Psychiatric Disorders of Obstetrical Patients: A Paradigm for Risk Assessment and Collaborative Management ()
1. Introduction
Obstetricians frequently care for women who have mood and anxiety disorders. These conditions include both new-onset disorders and recurrences of pre-pregnancy psychiatric illnesses [1]-[4]. Psychiatric diagnoses during pregnancy and the postpartum period are particularly common after trauma or undesirable events, such as unwanted pregnancy, miscarriage, traumatic delivery, dystocia, unexpected prenatal diagnosis, or unexpected/undesired caesarean section [5].
The most common psychiatric conditions dealt with by obstetricians are anxiety and mood disorders, either as individual diagnoses or in combination. Anxiety is identified in about 20% of pregnancies and depression in about 14% [5]-[7]. Less common psychiatric conditions—bipolar, obsessive, and psychotic disorders—also occur in women receiving obstetrical care; but are less common and more likely to present post-partum [8].
When psychiatric concerns arise during pregnancy, obstetricians, based on their training and experience, decide whether to diagnose and treat the problem themselves, whether to refer to a psychiatrist for co-management, and when to involve a neonatologist antepartum. Criteria for such referrals are lacking, and the need for such referrals should always be individualized.
The importance of engaging neonatology before birth is illustrated in a recent report from Sweden involving 1,308,487 infants, of whom 2677 (0.2%) were exposed to antipsychotics during pregnancy. Of the exposed infants, 516 (19.3%) were admitted to a neonatal intensive care unit compared with 98,976 (7.8%) of unexposed infants (adjusted risk ratio [ARR]: 1.7; 95% CI: 1.6 to 1.8). The highest risks were seen for withdrawal symptoms (17.7; 95% CI: 9.6 to 32.6), neurological disorders (3.4; 95% CI: 2.4 to 5.7), and pulmonary hypertension (2.1; 95% CI: 1.4 to 3.1) [9].
In this review, we provide a framework that we hope will assist obstetricians in caring for patients who manifest psychiatric illness. It includes assessment and management guidelines, and recommendations regarding when to consider psychiatric referral and when to involve a neonatologist antepartum. Our assessment/management paradigm begins with the obstetrician applying specific but simple criteria to characterize the severity of the psychiatric symptoms as either mild, moderate, or severe [10] [11]. While more diagnostic precision may be necessary for clinical research and psychiatric management, we maintain that beginning with the assessments and standardized rating scales we propose herein is practical and efficient in obstetrical practice.
2. Mild, Moderate, and Severe Depression/Anxiety
Mild depression/anxiety is characterized by symptoms that are apparent but manageable and without significant impairment in daily life (Table 1, first panel). Individuals with mild illness may report stress, worries, sadness, discouragement, restlessness, and/or irritability. These are more often intermittent than continuous and are commonly linked to life pressures and demands including those associated with the pregnancy. The Diagnostic and Statistical Manual of Mental Disorders, 5th edition and the International Statistical Classification of Diseases and Related Health Problems, 10th edition definitions of mild depression are similar; namely, “Few, if any, symptoms in excess of those required to make the diagnosis are present, the intensity of the symptoms is distressing but manageable, and the symptoms result in minor impairment in social or occupational functioning” [12] [13]. Obstetricians can proceed most confidently with a mild classification if there is no past or family history of depression, anxiety, bipolar, or a more severe psychiatric illness. However, a mild presentation could be the first phase of a moderate or severe condition.
Table 1. Treatment guidelines based on severity.
