Depression PROTOCOL 3

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1 PROTOCOL 3 Depression Kimberly Yonkers 1,2,3 1 Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA 2 Department of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine, New Haven, CT, USA 3 School of Epidemiology and Public Health, Yale University School of Medicine, New Haven, CT, USA Clinical significance Approximately 20% of women suffer from a depressive disorder at some point in their lives. The risk of being depressed is greatest for women during their reproductive years and thus clinicians may encounter a pregnant woman with pre-existing depression or a woman who becomes depressed during her pregnancy. Some research finds an association between maternal depression and particular perinatal complications, including preterm birth and/or delivery of a low-birth-weight baby, although there are dissenting results. These findings, along with the potentially devastating toll that a major depressive episode (MDE) has on a mother, underscore the need to treat depressed pregnant women. However, when the needed treatment is pharmacotherapy, there are additional concerns because antidepressants, and the anxiolytics that are often used concurrently, are linked with adverse perinatal and fetal outcomes. Researchers note a risk of fetal malformations although this appears to be a small risk that has largely centered on atrial and ventricular septal defects and only with some antidepressants. Other worrisome associations include delivery of an infant who is preterm or small for gestational age, as well as a very small increased likelihood of persistent pulmonary hypertension. The evidence for a number of these outcomes among women treated with antidepressants in pregnancy is mixed, with the strongest support for preterm birth. However, even the smallest risk can lead to apprehension on the part of patients and uneasiness for their prescribing physicians. Protocols for High-Risk Pregnancies: An Evidence-Based Approach, Sixth Edition. Edited by John T. Queenan, Catherine Y. Spong and Charles J. Lockwood John Wiley & Sons, Ltd. Published 2015 by John Wiley & Sons, Ltd. 27

2 28 Protocol 3 Pathophysiology As with many psychiatric disorders, the pathophysiology of a depressive disorder is unknown, although evidence suggests that underlying risk is determined by biology (e.g., genetic factors), stress, and trauma. Co-occurring general medical conditions and exposure to selected medications and other substances can also lead to development of depressive symptoms or an MDE. Brain imaging studies show that individuals with depression have changes in neurocircuitry and volume reductions in critical brain areas such as anterior cingulate cortex, amygdala, and hippocampus. These regions are also affected by elevations in glucocorticoids and there are longstanding theories that implicate dysregulation of the hypothalamic pituitary adrenal axis in depression. For example, the introduction of stress leads to secretion of cortisol. The integrity of the feedback systems between cortisol, adrenocorticotrophic hormone, and corticotrophin releasing hormone is compromised in many individuals with depression leading to overexpression of these hormones. Ongoing exposure to these hormones can lead to anatomic and dynamic (signaling) changes in the aforementioned brain regions. Diagnosis There are several mood disorders that fall under the category of depression and they are outlined in the Diagnostic and Statistical Manual version 5 (Association 2013). The prototypic depressive disorder is an MDE. There are nine candidate symptoms of an MDE including depressed mood, diminished interest, significant weight change, insomnia or hypersomnia, psychomotor retardation or agitation, fatigue, feelings of guilt or worthlessness, decreased concentration and recurrent thoughts of death or suicide. A woman should have at least five of these symptoms, including either depressed mood and/or diminished interest, most of the time for 2 weeks. If a woman has a history of manic/hypomanic episodes as well as MDEs, she suffers from bipolar disorder but is presenting in the depressed phase. Mania is characterized by elevated/expansive/irritable mood, increased energy, grandiosity, decreased need for sleep, pressured speech, and increased participation in goal-related or risky activities. If she has never had manic or hypomanic episodes, and she meets the above criteria, then her diagnosis is unipolar major depressive disorder. Management The management of a pregnant woman with an MDE will vary depending upon whether she has unipolar or bipolar illness. In either case, she may

