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PREPP: Postpartum Depression Prevention through the Mother-Infant Dyad

Authors:

Abstract

Most interventions to prevent postpartum depression (PPD) focus on the mother rather than the mother-infant dyad. As strong relationships between infant sleep and cry behavior and maternal postpartum mood have been demonstrated by previous research, interventions targeted at the dyad may reduce symptoms of PPD. The goal of the current study was to examine the effectiveness of Practical Resources for Effective Postpartum Parenting (PREPP). PREPP is a new PPD prevention protocol that aims to treat women at risk for PPD by promoting maternally mediated behavioral changes in their infants, while also including mother-focused skills. Results of this randomized control trial (RCT) (n = 54) indicate that this novel, brief intervention was well tolerated and effective in reducing maternal symptoms of anxiety and depression, particularly at 6 weeks postpartum. Additionally, this study found that infants of mothers enrolled in PREPP had fewer bouts of fussing and crying at 6 weeks postpartum than those infants whose mothers were in the Enhanced TAU group. These preliminary results indicate that PREPP has the potential to reduce the incidence of PPD in women at risk and to directly impact the developing mother-child relationship, the mother's view of her child, and child outcomes.
ORIGINAL ARTICLE
PREPP: postpartum depression prevention through
the motherinfant dyad
Elizabeth A. Werner
1
&Hanna C. Gustafsson
1
&Seonjoo Lee
3,4
&
Tianshu Feng
3
&Nan Jiang
1
&Preeya Desai
1
&Catherine Monk
1,2
Received: 2 March 2015 /Accepted: 5 July 2015
#Springer-Verlag Wien 2015
Abstract Most interventions to prevent postpartum depres-
sion (PPD) focus on the mother rather than the motherinfant
dyad. As strong relationships between infant sleep and cry
behavior and maternal postpartum mood have been demon-
strated by previous research, interventions targeted at the dyad
may reduce symptoms of PPD. The goal of the current study
was to examine the effectiveness of Practical Resources for
Effective Postpartum Parenting (PREPP). PREPP is a new
PPD prevention protocol that aims to treat women at risk for
PPD by promoting maternally mediated behavioral changes in
their infants, while also including mother-focused skills.
Results of this randomized control trial (RCT) (n=54) indicate
that this novel, brief intervention was well tolerated and effec-
tive in reducing maternal symptoms of anxiety and depres-
sion, particularly at 6 weeks postpartum. Additionally, this
study found that infants of mothers enrolled in PREPP had
fewer bouts of fussing and crying at 6 weeks postpartum than
those infants whose mothers were in the Enhanced TAU
group. These preliminary results indicate that PREPP has the
potential to reduce the incidence of PPD in women at risk and
to directly impact the developing motherchild relationship,
the mothers view of her child, and child outcomes.
Keywords Pregnancy .Postpartum depression .Anxiety .
Randomized control trial .Infant fuss and cry
Of the over 4 million live births each year in the USA, nearly
800,000or 20 %of these mothers will develop major or
minor depression within the first 3 months postpartum. These
numbers dwarf prevalence rates for gestational diabetes (25%)
and preterm birth (12.7 %) (Dabelea et al. 2005; Saigal and
Doyle 2008). Postpartum Depression (PPD) affects the mother
and her infant. It is associated with marital discord and impaired
occupational and social functioning, particularly with respect to
maternalinfant interactions that are characterized by disengage-
ment, hostility, and intrusion (Burke 2003;Lovejoyetal.2000;
Martins and Gaffan 2000;Murrayetal.1995). Child outcomes
include poor cognitive functioning, as well as emotional and
behavioral problems such as increased risk for externalizing
disorders and future psychopathology (Cicchetti et al. 1998;
Grace et al. 2003; Kurstjens and Wolke 2001). These deleterious
effects on child developmental trajectories have been shown
even when controlling for family SES and subsequent maternal
mental illness, indicating the importance of preventing PPD
during this critical period in development (Hay et al. 2001).
Existing clinical treatments for the prevention of PPD use
standard approaches that focus solely on the mother, e.g.,
pharmacologic and psychological interventions to reduce
womens symptoms. Given the complex genetic, biological,
and environmental etiology of depression, there is a need for
an array of intervention and treatment options; given the spe-
cific context in which PPD occurs, it is logical to exploit the
unique dyadic orientation of this period when designing new
treatment strategies. It also is important to consider the reasons
Hanna C. Gustafsson is co-first author.
*Elizabeth A. Werner
ew150@cumc.columbia.edu
1
Division of Behavioral Medicine, Department of Psychiatry,
Columbia University Medical Center, 622 West 168th Street,
PH1540-E, New York, NY 10032, USA
2
New York State Psychiatric Institute, New York, NY, USA
3
Division of Biostatistics, New York State Psychiatric Institute, New
York, NY, USA
4
Department of Biostatistics and Psychiatry, Columbia University,
New York, NY, USA
Arch Womens Ment Health
DOI 10.1007/s00737-015-0549-5
that PPD is significantly undertreated when developing a new
prevention protocol (Werner et al. 2014), e.g., time constraints
during the postpartum period and reluctance to take psycho-
tropic medications when breastfeeding (Ballestrem et al.
2005; Boath et al. 2004; Whitton et al. 1996).
This report describes a small, randomized control trial
(RCT) of a novel, brief, preventive intervention for PPD
called PREPP, Practical Resources for Effective Postpartum
Parenting, which aims to determine if a behavioral interven-
tion primarily targeting maternal caregiving of young infants
can increase infant sleep and reduce fuss/cry behavior, and
thereby reduce the incidence and/or severity of postpartum
maternal depression. PREPP integrates emerging, evidence-
based caregiving techniques, traditional psychotherapy ap-
proaches, psycho-education, as well as mindfulness medita-
tion training to treat at-risk women by promoting maternally
mediated behavioral changes in their infants.
Risks for PPD, including infant behaviors
Established risk factors for PPD include prenatal depres-
sion and anxiety, low social support, and a history of psy-
chopathology (OHara and Swain 1996; Beck 1996;
Seguin et al. 1999). Emerging data shows strong associa-
tions between infant behavior and maternal mood dysreg-
ulation. In several papers, greater infant fuss/cry and poor
sleep behavior were associated with maternal depression
(Armstrong et al. 1998; Bayer et al. 2007;Dennisand
Ross 2005; Hiscock and Wake 2001;Maxtedetal.2005;
Radesky et al. 2013;Viketal.2009). More specifically, in
a study of 55 dyads, infant crying at 3 months (based on
maternal report and laboratory observation) accounted for
30 % of the variance in PPD symptoms; the effect was
direct, and indirect, through the mediation of reducing
levels of parenting self-efficacy (Cutrona and Troutman
1986). In a prospective study of 180 women at risk for
PPD, objectively assessed neonatal irritability and poor
motor function predicted PPD at 2 months (estimated con-
tribution to log odds were 1.37 and 1.18, respectively,
p<0.0005); as these infant behaviors improved, so did ma-
ternal depression scores (Murray et al. 1996). Barr et al.
found that at 6 weeks postpartum, mother-reported infant
cry/fuss duration and frequency were positively associated
with postpartum distress (r(88)=0.45 and 0.28, p<0.01,
respectively) (Miller et al. 1993). Distress levels increased
pre- to postpartum in women whose infants met clinical
criteria for Bcolic^(Miller et al. 1993). There also is an
association between infant sleeping problems and PPD,
which may be mediated via disruption in womens sleep
(Armstrong et al. 1998; Bayer et al. 2007;DennisandRoss
2005; Hiscock and Wake 2001). To date, including the
treatment of infant behaviors in PPD interventions is only
beginning (Hiscock and Wake 2002; Hiscock et al. 2014).