Symptom Severity |
Characteristics & Presentation |
Rating Scales |
Treatment Guidelines |
Mild |
Feeling stressed, discouraged, upset, blue, worried. Evident symptoms and discomfort but of minor intensity. More intermittent than continuous Little to no functional impairment Often related to life pressures and
demands. |
PHQ-9 score 5 - 9 GAD-7 score 5 - 9 |
1) Avoid medication in the 1st trimester if
possible 2) Avoid recreational drugs and alcohol 3) Emphasize assurance, support, exercise,
sufficient sleep, nutritious diet 4) Counseling, psychotherapy, group therapy 5) Expectant mother classes, online resources 6) Screen for past and family hx of severe
psychiatric illness 7) Increased monitoring and vigilant
follow-up. Watch for escalation |
Moderate |
The above symptoms of greater intensity. More prominent anxiety and/or depression and heightened levels of distress causing impairment in work, home, marriage or
social functioning. Most continue to
function but with decreased satisfaction, increased effort, less efficiency and
functional deterioration. Symptoms more continuous than
intermittent. Absence of suicidal, homicidal or
psychotic features. |
PHQ-9 score
10 - 14 GAD-7 score
10 - 14 Edinburgh
Postnatal
Depression score ≥10 |
1) Outpatient treatment generally
appropriate 2) Psychiatric consultation for dx and
treatment 3) Classes and online resources 4) More intense psychotherapy 5) Psychiatric medications usually warranted 6) Medication guidelines as outlined in text 7) More frequent visits. Monitor for
escalation 8) Depending on medication used (see Table 5) involve neonatology prior to delivery |
Severe |
Serious, often critical, symptoms of anxiety, depression, psychosis, and/or obsessions. Often debilitating and hazardous to self
and others—risk of suicide and/or harm to others. Possible psychosis, such as delusions,
hallucinations, paranoia, grandiosity,
disorganized thinking/behavior, extreme
withdrawal, diminished emotional
expression. Possible extreme mood alteration, such as mania, guilt, worthlessness, hopelessness or suicidal ideation. Symptoms intense/distressing to self &
others. Inability to care for self or function in
usual roles. |
PHQ-9 score
15 - 27 GAD-7 score
15 - 21 Edinburgh
Postnatal
Depression score
≥13 Rapid Mood Screener score “yes” to 4 or more items |
1) Psychiatric referral for dx and
management 2) Inpatient treatment is usually necessary to assure safety 3) Rigorous treatment regimens commonly required, such as vigorous medication
protocols, ECT and supervised visits 4) Consider prophylactic treatment for
high-risk patients who have had previous
episodes 5) Involve neonatology prior to delivery |
ECT, electroconvulsive treatment; hx, history; dx, diagnosis.
Severity confirmation is available through simple self-administered patient rating scales. While there are numerous well-studied depression and anxiety rating scales, we recommend the Patient Health Questionnaire-9 (for depression) (PHQ-9, https://www.apa.org/depression-guideline/patient-health-questionnaire.pdf) and the Generalized Anxiety Disorder-7 (for anxiety) (GAD-7) https://patient.info/doctor/generalised-anxiety-disorder-assessment-gad-7. A single page containing both questionnaires is given in Table 2. The PHQ-9 is a nine-item questionnaire that commonly takes the patient less than two minutes to complete. It surveys depressive symptoms and is scored 0 to 27. Mild depression is indicated by scores of 5 – 9 [8] [10]. Generalized anxiety refers to a state of worry about life events and activities. The GAD-7 is a seven-item questionnaire assessing anxiety and is scored 0 to 21. Mild anxiety is indicated by scores of 5 – 9 [11] [12]. Questions on both the PHQ-9 and GAD-7 are followed by a query into the degree (‘not at all” to “extremely difficult”) to which symptoms are causing impairment in daily life. Functional impairment is a required criterion for a depression/anxiety diagnosis. Both questionnaires are in the public domain and can be freely reproduced and used.
Table 2. Patient health questionnaire and general anxiety disorder (PHQ-9 and GAD-7).
Date ___________ Patient Name ____________________________ Date of Birth _____________ |
Over the last 2 weeks, how often have you been bothered by any of the following problems? Please circle your answers. |
PHQ-9 |
Not at all |
Several days |
More than half the days |
Nearly every day |
1. Little interest or pleasure in doing things |
0 |
1 |
2 |
3 |
2. Feeling down, depressed, or hopeless |
0 |
1 |
2 |
3 |
3. Trouble falling or staying asleep, or sleeping too much |
0 |
1 |
2 |
3 |
4. Feeling tired or having little energy |
0 |
1 |
2 |
3 |
5. Poor appetite or overeating |
0 |
1 |
2 |
3 |
6. Feeling bad about yourself or that you are a failure or have let yourself or others down |
0 |
1 |
2 |
3 |
7. Trouble concentrating on things, such as reading the newspaper or watching television |
0 |
1 |
2 |
3 |
8. Moving or speaking so slowly that other people could have noticed. Or the opposite – being so fidgety or restless that you have been moving around a lot more than usual |
