Abstract
Objectives
(1) To assess the prevalence of depression and treatment rates in antepartum and postpartum women compared to a control group of reproductive-age women over a 12-year period, and (2) To determine demographic characteristics associated with depression.
Methods
National Health and Nutrition Examination Survey data (2007–2018) were used. 5412 controls, 314 antepartum women, and 455 postpartum women were analyzed. Outcomes included depression prevalence, defined as moderate to severe depressive symptoms measured by Patient Health Questionnaire-9 (PHQ-9) scores ≥10 or self-reported antidepressant use; and treatment, defined as antidepressant prescription and/or mental health care services in the past 12 months. Multivariable logistic regression adjusted for age, insurance, race/ethnicity, education, and marital status estimated odds ratios and 95% confidence intervals.
Results
Depression prevalence was 20.2% in controls (95% CI 18.5–21.9), 9.7% in antepartum (6.3–14.1), and 12.8% in postpartum women (9.3–17.1). Mental health care service utilization increased for postpartum women in 2017–2018 (22.0%, 10.6–37.7). In those with depression, control and postpartum groups had similar treatment rates (70%, p = 0.894) compared to antepartum women (51%, p = 0.051). Antidepressant use was the most common treatment reported in all groups. Those who were married or had private insurance had the lowest depression rates in their respective categories. After adjusting for confounders, antepartum and postpartum women had lower odds of depression compared to controls. When the outcome was PHQ-9 ≥ 10 alone, these associations persisted.
Conclusion
In a nationally representative sample, depression prevalence was lower in perinatal women compared to reproductive-age controls, and treatment rates were lowest in antepartum women with prevalent depression. Mental health care services may have increased for postpartum women due to the US Preventive Services Task Force 2016 recommendations, which endorsed psychotherapy for postpartum women. Even so, antidepressants were the most reported treatment among perinatal women, despite psychotherapy being the first-line recommended treatment for this population.
Introduction
Postpartum depression is the most common pregnancy-related complication worldwide and can lead to adverse maternal and child outcomes, including compromised mother-infant bonding, poorer infant cognitive outcomes, and shorter breastfeeding duration [1–4]. Likewise, antepartum depression is highly prevalent and tied to adverse birth outcomes, including preterm birth and low birthweight [5,6]. Both antepartum and postpartum depression are associated with increased risk for infant mortality and maternal suicide, which represents a leading cause of death in the perinatal period---prioritized nationally for prevention [7–10].
Depression prevalence has recently increased in the United States (US), largely driven by an increase in the incidence of depression in adolescents and young adults [11–13]. Globally, women demonstrate a two-fold higher risk of developing depression in their lifetime compared to men, and this gender gap has stayed constant over the last forty years [14,15], despite significant efforts to advance awareness and treatment.
Recent studies have documented an increase in depression and suicidal ideation in antepartum women in the US over the past two decades [16,17]. However, these findings are derived from analyses of commercial claims databases, which notably exclude mothers with public insurance. To our knowledge, no recent studies have assessed trends in the prevalence and treatment of antepartum or postpartum depression in a nationally representative US sample.
To address this gap in the literature, we analyzed trends in antepartum and postpartum depression prevalence and treatment compared to women of reproductive age, who were neither pregnant nor postpartum. We investigated trends over time and by key demographic characteristics known to be associated with risk and observed prevalence, including race and ethnicity, marital status, and education level. We harnessed data from 2007–2018 in the National Health and Nutrition Examination Survey (NHANES), a nationally representative and diverse population of the US conducted by the Centers for Disease Control and Prevention (CDC).
Methods
Study population
The study population included women of reproductive age between 20 and 44 years old, who underwent a urine pregnancy test, and were asked about their reproductive history and mental health from six NHANES cycles from 2007 to 2018 (each cycle comprises two years of data). NHANES, conducted by the Centers for Disease Control, is a nationally representative health survey of the non-institutionalized US population. Each year, the survey examines an estimated 5,000 individuals in counties across the country with both personal interviews conducted in the household and physical examinations performed in a mobile examination center. Interviews include demographic, socioeconomic, and health-related questions. This includes the Patient Health Questionnaire-9 (PHQ-9), a validated symptom instrument widely used for depression screening [18]. Female participants receive a reproductive health questionnaire as part of the interview [19].
Study groups
We defined three study groups: control, antepartum, postpartum. Women who had a positive pregnancy test were included in the antepartum group. Women who reported a birth within the past twelve months, identified with the question, “How many months ago did you have your baby?”, and had a negative pregnancy test, were included in the postpartum group. The control group was comprised of women who had a negative pregnancy test and were not in the 12-month postpartum period.
Outcome measurement
The primary outcome was depression prevalence, defined as PHQ-9 score ≥10 or self-reported current antidepressant use. Using a threshold of ≥ 10 is highly sensitive and specific for major depressive disorder, both in the general and perinatal populations [20–22]. Self-reported antidepressant use was defined as prescription medications taken in the past 30 days including bupropion, citalopram, desvenlafaxine, duloxetine, escitalopram, fluoxetine, imipramine, nortriptyline, paroxetine, sertraline, or venlafaxine. These antidepressants were chosen based on previous publications in perinatal depression [23,24]. Self-reported antidepressant use was included in the definition of prevalent depression because this may identify individuals living with depression whose symptoms are currently managed by their antidepressant treatment, as has been done in other studies assessing depression prevalence [25,26].
Additional outcomes included prevalence of: (i) moderate depressive symptoms or higher (PHQ-9 score ≥10), (ii) any depressive symptoms (PHQ-9 score ≥5) or antidepressant prescription, and (iii) total PHQ-9 score as a continuous outcome. Additional treatment outcomes evaluated included: (i) antidepressant prescription (with or without elevated PHQ-9 score) and (ii) mental health care service utilization, identified using the question, “During the past 12 months, have you seen or talked to a mental health professional such as a psychologist, psychiatrist, psychiatric nurse or clinical social worker about your health?” Throughout the manuscript, we refer to ‘moderate’ to ‘severe’ depressive symptoms, with or without antidepressant use, as depression.
A sensitivity analysis restricted to 2013–2019 leveraged the 2013 modification to NHANES where indication for each prescription was collected and coded according to International Classification of Diseases, Tenth Revision (ICD-10) codes. For this sensitivity outcome, depression was additionally defined as total PHQ-9 score of ≥ 10 or ICD-10 codes F32.9 (Major depressive disorder, single episode, unspecified) or F33.9 (Major depressive disorder, recurrent, unspecified) noted as prescription indications (regardless of antidepressant type) associated with a prescription.
Covariate assessment
Information on age, race/ethnicity, education level, marital status, family income, health insurance status, and pregnancy history were collected during interviews. Per NHANES data derivation guidelines, Hispanic individuals were included in the “Hispanic” category of race/ethnicity regardless of race. We used race/ethnicity categories determined by NHANES, which included Hispanic, non-Hispanic White, non-Hispanic Black, and Other Race/Multiracial. Ratio of family income to poverty was derived by NHANES by dividing total annual family (or individual) income by poverty guidelines specific to the survey year, family size, and geographic location. We created a categorical variable based on federal assistance program eligibility criteria, with ≤1.3 indicating low income [27]. Body measurements were collected during the physical examination by trained health technicians. Body mass index (BMI) was calculated as weight in kilograms divided by height in meters squared.
Statistical analysis
Descriptive statistics assessed participant characteristics and outcomes stratified by study group and aggregated across all data cycles. Weighted proportions and standard errors are reported for categorical variables, and means, standard deviations, medians, and interquartile ranges for continuous variables. We calculated 95% confidence intervals for all outcomes using the Korn-Graubald method for exact intervals [28,29].
