Medications Flashcards
ACEi - Donepezil, Rivastigmine, Galantamine
Efficacy
40-50% benefit
1/3 improve
1/3 plateau
1/3 don’t respond
Sodium Valproate - Teratogenicity
- 1/10 risk of malformation (2-3/100 baseline)
- Spina Bifida/NTDs - 1.5% risk (0.2-0.5% background)
- Deformities of limbs/kidneys/heart/urogenital tract possible
- Cleft lip/palate
- 30-40% have intellectual development difficulties e.g. autism/ADHD/low IQ
Sodium Valproate Side Effects - Common/Dose Related
- GI upset (anorexia, nausea and vomiting, diarrhoea, dyspepsia)
- Deranged LFTs
- Tremor
- Sedation
- Headache
- Irregular/delayed periods
- Dry mouth/swollen gums
Sodium Valproate - Initiation, Monitoring and Withdrawal
- Check FBC, LFTs and BMI before starting
- Dose depends on indication
- Plasma level monitoring not useful unless evidence of ineffectiveness, poor compliance or toxicity
- FBC/LFTs/BMI - 6 months after initiation and yearly thereafter
- Check FBC and clotting before surgery
- Avoid abrupt withdrawal - reduce dose gradually over at least 4 weeks
Lithium - Monitoring
- Lithium levels - weekly after initiation until dose stable
- Then every 3 months
- eGFR/TFTs every 6 months
- Weight/BMI when indicated
Lithium Toxicity - Symptoms
Occurs at levels >1.5 mmol/L
- Diarrhoea
- Vomiting
- Coarse tremor
- Hyperreflexia
- Muscle weakness
- Ataxia
- Confusion
- Seizures
- Kidney damage
Lithium Adverse Effects - Long Term
- Weight Gain
- Hypothyroidism
- Deranged renal function/kidney damage
- SIADH
- ECG changes (T-wave flattening)
- Skin changes - acne/psoriasis
Lithium Adverse Effects - Short-term/Common
- Thirst
- Polyuria
- Metallic taste
- Fine tremor
- Nausea/vomiting
Antidepressants - Efficacy
- 60-70% respond
Methylphenidate - Monitoring
- Cardiovascular status (HR/BP) - every 3/12
- Height/weight - every 6/12
Methylphenidate - Efficacy
- 70% respond
Sodium Valproate - Rare/Serious Side Effects
- Hepatic failure
- Pancreatitis
- Agranulocytosis
- Polycystic ovaries
- Increased suicidal thoughts - as early as one week after starting
Sodium Valproate - Side Effects (Unpredictable)
- Hair loss - with curly regrowth
- Peripheral oedema
- Leucopaenia/thrombocytopenia
- Weight gain
Lithium in Pregnancy/Teratogenicity
- Teratogenicity
- Possible risk of increased heart defects - now debated
- Ebstein’s anomaly 1:1000 risk (1:20000 baseline)
- Pregnant women taking lithium should have a level 2 USS at 6 + 18 weeks
- Lithium levels should be checked:
- Monthly during early pregnancy
- Weekly after 36 weeks
- Before and after delivery
Lithium During Pregnancy
- Best to stop
- Gradually reduce and stop over 4 weeks
- Switch to an alternative e.g. anyipsychotic
- Restart after delivery (but not if breastfeeding)
- Alternatively omit for first trimester only
Clozapine - Risk of Neutropenia/Agranlucytosis
- Neutropaenia 2-3/100
- Agranulocytosis <1/100
- Fatal 1/8000
Clozapine - Efficacy
- 60-70% of patients
- 30% respond after 6/52
- 20% after 3/12
- 20% after 6/12
- 30% never respond
ACE inhibitors - Side Effects
- Cholinergic
- Nausea
- Diarrhoea
- Urinary incontinence
- Insomnia
- Bradycardia
- Donepezil specifically contraindicated in asthma
Sodium Valproate - Indications and Contraindications
- Used for BPAD and epilepsy
- Avoid using in women of childbearing age if possible
- If no alternative must be enrolled in PREVENT pregnancy prevention program
- Use with caution in those with lupus
- Avoid in:
- Severe liver disease
- Personal/family history of drug related hepatic dysfunction
- Porphyria
- Mitochondrial disorders
Sodium Valproate Use In Women of Childbearing Age
- Avoid if at all possible
- Annual reviews under PREVENT pregnancy prevention program
- Regularly re-evaluate need for treatment - consider dose reduction or switch
- Complete and sign annual risk acknowledgement form - copies to patient/carer and GP
Sodium Valproate Use During Pregnancy
- If to be withdrawn recommend dose be slowly tapered down over a few weeks to reduce relapse risk
- In acute mania faster cross-taper to substitute
- If patient has to continue:
- High dose folic acid 5mg/day
- Use lowest dose possible
- Small split doses or extended release formulation to minimise peaks
- Plasma levels should not exceed 1g/day
- Present in small amounts in milk - avoid if baby premature or has kidney problems
Sodium Valproate Interactions
P450 Inhibitor
- Aspirin and Warfarin - displace valproate from albumin and may –> toxicity
- Cytochrome P450 inhibitors can increase levels:
- Erythromycin
- Fluoxetine
- Cimetidine
- TCAs - inhibits metabolism increasing levels
- Carbapenem antibiotics - decrease valproate levels
- Quetiapine - co-administration increases risk of neutropaenia/leucopaenia
- Lamotrigine - increases level of Lamotrigine
- Nimodipine - increases levels of Nimodipine
Clozapine - Initiation
- Prior to starting:
- FBC, LFTs, prolactin, CRP
- ECG - refer to cardiology if concerns
- Dose usually starts at 12.5mg and then titrated up
Clozapine - Monitoring
- Monitoring of FBC - registration through ZTAS
- FBC weekly for first 18 weeks
- Every 2 weeks for rest of year
- Every month thereafter
- Review treatment every 3-6 months
- Monitor for SEs including constipation and chest pain
- Risk of relapse if stopped suddenly