1 | Journal of Child and Family Studies 1 This is a post-peer-review, pre-copyedit version of an article published in Journal of Child and Family 2 Studies. The final authenticated version is available online at: http://dx.doi.org/10.1007/s10826-017-0889-z 3 4 5 Preventing and Treating Women’s Postpartum Depression: A Qualitative Systematic Review on Partner- 6 Inclusive Interventions 7 8 Stephanie Alves, Alexandra Martins, Ana Fonseca, Maria Cristina Canavarro, and Marco Pereira 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30
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1 | Journal of Child and Family Studies
1!
This is a post-peer-review, pre-copyedit version of an article published in Journal of Child and Family 2!
Studies. The final authenticated version is available online at: http://dx.doi.org/10.1007/s10826-017-0889-z 3!
4!
5!
Preventing and Treating Women’s Postpartum Depression: A Qualitative Systematic Review on Partner-6!
Inclusive Interventions 7!
8!
Stephanie Alves, Alexandra Martins, Ana Fonseca, Maria Cristina Canavarro, and Marco Pereira 9!
10!
11!
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2 | Journal of Child and Family Studies
Abstract 1!
Partner-related factors associated with the occurrence of Postpartum Depression (PPD) may justify the partner’s 2!
inclusion in preventive and treatment approaches. The aim of this qualitative systematic review was to 3!
synthesize the literature on partner-inclusive interventions designed to prevent or treat postpartum depression 4!
(PPD) in women. In accordance with the PRISMA guidelines, the systematic search of studies published 5!
between 1967 and May 2015 in PsycINFO and PubMed identified 26 studies that met the inclusion criteria, 6!
which reported on 24 interventions. The following partner parameters were analyzed: participation type, session 7!
content, mental health assessment, attendance assessment, and the effects of partner’s participation on the 8!
women’s response to the interventions. Total participation by the partner was mostly reported in the prevention 9!
studies, whereas partial participation was reported in the treatment studies. The session content was mostly 10!
based on psychoeducation about PPD and parenthood, coping strategies to facilitate the transition to parenthood 11!
such as the partner’s emotional and instrumental support, and problem-solving and communication skills. Some 12!
benefits perceived by the couples underscore the relevance of the partner’s inclusion in PPD interventions. 13!
However, the scarce information about the partner’s attendance and the associated effects on the women’s 14!
intervention outcomes, along with methodological limitations of the studies, made it difficult to determine if the 15!
partner’s participation was associated with the intervention’s efficacy. Conclusions about the clinical value of 16!
including partners in PPD interventions are still limited. More research is warranted to better inform health 17!
hecklist. * Participants attended the session(s) in addition to standard care (TA
U).
a Wom
en were classified as vulnerable if they scored tw
o on any one of the vulnerability questions in the LQ or scored 1 on m
ore than one question; b Total sam
ple included 258 mothers and 154 fathers/significant others (81 in the intervention group and 73 in the com
parison group). Although 2 m
others choose not to participate, the fathers of those infants w
ere enrolled; c A
ntenatal intervention delivered to pregnant wom
en with current depressive and anxiety sym
ptoms or at risk of developing PPD
; d O
f a total of eight groups delivered, the earlier programs com
prised five sessions (including one partner session), whilst the last four had six sessions (based on the feedback from
wom
en and partners an additional partner session w
as integrated).
!
4
Table 2 Intervention characteristics of included studies assessing treatm
ent interventions for PPD (n =
13)
Study (C
ountry) Sam
ple size
Intervention approach
Study D
esign
Control
type Intervention Form
at N
o. Sessions
Partner participation
Partner/Couple Session(s) C
ontent
Brandon et
al., 2012a;
USA
11 couples
PA-IPT
OT
NA
Individual
8 Total
Couple-based intervention that covered IPT strategies, including w
ays of partners being em
otionally and instrumentally supportive and respond to w
omen’s needs.
Chen et al.,
2011b;
SING
41
CB
T IPT C
ounseling Education
QE
NA
Individual
NS
Partial
Intervention program considered a second part for partners, w
hich included PPD
psychoeducation (e.g., adverse consequences, treatment options), counseling to
enhance support to the patient (e.g., facilitating the understanding of PPD, encouraging
support), and assessment of partner’s needs (brief exploration of partner’s coping and
counseling on resources available).
Danaher et
al., 2013; A
US
USA
53
CB
T
QE
NA
Individual (W
eb + Phone)
6 Partial
Separate Partner Support Website about inform
ation on PPD, overview
of M
omM
oodBooster Program
, and ways to be supportive.
