Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2019 Feb 1.
Published in final edited form as: J Affect Disord. 2017 Nov 21;227:731–738. doi: 10.1016/j.jad.2017.11.091

Factors associated with postpartum depression in women from low socioeconomic level in Argentina: A hierarchical model approach

Diana Pham a, Gabriela Cormick b,c,*, Melissa M Amyx d, Luz Gibbons b, Meitra Doty a, Asia Brown e, Angel Norwood f, Federico M Daray g, Fernando Althabe b, José M Belizán b
PMCID: PMC5805649  NIHMSID: NIHMS922745  PMID: 29179143

Abstract

Purpose

to estimate the prevalence of depression at 4-week postpartum using the Edinburgh postpartum Depression Scale (EPDS) in women who delivered in a public maternity hospital in Argentina.

Methods

This prospective cohort study was carried out from March to August 2016 in northwest Argentina. Eligibility included delivering a singleton live birth 28 weeks of gestational age or over, 18 years or older and resided within 1 hour from the maternity hospital. Women were excluded if they or their newborn were in the intensive care unit. We defined a positive screening as an EPDS score of 10 or higher or a positive response to item 10, which indicates thoughts of self-harm.

Results

A total of 587 women were enrolled and 539 women completed the home visit interview and the EPDS. A total of 167 (31.0%, 95% CI 27.1–35.1) mothers screened positive in the EPDS using a score ≥10 and 99 (18.4%, 95% CI 15.1%–21.6%) using a score ≥13, which indicate increased severity of depressive symptoms. In both cases, the 23 (4.3%) women that responded as having thoughts of self-harm were included.

Conclusion

Nearly a third of women who participated had depressive symptoms at four weeks postpartum in a public hospital in Tucumán, Argentina. Socio-demographic, particularly personal psychiatric history, factors and social and cultural influences can impact results.

Our results highlight the need for improved screening and better diagnostic tool for women with postpartum depression in Argentina and to investigate the impact of postpartum depressive symptoms on women’s health and their families.

Keywords: postpartum depression, Argentina, Edinburgh Postpartum Depression Scale, EPDS

Introduction

Perinatal maternal depression, defined as the onset of a nonpsychotic depressive episode of mild to major severity during pregnancy or the first 12 months postpartum,1, 2 can in turn result in impaired mother-to-child bonding 3, 4, adverse child development 3, and even suicide5 or infanticide.6 Unfortunately, despite its negative impact on maternal and child health, perinatal maternal depression is often under-diagnosed and under-treated.7

Postpartum depression (PPD) is considered one of the most frequent maternal morbidities after delivery, yet the published prevalence rates of PPD are difficult to compare across studies and countries. Initial reports of the World Health Organization described a prevalence of PPD of 10% for high-income countries (HICs) and 15% for low and middle-income countries (LMICs).8 A more recent a systematic review of PPD in 23 LMICs showed a pooled prevalence of 19.0% (15.5 – 23.0).7 However, studies from low to high-income countries show a wide variability that can be attributed to multiple factors such as the time of evaluation, the method of assessment, and the different assessment tools with various cutoff points.9, 10 Several literature reviews regarding PPD have shown that socioeconomic and cultural factors, such as dialects, perception and stigma of mental health and the utilization of a “Western” screening tool in a non-Western community, can also be driving forces for the wide range of PPD prevalence rates.7, 11, 12

Argentina’s healthcare system is comprised of 3 distinct sectors: the labor union, the private, and the public. There are two reported studies estimating PPD, which were conducted in the labor union and private sectors. Mathisen et al. found that 37.2% (27.7–47.7) of the 86 middle-class women interviewed from the labor union sector had depressive symptoms at 6-week postpartum, and the risk factors associated were cesarean section, pregnancy complications, labor complications, multiparity, and incomplete breast feeding.13 Rozic et al. estimated a prevalence of 17.8% (14.4–21.9) of the 398 women from the private sector at 5 days postpartum, and the risk factors included personal history of PPD or depression, maternal age less than 25 years old, tobacco consumption and complications in the newborn.14

It is relevant to provide information regarding the prevalence of PPD in the public sector. The public sector serves about 50% of the population, including those who lack formal work or cannot afford private insurance and are not eligible to receive labor union insurance funds. Women who receive care from the public hospitals are more likely to belong to a lower-middle socioeconomic level and prevalence of PPD in the public sector is expected to be higher due to the increased prevalence of risk factors (lower maternal age, multiparty, lower socioeconomic status (SES), and lesser access to health care).15, 16

Our primary objective is to estimate the prevalence of PPD using the Edinburgh Postpartum Depression Scale (EPDS) at 4-week postpartum in women who delivered in a public maternity hospital in Tucumán, Argentina and to examine the association between PPD and sociodemographic, medical and obstetric factors.

Materials and Methods

Study Design and Participants

This observational prospective cohort study was carried out from March to August 2016 in San Miguel de Tucumán at the Instituto Maternidad Provincial Nuestra Señora de las Mercedes, a public maternity hospital that serves as the referral ward for northwest Argentina with approximately 7,000 deliveries per year.17

Eligible women were those that had delivered a singleton live birth 28 weeks of gestational age or over, were 18 years or older, could provide at least 2 sources of contact information and resided within 1 hour from the maternity hospital. Women were excluded if they were in the intensive care unit (ICU) or had a newborn in the neonatal ICU (NICU) or with congenital abnormalities.

Procedures

Trained research personnel reviewed the Labor and Delivery book Mondays to Saturdays, with the exception of national holidays, to identify eligible candidates and inform them about the study’s objectives. Those agreeing to participate signed a written informed consent and completed a baseline survey. Medical and obstetric factors were collected from the participants’ clinical records.

Approximately four weeks after delivery, a trained social worker conducted a follow-up home visit to complete the survey, including administering the EPDS. Participants were considered lost to follow-up if they could not be located after two home visits and/or three phone calls. Women who screened “positive” or had thoughts of self-harm were then referred to the hospital mental health professional.