Trends in outcomes by data cycle were assessed using logistic regression to identify linear trends over time. The prevalence of depression was assessed and stratified by study group and according to participant characteristics pooled across all NHANES years. We subsequently performed logistic regression adjusted for age, insurance type, race/ethnicity, education level, and marital status to estimate the association between prevalent depression and study group. As a sensitivity analysis to distinguish the effects of antidepressant use and PHQ-9 score, we performed logistic regression with PHQ-9 ≥ 10 only as the outcome. Since missing data were minimal, with only 32 participants missing values for one or more variables in our regression analysis, complete case analyses were performed.
As an exploratory analysis, item-level descriptive statistics were generated for individual PHQ-9 questions for control, antepartum, and postpartum women with the primary outcome for all cycles combined.
All analyses accounted for complex survey design, including oversampling, survey nonresponse, and post-stratification of NHANES using sample weights, strata, and primary sampling units included in the NHANES data. For analyses pooled across years, we followed NHANES Analytic Guidelines to construct weights for combined NHANES survey cycles [30]. All tests were two-sided and performed at the 0.05 significance level. The research protocol and statistical analysis plan were pre-registered on Open Science Framework (OSF.io) prior to data analysis [31]. All analyses were performed with R version 4.2.2 [32].
Results
Across all data cycles, a total of 6181 participants met inclusion criteria, including: 5412 control group women, 314 antepartum women, and 455 postpartum women (STROBE diagram S1 Fig). Among the weighted study population participants, the median age was 32 [IQR = 25,38]. Fifty-nine percent of participants were White, 18.5% Hispanic, 13.4% Black, and 9.1% specified Other Race/Multiracial. The majority (78.3%) of participants reported having health insurance, with 58.8% reporting private insurance and 11.2% Medicaid. Twenty-seven percent had a family income 1.3 times the poverty level or lower (Table 1). Sixty-five percent of the control group reported ever being pregnant. The average time since delivery for postpartum women was 6.4 months (SD = 3.6).
Table 1. Descriptive characteristics by study group.
Overall | Control | Antepartum | Postpartum | |
---|---|---|---|---|
Unweighted Count | 6181 | 5412 | 314 | 455 |
Age in years (Median [IQR]) | 32 [25,38] | 32 [26,39] | 28 [24,33] | 28 [23,33] |
Age in Years | ||||
20-24 | 21.0 (1.0) | 19.7 (1.1) | 30.4 (3.1) | 31.3 (2.6) |
25-34 | 39.0 (0.9) | 37.5 (0.9) | 48 (3.5) | 52.2 (2.9) |
35-39 | 19.9 (0.6) | 20.6 (0.7) | 17.2 (2.7) | 12.8 (2.2) |
40-44 | 20.1 (0.8) | 22.3 (0.9) | 4.5 (2.0) | 3.8 (1.0) |
Race/Ethnicity | ||||
Hispanic | 18.5 (1.3) | 18.0 (1.3) | 22.2 (2.7) | 22.4 (2.2) |
Non-Hispanic White | 59.0 (1.7) | 59.7 (1.7) | 49.1 (4.1) | 56.2 (3.0) |
Non-Hispanic Black | 13.4 (0.9) | 13.2 (0.9) | 16.0 (2.0) | 13.8 (1.7) |
Other Race/Multiracial | 9.1 (0.5) | 9.0 (0.6) | 12.7 (2.2) | 7.5 (1.3) |
Language | ||||
English | 92.9 (0.6) | 93.0 (0.6) | 91.8 (1.6) | 92.1 (1.1) |
Spanish | 7.1 (0.6) | 7.0 (0.6) | 8.2 (1.6) | 7.9 (1.1) |
Education Level | ||||
Less than 9th Grade | 13.1 (0.6) | 12.6 (0.7) | 18.1 (2.2) | 16.7 (2.0) |
High School | 18.7 (0.8) | 18.3 (0.8) | 17.4 (2.2) | 24.5 (2.5) |
Some College or AA Degree | 36.4 (0.9) | 36.8 (1.0) | 34.0 (3.1) | 33.0 (2.4) |
College or above | 31.7 (1.3) | 32.3 (1.3) | 30.6 (3.3) | 25.8 (2.8) |
Body Mass Index1 (kg/m2) | ||||
<25 | 37.4 (1.0) | 38.5 (1.1) | 22.3 (2.4) | 33.5 (3.0) |
25- < 30 | 25.5 (0.7) | 24.8 (0.7) | 36.3 (4.0) | 26.0 (2.3) |
30- < 35 | 16.8 (0.5) | 16.7 (0.6) | 19.6 (2.7) | 16.1 (2.1) |
≥35 | 20.0 (0.7) | 19.6 (0.8) | 21.7 (2.7) | 24.4 (2.3) |
NA | 0.3 | 0.4 | 0 | 0 |
Marital Status | ||||
Married | 46.4 (1.1) | 44.3 (1.2) | 64.5 (3.5) | 60.3 (3.0) |
Widowed | 0.5 (0.1) | 0.5 (0.1) | 0 (0) | 0.1 (0.1) |
Divorced | 7.2 (0.4) | 7.8 (0.5) | 2.2 (0.9) | 2.7 (1.0) |
Separated | 2.9 (0.2) | 3.0 (0.2) | 2.2 (0.8) | 1.6 (0.5) |
Never Married | 29.8 (1.1) | 31.5 (1.1) | 16.6 (2.2) | 16.7 (2.0) |
Living With Partner | 13.3 (0.6) | 12.9 (0.6) | 14.4 (2.3) | 18.6 (1.9) |
NA | 0 | 0 | 0.1 | 0 |
Ratio Family Income to Poverty Level | ||||
≤1.3 | 26.9 (0.9) | 26.1 (1.0) | 25.7 (2.4) | 37.4 (2.4) |
>1.3-3.5 | 34.1 (0.9) | 34.3 (1.0) | 30.1 (3.4) | 35.6 (2.7) |
>3.5 | 32.9 (1.2) | 33.6 (1.2) | 35.8 (4.2) | 21.5 (2.5) |
NA | 6.1 | 6 | 8.3 | 5.6 |
Health Insurance | ||||
Yes | 78.3 (0.8) | 77.6 (0.9) | 86.6 (2.1) | 81.2 (2.0) |
No | 21.5 (0.8) | 22.2 (0.9) | 13.4 (2.1) | 18.6 (2.0) |
NA | 0.1 | 0.2 | 0 | 0.1 |
Health Insurance Type | ||||
Private | 58.8 (1.1) | 60.0 (1.1) | 51.0 (3.8) | 49 (3.2) |
Medicaid | 11.2 (0.7) | 9.4 (0.6) | 27.1 (3.0) | 23.1 (3.0) |
Other Insurance | 8.0 (0.5) | 7.9 (0.5) | 8.4 (1.9) | 8.9 (1.8) |
Medicare | 0.5 (0.1) | 0.5 (0.1) | 0 (0) | 0.5 (0.3) |
SCHIP | 0 (0) | 0 (0) | 0.3 (0.3) | 0 (0) |
Military | 1.5 (0.3) | 1.5 (0.3) | 0 (0) | 2.1 (1.1) |
State-Sponsored Health Plan | 3.5 (0.4) | 3.4 (0.4) | 5.6 (1.4) | 3.4 (1.0) |
Other Government | 2.1 (0.2) | 2.1 (0.3) | 1.7 (0.8) | 2.7 (0.7) |
Single Service Plan | 0.3 (0.1) | 0.3 (0.1) | 0.8 (0.7) | 0.2 (0.2) |
No Insurance | 21.5 (0.8) | 22.2 (0.9) | 13.4 (2.1) | 18.6 (2.0) |
NA | 0.5 | 0.5 | 0.2 | 0.4 |
Values are weighted percentages (SE) or median [IQR]. Missing values are presented as NA (not available).