Prevention of PPD
There have been many RCTs of psychological preventive in-
terventions for PPD. In a recent systematic review, Werner and
colleagues (2014) identified 37 psychological and psychoso-
cial intervention RCTs of which 17 were found to be effective.
Of these 17 effective RCTs, 13 were conducted with at-risk
populations, suggesting the importance of utilizing known
PPD risk factors as inclusion criteria when targeting women
for PDD preventive treatment. These authors (Werner et al.
2014) and others (Boath et al. 2004; Whitton et al. 1996;
Ballestrem et al. 2005) highlight several reasons that treat-
ments to prevent PPD may not be effective, including (1)
non-validated approaches to measure risk for PPD (Werner
et al. 2014), (2) emphasis on pharmacology when women
are breast feeding (Boath et al. 2004; Whitton et al. 1996),
and (3) high rates of attrition (Werner et al. 2014), which
may result from (a) stigma associated with receiving mental
health care (McIntosh 1993), (b) lack of accessibility, includ-
ing difficulty attending appointments with a new baby
(Ballestrem et al. 2005), and (c) a sole focus on the moth-
erwhich overlooks the child-centered orientation of the
perinatal period and the salience of maternalinfant interac-
tions to maternal well-being (Kochanska et al. 2000,2001,
2009; Kochanska and Aksan 2006; Feldman and Eidelman
2006;Feldman2007). Addressing these limitations is crucial
to developing successful PPD preventive interventions
(Werner et al. 2014).
Infant sleep and cry interventions
Largely independent of PPD interventions, several caregiving
techniques have been shown to positively affect infant sleep
and fuss/cry behavior (Meyer and Erler 2011; Pinilla and
Birch 1993; St. James-Roberts and Gillham 2001;Van
Sleuwen et al. 2007). For example, Pinilla and Birch (1993)
found that their intervention program was highly effective in
changing parent behavior and improving infant sleep duration
when delivered to parents in the home over multiple sessions
up to 8 weeks post-delivery, though parents were less compli-
ant with the same protocol when given instructions for it dur-
ing a home visit within 814 days post-birth, and there was
little effect on infant sleep (St. James-Roberts and Gillham
2001). In Pinilla and Birchs study of 26 first-time parents,
13 were assigned to a behavioral intervention, which, by
4 weeks postpartum, resulted in 38 % of infants sleeping
through the night (defined as sleeping without signaling for
attention between 12 and 5 A.M. for several consecutive nights)
compared to 7 % for the control group; by 8 weeks postpar-
tum, 100 % of the intervention group slept through the night
compared to 23 % (Pinilla and Birch 1993). This intervention
protocol encompassed several infant behavioral techniques to
increase nighttime sleeping in infants, including providing a
E.A. Werner et al.
focal feeding to the infant between 10 P. M . and midnight, ac-
centuating differences between day and night by providing
higher levels of stimulation during the day, and lengthening
the latency to feeding time in the middle of the night by en-
gaging in other attentive activities such as walking with the
baby and diapering, thereby extinguishing the association be-
tween night time waking and feeding (Pinilla and Birch 1993;
St. James-Roberts and Gillham 2001). In other research,
swaddling has been identified as a tool that can promote sleep
continuity, fewer awakenings, and more quiet sleep as evi-
denced in both laboratory and descriptive studies (Van
Sleuwen et al. 2007). In an RCT conducted in Germany
(Meyer and Erler 2011) of 85 healthy infants studied in a sleep
laboratory, swaddling was found to reduce the rate of sponta-
neous awakening, the number of sleep stage changes, and the
amount of time spent awake. It also was found to promote
quiet sleep and sleep efficiency (Meyer and Erler 2011).
There are other behavioral techniques to reduce infant
fussing and crying behavior. Barr et al. conducted a random-
ized controlled trial on the effects of increased carrying on
infant fuss/cry behavior (Hunziker and Barr 1986). At 3 weeks
postpartum, 99 dyads were randomly assigned to increased
carrying or no intervention; by 6 weeks post-delivery, the peak
age for crying, infants in the intervention group cried and
fussed 43 % less overall and 51 % less during 4 P.M .tomid-
night; similar but smaller differences were found at 4, 8, and
12 weeks (Hunziker and Barr 1986). However, these results
have not been consistently replicated. For example, when the
carrying intervention was taught to women in the hospital in
Britain immediately following birth, there were no effects of
increased carrying on infant cry/fuss behavior (St. James-
Roberts et al. 1995).
As indicated, few studies have examined whether these
caregiving techniques have an impact on maternal depressive
symptoms. In the first of its kind, Hiscock et al. (2014)pro-
vided 781 motherinfant dyads with written materials and an
educational DVD that presented information about infant
sleep cycles and crying patterns, strategies to promote inde-
pendent settling (e.g., swaddling), and information about self-
care for parents. Mothers in the intervention group were sig-
nificantly less likely to meet criteria for possible depression
(>9 on the Edinburgh Postnatal Depression Scale) when their
infant was 6 months old, though there were no differences
between the intervention and control groups at 4 months post-
partum. These caregiving techniques also were effective in
reducing daytime sleep and crying problems, but only for a
subset of their participants who they characterized as
Bfrequent feeders^by caregiver report. These findings provide
promising evidence that behavioral techniques targeting ma-
ternal care can be a useful component of PPD intervention
programs, though they require replication, and several ques-
tions remain. For example, maternal depressive symptoms
were studied at 4 and 6 months postpartum, yet the
Diagnostic and Statistical Manual of Mental Disorders (5th
ed.; American Psychiatric Association, 2013) specifies that
PPD has an onset within the first 4 weeks after birth. Given
the significance of this early developmental period for chil-
drens long-term functioning (e.g., Hay et al. 2001), examin-
ing maternal depressive symptoms earlier in development is
critical. Second, Hiscock et al.s intervention program recruit-
ed women 710 days postpartum, potentially after mothers
already had started to become symptomatic. It remains unclear
if intervening earlier (i.e., during pregnancy) would help to
prevent these symptoms from developing, resulting in differ-
ences in maternal well-being that are observable earlier in the
childs life. Third, these authorsand most other PPD preven-
tion studies (Werner et al. 2014)only focused on maternal
depressive symptoms when assessing postpartum mood.
However, there is evidence that women with PDD often have
severe anxiety and even panic attacks (Miller et al. 2006). The
extent to which these caregiving techniques also may improve
maternal anxiety in the postnatal period has been not been
studied.
Other tools for maternal mood intervention postpartum
The use of psychoeducation about the hormonal and psycho-
social changes that occur during the postpartum period has
been shown to be effective in the reduction of postpartum
depressive symptoms (Elliott et al. 2000; Matthey et al.
2004). In addition, programs like the Period of PURPLE cry-
ing (Barr et al. 2009) have been effective in improving mater-
nal knowledge about infant crying and developing coping
mechanisms to deal with the maternal upset caused by incon-
solable crying. Mindfulness meditation is another strategy that
can help women to cope better when their babies are distress-
ed and/or unsoothable. The success of a recent trial of a
mindfulness-based therapy for the prevention of perinatal de-
pressive relapse/recurrence suggests that the use of these types
of techniques may contribute to the prevention of PPD
(Dimidjian et al. 2014). To date, these therapeutic tools that
are aimed directly at helping the mother (e.g., mindfulness
meditation, psychoeducation about perinatal biological and
emotional changes) have not been added to an intervention
protocol focused on caregiving techniques.
The current study
The goal of the current study was to examine the effectiveness
of PREPP, a new PPD preventionprotocol that aims to treat at-
risk women by promoting maternally mediated behavioral
changes in their infants, while also including mother-focused
skills. In a sample of 54 dyads, we sought to test if PREPP
compared to an enhanced treatment as usual (ETAU) group
(1) reduces depression and anxiety symptoms during the early
postnatal period, (2) decreases infant fuss and cry behavior,
PREPP: postpartum depression prevention
and (3) has high rates of treatment compliance given the brief
number of sessions that are timed to perinatal medical sessions
and the description of the intervention as coaching.
