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The impact of intimate partner violence on the trajectory of perinatal depression: a cohort study in a Chinese sample

Published online by Cambridge University Press:  02 June 2020

Fengsu Hou
Affiliation:
Department of Public Health, Shenzhen Kangning Hospital, Shenzhen, Guangdong Province, China Department of Psychiatry, University of Rochester Medical Center, Rochester, NY, USA
Xingyu Zhang
Affiliation:
Department of Systems, Populations and Leadership, School of Nursing, University of MichiganSchool of Nursing, University of Michigan, Ann Arbor, MI, USA
Catherine Cerulli
Affiliation:
Department of Psychiatry, University of Rochester Medical Center, Rochester, NY, USA Injury Control Research Center for Suicide Prevention, University of Rochester Medical Center, Rochester, NY, USA Susan B. Anthony Center, University of Rochester, Rochester, NY, USA
Wenjun He
Affiliation:
Department of Medical Statistics and Epidemiology, School of Public Health, Sun Yat-sen University, Guangzhou, Guangdong Province, China
Yushi Mo
Affiliation:
Xiangya School of Public Health, Central South University, China
Wenjie Gong*
Affiliation:
Department of Psychiatry, University of Rochester Medical Center, Rochester, NY, USA Xiangya School of Public Health, Central South University, China
*
Author for correspondence: Wenjie Gong, E-mail: gongwenjie@csu.edu.cn
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Abstract

Abstract

Aims

Intimate partner violence (IPV) is an important risk factor for perinatal depression (PND). But IPV's impact on the natural prognosis of PND symptoms is not well understood. We tested two hypotheses: (1) pregnant women with IPV experiences will exhibit more severe PND symptoms than women without IPV experience; (2) IPV experience will impede the recovery prognosis of PND. We also explored the contribution of IPV to PND comparing with other risk factors.

Method

The sample is comprised of 813 pregnant women followed through perinatal period in Hunan, China. We assessed IPV experience using items from the Short Form of the Revised Conflict Tactics Scale (CTS2S), and PND symptoms via the Edinburgh Postnatal Depression Scale (EPSD). We conducted Linear Mixed-effects Model to compare the trajectories of PND symptoms between victims and non-victims and a multistage Generalised Estimating Equations Model to explore salient factors on the trajectory of PND symptoms.

Results

There were 90 participants (11.07%) who reported IPV experience in the past 12 months. With respect to physical, psychological and sexual violence, the prevalence was 4.55% (37/813), 9.23% (75/813) and 2.34% (19/813). Victims reported more severe PND symptoms (t = 5.30, p < 0.01) and slower decreasing slope of trajectories (t = 28.89, p < 0.01). The PND trajectory was associated with IPV experience (OR = 3.78; 95% CI 1.39–10.26), social support (OR = 0.93; 95% CI 0.88–0.97), positive coping strategies (OR = 0.85; 95% CI 0.80–0.91), negative coping strategies (OR = 1.25; 95% CI 1.14–1.37) and monthly income of $0.15–$298.36 (compared to no income, OR = 0.0075; 95% CI 0.00052–0.11).

Conclusions

The findings suggest the reported prevalence of IPV is lower in Hunan than most of the previous studies during perinatal period in other provinces of China, and IPV victimisation is associated with increased severity and slowed prognosis of PND symptoms. Future studies that screen for victimisation and establish its explicit mechanism to the poorer prognosis of PND symptoms would benefit the prevention and treatment of PND.

Information

Type
Original Articles
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s), 2020. Published by Cambridge University Press
Figure 0

Table 1. The content of assessments at each time point

Figure 1

Table 2. Demographic characteristics of 813 participants

Figure 2

Table 3. The comparison of EPDS scores between victims and non-victims during follow-ups

Figure 3

Fig. 1. The trajectories of perinatal depression between IPV victims and non-victims.

Figure 4

Table 4. The univariate GEE analysis of perinatal depression and associated factors

Figure 5

Table 5. The multivariate GEE analysis of perinatal depression and associated factors