Literature DB >> 34321738

An Assessment of the Risk Factors and Concerns of Postpartum Depression among Mothers Seeking Health Care in North Central Trinidad.

Shivananda B Nayak1, Sheneel Jaggernauth1, Ariana Jaggernauth1, Priyankaa Jadoo1, Nirdosh Jagmohansingh1, Vanessa Jaggernauth1, Rayhaan Hosein1, Britnee Issarie1, Jessica Jaikaran1.   

Abstract

BACKGROUND: Postpartum depression (PPD) is a debilitating mental disorder which affects mainly females usually after giving birth.
OBJECTIVES: We aimed to study the risk factors and concerns of PPD among mothers seeking health care at regional health authority hospitals in Trinidad.
MATERIALS AND METHODS: The cross-sectional study consisted of 360 mothers from the postnatal and neonatal clinics of the North Central Regional Health Authority, Trinidad. Data were collected via a questionnaire using convenience sampling to study the risk factors and concerns of PPD among mothers. Participants were asked to sign a consent form before filling out the questionnaire. The questions were geared toward obtaining mother's perspective on predisposing factors of PPD, identifying if they are at risk for perinatal depression, the outcomes of having PPD, and determining if they were screened and treated for it.
RESULTS: This study comprised 360 postnatal women among which 4.7% were diagnosed with postpartum while 40% scored ≥10 in the Edinburgh Postnatal Depression Scale which indicated a risk for PPD. This research revealed seven significant predictors of PPD: family history of mental illness, baby blues, mood swings during period, use of oral contraceptives, emotional support, life stress, and being diagnosed with depression (P < 0.05). Other characteristics like sociodemographics were not remarkably correlated but marginally indicative of depressive signs.
CONCLUSION: The study shows that many risk factors of PPD exist, and screening and treatment should be used to avoid the consequences of PPD. Copyright:
© 2021 Indian Journal of Community Medicine.

Entities:  

Keywords:  Concerns; Edinburgh Postnatal Depression Scale; postpartum depression; risk factors

Year:  2021        PMID: 34321738      PMCID: PMC8281835          DOI: 10.4103/ijcm.IJCM_628_20

Source DB:  PubMed          Journal:  Indian J Community Med        ISSN: 0970-0218


INTRODUCTION

Postpartum depression (PPD) is a debilitating mental disorder which affects mainly females usually after giving birth. It can typically manifest as difficulty sleeping, mood changes, appetite changes, anxiety, crying, trouble focusing, reduced interest in diurnal pastimes, and exhaustion, thus making it difficult to care for themselves or for others. According to Cheryl Beck, in a predictors of PPD article, approximately 13% of women experience PPD worldwide, and Psychiatrist Dr. Gerard Hutchinson, in Raising the Lid on PPD article, stated that studies done at Mt Hope and San Fernando General Hospital showed that after 2–3 weeks postlabor, PPD rates were as high as 35%.[12] A study done by Persad et al. with a sample size of 602 antenatal and postnatal patients asserted that the point prevalence of PPD was 38.5% in North Central Trinidad.[3] Predisposing factors increase the possibility of mothers acquiring PPD, some of which include lack of support, prior PPD, financial stress, a history of mood changes with menstrual cycles or oral contraceptives, and a family history of depression and mental illness. This illness can have longstanding consequences on a child causing the behavioral, cognitive, and academic development to be impaired. Currently, there is no screening for PPD at any health facilities in Trinidad and Tobago despite the probable adverse effects on both mother and infant. This results in numerous patients being undiagnosed and untreated. There are valid tools available for screening PPD such as the EPDS which was implemented in this study. This investigation aims to assess the risk factors and concerns of PPD that mothers face, as there are not many studies on the subject at present in Trinidad. Findings of this study can indicate risk factors in Trinidad that play a role in women having PPD as well as women at risk for developing PPD. Furthermore, increasing public awareness of PPD, as well as common concerns among mothers via targeted campaigning, can encourage mothers to not trivialize their mental health and seek help if necessary. The implementation of screening in public health facilities can aid in diagnosing and treating PPD, thus reducing the negative consequences of the illness in both mother and child.