0 |
1 |
2 |
3 |
9. Thoughts that you would be better off dead, or of hurting yourself in some way |
0 |
1 |
2 |
3 |
Add the score for each column |
|
|
|
|
Total score (add your column scores): ___________ |
If you checked off any problems, how difficult have these made it for you to do your work, take care of things at home, or get along with other people? (Circle one) 1) Not difficult at all; 2) Somewhat difficult; 3) Very difficult; 4) Extremely difficult |
Over the last 2 weeks, how often have you been bothered by any of the following problems? Please circle your answers. |
GAD-7 |
Not at all sure |
Several days |
Over half the days |
Nearly every day |
1. Feeling nervous, anxious, or on edge |
0 |
1 |
2 |
3 |
2. Not being able to stop or control worrying |
0 |
1 |
2 |
3 |
3. Worrying too much about different things |
0 |
1 |
2 |
3 |
4. Trouble relaxing |
0 |
1 |
2 |
3 |
5. Being so restless that it’s hard to sit still |
0 |
1 |
2 |
3 |
6. Becoming easily annoyed or irritable |
0 |
1 |
2 |
3 |
7. Feeling afraid as if something awful might happen |
0 |
1 |
2 |
3 |
Add the score for each column |
|
|
|
|
Total Score (add your column scores): ______________ |
If you checked off any problems, how difficult have these made it for you to do your work, take care of things at home, or get along with other people? (Circle one) 1) Not difficult at all; 2) Somewhat difficult; 3) Very difficult; 4) Extremely difficult |
Additional assistance can often be found in local resources, such as “Utah’s Maternal Mental Health Toolkit” available at https://mihp.utah.gov/mmhtoolkit. We recommend using rating scales and other assessments for mental health at least once antenatally, more frequently if indicated, and at least once at a post-partum office visit.
Moderate depression/anxiety is a significant escalation in symptom severity causing impairment in work, home, marriage, and/or social functioning (Table 1, second panel). Such individuals may be able to function in their daily lives, though their ability to do so is compromised. At this stage, the patient may find it more challenging to control fears, worries, and low moods, leading to sleep disturbance, appetite changes, difficulty concentrating, and social withdrawal. Severity is moderate when the number and intensity of symptoms and functional impairment fall between mild and severe. Such patients should be screened for suicide potential, psychotic symptoms, manic/hypomanic symptoms (“mood swings”), and substance use. If any of these are present the condition should be rated as “Severe”.
Rating scale scores in the 10 – 14 range on both the PHQ-9 and GAD-7 are consistent with illness of moderate severity [10] [11]. Question 9 on the PHQ-9 is a single question on suicidal thoughts, but not suicidal behaviors or impulses. Anyone who answers question 9 affirmatively requires further assessment of their suicidality.
Severe psychiatric symptoms in pregnancy and postpartum constitute the most debilitating and hazardous [8] [14] (Table 1, third panel). “Severe” is characterized by symptoms that are numerous, intense, cause significant distress, and are debilitating with significant impairment. Severe psychiatric symptoms include suicidal, homicidal, and/or infanticidal thoughts/intent, psychosis, mania, and immobilizing obsessions. Such patients may need hospitalization, rigorous medication regimens, and sometimes electroconvulsive therapy (ECT). Symptoms may include extreme guilt, worthlessness, hopelessness, intense anxiety, manic or hypomanic mood elevation, delusions, hallucinations, and fears of or urges toward harming the newborn or family. Unlike the “post-partum blues”, which affect the majority of women and are mild and transient, post-partum depression occurs in 10% - 15% of women following childbirth and up to 40% of those with a past history of major depressive disorder [14]. Risk factors include depression/anxiety during the pregnancy, bipolar disorder, and a history of recurrent major depression, post-partum depression, or post-partum psychosis [14].
If a woman has previously experienced post-partum psychosis, it is likely to recur after subsequent pregnancies [14] [15] and deserves close observation and prophylactic treatment. This is among the most threatening of all post-partum psychiatric conditions [16], occurring in 0.9-2.6 per 1000 deliveries [15] with onset usually within 1-2 weeks of delivery and bearing a high risk of harm to self and others [15]-[17]. One of the authors (DDC) managed a 39-year-old post-partum woman through a six-month psychiatric hospitalization after she poured gasoline on, and set fire to, herself and her sleeping children to “save them from the devil”. Even in those with less tragic outcomes, maternal depression and dysfunction has been shown to affect child development negatively [18] [19]. Those with post-partum obsessive states have recurrent fears of harming their newborn, but the risk of actual harm is low [20]-[22].