Hou et al.,
2014; C
HIN
249
CB
T SFT
RC
T TA
U
Individual 13 C
BT + 6
SFT*
Partial
Family therapy content included reconstruction of the m
ode of interaction (enhancing fam
ily relationships and support) among fam
ily mem
bers (e.g., couples, parents of couples), but it w
as not clear which person participated.
Lane et al.,
2002; A
US
23
C
BT
Q
E NA
G
roup 10 + 1 or 2 partner sessions
Partial
One or tw
o partner’s (only) evening sessions (content not reported).
Meager &
M
ilgrom,
1996; A
US
20
CB
T
RC
T W
L G
roup 10
Partial O
ne separate session for partners “to promote a better understanding of PPD
and to facilitate change”. It w
as not specified if the session was part of the 10 delivered and if
addressed both partners and the wom
en.
Milgrom
et al., 2005; A
US
192
CB
T
RC
T TA
U
Counselin
g
Group
9 + 3 couple sessions
Partial Partners attended three sessions w
ith wom
en (content not reported).
Milgrom
et al., 2015; A
US
45 R
CT
Sertraline Sertraline + C
BT
Misri et al.,
2000; C
AN
29
Education R
CT
Wom
en participation only
Group
7 Partial
Partners attended sessions 2, 4, 6 and 7 (content not reported) with w
omen. The
researcher encouraged positive interactions between the couple by focusing on
postpartum issues (e.g., involvem
ent in baby-tasks and housework).
!
5
M
organ et al., 1997; A
US
34c
CB
T
QE
NA
G
roup 8 + couple session
Partial
One evening session conjoint w
ith wom
en at week 6 organized in three parts: 1)
introductory meeting, w
here wom
en shared their difficulties followed by partner’s
perceptions; 2) meeting w
ith mothers and partners separately; 3) group discussion.
Puckering et al., 2010; U
K
20
CB
T Education
RC
T W
L G
roup 14 + 3 partner sessions
Partial
Three evening partner (only) sessions about information on PPD
and activities to prom
ote father-baby interactions.
Reay et al.,
2006; A
US
18
IPT-Group
QE
NA
B
oth
2 individual + 8 group + partner session
Partial
Partner (only) evening psychoeducational session about PPD (e.g., sym
ptoms, causes,
consequences) and practical and comm
unication strategies to support and respond to w
omen
d.
Mulcahy et
al., 2010; A
US
57
RC
T TA
U
Reay et al.,
2012 (follow-
up)
(50)
Note. U
SA = U
nited States; SING
= Singapore; AU
S = Australia; C
HIN
= China; C
AN
= Canada; U
K = U
nited Kingdom
; PA-IPT = Partner-A
ssisted Interpersonal Psychotherapy; CB
T = Cognitive-
Behaviour Therapy; IPT = Interpersonal Psychotherapy; SFT = System
ic Family Therapy; O
T = open trial; QE = quasi-experim
ental design; RC
T = randomized controlled trial; N
A = not applicable; TA
U =
treatment as usual; W
L = waiting list; B
oth = individual + group; NS = not specified.
* Participants attended the session(s) in addition to standard care (TAU
). a Treatm
ent delivered to pregnant and postpartum w
omen (72.7%
and 27.3%, respectively);
b Case m
anagement m
odel for PPD, w
ith screening and intervention components;
c One couple have a child 2-years old;
d Additional inform
ation retrieved from the descriptive study (R
eay, Mulcahy, et al., 2012).
!
6
Table 3 M
ethodological quality of included studies assessing preventive and treatment interventions for PPD
Study
Sample char
Sample pow
er IT
T C
ontrol A
ssess point Blind assess
Drop-out / R
eas Loss to FU
/ Reas
Excl curr treat
Preventive studies
Bernard et al., 2011
+ +
− +
− N
A
+ / + + / +
B
rugha et al., 2000 +
+ +
+ −
+ + / −
+ / −
Buist et al., 1999
+!−
− −
+ N
A
− / − + / −
Elliott et al., 2000
−!−
+ −
+ +
+ / − + / −
Fisher et al., 2010
+!+
+ +
− +
+ / + + / −
H
ayes & M
uller, 2004 +!
+ −
+ +
− − / −
+ / +
Hayes et al., 2001
+ +
− +
+ −
− / − + / −
K
ozinszky et al., 2012 +!
− +
+ −
+ − / −
+ / −
Mao et al., 2012
+!−
+ −
− +
+ / − + / +
M
atthey et al., 2004 +!
+ +
+ +
NS
+ / − + / −
M
elnyk et al., 2006 +!
+ +
+ −
NA
+ / −
+ / −
Milgrom
et al., 2011 +!
+ +
+ −
NA
+ / −
+ / −
Stamp et al., 1995
+!+
+ −
+ N
A
+ / − + / −
Thom
as et al., 2014 +
− −
− −
NA
+ / +
+ / −
Treatment studies
B
randon et al., 2012 +!
