Bipolar II Postpartum Depression: Detection, Diagnosis, and Treatment

Bipolar spectrum disorder generally includes bipolar I disorder, bipolar II disorder, and bipolar disorder not otherwise specified (1) . Bipolar I disorder is characterized by recurrent episodes of mania and depression, while bipolar II disorder is defined as recurrent episodes of depression and hypomania. The illness course in bipolar disorder not otherwise specified is also punctuated with manic and depressive symptoms, but the disorder does not reach the DSM-IV threshold criteria for bipolar I or II disorder. There is accumulating evidence that the majority of bipolarity exists beyond the realm of bipolar I disorder. The U.S. National Comorbidity Survey Replication Study reported lifetime prevalence estimates of 1.0% for bipolar I disorder, 1.1% for bipolar II disorder, and 2.4% for bipolar disorder not otherwise specified (2) .

Despite the combined high prevalence of bipolar II disorder and bipolar disorder not otherwise specified, research on postpartum mood disorders has focused primarily on major depressive disorder, mania, and puerperal psychosis. While the nosological status of postpartum psychosis remains a topic of debate, it is usually a manifestation of bipolar disorder triggered by childbirth. The study of postpartum bipolarity beyond bipolar I disorder has been largely ignored; consequently, there are scant data on the prevalence of depressive presentations in bipolar II disorder and bipolar disorder not otherwise specified. Freeman et al. (3) reported that 67% of 30 women with bipolar I and II disorder had a postpartum mood episode within 1 month of delivery; in the eight women who had experienced episodes following their first delivery, the recurrence rate following a subsequent delivery was 100%. Identified postpartum episodes were almost exclusively of the depressive type. Another study (4) found that approximately 20% of women with bipolar disorder retrospectively reported having postpartum mood episodes, mainly of the depressive type. Compared to women with major depressive disorder, those with bipolar disorder are more likely to have episodes of postpartum depression; however, no prospective studies have been conducted to ascertain the comparative prevalence of postpartum depression in women with major depression and those with bipolar disorder.

Misdiagnosis of bipolar depression as major depressive disorder during the postpartum period appears to be common. For example, Sharma et al. (5) reported that 54% of 56 outpatients seen consecutively with the referral diagnosis of postpartum depression were rediagnosed as having a lifetime diagnosis of bipolar disorder. In terms of frequency of occurrence, the primary diagnoses in this sample were major depressive disorder (46%), bipolar disorder not otherwise specified (29%), bipolar II disorder (23%), and bipolar I disorder (2%). Thirty percent of patients had a positive screen for bipolar spectrum disorder on the Mood Disorders Questionnaire, and 86% of those who screened positive met DSM-IV criteria for a diagnosis of bipolar disorder; however, only a small number (10%) of these patients reported receiving a past diagnosis of bipolar disorder.

Hypomanic symptoms are common after delivery, with various studies reporting rates in the range of 9%–20% (6 – 8) . While no comparative studies have been conducted on the prevalence of hypomania during the puerperium compared with the nonpuerperal periods, the rates of hypomania reported in various studies are higher than the lifetime prevalence of bipolar disorder. It has been suggested that postpartum hypomania does not simply reflect happiness at having a baby but is a manifestation of bipolar disorder (9) . Associated symptoms include increased goal-directed activity, overtalkativeness, racing of thoughts, decreased sleep requirement, distractibility, and irritability. In contrast, the “baby blues” denotes a brief period of mild emotional disturbance characterized by dysphoria, tearfulness, mood lability, insomnia, irritability, and anxiety. Symptoms of the baby blues occur in up to 80% of women in the few days after delivery and usually remit by the 10th day. Even though elation has been reported in some studies as a symptom of the baby blues, the symptoms of postpartum hypomania can be distinguished because of their onset on postpartum day 1 rather than day 3 or 4, as in the baby blues (9) . The peak prevalence of hypomanic symptoms is immediately after delivery, although the risk remains elevated for several weeks. Postpartum hypomania itself does not cause marked impairment in social or occupational functioning, but its clinical significance lies in its association with bipolar depression later in the postpartum period (10) .

Hypomania after delivery may be misconstrued as the normal joy related to the experience of motherhood. Because DSM-IV does not acknowledge hypomania as a postpartum-onset specifier, there is neither sufficient awareness of nor screening for this presentation. Consequently, clinicians may not inquire about episodes of mood elevation, and women may fail to report hypomanic symptoms and focus on symptoms of depression. There are no screening instruments designed specifically for use before or after delivery in women with bipolar disorder. Commonly used screening instruments, such as the Edinburgh Postnatal Depression Scale, have not been validated in women with bipolar disorder. Thus, women with bipolar II disorder and bipolar disorder not otherwise specified may be misdiagnosed as having major depressive disorder in the postpartum period. Brockington et al. (11) noted that unipolar postpartum depression can be distinguished from postpartum bipolar depression; he found that an early onset of depression (within 2 weeks of delivery) and a characteristic clinical profile—less anger, less self-rated emotion, and more animation—represent a clinical entity related to bipolar disorder.