Rating Scales. PHQ-9 scores 15 – 27 indicate severe depression, and GAD-7 scores of 15 – 21 indicate severe anxiety. The Edinburgh Postnatal Depression Scale was developed to screen for post-partum depression https://med.stanford.edu/content/dam/sm/ppc/documents/DBP/EDPS_text_added.pdf. It is a ten-item questionnaire scored from 0 to 30 where scores of 10 or more indicate “at risk” for post-partum depression, and scores of 13 or greater indicate “high risk”. An anxiety subscale, composed of items 3, 4, and 5, suggests “further exploration of post-partum anxiety” if the sum of these items is six or greater. The Rapid Mood Screener (RMS)
https://rapidmoodscreener.com is designed to detect bipolar disorder. Roughly 70% of bipolar patients are initially misdiagnosed with major depressive disorder, commonly leading to inappropriate treatment and a mean delay to correct diagnosis of 5 – 10 years [23]. A “positive” screen (“Yes” to 4 or more of 6 items) should be followed by a comprehensive evaluation by one experienced in bipolar disorder [24].
3. Treatment Guidelines Based on Illness Severity
We recommend that, whenever possible, a pre-pregnancy counseling session be scheduled for a woman currently taking psychotropic medications and planning to become pregnant. Each medication can be discussed with the obstetrician and/or, psychiatrist, to reevaluate the medications and dosages safest to use during pregnancy and postpartum.
Mild psychiatric conditions can be approached with interventions of lesser intensity and lower risk. Avoidance of psychotropic medication is desirable during the first trimester and advice should be given against the use of recreational drugs and alcohol. Remedies that center on reassurance and support are often helpful and sufficient, such as obtaining help with childcare and home duties, reducing employment hours, regular exercise, sufficient sleep, maintaining a varied and nutritious diet, increased engagement in rewarding activities, and seeking out the positive support of friends and family. Referral for counseling/psychotherapy may contribute to alleviating stress and fostering symptomatic improvement. Numerous online resources are available, such as groups, classes, and individual therapy (https://heidimcbain.com/pregnancy-mental-wellness-course, https://www.tinyhood.com/category/expecting?, https://www.betterhelp.com).
Increased frequency of prenatal visits contributes to reassurance and careful monitoring. Vigilant follow-up with recruitment of a spouse or partner to monitor and report is always desirable. Though these supportive interventions are often sufficient to alleviate mild distress and prevent its escalation, conservative psychotropic medication may be considered but is usually not necessary and may not be worth the associated risks in the first trimester.
Psychiatric conditions of moderate severity may also benefit from the above interventions. At this stage of severity, we recommend a referral for psychiatric consultation to establish a precise psychiatric diagnosis and recommend a treatment plan. Many, if not most, at this stage, will remain in the primary care of the obstetrician with any further outpatient psychiatric visits at the discretion of the psychiatrist-obstetrician alliance. Psychiatric medications, more frequent visits, and more intensive psychotherapy are common requirements for managing a moderately severe condition. A checklist such as the one given in (Table 3) is helpful when prescribing a psychotropic medication during pregnancy.
Table 3. Checklist to use when considering psychotropic medications during pregnancy and the postpartum period.
1 |
Hold a risk discussion with both patient and partner to secure a collaborative alliance, understand
risk-benefit issues under consideration, and obtain informed consent for medications and/or procedures where needed. |
|
2 |
Optimize non-medication options. Even if medication is prescribed, non-medication options can help
minimize the number of medications, facilitate lower drug doses and enhance the overall effectiveness of treatment. |
|
3 |
The risk of not using psychotropic medications should outweigh the risk of using them. Untreated or
undertreated psychiatric conditions pose risks to both mother and child. |
|
4 |
Avoid psychiatric medications in the first trimester and polypharmacy whenever possible. |
|
5 |
Avoid valproic acid, carbamazepine, benzodiazepines, and lithium. |
|
6 |
Use the lowest effective doses but do not undertreat. |
|
7 |
If medication is required, favor those with long track-records and the most available safety data. |
|
8 |
Once a psychotropic medication plan has been devised, establish clear and ongoing communication
between obstetrician, pediatrician/neonatologist, and psychiatrist. |
|
Online education and information sites are beneficial such as the National Alliance on Mental Illness (NAMI) webpage on Mental Health During Pregnancy (http://www.nami.org), Post-Partum Support International, https://www.postpartum.net and the MGH Center for Women’s Mental Health, http://www.womensmentalhealth.org.