Methods
Overview
Figure 1provides a schedule of participantsassessment and
PREPP sessions. Women were recruited and screened for
study eligibility by telephone (including PPD risk using the
Predictive Index of Postnatal Depression, Cooper et al. 1996)
in their third trimester of pregnancy. Between 34 and
38 weeksgestation, potential participants came to the labora-
tory to provide informed consent and complete mood ques-
tionnaires by self-report and interviewer administration
(Assessment 1). They also met with the clinical psychologist
who informed them of their treatment group assignment as
dictated by a computer-generated random assignment sched-
ule. Participants who were assigned to the PREPP group re-
ceived their first session of PREPP, while those in the ETAU
group were provided with an information session about PPD,
a brief clinical mood assessment, and a referral for treatment if
warranted or requested by the participant. Between 18 and
36 h after giving birth, all participants were visited by a re-
search assistant who collected medical information about their
delivery. Those in the PREPP intervention received their sec-
ond treatment session with the psychologist. At 2 weeks post-
partum, participants in the PREPP group received a check-in
telephone call from the psychologist with whom they had
been working. Those in the ETAU group received a brief
check-in call from the research assistant. At 6 weeks postpar-
tum, all participants returned to the laboratory to complete
mood assessments and meet with the psychologist
(Assessment 2). Women in the PREPP group received their
final PREPP session, while those in the ETAU group were
again given information about PPD and were clinically
assessed and referred to treatment when appropriate. At
10 weeks postpartum, participants were contacted by tele-
phone and completed the mood questionnaires via telephone
(Assessment 3). At 16 weeks postpartum, these questionnaires
were administered in person in the laboratory (Assessment 4).
Participants
Pregnant women ages 1845 in their second or third trimester
of pregnancy were recruited through the Department of
Obstetrics and Gynecology at Columbia University Medical
Center (CUMC) and via flyers posted at CUMC. Women who
reported smoking tobacco or using recreational drugs, lacking
fluency in English, currently receiving psychological/
psychiatric treatment, taking medication, having a medically
complicated pregnancy, or carrying a non-singleton pregnan-
cy were not eligible for enrollment in this study. This trial was
registered with clinicaltrials.gov: NCT01379781. All study
procedures were approved by the Institutional Review Board
of the New York State Psychiatric Institute/CUMC.
Participants were compensated for their assessment sessions,
and the travel to and from the meetings, but not for interven-
tion sessions.
Assessment measures
Predictive index of PPD
When women were 2838 weeks pregnant, potential partici-
pants were screened via telephone for their risk for PPD. PPD
risk was defined as scoring above 24 on the Predictive Index
of Postnatal Depression (Cooper et al. 1996). This 17-item
questionnaire asks women about factors that may predispose
them to PPD (e.g., BHave you felt particularly depressed or
miserable over the last few weeks?^BAfter any previous de-
livery were you particularly miserable or depressed at any
time during the following year?^BHas this pregnancy been
a positive experience for you?^). This widely used measure
has been shown to have adequate sensitivity and specificity
(Cooper et al. 1996).
Hamilton rating scales of depression and anxiety
Maternal depressive symptoms were measured by a trained
interviewer blind to the participantsgroup assignment
using the Hamilton Rating Scale for Depression (HRSD),
a1520-min rater-administered measure that indexes de-
pressive symptoms over the previous 2 weeks (Williams
1988). The HRSD values of 813 indicate mild depression,
Fig. 1 Assessment and treatment session schedule
E.A. Werner et al.
1418 indicate moderate depression, and 1922 indicate
severe depression (Hamilton 1960). Maternal symptoms
of anxiety were measured using the 1015-min Hamilton
Anxiety Rating Scale (HAM-A, Hamilton 1959), which
also indexes symptomatology over the previous 2 weeks.
Values less than 17 on this scale indicate mild severity, 18
24 indicates mild to moderate anxiety, and 2530 indicates
moderate to severe anxiety (Hamilton 1959). The validity
and reliability of the HRSD and HAM-A is well established
(Maier et al. 1988; Ramos-Brieva and Cordero-Villafafila
1988;Trajkovićet al. 2011).
Patient health questionnaire
Maternal depressive symptoms also were assessed using
the depression module of the patient health questionnaire
(PHQ-9; Kroenke and Spitzer 2002), a nine-item self-re-
port measure that assesses the DSM-IV diagnostic criteria
for depression (αranged from 0.72 to 0.77 at the various
assessment time points). Respondents are asked to rate on
a 3-point Likert-type scale (where 0=not at all and 3=
nearly every day) how frequently they were bothered by
specific symptoms over the past 2 weeks. An example
item reads Bfeeling down, depressed, or hopeless.^
Scores of 04 on this scale indicate minimal depression,
59 indicates mild depression, 1014 indicates moderate
depression, 1519 indicates moderately severe depression,
and 2027 indicates severe depression (Kroenke et al.
2001).
Infant fuss/cry episodes
Data about infant fussing and crying were obtained using
the BabysDayDiary(Barr 1985). Over four 24-h pe-
riods, mothers recorded the duration and frequency of
seven infant behavioral states: awake, alert, fussing, cry-
ing, inconsolable crying, feeding, and sleeping. Mothers
also recorded the duration and frequency of body contact
with their infants. A number of variables are produced
from these diaries, including the total number of episodes
during which the infant was fussing or crying. Following
previously published reports using this measure (e.g.,
Wol k e et al. 1994), the total number of episodes during
which the infant was fussing or crying was averaged over
the 4 days to arrive at an average daily frequency of fuss/
cry episodes. This measure has been well validated, as
evidenced by high correlations between its metrics and
audio recordings of fussing and crying (e.g., agreements
around 0.9) (Barr et al. 1988; St. James-Roberts et al.
1993). Importantly, previous research has found that the
quality of reporting using this measure is not biased by
caregiver depressive symptoms (Miller et al. 1993).
Intervention: PREPP and ETAU
PREPP
PREPP comprised a number of infant behavioral interven-
tions and targeted psychotherapy techniques. The partici-
pants in the PREPP arm of the study received three consec-
utive in-person sessions with a Ph.D.-level psychologist.
These sessions were described to the participants as
Bcoaching^sessions to minimize stigma that many women
associate with receiving mental healthcare during the peri-
natal period (Dennis and Chung-Lee 2006). The psycholo-
gist also contacted participants by telephone at 2 weeks
postpartum and, using motivational interviewing tech-
niques, encouraged the use of PREPP skills and answered
specific participant questions. To increase accessibility for
patients, the three in-person sessions were scheduled to
coincide with standard medical visits: (1) 3438 weeks
(third trimester ultrasound), (2) in the hospital post-
delivery (delivery), and (3) 6 weeks postpartum (6-week
well baby visit). Although this was a standardized protocol,
the instructional visits were personalized and varied in re-
sponse to womens needs and concerns.
