SSRIs, SNRIs and other antidepressant medications are commonly used for the treatment of conditions such as mood disorders. In the period from 2023 to 2024, 14% of the population in Australia was dispensed an antidepressant medication.4 Although most guidelines recommend that these medications be used for only 6–12 months for an episode of anxiety or depression, the average duration of use is four years.1
If you are considering prescribing these medications, you need to also understand when and how to deprescribe them, and the possibility of antidepressant withdrawal syndrome. Earlier descriptions of symptoms of this syndrome may have underemphasised the frequency and severity of the syndrome in some people.1
Deprescribing should be a process of planned and supervised dose reduction that leads to the cessation of the medication. It should be implemented when the potential harms of continuing outweigh the current or anticipated benefits of continuing, and may also be implemented if the patient indicates they would like to cease taking the medication.1,6
Before deciding whether to deprescribe or not, assess the patient's symptoms so that you can:
- determine whether there has been a significant improvement since beginning the medication and, if so, whether there are any ongoing symptoms of concern
- identify risk factors that might lead to a relapse.1,2
Risks of harm from continuing SSRIs/SNRIs are often greater where there is polypharmacy, pregnancy, advanced age or the patient is on a high dose.1,2
Patients should be told that:
- they may experience discontinuation and withdrawal symptoms
- such symptoms are commonly mild, but rarely may be severe, prolonged and debilitating1,6
- they should not stop taking antidepressants abruptly and should discuss stopping their antidepressant with their treating physician.6
The following resources are useful handouts and discussion tools:
Reviews of ongoing medication
Review intervals
The interval for review will depend on patient factors, such as their current symptoms, side effects, comorbid conditions, risk factors for relapse, severity of initial presentation and ongoing life stressors.1,2
Conducting the review
At each review:
- consider the ongoing need for the medication based on the patient’s individual circumstances1
- consider exploring the patient’s perceptions about their condition and the effectiveness of the medication
- consider educating the patient about antidepressants and exploring barriers to discontinuing
- encourage self-efficacy and maximising non-pharmacological management (decision aid tools and education, such as RELEASE resources, may be helpful).7
Continuing to prescribe
Continue to prescribe only if:
- there is shared decision-making with the patient
- it remains clinically indicated
- the benefits of continuing outweigh the potential risks of continuing.
Commencing deprescription
Discontinuation at 6–12 months may be appropriate for many patients, but patients with previous episodes or residual symptoms of depression have been shown to be at higher risk of relapse and may benefit from use beyond 12 months.2 There is no clinical trial evidence regarding maintaining antidepressant treatment beyond three years.2
If you decide to decrease or deprescribe the medication:
- explain and make sure the patient understands the risk of withdrawal and the recommendation to taper with medical supervision
- assess what supports the patient has or needs; ensure their family/carer understands the risks and what to look out for
- provide clear guidelines about the tapering (see Tapering below)
- establish regular follow-up appointments during and after weaning to monitor for risks, withdrawal and relapse.1,2
Tapering
The rate of reduction must be based on what the patient can tolerate. For many patients, this may be a 10% reduction (or less) of the previous dose every 2–4 weeks.1
If the patient does not tolerate any withdrawal symptoms they experience, halt any further weaning or increase the dose slightly until the patient’s symptoms settle.1
Follow guidelines (e.g. RELEASE tapering protocols from the University of Queensland) to ensure the tapering is appropriate.
Consider:
- how the tapering of the medication can be practically achieved (eg tablet cutters, liquid preparations, compounding1,7,8).
- the lower the current dose, the slower the tapering should be1,7
- ‘every other day dosing’ is not suitable unless the medication has a long elimination half-life.1
Withdrawal and relapse
Onset of withdrawal symptoms
Usually, withdrawal occurs within hours or days of a dose reduction, but if the drug has a longer half-life (eg fluoxetine), it can take weeks to occur.
Monitoring for withdrawal and relapse
Monitor the patient, and educate them to self-monitor, for withdrawal symptoms described below.
Physical symptoms:
- Changes in sleep (eg insomnia, excessive dreaming or nightmares)
- Flu-like symptoms (eg sweating, fatigue, malaise, headache)
- Gastrointestinal upset (eg anorexia, nausea, vomiting, diarrhoea)
- Neurological symptoms (eg tremor, paraesthesia, electric shock-like sensations, rushing noises, blurred vision, palinopsia, vertigo, disequilibrium)
- Mood changes (eg irritability, anxiety, agitation, low mood).1
Psychological symptoms:
- Psychological symptoms of withdrawal may differ from the original mood disorder presentation and can be severe in nature.
- Symptoms such as electric zaps are highly suggestive of withdrawal.1
- One of the most distressing withdrawal symptoms is akathisia, which is a neuropsychiatric presentation of severe restlessness, agitation and sense of terror.1
Assessing whether symptoms indicate withdrawal or relapse
Where symptoms occur, thoroughly assess the patient to decide whether the symptoms are likely related to withdrawal or relapse.
Taking a history of the time of onset, the physical and psychological symptoms and the patient’s response to reinstatement of the drug may help you differentiate between withdrawal symptoms and a relapse.1
What we understand about withdrawal syndrome
Withdrawal syndrome is not well understood, but we are beginning to understand that it can sometimes be severe and persistent, lasting months or even years. It seems that for some patients the effects of withdrawal syndrome can be extremely slow to resolve, or may even be permanent.1,9
Consequently, it may be that many studies overestimate the rate of relapse because they underestimate the duration of withdrawal syndrome.1