Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2019 Oct 1.
Published in final edited form as: Arch Womens Ment Health. 2018 Mar 13;21(5):543–551. doi: 10.1007/s00737-018-0825-2

How Obstetric Settings Can Help Address Gaps in Psychiatric Care for Pregnant and Postpartum Women with Bipolar Disorder

Nancy Byatt 1, Lucille Cox 1, Tiffany A Moore Simas 1, Nisha Kini, Kathleen Biebel 1, Padma Sankaran 1, Holly A Swartz 2, Linda Weinreb 1
PMCID: PMC6126942  NIHMSID: NIHMS950878  PMID: 29536256

Abstract

Purpose

To elucidate: 1) the challenges associated with under-recognition of bipolar disorder in obstetric settings; 2) barriers pregnant and postpartum women with bipolar disorder face when trying to access psychiatric care; and, 3) how obstetric settings can identify of such women and connect them with mental health services.

Methods

Structured, in-depth interviews were conducted with 25 pregnant and postpartum women recruited from obstetric practices who scored ≥ 10 on the Edinburgh Postnatal Depression Scale and met DSM-IV criteria for bipolar disorder I, II or not otherwise specified using the Mini International Neuropsychiatric Interview. Quantitative analyses included descriptive statistics. Interviews were transcribed, and resulting data were analyzed using a grounded theory approach.

Results

Most participants (n=19, 79.17%) did not have a clinical diagnosis of bipolar disorder documented in their medical records nor had received referral for treatment during pregnancy (n=15, 60%). Of participants receiving pharmacotherapy (n=14, 58.33%), most were treated with an antidepressant alone (n=10, 71.42%). Most medication was prescribed by an obstetric (n=4, 28.57%) or primary care provider (n=7, 50%). Qualitative interviews indicated that participants want their obstetric practices to proactively screen for, discuss, and help them obtain mental health treatment.

Conclusions

Women face challenges in securing mental health treatment appropriate to their bipolar illness. Obstetric providers provide the bulk of medical care for these women and need supports in place to: 1) better recognize bipolar disorder 2) avoid inappropriate prescribing practices for women with undiagnosed bipolar disorder; and, 3) ensure women are referred to specialized treatment when needed.

Keywords: Bipolar disorder, Perinatal, Pregnancy, Postpartum, Obstetric, Treatment

INTRODUCTION

Bipolar disorder affects 3% of the general population and 23% of perinatal (pregnant or within a year of giving birth) women who screen positive for perinatal depression (Wisner et al., 2013). Bipolar disorder has deleterious effects on birth and child outcomes (Rusner, Berg, & Begley, 2016) and is associated with self-injury, substance use (Geddes, 1999), disruption of mother-child bonding (Geddes, 1999), suicide, and infanticide (Lindahl, Pearson, & Colpe, 2005; Spinelli, 2004). The perinatal period is the time of highest risk for first onset or recurrence of bipolar disorder episodes (Kendell, Chalmers, & Platz, 1987; Munk-Olsen, Laursen, Pedersen, Mors, & Mortensen, 2006). Bipolar disorder is the most potent, best-established risk factor for postpartum psychosis (Jones & Craddock, 2001). Treatment access and adequacy during the perinatal time period is a critical issue because discontinuation of pharmacotherapy increases risk for illness relapse (Jones, Chandra, Dazzan, & Howard, 2014). Despite the negative impact of untreated illness and availability of effective evidence-based treatments, bipolar disorder is currently under-detected, not addressed effectively, or exacerbated through inappropriate treatment (Byatt et al., 2012; Byatt et al., 2017; Weinreb, Byatt, Moore Simas, Tenner, & Savageau, 2014).

Professional societies and policymakers that recommend screening for perinatal depression note that it must be accompanied by plans to ensure accurate diagnosis and appropriate treatment. This cannot be accomplished without screening, referral, and treatment of bipolar disorder (Wisner et al., 2013). In 2015, the American College of Obstetricians and Gynecologists (American College of Obstetricians and Gynecologists Committee on Obstetric Practice, 2015), the US Preventive Services Task Force (Siu et al., 2016), and the Center for Medicaid Services (Wachino & Center for Medicaid and CHIP Services, 2016 ) began recommending depression screening for all perinatal women. In response, obstetric practices are beginning to identify depression and provide treatment. While this is a major step forward, it poses new challenges. Because major depressive disorder is phenotypically identical to bipolar disorder when individuals are depressed, depression screening procedures that do not specifically assess for bipolar disorder do not distinguish between these illnesses. As depression screening becomes routine, resultant failure to identify and treat occult bipolar disorder in perinatal women constitutes an emerging and unmet health care need.

To develop approaches for identifying and treating bipolar disorder during the perinatal time-period that are acceptable to patients and providers, we need to better understand their perspectives regarding what would hinder, help, and be feasible. Obstetric providers are at the front line serving pregnant and postpartum women with bipolar disorder and may be able to play a critical role in helping them access appropriate mental health care. The purpose of the study is to elucidate in a sample of perinatal women with bipolar disorder: 1) the challenges associated with under-recognition of bipolar disorder in obstetric settings; 2) what barriers they face when trying to access psychiatric care; and, 3) their perspectives regarding how obstetric practices can facilitate the identification of bipolar disorder in this population and connect women with mental health care.

