1084 ANZJP Correspondence Australian & New Zealand Journal of Psychiatry, 47(11) Gentile S and Galbally M (2010) Prenatal expo- sure to antidepressant medications and neuro-developmental outcomes: A systematic review. Journal of Affective Disorders 128: 1–9. Grigoriadis S, Vonderporten EH, Mamisashvili L, et al. (2013) Antidepressant exposure during pregnancy and congenital malformations: is there an association? a systematic review and meta-analysis of the best evidence. Journal of Clinical Psychiatry 74: e293–e308. Lewis A, Galbally M and Bailey C (2012) Perinatal mental health, antidepressants and neonatal outcomes: Findings from the Longitudinal Study of Australian Children. Neonatal, Paediatric and Child Health Nursing 15: 22–28. Malm H, Artama M, Gissler M, et al. (2011) Selective serotonin reuptake inhibitors and risk for major congenital anomalies. Obstetrics & Gynecology 118: 111–120. Myles N, Newall H, Ward H and Large M (2013) Systematic meta-analysis of individual selective serotonin reuptake inhibitor medications and congenital malformations. Australian and New Zealand Journal of Psychiatry 47: 1001–1011. O’Brien L, Einarson TR, Sarkar M, et al. (2008) Does paroxetine cause cardiac malformations? Journal of Obstetrics and Gynaecology Canada 30: 696–701. Rahimi R, Nikfar S and Abdollahi M (2006) Pregnancy outcomes following exposure to serotonin reuptake inhibitors: A meta-analy- sis of clinical trials. Reproductive Toxicology 22: 571–575. Wurst KE, Poole C, Ephross SA, et al. (2010) First trimester paroxetine use and the prevalence of congenital, specifically cardiac, defects: A meta-analysis of epidemiological studies. Birth Defects Research. Part A, Clinical and Molecular Teratology 88: 159–170. Use of quetiapine in child and adolescent populations – Response to letter from Dr Lambe Erik Monasterio and Andrew McKean Hillmorton Hospital, Christchurch, New Zealand Corresponding author: Erik Monasterio, Hillmorton Hospital, Annex Road, Christchurch 8140, New Zealand. Email: erik.monasterio@cdhb.govt.nz DOI: 10.1177/0004867413498274 We are grateful to be given an opportu- nity to comment on the letter by Dr Lambe (Lambe, 2013) in response to our previous correspondence (Monasterio and McKean, 2013), which outlined our concern about the exten- sive off-label use of quetiapine in primary and specialist psychiatric care, despite the limited evidence base for its safety and efficacy (Monasterio and McKean, 2011). Dr Lambe acknowledges that there are many potential adverse effects associated with the use of quetiapine, particularly in child and adolescent psychiatry, but, despite this, comments that: ‘off-label prescribing of quetiapine for excessive anxiety and insomnia is often the best alternative, as long as one monitors for side effects’ (Lambe, 2013). In considering the appropriateness of off-label prescribing of atypical antipsychotic (AAP) medications in child and adolescent psychiatry, we encourage close attention to recent findings in the literature, which indi- cate that there has been a particularly rapid expansion in the use of these agents in this age group for reasons which remain largely unknown. • An analysis of drug dispensing data from community pharmacies in The Netherlands found that between 1997 and 2005 the use of antipsychotics increased from 3.0 to 6.8 per thousand for youths to 19 years of age; the use of AAPs increased almost ninefold. The increase in AAPs was most pro- nounced for 5–9 year olds (almost 10-fold) and for 10–14 year olds (almost 12-fold). The median duration of AAP use across all age groups was 2.9 years and longest for 5-9 year olds, at 5.1 years. (Kalverdijk et al., 2008). • An analysis of Medical Expen- ditures Panel Survey (MEPS) data on non-institutionalized individu- als in the USA found that the pro- portion of antipsychotic users who were under age 18 doubled between 1996/1997 and 2004/ 2005 from 7% to 15% of all users (Domino and Swartz, 2008). Analysis of data from the National Ambulatory Medical Care Survey (NAMCS), which collects informa- tion from office-based physician practices, found that the annual number of US office visits by those under age 21 that included pre- scription of an antipsychotic medi- cation jumped more than fivefold from 1993/1995 to 2002 (Olfson et al., 2006). Amongst privately insured 2–5-year-old children in the USA, the rate of antipsychotic use doubled in the period of 1999/2001 to 2007; this occurred at the same time that the use of antidepressants decreased (1.6 times less common in 2007) in this age group (Olfson et al., 2010). Data from long-term US trends in office-based physician use of antip- sychotic medications found that there was an eightfold increase in the number of treatment visits for children between 1995 and 2008 (Alexander et al., 2011). In British Columbia, there has been a 10-fold increase in the prescrip- tion of AAPs to children under 14 between 1997 and 2007 (Panagiotopoulos et al., 2010). • Data supplied by PHARMAC (the pharmaceutical funding agency in New Zealand) indicates that there has been a 56% increase in the use of antipsychotic medications in 10–19 year olds from 2008 to 2012 in New Zealand. • Children and adolescents may be at a higher risk of antipsychotic- associated weight gain, as well as sedation and movement disorders, when compared to adults (McKinney and Renk, 2011). Among 257 children taking sec- ond-generation antipsychotics for the first time, weight increased during the first 12 weeks of treat- ment. Among subjects taking olan- zapine, the mean weight gain was