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ORIGINAL RESEARCH article

Front. Psychiatry, 13 October 2022
Sec. Anxiety and Stress Disorders
This article is part of the Research Topic Monitoring Depression and Anxiety Symptoms: Scales and Measurements View all 17 articles

The symptoms of postpartum depression observed by family members: A pilot study

\nHuong Thi Thanh NguyenHuong Thi Thanh Nguyen1Ly Thi Kim DoLy Thi Kim Do2Huong Thi Thu Pham,,Huong Thi Thu Pham3,4,5Anh Phuong Hoang,
Anh Phuong Hoang1,3*Hoa Thi TruongHoa Thi Truong1Huyen Thi Hoa NguyenHuyen Thi Hoa Nguyen1
  • 1College of Health Sciences, VinUniversity, Hanoi, Vietnam
  • 2General Surgical Department, University Medical Center Schleswig-Holstein, Lübeck, Germany
  • 3Faculty of Nursing and Midwifery, Hanoi Medical University, Hanoi, Vietnam
  • 4School of Nursing, College of Medicine, National Taiwan University, Taipei, Taiwan
  • 5National Institute of Mental Health, Bach Mai Hospital, Hanoi, Vietnam

Postpartum Depression (PPD) is a burden on women's mental health after delivery, predominantly occurring in the 1st year. PPD poses a threat to the mother's life and affects the quality of childcare. Early detection by family members of depressive symptoms is critical. This study aimed to examine the role of family members in reporting depressive symptoms of PPD among new mothers. A cross-sectional study was conducted, where 56 family members were asked to report depressive symptoms observed in new mothers. At the same time, the new mothers were also screened for PPD using the Edinburgh Postpartum Depression Scale (EPDS). Binary logistic regression was performed. Depressive symptoms of new mothers reported by family members, including emotional and behavioral disturbance, being under stress, high anxiety, isolation, changing lifestyle, and inability to take care of their children, were found as predictors of PPD.

Background

Postpartum Depression (PPD) is a major maternal health problem. The prevalence of PPD ranges from 1.9 to 82.2% in developing countries and from 5.3 to 74% in developed countries (1). In Viet Nam, a study discovered that the prevalence of women suffering from PPD was 20.4% in urban areas and 15.8% in rural areas (2). PPD is associated with a reduction in women's physical and mental health, and depressed women experience a lower quality of life (3). If a mother is depressed, anxious, or stressed, her children are more likely to have a wide range of adverse outcomes, including emotional problems, attention deficit hyperactivity disorder (ADHD), or impaired cognitive development (4). Social and/or family support plays a significant role in detecting PPD. When women receive support and care from their husbands, the percentage of those with depression reduces significantly (5). However, limited studies are available on the role of family members in screening for PPD. The sooner the PPD is detected, the better the outcome is achieved. This study, therefore, aims to explore the feasibility of family members of women with PPD helping detect early symptoms of PPD.

Methods

This study is cross-sectional, piloted in a small group of families with new mothers whose child anywhere from birth to 1 year old. A convenience sampling method was used. The research team conducted home visits with new mothers whose children were under 1 year old to invite them to participate in this study. A brief introduction of this study and a consent form was sent out to all new mothers who gave birth within one previous year during the home visits in a commune of Thuong Tin district, Hanoi. In case mothers were not available at home during visiting time, the researchers would leave a message and return within that day. If the new mothers agreed to participate in the study, they were asked to complete the Edinburgh Postpartum Depression Scale (EPDS). The EPDS includes 10 items measured on a Likert scale of 0–3. A score of 12 and above indicates the risk of depression. The sensitivity and specificity of EPDS were 65–100% and 49–100% respectively (6). The validated Vietnamese version of EPDS is the most common screening tool for perinatal common mental disorders used in Vietnam with an internal consistency of 0.77 (7).

During home visits, researchers paid attention to the living environments and family members involved in caring for new mothers to identify the closest caregiver to that mother. The family members were asked to complete the second part of the questionnaire with 9 items to report any depressive symptoms they could observe in the new mothers. This part of the questionnaire was developed by the research team based on guidelines in DSM-V, including common items relating to the possibility of observing signs and symptoms of PPD among these new mothers (8). The evidenced-based items were developed based on DSM-V by the American Psychiatric Association and previous studies (5, 9, 10).

Although 116 families were reached out in total, only 56 families responded with both the answers of the new mothers and her family members.

SPSS software version 23.0 was employed for data management and analysis. Binary logistic regression was also performed to investigate the relationship between PPD among new mothers and depressive symptoms observed by family members. The proposal, including ethical considerations, was approved by Hanoi Medical University Research Proposal Committee, Decision No 5042/Q-HYHN.

