Antidepressant medication should be continued for a minimum of 6 months after symptoms have remitted to reduce the risk of relapse. Therefore, the correct course of action is to continue treatment for 6 more months from the point of remission. Continuing for only 2 or 3 more months would not meet the recommended duration of treatment. Gradually reducing doses over 4 weeks is a suitable approach for weaning off SSRIs, but it should only be done after the 6-month period of treatment. Stopping citalopram abruptly is not safe and could lead to discontinuation syndrome or a relapse of depression.

Selective serotonin reuptake inhibitors (SSRIs) are commonly used as the first-line treatment for depression. Citalopram and fluoxetine are the preferred SSRIs, while sertraline is recommended for patients who have had a myocardial infarction. However, caution should be exercised when prescribing SSRIs to children and adolescents. Gastrointestinal symptoms are the most common side-effect, and patients taking SSRIs are at an increased risk of gastrointestinal bleeding. Patients should also be aware of the possibility of increased anxiety and agitation after starting a SSRI. Fluoxetine and paroxetine have a higher propensity for drug interactions.

The Medicines and Healthcare products Regulatory Agency (MHRA) has issued a warning regarding the use of citalopram due to its association with dose-dependent QT interval prolongation. As a result, citalopram and escitalopram should not be used in patients with congenital long QT syndrome, known pre-existing QT interval prolongation, or in combination with other medicines that prolong the QT interval. The maximum daily dose of citalopram is now 40 mg for adults, 20 mg for patients older than 65 years, and 20 mg for those with hepatic impairment.

When initiating antidepressant therapy, patients should be reviewed by a doctor after 2 weeks. Patients under the age of 25 years or at an increased risk of suicide should be reviewed after 1 week. If a patient responds well to antidepressant therapy, they should continue treatment for at least 6 months after remission to reduce the risk of relapse. When stopping a SSRI, the dose should be gradually reduced over a 4 week period, except for fluoxetine. Paroxetine has a higher incidence of discontinuation symptoms, including mood changes, restlessness, difficulty sleeping, unsteadiness, sweating, gastrointestinal symptoms, and paraesthesia.

When considering the use of SSRIs during pregnancy, the benefits and risks should be weighed. Use during the first trimester may increase the risk of congenital heart defects, while use during the third trimester can result in persistent pulmonary hypertension of the newborn. Paroxetine has an increased risk of congenital malformations, particularly in the first trimester.

Anxiety is a common disorder that can manifest in various ways. According to NICE, the primary feature is excessive worry about multiple events associated with heightened tension. It is crucial to consider potential physical causes when diagnosing anxiety disorders, such as hyperthyroidism, cardiac disease, and medication-induced anxiety. Medications that may trigger anxiety include salbutamol, theophylline, corticosteroids, antidepressants, and caffeine.

NICE recommends a step-wise approach for managing generalised anxiety disorder (GAD). This includes education about GAD and active monitoring, low-intensity psychological interventions, high-intensity psychological interventions or drug treatment, and highly specialist input. Sertraline is the first-line SSRI for drug treatment, and if it is ineffective, an alternative SSRI or a serotonin-noradrenaline reuptake inhibitor (SNRI) such as duloxetine or venlafaxine may be offered. If the patient cannot tolerate SSRIs or SNRIs, pregabalin may be considered. For patients under 30 years old, NICE recommends warning them of the increased risk of suicidal thinking and self-harm and weekly follow-up for the first month.

The management of panic disorder also follows a stepwise approach, including recognition and diagnosis, treatment in primary care, review and consideration of alternative treatments, review and referral to specialist mental health services, and care in specialist mental health services. NICE recommends either cognitive behavioural therapy or drug treatment in primary care. SSRIs are the first-line drug treatment, and if contraindicated or no response after 12 weeks, imipramine or clomipramine should be offered.

Severe depression is often linked to Cotard syndrome, a rare form of nihilistic delusions where individuals believe they are dead or non-existent. This condition can also be observed in individuals with schizophrenia.