Instrument and study variables

Edinburg Postnatal Depression Scale (EPDS)

Our primary outcome was PPD, as measured by the Edinburgh Postnatal Depression Scale (EPDS)18 at 4-week postpartum. The EPDS is a 10-item self-reported questionnaire that measures depressive symptoms in the past 7 days. Each item is scored on a 4-point scale (0–3), with higher scores reflecting increasing severity of depressive symptoms. We defined a positive screening of PPD as an EPDS score of 10 or higher or a positive response to item 10, which indicates thoughts of self-harm. This definition was used in the two previous studies in Argentina, which permits their comparison with our results.7,11 The EPDS version validated in Chile showed that a cutoff point of 10 or 11 has a good accuracy; however, we also report the cutoff point of 13 or higher, as the EPDS accuracy was maximized with a cutoff point of 12 or 13.19, 20

The 4-week postpartum follow-up was chosen based on the DSM-V definition (Diagnostic and Statistical Manual of Mental Disorders) of the postpartum period. A study by Cox et al also demonstrated a threefold increase in the rate of onset of depression one month after delivery.21

Baseline characteristics

Self-reported variables collected at baseline included sociodemographic characteristics (education, birthplace, occupation, and with whom the mother lives), self-reported maternal and familial psychiatric history, family planning22, and pregnancy birth experience (hospitalization during pregnancy, if the woman heard her baby’s first cry at delivery and skin to skin contact with the mother).

Information extracted from clinical records included: gestational history, history of chronic diseases, first prenatal screening, number of prenatal visits, complications during pregnancy, delivery mode and indications for cesarean delivery, Apgar scores, newborn resuscitation requirements, gestational age at birth, birth weight and sex of the baby.

Postpartum Experience at 4 weeks

Data collected regarding maternal experience after birth included: help with the baby’s care, breastfeeding, complications with the baby or the mother immediately after delivery or after discharge, and experience of disrespect from a healthcare professional during delivery (defined as someone who made ironic, disqualifying or sarcastic comments to the woman or if the way the woman was attended to make her feel vulnerable, guilty or insecure).

Statistical Analysis

Sample Size

Taking into account a prior Argentine study 14 which found a prevalence of PPD of 17.8%, we determined the sample size required to estimate the prevalence of PPD with a desired precision of 5% at alpha=0.05 was 227 women. However, due to our strong interest in the secondary outcome of assessing the relationship between sociodemographic, medical and obstetric factors and PPD, we increased the sample size to have sufficient power to address this objective. A total of 516 participants was required to include in a multivariate model up to four factors described to be associated with PPD (age, education, parity and history of depression) with a power of 80%. After adjusting for potential loss to follow up (10%), we targeted a sample size of 570 participants. (http://sampsize.sourceforge.net/iface/).

Data Analysis

A descriptive analysis of the maternal characteristics was performed and the absolute number and proportion were calculated. The prevalence of PPD and its precision (reported as 95% Confidencial Interval [CI]) was determined. Next, a bivariate analysis was performed to examine the relationship between PPD and covariates of interest; for each covariate category, the number and proportion of women with PPD was reported. Subsequently, crude odds ratios (ORs) and 95% CIs were computed to measure the association between PPD and each covariate.

Finally, we conducted a multivariate analysis using hierarchical modeling following the recommendations about the design. 23 This conceptual hierarchical framework was constructed using knowledge of the demographic and biological determinants of PPD looking for an explanatory or causal model. The relationship between PPD and the study variables was conceptually based on a theoretical hierarchical model designed by the study investigators (see Figure 2). 20 According to this model, socio-demographic data in the first level may directly or indirectly determine all the other factors under study. The second hierarchical level comprised maternal medical history and maternal and familial psychiatric history, which can be partially explained by socio-demographic factors. The third level includes maternal medical data of the current pregnancy and the fourth level combines the experience of hospital stay and newborn data. At the last level, the postpartum experience until 4 weeks may be affected by preceding variables, and directly influence PPD.

Figure 2.

Figure 2

Hierarchical Model explaining the relationship between the study variables and Postpartum Depression

We considered determinants of PPD to be those variables that showed a statistically significant association (p<0.05) with PPD in each respective level of the hierarchical model. In the first step all variables were entered and all statistically significant variables were kept. The variables in the second level were then added keeping only those that were significant. A similar procedure was repeated for the variables for the other levels. The reported crude ORs were those corresponding to the level in which the risk factor of interest was first entered, and the adjusted ORs were those corresponding to the final full model with all the variables.

Data was entered in the REDCap Software, Version 6.5.20 and analysis was performed using SAS 9.3. P-value <0.05 was considered statistically significant.

Ethics

The protocol, study instruments and informed consents were approved by the ethics committee of the University of North Carolina at Chapel Hill (Chapel Hill, NC, USA) and the local ethics committee, El Centro de Educación Médica e Investigaciones Clínicas (CEMIC; Buenos Aires, Argentina).

Results

1042 women were screened consecutively from the Labor and Delivery book and 706 were classified as potentially eligible (see Figure 1). However, 119 were further excluded as they could not provide two sources of contact information (n=1), lived more than 1 hour from the maternity hospital (n=42), were discharged from the maternity before study personnel could invite them (n=5), refused (n=10), were unable to be located (n=53), or were not invited because the desired sampled size had been reached (n=8). A total of 587 women were enrolled in the study and 559 women completed the home visit interview (95.9% follow-up rate). Of the 28 women lost to follow up, 4 dropped out of the study, 6 moved outside the city and 18 could not be located. Twenty additional women were excluded due to incomplete outcome data, leaving a total of 539 participants for analysis.

Figure 1.

Figure 1

Flow Diagram

Participant characteristics are described in Table 1. Most participants had at least started (n=176, 32.7%) or completed secondary education or higher (n=237, 44.1%). All but 4 participants (0.7%) were born in Argentina. The majority had a stable partner (n=388, 72.0%), were housewives (n=459, 85.2%) and lived with a partner (n=231, 42.9%) while about a third lived with parents (n=194, 36.0%). Most women reported not suffering from chronic diseases (n=478, 88.7%). Regarding maternal psychiatric history, 15.4% (n=83) self-reported family history of depression and 11.9% (n=64) a personal history of depression. Almost half of pregnancies were reported as unwanted or mistimed. Most women had their first prenatal visit during the first trimester (n=445, 84.3%) and had more than four prenatal visits (n=443, 89.1%). 28.8% (n=155) reported experiencing some complications during pregnancy while 44.3% (n=239) of deliveries were by Cesarean-section.

Table 1.

