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Published 21 October 2009, doi:10.1136/bmj.b4295
Cite this as: BMJ 2009;339:b4295
| The first 150 words of the full text of this article appear below. |
I did not intend my comments to be interpreted as minimising the risk.1 2 Rather, I intended to place the risks in context in terms of both size (which is estimated to be comparatively small compared with other known teratogens such as isotretinoin, which can affect more than 20% of exposed pregnancies) and the concomitant risks of no treatment or undertreatment.
Healy mentions our California data on pregnancy outcomes with prenatal exposure to paroxetine.2 This is a perfect example of the difficulty in drawing conclusions from studies with inadequate sample sizes. Our data on paroxetine were drawn from an ongoing open cohort study with an increasing but still extremely small sample size. Preliminary results were published in abstract form several years ago,3 and updated results were provided for and included in the meta-analysis recently published by Wurst et al.4 These same data were also included in a published paper on the
Christina Chambers, associate professor1
1 Division of Dysmorphology and Teratology, Departments of Pediatrics and Family and Preventive Medicine, School of Medicine, University of California San Diego, 9500 Gilman Drive, MC 0828, La Jolla, CA 92093-0828, USA
chchambers@ucsd.edu