Understanding Cotard Syndrome

Cotard syndrome is a mental disorder that is characterized by the belief that the affected person or a part of their body is dead or non-existent. This rare condition is often associated with severe depression and psychotic disorders, making it difficult to treat. Patients with Cotard syndrome may stop eating or drinking as they believe it is unnecessary, leading to significant health problems.

The delusion experienced by those with Cotard syndrome can be challenging to manage, and it can have a significant impact on their quality of life. The condition is often accompanied by feelings of hopelessness and despair, which can make it challenging for patients to seek help. Treatment for Cotard syndrome typically involves a combination of medication and therapy, but it can take time to find an effective approach.

Hyperparathyroidism and subsequent hypercalcaemia can occur with prolonged use of lithium. This can lead to the formation of kidney stones due to excessive calcium concentration. Amitriptyline, a sedative tricyclic antidepressant, is not likely to cause nephrolithiasis or explain the patient’s elevated calcium and parathyroid hormone levels. Similarly, clozapine, a second-generation antipsychotic, is not known to cause hypercalcaemia or hyperparathyroidism. Sertraline, a selective serotonin reuptake inhibitor, typically causes side effects during initiation or discontinuation, such as sexual dysfunction and gastrointestinal issues. Checking thyroid function tests may also be helpful as lithium use can lead to hypothyroidism.

Lithium is a medication used to stabilize mood in individuals with bipolar disorder and as an adjunct in treatment-resistant depression. It has a narrow therapeutic range of 0.4-1.0 mmol/L and is primarily excreted by the kidneys. The mechanism of action is not fully understood, but it is believed to interfere with inositol triphosphate and cAMP formation. Adverse effects may include nausea, vomiting, diarrhea, fine tremors, nephrotoxicity, thyroid enlargement, ECG changes, weight gain, idiopathic intracranial hypertension, leucocytosis, hyperparathyroidism, and hypercalcemia.

Monitoring of patients taking lithium is crucial to prevent adverse effects and ensure therapeutic levels. It is recommended to check lithium levels 12 hours after the last dose and weekly after starting or changing the dose until levels are stable. Once established, lithium levels should be checked every three months. Thyroid and renal function should be monitored every six months. Patients should be provided with an information booklet, alert card, and record book to ensure proper management of their medication. Inadequate monitoring of patients taking lithium is common, and guidelines have been issued to address this issue.

The woman’s alternating episodes of hypomania and severe depression suggest that she has type 2 bipolar disorder. There are no indications of an anxiety disorder, and the severity of her symptoms is not consistent with cyclothymia. Major depressive disorder is also not a likely diagnosis, as she experiences ‘highs’ consistent with hypomania. Type 1 bipolar disorder is also unlikely, as her ‘high’ periods are more in line with hypomania rather than full-blown mania.

Understanding Bipolar Disorder

Bipolar disorder is a mental health condition that is characterized by alternating periods of mania/hypomania and depression. It typically develops in the late teen years and has a lifetime prevalence of 2%. There are two recognized types of bipolar disorder: type I, which involves mania and depression, and type II, which involves hypomania and depression.

Mania and hypomania both refer to abnormally elevated mood or irritability, but mania is more severe and can include psychotic symptoms for 7 days or more. Hypomania, on the other hand, involves decreased or increased function for 4 days or more. The presence of psychotic symptoms suggests mania.

Management of bipolar disorder may involve psychological interventions specifically designed for the condition, as well as medication. Lithium is the mood stabilizer of choice, but valproate can also be used. Antipsychotic therapy, such as olanzapine or haloperidol, may be used to manage mania/hypomania, while fluoxetine is the antidepressant of choice for depression. It is important to address any co-morbidities, as there is an increased risk of diabetes, cardiovascular disease, and COPD in individuals with bipolar disorder.