SE, standard error; IQR, interquartile range; AA, Associate in Arts; SCHIP, State Children’s Health Insurance Program.
1 Body mass index measured at physical examination.
Compared to the control group, antepartum and postpartum groups were younger, more likely to be married, have health insurance, and be on Medicaid. Postpartum women were less likely to be college educated and had lower family incomes.
Outcomes among the entire study population
The prevalence of depression was 20.2% (95% CI 18.5–21.9), 9.7% (6.3–14.1), 12.8% (9.3–17.1) in the control, antepartum, and postpartum groups, respectively, pooled across all cycles. Moderate or severe depression defined by PHQ-9 ≥ 10 was 11.1% (9.9–12.4), 6.5% (4.0–9.7), and 6.4% (3.7–10.0) in the three groups, respectively. Overall, antidepressant use and mental health care service utilization were highest in the controls, followed by postpartum women, and lowest in antepartum women (Table 2). Depression prevalence varied by parity: among pregnant women, it was 11.0% in nulliparous and 6.4% in multiparous women. Among postpartum women, depression was 14.9% in first-time mothers and 11.7% in mothers with two or more live births.
Table 2. Outcomes stratified by study group.
Control | Antepartum | Postpartum | |
---|---|---|---|
Overall | 5412 | 314 | 455 |
PHQ-9 ≥ 10 or Antidepressant | 20.2 (18.5-21.9) | 9.7 (6.3-14.1) | 12.8 (9.3-17.1) |
PHQ-9 ≥ 10 | 11.1 (9.9-12.4) | 6.5 (4.0-9.7) | 6.4 (3.7-10.0) |
PHQ-9 ≥ 5 or Antidepressant | 34.0 (32.2-35.8) | 28.3 (21.4-36.0) | 28.5 (23.7-33.7) |
Antidepressant Use | 12.2 (10.8-13.7) | 4.6 (2.1-8.6) | 7.4 (4.6-11.1) |
Mental Health Services Past 12 Months | 12.1 (10.9-13.5) | 6.4 (3.5-10.4) | 8.7 (5.8-12.6) |
Total PHQ-9 Score | |||
Median [IQR] | 2 [1,5] | 3 [1,5] | 2 [0, 5] |
Mean (SD) | 3.7 (4.4) | 3.4 (3.6) | 3.2 (3.8) |
Count in 2013–20181 | 2690 | 157 | 231 |
PHQ-9 ≥ 10 or Antidepressant | 19.9 (17.6-22.3) | 12.2 (6.8-19.8) | 11.5 (6.5-18.3) |
Antidepressant Use | 11.8 (9.8-14.0) | 7.0 (2.7-14.5) | 8.0 (3.7-14.5) |
PHQ-9 ≥ 10 or Antidepressant (Sensitivity2) | 16.3 (14.2-18.6) | 11.4 (6.2-18.6) | 7.3 (3.7-12.6) |
Antidepressant Use (Sensitivity2) | 7.6 (6.1-9.4) | 5.8 (1.9-13.1) | 3.6 (1.1-8.6) |
PHQ-9, Patient Health Questionnaire-9; IQR, interquartile range; SD, standard deviation.
All counts are unweighted. Values are weighted percentages with 95% confidence intervals, unless otherwise noted.
1The bottom panel shows outcomes for the data in 2013–2018 when medication indication (ICD-10 code) was provided.
2Sensitivity outcome is defined as PHQ-9 ≥ 10 or Antidepressant with ICD-10 code for depression.
Treatment among women with prevalent depression
Among those with prevalent depression, 69.9% control, 51% antepartum, and 68.9% postpartum women reported treatment with antidepressant use, mental health care services, or both. Antidepressant use alone was the most reported treatment among all groups (Fig 1). The differences in treatment rates were not statistically significant between control and antepartum women (p = 0.051), nor between control and postpartum women (p = 0.894). Mental health care service use was relatively low for individuals with PHQ-9 ≥ 10 without antidepressants (45.3% controls, 26.3% antepartum group, 37.4% postpartum group).
Fig 1. Treatment among women with prevalent depression (PHQ-9 ≥ 10 or antidepressant prescription).
Temporal trends in depression prevalence and treatment
Fig 2 shows trends in depression prevalence, antidepressant prescription, and mental health care utilization over a 12-year period. For the antepartum and postpartum groups, depression prevalence varied considerably across NHANES data cycles, as expected due to the relatively small sample sizes for both groups. For antepartum women, the highest prevalence of depression was in 2015–2016 (N = 58, 15.9%, 4.1–37.2), but we found no significant temporal trends. Antidepressant use increased significantly over time, peaking in 2015–2016 (N = 58, 12.4%, 2.5–32.9; linear trend p < 0.001).
Fig 2. Temporal trends in primary and secondary depression outcomes, weighted percentages and 95% CIs.
In postpartum women, prevalence of depression was highest in 2011–2012 (N = 68, 20.7%, 11.2–33.3) and lowest in 2013–2014 (N = 76, 7.5%, 4.0–12.6), though these differences may reflect chance fluctuations given the small sample sizes. Use of antidepressants and mental health services similarly fluctuated, and we found no significant linear trend across the years, except for higher use of mental health care services in 2017–2018 (22.0% N = 76, 10.6–37.7, p = 0.021) (S1 Table).
In the control group, prevalence of depression and antidepressant use stayed constant over time. In contrast, mental health care service utilization increased linearly over time (p = 0.010), starting at 10.9% (9.2–12.7) in 2007–2008 and gradually increasing to 14.4% (11.1–18.2) in 2017–2018. All three outcomes were higher at almost every timepoint compared to the antepartum and postpartum groups. There were no statistically significant trends in total PHQ-9 score over time across all groups.
Trends in depression prevalence by individual characteristics
Higher prevalence of depression was associated with increasing age, lower educational attainment, and White race. Those who were married or had private insurance had the lowest depression prevalence within their respective categorical variables. Hispanic ethnicity was associated with lower depression prevalence across the three groups, although the confidence intervals were imprecise for antepartum and postpartum women (Table 3).
Table 3. Depression prevalence (PHQ-9 ≥ 10 or antidepressant prescription) by study group characteristics.