The misdiagnosis of bipolar disorder as major depressive disorder frequently results in a delay in the initiation of appropriate treatment. The consequences of misdiagnosis can be particularly serious as treatment with antidepressants may precipitate mania, a mixed state, or rapid cycling and thereby increase the risk for psychiatric hospitalization. The injudicious use of antidepressants in patients with a bipolar diathesis has also been linked to polypharmacy and treatment refractoriness (12) .

Postpartum treatment of women with bipolar II disorder and bipolar disorder not otherwise specified is challenging because of the lack of diagnostic instruments designed for postpartum mood presentations and a paucity of psychopharmacological data to guide clinical decision making. Given the prevalence of bipolarity and the potentially serious consequences of its misdiagnosis, pregnant women should be universally screened for bipolar disorder by inquiring about personal and family history of bipolar disorder. This will permit early identification, formal risk assessment, and management planning, including close follow-up during the period of risk. It can provide an opportunity to address avoidable risk factors, such as general stress and sleep disruption, in late pregnancy and the early postpartum period. Women with postpartum depression in particular should be routinely screened for mania and hypomania. Until a validated assessment tool is established, the Mood Disorder Questionnaire may be useful for screening for bipolar disorder in pregnant and postpartum women (1) . The Highs scale (9) is not a diagnostic instrument, but it can be valuable in eliciting the symptoms of hypomania. The presence of clinical features, such as atypical features (DSM-IV criteria), racing of thoughts, and psychotic symptoms, during a depressive episode should serve as a clue to the bipolar nature of depression. Screening should include questions about a family history of bipolar disorder. Early initiation of appropriate management can improve the patient’s quality of life, which can significantly affect her family and her child’s early development.

Because insufficient research has been conducted on the treatment of postpartum bipolar II disorder, definitive recommendations cannot be made. Until there is more research and stronger evidence, the treatment of bipolar postpartum depression should follow the same guidelines as the treatment of nonpuerperal bipolar II depression (18), provided the selected medications are compatible with lactation. For acute management, treatment options include quetiapine, lamotrigine, lithium, valproate, quetiapine plus lamotrigine, and lithium plus lamotrigine. For prophylactic treatment, lithium, lamotrigine, or an atypical antipsychotic, such as olanzapine and quetiapine, should be considered. Antidepressant monotherapy should be avoided for prophylactic and acute treatment. For women with bipolar disorder who are already receiving an antidepressant, the need for its continued use in the maintenance treatment of depression should be evaluated because antidepressants may perpetuate instability of the illness course.

For women who appear to have significant bipolar illness in the postpartum setting, consideration should be given to the continued use of stabilizing medication after the first postpartum year. If medication is discontinued, it is advisable to continue psychiatric monitoring beyond the first postpartum year in order to ensure ongoing maternal emotional stability. Women should be carefully monitored for mood stability during subsequent pregnancies and postpartum periods. Consideration should be given to whether to use prophylactic management with previously effective medications or careful monitoring and prompt initiation of medications that have been effective in the past.

In the case vignette, the patient was thought to have bipolar II disorder, depressed phase, with postpartum onset. Clues to the bipolar nature of the depression included a history of postpartum hypomania, atypical symptoms of depression (hypersomnia and psychomotor retardation), family history of bipolar disorder, and a loss of antidepressant response. Collateral history obtained from her husband confirmed the diagnosis of bipolar II disorder. The venlafaxine dose was gradually tapered off and she was started on lamotrigine. During withdrawal from venlafaxine the patient’s insomnia worsened, leading her treatment team to substitute 25 mg of quetiapine for the zopiclone she had been taking at bedtime. She was unable to tolerate a higher dose of quetiapine because of excessive sedation and postural hypotension. The treatment team decided to try lamotrigine, at 150 mg daily, because of its ease of use (no laboratory monitoring) and safety during lactation compared to lithium. The patient reported a significant and sustained improvement in her condition after the addition of lamotrigine.

Received Dec. 29, 2008; revision received Feb. 11, 2009; accepted Feb. 23, 2009 (doi: 10.1176/appi.ajp.2009.08121902). From the Departments of Psychiatry and of Obstetrics and Gynecology, University of Western Ontario, London; the Perinatal Clinic, St. Joseph’s Health Care, London, Ontario; the Department of Psychiatry, Geffen School of Medicine at UCLA, Los Angeles; and the Women’s Life Center, Resnick Neuropsychiatric Hospital at UCLA. Address correspondence and reprint requests to Prof. Sharma, Specialized Adult Program, Regional Mental Health Care London, 850 Highbury Avenue North, P.O. Box 5532, Station B, London, Ont., Canada N6A 4H1; [email protected] (e-mail).

Dr. Sharma has received grant support from, participated on scientific advisory boards for, or served on the speakers bureaus of AstraZeneca, Bristol-Myers Squibb, Eli Lilly, Janssen, Lundbeck, the Ontario Mental Health Foundation, Pfizer, Servier, and the Stanley Foundation. Dr. Burt has served as an advisor or consultant to, or on the speakers bureaus of, AstraZeneca, Eli Lilly, Noven Pharmaceuticals, Takeda Pharmaceuticals, and Wyeth Ayerst. Dr. Ritchie reports no financial relationships with commercial interests.

Supported by a grant from the Ontario Mental Health Foundation.

The authors thank Christine Drake for her help in the preparation of the manuscript.