The intervention protocol encompassed the following five
specific infant behavioral techniques, supported by emerging
research and aimed at reducing infant fuss/cry behavior and
promoting sleep (Barr et al. 2009; Meyer and Erler 2011;
Pinilla and Birch 1993; St. James-Roberts and Gillham
2001; Van Sleuwen et al. 2007): (1) feeding the infant between
10 P.M. and midnight, even if s/he must be awakened (Bafocal
feed^) (Pinilla and Birch 1993; St. James-Roberts and
Gillham 2001); (2) accentuating differences between day
and night by providing higher levels of stimulation during
the day (Pinilla and Birch 1993; St. James-Roberts and
Gillham 2001); (3) lengthening the latency to feeding time
in the middle of the night by engaging in other attentive ac-
tivities such as walking with the baby and diapering, thereby
extinguishing the association between night time waking and
feeding (Pinilla and Birch 1993; St. James-Roberts and
Gillham 2001); (4) carrying infants for a minimum of 3 h a
day, throughout the day, in addition to the carrying that occurs
in response to crying and feeding (Barr et al. 2009); and (5)
learning to swaddle the baby (Van Sleuwen et al. 2007). As
part of the intervention, women also were provided with (1)
supportive psychological interviewing that encourages reflec-
tion on their own childhood and how it will inform the devel-
opment of their parental identity, (2) psychoeducation about
the postpartum period (e.g., hormone levels, Baby Blues, in-
fant cry behavior/patterns based on materials from the Period
of Purple Crying campaign; Barr et al. 2009), and (3) various
mindfulness techniques aimed at (a) helping them to cope
better when their babies are distressed and/or unsoothable
and (b) aiding them to return to sleep after tending to their
PREPP: postpartum depression prevention
babies during the nighttime. In the first visit, participants are
given a carrier and a swaddling blanket to use with their
babies.
Enhanced TAU
Participants in the ETAU condition met with a Ph.D.-level
clinical psychologist on two occasions: (1) 3438 weeksges-
tation and (2) 6 weeks postpartum. During these visits, the
psychologist discussed PPD symptoms with participants and
offered referrals for mental health care. The psychologist pro-
vided suitable referrals and clinical follow-up for all partici-
pants who reported symptoms of depression or anxiety or if
the participant expressed interest in such a referral.
Participants also were provided with printed educational ma-
terials about the symptoms of PPD and supportive services in
the community.
Analytic strategy
A series of linear mixed effects models (McCulloch and
Neuhaus 2001) were used to assess the effect of the PREPP
intervention on participantspsychiatric symptomatology.
Specifically, three linear mixed effects models were conducted,
one for each of the maternal mood measures (i.e., HRSD,
HAM-A, and PHQ-9). In each of these models, the partici-
pants intervention status (0=ETAU, 1 = PREPP) was entered
as a predictor of change in maternal mood over time. Linear
mixed effects models can accommodate missing data, and
therefore no participants were excluded from analyses due to
missing data. A univariate analysis of variance (ANOVA) was
used to test whether women in the PREPP and ETAU groups
differed in their report of infant fuss/cry behaviors. All analyses
were conducted using SPSS version 22.0 (IBM Corporation,
Armonk, NY) and adhered to intention-to-treat principles with
one exception: one participant who was randomized to the
PREPP condition was immediately referred to intensive psy-
chiatric treatment during the first intervention session and sub-
sequently attended twice-weekly treatment throughout the du-
ration of the study. As current mental health treatment was an
exclusion criterion for the study (and in an effort not to overes-
timate the effectiveness of the study treatments), we made an a
priori decision to exclude her from analyses.
Results
Recruitment and enrollment
Of the 619 individuals who were screened for this study
between July 2011 and December 2013, 95 (15 %) were
eligible to enroll. The majority of individuals who were
deemed ineligible did not score high enough on the
Predictive Index of Postnatal Depression to be considered
at risk for PPD (n=261); other common reasons for ineli-
gibility were if they were having a medically complicated
pregnancy (n=54), if they delivered their child prior to
being screened for the study (n=52), and if they were not
interested in participating in research (n=50). Of the 95
women who were eligible for the current study, 54 (57 %)
were enrolled and randomized to either the PREPP (n=27)
or ETAU (n=27) condition. The majority of women who
were eligible but did not enroll were lost to follow-up (n=
22) or did not show to their consent appointment (n=13).
More detailed information about screening, eligibility, and
enrollment can be found in Fig. 2.
Demographics and baseline mood measures
Demographic information about the sample appears in
Tab le 1. The groups did not differ significantly from one an-
other on any of these variables.
Treatment adherence and assessment attrition
All participants who were randomized to the PREPP interven-
tion condition received the entire treatment. That is, they all
attended and completed the prenatal, newborn, and 6-week
postpartum treatment sessions and had a phone session with
the psychologist at 2 weeks postpartum. With respect to as-
sessment sessions, there are missing data.
Of the 54 participants who were randomized to either the
PREPP or the ETAU conditions, all completed the first assess-
ment. The participant (described above) who was randomized
to the PREPP condition but who was immediately referred to
intensive psychiatric treatment discontinued participation at
this session. Eight individuals did not complete the 6-week
postpartum session, 13 did not complete the 10-week postpar-
tum session, and 18 did not complete the 4-month postpartum
session. Individuals who did or did not participate in these
assessments did not differ from one another on any of the
demographic or pre-randomization mood variables, with one
exception: participants who did not complete the 6-week as-
sessment (n=8), on average, had lower Predictive Index of
Postnatal Depression scores at screening (m=27, SD=2.5)
than those who did participate (m=30.7, SD=2.5), p<0.05.
Figure 2presents more detailed information about participant
attrition for assessment sessions.
Treatment effects
Clinical relevance of average maternal mood by group
at each session
Participant scores on the Predictive Index of Postnatal
Depression at screening and descriptive information (i.e.,
E.A. Werner et al.
means, standard deviations, range) about womens HRSD,
HAM-A, and PHQ-9 scores prior to randomization (at 36
38 gestational weeks) and at the various assessment time
points appear in Table 2. At the pre-randomization assess-
ment, participants (n=53), on average, scored in the
Bmoderate depression^range on the HRSD (m=16.11, SD=
11.86), in the Bmild anxiety^range on the HAM-A (m=16.45,
SD= 12.26), and in the Bmild depression^range on the PHQ-9
(m=7.12, SD=3.97). The PREPP and ETAU groups did not
differ statistically from one another on any of these variables
at study entry, although the mean of the PREPP group fell in
the Bmoderate depression^range and the ETAU groupsmean
was in the Bmild depression^range.
At the 6-week postpartum session, participants in the
PREPP group, on average, scored in the Bmild depression^
range on the HRSD (m= 12.09, SD= 7.31), whereas those in
the ETAU group scored in the Bmoderate depression^range
(m=17.17, SD=9.81). As can be seen in Table 2,bothgroups,
on average, scored in the Bmild depression^range at the 10-
and 16-week postpartum sessions. At 10 weeks postpartum,
the average PHQ-9 score for the PREPP group indicated
Bmild depression^; the average score was at the Bmoderate
Fig. 2 Consort diagram
PREPP: postpartum depression prevention
Tabl e 1 Participant demographic
information and mood variables
prior to randomization
PREPP Enhanced TAU
Mean (SD) or % nMean (SD) or % n
Maternal age (years) 30.87 (6.51) 26 29.60 (5.67) 27
Relationship status
Living together 34.60 % 9 33.33 % 9
Married 38.50 % 10 29.63 % 8
Not living together 7.69 % 2 11.11 % 3
Single 15.40 % 4 18.52 % 5
Divorced 0.00 % 0 7.41 % 2
Race
Asian 7.70 % 2 7.41 % 2
Black/African American 15.40 % 4 22.22 % 6
White/Caucasian 15.40 % 4 7.41 % 2
Biracial 3.80 % 1 0.00 % 0
Other 53.80 % 14 62.96 % 17
Ethnicity
Hispanic 57.70 % 15 59.26 % 16
Not Hispanic 38.50 % 10 37.04 % 10
Maternal education (years) 15.94 (4.19) 25 14.82 (2.53) 27
Number of other children 0.44 (0.65) 25 0.67 (.83) 27
Employment status
Not working outside of home 38.50 % 10 48.15 % 13
Full time 38.50 % 10 25.93 % 7
Part time 19.20 % 5 25.93 % 7
Paternal age (years) 35.25 (8.41) 24 31.15 (6.71) 27
Tabl e 2 Means and standard deviations of maternal mood variables
PREPP intervention Enhanced TAU
Mean (SD) Range Severity Mean (SD) Range Severity
Predictive index of postnatal depression
2838 weeks GA 31.19 (6.09) 2547 29.07 (2.81) 2535
HRSD
3638 weeks GA 18.48 (12.82) 048 Moderate 13.83 (10.64) 144 Mild
6 weeks postpartum 12.09 (7.31) 124 Mild 17.17 (9.81) 235 Moderate
10 weeks postpartum 11.48 (8.45) 027 Mild 13.44 (10.48) 040 Mild
16 weeks postpartum 10.48 (10.31) 033 Mild 11.12 (9.43) 030 Mild
HAM-A
3638 weeks GA 19.35 (13.79) 144 Mild/moderate 13.67 (10.11) 136 Mild
6 weeks postpartum 11.73 (8.20) 126 Mild 14.17 (8.49) 331 Mild
10 weeks postpartum 11.07 (8.22) 028 Mild 12.00 (8.96) 133 Mild
16 weeks postpartum 9.33 (9.77) 033 Mild 11.53 (9.10) 033 Mild
PHQ-9
3638 weeks GA 6.45 (3.57) 015 Mild 7.79 (4.31) 118 Mild
6 weeks postpartum 7.16 (4.39) 014 Mild 10.08 (5.03) 116 Moderate
10 weeks postpartum 7.06 (5.04) 121 Mild 8.29 (4.06) 117 Mild
16 weeks postpartum 4.00 (3.30) 011 Minimal 7.22 (4.13) 017 Mild
E.A. Werner et al.