If symptoms suggest hypomania, routine referral to the community mental health team (CMHT) is recommended. However, if there are features of mania or severe depression, an urgent referral to the CMHT should be made. Understanding bipolar disorder and its management is crucial for healthcare professionals to provide appropriate care and support for individuals with this condition.

Acute stress disorder is a type of acute stress reaction that occurs within four weeks of a traumatic event, while PTSD is diagnosed after four weeks have passed. Although this patient’s symptoms have the potential to develop into PTSD, they currently meet the criteria for acute stress disorder. It is important to monitor their progress and reassess in two weeks.

Panic disorder is characterized by recurrent panic attacks and is often accompanied by agoraphobia. To be diagnosed with panic disorder, the individual must experience persisting anxiety about the recurrence of attacks for at least one month after the initial episode.

Depression is characterized by persistent feelings of sadness or loss of pleasure in activities, along with a range of emotional, cognitive, physical, and behavioral symptoms.

Generalized anxiety disorder is characterized by excessive and uncontrollable worry that is pervasive and persistent, along with a range of somatic, cognitive, and behavioral symptoms. This disorder must be present for longer than two weeks and is typically experienced on a continuum of severity.

Acute stress disorder is a condition that occurs within the first four weeks after a person has experienced a traumatic event, such as a life-threatening situation or sexual assault. It is characterized by symptoms such as intrusive thoughts, dissociation, negative mood, avoidance, and arousal. These symptoms can include flashbacks, nightmares, feeling disconnected from reality, and being hypervigilant.

To manage acute stress disorder, trauma-focused cognitive-behavioral therapy (CBT) is typically the first-line treatment. This type of therapy helps individuals process their traumatic experiences and develop coping strategies. In some cases, benzodiazepines may be used to alleviate acute symptoms such as agitation and sleep disturbance. However, caution must be taken when using these medications due to their addictive potential and potential negative impact on adaptation. Overall, early intervention and appropriate treatment can help individuals recover from acute stress disorder and prevent the development of more chronic conditions such as PTSD.

Differentiating Panic Disorder from Other Conditions

Panic disorder is a mental health condition characterized by intense anxiety episodes with somatic symptoms and an exaggerated sense of danger. However, it can be challenging to distinguish panic disorder from other conditions that share similar symptoms. Here are some examples:

Panic Disorder vs. Somatisation Disorder

Patients with somatisation disorder also experience physical symptoms, but they fall into four different clusters: pain, gastrointestinal, urogenital, and neurological dysfunction. In contrast, panic disorder symptoms are more generalized and not limited to specific bodily functions.

Panic Disorder vs. Hypoglycemia

Hypoglycemia rarely induces severe panic or anticipatory anxiety, except in cases of insulin reactions. Patients with hypoglycemia typically experience symptoms such as sweating and hunger, which are not necessarily associated with panic disorder.

Panic Disorder vs. Paroxysmal Atrial Tachycardia

Paroxysmal atrial tachycardia is a heart condition that causes a doubling of the pulse rate and requires electrocardiographic evidence for diagnosis. While it may cause some anxiety, it is not typically accompanied by the intense subjective anxiety seen in panic disorder.

Panic Disorder vs. Specific Phobia

Specific phobias involve reactions to limited cues or situations, such as spiders, blood, or needles. While they may trigger panic attacks and avoidance, they are not as generalized as panic disorder and are limited to specific feared situations.

Grief is a natural response to the death of a loved one and does not always require medical intervention. However, understanding the potential stages of grief can help determine if a patient is experiencing a normal reaction or a more significant problem. The most common model of grief divides it into five stages: denial, anger, bargaining, depression, and acceptance. It is important to note that not all patients will experience all five stages. Atypical grief reactions are more likely to occur in women, sudden and unexpected deaths, problematic relationships before death, and lack of social support. Delayed grief, which occurs when grieving does not begin for more than two weeks, and prolonged grief, which is difficult to define but may last beyond 12 months, are features of atypical grief reactions.