Severe psychiatric symptoms during the pregnancy and postpartum period are perilous and often incapacitating. Close supervision, such as hospitalization, is usually required to ensure safety, well-being, and self-care. Psychiatric referral is warranted, with the psychiatrist assuming responsibility for the psychiatric diagnosis and treatment. Hospital protocols commonly encompass intensive and exacting endeavors such as risk/lethality assessments, suicide precautions, supervision of visits, intensive medication regimens, and possibly ECT. Such severe symptoms may occur pre- or post-partum and frequently center on depression, anxiety, psychosis, and/or mania. The most reliable predictor of a severe pre-or post-partum condition is a past or family history of the disorder. Be alert to ancillary symptoms such as insomnia, anxiety, panic attacks, and impaired functioning progressing to more overt major depression. Post-partum depression is generally defined as beginning within 4 weeks of delivery [15] [18] though initial depressive symptoms may begin in the final weeks of pregnancy. Recognition of a patient at high risk of perinatal psychiatric illness should prompt a discussion of prophylactic medication throughout the pregnancy and post-natal period, preferably beginning after the first trimester. If one has a history of bipolar disorder and their mood stabilizer has been discontinued, there is a particularly high rate of recurrence (71%) in the perinatal period [24].
4. Neonatal Complications of Antipsychotic/Antidepressant Use during Pregnancy
Large studies conclude that antipsychotic medications are associated with risk to the fetus and neonate (Table 4) [25]-[35]. For instance, a recent 14-year Finnish study of over 36,000 women, concluded that; 1) the use of antipsychotic medications during pregnancy increased from 2002 to 2016, and 2) infants born to these patients were statistically more likely to need NICU admission and a hospital stay over five days (OR 1.54; 95% CI 1.10 – 2.15) [21]. Similarly, a cross-sectional study of delivery records in Los Angeles published in 2020 found that maternal mental illness was independently associated with adverse fetal and neonatal outcomes (OR 1.12; 95% CI 1.09 – 1.14) [22].
Table 4. Psychotherapeutics and associations with fetal/neonatal disorders.
Medication |
Indication |
Associations with Fetal/Neonatal Disorders |
Reference |
Brexanolone |
Post-partum
depression |
Little data on use in pregnant women to determine
drug-induced risks of major birth defects or adverse fetal
outcomes. Animal reproductive studies identified serious
adverse outcomes. |
[26] |
Zuranolone |
Post-partum
depression |
Advise pregnant women of the potential risk to a fetus.
Available data on use in pregnant women are insufficient to evaluate for a drug-associated risk of major birth defects,
miscarriage, or adverse fetal outcomes. |
[27] |
Benzodiazepines |
Anxiety, insomnia, panic disorders |
Withdrawal symptoms, hypotonia, seizures. Best to avoid during pregnancy, if possible. |
[28] |
Lithium |
Bipolar and major
depressive disorder |
Avoid during pregnancy. Risk of spontaneous preterm birth (8.7% vs 3.0%, RR 2.80 (95% CI 2.02, 3.88)) higher incidence of neonates with cardiac malformations (2.1% vs 0.8% RR 3.17 (95% CI 1.64, 6.13) the majority (66.6%) are malformations of the cardiac septa. |
[29] |
Paroxetine |
Major depressive
disorder, panic
disorder, anxiety with or without depression |
Favor other SSRTs when possible. Risk of cardiac
malformation. Withdrawal; jitteriness, increased tone, irritability, tremors, trouble eating, trouble breathing. |
[30] [31] |
Valproate |
Bipolar disorder |
Avoid during pregnancy. Fetal valproate syndrome caused by exposure during the first trimester. Neural tube defects such as spina bifida, distinctive facial features, congenital heart defects and other musculoskeletal abnormalities. |
[32] |
Carbamazepine |
Mania with bipolar disorder |
Avoid during pregnancy. Increased NICU admission
(especially for respiratory care). Adverse effects on infant
neurodevelopment, poor cognitive and language development and negative behavioral traits. |
[33] |
Lamotrigine |
Bipolar disorder |
Appears to be the safest mood stabilizer to use during
pregnancy. Not found to be statistically associated with
neurodevelopmental disorders as a whole, language disorders or delay, diagnosis or risk of ASD and diagnosis or risk of
ADHD. |
[34] |
SSRIs |
Depression |
Generally accepted as safe during pregnancy. Withdrawal;
jitteriness, increased tone, irritability, tremors, trouble eating, trouble breathing. |
[25] [30] [31] |
ECT |
Severe treatment-
resistant depression, severe mania |
Uterine contractions are the most common (low-grade)
complication, fetal heart rate abnormalities (transient) in a few cases. No proven significant fetal or neonatal effects. |
[35] |
Antipsychotic use early in pregnancy is associated with a higher risk of adverse outcomes to infants than if used only later in pregnancy. Lin et al. [36], in a seven-year study from Taiwan region, found a higher risk of preterm birth (1.29; 95% CI 1.04 – 1.6) and concluded that when women need antipsychotics early in pregnancy, they should be monitored carefully for preterm birth and low infant birth weight. Whether antipsychotic use in pregnancy is a risk factor for gestational diabetes is debated. A 12-year Swedish national registry controlled for maternal factors including body mass index, and concluded that the risk was indeed elevated, with exposed infants at risk for being large for gestational age (1.6; 1.3 - 1.9) [9].