Sociodemographic characteristics, maternal medical, psychiatric and obstetric history

Variables n (%)
Maternal Age (years)
 18 - less than 20 63/539 (11.7%)
 20 – less than 35 429/539 (79.6%)
 ≥ 35 47/539 (8.7%)
Level of Education
 Incomplete primary 31/538 (5.8%)
 Complete Primary 94/538 (17.5%)
 Incomplete Secondary 176/538 (32.7%)
 Complete Secondary or more 237/538 (44.1%)
Nationality
 Argentina 535/539 (99.3%)
 Others 4/539 (0.7%)
Marital Status
 Married 63/539 (11.7%)
 With a stable partner 388/539 (72.0%)
 Single/separated 88/539 (16.3%)
Occupation
 Housewife 459/539 (85.2%)
 Student 32/539 (5.9%)
 Dependent Job 23/539 (4.3%)
 Independent Job 25/539 (4.6%)
Live with:
 Alone 1/539 (0.2%)
 With partner (with or without kids) 231/539 (42.9%)
 With parents (with or without others) 194/539 (36.0%)
 Others 113/539 (21.0%)
Total number of previous births
 0 176/539 (32.7%)
 1–2 276/539 (51.2%)
 More than 2 87/539 (16.1%)
Chronic Disease
 Yes 61/539 (11.3%)
 No 478/539 (88.7%)
History of Depression
 Yes 64/539 (11.9%)
 No 475/539 (88.1%)
History of Depression in Previous Pregnancies
 Yes 38/536 (7.1%)
 No 498/536 (92.9%)
History of Postpartum Depression
 Yes 37/537 (6.9%)
 No 500/537 (93.1%)
Family History of Depression
 Yes 83/538 (15.4%)
 No 455/538 (84.6%)
Family History of Psychiatric Illness
 Yes 37/539 (6.9%)
 No 502/539 (93.1%)
Planned Pregnancy
 Intended 252/539 (46.8%)
 Mistimed 51/539 (9.5%)
 Unwanted 236/539 (43.8%)
Complications during pregnancy *
 Yes 155/539 (28.8%)
 No 384/539 (71.2%)
Type of Delivery
 Vaginal Delivery 300/539 (55.7%)
 C-Section 239/539 (44.3%)
*

Threat of premature birth, anemia, urinary tract infection.

A total of 167 (31.0%, 95% CI 27.1–35.1) mothers screened positive on the EPDS using a score ≥10 and 99 (18.4%, 95% CI 15.1%–21.6%) using a score ≥13, which indicates increased severity of depressive symptoms. In both cases, the 23 (4.3%) women that responded having thoughts of self-harm were included. The results of the EPDS by item are shown in Table 2.

Table 2.

Edinburg Postnatal Depression Scale - EPDS

Outcome Outcome (Edinburg Postnatal Depression Scale - EPDS): Number of women reporting positive for each idem *
n (%)
1 I have been able to laugh and see the funny side of things 55 (10.2)
2 I have looked forward with enjoyment to things 29 (5.4)
3 I have blamed myself unnecessarily when things went wrong 279 (51.8)
4 I have been anxious or worried for no good reason 273 (50.6)
5 I have felt scared or panicky for no very good reason 192 (35.6)
6 Things have been getting on top of me 230 (42.7)
7 I have been so unhappy that I have had difficulty sleeping 159 (29.5)
8 I have felt sad or miserable 89 (16.5)
9 I have felt sad or miserable that I have been crying 70 (13.0)
10 The thought of harming myself has occurred to me 23 (4.3)
*

Scoring 2 or 3 for that question.

Looking at socio-demographic variables, PPD was inversely related to education level. Women with incomplete primary (OR 2.43, 95% CI 1.13–5.22) or complete primary (OR 2.28, 95% CI 1.38–3.77) were more likely to develop PPD compared to women with higher levels of education. Women reporting being housewives were most likely to have PPD symptoms (OR 3.40, 95% CI 1.17–9.86). Maternal age, marital status, living alone or accompanied were not associated with PPD (Table 3).

Table 3.

Variables significantly associated with Postpartum Depression.

PPD (%) Cases/Total
Crude OR P-Value OR Adjusted 1 P-Value
Level 1. Sociodemographic Data
Level of Education
  Incomplete primary 14/31 (45.2%) 2.43 (1.13–5.22) 0.023 2.43 (1.13–5.22) 0.023
  Complete Primary 41/94 (43.6%) 2.28 (1.38–3.77) 0.0013 2.28 (1.38–3.77) 0.0013
  Incomplete Secondary 51/176 (29.0%) 1.20 (0.78–1.86) 0.407 1.20 (0.78–1.86) 0.407
  Complete Secondary or more 60/237 (25.3%) 1 - 1.00a -
Occupation
  Housewife 150/459 (32.7%) 3.40 (1.17–9.86) 0.0245
  Student 4/32 (12.5%) 1 -
  Dependent Job 8/23 (34.8%) 3.73 (0.96–14.5) 0.0566
  Independent Job 5/25 (20.0%) 1.75 (0.42–7.34) 0.4447
LEVEL 2. Maternal Medical History
Total number of previous births
  0 42/176 (23.9%) 1 - 1.00b -
  1–2 88/276 (31.9%) 1.49 (0.97–2.29) 0.0671 1.36 (0.87–2.12) 0.1768
  More than 2 37/87 (42.5%) 2.36 (1.36–4.09) 0.0021 1.79 (1.00–3.22) 0.0515
Maternal and Familial Psychiatric History
History of Depression
  Yes 39/64 (60.9%) 4.23 (2.46–7.27) <0.0001 3.78 (2.16–6.59) <0.0001
  No 128/475 (26.9%) 1 - 1.00b -
History of Depression in Previous Pregnancies
  Yes 23/46 (50.0%) 2.22 (1.19–4.14) 0.012
  No 104/335 (31.0%) 1 -
Family History of Depression
  Yes 35/83 (42.2%) 1.78 (1.10–2.88) 0.0181
  No 132/455 (29.0%) 1 -
Family History of Psychiatric Illness
  Yes 17/37 (45.9%) 1.99 (1.02–3.91) 0.0447
  No 150/502 (29.9%) 1 -
LEVEL 4. Experience of Hospital stay
Made ironic, disqualifying or joking comments
  Yes 14/24 (58.3%) 3.32 (1.45–7.65) 0.0047 2.91 (1.15–7.36) 0.0236
  No 152/513 (29.6%) 1 - 1.00c -
Feelings of vulnerability, guiltiness or insecurity
  Yes 25/44 (56.8%) 3.26 (1.74–6.11) 0.0002 3.21 (1.62–6.37) 0.0009
  No 142/494 (28.7%) 1 - 1.00c -
Recent Newborn Data (LEVEL 4)
Sex
  Male 74/281 (26.3%) 1 - 1.00c -
  Female 90/251 (35.9%) 1.56 (1.08–2.26) 0.0179 1.60 (1.07–2.38) 0.0209
LEVEL 5. Postpartum Experience until 4 weeks
Help with Baby Care
 With no help 28/53 (52.8%) 3.97 (1.96–8.02) 0.0001 3.54 (1.62–7.74) 0.0016
 With help from only partner 48/151 (31.8%) 1.65 (0.94–2.91) 0.0838 1.70 (0.90 –3.18) 0.0997
 With help from only mother 27/73 (37.0%) 2.08 (1.08–4.01) 0.0289 2.36 (1.15–4.87) 0.0199
 With help only from partner and mother 24/109 (22.0%) 1 - 1.00d -
 Help from other 40/153 (26.1%) 1.25 (0.70–2.24) 0.4441 1.23 (0.65–2.34) 0.5246
1