METHODS

A descriptive exploratory study was conducted with a convenience sample of English- speaking pregnant or postpartum women aged 18–55 recruited from November 2014 – July 2016. Women were recruited during pregnancy and up to 24 months after birth from five obstetric practices associated with a large tertiary care center. The study was approved by University of Massachusetts Institutional Review Board.

Each practice’s depression screening protocol included administering the Edinburgh Postnatal Depression Scale (EPDS) (Cox, Holden, & Sagovsky, 1987) at 12–14 and/or 26–28 weeks gestational age and 6 weeks postpartum. Each practice informed patients of the study during depression screening and gave patients the opportunity to opt out of being contacted by a Research Coordinator. Patients that did not opt out and were deemed eligible based on prescreening were contacted by telephone and screened for eligibility using the 3-question Composite International Diagnostic Interview Based Bipolar Disorder (CIDI) Screening (Kessler et al., 2006). If the CIDI screen was positive, patients were invited to meet in-person and written informed consent was obtained from eligible patients. Women were eligible if they: 1) had an EPDS ≥ 10 when screened by the practice; 2) were 18–55 years old; 3) were English-speaking; 4) were pregnant or < 24 months postpartum; and, 5) met criteria for bipolar illness as determined by the Mini International Neuropsychiatric Interview at the time of the interview (M.I.N.I.) (Sheehan et al., 1998). The minimum cut-off on the EPDS used to indicate possible depression ranges from 9–13 in relevant literature. Consistent with recommendations by Gibson et al. (Gibson, McKenzie-McHarg, Shakespeare, Price, & Gray, 2009) and many studies in the peer reviewed literature (Burton et al., 2011; Chaudron et al., 2005; Chen et al., 2011; Flynn, O’Mahen, Massey, & Marcus, 2006; Glavin, Smith, & Sorum, 2009; Glavin, Smith, Sorum, & Ellefsen, 2010; Goodman & Tyer-Viola, 2010), we used a cut-off of 10 to ensure that we captured most or all women with scores requiring further assessment. Women who completed the study received a $15 gift card.

Participants also completed the Barriers to Access to Care Evaluation (BACE). The BACE is a 30 item self-administered tool, with demonstrated reliability, validity, and acceptability (Sarah Clement et al., 2012), that assesses barriers to accessing mental health care, including a ‘treatment stigma’ subscale (S. Clement et al., 2012). BACE scores range from 0 to 3 with higher scores indicating more barriers or stigma. The EPDS (Cox et al., 1987) is a validated, self-administered 10-item screening questionnaire for which the scores range from 0–30, with higher scores reflecting greater symptom severity (Cox et al., 1987). The structured interview obtained demographics and factors associated with mental health treatment participation. After excluding one participant due to the medical record being unavailable, pharmacotherapy during pregnancy and within one year postpartum was abstracted from the medical record for 24 participants.

Twenty-minute in-depth interviews in which participants responded to study probes regarding the barriers and facilitators to mental health treatment were also conducted. Recordings were cleaned of any identifying data, transcribed, and checked for accuracy. Transcripts were uploaded into Dedoose (“Dedoose,” 2012), a web-based software program that facilitates mixed methods data management for further coding, elaboration and specification of concepts and relationships. Interview content was organized theoretically, using a modified grounded theory approach with a phenomenological emphasis (Morgan, 1988). Using methods described by Miles & Huberman (Miles, 1994), categorizing began with an initial set of preliminary codes for themes suggested from the literature, research aims and previous work. Codes were added as they emerged from the data until saturation was achieved, and initial transcript sections were re-categorized using the reformulated codes. Each transcript was coded by two researchers, who achieved at least a 90% agreement rate in independent coding. Dedoose allows for the assembling of coded segments into selected configurations that facilitates identification of recurring patterns/clusters.

Mean and standard deviation was calculated for continuous variables and percentages for categorical variables. Mean BACE scores were calculated for 3 subscales (stigma, instrumental barrier, and attitudinal barrier) and total score. Reliability of the BACE was measured using Cronbach’s alpha for the BACE total scale (0.91), BACE stigma sub-scale (0.91), BACE instrumental barriers scale (0.77), and BACE attitudinal barriers scale (0.82). Reliability for the EPDS was (0.86).

RESULTS

The population studied represented a diverse sample (Table 1). Based on the M.I.N.I, all participants met diagnostic criteria for bipolar illness and most had comorbid illnesses (Table 2). The total BACE score and stigma, instrumental barriers and attitudinal barriers and access to care subscales were low. While the majority had received a mental health diagnosis (n=21, 84.0%) or psychiatric treatment (n=21, 84.0%) in their lifetime, only seven (28.0%) were referred for treatment during pregnancy and only six (20.83%) had a clinical diagnosis of bipolar disorder documented in their medical record (Table 3). Of those who were prescribed medication (n=14, 58.33%), most were treated with an antidepressant alone (n=10, 71.42%), a management approach that is not consistent with current treatment guidelines for bipolar disorder (Bipolar disorders in adults: NICE Guideline, 2015).

Table 1.