depression^level for the ETAU group; at 16 weeks, PHQ
results showed the PREPP participants at the Bminimal level^
of depression, while those in the ETAU sample had an average
score that remained in the Bmild^range.
Change in maternal mood by treatment group
Results from the mixed effects models that were used to test
whether the PREPP intervention had an effect on maternal
symptoms of depression or anxiety are presented in Table 3.
Consistent with expectation, these results indicate that women
who underwent PREPP compared to those who received the
ETAU differed significantly from one another in their change
in symptomatology over time.
Specifically, HRSD and HAM-A results show women who
received the PREPP intervention decreased significantly in their
HRSD-rated depressive symptoms (B=6.54, p=0.01) between
the pre-randomization assessment (i.e., at 3638 weeksgesta-
tion) and the 6-week postpartum session. In contrast, women in
the ETAU group had no significant change between the prenatal
and 6-week postpartum assessment (B=3.02, p=0.22). The re-
sults for anxiety are consistent with those for depression, such
that women in PREPP decreased significantly in their HAM-A-
rated symptoms of anxiety between the pre-randomization as-
sessment and 6 weeks postpartum (B=7.84, p<0.01), whereas
those in the ETAU group did not change significantly over this
period of time (B=0.24, p=0.94). These PREPP effects
remained marginally significant (p<0.10) at the 10-week as-
sessment for both HRSD and HAM-A findings and were statis-
tically significant for HAM-A scores at 16 weeks postpartum
(p<0.05). As a complement to the results from these mixed
effects models, Figs. 3and 4present the average change scores
(presented separately by treatment condition) for HRSD and
HAM-A scores, respectively.
For the PHQ-9, results from the mixed effects model were as
follows. The PREPP group did not change significantly be-
tween the prenatal and 6-week postpartum session (B=0.61,
p=0.58). The ETAU group, however, reported significantly
more depressive symptoms at the 6-week postpartum session,
relative to the pre-randomization assessment (B= 2.44, p=
0.02). Figure 5presents the average change scores for the
PHQ-9 scores, presented separately by treatment condition.
Effects on infant fuss/cry behavior
Data from the Babys Day Diary was available on a subset of
participants enrolled in the current study (n=30);this subsam-
ple did not differ significantly from the complete sample on
any of the demographic variables, but did differ significantly
on their score on the PHQ-9 prior to randomization, with the
respondents scoring higher than the non-respondents. Results
from the ANOVA used to test whether infants in the PREPP
versus ETAU conditions differed from one another in the fre-
quency of their fuss/cry behavior are visually depicted in
Fig. 6. Consistent with expectation, mothers who received
the PREPP intervention reported fewer bouts of fuss/cry be-
havior (m=4.07, SD= 2.50) than those in the ETAU condition
(m=6.30, SD=2.63), F(1, 28)=5.68, p=0.02.
Discussion
The current study provides preliminary evidence in support of
the effectiveness of PREPP in preventing the development of
Tabl e 3 Results of linear mixed effects models
HRSD HAM-A PHQ-9
Va r i ab l e BSE BB SE BB SE B
Intercept 14.21** 2.00 14.01** 1.95 7.78** 0.84
Main effects
Intervention group
a
4.27 2.87 5.342.79 1.26 1.18
Time
b
6 weeks postpartum 3.02 2.46 0.24 2.41 2.44* 1.05
10 weeks postpartum 1.06 2.53 2.10 2.47 0.41 1.07
16 weeks postpartum 3.42 2.43 2.43 2.67 0.82 1.18
Interaction effects
Intervention group× time 6 weeks postpartum 9.56** 3.51 8.07* 3.44 1.83* 1.52
10 weeks postpartum 6.173.47 6.673.60 0.11 1.55
16 weeks postpartum 4.11 3.94 7.69* 3.60 2.20 1.75
HRSD Hamilton Rating Scales for Depression, HAM-A Hamilton Rating Scales for Anxiety, PHQ-9 Patient Health Questionnaire
*p<0.05, **p<0.01, p<0.10
a
0= Enhanced Treatment as Usual, 1= PREPP
b
The reference group for all time effects is 3638 weeksgestation (prior to randomization)
PREPP: postpartum depression prevention
PPD symptoms. These effects were most consistently observed
at 6 weeks postpartum; given that the DSM-V specifies that
symptoms of PPD must first occur within the first 4 weeks post-
partum, these findings indicate that PREPP is a useful tool
consistent with the clinical focus on this time period for mothers,
as well as their infants. In addition, the study also found that
mothers who received PREPP reported having infants who
fussed and cried fewer times per day at 6 weeks postpartum than
Note: Change scores are calculated with respect to the previous assessment timepoint.
The mood assessment at 36-38 weeks gestation occurred prior to randomization.
Fig. 3 Hamilton rating scales for
depression change scores: ETAU
versus PREPP
Note: Change scores are calculated with respect to the previous assessment timepoint.
The mood assessment at 36-38 weeks gestation occurred prior to randomization.
Fig. 4 Hamilton rating scales for
anxiety change scores: ETAU
versus PREPP
E.A. Werner et al.
infants of the ETAU mothers. These data, along with the 0 %
attrition rate for PREPP treatment sessions, suggest that PREPP
is a well-tolerated intervention, and one with promising results
for preventing PPD in those at risk for it.
Specifically, we found that women at risk for PPD who re-
ceived the dyadically oriented preventive intervention, on aver-
age, reduced symptoms of depression and anxiety judged by
blinded, clinician report (HRSD, HRSA) at 6 weeks postpartum,
while those at-risk women who were assigned to the ETAU
group did not. Additionally, there was a significant increase in
self-reported depression in the ETAU group and no change in the
PREPP intervention group on this index. PREPPseffectson
blind-clinician ratings of maternal depression approached signif-
icance at the 10-week assessment. Blind-clinician ratings of anx-
iety approached significance at the 10-week assessment and were
significantly lower than baseline at 16 weeks postpartum.
