TY - JOUR
T1 - Oregon PRAMS 2012–2018
T2 - Revealing racial inequity in postpartum depression
AU - Docherty, Angie
AU - Stoyles, Sydnee
AU - Najjar, Rana
AU - Woolley, Rachel
N1 - Funding Information:
The authors would like to acknowledge the Oregon Public Health Division and Centers for Disease Control and Prevention.
Publisher Copyright:
© 2022 Wiley Periodicals LLC
PY - 2022/4
Y1 - 2022/4
N2 - Researchers have suggested that some women are undiagnosed and untreated for postpartum depression (PPD). However, there are mixed findings of the factors most likely to predict those most at risk. Recognizing historical racial and ethnic disparities existing in health outcomes, we sought to determine the extent of PPD inequity in Oregon. Using data from the Oregon pregnancy risk assessment monitoring system 2012–2018 and univariate weighted logistic regression models, we explored the relationship between PPD, maternal characteristics, and social variables. These variables included race/ethnicity, social support, life stressors, financial security, and perceived healthcare discrimination. A further phased analysis examined whether race/ethnicity remained a predictor of PPD when combined with other significant variables. Over 8000 respondents were included in the full phased analysis. Almost 17% of women reported they did not discuss depression with a provider during pregnancy, including over 12% who reported PPD symptoms. Black, Asian/Pacific Islander (API), American–Indian, and mixed race mothers had increased odds of PPD compared to White women (odds ratio ranged from 1.55 to 1.87). Less than baccalaureate education, lack of social support, and perceived healthcare discrimination also increased the odds of PPD. The phased analysis showed that significant differences in odds of PPD symptoms remained between Black, APIs, and American–Indian mothers compared to White mothers. Our analysis suggests that race is an important predictor of PPD. The knowledge of who is most at risk, and the provision of adequate assessment and screening, is of fundamental importance in today's society.
AB - Researchers have suggested that some women are undiagnosed and untreated for postpartum depression (PPD). However, there are mixed findings of the factors most likely to predict those most at risk. Recognizing historical racial and ethnic disparities existing in health outcomes, we sought to determine the extent of PPD inequity in Oregon. Using data from the Oregon pregnancy risk assessment monitoring system 2012–2018 and univariate weighted logistic regression models, we explored the relationship between PPD, maternal characteristics, and social variables. These variables included race/ethnicity, social support, life stressors, financial security, and perceived healthcare discrimination. A further phased analysis examined whether race/ethnicity remained a predictor of PPD when combined with other significant variables. Over 8000 respondents were included in the full phased analysis. Almost 17% of women reported they did not discuss depression with a provider during pregnancy, including over 12% who reported PPD symptoms. Black, Asian/Pacific Islander (API), American–Indian, and mixed race mothers had increased odds of PPD compared to White women (odds ratio ranged from 1.55 to 1.87). Less than baccalaureate education, lack of social support, and perceived healthcare discrimination also increased the odds of PPD. The phased analysis showed that significant differences in odds of PPD symptoms remained between Black, APIs, and American–Indian mothers compared to White mothers. Our analysis suggests that race is an important predictor of PPD. The knowledge of who is most at risk, and the provision of adequate assessment and screening, is of fundamental importance in today's society.
KW - health equity
KW - postpartum depression
KW - race/ethnicity
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U2 - 10.1002/nur.22214
DO - 10.1002/nur.22214
M3 - Article
C2 - 35128706
AN - SCOPUS:85124469495
SN - 0160-6891
VL - 45
SP - 163
EP - 172
JO - Research in Nursing and Health
JF - Research in Nursing and Health
IS - 2
ER -