SSRI discontinuation syndrome can cause gastrointestinal side-effects such as diarrhoea, with paroxetine having a particularly high risk of such symptoms. Withdrawal of SSRIs should be done gradually over several weeks to reduce the incidence of discontinuation symptoms. Colchicine, a gout medication, is associated with gastrointestinal side effects but does not cause significant symptoms upon withdrawal. Levothyroxine withdrawal does not cause any particular symptoms, but stopping long-term use can lead to hypothyroidism symptoms such as constipation. Metformin withdrawal does not cause acute symptoms, but stopping long-term use can worsen diabetic control, and diarrhoea is a side effect of metformin treatment.

Selective serotonin reuptake inhibitors (SSRIs) are commonly used as the first-line treatment for depression. Citalopram and fluoxetine are the preferred SSRIs, while sertraline is recommended for patients who have had a myocardial infarction. However, caution should be exercised when prescribing SSRIs to children and adolescents. Gastrointestinal symptoms are the most common side-effect, and patients taking SSRIs are at an increased risk of gastrointestinal bleeding. Patients should also be aware of the possibility of increased anxiety and agitation after starting a SSRI. Fluoxetine and paroxetine have a higher propensity for drug interactions.

The Medicines and Healthcare products Regulatory Agency (MHRA) has issued a warning regarding the use of citalopram due to its association with dose-dependent QT interval prolongation. As a result, citalopram and escitalopram should not be used in patients with congenital long QT syndrome, known pre-existing QT interval prolongation, or in combination with other medicines that prolong the QT interval. The maximum daily dose of citalopram is now 40 mg for adults, 20 mg for patients older than 65 years, and 20 mg for those with hepatic impairment.

When initiating antidepressant therapy, patients should be reviewed by a doctor after 2 weeks. Patients under the age of 25 years or at an increased risk of suicide should be reviewed after 1 week. If a patient responds well to antidepressant therapy, they should continue treatment for at least 6 months after remission to reduce the risk of relapse. When stopping a SSRI, the dose should be gradually reduced over a 4 week period, except for fluoxetine. Paroxetine has a higher incidence of discontinuation symptoms, including mood changes, restlessness, difficulty sleeping, unsteadiness, sweating, gastrointestinal symptoms, and paraesthesia.

When considering the use of SSRIs during pregnancy, the benefits and risks should be weighed. Use during the first trimester may increase the risk of congenital heart defects, while use during the third trimester can result in persistent pulmonary hypertension of the newborn. Paroxetine has an increased risk of congenital malformations, particularly in the first trimester.

Knowing the side effects of ECT is crucial as it is a treatment that is often viewed with apprehension by the public. ECT is typically used to treat depression that is resistant to other treatments, as well as severe mania and catatonic schizophrenia. While it was once a feared treatment due to its use of high strengths and lack of anesthesia, it is now considered to be a relatively safe intervention. Short-term side effects of ECT include headaches, nausea, memory problems, and cardiac arrhythmias. There are few long-term effects, although some patients may experience long-term memory issues. ECT is used to treat mania and is being studied as a potential treatment for Parkinson’s disease. It induces a generalized seizure but is not associated with epilepsy or glaucoma.

Electroconvulsive therapy (ECT) is a viable treatment option for patients who suffer from severe depression that does not respond to medication, such as catatonia, or those who experience psychotic symptoms. The only absolute contraindication for ECT is when a patient has raised intracranial pressure.

Short-term side effects of ECT include headaches, nausea, short-term memory impairment, memory loss of events prior to the therapy, and cardiac arrhythmia. However, these side effects are typically temporary and resolve quickly.

Long-term side effects of ECT are less common, but some patients have reported impaired memory. It is important to note that the benefits of ECT often outweigh the potential risks, and it can be a life-changing treatment for those who have not found relief from other forms of therapy.