MATERIALS AND METHODS

The cross-sectional study consisted of 360 mothers from the postnatal and neonatal clinics of the North Central Regional Health Authority. This study was conducted from January 2019 to August 2019. The study was approved by the Campus Ethics Committee of the University of the West Indies (CEC776/11/18). Written informed consent was obtained from the participants prior to completing the questionnaire (all patients agreed to participate in the study and fill the study questionnaire). Data were collected using a questionnaire via convenience sampling consisting of 35 questions via single-point cluster sampling in the postnatal and neonatal clinics of Mount Hope Women's Hospital, Chaguanas District Health Facility, St. Joseph and Macoya Health Centers. The annual attendance rate of these clinics comprises approximately 56,000 mothers who attend for postnatal and neonatal care in which both mother and baby are assessed together and is representative of the population. The first 25 questions consisted of demographic questions which included age, marital status, ethnicity, and employment status and closed-ended questions specific to assessing possible risk factors and concerns that mothers can have after giving birth, as well as the effects of any PPD that develops. The remaining questions were those of the Edinburgh Postnatal Depression Scale (EPDS). The American College of Obstetricians and Gynecologists recommends a standardized validated tool and cites both the EPDS and the Patient Health Questionnaire-9 as appropriate to screen for postnatal depression.[4] We chose the EPDS as the study was conducted in a primary care setting, having been validated in primary care postnatal and nonpostal women. The EPDS is a versatile tool that is used to assist health professionals in detecting mothers that are at risk for PPD. Elements of the scale correspond to numerous clinical depression symptoms, such as guilt feeling, sleep disturbance, low energy, anhedonia, and suicidal ideation. For each question, the patient will choose one of four possible replies that reflect how she has been feeling over the past 7 days. Responses are scored as 0, 1, 2, or 3 for a maximum score of 30. Higher scores ≥10 indicate more depressive symptoms.[4] Cox et al. found that the diagnostic validity of the EPDS scores ≥10 had satisfactory sensitivity (79%) and specificity (85%) for PPD.[5] The sample size was determined based on the formula: n = (Z1−α) 2× (P [(1 − P)]/D2), where Z = 1.96 corresponding to 95% confidence level, P was 0.295, and D (the margin of error) = 0.05. Using the formula, the minimum sample size needed was 320 mothers seeking health care at regional health authority hospitals. The size taken was 360 mothers seeking health care at regional health authority hospitals.

RESULTS

The prevalence of PPD was 4.7%, and 40% of the participants had an EPDS score ≥10. Of the 4.7% diagnosed with PPD [Table 1], 3.6% of the participants had an EPDS score ≥10. 95.3% of the participants were not diagnosed with PPD by a doctor, and of this, 36.4% of the participants had an EPDS score ≥10.
Table 1

Participants diagnosed and not diagnosed with postpartum depression and the Edinburgh Postnatal Depression Scale scores of participants

EPDS score <10 (%)EPDS score ≥10 (%)Total (%)
Diagnosed with PPD4 (1.1)13 (3.6)17 (4.7)
Not diagnosed with PPD212 (58.9)131 (36.4)343 (95.3)
Total (%)216 (60.0)144 (40.0)360 (100)

EPDS: Edinburgh Postnatal Depression Scale, PPD: Postpartum depression

Participants of 73.7% were not asked questions about PPD. Participants of 43.1% with an EPDS score <10 were not asked questions about PPD by their doctor. For those with an EPDS score ≥10, 9.4% of the participants were asked questions about PPD while 30.6% were not. Participants diagnosed and not diagnosed with postpartum depression and the Edinburgh Postnatal Depression Scale scores of participants EPDS: Edinburgh Postnatal Depression Scale, PPD: Postpartum depression Participants with PPD were more likely to have a family history of mental illness compared to those who did not have a family history of mental illness (odds ratio [OR]: 3.369; confidence interval [CI] 95%: 1.232–9.212). There was no statistical significance between there being a recent death in the family and having PPD as well as for if there were complications during or after birth, if the pregnancy was planned or not, and if participants had mood swings when taking oral contraceptives as P > 0.05. For those with PPD, the odds were higher that participants experienced baby blues (OR: 5.727; CI 95%: 1.617–20.29). Participants with PPD were more likely to be diagnosed with depression (OR: 22.992; CI 95%: 7.835–67.46) [Table 2].
Table 2