OR Adjusted by all variables in the same level.

Women with more than 2 previous births had a higher risk of PPD when compared to women with no previous births (OR 2.36, 95% CI 1.36–4.09). Women reporting a personal history of depression (OR 4.23, 95% CI 2.46–7.27), history of depression in previous pregnancies (OR 2.22, 95% CI 1.1–4.14), family history of depression (OR 1.78, 95% CI 1.1–2.88) or family history of psychiatric illness (OR 1.99, 95% CI 1.02–3.91) were shown to have an increased risk for PPD.

History of previous abortions, or variables related to the current pregnancy such as unwanted or unintended pregnancy, gestational age at first prenatal visit, number of prenatal checks or complications during pregnancy showed no significant association with PPD in the bivariate analysis.

Regarding the hospital experience, women who reported a negative interaction with their healthcare professional (OR 3.32, 95% CI 1.45–7.65) or felt vulnerable, guilty or insecure during their delivery (OR 3.26, 95% CI 1.74–6.11) had a significantly higher risk of PPD in the bivariate model.

Giving birth to a female newborn was significant positive association with PPD (OR 1.56, 95% CI 1.08–2.26). Women who reported receiving no help with baby care and women who reported receiving help from only her mother were most likely to have PPD when compared to women with help from both her partner and her mother (OR 3.97, 95% CI 1.96–8.02 and OR 2.08, 95% 1.08–4.01, respectively). Breastfeeding or complications of the newborn or the mother after discharge showed no association with PPD.

Results of the hierarchical model are shown in Table 3. Education was the only variable from the first level that remained significantly associated to PPD and was kept in the model. When variables from the second level were added, number of previous births (OR 1.79, 95% CI 1.00–3.22) and maternal history of depression (OR 3.78, 95% CI 2.16–6.59) remained significant. In the third level, perceived negative comments (OR 2.91, 95% CI 1.15–7.36), feelings of insecurity (OR 3.21, 95% CI 1.62–6.37), and having a female newborn (OR 1.60, 95% CI 1.07–2.38) remained significant.

Discussion

We found that the prevalence of PPD was 31.0% (95% CI 27.1–35.1) and 18.4% (95% CI 15.1%–21.6%), using the cutoff score ≥ 10 and ≥13, respectively. The analysis from the hierarchical model showed that lower education level, higher parity, personal history of depression, perceived negative interaction with health care professionals, or feelings of vulnerability or insecurity at delivering, having a female newborn, or lacking childcare help were risk factors for screening positive for PPD.

Maternal depression is one of the major contributors of pregnancy-related morbidity and mortality. Despite its enormous burden, maternal depression in LMICs remains under-recognized and under-treated.24 Considering a cut-off of 10 our study found a higher prevalence than the recent systematic review in 23 LMICs, however, using the cutoff point of 13 or higher, the PPD prevalence is similar.25 The systematic review included studies using different depression scales including the Patient Health Questionare-9 (PHQ-9), the Beck Depression Inventory II (BDI-II), the Mini International Neuropsychiatric Interview (MINI) and the EPDS among others, that measure different factors of depressive symptoms.26 Moreover, studies using the EPDS report different cutoff points, even within the same country27, 28 leading to different prevalence of depressive symptoms. Additionally, the population used in the studies included in the review varied. As one of the main determinants of PPD symptoms is socioeconomic status; the way the sample is selected can lead to different prevalence values. Our aim was to determine the prevalence of PPD in the public sector, and therefore, higher levels of PPD were expected.

A cutoff point of 10, though it increased the false positive rate enabled comparison with the two previous studies in Argentina. In the Rozic et al study. PPD prevalence in the private sector measured at 5 days postpartum is lower than that reported in our study.14 These differences could be explained by their shorter time frame to assess PPD, when higher risk of PPD is between 4 and 5 weeks; and a sample with more than 97% of women with >12 years of education, reflecting a higher socio-economic status. Mathisen et al. reported that 37.2% (27.7–47.7) of middle-class women had depressive symptoms at 6-week postpartum that are within the range described in our study.13 While previous studies evaluated PPD at the health facilities, we chose to administer the EPDS outside the hospital to control for courtesy bias; however, we had difficulty limiting the influence of a family member, potentially exaggerating or minimizing the respondent’s psychiatric symptoms.18

Consistent with the epidemiological literature, we observed that a low educational level was associated with a higher prevalence of PPD. 8, 29 The same association has been described in the general population in Argentina.30 The relationship between education and depression is poorly understood. Education may influence the subjective experience, self-awareness or the acceptance of depressive feelings, and therefore delay disclosure of psychiatric symptoms and help seeking behaviors.31 Moreover, education combined with other socio-economic factors may also modulate the maturation of specific brain regions involved in mood disorders, such as the prefrontal cortex.32

A review of the prevalence of self-harming thoughts using the EDPS found a range between 4% and 15.4 %.33 In our study, 23 (4.3%) women responded as having thoughts of self-harm, which is within the range reported in the literature. Although it is a single item within the scale, which may or may not reflect intention to die, it could be useful to develop new studies exploring other dimensions of suicidal behavior during the postpartum period. Women with postpartum psychiatric disorders present approximately four times higher mortality rate ratios when compared to mothers with no previous psychiatric history and suicide is one of the main unnatural causes of death in this vulnerable group, especially during the first year after diagnosis.34 To develop a comprehensive prevention strategy for suicide, the first step is the identification of high-risk groups and precipitating factors that lead to attempted or completed suicide. One of the strongest predictors of suicide attempt and completion is the presence of suicidal ideation.35 Therefore, identifying individuals who endorse suicidal ideation presents an important opportunity for directing suicide prevention efforts to those at highest risk.