3 Depression 29 benefit from psychotherapy although she should be monitored to ensure that this treatment is sufficient for response. If she requires pharmacotherapy, she should be apprised of the risks and benefits and this should be documented in her medical chart. Along with her obstetrician, it may be prudent to have her evaluated and followed concurrently by a psychiatrist. If she experiences thoughts of self-harm or suicide, she should be evaluated by a psychiatrist or clinical psychologist as soon as possible. Women with MDE, who suffer from bipolar disorder, will require treatment with a mood stabilizer and an antidepressant. Valproate and carbamazepine are effective mood stabilizers but also established teratogens and should not be used early in pregnancy. Lamotrigine is FDA approved for treatment of individuals with bipolar disorder and may be useful although it must be titrated up slowly. Lithium has been associated with cardiac defects and should be avoided early in pregnancy, although the risk is now considered to be smaller than it was after publication of results from the lithium registry. It is currently thought that the risk of the heart malformation, Ebstein s anomaly is 1 2 per thousand for lithium-exposed babies. However, the risk of other types of cardiac malformations has been reported to be nearly 8-fold higher for lithium-exposed offspring as compared to those nonexposed in the first trimester. First- and second-generation antipsychotics have good mood stabilizing properties and appear to have lower teratogenic risk than anticonvulsants and lithium. If mood improves, there is no need to add an antidepressant. Women with unipolar MDE who are not sufficiently treated with psychotherapy or women with bipolar disorder who did not respond to a mood stabilizer alone will need treatment with an antidepressant agent. The reproductive safety profile for the older tricyclic antidepressants is no better than for the newer, serotonin or serotonin-norepinephrine reuptake inhibitors. However, older agents have more side effects. It is reasonable to start with either a selective serotonin reuptake inhibitor or bupropion. If a woman is struggling to avoid nicotine cigarettes, use of bupropion may help treat her nicotine addiction and her depression. Given data associating paroxetine use in pregnancy with malformations of the heart, many experts recommend that this agent not be prescribed to pregnant women in the first trimester. However, if a woman presents well into her first trimester of pregnancy, there may be little benefit to switching to a different agent since exposure has already occurred. In any case, women should be counseled to minimize use of other harmful licit and illicit substances such as cigarettes, alcohol or recreational drugs. Use of substances is more common in women with depression as compared to without depression and patients may not realize that cigarettes, alcohol or other drugs are as harmful, if not more problematic than antidepressant agents.

4 30 Protocol 3 Follow up It is ideal to see a woman a week after initiation of pharmacotherapy for MDE to determine side effects to the medication and assess further deterioration in psychiatric status. Subsequently, she can be seen again after 2 weeks and then monthly. Some degree of mood improvement may be noticeable within a few weeks. However, it may take 6 8 weeks to see full response to treatment. The patient should be assessed for suicidal thoughts at each visit. While some clinicians have concerns that asking about suicidal thoughts will suggest this action to patients, this is not the case. Appropriate emergency medical care can be arranged if the patient endorses suicidal thoughts. If the obstetrician is unable to provide follow-up care at these intervals, the patient may be referred to a psychiatrist who can communicate with the obstetrician with regard to the patient s progress. Once response has been obtained, the patient s mood can be re-evaluated at routine obstetrical visits. Conclusion The risk period for an episode of MDE coincides with the period of women s fertility. While some women benefit from psychotherapy and can avoid pharmacotherapy in pregnancy, this is not always the case. Women who have underlying bipolar disorder and those with severe recurrent major depressive disorder will likely require medication management. Antipsychotic agents have a lower risk profile than anticonvulsant mood stabilizers, which should be avoided early in pregnancy. Antidepressants are not major teratogens but clinicians need to apprise patients of potential risks and benefits of treatment, including perinatal complications such as preterm birth or transient neonatal distress. Suggested reading American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition. Washington, DC, American Psychiatric Association, Chambers C, Hernandez-Diaz H, Marter LV, Werler M, Louik C, Jones K, Mitchell A. Selective serotonin-reuptake inhibitors and risk of persisitent pulmonary hypertension of the newborn. New Eng J Med 2006;354: Kallen B, Reis M. Neonatal complications after maternal concomitant use of SSRI and other central nervous system active drugs during the second or third trimester of pregnancy. Journal Of Clinical Psychopharmacology 2012;32(5): McKenna K, Koren G, Tetelbaum M, Wilton L, Shakir S, Diav-Citrin O, Levinson A, Zipursky RB, Einarson A. Pregnancy outcome of women using atypical antipsychotic drugs: a prospective comparative study. J Clin Psych 2005;66(4): ; quiz 546.

5 Depression 31 Moore JA. An assessment of lithium using the IEHR evaluative process for assessing human developmental and reproductive toxicity of agents. Reprod Tox 1995;9(2): Ross LE, Grigoriadis S, Mamisashvili L, Vonderporten EH, Roerecke M, Rehm J, Dennis CL, Koren G, Steiner M, Mousmanis P, Cheung A. Selected pregnancy and delivery outcomes after exposure to antidepressant medication: a systematic review and meta-analysis. JAMA Psychiatry 2013;70(4): Yonkers K, Blackwell K, Glover J, Forray A. Antidepressant use in pregnant and postpartum women. Ann Rev Clin Psyc 2014;10: Yonkers KA, Norwitz ER, Smith MV, Lockwood CJ, Gotman N, Luchansky E, Lin H, Belanger K. Depression and serotonin reuptake inhibitor treatment as risk factors for preterm birth. Epidemiology 2012;23(5):