Results

Fifty-six new mothers participated in the screening with EPDS, and 20 (35.7%) of them were detected to be at risk of PPD (with an EPDS score of 12 and above). A family member of these mothers was also invited to an interview to report depressive symptoms observed from the mothers. Of the 56 family members, husbands were the majority (n = 29, accounting for 51.8%), followed by relatives and close friends (n = 17, accounting for 30.4%). There were only 5 maternal parents (8.9%) and 5 parents-in-law (8.9%) that participated in the interview (Table 1).

TABLE 1
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Table 1. The percentage of family members participating in the study.

The relationships between observed depressive symptoms by family members and the risk of PPD among new mothers were reported. The results (Table 2) indicated that many symptoms and signs of PPD could be observed by family members. “Being sad unreasonably” was the most prevalent sign of PPD. As shown below, new mothers whom family members observed with the symptom “being sad unreasonably” experienced the risk of PPD (EPDS ≥ 12) 11.3 times higher than that of a new mother without this symptom (OR = 11.3; p < 0.05). Other significant depressive symptoms/signs observed by family members included “Separated to the outside” (OR = 8.8; p < 0.05); “Changing lifestyle” (OR = 7.6; p < 0.05); “Under stress and anxiety” (OR = 6.1; p < 0.05); “Uncontrolled emotion and behavior” (OR = 5.3; p < 0.05); and “Over-taking care of and being concerned about the child(ren)” (OR = ; p < 0.05).

TABLE 2
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Table 2. Depression symptoms reported by family members.

Discussion

Depressive symptoms/ signs observed by family members in our study were consistent with the literature on signs and symptoms of PPD, including sleep disturbances, emotional disorders, and separating from society (2, 11, 12). Emotional and behavioral disturbance, being under stress and anxiety, isolation, changing lifestyle, and inability to take care of their child(ren) are likely predictors of PPD. These are similar to studies summarizing PPD psychosocial predictors such as stress, social support, and family connection (13), or factors of food intake patterns, sleep status, exercise, and physical activities (14) were also commonly reported. An explanation could be that the biological changes after delivery lead to fatigue and changes in emotions, behaviors, and daily activities (15). However, without early detection and/or proper treatment and care, psychoses occur in 1 to 2 per 1,000 postpartum women, and they may present as schizophrenic or affective disorders or as confused states (16).

Changing lifestyles reported by family members, such as eating habits or sleeping patterns, which were significantly associated with the risk of PPD, were also commonly found in women with PPD in other previous studies. It is not denied that we frequently observed the signs or symptoms of eating disorders related to depression among postpartum women. Typically, our results found a clear association between PPD and changing lifestyles (p < 0.001). Similarly, in another study, taking unhealthy food, and performing an unhealthy lifestyle, were found to have a significant relationship with depression, with 26.1% changing their daily lifestyle (17). Sleeping disorder is not only a predictor of PPD but also is a consequence of increasing PPD (18). Recently researchers examined the links between maternal sleep, maternal depressive symptoms, and mothers' perceptions of their emotional relationship with their infant in a self-recruited sample of mothers (11). Some studies described the association between serotonin and anxiety and depressive symptoms would be consistent with numerous observations indicating abnormal functioning of the serotoninergic system in depression for people experiencing anorexia or overeating (19).

Conclusion

A larger-scale study with a bigger sample size is recommended to provide more substantial evidence that many symptoms/ signs of PPD can be reported by family members. It will then be followed by strategies to raise awareness that family members can play a crucial role in early screening for PPD.

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving human participants were reviewed and approved by Hanoi Medical University Research Proposal Committee, Decision No. 5042/Q-HYHN. Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements.

Author contributions

All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Abbreviations

PPD, postpartum depression; EPDS, Edinburgh Postpartum Depression Scale; DSM-V, Diagnostic and Statistical Manual of Mental Disorder V.

References

1. Norhayati M, Hazlina NN, Asrenee A, Emilin WW. Magnitude and risk factors for postpartum symptoms: a literature review. J Affect Disord. (2015) 175:34–52. doi: 10.1016/j.jad.2014.12.041

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Murray L, Dunne MP, Van Vo T, Anh PNT, Khawaja NG, Cao TN. Postnatal depressive symptoms amongst women in Central Vietnam: a cross-sectional study investigating prevalence and associations with social, cultural and infant factors. BMC Pregnancy Childbirth. (2015) 15:234. doi: 10.1186/s12884-015-0662-5

PubMed Abstract | CrossRef Full Text

3. Tungchama FP, Piwuna CG, Armiya'u AY, Maigari YT, Davou FJ, Umar MU, et al. Relationship between quality of life and postpartum depression among women in North-Central, Nigeria. Highland Med Res J. (2017) 17:11–8.

