Literature DB >> 15900008

Neonatal signs after late in utero exposure to serotonin reuptake inhibitors: literature review and implications for clinical applications.

Eydie L Moses-Kolko1, Debra Bogen, James Perel, Amy Bregar, Kathleen Uhl, Bob Levin, Katherine L Wisner.   

Abstract

CONTEXT: A neonatal behavioral syndrome linked to in utero serotonin reuptake inhibitor (SRI) exposure during the last trimester of pregnancy has been identified. The US Food and Drug Administration (FDA) and drug manufacturers have recently agreed to a class labeling change for SRIs, which include selective serotonin reuptake inhibitors (SSRIs) and serotonin and norepinephrine reuptake inhibitors (SNRIs), to include information about potential adverse events in neonates exposed in utero. Integration of data about the neonatal behavioral syndrome into the management of pregnancy in women who take SRIs is a current challenge for physicians.
OBJECTIVES: To review evidence regarding the SRI-related neonatal syndrome and to help clinicians guide their patients in a risk-benefit decision-making process. DATA SOURCES: We searched MEDLINE (1966-February 2005) and PsycINFO (1974-February 2005). All articles related to neonatal signs after in utero SRI exposure were acquired, as well as unpublished data on this topic from the FDA advisory committee meeting of June 2004. References cited in case reports and studies were reviewed. Foreign-language literature was included and translated to English. STUDY SELECTION AND DATA EXTRACTION: Studies were included if they had clearly identified maternal SRI exposure for a minimum of the final trimester of pregnancy through delivery and assessed neonatal outcomes. We identified 13 case reports describing a total of 18 cases. Nine cohort studies met criteria. When not included in the published article, relative risks and 95% confidence intervals (CIs) were computed from raw data and summary risk ratios and 95% CIs were determined with Mantel-Haenszel estimates. DATA SYNTHESIS: Compared with early gestational SRI exposure or no exposure, late SRI exposure carries an overall risk ratio of 3.0 (95% CI, 2.0-4.4) for a neonatal behavioral syndrome. The most SRI-related neonatal case reports involved fluoxetine and paroxetine exposures. Neonates primarily display central nervous system, motor, respiratory, and gastrointestinal signs that are usually mild and disappear by 2 weeks of age. Medical management has consisted primarily of supportive care in special care nurseries. A severe syndrome that consists of seizures, dehydration, excessive weight loss, hyperpyrexia, or intubation is rare in term infants (1/313 quantifiable cases). There have been no reported neonatal deaths attributable to neonatal SRI exposure.
CONCLUSIONS: Available evidence indicates that in utero exposure to SRIs during the last trimester through delivery may result in a self-limited neonatal behavioral syndrome that can be managed with supportive care. The risks and benefits of discontinuing an SRI during pregnancy need to be carefully weighed for each individual patient. Development and validation of assessment methods and clinical management strategies are critical to advancing this research.

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Year:  2005        PMID: 15900008     DOI: 10.1001/jama.293.19.2372

Source DB:  PubMed          Journal:  JAMA        ISSN: 0098-7484            Impact factor:   56.272


  117 in total

Review 1.  Investigating outcomes following the use of selective serotonin reuptake inhibitors for treating depression in pregnancy: a focus on methodological issues.

Authors:  Luke E Grzeskowiak; Andrew L Gilbert; Janna L Morrison
Journal:  Drug Saf       Date:  2011-11-01       Impact factor: 5.606

2.  Neonatal seizures on EEG after in utero exposure to venlafaxine.

Authors:  Chris J C Hoppenbrouwers; Jacob Bosma; Hanneke J M B Wennink; Antonius A J Hilgevoord; Marion Heres; Adriaan Honig
Journal:  Br J Clin Pharmacol       Date:  2010-09       Impact factor: 4.335

3.  Three cases of lithium exposure and exclusive breastfeeding.

Authors:  Debra L Bogen; Dorothy Sit; Adrienne Genovese; Katherine L Wisner
Journal:  Arch Womens Ment Health       Date:  2012-01-26       Impact factor: 3.633

4.  Treatment with selective serotonin reuptake inhibitors during pregnancy: deceleration of weight gain because of depression or drug?

Authors:  Lisa M Bodnar; Keerthy R Sunder; Katherine L Wisner
Journal:  Am J Psychiatry       Date:  2006-06       Impact factor: 18.112

5.  Mood disorders and their pharmacological treatment during pregnancy: is the future child affected?

Authors:  Catherine Monk; Elizabeth M Fitelson; Elizabeth Werner
Journal:  Pediatr Res       Date:  2011-05       Impact factor: 3.756

6.  Length of prenatal exposure to selective serotonin reuptake inhibitor (SSRI) antidepressants: effects on neonatal adaptation and psychomotor development.

Authors:  Regina C Casper; Allyson A Gilles; Barry E Fleisher; Joan Baran; Gregory Enns; Laura C Lazzeroni
Journal:  Psychopharmacology (Berl)       Date:  2011-04-16       Impact factor: 4.530

Review 7.  [Affective disorders during pregnancy : Therapy with antidepressants and mood stabilizers].

Authors:  N Bergemann; W E Paulus
Journal:  Nervenarzt       Date:  2016-09       Impact factor: 1.214

Review 8.  Interpreting the pharmacoepidemiology literature in obstetrical studies: A guide for clinicians.

Authors:  Laura J Rasmussen-Torvik; Katelyn B Zumpf; Hannah K Betcher; Jody D Ciolino
Journal:  Semin Perinatol       Date:  2020-02-28       Impact factor: 3.300

9.  The effects of maternal depression and use of antidepressants during pregnancy on risk of a child small for gestational age.

Authors:  Hans Mørch Jensen; Randi Grøn; Ojvind Lidegaard; Lars Henning Pedersen; Per Kragh Andersen; Lars Vedel Kessing
Journal:  Psychopharmacology (Berl)       Date:  2013-03-02       Impact factor: 4.530

10.  Omega-3 fatty acids and supportive psychotherapy for perinatal depression: a randomized placebo-controlled study.

Authors:  Marlene P Freeman; Melinda Davis; Priti Sinha; Katherine L Wisner; Joseph R Hibbeln; Alan J Gelenberg
Journal:  J Affect Disord       Date:  2008-02-21       Impact factor: 4.839

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