Control | Antepartum | Postpartum | ||||
---|---|---|---|---|---|---|
Counts1 | Weighted %, (95% CI) |
Counts | Weighted %, (95% CI) |
Counts | Weighted %, (95% CI) |
|
Overall | 5412 | 20.2 (18.5-21.9) | 314 | 9.7 (6.3-14.1) | 455 | 12.8 (9.3-17.1) |
Age in Years | ||||||
20-24 | 1002 | 16.5 (13.5-19.9) | 102 | 8.0 (3.2-15.9) | 148 | 13.6 (7.1-22.7) |
25-34 | 2015 | 16.7 (14.7-18.7) | 153 | 9.0 (4.2-16.4) | 230 | 13.4 (7.9-20.8) |
35-39 | 1126 | 23.2 (20.4-26.3) | 45 | 15.5 (4.3-35.6) | 53 | 10.0 (0.5-39.0) |
40-44 | 1269 | 26.5 (22.4-30.9) | 14 | 6.4 (NA) | 24 | 10.1 (NA2) |
Race/Ethnicity | ||||||
Hispanic | 1493 | 14.2 (12.3-16.3) | 101 | 6.8 (2.5-14.3) | 157 | 6.6 (3.0-12.3) |
Non-Hispanic White | 2032 | 23.6 (21.4-25.8) | 89 | 10.3 (4.7-19.0) | 159 | 16.7 (10.6-24.5) |
Non-Hispanic Black | 1151 | 17.1 (14.6-19.8) | 75 | 11.7 (4.4-23.9) | 91 | 10.4 (4.6-19.4) |
Other Race/Multiracial | 736 | 14.3 (10.5-18.7) | 49 | 9.8 (1.5-29.2) | 48 | 7.1 (0.8-24.0) |
Language | ||||||
English | 4776 | 20.9 (19.2-22.6) | 275 | 10.2 (6.6-14.9) | 393 | 13.1 (9.3-17.8) |
Spanish | 636 | 10.9 (8.3-14.0) | 39 | 3.6 (0-31.7) | 62 | 9.7 (2.2-24.8) |
Education Level | ||||||
Less than 9th Grade | 957 | 24.5 (21.0-28.3) | 71 | 16.6 (7.4-30.1) | 100 | 11.9 (5.0-2.7) |
High School | 1022 | 23.3 (19.5-27.5) | 65 | 4.2 (0.6-13.7) | 110 | 21.3 (12.2-33.0) |
Some College or AA Degree | 1989 | 21.3 (18.9-23.9) | 108 | 11.3 (5.1-20.7) | 146 | 14.6 (8.4-23.0) |
College Degree or above | 1443 | 15.3 (12.6-18.4) | 70 | 7.0 (1.7-18.0) | 99 | 3.2 (0.3-11.7) |
Body Mass Index | ||||||
<25 | 1949 | 16.1 (14.2-18.2) | 84 | 4.3 (1.1-10.9) | 144 | 12.4 (5.9-21.9) |
25- < 30 | 1342 | 19.7 (16.8-22.7) | 98 | 10.2 (3.9-20.7) | 130 | 8.1 (3.6-15.1) |
30- < 35 | 967 | 24.2 (20.8-27.9) | 65 | 13.2 (3.2-32.7) | 79 | 11.4 (4.0-24.0) |
≥35 | 1127 | 25.3 (21.9-29.0) | 67 | 11.2 (4.5-22.0) | 102 | 19.5 (8.9-34.8) |
Marital Status | ||||||
Married | 2264 | 16.9 (14.8-19.1) | 170 | 7.1 (3.2-13.2) | 246 | 8.4 (4.3-14.6) |
Widowed | 32 | 45.1 (4.6-92.0) | 0 | NA | 1 | 0 (NA) |
Divorced | 410 | 34.7 (28.6-41.1) | 10 | 33.2 (NA) | 13 | 30.7 (NA) |
Separated | 217 | 39.9 (32.0-48.3) | 9 | 28.9 (NA) | 10 | 17.4 (NA) |
Never Married | 1795 | 18.2 (15.9-20.7) | 67 | 8.9 (2.4-21.6) | 87 | 22.9 (10.6-40.1) |
Living With Partner | 693 | 21.9 (18.2-26.0) | 57 | 15.9 (7.1-29.0) | 98 | 15.2 (6.9-27.5) |
Ratio of Family Income to Poverty Level | ||||||
≤1.3 | 1843 | 26.0 (23.3-28.8) | 109 | 15.7 (8.9-24.9) | 209 | 12.2 (7.1-19.1) |
>1.3-3.5 | 1818 | 19.3 (16.4-22.5) | 99 | 11.8 (4.5-23.8) | 145 | 8.0 (3.3-15.7) |
>3.5 | 1351 | 17.2 (14.7-20.0) | 73 | 2.9 (0.2-12.3) | 74 | 16.6 (5.6-34.5) |
Health Insurance | ||||||
Yes | 3922 | 20.3 (18.5-22.1) | 261 | 9.3 (5.6-14.3) | 343 | 12.7 (8.5-18.1) |
No | 1483 | 19.8 (17.1-22.8) | 53 | 12.4 (3.8-27.8) | 111 | 13.3 (6.1-24.2) |
Health Insurance Type | ||||||
Private | 2770 | 17.6 (15.7-19.8) | 131 | 7.5 (3.1-14.8) | 181 | 8.3 (3.6-15.9) |
Medicaid | 670 | 32.4 (27.3-37.8) | 101 | 9.6 (3.8-19.2) | 117 | 14.3 (6.8-25.2) |
Other Insurance | 461 | 26.3 (21.2-31.9) | 28 | 19.5 (NA) | 44 | 33.6 (10.6-64.5) |
No Insurance | 1485 | 19.9 (17.1-22.8) | 53 | 12.4 (3.8-27.8) | 111 | 13.3 (6.1-24.2) |
1Counts are unweighted. Weighted percentages are shown with 95% confidence intervals (CI).
2NA: Confidence intervals are suppressed for cells with counts less than 30.
After adjusting for these potential confounders in a multivariable regression, antepartum and postpartum women both had lower odds of prevalent depression compared to controls (Table 4; Antepartum: aOR 0.52, 0.33–0.81; Postpartum: aOR 0.67, 0.46–0.99). When the outcome was PHQ-9 ≥ 10 alone, these associations persisted (Antepartum: aOR 0.54, 0.32–0.89, Postpartum: aOR 0.50, 0.28–0.90).
Table 4. Adjusted logistic regression results for primary outcome of depression prevalence.
aOR | Lower 95% CI | Upper 95% CI | p | |
---|---|---|---|---|
Study Group | ||||
Control | Reference | |||
Antepartum | 0.52 | 0.33 | 0.81 | 0.005 |
Postpartum | 0.67 | 0.46 | 0.99 | 0.042 |
Age in Years | ||||
20-24 | Reference | |||
25-34 | 1.17 | 0.91 | 1.51 | 0.224 |
35-39 | 1.78 | 1.36 | 2.34 | <0.001 |
40-44 | 2.12 | 1.59 | 2.83 | <0.001 |
Health Insurance | ||||
Private | Reference | |||
Medicaid | 1.89 | 1.44 | 2.48 | <0.001 |
Other Insurance | 1.67 | 1.26 | 2.21 | <0.001 |
No Insurance | 1.18 | 0.96 | 1.45 | 0.114 |
Race/Ethnicity | ||||
Hispanic | Reference | |||
Non-Hispanic White | 2.46 | 1.99 | 3.03 | <0.001 |
Non-Hispanic Black | 1.21 | 0.95 | 1.54 | 0.119 |
Other Race/Multiracial | 1.38 | 0.96 | 1.97 | 0.081 |
Education Level | ||||
Less than High School | Reference | |||
High School | 0.95 | 0.74 | 1.22 | 0.712 |
Some College | 0.86 | 0.67 | 1.11 | 0.240 |
College or above | 0.58 | 0.44 | 0.77 | <0.001 |
Marital Status | ||||
Married | Reference | |||
Widowed | 2.92 | 1.09 | 7.8 | 0.033 |
Divorced | 2.24 | 1.64 | 3.06 | <0.001 |
Separated | 3.15 | 2.21 | 4.49 | <0.001 |
Never Married | 1.48 | 1.2 | 1.84 | 0.001 |
Living With Partner | 1.56 | 1.21 | 2.02 | 0.001 |
Unweighted sample size for regression is 6,149 participants (32 excluded missing values for one or more variables).
aOR, adjusted odds ratio; CI, confidence interval.