The relationship between number of previous birth and PPD is controversial. Most studies reported an association between multiparity and PPD,36, 37 others showed no association, 38 while some found primiparous were at higher risk.39 In the present study, we found a positive association between higher parity and the risk of PPD. This could reflect higher care burden and psychological stress. Similar results have been observed in the previous study in the labor union sector in Argentina. 13

An association between PPD and personal history of a previous depressive episode has been described before.9, 40, 41 Accordingly, we observed that personal history of depression had the strongest association with developing depressive symptoms by a factor of 4 in comparison with mothers without personal history of depression. This could reflect an interaction between psychiatric vulnerability and pregnancy as a stressor leading to acute depression during the postpartum period. The personal history of depression could be useful to identify women at high risk of PPD.

In the present study, women who received no help with baby care were at highest risk of postpartum depression. The association between lack of social support and PPD has been previously reported by studies from both developing and developed countries.42, 43 These studies have shown that social support plays a buffering role from stressful life events by providing resources, support and strength during pregnancy.

In some Asian cultures such as China and India there is preference for a first-born male child 44 and this gender preference has been reported to be stressful for the mothers giving birth to a female child.45 In the present study having a female newborn also presented a risk for PPD. This finding was unexpected since there are no reports in Argentina about gender preference.

From our study, we observed how educational level, multi-parity, history of psychiatric illnesses, negative experience during pregnancy and labor, newborn gender and social support can influence the development of PPD in Tucuman mothers. While the focus of this study was to examine the social and cultural factors associated with developing PPD, there has been increasing evidence that hormonal changes during and after pregnancy can make women more susceptible to developing PPD.46, 47 In our study sample, women at risk for postpartum depression may have been more vulnerable to the effects of hormonal changes than their non-depressed counterparts and that their social circumstances triggered their susceptibility for having depressive symptoms. Future studies can further evaluate and analyze the influence of hormonal changes around delivery as a marker for developing PPD.48 In summary, pregnancy is a major life event that is inevitably accompanied by social, psychological and biological changes49 and these changes can trigger depressive episodes with serious implications for both maternal and infant outcomes.50, 51, 52

Strengths and Weaknesses

We minimized potential selection bias by conducting a consecutive cohort study where all eligible women were invited to enroll. We achieved a high response rate by administering the EPDS at the participants’ homes. Thus, our study sample is more representative than if we had conducted the follow-up at a postpartum clinic visit because it would potentially underrepresent mothers who may not have access to attend their postpartum checkup. One limitation of the study is that we excluded women with severe health complication or adverse neonatal outcomes as it is known to increase risk of PPD 53, 54 and we only recruited women who lived less than 1 hour away from the capital city, excluding mothers from rural areas, who may be poorer and have less access to health care. Another limitation of this study is no data was collected about different substances of abuse like nicotine, alcohol or other hard drugs. A further limitation is that we did not collect the data about the pharmacological lifetime, recent history of antidepressants use or data of bipolarity that would provide the prevalence of women with diagnosis and treatment of depression.

The EPDS has been widely accepted as a useful and quick screening tool for PPD due to its ease of use and has been validated across different cultures and languages. 55,56,57,58 However, it must be emphasized that the EPDS is not a diagnostic tool and it can overestimate the prevalence of PPD in comparison to well-structured interview-based methods.9, 59, 60 Comparing the available validated Spanish versions, we adopted the Chilean version with 100% sensitivity, 80% specificity and 37% positive predictive value (cutoff score ≥ 10). The Chilean version is applicable for middle- and working-class women, the language is most similar to that of Argentina, and the previous studies in Argentina had used this version as well.13, 14, 19, 61

While this allows comparing the results, subtle language differences were noted and even though they were addressed at the interviews, this could lead to misinterpretation, potentially affecting the results.

We found that demeaning comments made by a healthcare professional or feelings of vulnerability, guiltiness or insecurity in the mother were associated with reporting symptoms of PPD. Questions regarding the inter-relationship with healthcare provider or the amount of childcare support received was based on the woman’s perception. In other words, people with depression are more likely to perceive their relationship with others or their level of support more negatively compared to their non-depressed counterparts.62 Our method of measuring support was over-simplified. We did not measure social support as a multi-dimensional construct, as the mother may be receiving other types of support, such as informational, financial or emotional.

Conclusion

Our prospective cohort study shows that nearly a third of women had depressive symptoms at four weeks postpartum in a public hospital in Tucumán, Argentina and further revealed that socio-demographic factors, particularly personal psychiatric history, and social and cultural influences can impact results. Due to the limited evidence in Argentina, our results highlight the need for improved screening and a better diagnostic tool for women with PPD. In addition, it would be prudent to further investigate the impact of postpartum depressive symptoms and measure the burden on women’s health and their families. The impact of improved provider and patient inter-relationship on PPD should be further explored. A formal validated version of the EPDS in Argentina is warranted to determine the appropriate language and threshold score. Future studies including hospitals from different regions of the country are also needed in order to estimate the prevalence of PPD in Argentina and to further elucidate potential risk factors in order to aid future community interventions to prevent and treat PPD.

Highlights.

  • At four weeks postpartum, a total of 167 (31.0%, 95% CI 27.1–35.1) mothers screened positive in the Edinburgh Postpartum Depression Scale using a score >10, in a public hospital in Tucumán, Argentina.

  • 23 (4.3%) women that responded as having thoughts of self-harm were included.

  • There is a need for improved screening and better diagnostic tool for women with postpartum depression in Argentina.

Acknowledgments

The authors wish to thank the contribution of the Instituto de Ginecología y Obstetricia Nuestra Señora de las Mercedes in Tucumán, the research assistants, Sebastian Diaz and Valeria Bosio, El Centro de Educación Médica e Investigaciones Clínicas, and Instituto de Efectividad Clinica y Sanitaria. We would also like to express personal gratitude to the Tucuman community, especially the social workers including Adriana Diaz, Belén Villarreal, Luciana Villareal, Ana Silvia Naharro, Ayelén Villareal, Pablo Palavecino, Franco Lobo, Irma Diaz and Maria Soledad Diaz for their dedication in finding the study participants as well as providing us local insight into their culture. We would also like to thank Dr. Benjamin Chi for his guidance throughout the entire process—from IRB approval to finalizing the manuscript. I would also like to give a personal thank you to Dr. Johnson for being a part of my thesis committee and Joyce Chen and Ben Sutton for assisting me during the editing stage.

