimal sequence of the options listed below):
-
additional CBT (including ERP) or cognitive therapy
-
adding an antipsychotic to an SSRI or clomipramine
-
combining clomipramine and citalopram.
Note that this is an off-label use of citalopram. See NICE's information on prescribing medicines.
1.5.4.8
Following multidisciplinary review, for adults with BDD, if there has been no response to a full trial of at least 1 SSRI alone, a full trial of combined treatment with CBT (including ERP) and an SSRI, and a full trial of clomipramine alone, the following treatment options should also be considered (note, there is no evidence of the optimal sequence of the options listed below):
-
additional CBT or cognitive therapy by a different multidisciplinary team with expertise in BDD
-
adding buspirone to an SSRI.
Note that this is an off-label use of buspirone. See NICE's information on prescribing medicines.
1.5.4.9
For adults with BDD, if there has been no response to treatment, or the patient is not receiving appropriate treatment, more intensive monitoring is needed because the risk of suicide is high in people with BDD.
1.5.4.10
Treatments such as combined antidepressants and antipsychotic augmentation should not be routinely initiated in primary care.
How to use clomipramine in adults
1.5.4.11
For adults with OCD or BDD who are at a significant risk of suicide, healthcare professionals should only prescribe small amounts of clomipramine at a time because of its toxicity in overdose (see the summary of product characteristics for details of dosage). The patient should be monitored regularly until the risk of suicide has subsided.
1.5.4.12
An electrocardiogram (ECG) should be carried out and a blood pressure measurement taken before prescribing clomipramine for adults with OCD or BDD at significant risk of cardiovascular disease.
1.5.4.13
For adults with OCD or BDD, if there has not been an adequate response to the standard dose of clomipramine, and there are no significant side effects, a gradual increase in dose should be considered in line with the schedule suggested by the summary of product characteristics.
1.5.4.14
For adults with OCD or BDD, treatment with clomipramine should be continued for at least 12 months if it appears to be effective and because there may be further improvement.
1.5.4.15
For adults with OCD or BDD, when discontinuing clomipramine, doses should be reduced gradually in order to minimise potential discontinuation or withdrawal symptoms.
1.5.5 Poor response to initial treatment in children and young people
Current published evidence suggests that SSRIs are effective in treating children and young people with OCD. The only SSRIs licensed for use in children and young people with OCD are fluvoxamine and sertraline. When used as a treatment for depression, SSRIs can cause significant adverse reactions, including increased suicidal thoughts and risk of self‑harm, but it is not known whether this same risk occurs with their use in OCD. SSRIs may be safer in depression when combined with psychological treatments (see NICE's guideline on depression in children and young people). Given that the UK regulatory authority has advised that similar adverse reactions cannot be ruled out in OCD, appropriate caution should be observed, especially in the presence of comorbid depression.
1.5.5.1
For a child or young person with OCD or BDD, if there has not been an adequate response within 12 weeks to a full trial of CBT (including ERP) involving the family or carers, a multidisciplinary review should be carried out.
1.5.5.2
Following multidisciplinary review, for a child (aged 8 to 11 years) with OCD or BDD with moderate to severe functional impairment, if there has not been an adequate response to CBT (including ERP) involving the family or carers, the addition of an SSRI to ongoing psychological treatment may be considered. Careful monitoring should be undertaken, particularly at the beginning of treatment.
1.5.5.3
Following multidisciplinary review, for a young person (aged 12 to 18 years) with OCD or BDD with moderate to severe functional impairment, if there has not been an adequate response to CBT (including ERP) involving the family or carers, the addition of an SSRI to ongoing psychological treatment should be offered. Careful monitoring should be undertaken, particularly at the beginning of treatment.
1.5.5.4
For a child or a young person with OCD or BDD, if treatment with an SSRI in combination with CBT (including ERP) involving the family or carers is unsuccessful or is not tolerated because of side effects, the use of another SSRI or clomipramine with careful monitoring may be considered, especially if the child or young person has had a positive response to these alternatives in the past. This should also be in combination with CBT (including ERP).
Note that this is an off-label use of clomipramine. See NICE's information on prescribing medicines.
1.5.6 How to use pharmacological treatments in children and young people
In adults with OCD treated by medication, there is some clinical trial evidence regarding the onset of therapeutic response, the dose needed, the rate of increase of dose, the duration of treatment and the likelihood of relapse on discontinuation. Trials of these aspects have not been done in children and/or young people, but the following good practice for prescribing SSRIs or clomipramine is based on adult trials and clinical experience.
How to use SSRIs in children and young people
1.5.6.1
An SSRI should only be prescribed to children and young people with OCD or BDD following assessment and diagnosis by a child and adolescent psychiatrist who should also be involved in decisions about dose changes and discontinuation.