Google Scholar

4. Glover V. Maternal depression, anxiety and stress during pregnancy and child outcome; what needs to be done. Best Practice Res Clin Obstetrics Gynaecol. (2014) 28:25–35. doi: 10.1016/j.bpobgyn.2013.08.017

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Stewart DE, Vigod S. Postpartum depression. N Engl J Med. (2016) 375:2177–86. doi: 10.1056/NEJMcp1607649

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Kozinszky Z, Dudas RB. Validation studies of the edinburgh postnatal depression scale for the antenatal period. J Affect Disord. (2015) 176:95–105. doi: 10.1016/j.jad.2015.01.044

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Tran TD, Tran T, Fisher J. Validation of three psychometric instruments for screening for perinatal common mental disorders in men in the north of Vietnam. J Affect Disord. (2012) 136:104–9. doi: 10.1016/j.jad.2011.08.012

PubMed Abstract | CrossRef Full Text | Google Scholar

8. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders (DSM-5®): American Psychiatric Pub (2013). doi: 10.1176/appi.books.9780890425596

PubMed Abstract | CrossRef Full Text | Google Scholar

9. 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) 14:402. doi: 10.1186/s12884-014-0402-2

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Marshall EM, Simpson JA, Rholes WS. Personality, communication, and depressive symptoms across the transition to parenthood: A dyadic longitudinal investigation. Eur J Pers. (2015) 29:216–34. doi: 10.1002/per.1980

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Haddad S, Brown D, Dennis C, Lee K, Murray B, Pullenayegum E, et al. 1104 Maternal depression and sleep quality in early postpartum: Do maternal sleep-related cognitions and nighttime behaviours mediate the relationship? J Sleep Sleep Disord Res. (2017) 40(suppl_1):A411–2. doi: 10.1093/sleepj/zsx050.1103

CrossRef Full Text | Google Scholar

12. Hatton DC, Harrison-Hohner J, Coste S, Dorato V, Curet LB, McCarron DA. Symptoms of postpartum depression and breastfeeding. J Human Lactation. (2005) 21:444–9. doi: 10.1177/0890334405280947

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Yim IS, Stapleton LRT, Guardino CM, Hahn-Holbrook J, Schetter CD. Biological and psychosocial predictors of postpartum depression: systematic review and call for integration. Annu Rev Clin Psychol. (2015) 11:99. doi: 10.1146/annurev-clinpsy-101414-020426

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Ghaedrahmati M, Kazemi A, Kheirabadi G, Ebrahimi A, Bahrami M. Postpartum depression risk factors: A narrative review. J Educ Health Promot. (2017) 6.

PubMed Abstract | Google Scholar

15. Sacher J, Rekkas PV, Wilson AA, Houle S, Romano L, Hamidi J, et al. Relationship of monoamine oxidase-A distribution volume to postpartum depression and postpartum crying. Neuropsychopharmacology. (2015) 40:429–35. doi: 10.1038/npp.2014.190

PubMed Abstract | CrossRef Full Text | Google Scholar

16. VanderKruik R, Barreix M, Chou D, Allen T, Say L, Cohen LS. The global prevalence of postpartum psychosis: a systematic review. BMC Psychiatry. (2017) 17:272. doi: 10.1186/s12888-017-1427-7

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Wan Mohamed Radzi CWJB, Salarzadeh Jenatabadi H, Samsudin N. Postpartum depression symptoms in survey-based research: a structural equation analysis. BMC Public Health. (2021) 21:1–12. doi: 10.1186/s12889-020-09999-2

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Park EM, Meltzer-Brody S, Stickgold R. Poor sleep maintenance and subjective sleep quality are associated with postpartum maternal depression symptom severity. Arch Women's Mental Health. (2013) 16:539–47. doi: 10.1007/s00737-013-0356-9

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Gauthier C, Hassler C, Mattar L, Launay JM, Callebert J. Symptoms of depression and anxiety in anorexia nervosa: Links with plasma tryptophan and serotonin metabolism. Psychoneuroendocrinology. (2014) 39:170–8. doi: 10.1016/j.psyneuen.2013.09.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: symptoms, postpartum depression, role of family members, postpartum, family role attitudes

Citation: Nguyen HTT, Do LTK, Pham HTT, Hoang AP, Truong HT and Nguyen HTH (2022) The symptoms of postpartum depression observed by family members: A pilot study. Front. Psychiatry 13:897175. doi: 10.3389/fpsyt.2022.897175

Received: 15 March 2022; Accepted: 02 September 2022;
Published: 13 October 2022.

Edited by:

Michael Noll-Hussong, Saarland University, Germany

Reviewed by:

Rebecca Pearson, Manchester Metropolitan University, United Kingdom
Grace Lim, University of Pittsburgh, United States

Copyright © 2022 Nguyen, Do, Pham, Hoang, Truong and Nguyen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Anh Phuong Hoang, anh.hp@vinuni.edu.vn

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.