Funding source

This project was supported by NIH Research Training Grant Number R25 TW009340 funded by the Fogarty International Center, the NIH Office of the Director Office of AIDS Research, the NIH Office of the Director Office of Research on Women’s Health, the NIH Office of the Director Office of Behavioral and Social Science Research, the National Cancer Institute, and the National Heart, Lung and Blood Institute and by the Grant Number T37MD001424 from the National Center for Minority Health and Health Disparities (NCMHD).

Footnotes

Authors’ contributions

DP, MD, JB and FA conceived the idea of the study. DP, GC, JB, FA, MD and MA participated in its design and DP, GC, AB and AN were involved in the coordination. DP, GC wrote the first draft of the manuscript. MA, FD helped to draft the manuscript. LG, FD performed the analysis. All authors reviewed, made contributions and approved the final manuscript.

Conflict of interests

The authors declare that they have no conflict of interests.

Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

References

  • 1.Gavin NI, Gaynes BN, Lohr KN, Meltzer-Brody S, Gartlehner G, Swinson T. Perinatal depression: a systematic review of prevalence and incidence. Obstet Gynecol. 2005;106:1071–83. doi: 10.1097/01.AOG.0000183597.31630.db. [DOI] [PubMed] [Google Scholar]
  • 2.Depressive Disorders, in Diagnostic and Statistical Manual of Mental Disorders. 5. Washington DC: American Psychitric Association; 2013. [Google Scholar]
  • 3.Beck CT. The effects of postpartum depression on child development: a meta-analysis. Arch Psychiatr Nurs. 1998;12:12–20. doi: 10.1016/s0883-9417(98)80004-6. [DOI] [PubMed] [Google Scholar]
  • 4.Stein A, Gath DH, Bucher J, Bond A, Day A, Cooper PJ. The relationship between post-natal depression and mother-child interaction. Br J Psychiatry. 1991;158:46–52. doi: 10.1192/bjp.158.1.46. [DOI] [PubMed] [Google Scholar]
  • 5.Tabb KM, Gavin AR, Guo Y, Huang H, Debiec K, Katon W. Views and experiences of suicidal ideation during pregnancy and the postpartum: findings from interviews with maternal care clinic patients. Women Health. 2013;53:519–35. doi: 10.1080/03630242.2013.804024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Barr JA, Beck CT. Infanticide secrets: qualitative study on postpartum depression. Can Fam Physician. 2008;54:1716–1717. e5. [PMC free article] [PubMed] [Google Scholar]
  • 7.Gelaye B, Rondon MB, Araya R, Williams MA. Epidemiology of maternal depression, risk factors, and child outcomes in low-income and middle-income countries. Lancet Psychiatry. 2016;3:973–982. doi: 10.1016/S2215-0366(16)30284-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Fisher J, Cabral de Mello M, Patel V, Rahman A, Tran T, Holton S, Holmes W. Prevalence and determinants of common perinatal mental disorders in women in low- and lower-middle-income countries: a systematic review. Bull World Health Organ. 2012;90:139G–149G. doi: 10.2471/BLT.11.091850. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Halbreich U, Karkun S. Cross-cultural and social diversity of prevalence of postpartum depression and depressive symptoms. J Affect Disord. 2006;91:97–111. doi: 10.1016/j.jad.2005.12.051. [DOI] [PubMed] [Google Scholar]
  • 10.O’Hara MW, Swain AM. Rates and risk of postpartum depression -- a meta-analysis. Int Rev Psyciatry. 1996;8:37–54. [Google Scholar]
  • 11.Zubaran C, Schumacher M, Roxo MR, Foresti K. Screening tools for postpartum depression: validity and cultural dimensions. Afr J Psychiatry (Johannesbg) 2010;13:357–65. doi: 10.4314/ajpsy.v13i5.63101. [DOI] [PubMed] [Google Scholar]
  • 12.Bashiri N, Spielvogel AM. Postpartum depression: a cross-cultural perspective. Primary Care Update for OB/GYNS. 1999;6:82–87. [Google Scholar]
  • 13.Mathisen SE, Glavin K, Lien L, Lagerløv P. Prevalence and risk factors for postpartum depressive symptoms in Argentina: a cross-sectional study. Int J Womens Health. 2013;21(5):787–93. doi: 10.2147/IJWH.S51436. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Rozic PR, Schvartzman JA, Paolini CI, Gadow A, Calvo DA, Paesani F, Pieczanski P, Vázquez GH, Lolich M, Krupitzki HB. Screening for symptoms of depression during postpartum and the long term follow up: temporal stability and associated factors. Vertex. 2012;23:409–17. Spanish. [PubMed] [Google Scholar]
  • 15.Argentina. Instituto Nacional de Estadística y Censos. Censo nacional de población, hogares y viviendas 2010: censo del Bicentenario: resultados definitivos, Serie B no 2. 1. Vol. 1. Buenos Aires: Instituto Nacional de Estadística y Censos - INDEC; 2012. [Accessed August 8, 2017]. pp. 378pp. 23–32. www.indec.gob.ar/ftp/cuadros/poblacion/censo2010_tomo1.pdf. [Google Scholar]
  • 16.Schwarcz A, Karolinski A, Jaquenod M. Encuesta Perinatal 2008: Resultados en Hospitales Públicos de la Provincia de Buenos Aires y Ciudad Autónoma de Buenos Aires. [Accessed August 8, 2017];Ministerio de Salud de la Provincia de Buenos Aires. 2008 salud.ciee.flacso.org.ar/files/flacso/AMBA/pdf/
  • 17.Cormick G, Ciganda A, Cafferata ML, Ripple MJ, Sosa-Estani S, Buekens P, Belizán JM, Althabe F. Text message interventions for follow up of infants born to mothers positive for Chagas disease in Tucumán, Argentina: a feasibility study. BMC Res Notes. 2015;29:508. doi: 10.1186/s13104-015-1498-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Cox JL, Holden JM, Sagovsky R. Detection of postnatal depression. Development of the 10-item Edinburgh Postnatal Depression Scale. Br J Psychiatry. 1987;150:782–6. doi: 10.1192/bjp.150.6.782. [DOI] [PubMed] [Google Scholar]