Risk factors and diagnosis of postpartum depression and Edinburgh Postnatal Depression Scale scores

Risk factors (n=360)Diagnosis of PPD
EPDS score
Yes (%)No (%)PORCI 95%≥10 (%)<10 (%)PORCI 95%
Experience baby blues
 Yes14 (3.9)154 (42.8)0.0035.7271.617-20.29294 (26.1)74 (20.6)<0.0013.6082.315-5.621
 No3 (0.8)189 (52.5)50 (13.9)142 (39.4)
Complications during/after birth giving
 Yes11 (3.1)147 (40.8)0.0762.4440.884-6.76268 (18.9)90 (25)0.2981.2530.819-1.915
 No6 (1.7)(54.4)76 (21.1)126 (35)
Planned pregnancy
 Yes2 (0.6)94 (26.1)0.2590.3530.079-1.57432 (8.9)64 (17.8)0.1190.6790.416-1.107
 No15 (4.2)249 (69.1)112 (31.1)152 (42.2)
Mood swings during period
 Yes14 (3.9)193 (53.6)0.0343.6271.024-12.851102 (28.3)105 (29.2)<0.0012.5671.641-4.017
 No3 (0.8)150 (41.7)42 (11.7)111 (30.8)
Oral contraceptives
 Yes1 (0.3)134 (37.2)0.0103.7431.290-10.86564 (0.017)82 (22.7)0.2201.3070.852-2.007
 No5 (1.4)209 (58.1)80 (22.2)134 (37.2)
Mood swings when taking oral contraceptives (*n=146)
 Yes7 (4.8)44 (30.1)0.1122.8640.860-9.53625 (17.1)26 (17.8)0.3551.3810.696-2.737
 No5 (3.4)90 (61.7)39 (26.7)56 (38.3)
Diagnosed with depression
 Yes9 (2.5)16 (4.4)<0.00122.9927.835-67.46818 (5)7 (1.9)0.0014.2651.733-10.497
 No8 (2.2)327 (90.8)126 (35)209 (58.1)

OR: Odds ratio, CI: Confidence interval, EPDS: Edinburgh Postnatal Depression Scale, PPD: Postpartum depression

Risk factors and diagnosis of postpartum depression and Edinburgh Postnatal Depression Scale scores OR: Odds ratio, CI: Confidence interval, EPDS: Edinburgh Postnatal Depression Scale, PPD: Postpartum depression Participants with an EPDS score ≥10 were more likely to have a family history of mental illness (OR: 2.041; CI 95%: 1.751–5.282). Participants with an EPDS score ≥10 were more likely to have a recent death in the family (OR: 2.488; CI 95%: 1.553–3.984). For those with an EPDS score ≥10, the odds were higher that participants experienced baby blues (OR: 3.608; CI 95%: 2.315–5.621 respectfully). There was no statistical significance between whether participants had an EPDS score ≥10 and if they had complications during and after giving birth, if the pregnancy was planned or not, if participants used oral contraceptives, and if they had mood swings while using oral contraceptives as P > 0.05. Participants with an EPDS score ≥10 were more likely to have mood swings during their period (OR: 2.567; CI 95%: 1.641–4.017) and be diagnosed with depression (OR: 4.265; CI 95%: 1.733–10.497).