Sensitivity analysis
When antidepressant use was defined using ICD-10 codes for depression available in 2013–2018, lower depression prevalence was observed across all groups. During this period, depression prevalence using the primary outcome was 19.9% (17.6–22.3), 12.2% (6.8–19.8), and 11.5% (6.5–18.3) in the control, antepartum, and postpartum groups, respectively. In the sensitivity analysis, depression prevalence decreased to 16.3% (14.2–18.6), 11.4% (6.2–18.6), and 7.3% (3.7–12.6) in the three groups, respectively (Table 2, bottom panel). Out of the 274 participants with antidepressant prescriptions during this period, 63.5% had an accompanying depression ICD-10 code. In most cases where depression was not coded as the reason for prescription, anxiety disorder was cited.
The relationships between prevalent depression and educational attainment, income, race/ethnicity, and marital status remained the same. Depression prevalence no longer differed substantially by age (S2 Table). In the adjusted regression, postpartum women had lower odds of prevalent depression compared to the control (aOR 0.41, 0.20–0.84), while antepartum women had imprecise odds (aOR 0.71, 0.37–1.36) (S3 Table).
PHQ-9 itemized responses
In the exploratory analysis of item-level PHQ-9 responses from women with prevalent depression (n = 1007 control, n = 33 antepartum, and n = 54 postpartum), the two most common symptoms of depression across study groups were feeling tired or having little energy (85.2%, 81.8%, and 87.0% in control, antepartum, and postpartum women, respectively) and trouble sleeping or sleeping too much (74.3%, 75.6%, 75.3%) (Table 5).
Table 5. PHQ-9 individual item responses by group for women with prevalent depression.
Control | Antepartum | Postpartum | ASD1 | |
---|---|---|---|---|
Unweighted Count w/ Primary Outcome | 1007 | 33 | 54 | |
Have little interest in doing things | 0.407 | |||
Not at all | 37.2 (2.0) | 33.5 (9.9) | 32.8 (8.5) | |
Several days | 35.9 (1.8) | 30.9 (9.6) | 44.7 (9.3) | |
More than half the days | 15.6 (1.2) | 7.8 (6.1) | 14.3 (6.0) | |
Nearly every day | 11.3 (1.3) | 27.7 (9.1) | 8.2 (4.1) | |
Feeling down, depressed, or hopeless | 0.300 | |||
Not at all | 33.6 (2.2) | 20.7 (8.7) | 34.1 (8.7) | |
Several days | 36.3 (1.7) | 36.4 (9.4) | 38.4 (8.4) | |
More than half the days | 14.5 (1.4) | 13.3 (3.6) | 10.5 (3.6) | |
Nearly every day | 15.6 (1.4) | 29.5 (8.4) | 17.0 (6.5) | |
Trouble sleeping or sleeping too much | 0.236 | |||
Not at all | 25.7 (1.7) | 24.4 (10.0) | 24.6 (6.3) | |
Several days | 26.2 (1.4) | 26.7 (8.2) | 21.2 (6.0) | |
More than half the days | 18.4 (1.3) | 11.1 (4.5) | 22.6 (7.1) | |
Nearly every day | 29.7 (2.0) | 37.8 (9.2) | 31.5 (8.2) | |
Feeling tired or having little energy | 0.267 | |||
Not at all | 14.9 (1.4) | 18.2 (9.7) | 11.0 (6.1) | |
Several days | 32.1 (1.6) | 25.5 (7.9) | 34.0 (9.3) | |
More than half the days | 21.1 (1.4) | 12.2 (5.6) | 19.2 (6.4) | |
Nearly every day | 32.0 (1.6) | 44.1 (9.4) | 35.8 (8.2) | |
Poor appetite or overeating | 0.379 | |||
Not at all | 37.2 (2.1) | 35.6 (10.5) | 35.5 (7.8) | |
Several days | 25.6 (1.9) | 18.3 (6.8) | 37.0 (7.1) | |
More than half the days | 17.6 (1.5) | 14.4 (8.3) | 14.8 (6.0) | |
Nearly every day | 19.6 (1.3) | 31.7 (8.9) | 12.7 (5.7) | |
Feeling bad about yourself | 0.457 | |||
Not at all | 42.5 (2.0) | 40.6 (10.4) | 38.4 (8.6) | |
Several days | 28.8 (1.8) | 38.7 (9.7) | 39.1 (8.1) | |
More than half the days | 14.5 (1.2) | 1.9 (1.9) | 15.3 (5.8) | |
Nearly every day | 14.1 (1.3) | 18.8 (7.8) | 7.2 (5.3) | |
Trouble concentrating on things | 0.323 | |||
Not at all | 46.4 (2.3) | 51.2 (9.5) | 39.0 (7.9) | |
Several days | 27.0 (1.9) | 29.0 (7.6) | 29.9 (7.5) | |
More than half the days | 13.7 (1.2) | 4.4 (3.2) | 7.3 (3.8) | |
Nearly every day | 13.0 (1.1) | 15.3 (6.0) | 23.9 (7.5) | |
Moving or speaking slowly or too fast | 0.389 | |||
Not at all | 64.4 (1.6) | 74.7 (7.5) | 60.7 (8.4) | |
Several days | 19.5 (1.3) | 22.2 (7.1) | 26.5 (7.6) | |
More than half the days | 10.3 (1.1) | 0 (0) | 5.9 (3.4) | |
Nearly every day | 5.7 (0.7) | 3.1 (2.2) | 6.8 (3.9) | |
Thoughts you would be better off dead | 0.228 | |||
Not at all | 85.9 (1.4) | 91.0 (3.9) | 89.7 (4.4) | |
Several days | 9.8 (1.2) | 5.1 (2.9) | 9.0 (4.2) | |
More than half the days | 2.5 (0.6) | 2.1 (2.1) | 0 (0) | |
Nearly every day | 1.7 (0.4) | 1.9 (1.9) | 1.2 (1.2) |
Values are weighted percentages (standard error).
1Absolute standardized difference (ASD). Values of 0.2, 0.5, and 0.8 correspond to small, moderate, and large differences between groups.
“Thoughts you would be better off dead” was present in some degree (answers ranging from several days to nearly every day the past two weeks) in 3.7%, 1.7%, and 2.9% of the overall population of control, antepartum, and postpartum women, respectively. In contrast, suicidal ideation was much higher in those with prevalent depression: 14.1%, 9.0%, 10.3%, in the three groups, respectively.
Discussion
In a nationally representative sample of reproductive age women in 2007–2018, we found that the prevalence of depression, defined as PHQ-9 ≥ 10 or current antidepressant prescription, was 20.2% in controls (95% CI 18.5–21.9), 9.7% in antepartum women (6.3–14.1), and 12.8% in postpartum women screened within 12 months of childbirth (9.3–17.1). These differences persisted in adjusted analyses and sensitivity analyses. For those meeting criteria for prevalent depression, control and postpartum groups showed similar rates of antidepressant or mental health care service utilization (70%), while antepartum women had the lowest treatment rate (51%).
No significant temporal trends in depression prevalence were observed across assessment waves, though we lacked statistical power to detect trends in antepartum and postpartum women. Mental health care service utilization increased substantially for postpartum women in the last data cycle (2017–2018). Across both primary and sensitivity analyses, married status was protective against depression for control and postpartum women.
