Common Mental Disorders Depression - New Zealand Doctor
Common Mental Disorders Depression - New Zealand Doctor
Common Mental Disorders Depression - New Zealand Doctor
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Chapter 7 Special issues: women with mental disorders in the antenatal and postnatal period<br />
Pharmacological therapies<br />
A search was conducted for RCTs of antidepressant use in women with depression in<br />
the antenatal or postnatal period. The evidence comprised one guideline 101 with three<br />
relevant studies conducted in mixed primary and secondary care populations. 479,486,490<br />
Given the dearth of evidence from controlled studies on the safety of antidepressants<br />
in this population, recent reviews of relevant observational evidence were also<br />
retrieved. Three narrative reviews 453,456,470 were identified and studies from their lists of<br />
references were accessed. Advice on relevant studies was also sought from a maternal<br />
mental health specialist.<br />
Efficacy<br />
There was some evidence (from a single RCT) 486 of the efficacy of the SSRI fluoxetine<br />
with a single session of CBT in the postnatal period. However, fluoxetine with six<br />
sessions of CBT was only as effective as 6 sessions of CBT alone. This finding was<br />
supported by low-quality evidence from uncontrolled trials. 65<br />
Safety and adverse effects on the infant/foetus<br />
Selective serotonin reuptake inhibitors in pregnancy<br />
Small prospective cohort studies in the 1990s found no association between maternal<br />
SSRI use and birth defects. 453 However, more recently large case-control studies 464,491<br />
and a population-based cohort study 492 found a significant association between<br />
maternal SSRI use in early pregnancy and major birth defects. In two studies, 464,491 the<br />
increase associated with SSRIs applied only to specific rare defects (eg, omphalocele),<br />
with no increase in the overall rate, but in the third 492 there was a moderate increase<br />
in overall risk of birth defects (RR 1.34, 95% CI 1.00 – 1.79). There has been concern<br />
about a possible increase in the risk of cardiovascular malformations associated<br />
with the use of paroxetine during the first trimester. 465,493 A Canadian study linking<br />
databases of medications and hospital discharges involving International Classification<br />
of Diseases, Ninth Revision (ICD9) codes for malformations, also showed an<br />
association between major cardiac malformations and exposure to paroxetine, though<br />
only at daily doses of greater than 25 mg (adjusted odds ratio 3.07; 95% CI 1.00 –<br />
9.42). 494 However, a recent study identified outcomes in over 3000 infants exposed to<br />
paroxetine during the first trimester and found that the rate of malformations was well<br />
within incidence in the general population, at around 1%. 495 Current Medsafe advice<br />
recommends avoiding the use of paroxetine in pregnancy. 462<br />
A systematic review of more than 20 small observational studies reported a neonatal<br />
syndrome with symptoms of increased muscle tone, tremulousness, and difficulty<br />
with respiration, feeding, and sleep in infants who had third-trimester exposure to<br />
SSRIs. 496 A large study using British Columbian population health data over a 3-year<br />
period found that prenatal exposure to SSRIs was associated with an increased risk of<br />
neonatal respiratory distress, even after accounting for maternal illness severity. 496,497<br />
Identification of <strong>Common</strong> <strong>Mental</strong> <strong>Disorders</strong> and Management of <strong>Depression</strong> in Primary Care 105