Description of study participants (N=25) demographics

Variable Mean Std Dev
Age 30.96 5.84
Postpartum weeks (N=13) 36.23 25.71
Weeks pregnant (N=12) 21.75 6.78
Number of pregnancies (Median, IQR) 3 1.5–5
Number of births (Median, IQR) 2 1–3

N %

Race
 Black or African-American 2 8.0
 White 16 64.0
 Other/ Unknown 7 28.0
Hispanic/ Latina 9 36.0
Pregnant 12 48.0
Living with partner 19 76.0
Health insurance
 Medicaid or Medicare 12 48.0
 Private health insurance 11 44.0
 Combination 2 8.0
Household Income
 Less than $15000 4 16.0
 $15000 – $30000 7 28.0
 $30000 – $60000 4 16.0
 More than $60000 7 28.0
 Don’t know 3 12.0
Relationship status
 Married 9 36.0
 Divorced 4 16.0
 Separated 1 4.0
 Never Married 2 8.0
 Not married but in a long-term relationship 8 32.0
 Other 1 4.0
Education
 Less than high school 4 16.0
 High school diploma or GED equivalent 5 20.0
 Some college or technical/trade school 6 24.0
 Associate Degree or higher 10 40.0

Percentages may not add up due to missing values

Std Dev=Standard Deviation

Table 2.

Psychiatric history of study participants based on MINI (N=25)

Variable Mean Std Dev
EPDS Sum Score 15.84 5.90

N %

Bipolar disorder, type I 14 58.33
Bipolar disorder, type II 5 20.83
Bipolar disorder, not otherwise specified 5 20.83
Major depressive episode, current 15 60.0
Manic episode, lifetime 14 56.0
Hypomanic episode, lifetime 15 60.0
Dysthymia, current 1 4.0
Ever made a suicide attempt 13 52.0
Past psychiatric hospitalization 8 32.0
Lifetime panic disorder 13 52.0
Social phobia, current 10 40.0
 Generalized 9 90.0
 Non-generalized 1 10.0
Post-traumatic stress disorder 9 36.0

Percentages may not add up due to missing values

Std Dev=Standard Deviation

Table 3.

Access to mental health treatment and satisfaction study (n=25)

Variable Mean Std Dev
BACE, total score, mean 0.90 0.57
BACE, stigma score, mean 0.97 0.75
BACE, instrumental barrier, mean 0.73 0.62
BACE, attitudinal barrier, mean 0.94 0.65

n %

Seen a psychiatrist 7 28.00
Medication provider during pregnancy or postpartum
 Primary care provider 3 27.27
 Obstetric provider 2 18.18
 Mental Health provider 6 54.55
Received a mental health diagnosis from a provider during lifetime 21 84.00
 Depression 18 72.00
 Bipolar 7 28.00
Received any treatment for depression / mania / psychosis during lifetime
 Yes 21 84.00
 Medication 2 9.09
 Counseling 2 9.09
 Both 18 81.82
Talked to provider about treatment during pregnancy 10 40.00
Referred for treatment during pregnancy 7 28.00
Currently receiving psychotherapy 9 37.50
Currently receiving pharmacotherapy 7 28.00
The risks, benefits and alternatives to psychiatric medication treatment in pregnancy were discussed
 Strongly disagree 1 4.17
 Disagree 8 33.33
 Agree 7 29.17
 Strongly Agree 8 33.33
The risks, benefits and alternatives to psychiatric medication treatment during breastfeeding were discussed
 Strongly disagree 2 8.00
 Disagree 5 20.00
 Agree 6 24.00
 Strongly Agree 6 24.00
 N/A (because still pregnant) 6 24.00
Did not receive help for emotional / mental health 3 months prior to pregnancy 10 40.00
Among those who saw a doctor (n=16)
Satisfaction level with treatment and services from health care provider prior to becoming pregnant
 Satisfied 10 62.50
 Neither satisfied or dissatisfied 1 6.25
 Very dissatisfied 3 18.75
Help received from healthcare provider
 A lot 4 25.00
 Some 7 43.75
 A little 2 12.50
 Not at all 2 12.50
 Don’t know/remember 1 6.25
 Prescribed medication during pregnancy or postpartum period 14 58.33
  Medication prescribed by obstetric provider 11 78.57
  Medication prescribed by primary care provider 7 50.0
  Medication prescribed by psychiatric provider 2 14.29
No diagnosis of bipolar disorder documented in medical record 19 79.17
Treated with antidepressant alone 10 41.67
Treated with antidepressant medication in conjunction with a mood stabilizer or antipsychotic medication 3 12.50
Treated with a mood stabilizer alone 1 4.17
Prescribed a benzodiazepine 5 20.83
Prescribed a non-benzodiazepine sedative-hypnotic 1 4.17
Discontinued medication during pregnancy 6 25.0

Qualitative Data

Participant interviews revealed themes that reflect barriers and facilitators to their obstetric providers addressing mental health during perinatal period. While all participants had a diagnosis of bipolar disorder based on the M.I.N.I., most were unaware of their diagnosis and thus focused on concerns about depression rather than bipolar disorder.

Patient-level Barriers

Self-blame, stigma, fear, and lack of support prevent women from seeking help

Participants felt embarrassed that they were experiencing psychiatric symptoms due to a perception that women should not need emotional support during pregnancy or the postpartum period. They reported being scared to reach out for help due to fear of being judged.

“I don’t think that it was that no one was there… it was more of me being scared of reaching out to people and letting them know that I don’t have the perfect family. I think it was that fear.”

Lack of support from their spouse or partner contributed to these fears and made it even more challenging to seek help. Several women reported that their partner discouraged them from seeking help because their partner said they, “don’t need it… and just need to calm down and stop crying.”