Perinatal women have lower depression prevalence and lower rates of treatment
We found that antepartum and postpartum women had lower rates of depression compared to the control group, even after adjusting for confounding factors. This finding persisted even when examining PHQ-9 ≥ 10 alone, indicating that higher antidepressant use in the control group does not completely explain the findings. Two previous studies that used nationally representative data from 2005–2009 also found higher rates of depression in non-pregnant women compared to pregnant women, but the difference was not statistically significant [33,34]. However, both studies did not distinguish postpartum from non-pregnant, which could have artificially decreased depression prevalence in non-pregnant women. Similar to our study, a cross-sectional study in China found that pregnant women had 77% lower odds of PHQ-9 ≥ 10 than non-pregnant women, although this was specifically during the COVID-19 pandemic [35]. Our findings indicate lower prevalence of depressive symptoms among pregnant and postpartum women compared to non-pregnant controls. The PHQ-9 may not be adequate at screening for depression in perinatal populations, potentially underestimating the depression burden in antepartum and postpartum women [36]. Cohort studies with longitudinal follow-up are needed to explain these findings. Finally, note that most women with postpartum depression experience onset in the early postpartum period, which could lead to an underestimate of PPD prevalence in our sample, given that the average postpartum time in our sample was 6 months [37,38]. However, our prevalence estimates line up with past studies, suggesting instead that PPD identified in our study is unresolved.
Pregnant women with depression used antidepressant or mental health care services less compared with non-pregnant women in our study. Ko et al. found that 50% of pregnant women with prevalent depression reported mental health treatment (defined as prescription medication, counseling, or inpatient care), compared to 54% of non-pregnant women in 2005–2009 [33]. Our more recent data suggest that this treatment gap has widened substantially over time, with treatment rates in pregnant women still at only 51% compared to 70% for non-pregnant women, although we were not powered to see a statistically significant effect (p = 0.051). While most postpartum women are screened for depression at least once after birth, antepartum women do not generally receive screening as part of prenatal care, which could be a factor in treatment rates. Concern around the potential negative effects of maternal antidepressant use on the growing fetus likely also plays a role in lower pharmacological treatment rates [39–41].
Mental health care services increased substantially for postpartum women
We found that mental health care services utilization doubled from less than 10% in previous data cycles to 22% in 2017–2018 for postpartum women. In January 2016, the US Preventive Services Task Force (USPSTF) recommended universal depression screening for pregnant and postpartum women [42]. Additionally, the USPSTF, noting potential harms to the fetus and breastfeeding newborn from antidepressants, encouraged clinicians to consider evidence-based psychosocial treatments, such as cognitive behavioral therapy, as a first-line treatment for perinatal depression. This may have contributed to the increase in mental health services we observed in the ensuing years, but most perinatal women with prevalent depression continued to report antidepressant use without additional mental health care.
Psychological treatments remain far from universally accessible. We found that across all years, utilization of mental health care services in the past 12 months among those with prevalent depression was 34.7%, 26.8%, and 25.6% for control, antepartum, and postpartum women, respectively. In response to the USPSTF guidelines, one article outlines the need for infrastructure changes in health care settings to meet mental health care demands for perinatal women, similar to how obstetric clinics screen for and treat gestational diabetes mellitus [43].
Married women have lower depression prevalence
We found that married women had lower depression prevalence than unmarried women in postpartum and control groups, even after accounting for confounding variables. For many mothers, an intimate partner is the primary source of social support after childbirth. Low levels of social support are one of the predominant risk factors for postpartum depression, and are even more impactful than pregnancy- and delivery-related complications and socioeconomic status [44–49].
Consistent with our findings, previous research has found that mothers in stable marriages have superior physical and mental health compared to unmarried mothers within a year of childbirth, which was not explained by greater socioeconomic resources [49]. A meta-analysis found that lower marital satisfaction and being unmarried are linked to higher rates of postpartum depression [45]. This aligns with the broader narrative around the positive effects of marriage on health outcomes beyond parenthood, including better mental health over the life course [50,51]. Future studies should consider marital status as a proxy for social support, especially in datasets where more precise social support measurements are difficult or impossible to obtain, such as administrative claims data and electronic health records.
Suicidal ideation
We found that suicidal ideation was present in about 10% of perinatal women with prevalent depression, compared to 2–3% of perinatal women in the overall population. We also found high rates of sleep disturbance in our sample, which is an evidence-based risk factor for suicidal behaviors across the lifespan, and associated with postpartum depression [52–54]. Adequate sleep and good self-reported sleep quality are important factors in assessing quality of postpartum recovery [55], and may be a novel opportunity for prevention [52,56]. Given that mental health conditions are now the leading cause of pregnancy-related mortality in the US, future research is critical to enhance novel screening, treatment, and referral strategies that may guide depression and suicide prevention efforts in perinatal women specifically [57].
Limitations and strengths
Limitations included reduced power to analyze trends across time due to small sample sizes of postpartum and pregnant women with prevalent depression per data cycle, and a cross-sectional study design. Future prospective study of epidemiological trends in depression prevalence are recommended to establish temporality between perinatal status and depression onset. Next, our primary analysis defined antidepressant use broadly, allowing for some amount of misclassification given antidepressant medications have other indications, especially in non-perinatal populations. However, in a sensitivity analysis of years that included diagnosis codes for antidepressant prescriptions, our conclusions were similar compared to defining antidepressant use broadly. As an additional limitation, mental health care services were defined dichotomously (yes/no) and over a 12-month period, preventing study of treatment linked to pregnancy or postpartum directly. Given the well-established link between socioeconomic status and depression, we initially planned to adjust for the income-to-poverty ratio from NHANES data. However, because this variable had a relatively high rate of missingness, we used insurance type as a proxy instead. Finally, several measurements were limited to self-report, and key confounding factors, such as a history of mental health conditions and adverse pregnancy and delivery outcomes that increase depression risk, were not collected.
Despite these limitations, our study’s greatest strength is that the participants comprise a socioeconomically, racially, and ethnically diverse group of individuals that are representative of reproductive-age women in the United States. This is the first study to evaluate antepartum and postpartum depression trends in a cohort of women with private and public insurance, increasing the generalizability of our findings. NHANES is known for its comprehensive data collection and rigorous standards, which allow for the analysis of various health indicators with limited information bias. All analyses were pre-registered to limit false positives in our findings.
Conclusion
In conclusion, over a twelve-year period in the US, the prevalence of antepartum depression was 10% and postpartum depression was 13%, both of which were significantly lower compared to depression in reproductive-age women who were neither pregnant nor postpartum (20%). Rates of recent mental health care services doubled in postpartum women over time, perhaps reflecting the impact of USPSTF guidelines on treatment for depression. Married women had significantly lower rates of prevalent depression: marital status may be acting as a proxy for social support, one of the most important predictors of postpartum depression.
Future research should evaluate the causal effect of USPSTF and American College of Obstetrics and Gynecology depression screening guidelines on depression and treatment trends in perinatal populations within the US, particularly whether such guidelines led to meaningful change in mental health services access and uptake and ultimately decreased depressive symptoms for antepartum and postpartum individuals with depression.
Supporting Information
(TIF)
(DOCX)
(DOCX)
(DOCX)
Acknowledgments
The authors thank Dr. Kristin Sainani for editing the manuscript and critically evaluating the statistical analyses and conclusions.
Data Availability
All data files used in this study are publicly available from the National Center for Health Statistics and can be accessed at https://wwwn.cdc.gov/nchs/nhanes/Default.aspx.