Understanding Different Types of Anxiety Disorders

Post-traumatic stress disorder (PTSD) is characterized by a mix of anxiety and dissociative symptoms that persist for several months. Patients with PTSD often experience unintentional recollection, flashbacks, and nightmares of the traumatic event. They may also exhibit symptoms of chronic hyperarousal, such as sleep disruptions, irritability, and hypervigilance.

Panic disorder with agoraphobia is diagnosed in patients who avoid situations that they believe may trigger a panic attack or where it would be dangerous or embarrassing to have one.

Acute stress disorder is a condition that typically subsides within a month and is most common in patients who use dissociation to separate the events from the associated painful emotions.

Generalized anxiety disorder is characterized by a mental state of dread or fear and somatic manifestations, such as palpitations, churning stomach, and muscle tension. Patients with this disorder often have fears concerning many aspects of their personal security.

Somatization disorder is a condition where patients seek medical attention for cryptic physical symptoms that are difficult to explain. Patients with this disorder complain of problems in at least four different organ systems, usually without clear physical cause. They often deny anxiety or psychic distress, except for distress about their physical condition.

Overall, understanding the different types of anxiety disorders and their symptoms can help with proper diagnosis and treatment.

The patient’s symptoms suggest pseudodementia caused by depression rather than dementia. Managing the depression should reverse the cognitive impairment.

Differentiating between Depression and Dementia

Depression and dementia are two conditions that can have similar symptoms, making it difficult to distinguish between the two. However, there are certain factors that can suggest a diagnosis of depression over dementia.

One of the key factors is the duration and onset of symptoms. Depression often has a short history and a rapid onset, whereas dementia tends to develop slowly over time. Additionally, biological symptoms such as weight loss and sleep disturbance are more commonly associated with depression than dementia.

Patients with depression may also express concern about their memory, but they are often reluctant to take tests and may be disappointed with the results. In contrast, patients with dementia may not be aware of their memory loss or may not express concern about it.

The mini-mental test score can also be variable in patients with depression, whereas in dementia, there is typically a global memory loss, particularly in recent memory.

In summary, while depression and dementia can have overlapping symptoms, careful consideration of the duration and onset of symptoms, biological symptoms, patient concerns, and cognitive testing can help differentiate between the two conditions.

Treatment for Clozapine-Induced Hypersalivation: Hyoscine and Other Options

Hypersalivation, or excessive saliva production, is a common side effect of clozapine treatment. While it usually subsides over time, it can be distressing for patients and may even pose a risk of aspiration pneumonia. Limited trial data exists on treatments for clozapine-induced hypersalivation, but hyoscine, a type of anticholinergic medication, is commonly used. Other options include pirenzepine and benzhexol. It’s important to note that procyclidine is typically used for acute dystonia, not hypersalivation, and medications like propranolol, risperidone, and lorazepam are not indicated for this side effect.

Understanding Sleep Paralysis

Sleep paralysis is a condition that affects many people and is characterized by a temporary inability to move the skeletal muscles when waking up or falling asleep. It is believed to be linked to the natural paralysis that occurs during REM sleep. This phenomenon is recognized in various cultures and is often accompanied by hallucinations or vivid images.

The paralysis occurs either before falling asleep or after waking up, and it can be a frightening experience for those who are not familiar with it. However, it is a relatively harmless condition that does not require medical attention in most cases. If the symptoms are particularly bothersome, medication such as clonazepam may be prescribed to alleviate the symptoms.

In summary, sleep paralysis is a common occurrence that affects many people. It is characterized by temporary paralysis of the skeletal muscles and is often accompanied by hallucinations. While it can be a frightening experience, it is generally harmless and does not require medical attention.

Coping Mechanisms: Understanding Different Approaches to Dealing with Stress

When faced with stress, individuals often employ coping mechanisms to manage their emotions and reactions. Here are some common coping mechanisms and their definitions:

Avoidance: This coping mechanism involves denying the existence of a stressor and continuing with one’s usual behavior without making any changes. It is often used when the stressor is too overwhelming to deal with immediately.