  • 19.Alvarado R, Jadresic E, Guajardo V, Rojas G. First validation of a Spanish-translated version of the Edinburgh postnatal depression scale (EPDS) for use in pregnant women. A Chilean study. Arch Womens Ment Health. 2015;18:607–12. doi: 10.1007/s00737-014-0466-z. [DOI] [PubMed] [Google Scholar]
  • 20.Victora CG, Fuchs SC, Flores JA, Fonseca W, Kirkwood B. Risk factors for pneumonia among children in a Brazilian metropolitan area. Pediatrics. 1994;93:977–85. [PubMed] [Google Scholar]
  • 21.Cox JL, Chapman G. A controlled Study of the Onset, Duration and Prevalence of Postnatal Depression. Br J Psychiatry. 1993;163:27–31. doi: 10.1192/bjp.163.1.27. [DOI] [PubMed] [Google Scholar]
  • 22.Mosher WD, Jones J, Abma JC. Intended and unintended births in the United States: 1982–2010. Natl Health Stat Report. 2012;(55):1–28. [PubMed] [Google Scholar]
  • 23.Victora CG, Huttly SR, Fuchs SC, Olinto MT. The role of conceptual frameworks in epidemiological analysis: a hierarchical approach. Int J Epidemiol. 1997;26:224–7. doi: 10.1093/ije/26.1.224. [DOI] [PubMed] [Google Scholar]
  • 24.Oates M. Perinatal psychiatric disorders: a leading cause of maternal morbidity and mortality. BrMed Bull. 2003;67:219–29. doi: 10.1093/bmb/ldg011. [DOI] [PubMed] [Google Scholar]
  • 25.Gelaye B, Rondon MB, Araya R, Williams MA. Epidemiology of maternal depression, risk factors, and child outcomes in low-income and middle-income countries. Lancet Psychiatry. 2016;3:973–982. doi: 10.1016/S2215-0366(16)30284-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Shafer AB. Meta-analysis of the factor structures of four depression questionnaires: Beck, CES-D, Hamilton, and Zung. J Clin Psychol. 2006;62:123–46. doi: 10.1002/jclp.20213. [DOI] [PubMed] [Google Scholar]
  • 27.Santos IS, Matijasevich A, Tavares BF, Barros AJ, Botelho IP, Lapolli C, Magalhães PV, Barbosa AP, Barros FC. Validation of the Edinburgh Postnatal Depression Scale (EPDS) in a sample of mothers from the 2004 Pelotas Birth Cohort Study. Cad Saúde Pública. 2007;23:2577–88. doi: 10.1590/s0102-311x2007001100005. [DOI] [PubMed] [Google Scholar]
  • 28.Tannous L, Gigante LP, Fuchs SC, Busnello ED. Postnatal depression in Southern Brazil: prevalence and its demographic and socioeconomic determinants. BMC Psychiatry. 2008;8:1. doi: 10.1186/1471-244X-8-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Séguin L, Potvin L, St-Denis M, Loiselle J. Depressive symptoms in the late postpartum among low socioeconomic status women. Birth. 1999;26:157–63. doi: 10.1046/j.1523-536x.1999.00157.x. [DOI] [PubMed] [Google Scholar]
  • 30.Daray FM, Rubinstein AL, Gutierrez L, Lanas F, Mores N, Calandrelli M, Poggio R, Ponzo J, Irazola VE. Determinants and geographical variation in the distribution of depression in the Southern cone of Latin America: A population-based survey in four cities in Argentina, Chile and Uruguay. J Affect Disord. 2017;220:15–23. doi: 10.1016/j.jad.2017.05.031. [DOI] [PubMed] [Google Scholar]
  • 31.Cook TM, Wang J. Descriptive epidemiology of stigma against depression in a general population sample in Alberta. BMC Psychiatry. 2010;10:29. doi: 10.1186/1471-244X-10-29. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Shonkoff JP, Boyce WT, McEwen BS. Neuroscience, molecular biology, and the childhood roots of health disparities: building a new framework for health promotion and disease prevention. JAMA. 2009;301:2252–9. doi: 10.1001/jama.2009.754. [DOI] [PubMed] [Google Scholar]
  • 33.Lindahl V, Pearson JL, Colpe L. Prevalence of suicidality during pregnancy and the postpartum. Arch Womens Ment Health. 2005;8:77–87. doi: 10.1007/s00737-005-0080-1. [DOI] [PubMed] [Google Scholar]
  • 34.Johannsen BM, Larsen JT, Laursen TM, Bergink V, Meltzer-Brody S, Munk-Olsen T. All-Cause Mortality in Women With Severe Postpartum Psychiatric Disorders. Am J Psychiatry. 2016;173:635–642. doi: 10.1176/appi.ajp.2015.14121510. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Joiner TE, Jr, Rudd MD, Rouleau MR, Wagner KD. Parameters of suicidal crises vary as a function of previous suicide attempts in youth inpatients. J Am Acad Child Adolesc Psychiatry. 2000;39:876–80. doi: 10.1097/00004583-200007000-00016. [DOI] [PubMed] [Google Scholar]
  • 36.Mayberry LJ, Horowitz JA, Declercq E. Depression symptom prevalence and demographic risk factors among U.S. women during the first 2 years postpartum. J Obstet Gynecol Neonatal Nurs. 2007;36:542–9. doi: 10.1111/j.1552-6909.2007.00191.x. [DOI] [PubMed] [Google Scholar]
  • 37.Righetti-Veltema M1, Conne-Perréard E, Bousquet A, Manzano J. Risk factors and predictive signs of postpartum depression. J Affect Disord. 1998;49:167–80. doi: 10.1016/s0165-0327(97)00110-9. [DOI] [PubMed] [Google Scholar]
  • 38.Chi X1, Zhang P2, Wu H3, Wang J4. Screening for Postpartum Depression and Associated Factors Among Women in China: A Cross-Sectional Study. Front Psychol. 2016;7:1668. doi: 10.3389/fpsyg.2016.01668. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Kheirabadi GR, Maracy MR, Barekatain M, Salehi M, Sadri GH, Kelishadi M, Cassy P. Risk factors of postpartum depression in rural areas of Isfahan Province, Iran. Arch Iran Med. 2009;12:461–7. [PubMed] [Google Scholar]