Despite having robust findings at the 6-week assessment,
the current study did not consistently observe statistically sig-
nificant long-term effects on the clinician-rated and self-report
measures administered at 10 and 16 weeks postpartum. These
less consistent results may be due to several factors. First, this
is a small pilot study, so our analyses may have been under-
powered. Additionally, as indicated, not all participants com-
pleted all assessment sessions, which may have contributed
further to issues of power. Second, post hoc analyses revealed
that there was differential attrition for the ETAU group only,
such that participants in this group who did not complete the
16-week assessment had significantly higher HRSD scores
pre-randomization. This may have created an artificial appear-
ance of improvement in the symptomatology of the ETAU
group, thereby reducing our ability to detect an effect at this
later time point. Third, previous research by Hiscock et al.
(2014) found that their treatment to prevent infant sleep and
cry problems had effects on maternal report of depression
symptoms at 6 months but not on these symptoms at 4 months
postpartum. Perhaps, if we had followed our sample for an
additional 2 months, we, too, may have seen PREPP having a
sustained effect on maternal mood 6 months postpartum even
though we saw no 16-week effect. If, in future studies, we
confirm a lack of effect at these later postpartum assessments,
Note: Change scores are calculated with respect to the previous assessment timepoint.
The mood assessment at 36-38 weeks gestation occurred prior to randomization.
Fig. 5 Patient health
questionnaire change scores:
ETAU versus PREPP
0
1
2
3
4
5
6
7
8
Average Daily Frequency of
Fuss/Cry Episodes
PREPP Enhanced
TAU
*p< .05
Fig. 6 Infants of mothers in the PREPP fuss/cry significantly fewer times
per day than those in the ETAU condition
PREPP: postpartum depression prevention
it may suggest that PREPP would be enhanced by providing
infant behavioral interventions that are focused on the care-
giving of older babies.
This study also found that the PREPP intervention was
effective in reducing the number of episodes of infant fuss/
cry behavior by maternal report. On average, women who
received PREPP reported over two fewer bouts of fuss/cry
per day. These results add support to previous findings that
demonstrated that the use of specific infant care techniques is
effective at reducing infant fuss/cry behavior (Hunziker and
Barr 1986; Hiscock et al. 2014). Unlike Hiscock et al. (2014),
who found that their intervention reduced crying problems
only in babies classified as Bfrequent feeders,^the current
study found that the effects on maternal report of cry behavior
were not limited to a subset of infants. However, it is impor-
tant to note that our infants actually may represent a subset
because we only recruited women at risk for PPD for this
study. Although this study did not have the power to test
whether reductions in infant crying is the mechanism through
which maternal mood was improved, the fact that reductions
in distressed mood and in infant fuss/cry behaviors both oc-
curred at 6 weeks supports our theoretical prediction of the
dyadic influence of mother and infant behavior.
In addition to finding that this treatment can affect maternal
mood and infant fuss/cry behavior, we also found that PREPP
is a well-tolerated and accessible treatment for PPD. All par-
ticipants who were randomized to the PREPP condition com-
pleted all treatment sessions, yielding a 0 % attrition rate. This
rate is much lower than those reported by many other PPD
prevention programs (Stamp et al. 1995; Brugha et al. 2000;
Le Strat et al. 2011), some of which describe attrition rates
over 50 % (e.g., Lara et al. 2010). We attribute our 0 % attri-
tion rate to our careful attention to the barriers to PPD treat-
ment, including calling our intervention Bcoaching sessions^
to address the stigma associated with receiving mental health
care (McIntosh 1993) and improving the accessibility of this
treatment by offering it at the same time women are receiving
routine medical care. In addition, we hypothesize that
targeting the dyad and teaching infant care techniques in ad-
dition to the use of traditional psychotherapeutic techniques
may have increased engagement in the treatment.
Strengths
There were several methodological strengths of this study. For
example, we utilized both blind, clinician-rated assessments
and self-report measures of maternal mood. In addition, this
study also benefits from assessing both symptoms of depres-
sion and anxiety as outcome measures. As PPD often encom-
passes symptoms of anxiety as well as depression (Miller et al.
2006), the inclusion of anxiety assessment is essential when
determining the effectivity of a preventive PPD intervention.
Limitations
This study also had a number of limitations. Most notably, this
pilot study had a small sample size, which may have reduced
our ability to detect certain findings. Despite its small sample
size, the current study reports several statistically significant
findings, a fact that may reflect the robust nature of these ef-
fects. We also had a differential attrition rate for the assessment
sessions in the ETAU group, such that the most depressed
(those with highest HRSD scores pre-randomization) dropped
out of the study, which artificially reduced the severity of the
mood scores in the ETAU group over time. As described above,
thismayhaveprovidedanoverlyconservativeassessmentof
the effectiveness of PREPP over time. However, there still were
trends at 10 weeks postpartum for the HRSD and HAM-A, and
a significant result for the HAM-A at 16 weeks postpartum.
Future research with a larger sample may provide further sup-
port for the effectiveness of PREPP in reducing symptoms over
time. Another weakness of this study is that crying and fussing
bouts were assessed by maternal report. However, they were
assessed using the BabysDayDiary(Barr 1985), a widely used
tool that has been shown to be highly reliable and valid (St.
James-Roberts and Gillham 2001). Further, as Radesky et al.
recently suggested (2013), because we are aiming to reduce
maternal depression/anxiety symptoms by reducing fussing/
crying behavior in infants, an alteration in maternal perception
of these infant behaviors, a Bdyadic measure,^may be effective
on its own in improving maternal mood via improvement in
self-efficacy. Last, the current study did not include a self-report
measure of anxiety and only relied on a clinician rating, despite
the fact that anxiety symptoms are a major feature of PPD.
However, clinician assessments are often considered a more
valid assessment of symptomatology than self-report measures.
Summary and conclusions
Building on developmental data showing the profound bi-
directionality of emotional and behavioral influences between
mother and infant (Kochanska et al. 2000,2001,2009;
Kochanska and Aksan 2006; Feldman and Eidelman 2006;
Feldman 2007), PREPP takes a dyadic behavioral approach
to the prevention of PPD. The current pilot study indicates that
this novel, brief intervention, which also includes
psychoeducation and mindfulness skills, was well tolerated
and effective in reducing maternal symptoms of anxiety and
depression, particularly at 6 weeks postpartum. Additionally,
this study found that infants of mothers enrolled in PREPP had
fewer bouts of fussing and crying at 6 weeks postpartum than
those infants whose mothers were in the Enhanced TAU
group. Significantly, reports show that remission from PPD
using standard treatment does not improve womensratingsof
their childrens behavior, nor child outcomes (Forman et al.
E.A. Werner et al.
2007). These preliminary results indicate that PREPP has the
potential to reduce the incidence of PPD in women at risk and
to directly impact the developing motherchild relationship,
the mothers view of her child, and child outcomes.
Acknowledgements This study was supported by the National Institute
of Mental Health (R21MH092665), the Robin Hood Foundation, and by
a postdoctoral fellowship in behavioral medicine awarded by the Herbert
H.andRuthS.Reinerfellowshipfund.
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E.A. Werner et al.
... Studies have shown that exercise to prevent postpartum depression, prenatal training, and a peer support program provided by telephone or message have positive effects on postpartum depression. [34][35][36][37][38][39][40][41][42] In addition, progressive relaxation exercises have been reported to positively affect mood and reduce depression. [43][44][45] Regular use of progressive muscle relaxation exercises can reduce the body's sensitivity to fatigue through relaxation and provide more comfortable sleep. ...
... 36 Studies have shown that a training program designed to both enhance the mother-infant relationship and prevent postpartum depression by creating behavioral changes in mothers reduces postpartum depression. [37][38][39] Several studies, meanwhile, suggest that peer support and telehealth applications delivered to pregnant women by phone or text also reduce postpartum depression. [40][41][42] Although some of the findings in the literature on the preven- The health training/counseling content in our study included suggestions for increasing attachment, participating in baby care, and communicating effectively with the baby. ...