Regarding the neonatal effects of schizophrenia and its treatment during pregnancy, Kulkarni et al. from Australia reported a case-control study focused on women taking clozapine and reported a statistically significant risk of miscarriages, maternal gestational diabetes, and lower birth weight [37].
Antidepressant use during pregnancy is common [25]. Guidelines for using antidepressants in pregnancy have been issued by at least six advocate societies (Table 5). Four of the six specifically advise using pharmacologic treatment for “new onset” depression during pregnancy [38]-[43]. One (German) advises to “continue” antidepressants during pregnancy [44]. The most commonly prescribed antidepressants during pregnancy are selective serotonin reuptake inhibitors (SSRIs) or serotonin-norepinephrine reuptake inhibitors (SNRIs) [25]. Subtle adverse effects were reported in a meta-analysis of 11 studies, by Lattimore et al. [25]. They concluded that neonates exposed to SSRIs in utero are somewhat more likely to have low birth weight and to be admitted to a NICU. In one meta-analysis, paroxetine use during the first trimester was associated with a 1.28-fold increased risk of cardiac malformations (in the cardiac septum, bulbus cordis, and right ventricular outflow tract) [31]. Nevertheless, SSRIs and SNRIs are among the best-studied antidepressants in pregnancy and are considered to be the safest. We suggest involving the neonatology service to evaluate whether delivery should occur in a facility that has a NICU.
Table 5. Guidelines for managing depression during pregnancy. (Modified from Eleftheriou et al. Int J Environ Res Public Health. 2023 [38]).
Advocate Society |
Year |
Country |
Recommendations |
Reference |
Dutch Society Ob Gyn |
2012 |
Netherlands |
No clear advice to continue
antidepressants in pregnancy |
[40] |
National Institute for Health & Care Excellence |
2014 |
UK |
Advise psychotherapy and
pharmacologic treatment for
new-onset depression |
[41] |
Royal Australian and New Zealand College of Psychiatrists |
2015 |
Australia & New Zealand |
Advise psychotherapy for new-onset depression |
[42] |
Canadian Network for Mood &
Anxiety Treatments |
2016 |
Canada |
Advise psychotherapy and
pharmacologic treatment for
new-onset depression |
[43] |
German Society for Psychiatry and Psychotherapy, Psychosomatics and Neurology |
2017 |
Germany |
Advise to continue antidepressants in pregnancy |
[44] |
American College Ob-Gyn |
2023 |
USA |
Advise pharmacologic treatment for new-onset depression |
[39] |
5. Conclusion
Psychiatric disorders are common during pregnancy and the postpartum period. If unrecognized and untreated, these can lead to symptom escalation, patient and family dysfunction, and in the most severe instances, suicide, homicide, or infanticide. We propose an approach where the obstetrician can assess psychiatric problems based on symptom severity, aided by simple patient self-assessment questionnaires. We propose guidelines to inform the treatment of mild psychiatric conditions by the obstetrician, for more severe psychiatric disorders to trigger a referral to mental health specialists, and to involve a neonatologist as a team member when the maternal condition or therapeutics may increase the risk of NICU admission (Table 6). This approach can simplify patient assessment by the obstetrician, help direct decision-making, and facilitate appropriate treatment.
Table 6. Representation of how assigning a symptom severity of “mild, moderate, or severe” might influence the management and therapy of an obstetrical patient who has a psychiatric disorder.
Symptom Severity |
Management |
Therapeutic Strategy |
Mild |
OBSTETRICIAN |
Counseling, education, support, monitoring closely, online resources |
Moderate |
OBSTETRICIAN with PSYCHIATRIC consultation |
All of the above plus: Psychiatric medications, psychotherapy (NEONATOLOGY involvement depending on the psychotropic medications used) |
Severe |
PSYCHIATRIC inpatient. When no longer severe, outpatient management by OBSTETRICIAN with
PSYCHIATRIST co-management |
All of the above plus: Assure safety of patient and family. NEONATOLOGY involvement prior to delivery (See Table 1 and Table 4) |