Limited time and resources, competing demands, child care responsibilities, and being pregnant made it even harder for women to prioritize and take care of themselves and their mental health so they, “put it on the backburner… because there is no time for me.” Women also blamed themselves and wondered, “why am I feeling like that? Is it because I want attention or am being dramatic?”

Provider-level Barriers

Mood disorders and the risks and benefits of treatment are not discussed or addressed by obstetric providers

Participants perceived lack of discussion of options as a major omission in their prenatal care.

“They didn’t offer much advice or anything about the medication… they just kind of said what medication are you on and put it in the computer, and didn’t really talk to me about it or anything. I would like to hear his opinion, how he feels about the medication… and the depression and all those kinds of things… I didn’t really get that.”

Several participants noted that their provider did not ask questions about or provide information about their mood disorder or the risks and benefits of the psychiatric medications they were taking during pregnancy or breastfeeding. One participant stated, “I do wanna breastfeed, but I get scared because I don’t know… what that [medication] is going to do my child and I don’t want my child to have issues any issues with the medication going through my breast.’”

Lack of follow-through of screening results among providers

Participants felt discouraged when their provider did not pay attention to the answers to the depression screen or did not discuss the results. One participant shared her experience:

“They do the survey… but they don’t discuss [it]… they just give you the survey, “Here fill this out.” There’s no discussion about it…”

Multiple participants felt they filled out the screen and “that was it.” They also noted that other important topics related to their emotional health and overall well-being were not discussed such as “the obvious, are you nauseous, gain weight, lose weight, whatever... it is never really [discussed].”

System-level Barriers

Unable to find providers who treat pregnant women with mood disorders

Participants noted that depression screening had limited utility because they did not know where to go for help. One participant noted:

“I saw that some other women in the group had problems with like waiting times to get into groups or services, which seemed unreasonable. Especially during postpartum when time is very important.”

Barriers to accessing mental health care included participants’ limited knowledge regarding available providers, in addition to encountering unresponsive providers, and long wait times for appointments.

Patient-level Facilitators

Feeling empowered by knowledge about illness and importance of treatment

Women felt empowered when they had information and knowledge about mental health complications during pregnancy and available treatments. They noted that it helped when friends, family members, or partners checked in on them periodically and asked about their mental health or suggested they reach out for help.

“The knowledge of mental health. I think it is probably the biggest thing, knowing, recognizing the signs and symptoms. Just knowing that I needed to seek help before it got worse.”

Openness to discussing their mental health concerns among themselves and other women was greatly valued by many participants and was noted to help them feel better that they “feel the same that I am [feeling].”

Provider-level Facilitators

Obstetric providers detecting and discussing mood disorders and referring women for treatment

Participants suggested obstetric providers encourage women to disclose their concerns about their mental health and let them know where they can go to seek help. Women wanted their obstetric provider to refer them for treatment and be the gateway for more specialized treatment when needed.

“It is more not [being] sure what the first step is... whether you should… call my primary care or do I call my OB and ask him to refer me to someone. Or how do I know [whether] it’s covered by insurance. It’s just not really clear what the steps are in doing that. Maybe if someone talked to me about some the options and I… had some supports as to who to who I go to and what the steps [are] to get the help that I need, that would help.”

Women also wanted their obstetric provider to be more insistent about them getting treatment. Participants suggested that obstetric providers discuss mental health disorders that that can occur before, during and after birth with women and their partners or family. They noted this would help them seek help and act on any concerns that may arise.

System-level Facilitators

Increasing awareness of mood disorders through education and provision of resources

Participants wanted to be informed about the available treatment for mood disorders and how to seek help should they occur. Several noted that, “doctors should have something [to give them] and should talk about it at every visit,” even when there is no psychiatric history. Participants noted how helpful it would be if obstetric providers routinely discussed mental health resources and treatment options and start this early in pregnancy to help women and their supports recognize mood disorder symptoms and seek help.

“Every time they go to doctor visits, the Ob/Gyn needs to talk about it, at every visit. Even if the woman looks happy, there’s always something. I think if the doctors would mention it all the time, every pregnancy, it would get through their head that maybe it’s a serious thing.”

Screening coupled with coordination and consistent follow-up of care

To engage and support women getting treatment, participants suggested that screening should be coupled with a follow-up discussion, education, coordination of treatment and periodic check-ins and/or follow-up phone calls to ensure that women got connected with treatment.

“…especially when I was having trouble and there was a lot of pressure on my husband. I feel like that shouldn’t be only for people who can afford it, I think that should be somehow accessible to everybody with a psychiatric problem.”

DISCUSSION AND CONCLUSION

While all women in our sample met the criteria for bipolar disorder based on the MINI, they: 1) were not clinically diagnosed with bipolar disorder; and, 2) did not receive targeted treatment for bipolar disorder. Despite having met the criteria for bipolar disorder on the M.I.N.I., most women had not been given a clinical diagnosis of bipolar disorder (72.0%). This is consistent with prior work in general adult populations in which misdiagnosis of bipolar disorder is common (Hirschfeld, Lewis, & Vornik, 2003; Hirschfeld & Vornik, 2004), with typically a 10 year lag between onset of illness and receipt of correct diagnosis (N. Ghaemi, Sachs, & Goodwin, 2000; S. N. Ghaemi, Boiman, & Goodwin, 2000). Almost half the sample (42%) received inappropriate / relatively contraindicated medication treatment (i.e., antidepressant monotherapy) (Bipolar disorders in adults: NICE Guideline, 2015). Similarly, almost half (42%) received no medication treatment, which is also inconsistent with current treatment guidelines.