... Only one study including postpartum PMRE could be found in the literature, which found that progressive muscle relaxation exercises performed for 8 weeks postpartum reduced postpartum depression and positively affected women's comfort level. 51 Apart from this, there are studies in the literature using various applications to prevent postpartum depression.[34][35][36][37]40 ...
Article
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Objective To evaluate the effect of online health training/counseling and a progressive muscle relaxation exercise (PMRE) program on postpartum depression and maternal attachment. Methods The present study was a randomized, controlled, experimental trial. Participants were asked to complete the Prenatal Attachment Inventory (PAI) and the Edinburgh Postpartum Depression Scale (EPDS) at 35 weeks of pregnancy. Group assignment was done by stratified block randomization according to EPDS score (0–9, 10–30) and parity. Women in the experimental group received training in progressive muscle relaxation, postpartum depression, and maternal attachment via online video calls twice a week starting at 36–37 weeks of pregnancy. They were asked to complete the PMRE program from 36 weeks of pregnancy until 6 months postpartum, and online counseling was provided throughout this period. Participants completed the Maternal Postpartum Attachment Scale (MPAS) and the EPDS at 6 weeks postpartum. Results Mean PAI score was 64.24 ± 9.61 in the experimental group before the intervention and 62.14 ± 10.13 in the control group. The mean EPDS score of the experimental group was 9.12 ± 5.05 and the mean score of the control group was 9.77 ± 6.30 (P > 0.05). The mean MPAS score after the intervention was 13.92 ± 5.54 in the experimental group and 17.51 ± 6.12 in the control group. The mean EPDS score of the experimental group was 3.40 ± 3.00 and the mean score of the control group was 11.40 ± 5.91 (P < 0.05). Conclusion Online health training/counseling and PMRE reduce the risk of postpartum depression and increase maternal attachment.
... In the literature, the majority of published plasma oxytocin studies support an inverse relationship between endogenous oxytocin levels and depressive symptoms, though results are inconsistent and causality has not been determined. A systemic review found that, of the twelve studies focused on endogenous oxytocin, eight suggested an inverse relationship between plasma oxytocin levels and depressive symptoms, three found no significant relationship, and one actually showed a positive relationship [32]. Taken together, discrepancies in oxytocin levels could be attributed to differences in laboratory measurement procedures, including extraction protocols, consideration of covariates, and individual study limitations. ...
... While salivary oxytocin levels are more than 10-fold lower than plasma values [33], our samples were analyzed in triplicate using an ECL method, which is highly sensitive, specific, and rapid, with a low background signal compared to the commonly used enzyme-linked immunosorbent assay technique [34][35][36]. Furthermore, given that reference ranges for normal endogenous oxytocin levels in postpartum women have not been established, the most useful comparisons come from relative oxytocin differences within the same sample rather than absolute values [32]. More refined research needs to be carried out on this prosocial neuropeptide, controlling for variables such as exposure to exogenous oxytocin (i.e., Pitocin, which is often used to strengthen uterine contractions during labor); specific collection, storage, and extraction protocols; and the timing of collection to make meaningful conclusions about its contribution to social connectedness in the PPD population. ...
Article
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Postpartum depression (PPD) can interfere with the establishment of affective bonds between infant and mother, which is important for the cognitive, social–emotional, and physical development of the child. Rates of PPD have increased during the COVID-19 pandemic, likely due to the added stress and limited support available to new parents. The present study examined whether parenting-related stress, perceived bonding impairments, the quality of observed mother–infant interactions, and salivary oxytocin levels differ between depressed and non-depressed mothers, along with differential impacts of COVID-19 on depressed mothers. Participants included 70 mothers (45 depressed, 25 controls) with infants aged 2–6 months. All data were collected remotely to ease participant burden during the pandemic. Depression was associated with experiences of heightened parenting-related stress and bonding difficulties. These differences were not observed during mother–infant interactions or in salivary oxytocin levels. Differences in COVID-19-related experiences were minimal, though depressed mothers rated slightly higher stress associated with returning to work and financial impacts of the pandemic. Findings highlight the importance of early intervention for PPD to mitigate long-term effects on mothers, children, and families. Additionally, they underscore the need for early intervention to support the developing mother–infant dyad relationship during this crucial time.
... 16 Evidence-based psychotherapies including cognitive behavior therapy (CBT), and interpersonal therapy (IPT) are effective and are often recommended as first-line treatments for mildto-moderate PPD. [17][18][19] Evidence-based Reach Out, Stay Strong, Essentials protocol [19][20][21] and Practical Resources for Effective Postpartum Parenting protocol 22 may be cost-effective preventative interventions. 23 There is increasing evidence for alternative and complementary therapies, with modalities including bright light therapy, 24 physical activity, 25 and yoga, 26 having the most safety and efficacy evidence in PPD. ...
Article
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Peripartum depression (PPD) affects approximately one in every eight birthing individuals. Despite a high prevalence, PPD is underdiagnosed and undertreated. Several PPD treatment options exist including psychotherapies, conventional serotonergic-based antidepressants and alternative and integrative medicine approaches. Rapid-acting neuroactive steroid-based antidepressants have been studied and approved in the United States (US) for the treatment of adult females with PPD. Zuranolone is the first US Food and Drug Administration approved oral antidepressant for adult females with PPD. This narrative review reports on the evidence for the clinical utility of zuranolone in PPD treatment. In double-blind, randomized, placebo-controlled, clinical trials, zuranolone demonstrated rapid, statistically significant and clinically meaningful improvements in depressive symptoms. Most common adverse events reported with zuranolone use were somnolence, dizziness, sedation, and headache. No clinically significant changes in vital signs, electrocardiogram or clinical lab parameters were observed. No loss of consciousness and no increase in suicidal ideation from baseline or deaths were seen in the studies. Secondary analyses demonstrated that zuranolone improves comorbid symptoms of anxiety and insomnia and some measures of health-related quality of life. Zuranolone relevant infant dose lactation data suggest that its use is compatible with breastfeeding, though future research is needed to measure potential adverse effects on the breastfed infant. Key aspects of clinical decision-making in patients with PPD are discussed.
... • Maternal postpartum depression can be effectively targeted through dyadic-focused interventions for the parent and the child.140 • Multifamily parenting interventions can improve mental health and parenting among high-risk mothers with young children.141 ...
Technical Report
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This report provides a theoretical and research foundation for "early relational health", which underpins relational practices and the significant of small, simple, and ordinary interactions.
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Background: Postpartum depression (PPD) is a prevalent and debilitating disorder that occurs in 14% of women after giving birth. Objectives: We aimed to assess the efficacy and safety of perioperative esketamine for preventing PPD in women undergoing cesarean section. Search strategy: We performed a systematic literature search in five medical databases - MEDLINE, Cochrane Library, Embase, Scopus, and Web of Science on the 12th of January 2025. Selection criteria: We searched for trials on the efficacy and safety of esketamine for preventing PPD. Data collection and analysis: We collected data on rates of PPD, Edinburgh Postnatal Depression Scale (EPDS) scores, and adverse effects. Pooled odds ratios (OR) and mean differences (MD) with 95% confidence intervals (CI) were calculated using a random-effects model. Results: Our systematic search provided 2681 records; we screened 1336 duplicate-free records. A total of 17 eligible studies were identified after title, abstract, and full-text selection. Esketamine administration was associated with a lower rate of PPD at postpartum days 3–7 and 28–42 (OR = 0.43; 95% CI: 0.31–0.59 and OR = 0.59; 95% CI: 0.39–0.87, respectively). Esketamine administration was associated with significantly lower EPDS scores at postpartum days 3–7 (MD = −1.32; 95% CI: 1.84 to −0.80). Conclusions: Our findings suggest that perioperative administration of esketamine was associated with lower PPD rates and lower scores on the EPDS questionnaire and was considered safe compared to placebo/standard care.
