1 Perinatal Mental Health Azlan Luk TARGET Session 22092016
1 Perinatal Mental Health Azlan Luk TARGET Session 22092016
1 Perinatal Mental Health Azlan Luk TARGET Session 22092016
Perinatal Psychiatry
Dr Azlan Luk
Consultant Psychiatrist
Guildford CMHRS
Disclosures
I am not a perinatal psychiatrist.
I am a General Adult Psychiatrist
Attended BAP, Maudsley Simulation day
Read NICE, Confidential enquiry into maternal
deaths etc
Structure
Psychiatric disorders
Brief epidemiology
Specific prescribing
Antidepressants
Antipsychotics
Mood stabilisers
Anxiolytics / Hypnotics
2.5 9 % vs 1.1%
(gen pop)
3-5%
3 - 5%
10 15%
Postpartum Psychosis
2%
Working to deliver excellence in mental health simulation as part of South London and Maudsley NHS Foundation Trust
Working to deliver excellence in mental health simulation as part of South London and Maudsley NHS Foundation Trust
Domestic Violence
Systematic review: high prevalence and increased odds (2-3)
among pregnant women across all diagnoses
19% experienced domestic violence in pregnancy (CRIS SLAM)
Identification of domestic violence by clinicians occurs in 1030% of cases
(Feder et al 2011; Howard et al 2010, 2013)
Postpartum Psychosis
Psychiatric emergency
1 in every 1000 births
30 50% of women with BPAD, schizoaffective
disorder, psychotic depression, previous post
partum psychosis or schizophrenia develop it
> 60 % of BPAD with FHx / PHx of post partum
psychosis
Onset greatest in first 30 days (50 60% by day
14)
Approx. 50% are first episodes
60% will have future psychotic episode
30 50% risk of future postpartum psychosis
Uncertainty
Evidence is uncertain about
benefits, risks and harm of
treatments
Balance the risks of harm to
mother and fetus / baby
Likely benefits of treatment
Previous history
Risks to mother and fetus of treating
Potential effect of untreated mental
illness
Risks or harms to mother and fetus /
baby associated with stopping or
changing treatment
Prescribing in pregnancy
Identify risk factors
Optimise non-pharmacological treatments
Talking therapy provide within one month of assessment
(NICE)
Breastfeeding
All psychotropic drugs transferred into breast
milk
Exposure less than pregnancy
Few data for most psychotropics
Most psychotropics are well below 10% RID
(relative infant dose) but some exceptions
Half life of drugs should be considered
Lowest effective dose
Avoid polypharmacy
Time dose to avoid peak levels
Antidepressants - outcomes
All commonly used SSRIs implicated (with malformations) but residual
confounding factors (including depression itself) not controlled for
Persistent pulmonary Hypertension - OR 1.1 2.1
Premature delivery 0.45 weeks earlier
Birthweight 74 grams lower (though not significant if compared to
women with depression)
Apgar scores - significant outcome 0.37 1min and 0.16 at 5 min
Postnatal Adaptation syndrome OR 5.07
Respiratory distress OR 2.2
Tremors OR 7.89
ASD unclear
Antidepressants
Pregnancy
Commonly used 10% in USA
Relapse rates are high with stopping antidepressants in
women with a history of depression (68% vs 26%)
Absolute risk low
Most evidence with Amitriptyline, Imipramine ( both
constipation, withdrawals), Sertraline (low infant exposure),
Fluoxetine (earlier delivery, reduced birth weight)
Paroxetine ?less safe - 1.5 2 x risk cardiac defects
Breastfeeding
Differences between antidepressants are small
Sertraline (low infant serum levels)
Antipsychotics
Current evidence antipsychotics not major teratogens
Small increase in major congenital anomalies mostly
cardiovascular could be due to confounding factors
Small increase pre-term birth and small for gestational
age
Possibly small increase in still births
Uncertain association with gestational diabetes
No indication of significant long term
neurodevelopmental effect
Most experience with chlorpromazine,
trifluoperazine, haloperidol, olanzapine,
quetiapine and clozapine
Antipsychotics - Breastfeeding
Olanzapine (Maudsley)
Not seem to be affected by prolactin raising
antipsychotics
Avoid clozapine (agranulocytosis)
Avoid depots
Mood stabilisers
Valproate 3 fold increase in major congenital malformations
Spina bifida OR 12.7
Associated with hypospadias, cleft palate, atrial septal defects,
polydactyly, craniosynostosis
Cognitive development IQ difference 8 points
Effect of folate effect at best is uncertain
No safe time and no known safe dose
Lithium
Conflicted data potentially a small increase (2
fold) in major congenital malformations
Ebstein Anomaly currently no evidence for
increased risk but low number of events.
Cases of maternal lithium toxicity at delivery
Case reports of
Lithium - considerations
Only continue in preconception and 1 st trimester if switch means
high risk of occurrence
Replace lithium with antipsychotic agent until 2 nd trimester or until
after delivery
Adjust lithium dose
Structural ultrasound and fetal echocardiogram
Delivery in hospital, obstetrician-led care
Stop lithium when labour starts
Breast feeding
dont offer lithium (serum levels 10 50%) - NICE
Dont offer valproate or carbamazepine (NICE)
Z- drugs
Not teratogenic
Zolpidem possibly some increase risk preterm birth,
small for
gestational age, low birthweight
Use short term avoid Zolpidem
Structure
Psychiatric disorders
Brief epidemiology
Specific prescribing
Antidepressants
Antipsychotics
Mood stabilisers
Anxiolytics / Hypnotics
Remember - Uncertainty
Information
Patients
UK teratology information service
www.uktis.org
Bumps best use of medicines in pregnancy
www.medicinesinpreganancy.org
Professionals
TOXBASE 0344 892 0111 www.toxbase.org
The Maudsley Pharmacy - Specialist Prescriber Advice
020 3228 2317
Questions
References
Confidential Enquiry into Maternal Death, MBRRACE-UK Report 2015 https://www.npeu.ox.ac.uk/mbrrace-uk
Antenatal and postnatal mental health: Clinical management and service guidance, NICE
guidelines (CG192) 2014
The Maudsley Prescribing Guidelines in Psychiatry 13 th Edition 2015: Taylor, Paton,
Kapur Wiley Blackwell
Course material British Association for Psychopharmacology Perinatal Masterclass 28 th
April 2016
Course material Maudsley Perinatal Mental Health Simulation Day 11th February 2016
Presentation implications of the Barker Hypothesis (what can we do about modifiable
in utero risk factors L Howard - http://www.rcpsych.ac.uk/pdf/IC14%20S32%20Howard
%20Louise.pdf