PUBLICATION #2 — Women’s mental health
Trajectories of Depressive and Anxiety Symptoms Across Pregnancy and Postpartum in Selective Serotonin Reuptake Inhibitor‐Treated Women.
Gabrielle A. Mesches, M.S., Jody D. Ciolino, Ph.D., Catherine S. Stika, M.D., Dorothy K. Sit, M.D., Katelyn Zumpf, M.S., Sheehan Fisher, Ph.D., Crystal T. Clark, M.D., M.Sc., Alfred L. George Jr.,, M.D., Michael J. Avram, Ph.D., Laura J. Rasmussen‐Torvik, Ph.D., M.P.H., Daniel L. Erickson, M.B.A., Steven Caritis, M.D., Dawn Fischer, B.S.N., Raman Venkataramanan, Ph.D., Maged Costantine, M.D., Holly West, D.H.Ed., P.A.‐C., Elizabeth Welch, RN., Shannon Clark, M.D., M.M.S., Katherine L. Wisner, M.D., M.S., Jacqueline K. Gollan, Ph.D.
Objective:
Tracking perinatal mood and anxiety disorders is championed by the American Psychiatric Association and the International Marcé Society for Perinatal Mental Health. We conducted this study to examine trajectories of monthly depressive and anxiety symptoms through pregnancy and postpartum.
Methods:
This is a prospective longitudinal observational cohort study of pregnant women interviewed at baseline (≤18th gestational week), every four weeks through delivery and at 6 and 14 weeks postpartum at three urban academic medical centers (N = 85) and a single rural health center (N = 3) from 2016 to 2020. Pregnant women had at least one prior episode of major depressive disorder, were not in a current episode, and were treated with sertraline, fluoxetine, citalopram, or escitalopram. Of 192 women screened, 88 (46%) women enrolled, and 77 (88%) women completed the postpartum follow‐up. Symptom trajectories were generated with scores from the Edinburgh Postnatal Depression Scale, the Quick Inventory of Depressive Symptoms, the Generalized Anxiety Disorder Scale, 7‐item, and the Patient‐Reported Outcomes Measurement Information System Global Health measure. A semi‐parametric, group‐based mixture model (trajectory analysis) was applied.
Results:
Three relatively stable depression trajectories emerged, described as Minimal, Mild, and Subthreshold, in each group across pregnancy. Two of the four anxiety trajectories were stable, including Asymptomatic and Minimal, while the third, termed Breakthrough, was ascending with increasing symptoms and the fourth trajectory, described as Mild, had descending symptoms.
Conclusions:
Screening for anxiety with depression for pregnant women will yield a comprehensive view of psychiatric symptoms and treatment targets in perinatal women.
Annotation
The finding:
This is a prospective longitudinal observational cohort study—Optimizing Medication Management for Mothers with Depression (OPTI‐MOM)—of 88 pregnant women. Questions addressed through the study were, What is the symptom course of SSRI‐treated women across childbearing? Do depressive and anxiety symptoms vary together? Do symptoms increase after birth? Women completed assessments every 4 weeks from study entry until delivery and until 6-14 weeks postpartum.Inclusion criteria were -18 to 45 years of age, singleton pregnancy less than 18 weeks, a lifetime DSM‐IV diagnosis of MDD (any subtype), and current treatment with sertraline, fluoxetine, citalopram, or escitalopram with the intent to continue through pregnancy and postpartum. Exclusions were defined as bipolar or psychotic illness, ongoing substance use, Edinburgh postnatal depression scale (EDPS) >25 and response of 3 on self-harm thoughts question on EPDS. The scales used were the EPDS, Quick Inventory of Depressive Symptoms (QIDS), Generalized Anxiety Disorder Scale, (GAD‐7) and Patient‐Reported Outcomes Measurement Information System Global Health (PROMIS‐GH). Upon study entry, most participants were not in remission despite maintenance drug treatment. Three relatively stable depression trajectories emerged: Minimal (EPDS<5), Mild (EPDS=5), and Subthreshold (EPDS 8 or higher). Anxiety varied across 4 trajectories; 2 of the 4 anxiety trajectories were stable, including Asymptomatic and Minimal, while the third, termed Breakthrough, was ascending with increasing symptoms. A fourth anxiety trajectory, described as Mild, had descending symptoms.
Strength and weaknesses:
This study’s strengths included obtaining novel data from monthly self‐report symptom assessments through pregnancy and after birth in women who were treated with an SSRI at enrollment. The sample was limited: all were SSRI‐treated women and predominantly white, married, and educated women. Secondly, because only SSRI-treated women were included, symptom trajectories for women treated with other classes of antidepressants were not described.
Relevance:
This study demonstrates that the treatment goal to achieve full resolution of maternal depression and anxiety symptoms remains a clinical challenge despite maintenance pharmacological treatment. In the setting of incomplete treatment, the fetus remains exposed to both the illness and the drug. The majority of women also had coexisting anxiety symptoms, which underscores the importance of screening for and treating anxiety in this population. These findings also encourage psychiatrists to implement measures of anxiety and depression throughout the perinatal period to monitor for residual symptoms.