Given that all the women in our sample screened positive for depression and were not diagnosed with bipolar disorder, it is understandable that some received treatment with antidepressant medication. Antidepressant medication is an appropriate, evidence-based treatment for unipolar depression but not for bipolar disorder. Research suggests a lack of efficacy of antidepressant treatment for bipolar depression (Sachs et al., 2007; Sidor & MacQueen, 2011) with concomitant risk of cycling / switching between episodes of depression or hypomania / mania (Leverich et al., 2006; Schneck et al., 2008). Use of antidepressant monotherapy in bipolar disorder, type II has more supporting evidence (Amsterdam & Shults, 2010; Amsterdam, Wang, & Shults, 2010) with lower risk of switching in bipolar disorder, type II relative to type I (Altshuler et al., 2017) (Altshuler et al., 2006). However, increased rates of suicidal ideation and attempts are associated with antidepressant exposure (Bauer et al., 2006; Pacchiarotti et al., 2011). Currently, evidence-based guidelines recommend use of antidepressants only in conjunction with mood stabilizers (Bipolar disorders in adults: NICE Guideline, 2015). Thus, in our study, most women with bipolar illness were neither correctly identified nor offered evidence-based treatment for bipolar disorder because they were either not treated or treated with antidepressants alone (68.0%). Although this was a severely ill population in which most participants had a history of psychiatric treatment with pharmacotherapy and a past suicide attempt, most also reported that they were not given the opportunity to discuss medication treatment options during pregnancy.

Despite these challenges, women reported experiencing low stigma and the majority received at least some form of mental health treatment. Most treatment was provided by non-psychiatric providers, suggesting that obstetric practices play a critical role in providing psychiatric care to this population. This is major progress and an important step in increasing access to mental health care for perinatal mood disorders. Our qualitative data suggest that women want their obstetric providers to proactively screen for, discuss, and help them obtain mental health treatment.

Although obstetric providers’ increased comfort in treating perinatal depression is a major advance, our data suggest that it also may be associated with an increased risk of delivering inappropriate treatment to women with undiagnosed bipolar disorder, including antidepressant monotherapy. Our data are particularly concerning because our study sample was a high-risk population in which the majority had attempted suicide or had been psychiatrically hospitalized, both of which are predictors of poor course and outcomes.

Bipolar disorder is complicated illness that can be difficult to diagnose (Smith et al., 2011). Patients that screen positive for bipolar disorder will generally need to be assessed by a psychiatric provider for diagnostic clarification. While it may not be appropriate or feasible for obstetric providers to diagnose bipolar disorder, it is imperative that they screen for it before initiating treatment with an antidepressant. Screening with a validated screening tool would allow obstetric providers to determine when it is appropriate to initiate treatment with an antidepressant versus refer for assessment and treatment with a psychiatric provider. This approach is consistent with the Maternal Mental Health Safety Bundle (Kendig et al., 2017) which recommends screening for bipolar disorder in obstetric settings.

Study strengths include that we obtained both qualitative and quantitative data, allowing for more in depth understanding of participants’ experiences. Our study is limited by a small sample of women with severe psychiatric illness drawn from a single geographic region, which limits generalizability. Further investigation in larger and more diverse samples in different geographic regions is needed to increase the generalizability of our findings.

Although we purposefully sampled women with bipolar disorder, our qualitative findings may also apply to other psychiatric illnesses that occur during pregnancy and the postpartum period. For example, because there was no comparison group, it is possible that the barriers to care in our sample are similar to those experienced by women who do not meet criteria for bipolar disorder. Differentiating the barriers experienced by women with and without unrecognized bipolar disorder would also have allowed us to better understand the different barriers experienced by these subsets of women in our sample. Including data on the perspectives of obstetric providers would also have enhanced our findings. Regardless, our study builds on previous research to better understand the experiences of perinatal women with bipolar disorder.

Our data suggest that pregnant women with bipolar face many challenges in securing mental health care treatment appropriate to their needs. To promote maternal, and ultimately child health, bipolar disorder must be recognized, treated and carefully monitored. Obstetric providers are at the front line serving these vulnerable women with complex conditions. As recommended in the Maternal Mental Health Safety Bundle (Kendig et al., 2017), these settings can and should be leveraged as a place to detect bipolar disorder and refer patients for treatment. Obstetric providers play a pivotal role in this process. Our data suggests that obstetric providers need to identify women with bipolar disorder and help link women with needed psychiatric care to: 1) avoid inappropriate and potentially dangerous prescribing practices for the women who have undiagnosed bipolar disorder; and, 2) ensure women are referred to the specialized treatment they need.

Acknowledgments

Funding: This work was supported by the National Center for Research Resources and the National Center for Advancing Translational Sciences, National Institutes of Health (NIH), [Grant numbers KL2TR000160, UL1TR000161]. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.

Footnotes

Ethical Approval: All procedures performed in studies involving human participants were in accordance with the ethical standards of The University of Massachusetts Institutional Review Board (who approved the study) and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Informed Consent: Informed consent was obtained from all study participants before they participated in the study.