Appraisal: Appraisal involves assessing past events and experiences to make decisions for future arrangements. This coping mechanism can help individuals feel more in control of their situation.

Projection: Projection is when an individual attributes unwanted thoughts and feelings onto someone else. This can be a way to avoid dealing with one’s own emotions.

Problem-focused: This coping mechanism involves identifying the causes of a stressor and taking action to reduce or eliminate it. It is a proactive approach to dealing with stress.

Emotion-focused: Emotion-focused coping involves managing the emotions that a stressor creates. This can involve using drugs or other methods to regulate one’s emotional response.

Understanding these coping mechanisms can help individuals choose the most effective approach for dealing with stress in their lives.

Management of ADHD: First-Line Treatment and Other Options

Attention-deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder that affects young people. While group-based support and environmental modifications can be helpful, medication and therapy are often necessary for ongoing, persistent impairment. Here are some options for managing ADHD:

First-Line Treatment: Methylphenidate
Methylphenidate is a central nervous system stimulant that is considered first-line treatment for young people with ADHD who still have significant symptoms despite other interventions. However, it is not approved for use in children under six years and requires monitoring of height, weight, heart rate, blood pressure, and ECG.

Therapy: Cognitive Behavioural Therapy (CBT)
CBT can be helpful for patients who have already tried medication but continue to have significant symptoms. It can cover topics such as social skills, active listening, self-control, and expression of feelings.

Alternative Medication: Dexamphetamine
Dexamphetamine is an option for patients who cannot tolerate or do not respond to methylphenidate. However, it is not first-line treatment.

Not Recommended: Diazepam and Melatonin
Diazepam is not recommended for sedation in patients with ADHD. Melatonin can be used for regulating sleep in patients with learning difficulties, but it is not routinely used for ADHD management.

In summary, ADHD management requires a tailored approach that may involve medication, therapy, or both. Methylphenidate is the first-line treatment, but other options are available for patients who do not respond or cannot tolerate it.

Knight’s move thinking involves illogical leaps from one idea to another without any discernible link between them, while flight of ideas involves moving from one idea to another with discernible links between them. In this scenario, the patient is exhibiting Knight’s move thinking, which is a thought disorder associated with schizophrenia. This is different from circumstantiality, which involves giving excessive, unnecessary detail without returning to the original point, and clang associations, which involves linking ideas based on their sound or rhyme. Flight of ideas, on the other hand, involves rapid and pressured speech with discernible links between ideas.

Thought disorders can manifest in various ways, including circumstantiality, tangentiality, neologisms, clang associations, word salad, Knight’s move thinking, flight of ideas, perseveration, and echolalia. Circumstantiality involves providing excessive and unnecessary detail when answering a question, but eventually returning to the original point. Tangentiality, on the other hand, refers to wandering from a topic without returning to it. Neologisms are newly formed words, often created by combining two existing words. Clang associations occur when ideas are related only by their similar sounds or rhymes. Word salad is a type of speech that is completely incoherent, with real words strung together into nonsensical sentences. Knight’s move thinking is a severe form of loosening of associations, characterized by unexpected and illogical leaps from one idea to another. Flight of ideas is a thought disorder that involves jumping from one topic to another, but with discernible links between them. Perseveration is the repetition of ideas or words despite attempts to change the topic. Finally, echolalia is the repetition of someone else’s speech, including the question that was asked.

Lithium, a mood-stabilizing drug commonly used in bipolar disorder, can lead to various health complications such as thyroid, cardiac, renal, and neurological issues. One of the common side effects of lithium is benign leucocytosis, which is also associated with other drugs like corticosteroids and beta-blockers. In this case, it is appropriate to continue with the normal monitoring schedule and safety netting for any signs of infection or malignancy, as there are no indications of either. Antibiotics would not be necessary. Malignant leucocytosis is unlikely as there are no accompanying symptoms such as night sweats, weight loss, bleeding, lymphadenopathy, or bone pain. Withholding lithium would not be advisable as it is effectively managing the patient’s condition. The psychiatric team should be consulted before making any decisions regarding the medication.