Funding Statement
Ms. Gardner's effort was supported by the T32 Training in Advanced Data and Analytics for Behavioral and Social Sciences Research (TADA-BSSR) training grant from the NIH National Heart, Lung, and Blood Institute (grant number 1T32HL1513232). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
References
- 1.Shorey S, Chee CYI, Ng ED, Chan YH, Tam WWS, Chong YS. Prevalence and incidence of postpartum depression among healthy mothers: A systematic review and meta-analysis. J Psychiatr Res. 2018;104:235–48. doi: 10.1016/j.jpsychires.2018.08.001 [DOI] [PubMed] [Google Scholar]
- 2.Dadi AF, Miller ER, Mwanri L. Postnatal depression and its association with adverse infant health outcomes in low- and middle-income countries: a systematic review and meta-analysis. BMC Pregnancy Childbirth. 2020;20(1):416. doi: 10.1186/s12884-020-03092-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Murray L, Fiori-Cowley A, Hooper R, Cooper P. The impact of postnatal depression and associated adversity on early mother-infant interactions and later infant outcome. Child Dev. 1996;67(5):2512–26. doi: 10.2307/1131637 [DOI] [PubMed] [Google Scholar]
- 4.Dias CC, Figueiredo B. Breastfeeding and depression: a systematic review of the literature. J Affect Disord. 2015. Jan 15;171:142–54. doi: 10.1016/j.jad.2014.09.022 [DOI] [PubMed] [Google Scholar]
- 5.Yin X, Sun N, Jiang N, Xu X, Gan Y, Zhang J, et al. Prevalence and associated factors of antenatal depression: Systematic reviews and meta-analyses. Clinical Psychology Review 2021 Feb 1; 83:101932. [DOI] [PubMed]
- 6.Accortt EE, Cheadle ACD, Dunkel Schetter C. Prenatal depression and adverse birth outcomes: an updated systematic review. Matern Child Health J. 2015;19(6):1306–37. doi: 10.1007/s10995-014-1637-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Chin K, Wendt A, Bennett IM, Bhat A. Suicide and Maternal Mortality. Curr Psychiatry Rep. 2022 Apr 1; 24(4):239–75. [DOI] [PMC free article] [PubMed]
- 8.Goldman-Mellor S, Margerison CE. Maternal drug-related death and suicide are leading causes of postpartum death in California. Am J Obstetrics and Gynecology. 2019. Nov 1; 221(5):489.e1–489.e9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Jacques N, de Mola CL, Joseph G, Mesenburg MA, da Silveira MF. Prenatal and postnatal maternal depression and infant hospitalization and mortality in the first year of life: A systematic review and meta-analysis. J Affective Disorders. 2019. Jan 15; 243:201–8. [DOI] [PubMed] [Google Scholar]
- 10.Health (OASH) O of the AS for. Biden-Harris Administration Announces Maternal Mental Health Task Force’s National Strategy to Improve Maternal Mental Health Care Amid Urgent Public Health Crisis [Internet]. 2024. [cited 2024 Oct 17]. Available from: https://www.hhs.gov/about/news/2024/05/14/biden-harris-administration-announces-maternal-mental-health-task-force-national-strategy-improve-maternal-mental-health-care-amid-urgent-public-health-crisis.html [Google Scholar]
- 11.Weinberger AH, Gbedemah M, Martinez AM, Nash D, Galea S, Goodwin RD. Trends in depression prevalence in the USA from 2005 to 2015: widening disparities in vulnerable groups. Psychological Medicine. 2018. Jun;48(8):1308–15. doi: 10.1017/S0033291717002781 [DOI] [PubMed] [Google Scholar]
- 12.Iranpour S, Sabour S, Koohi F, Saadati HM. The trend and pattern of depression prevalence in the U.S.: Data from National Health and Nutrition Examination Survey (NHANES) 2005 to 2016. J Affective Disorders. 2022. Feb 1; 298:508–15. [DOI] [PubMed] [Google Scholar]
- 13.Mojtabai R, Olfson M, Han B. National Trends in the Prevalence and Treatment of Depression in Adolescents and Young Adults. Pediatrics. 2016. Dec 1;138(6):e20161878. doi: 10.1542/peds.2016-1878 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Kuehner C. Gender differences in unipolar depression: an update of epidemiological findings and possible explanations. Acta Psychiatrica Scandinavica. 2003;108(3):163–74. [DOI] [PubMed] [Google Scholar]
- 15.Platt JM, Bates L, Jager J, McLaughlin KA, Keyes KM. Is the US Gender Gap in Depression Changing Over Time? A Meta-Regression. Am J Epidemiol. 2021. Jul 1;190(7):1190–206. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Tabb KM, Dalton VK, Tilea A, Kolenic GE, Admon LK, Hall SV, et al . Trends in antenatal depression and suicidal ideation diagnoses among commercially insured childbearing individuals in the United States, 2008–2018. J Affective Disorders. 2023. Jan 1; 320: 263–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Admon LK, Dalton VK, Kolenic GE, Ettner SL, Tilea A, Haffajee RL, et al. Trends in Suicidality 1 Year Before and After Birth Among Commercially Insured Childbearing Individuals in the United States, 2006-2017. JAMA Psychiatry. 2021. Feb 1; 78(2):171–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Spitzer RL, Kroenke K, Williams JBW, and the Patient Health Questionnaire Primary Care Study Group. Validation and Utility of a Self-report Version of PRIME-MD: The PHQ Primary Care Study. JAMA. 1999. Nov 10; 282(18):1737–44. [DOI] [PubMed] [Google Scholar]
- 19.Centers for Disease Control and Prevention (CDC), National Center for Health Statistics (NCHS). National Health and Nutrition Examination Survey Data. [Internet]. Hyattsville, MD: U.S. Department of Health and Human Services, Centers for Disease Control and Prevention; 2007. [cited 2023 Aug 17]. Available from: https://www.cdc.gov/nchs/ [Google Scholar]
- 20.Wang L, Kroenke K, Stump TE, Monahan PO. Screening for perinatal depression with the Patient Health Questionnaire depression scale (PHQ-9): A systematic review and meta-analysis. General Hospital Psychiatry. 2021. Jan 1; 68(1):74–82. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Gjerdingen D, Crow S, McGovern P, Miner M, Center B. Postpartum Depression Screening at Well-Child Visits: Validity of a 2-Question Screen and the PHQ-9. Ann Family Med. 2009. Jan 1; 7(1):63–70. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Levis B, Benedetti A, Thombs BD. Accuracy of Patient Health Questionnaire-9 (PHQ-9) for screening to detect major depression: individual participant data meta-analysis. BMJ. 2019. Apr 9; 365:l1476. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Slezak J, Sacks D, Chiu V, Avila C, Khadka N, Chen J-C, et al. Identification of Postpartum Depression in Electronic Health Records: Validation in a Large Integrated Health Care System. JMIR Med Inform. 2023. Mar 1;11(1):e43005. doi: 10.2196/43005 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Jimenez-Solem E, Andersen JT, Petersen M, Broedbaek K, Andersen NL, Torp-Pedersen C, et al. Prevalence of antidepressant use during pregnancy in Denmark, a nation-wide cohort study. PLOS ONE. 2013. Apr 25;8(4):e63034. doi: 10.1371/journal.pone.0063034 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Wang Y, Lopez JMS, Bolge SC, Zhu VJ, Stang PE. Depression among people with type 2 diabetes mellitus, US National Health and Nutrition Examination Survey (NHANES), 2005–2012. BMC Psychiatry. 2016. Apr 5; 16(1):88. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Svardal CA, Waldie K, Milne B, Morton SM, D’Souza S. Prevalence of antidepressant use and unmedicated depression in pregnant New Zealand women. Aust N Z J Psychiatry. 2022. May 1;56(5):489–99. [DOI] [PubMed] [Google Scholar]