DISCUSSION

PPD causes great harm to the female population and their families, and early detection is quite a challenge. Participants diagnosed and not diagnosed with PPD and EDPS scores of participants showed that the incidence of PPD detection was higher using the EPDS ≥10 as compared to the incidence of PPD with only routine clinical evaluation. This is concurrent with the study done by Evins et al.[6] which found that the incidence of PPD detection was higher using EPDS as compared to the incidence of PPD with only routine clinical evaluation. Our study indicated that 73.7% of the participants were not asked about PPD and 30.6% scoring over 10 on the EPDS were not inquired about PPD either. Therefore, we can conclude that many patients' diagnosis is overlooked, thus underscoring the need for increased awareness, and the use of screening techniques like EPDS will increase the likeliness of detection and treatment. This study revealed that sociodemographics such as ethnicity, age, marital status, and employment had no significant impact in producing PPD. A similar study by the Institute of Social Medicine indicated that advanced maternal age has lower rates of PPD than younger women.[7] In another study from Portugal, it was found that young mothers exhibited more depressive signs as well as more EPDS > 12 scores than adult mothers in the postpartum period.[8] The current study did not find any ethnic disparity in the occurrence of PPD. Research done by Wei et al. disclosed that there was a high frequency of depression among African Americans.[9] Women from different ethnic backgrounds seem to have varying levels of emotional health. In our study, employment was found to be protective of PPD, and this discovery was validated by Lewis et al.[10] Most of the participants were married, common-law, and single where the highest (9%) diagnosis of PPD belonged to married women and 4% to single women. This is inconsistent with a study done in Jamaica which reported a frequency of 71% of PPD among single mothers.[11] Another meta-analysis found that single marital status is a predictor of PPD.[1] Our study found that 7.8% of people with EPDS ≥10 and 1.6% of people with PPD had insufficient emotional support whereas the majority who were undiagnosed and scored < 10 had sufficient emotional support, thus stipulating that inadequate support is a predisposing component for PPD. Contrastingly, in our research, only 1.1% with PPD agreed to having marital problems while 10.8% had EPDS scores ≥10 which showed that marital problems did not have a discernible impact on PPD. This finding contradicts with the phenomena of previous research exhibiting that marital problems are an influential factor of PPD.[12] The study reported a notable interrelation between a family history of mental illness, PPD, and EPDS ≥10. These data were supported by Franks in 1934 and John Hopkins School of Medicine as it affirmed that women who have a family history of mental disorder, particularly PPD, major depression, anxiety, and panic attacks (53.3%), are more likely to develop PPD than women with no historical factors.[1314] Women with a history of major depression or a family history of psychiatric illness should be acknowledged in pregnancy and closely monitored in the postpartum period to avoid developing PPD.[15] We explored the association between recent death in the family, complications during or after giving birth, and having a planned or unplanned pregnancy and PPD and established no substantial relation (P > 0.05). Nonetheless, the correlation between a recent death in the family and EPDS ≥10 was noted where 15.6% of the participants scored above 10 (P < 0.001), implying that recent death in the family poses a risk. We also found that women who experienced baby blues had higher odds of acquiring PPD. Manjunath et al. suggested that 60%–80% of all new mothers suffer from postpartum blues (PPB) and should be monitored as 20% of these mothers can develop PPD.[16] This notion is further supported by Horibe et al. which stated that primiparas tend to have significantly higher EPDS scores than multiparas.[17] It was proposed that a mentally ill history and natural irritants may determine if baby blues lead to depression. Sociodemographics with EPDS scores ≥10 can also contribute to PPB developing into PPD.[18] Mood swings during period, oral contraceptives, and being diagnosed with depression were all found to have a connection with PPD and EPDS ≥10 (P < 0.05). This finding supports the argument by Petrick and Boyer that these were strong threats of PPD.[1920] Furthermore, Horibe et al. proposed that the relationship between regular oral contraceptive use prior to pregnancy and PDD may be due to negative hormonal effects experienced while using oral contraceptives.[17] Pluchino et al. also stated that a possible reason for contraceptives causing PPD is due to the effects of testosterone, progesterone, and estradiol on the central nervous system, however, the mechanism is not well understood.[21] According to the Harvard study of Moods and Cycle, women who also took oral contraceptives were at risk of worsening their mood.[22] Participants of 14.7% with an EPDS score ≥10 strongly agreed of having financial problems. Prior studies done by Maryam Ghaedrahmati and Qobadi et al. found that stressful life events such as financial struggles exacerbate the risk of PPD.[2324] An important finding of this study is the concerns of mothers diagnosed with PPD. We found that majority was perturbed that their depression would negatively affect their relationship with their children and partner (35.5% and 23.5%). Only 17.6% almost always worried that their depression would impact the development of their child and compromise their caregiving abilities. The participants rarely thought of harming their children and that their depression would make it difficult to have a connection with their child. A comparable study by Field showed how PPD impinges on early interactions with their child and caregiving abilities.[25]