Conflict of Interest: The first, third, fourth, and eighth authors have received salary and/or funding support from Massachusetts Department of Mental Health via the Massachusetts Child Psychiatry Access Program for Moms (MCPAP for Moms). The first author is also the statewide Medical Director of MCPAP for Moms. The first author has served on the Perinatal Depression Advisory Board for the Janssen Disease Interception Accelerator Program and Advisory Boards for Sage Therapeutics. She is also a council member of the Gerson Lerhman Group. The third author is the Lead Obstetric Liaison for MCPAP for Moms and has served on a Physician Advisory Board for Sage Therapeutics and is a consultant for two research projects. The fifth author has been the Program Director of MCPAP for Moms, and the eight author has served as a Consultant for MCPAP for Moms. The seventh author serves as a consultant for Myriad Genetic, Inc. The second, fourth, and sixth authors declare that they do not have conflicts of interest.

References

  1. Altshuler LL, Sugar CA, McElroy SL, Calimlim B, Gitlin M, Keck PE, Jr, … Suppes T. Switch Rates During Acute Treatment for Bipolar II Depression With Lithium, Sertraline, or the Two Combined: A Randomized Double-Blind Comparison. American Journal of Psychiatry. 2017;174(3):266–276. doi: 10.1176/appi.ajp.2016.15040558. [DOI] [PubMed] [Google Scholar]
  2. Altshuler LL, Suppes T, Black DO, Nolen WA, Leverich G, Keck PE, Jr, … Post R. Lower switch rate in depressed patients with bipolar II than bipolar I disorder treated adjunctively with second-generation antidepressants. American Journal of Psychiatry. 2006;163(2):313–315. doi: 10.1176/appi.ajp.163.2.313. [DOI] [PubMed] [Google Scholar]
  3. American College of Obstetricians and Gynecologists Committee on Obstetric Practice. Committee opinion no. 630: Screening for Perinatal Depression. 2015;(631) doi: 10.1097/01.AOG.0000465192.34779.dc. Retrieved from http://www.acog.org/Womens-Health/Depression-and-Postpartum-Depression. [DOI] [PubMed]
  4. Amsterdam JD, Shults J. Efficacy and safety of long-term fluoxetine versus lithium monotherapy of bipolar II disorder: a randomized, double-blind, placebo-substitution study. The American Journal of Psychiatry. 2010;167(7):792–800. doi: 10.1176/appi.ajp.2009.09020284. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Amsterdam JD, Wang G, Shults J. Venlafaxine monotherapy in bipolar type II depressed patients unresponsive to prior lithium monotherapy. Acta Psychiatrica Scandinavica. 2010;121(3):201–208. doi: 10.1111/j.1600-0447.2009.01462.x. [DOI] [PubMed] [Google Scholar]
  6. Bauer MS, Wisniewski SR, Marangell LB, Chessick CA, Allen MH, Dennehy EB, … Sachs GS. Are antidepressants associated with new-onset suicidality in bipolar disorder? A prospective study of participants in the Systematic Treatment Enhancement Program for Bipolar Disorder (STEP-BD) The Journal of clinical psychiatry. 2006;67(1):48–55. doi: 10.4088/jcp.v67n0108. [DOI] [PubMed] [Google Scholar]
  7. Bipolar disorders in adults: NICE Guideline. 2015 Retrieved from https://www.nice.org.uk/guidance/qs95.
  8. Burton A, Patel S, Kaminsky L, Rosario GD, Young R, Fitzsimmons A, Canterino JC. Depression in pregnancy: time of screening and access to psychiatric care. J Matern Fetal Neonatal Med. 2011;24(11):1321–1324. doi: 10.3109/14767058.2010.547234. [DOI] [PubMed] [Google Scholar]
  9. Byatt N, Biebel K, Debordes-Jackson G, Lundquist RS, Moore Simas TA, Weinreb L, Ziedonis D. Community Mental Health Provider Reluctance to Provide Pharmacotherapy May Be a Barrier to Addressing Perinatal Depression: A Preliminary Study. The Psychiatric quarterly. 2012 doi: 10.1007/s11126-012-9236-0. [DOI] [PubMed] [Google Scholar]
  10. Byatt N, Cox L, Moore Simas TA, Biebel K, Sankaran P, Swartz HA, Weinreb L. Access to Pharmacotherapy Amongst Women with Bipolar Disorder during Pregnancy: a Preliminary Study. Psychiatric Quartely. 2017 doi: 10.1007/s11126-017-9525-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Chaudron LH, Kitzman HJ, Peifer KL, Morrow S, Perez LM, Newman MC. Prevalence of maternal depressive symptoms in low-income Hispanic women. Journal of Clinical Psychiatry. 2005;66(4):418–423. doi: 10.4088/jcp.v66n0402. [DOI] [PubMed] [Google Scholar]
