THE LEVEL OF DEPRESSIVE SYMPTOMS IN POSTPARTUM INDIVIDUALS: AN EXPLORATORY PRELIMINARY STUDY

do Amaral Rocha L1, Amaral Pequeno S1, Cecchi Salata M2, Shimohara Bradaschia J1, Martinez David M1, da Silva Souza S1, Tirolli Rett M3, Lucena da Silva M1, Azevedo Garcia P1, Barbaresco Gomide Matheus L1, Armando Nunes de Lima E1, Henriques Jácomo R4, Paplinskie S5, Mottola M5, Teixeira Alves A1

Research Type

Clinical

Abstract Category

Pregnancy and Pelvic Floor Disorders

Abstract 682
Open Discussion ePosters
Scientific Open Discussion Session 36
Friday 29th September 2023
15:55 - 16:00 (ePoster Station 3)
Exhibit Hall
Female Prevention Questionnaire Quality of Life (QoL)
1. University of Brasilia - UnB, 2. Uniceplac, 3. University of Sergipe - UFS, 4. University Hospital of Brasilia - HUB, 5. University of Western Ontario - UWO
Presenter
Links

Abstract

Hypothesis / aims of study
The perinatal period offers a window of opportunity for the early identification of depressive symptoms, and the implementation of health promotion and prevention actions. From this perspective, knowing the clinical and sociodemographic profile of women who are at risk of developing postpartum depression (PPD) is essential to reduce its consequences and identify early those who need more detailed evaluation and treatment. 
The aim of this study was to analyze the level of depressive symptoms in postpartum women according to the Edinburgh Postnatal Depression Scale (EPDS) and to describe their clinical and sociodemographic profiles.
Study design, materials and methods
This was a preliminary, descriptive, exploratory, and cross-sectional study that was part of broader development research. Data were collect between June and September 2021 through an online form containing a sociodemographic, clinical questionnaire, and the EPDS. 
The inclusion criteria were adult individuals in the postpartum period (until 12 months postpartum); 18 years old or older; to write, comprehend, and speak Portuguese (Brazil). Exclusion criteria were refusal to participated, and the inability to provide consent. 
The variables analyzed were: EPDS score (mild < 8; moderate = 9-12; severe > 13), maternal age, parity, days after delivery, education level, marital status, household income, and perinatal depression symptoms. 
Data analysis was perform based on descriptive statistics.
Results
All participants who answered the form were included and had an average EPDC score of 10.06 ± 6.50. Classifying the sample according to the EPDC, 25 participants (31%) were at high risk for PPD, while 22 (27%) were at moderate risk and 34 (42%) were at low risk, as shown in Table 1. The average score of participants of high, moderate and low risk in EPDC was 18.08 ± 4.03, 10.00 ± 0.98 and 4.21 ± 2.47, respectively. 
Of those who exhibited a high risk of PPD (N=25), 44% were between 25 and 34 years old (N=11), 28% did not complete higher education (N=7), 84% were married (N=21), 44% had an income between $200-600 USD (N=11), 88% were more than 45 days postpartum (n=22), 52% were multiparous (N=13) and 72% had reported symptoms of depression during the prenatal period (N=18). 
Of those whose indicated moderate risk of PPD, 50% were between 25 and 34 years old (N=11), 32% completed higher education (N=7), 77% were married (N=17), 27% had an income between $200-600 USD (N=6), 68% were primiparous (N = 15), 95% were more than 45 days postpartum (N=21), and 91% had not presented symptoms of depression during pregnancy (N=20). 
Of those with low risk of PPD, 47% were between 25 to 34 years old (N=16), 32% had completed a graduation degree – "specialization" (N=11), 88% were married (N=30), 32% had a household income between $1,000-1,400 US dollars (N=11), and 79% were primiparous (N=27), 79% were 45 days postpartum (N=34) and 91% had not presented symptoms of depression during the prenatal period (N=31).
Interpretation of results
The profile of postpartum individuals was comparable to that presented in the literature, with regards to postpartum depression and low educational levels and lower household incomes. 
The literature also suggests that multiparous individuals will be more likely to report symptoms of depression, which were similar to the data collected in our study. Most participants in the low- to moderate- postpartum depression groups were primiparous and, similarly, both groups reported mild symptoms of depression during the prenatal period.
Concluding message
Severe postpartum depression can be prevented with early screening, which will allow for more appropriate management of symptoms. Factors that influence early detection in those at a higher risk of postpartum depression are, previous depressive symptoms before or during the pregnancy, family history, stress factors through life, and inadequate family support. 
With proper screening tools, health professionals could identify those at a higher risk for postpartum depression before, during, and after childbirth, resulting in a lower prevalence of postpartum depression and, thus, enhancing the health of the mother and the newborn.
Figure 1
References
  1. Shorey Shefaly, Ing Cornelia Chee Yin, Ng Esperanza Debby, Huak Chan Yiong, San Wilson Tam Wai, Seng Chong Yap. Prevalence and incidence of postpartum depression among healthy mothers: A systematic review and meta-analysis. Journal of Psychiatric Research. 2021 Aug 01;104:235-248. DOI: 10.1016/j.jpsychires.2018.08.001.
  2. Josefsson A, Berg G, Nordin C, Sydsjö G. Prevalence of depressive symptoms in late pregnancy and postpartum. Acta Obstetricia et Gynecologica Scandinavica. 2001 Mar;80:251-5. DOI 0.1034/j.1600- 0412.2001.080003251.x.
  3. Lancaster Christie A., Gold Katherine J., Flynn Heather A., Yoo Harim, Marcus Sheila M., Davis Matthew M. Risk factors for depressive symptoms during pregnancy: a systematic review. American Journal of Obstetrics and Gynecology. 2010 Jan 202:5-14. DOI 10.1016/j.ajog.2009.09.007.
Disclosures
Funding None Clinical Trial No Subjects Human Ethics Committee Comitê de Ética da Faculdade de Ceilândia da Universidade de Brasília - CAAE: 45304021.4.0000.8093 Helsinki Yes Informed Consent Yes
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