  • 40.Beck CT. Predictors of postpartum depression: an update. Nurs Res. 2001;50:275–85. doi: 10.1097/00006199-200109000-00004. [DOI] [PubMed] [Google Scholar]
  • 41.Kimmel M, Hess E, Roy PS, Palmer JT, Meltzer-Brody S, Meuchel JM, Bost-Baxter E, Payne JL. Family history, not lack of medication use, is associated with the development of postpartum depression in a high-risk sample. Arch Womens Ment Health. 2015;18:113–21. doi: 10.1007/s00737-014-0432-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Dibaba Y, Fantahun M, Hindin MJ. The association of unwanted pregnancy and social support with depressive symptoms in pregnancy: evidence from rural Southwestern Ethiopia. BMC Pregnancy Childbirth. 2013;13:135. doi: 10.1186/1471-2393-13-135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Dennis CL, Janssen PA, Singer J. Identifying women at-risk for postpartum depression in the immediate postpartum period. Acta Psychiatr Scand. 2004 Nov;110(5):338–46. doi: 10.1111/j.1600-0447.2004.00337.x. [DOI] [PubMed] [Google Scholar]
  • 44.Mithra A. Son preference in India: implications. [Accessed August 8, 2017];For gender development. 2016 Available at: http://www.socialeconomics.org/Papers/Mitra4A.pdf.
  • 45.Patel V, Rodrigues M, DeSouza N. Gender, poverty, and postnatal depression: a study of mothers in Goa, India. Am J Psychiatry. 2002;159:43–7. doi: 10.1176/appi.ajp.159.1.43. [DOI] [PubMed] [Google Scholar]
  • 46.Bloch M, Schmidt PJ, Danaceau M, Murphy J, Nieman L, Rubinow DR. Effects of gonadal steroids in women with a history of postpartum depression. Am J Psychiatry. 2000;157(6):924. doi: 10.1176/appi.ajp.157.6.924. [DOI] [PubMed] [Google Scholar]
  • 47.Schiller CE, Meltzer-Brody S, Rubinow DR. The role of reproductive hormones in postpartum depression. CNS Spectr. 2015 Feb;20(1):48–59. doi: 10.1017/S1092852914000480. Epub 2014 Sep 29. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Bennett HA, Einarson A, Taddio A, Koren G, Einarson TR. Prevalence of depression during pregnancy: systematic review. Obstet Gynecol. 2004;103:698–709. doi: 10.1097/01.AOG.0000116689.75396.5f. [DOI] [PubMed] [Google Scholar]
  • 50.Field T, Diego M, Hernandez-Reif M. Prenatal depression effects on the fetus and newborn: a review. Infant Behav Dev. 2006;29:445–5. doi: 10.1016/j.infbeh.2006.03.003. [DOI] [PubMed] [Google Scholar]
  • 51.Dayan J, Creveuil C, Marks MN, et al. Prenatal depression, prenatal anxiety, and spontaneous preterm birth: a prospective cohort study among women with early and regular care. Psychosom Med. 2006;68:938–46. doi: 10.1097/01.psy.0000244025.20549.bd. [DOI] [PubMed] [Google Scholar]
  • 52.Hollins K. Consequences of antenatal mental health problems for child health and development. Curr Opin Obstet Gynecol. 2007;19:568–72. doi: 10.1097/GCO.0b013e3282f1bf28. [DOI] [PubMed] [Google Scholar]
  • 53.Nelson DB, Freeman MP, Johnson NL, McIntire DD, Leveno KJ. A prospective study of postpartum depression in 17 648 parturients. J Matern Fetal Neonatal Med. 2013;26:1155–61. doi: 10.3109/14767058.2013.777698. [DOI] [PubMed] [Google Scholar]
  • 54.Nelson DB, Doty M, Mcintire DD, Leveno KJ. Rates and precipitating factors for postpartum depression following screening in consecutive births. J Matern Fetal Neonatal Med. 2016;29:2275–9. doi: 10.3109/14767058.2015.1083004. [DOI] [PubMed] [Google Scholar]
  • 55.Alvarado-Esquivel C, Sifuentes-Alvarez A, Salas-Martinez C, Martínez-García S. Validation of the Edinburgh Postpartum Depression Scale in a population of puerperal women in Mexico. Clin Pract Epidemiol Ment Health. 2006;2:33. doi: 10.1186/1745-0179-2-33. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Vega-Dienstmaier JM, Mazzotti Suárez G, Campos Sánchez M. Validation of a Spanish version of the Edinburgh Postnatal Depression Scale. Actas Esp Psiquiatr. 2002;30:106–11. Spanish. [PubMed] [Google Scholar]
  • 57.Garcia-Esteve L, Ascaso C, Ojuel J, Navarro P. Validation of the Edinburgh Postnatal Depression Scale (EPDS) in Spanish mothers. J Affect Disord. 2003;75:71–6. doi: 10.1016/s0165-0327(02)00020-4. [DOI] [PubMed] [Google Scholar]
  • 58.Jadresic E, Araya R, Jara C. Validation of the Edinburgh Postnatal Depression Scale (EPDS) in Chilean postpartum women. J Psychosom Obstet Gynaecol. 1995;16:187–91. doi: 10.3109/01674829509024468. [DOI] [PubMed] [Google Scholar]
  • 59.Katon W, Russo J, Gavin A. Predictors of postpartum depression. J Womens Health (Larchmt) 2014;23:753–9. doi: 10.1089/jwh.2014.4824. [DOI] [PubMed] [Google Scholar]
  • 60.Santos IS, Franck Tavares B, Munhoz TN, Manzolli P, Bartz de Ávila G, Jannke E, Matijasevich A. Patient health questionnaire-9 versus Edinburgh postnatal depression scale in screening for major depressive episodes: a cross-sectional population-based study. BMC Res Notes. 2016;9:453. doi: 10.1186/s13104-016-2259-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Alvarado R, Jadresic E, Guajardo V, Rojas G. First validation of a Spanish-translated version of the Edinburgh postnatal depression scale (EPDS) for use in pregnant women. A Chilean study. Arch Womens Ment Health. 2015;18:607–12. doi: 10.1007/s00737-014-0466-z. [DOI] [PubMed] [Google Scholar]
  • 62.Logsdon MC, Birkimer JC, Usui WM. The link of social support and postpartum depressive symptoms in African-American women with low incomes. MCN Am J Matern Child Nurs. 2000;25:262–6. doi: 10.1097/00005721-200009000-00009. [DOI] [PubMed] [Google Scholar]

RESOURCES