  12. Chen H, Wang J, Ch’ng YC, Mingoo R, Lee T, Ong J. Identifying mothers with postpartum depression early: integrating perinatal mental health care into the obstetric setting. ISRN obstetrics and gynecology. 2011;2011:309189. doi: 10.5402/2011/309189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Clement S, Brohan E, Jeffery D, Henderson C, Hatch SL, Thornicroft G. Development and psychometric properties the Barriers to Access to Care Evaluation scale (BACE) related to people with mental ill health. BMC Psychiatry. 2012;12(1):1–11. doi: 10.1186/1471-244x-12-36. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Clement S, Brohan E, Jeffery D, Henderson C, Hatch SL, Thornicroft G. Development and psychometric properties the Barriers to Access to Care Evaluation scale (BACE) related to people with mental ill health. BMC psychiatry. 2012;12:36. doi: 10.1186/1471-244X-12-36. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Cox JL, Holden JM, Sagovsky R. Detection of postnatal depression. Development of the 10-item Edinburgh Postnatal Depression Scale. British Journal of Psychiatry. 1987;150:782–786. doi: 10.1192/bjp.150.6.782. [DOI] [PubMed] [Google Scholar]
  16. Dedoose. Los Angeles, CA: SocioCultural Research Consultants, LLC; 2012. [Google Scholar]
  17. Flynn HA, O’Mahen HA, Massey L, Marcus S. The impact of a brief obstetrics clinic-based intervention on treatment use for perinatal depression. J Womens Health (Larchmt) 2006;15(10):1195–1204. doi: 10.1089/jwh.2006.15.1195. [DOI] [PubMed] [Google Scholar]
  18. Geddes J. Prenatal and perinatal and perinatal risk factors for early onset schizophrenia, affective psychosis, and reactive psychosis. BMJ. 1999;318(7181):426. [PubMed] [Google Scholar]
  19. Ghaemi N, Sachs GS, Goodwin FK. What is to be done? Controversies in the diagnosis and treatment of manic-depressive illness. World Journal of Biological Psychiatry. 2000;1(2):65–74. doi: 10.3109/15622970009150569. [DOI] [PubMed] [Google Scholar]
  20. Ghaemi SN, Boiman EE, Goodwin FK. Diagnosing bipolar disorder and the effect of antidepressants: a naturalistic study. Journal of Clinical Psychiatry. 2000;61(10):804–808. doi: 10.4088/jcp.v61n1013. quiz 809. [DOI] [PubMed] [Google Scholar]
  21. Gibson J, McKenzie-McHarg K, Shakespeare J, Price J, Gray R. A systematic review of studies validating the Edinburgh Postnatal Depression Scale in antepartum and postpartum women. Acta Psychiatrica Scandinavica. 2009;119(5):350–364. doi: 10.1111/j.1600-0447.2009.01363. [DOI] [PubMed] [Google Scholar]
  22. Glavin K, Smith L, Sorum R. Prevalence of postpartum depression in two municipalities in Norway. Scandinavian Journal of Caring Sciences. 2009;23(4):705–710. doi: 10.1111/j.1471-6712.2008.00667.x. SCS667 [pii] [DOI] [PubMed] [Google Scholar]
  23. Glavin K, Smith L, Sorum R, Ellefsen B. Redesigned community postpartum care to prevent and treat postpartum depression in women--a one-year follow-up study. Journal of Clinical Nursing. 2010;19(21–22):3051–3062. doi: 10.1111/j.1365-2702.2010.03332.x. [DOI] [PubMed] [Google Scholar]
  24. Goodman JH, Tyer-Viola L. Detection, treatment, and referral of perinatal depression and anxiety by obstetrical providers. J Womens Health (Larchmt) 2010;19(3):477–490. doi: 10.1089/jwh.2008.1352. [DOI] [PubMed] [Google Scholar]
  25. Hirschfeld RM, Lewis L, Vornik LA. Perceptions and impact of bipolar disorder: how far have we really come? Results of the national depressive and manic-depressive association 2000 survey of individuals with bipolar disorder. Journal of Clinical Psychiatry. 2003;64(2):161–174. [PubMed] [Google Scholar]
  26. Hirschfeld RM, Vornik LA. Recognition and diagnosis of bipolar disorder. The Journal of clinical psychiatry. 2004;65(Suppl 15):5–9. [PubMed] [Google Scholar]
  27. Jones I, Chandra PS, Dazzan P, Howard LM. Bipolar disorder, affective psychosis, and schizophrenia in pregnancy and the post-partum period. Lancet. 2014;384(9956):1789–1799. doi: 10.1016/S0140-6736(14)61278-2. [DOI] [PubMed] [Google Scholar]
  28. Jones I, Craddock N. Familiality of the puerperal trigger in bipolar disorder: results of a family study. American Journal of Psychiatry. 2001;158(6):913–917. doi: 10.1176/appi.ajp.158.6.913. [DOI] [PubMed] [Google Scholar]
  29. Kendell RE, Chalmers JC, Platz C. Epidemiology of puerperal psychoses. British Journal of Psychiatry. 1987;150:662–673. doi: 10.1192/bjp.150.5.662. [DOI] [PubMed] [Google Scholar]