Lithium is a medication used to stabilize mood in individuals with bipolar disorder and as an adjunct in treatment-resistant depression. It has a narrow therapeutic range of 0.4-1.0 mmol/L and is primarily excreted by the kidneys. The mechanism of action is not fully understood, but it is believed to interfere with inositol triphosphate and cAMP formation. Adverse effects may include nausea, vomiting, diarrhea, fine tremors, nephrotoxicity, thyroid enlargement, ECG changes, weight gain, idiopathic intracranial hypertension, leucocytosis, hyperparathyroidism, and hypercalcemia.

Monitoring of patients taking lithium is crucial to prevent adverse effects and ensure therapeutic levels. It is recommended to check lithium levels 12 hours after the last dose and weekly after starting or changing the dose until levels are stable. Once established, lithium levels should be checked every three months. Thyroid and renal function should be monitored every six months. Patients should be provided with an information booklet, alert card, and record book to ensure proper management of their medication. Inadequate monitoring of patients taking lithium is common, and guidelines have been issued to address this issue.

The patient is exhibiting symptoms of acute dystonia, which is characterized by sustained muscle contractions such as torticollis or oculogyric crisis. In this case, the patient’s symptoms are likely a result of starting a typical antipsychotic medication, specifically haloperidol. Torticollis, or a wry neck, is present with unilateral pain and deviation of the neck, restricted range of motion, and pain upon palpation. While neuroleptic malignant syndrome is a medical emergency that can occur in patients taking antipsychotics, the patient’s lack of altered mental state and normal observations make it unlikely. An oculogyric crisis, which involves sustained upward deviation of the eyes, clenched jaw, and hyperextension of the back/neck with torticollis, is another example of acute dystonia, but the patient does not exhibit any facial signs or symptoms. Tardive dyskinesia, on the other hand, is a condition that occurs in patients on long-term typical antipsychotics and is characterized by uncontrolled facial movements such as lip-smacking.

Antipsychotics are a group of drugs used to treat schizophrenia, psychosis, mania, and agitation. They are divided into two categories: typical and atypical antipsychotics. The latter were developed to address the extrapyramidal side-effects associated with the first generation of typical antipsychotics. Typical antipsychotics work by blocking dopaminergic transmission in the mesolimbic pathways through dopamine D2 receptor antagonism. They are associated with extrapyramidal side-effects and hyperprolactinaemia, which are less common with atypical antipsychotics.

Extrapyramidal side-effects (EPSEs) are common with typical antipsychotics and include Parkinsonism, acute dystonia, sustained muscle contraction, akathisia, and tardive dyskinesia. The latter is a late onset of choreoathetoid movements that may be irreversible and occur in 40% of patients. The Medicines and Healthcare products Regulatory Agency has issued specific warnings when antipsychotics are used in elderly patients, including an increased risk of stroke and venous thromboembolism. Other side-effects include antimuscarinic effects, sedation, weight gain, raised prolactin, impaired glucose tolerance, neuroleptic malignant syndrome, reduced seizure threshold, and prolonged QT interval.

Understanding the Symptoms and Causes of Lithium and Clozapine Toxicity

Lithium toxicity occurs when levels exceed 1.5 mmol/l, leading to gastrointestinal and central nervous system symptoms. At levels above 2.0 mmol/l, confusion, coma, and death may occur. Clozapine and lithium are not commonly co-prescribed, and lithium is not typically used to augment clozapine for psychotic symptoms. Clozapine toxicity causes lethargy, confusion, tachycardia, hypotension, and hypersalivation. Gastrointestinal infection due to clozapine-induced neutropenia is unlikely if the neutrophil count is normal. Hypoglycemia is not suggested with a blood sugar level of 6.1. Serotonin syndrome presents with tachycardia, hypertension, tachypnea, confusion, seizures, fever, disseminated intravascular coagulation, and renal failure.