Article
Background: Parents exposed to psychosocial adversities often experience challenges which, combined with the needs of a new-born infant, can be difficult to manage and increase the risk of poor outcomes for both parents and infants. Psychosocial adversity can disrupt the development of parental-foetal attachment to the baby during pregnancy, which can have a negative effect on parental care and quality of interaction during the postnatal period. This intervention is based on the proposition that enhanced parental capacity to mentalise and emotionally connect to unborn children during pregnancy, and better understanding about how to manage distressing infant behaviour (i.e., persistent crying and sleep problems) will: (i) promote the development of secure parent-infant attachment; (ii) improve antenatal bonding and postnatal parenting; and, (ii) reduce parental distress. Method: This protocol is for a pilot randomised control trial evaluating a new intervention, which makes use of innovative technologies to support parents experiencing moderate psychosocial adversity (Australian New Zealand Clinical Trials Registry: ACTRN12622000287730). The New Technology for New Parents (NTNP) intervention provides support using antenatal ultrasound scans and 'virtual home visits' during the perinatal period. Quantitative outcomes include mentalising capacity, parental-foetal/infant attachment, and parental competence. Conclusion: To the best of our knowledge, no study has evaluated the combined effectiveness of two novel technologies (3D/4D ultrasound scans and virtual home visits) to support parents across the antenatal and postnatal periods. This protocol, which includes the rationale for this innovative intervention, addresses a gap in services for parents experiencing moderate psychosocial adversity.
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The course, antecedents, and implications for social development of effortful control were examined in this comprehensive longitudinal study. Behavioral multitask batteries and parental ratings assessed effortful control at 22 and 33 months (N = 106). Effortful control functions encompassed delaying, slowing down motor activity, suppressing/initiating activity to signal, effortful attention, and lowering voice. Between 22 and 33 months, effortful control improved considerably, its coherence increased, it was stable, and it was higher for girls. Behavioral and parent-rated measures converged. Children's focused attention at 9 months, mothers' responsiveness at 22 months, and mothers' self-reported socialization level all predicted children's greater effortful control. Effortful control had implications for concurrent social development. Greater effortful control at 22 months was linked to more regulated anger, and at 33 months, to more regulated anger and joy and to stronger restraint.
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Pregnant women with histories of depression are at high risk of depressive relapse/recurrence during the perinatal period, and options for relapse/recurrence prevention are limited. Mindfulness-based cognitive therapy (MBCT) has strong evidence among general populations but has not been studied among at-risk pregnant women to prevent depression. We examined the feasibility, acceptability, and clinical outcomes of depression symptom severity and relapse/recurrence associated with MBCT adapted for perinatal women (MBCT-PD). Pregnant women with depression histories were recruited from obstetrics clinics in a large health maintenance organization at two sites and enrolled in MBCT-PD (N = 49). Self-reported depressive symptoms and interview-based assessments of depression relapse/recurrence status were measured at baseline, during MBCT-PD, and through 6-months postpartum. Pregnant women reported interest, engagement, and satisfaction with the program. Retention rates were high, as were rates of completion of daily homework practices. Intent to treat analyses indicated a significant improvement in depression symptom levels and an 18 % rate of relapse/recurrence through 6 months postpartum. MBCT-PD shows promise as an acceptable, feasible, and clinically beneficial brief psychosocial prevention option for pregnant women with histories of depression. Randomized controlled trials are needed to examine the efficacy of MBCT-PD for the prevention of depressive relapse/recurrence during pregnancy and postpartum.
Article
Nearly 20 % of mothers will experience an episode of major or minor depression within the first 3 months postpartum, making it the most common complication of childbearing. Postpartum depression (PPD) is significantly undertreated, and because prospective mothers are especially motivated for self-care, a focus on the prevention of PPD holds promise of clinical efficacy. This study is a qualitative review of existing approaches to prevent PPD. A PubMed search identified studies of methods of PPD prevention. The search was limited to peer-reviewed, published, English-language, randomized controlled trials (RCTs) of biological, psychological, and psychosocial interventions. Eighty articles were initially identified, and 45 were found to meet inclusion criteria. Eight RCTs of biological interventions were identified and 37 RCTs of psychological or psychosocial interventions. Results were mixed, with 20 studies showing clear positive effects of an intervention and 25 showing no effect. Studies differed widely in screening, population, measurement, and intervention. Among biological studies, anti-depressants and nutrients provided the most evidence of successful intervention. Among psychological and psychosocial studies, 13/17 successful trials targeted an at-risk population, and 4/7 trials using interpersonal therapy demonstrated success of the intervention versus control, with a further two small studies showing trends toward statistical significance. Existing approaches to the prevention of PPD vary widely, and given the current literature, it is not possible to identify one approach that is superior to others. Interpersonal therapy trials and trials that targeted an at-risk population appear to hold the most promise for further study.
Article
Objective: While considerable attention has focused on improving the detection of depression, assessment of severity is also important in guiding treatment decisions. Therefore, we examined the validity of a brief, new measure of depression severity. Measurements: The Patient Health Questionnaire (PHQ) is a self-administered version of the PRIME-MD diagnostic instrument for common mental disorders. The PHQ-9 is the depression module, which scores each of the 9 DSM-IV criteria as "0" (not at all) to "3" (nearly every day). The PHQ-9 was completed by 6,000 patients in 8 primary care clinics and 7 obstetrics-gynecology clinics. Construct validity was assessed using the 20-item Short-Form General Health Survey, self-reported sick days and clinic visits, and symptom-related difficulty. Criterion validity was assessed against an independent structured mental health professional (MHP) interview in a sample of 580 patients. Results: As PHQ-9 depression severity increased, there was a substantial decrease in functional status on all 6 SF-20 subscales. Also, symptom-related difficulty, sick days, and health care utilization increased. Using the MHP reinterview as the criterion standard, a PHQ-9 score > or =10 had a sensitivity of 88% and a specificity of 88% for major depression. PHQ-9 scores of 5, 10, 15, and 20 represented mild, moderate, moderately severe, and severe depression, respectively. Results were similar in the primary care and obstetrics-gynecology samples. Conclusion: In addition to making criteria-based diagnoses of depressive disorders, the PHQ-9 is also a reliable and valid measure of depression severity. These characteristics plus its brevity make the PHQ-9 a useful clinical and research tool.
Article
Objective: To evaluate a prevention program for infant sleep and cry problems and postnatal depression. Methods: Randomized controlled trial with 781 infants born at 32 weeks or later in 42 well-child centers, Melbourne, Australia. Follow-up occurred at infant age 4 and 6 months. The intervention including supplying information about normal infant sleep and cry patterns, settling techniques, medical causes of crying and parent self-care, delivered via booklet and DVD (at infant age 4 weeks), telephone consultation (8 weeks), and parent group (13 weeks) versus well-child care. Outcomes included caregiver-reported infant night sleep problem (primary outcome), infant daytime sleep, cry and feeding problems, crying and sleep duration, caregiver depression symptoms, attendance at night wakings, and formula changes. Results: Infant outcomes were similar between groups. Relative to control caregivers, intervention caregivers at 6 months were less likely to score >9 on the Edinburgh Postnatal Depression Scale (7.9%, vs 12.9%, adjusted odds ratio [OR] 0.57, 95% confidence interval [CI] 0.34 to 0.94), spend >20 minutes attending infant wakings (41% vs 51%, adjusted OR 0.66, 95% CI 0.46 to 0.95), or change formula (13% vs 23%, P < .05). Infant frequent feeders (>11 feeds/24 hours) in the intervention group were less likely to have daytime sleep (OR 0.13, 95% CI 0.03 to 0.54) or cry problems (OR 0.27, 95% CI 0.08 to 0.86) at 4 months. Conclusions: An education program reduces postnatal depression symptoms, as well as sleep and cry problems in infants who are frequent feeders. The program may be best targeted to frequent feeders.