  30. Kendig S, Keats JP, Hoffman MC, Kay LB, Miller ES, Moore Simas TA, … Lemieux LA. Consensus Bundle on Maternal Mental Health: Perinatal Depression and Anxiety. Obstetrics and Gynecology. 2017;129(3):422–430. doi: 10.1097/AOG.0000000000001902. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Kessler RC, Akiskal HS, Angst J, Guyer M, Hirschfeld RM, Merikangas KR, Stang PE. Validity of the assessment of bipolar spectrum disorders in the WHO CIDI 3.0. Journal of Affective Disorders. 2006;96(3):259–269. doi: 10.1016/j.jad.2006.08.018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Leverich GS, Altshuler LL, Frye MA, Suppes T, McElroy SL, Keck PE, Jr, … Post RM. Risk of switch in mood polarity to hypomania or mania in patients with bipolar depression during acute and continuation trials of venlafaxine, sertraline, and bupropion as adjuncts to mood stabilizers. American Journal of Psychiatry. 2006;163(2):232–239. doi: 10.1176/appi.ajp.163.2.232. [DOI] [PubMed] [Google Scholar]
  33. Lindahl V, Pearson JL, Colpe L. Prevalence of suicidality during pregnancy and the postpartum. Arch Womens Ment Health. 2005;8(2):77–87. doi: 10.1007/s00737-005-0080-1. [DOI] [PubMed] [Google Scholar]
  34. Miles MH, AM . Qualitative Data Analysis. 2. Thousand Oaks, CA: Sage Publications; 1994. [Google Scholar]
  35. Morgan D. Focus Groups as Qualitative Research. Thousand Oaks, CA: Sage Publications; 1988. [Google Scholar]
  36. Munk-Olsen T, Laursen TM, Pedersen CB, Mors O, Mortensen PB. New parents and mental disorders: a population-based register study. JAMA. 2006;296(21):2582–2589. doi: 10.1001/jama.296.21.2582. 296/21/2582 [pii] [DOI] [PubMed] [Google Scholar]
  37. Pacchiarotti I, Valenti M, Colom F, Rosa AR, Nivoli AM, Murru A, … Vieta E. Differential outcome of bipolar patients receiving antidepressant monotherapy versus combination with an antimanic drug. J Affect Disord. 2011;129(1–3):321–326. doi: 10.1016/j.jad.2010.07.036. [DOI] [PubMed] [Google Scholar]
  38. Rusner M, Berg M, Begley C. Bipolar disorder in pregnancy and childbirth: a systematic review of outcomes. BMC Pregnancy Childbirth. 2016;16(1):331. doi: 10.1186/s12884-016-1127-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Sachs GS, Nierenberg AA, Calabrese JR, Marangell LB, Wisniewski SR, Gyulai L, … Thase ME. Effectiveness of adjunctive antidepressant treatment for bipolar depression. New England Journal of Medicine. 2007;356(17):1711–1722. doi: 10.1056/NEJMoa064135. [DOI] [PubMed] [Google Scholar]
  40. Schneck CD, Miklowitz DJ, Miyahara S, Araga M, Wisniewski S, Gyulai L, … Sachs GS. The prospective course of rapid-cycling bipolar disorder: findings from the STEP-BD. Am J Psychiatry. 2008;165(3):370–377. doi: 10.1176/appi.ajp.2007.05081484. quiz 410. [DOI] [PubMed] [Google Scholar]
  41. Sheehan DV, Lecrubier Y, Sheehan KH, Amorim P, Janavs J, Weiller E, … Dunbar GC. The Mini-International Neuropsychiatric Interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. Journal of Clinical Psychiatry. 1998;59(Suppl 20):22–33. quiz 34–57. [PubMed] [Google Scholar]
  42. Sidor MM, MacQueen GM. Antidepressants for the acute treatment of bipolar depression: A systematic review and meta-analysis. Journal of Clinical Psychiatry. 2011;72(2):156–167. doi: 10.4088/JCP.09r05385gre. [DOI] [PubMed] [Google Scholar]
  43. Siu AL, Bibbins-Domingo K, Grossman DC, Baumann LC, Davidson KW, Ebell M, … Pignone MP. Screening for Depression in Adults: US Preventive Services Task Force Recommendation Statement. JAMA. 2016;315(4):380–387. doi: 10.1001/jama.2015.18392. [DOI] [PubMed] [Google Scholar]
  44. Smith DJ, Griffiths E, Kelly M, Hood K, Craddock N, Simpson SA. Unrecognised bipolar disorder in primary care patients with depression. British Journal of Psychiatry. 2011;199(1):49–56. doi: 10.1192/bjp.bp.110.083840. [DOI] [PubMed] [Google Scholar]
  45. Spinelli MG. Maternal infanticide associated with mental illness: prevention and the promise of saved lives. American Journal of Psychiatry. 2004;161(9):1548–1557. doi: 10.1176/appi.ajp.161.9.1548. [DOI] [PubMed] [Google Scholar]
  46. Wachino V Center for Medicaid and CHIP Services. Maternal Depression Screening and Treatment: A Critical role for Medicaid in the Care of Mothers and Families. Baltimore, MD: Centers for Medicare and Medicaid Services; 2016. [Google Scholar]
  47. Weinreb L, Byatt N, Moore Simas TA, Tenner K, Savageau JA. What happens to mental health treatment during pregnancy? Women’s experience with prescribing providers. Psychiatric Quartely. 2014;85(3):349–355. doi: 10.1007/s11126-014-9293-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Wisner KL, Sit DK, McShea MC, Rizzo DM, Zoretich RA, Hughes CL, … Hanusa BH. Onset timing, thoughts of self-harm, and diagnoses in postpartum women with screen-positive depression findings. JAMA Psychiatry. 2013;70(5):490–498. doi: 10.1001/jamapsychiatry.2013.87. [DOI] [PMC free article] [PubMed] [Google Scholar]

RESOURCES