1.5.6.2
When an SSRI is prescribed to children and young people with OCD or BDD, it should be in combination with concurrent CBT (including ERP). If children and young people are unable to engage with concurrent CBT, specific arrangements should be made for careful monitoring of adverse events and these arrangements should be recorded in the notes.
1.5.6.3
Children and young people with OCD or BDD starting treatment with SSRIs should be carefully and frequently monitored and seen on an appropriate and regular basis. This should be agreed by the patient, his or her family or carers and the healthcare professional, and recorded in the notes.
1.5.6.4
A licensed medication (sertraline or fluvoxamine) should be used when an SSRI is prescribed to children and young people with OCD, except in patients with significant comorbid depression when fluoxetine should be used, because of current regulatory requirements.
Note the uses of sertraline for under 6s, fluvoxamine for under 8s, and fluoxetine for children and young people are off-label. See NICE's information on prescribing medicines.
1.5.6.5
Fluoxetine should be used when an SSRI is prescribed to children and young people with BDD.
Note that this is an off-label use. See NICE's information on prescribing medicines.
1.5.6.6
For children and young people with OCD or BDD who also have significant depression, the NICE recommendations for the treatment of childhood depression should be followed and there should be specific monitoring for suicidal thoughts or behaviours.
See NICE's guideline on depression in children and young people.
1.5.6.7
Children and young people with OCD or BDD starting treatment with SSRIs should be informed about the rationale for the drug treatment, the delay in onset of therapeutic response (up to 12 weeks), the time course of treatment, the possible side effects and the need to take the medication as prescribed. Discussion of these issues should be supplemented by written information appropriate to the needs of the child or young person and their family or carers.
1.5.6.8
The starting dose of medication for children and young people with OCD or BDD should be low, especially in younger children. A half or quarter of the normal starting dose may be considered for the first week.
1.5.6.9
If a lower dose of medication for children and young people with OCD or BDD is ineffective, the dose should be increased until a therapeutic response is obtained, with careful and close monitoring for adverse events. The rate of increase should be gradual and should take into account the delay in therapeutic response (up to 12 weeks) and the age of the patient. Maximum recommended doses for children and young people should not be exceeded.
1.5.6.10
Children and young people prescribed an SSRI, and their families or carers, should be informed by the prescribing doctor about the possible appearance of suicidal behaviour, self‑harm or hostility, particularly at the beginning of treatment. They should be advised that if there is any sign of new symptoms of these kinds, they should make urgent contact with their medical practitioner.
1.5.6.11
Where children or young people with OCD or BDD respond to treatment with an SSRI, medication should be continued for at least 6 months post‑remission (that is, symptoms are not clinically significant and the child or young person is fully functioning for at least 12 weeks).
How to use clomipramine in children and young people
1.5.6.12
Children and young people with OCD or BDD and their families or carers should be advised about the possible side effects of clomipramine, including toxicity in overdose.
1.5.6.13
Before starting treatment with clomipramine in children and young people with OCD or BDD, an ECG should be carried out to exclude cardiac conduction abnormalities.
1.5.6.14
For a child or young person with OCD or BDD, if there has not been an adequate response to the standard dose of clomipramine, and there are no significant side effects, a gradual increase in dose may be cautiously considered.
1.5.6.15
Treatment of a child or young person with OCD or BDD with clomipramine should be continued for at least 6 months if the treatment appears to be effective, because there may be further improvement in symptoms.
Stopping or reducing SSRIs and clomipramine in children and young people
1.5.6.16
In children and young people with OCD or BDD, an attempt should be made to withdraw medication if remission has been achieved (that is, symptoms are no longer clinically significant and the child or young person is fully functioning) and maintained for at least 6 months, and if that is their wish. Patients and their family or carers should be warned that relapse and/or discontinuation or withdrawal symptoms may occur. They should be advised to contact their medical practitioner should symptoms of discontinuation or withdrawal arise.
1.5.6.17
For children and young people with OCD or BDD, to minimise discontinuation or withdrawal symptoms on reducing or stopping antidepressants, particularly SSRIs, the dose should be tapered gradually over several weeks according to the individual's need. The rate of reduction should take into account the starting dose, the drug half‑life and particular profiles of adverse effects.
1.5.6.18
Children and young people with OCD or BDD should continue with psychological treatment throughout the period of drug discontinuation because this may reduce the risk of relapse.
Other drugs
1.5.6.19
Tricyclic antidepressants other than clomipramine should not be used to treat OCD or BDD in children and young people.
1.5.6.20
Other antidepressants (MAOIs, SNRIs) should not be used to treat OCD or BDD in children and young people.
1.5.6.21
Antipsychotics should not be used alone in the routine treatment of OCD or BDD in children or young people, but may be considered as an augmentation strategy.