- 27.Alaimo K, Briefel RR, Frongillo EA, Olson CM. Food insufficiency exists in the United States: results from the third National Health and Nutrition Examination Survey (NHANES III ). Am J Public Health. 1998. Mar;88(3):419–26. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Korn Edward L. Barry I. Confidence intervals for proportions with small expected number of positive counts estimated from survey data. Survey Methodology. 1998; 24:193–201. [Google Scholar]
- 29.National Center for Health Statistics data presentation standards for proportions [Internet]. [cited 2023 Sep 5]. Available from: https://stacks.cdc.gov/view/cdc/47786 [PubMed] [Google Scholar]
- 30.NHANES Tutorials - Weighting Module [Internet]. [cited 2023 Sep 8]. Available from: https://wwwn.cdc.gov/nchs/nhanes/tutorials/Weighting.aspx [Google Scholar]
- 31.Gardner RM, Simard JF. Trends in depression prevalence for pregnant and postpartum women in the United States: Data from the National Health and Nutrition Examination Survey (NHANES) 2007 to 2018 [Internet]. OSF; 2023. Available from: osf.io/fe3w4 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.R Core Team. R: A language and environment for statistical computing [Internet]. Vienna, Austria: R Foundation for Statistical Computing; 2022. Available from: https://www.R-project.org/. [Google Scholar]
- 33.Ko JY, Farr SL, Dietz PM, Robbins CL. Depression and Treatment Among U.S. Pregnant and Nonpregnant Women of Reproductive Age, 2005–2009. J Womens Health (Larchmt) 2012 Aug; 21(8):830–6 [DOI] [PMC free article] [PubMed]
- 34.Ashley JM, Harper BD, Arms-Chavez CJ, LoBello SG. Estimated prevalence of antenatal depression in the US population. Arch Womens Ment Health. 2016. Apr 1; 19(2):395–400. doi: 10.1007/s00737-015-0593-1 [DOI] [PubMed] [Google Scholar]
- 35.Zhou Y, Shi H, Liu Z, Peng S, Wang R, Qi L, et al. The prevalence of psychiatric symptoms of pregnant and non-pregnant women during the COVID-19 epidemic. Transl Psychiatry. 2020. Sep 19; 10:1 1–7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Sultan P, Ando K, Elkhateb R, George RB, Lim G, Carvalho B, et al. Assessment of Patient-Reported Outcome Measures for Maternal Postpartum Depression Using the Consensus-Based Standards for the Selection of Health Measurement Instruments Guideline: A Systematic Review. JAMA Network Open. 2022. Jun 24;5(6):e2214885. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Stowe ZN, Hostetter AL, Newport DJ. The onset of postpartum depression: Implications for clinical screening in obstetrical and primary care. Am J Obstet Gynecol. 2005. Feb 1;192(2):522–6. doi: 10.1016/j.ajog.2004.07.054 [DOI] [PubMed] [Google Scholar]
- 38.Kettunen P, Koistinen E, Hintikka J. Is postpartum depression a homogenous disorder: time of onset, severity, symptoms and hopelessness in relation to the course of depression. BMC Pregnancy Childbirth. 2014. Dec 10;14(1):402. doi: 10.1186/s12884-014-0402-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Williams M, Wooltorton E. Paroxetine (Paxil) and congenital malformations. CMAJ. 2005. Nov 22; 173(11):1320–1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Bérard A, Iessa N, Chaabane S, Muanda FT, Boukhris T, Zhao J-P. The risk of major cardiac malformations associated with paroxetine use during the first trimester of pregnancy: a systematic review and meta-analysis. Br J Clin Pharmacol. 2016;81(4):589–604. doi: 10.1111/bcp.12849 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Huang H, Coleman S, Bridge JA, Yonkers K, Katon W. A meta-analysis of the relationship between antidepressant use in pregnancy and the risk of preterm birth and low birth weight. Gen Hosp Psychiatry. 2014;36(1):13–8. doi: 10.1016/j.genhosppsych.2013.08.002 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Siu AL, and the US Preventive Services Task Force . Screening for Depression in Adults: US Preventive Services Task Force Recommendation Statement. JAMA. 2016. 315(4):380–7. [DOI] [PubMed] [Google Scholar]
- 43.Felder JN. Implementing the USPSTF Recommendations on Prevention of Perinatal Depression-Opportunities and Challenges. JAMA Intern Med. 2019;179(4):467–8. doi: 10.1001/jamainternmed.2018.7729 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Robertson E, Grace S, Wallington T, Stewart DE. Antenatal risk factors for postpartum depression: a synthesis of recent literature. Gen Hosp Psychiatry. 2004;26(4):289–95. doi: 10.1016/j.genhosppsych.2004.02.006 [DOI] [PubMed] [Google Scholar]
- 45.Beck CT. Predictors of Postpartum Depression: An Update. Nurs Res. 2001. Oct;50(5):275. [DOI] [PubMed] [Google Scholar]
- 46.O’hara MW, Swain AM. Rates and risk of postpartum depression—a meta-analysis. Int Rev Psychiatry. 1996;8(1):37–54. doi: 10.3109/09540269609037816 [DOI] [Google Scholar]
- 47.Séguin L, Potvin L, St-Denis M, Loiselle J. Depressive symptoms in the late postpartum among low socioeconomic status women. Birth. 1999;26(3):157–63. doi: 10.1046/j.1523-536x.1999.00157.x [DOI] [PubMed] [Google Scholar]
- 48.Reid KM, Taylor MG. Social support, stress, and maternal postpartum depression: A comparison of supportive relationships. Social Sci Res. 2015. Nov 1; 54: 246–62. [DOI] [PubMed] [Google Scholar]
- 49.Meadows S.O., McLanahan S.S., Brooks-Gunn J. Stability and Change in Family Structure and Maternal Health Trajectories. Am Sociol Rev. 2008. Apr 1;73(2):314–34. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.MARKS NF, LAMBERT JD. Marital Status Continuity and Change Among Young and Midlife Adults: Longitudinal Effects on Psychological Well-Being. J Family Issues. 1998. Nov 1; 19(6):652–86. [Google Scholar]
- 51.Brown SL. The Effect of Union Type on Psychological Well-Being: Depression among Cohabitors versus Marrieds. Journal of Health and Social Behavior. 2000;41(3):241–55. [PubMed] [Google Scholar]
- 52.Bernert RA, Kim JS, Iwata NG, Perlis ML. Sleep Disturbances as an Evidence-Based Suicide Risk Factor. Curr Psychiatry Rep. 2015. Feb 21; 17(3):15. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.Sultan P, Guo N, Kawai M, Barwick FH, Carvalho B, Mackey S, et al. Prevalence and predictors for postpartum sleep disorders: a nationwide analysis. J Matern Fetal Neonatal Med. 2023. Dec 31;36(1):2170749. doi: 10.1080/14767058.2023.2170749 [DOI] [PubMed] [Google Scholar]
- 54.Bernert RA, Turvey CL, Conwell Y, Joiner TE Jr. Association of Poor Subjective Sleep Quality With Risk for Death by Suicide During a 10-Year Period: A Longitudinal, Population-Based Study of Late Life. JAMA Psychiatry. 2014. Oct 1;71(10):1129–37. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Gowin JL, Stoddard J, Doykos TK, Sammel MD, Bernert RA. Sleep Disturbance and Subsequent Suicidal Behaviors in Preadolescence. JAMA Netw Open. 2024. Sep 16;7(9):e2433734. doi: 10.1001/jamanetworkopen.2024.33734 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56.Sultan P, Carvalho B. Postpartum recovery: what does it take to get back to a baseline? Current Opinion in Obstetrics and Gynecology. 2021. Apr; 33(2):86. [DOI] [PubMed] [Google Scholar]
- 57.CDC. Pregnancy-Related Deaths: Data From Maternal Mortality Review Committees in 36 U.S. States, 2017–2019 [Internet]. Maternal Mortality Prevention. 2024. [cited 2024 Jun 10]. Available from: https://www.cdc.gov/maternal-mortality/php/data-research/mmrc-2017-2019.html [Google Scholar]