CONCLUSION

Findings show that many participants were at risk for developing PPD. The prominent risk factors of PPD identified for mothers diagnosed with PPD were a family history of mental illness, baby blues, mood swings during periods, use of oral contraceptives, emotional support, life stress, and being diagnosed with depression. For those at risk for developing PPD (EPDS score ≥10), the risk factors were family history of mental illness, recent death in the family, mood swings during period, baby blues, life stress, financial and marital problems, and being diagnosed with depression. Other characteristics like sociodemographics were not significantly correlated but marginally indicative of depressive symptoms.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.
  20 in total

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Authors:  N Pluchino; A Cubeddu; A Giannini; S Merlini; V Cela; S Angioni; A R Genazzani
Journal:  Maturitas       Date:  2009-01-22       Impact factor: 4.342

2.  Family history, not lack of medication use, is associated with the development of postpartum depression in a high-risk sample.

Authors:  Mary Kimmel; Edward Hess; Patricia S Roy; Jennifer Teitelbaum Palmer; Samantha Meltzer-Brody; Jennifer M Meuchel; Emily Bost-Baxter; Jennifer L Payne
Journal:  Arch Womens Ment Health       Date:  2014-07-01       Impact factor: 3.633

3.  Prevalence and predictors of depressive symptoms in older premenopausal women: the Harvard Study of Moods and Cycles.

Authors:  B L Harlow; L S Cohen; M W Otto; D Spiegelman; D W Cramer
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4.  Reappraising the relationship between maternal age and postpartum depression according to the evolutionary theory: Empirical evidence from a survey in primary health services.

Authors:  Marcela N Bottino; Paulo Nadanovsky; Claudia L Moraes; Michael E Reichenheim; Gustavo Lobato
Journal:  J Affect Disord       Date:  2012-07-25       Impact factor: 4.839

5.  Postpartum depression: racial differences and ethnic disparities in a tri-racial and bi-ethnic population.

Authors:  Guo Wei; Linda B Greaver; Stephen M Marson; Cynthia H Herndon; James Rogers
Journal:  Matern Child Health J       Date:  2007-10-23

6.  Validation of the Edinburgh Postnatal Depression Scale (EPDS) in non-postnatal women.

Authors:  J L Cox; G Chapman; D Murray; P Jones
Journal:  J Affect Disord       Date:  1996-07-29       Impact factor: 4.839

7.  Detection of postnatal depression. Development of the 10-item Edinburgh Postnatal Depression Scale.

Authors:  J L Cox; J M Holden; R Sagovsky
Journal:  Br J Psychiatry       Date:  1987-06       Impact factor: 9.319

8.  Depression during pregnancy and the postpartum period in adolescent and adult Portuguese mothers.

Authors:  B Figueiredo; A Pacheco; R Costa
Journal:  Arch Womens Ment Health       Date:  2007-05-18       Impact factor: 3.633

9.  The effects of postpartum depression on maternal-infant interaction: a meta-analysis.

Authors:  C T Beck
Journal:  Nurs Res       Date:  1995 Sep-Oct       Impact factor: 2.381

10.  The Effect of Stressful Life Events on Postpartum Depression: Findings from the 2009-2011 Mississippi Pregnancy Risk Assessment Monitoring System.

Authors:  Mina Qobadi; Charlene Collier; Lei Zhang
Journal:  Matern Child Health J       Date:  2016-11
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