Journal of Obstetric, Gynecologic & Neonatal Nursing
RESEARCHA Community‐Based Screening Initiative to Identify Mothers at Risk for Postpartum Depression
Section snippets
Background and Significance
Postpartum depression is a common childbirth complication with documented prevalence estimated at 13% (13, 14, 22, 23). Although combinations of risk factors are likely to contribute to any individual woman's vulnerability to PPD, accumulating evidence suggests that PPD affects a cross‐section of women and that factors such as prenatal depression and history of maternal depression, current stress, poor quality of relationships, young age, very low socioeconomic status or education, and possibly
Theoretical Framework
The CARE screening design followed the Agency for Healthcare Research and Quality (AHRQ) framework recommended by Gaynes et al. (2005) in their evidence report on the impact of PPD screening, intervention, and patient outcomes. This framework begins by identifying a cohort of mothers in the postpartum period with unknown mood state, follows with formal postpartum screening using a valid measure, proceeds with clinical diagnostic evaluation for those with positive screens, employs random group
Methods
The research reported here makes up Phase 1 of the study, CARE Intervention for Depressed Mothers and Their Infants. Phase 1 involved recruiting, screening, and diagnostic evaluation of postpartum women to determine depression status and eligibility for enrollment in the randomized clinical trial (RCT). Results presented here include a description of the key features of an effective PPD screening protocol for women in the community, prevalence rates obtained for telephone and mail‐in screening
Measures
Edinburgh Postnatal Depression Scale (EPDS). The EPDS (Cox, 1986; Cox et al., l987) was designed specifically to identify symptoms of PPD and is the most widely used PPD screening instrument with community‐based populations in the United States and internationally (13, 14). The EPDS was used in the current study to identify mothers who were at risk for PPD. The EPDS consists of 10 statements describing depressive symptoms with some reverse‐coded items with four possible responses, each scored
Procedures
The study protocol was approved by Partners Health Care Human Subjects Committee and the Boston College Human Subjects Committee. Following PPD screening for possible RCT eligibility, the research nurse explained the study and asked mothers with positive PPD screening scores if they were willing to have an advanced practice registered nurse (APRN) make a home visit for a follow‐up assessment interview (i.e., the SCID). For willing mothers, formal informed consent was obtained by the APRN at
Follow‐Up Procedures
During screening, and at any point in the 9‐month clinical trial, whenever a mother's depression score was in the moderate to severe symptom range (i.e., EPDS ≥13) or her response to EPDS Item 10 (that indicated thoughts of self‐harm) was positive (i.e.,hardly ever, sometimes, oryes quite often), the research nurse determined whether the mother was currently receiving any mental health treatment and subsequently encouraged the mother to contact her clinician immediately. If the mother was not
PPD Screening and Prevalence
CARE study nurses received signed PCFs from 7,212 mothers that indicated permission to contact these mothers at 4 weeks postpartum. Figure 1 details the disposition of the 7,212 mothers. Of these 7,212 mothers, 3,018 (42%) mothers received their questionnaires in the mail and 3,806 (53%) were screened by telephone. Of those who received mailed forms, 1,363 (19% of the total population) sent them back and 1,655 (23% of the total population) did not. In addition, 88 (1.2%) women returned opt‐out
SCID Diagnostic Interview Results
Of the 674 mothers with positive screens, 268 (39%) agreed to be considered for the Phase 2 9‐month RCT and 267 (39%) declined, 74 (11%) mothers were deemed to be too late with respect to study timelines, 52 (9%) mothers were not reached by phone or mail, and 16 (2%) mothers did not meet inclusion criteria. The available data elicited from mothers indicated that reasons for declining to participate and/or not completing the diagnostic interview visit included being unable to schedule the home
Discussion and Implications
In the screening (Phase 1) of the CARE study mothers with unknown mood state were screened for PPD and those with positive screens who agreed then participated in diagnostic evaluation. Willing mothers who qualified were subsequently randomly assigned for participation in the RCT (Phase 2), and referred for treatment options as necessary during follow‐up. Feasibility of the AHRQ framework was validated, as more than 5,000 mothers were willingly screened for PPD with the EPDS. Because mothers in
Conclusions
In summary, results presented here demonstrate that mothers were receptive to PPD screening, by telephone and by mail. The risk factors identified add to the growing knowledge about mothers who may be at increased risk for PPD. Our findings reinforce the recommendations of Gaynes et al. (2005) for continued research to test the effectiveness of methods for routine PPD screening, including examination of whether health outcomes are improved through such screening efforts. The success of our PPD
Acknowledgments
Funded by CARE Intervention for Depressed Mothers and Their Infants, National Institutes of Health, National Institute for Nursing Research Grant #R01 NR008033 (2004‐2010).
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