− −
− +
+ + / −
+ / +
+ C
hen et al., 2011 +!
− −
− −
NA
− / −
− / −
+ D
anaher et al., 2013 +!
− +
− +
− + / −
+ / −
+ H
ou et al., 2014 +!
− −
− +
NA
− / −
+ / +
− Lane et al., 2002
−!−
− −
− N
A
+ / +
+ / − N
S M
eager & M
ilgrom, 1996
+!−
− −
− N
A
+ / +
+ / − −
Milgrom
et al., 2005 +!
+ +
+ +
NA
+ / −
+ / −
+ M
ilgrom et al., 2015
+!+
+ +
+ N
A
+ / −
− / − +
Misri et al., 2000
+!−
− −
+ N
S + / −
+ / −
− M
organ et al., 1997 +!
− −
− +
NA
+ / −
− / −
− Puckering et al., 2010
−!−
− −
− N
A
+ / −
+ / − −
Reay et al., 2006
+!−
+ −
+ +
+ / +
+ / − −
Mulcahy et al., 2010
+!−
+ −
+ +
+ / +
+ / − −
Reay et al., 2012 +!
− −
+ N
A
NA
N
A
+ / + N
A
Note. Sam
ple char = describe sample’s characteristics; Sam
ple power = report pow
er analysis; ITT = report intention-to-treat analysis; Control = report control of confounders in data analyses; A
ssess point = tw
o or more assessm
ent time points; B
lind assess = interviewers w
ere blind to group condition; Drop-out/R
eas = specify the number of participants w
ho dropped-out/specify the reasons for drop-out; Loss to FU
/Reas = specify the num
ber of participants who w
ere loss to follow-up/specify the reasons for loss to follow
-up; Excl curr treat = exclusion of wom
en receiving current treatment (e.g., pharm
acotherapy,
!
7
psychotherapy) at baseline; + = yes; − = no; NA
= not applicable; NS = not specified.
!
8
Table 4 Assessm
ent characteristics of included studies assessing preventive interventions for PPD (n =
13) Study
Method of outcom
e assessm
ent O
utcome m
easure + C
ut-off/Diagnostic criteria
Postpartum assessm
ent tim
ings (weeks)
Wom
en’s attendance Partner/C
ouple’s attendance
Bernard et al., 2011
Self-report W
omen:
BD
I-II 4 w
eeks after infant’s discharge from
NIC
U
26/31 mothers received all 3 sessions.
NS
Brugha et al., 2000
Both
Wom
en: G
HQ
-D ≥
2 EPD
S!≥11
SCA
N IC
D-10
12 42/94 (45%
) of the intervention group wom
en (w
ho completed the 3-m
onth assessment)
attended 2 or more sessions in addition to
session 3.
NS
Buist et al., 1999
Self-report
Wom
en: B
DI
EPDS
6 24 N
S N
S
Elliott et al., 2000
B
oth W
omen:
EPDS
PSE C
CEI
SRQ
12 48
18/21 first-time m
others and 15/26 second-tim
e mothers attended an average of 7 and 4
sessions, respectively.
NS
Fisher et al., 2010
Clinician-adm
inistrated m
easure
Wom
en: C
IDI a
24 120/189 (64%
) wom
en attended the session. U
nclear
Hayes &
Muller,
2004
Clinician-adm
inistrated m
easure W
omen:
SAD
S-M!
8-12 16-24
NS
NS
Hayes et al., 2001
Wom
en: PO
MS
Kozinszky et al.,
2012
Clinician-adm
inistrated m
easure W
omen:
LQ!≥12
6-8
NS
NS
Mao et al., 2012
B
oth W
omen:
PHQ
-9 ≥10
* EPD
S!≥11
SCID
(DSM
-IV-TR
)
6 A
ll participants completed the intervention.
Unclear
!
9
Matthey et al., 2004
Both
Wom
en and partner: EPD
S (various cut-offs) PO
MS
DIS (D
SM-IV
) C
ES-D (partners only)
Wom
en and partner: 6 24
246/268 couples (92%
) b
Melnyk et al., 2006
Self-report W
omen and partner:
BD
I-II W
omen and partner c:
8 week’s corrected infant
age
Unclear
U
nclear
Milgrom
et al., 2011 Self-report
Wom
en: B
DI-II!≥
14 Partner: D
ASS
12 50.7%
of wom
en in the intervention group participated in all 8 Phone sessions.
NS
Stamp et al., 1995
Self-report W
omen:
EPDS!>
9 (minor depression)
and > 12 (m
ajor depression
6 12 24
31% of w
omen attended the three
intervention groups. 3/71 (4%
) partners attended at least one of the three groups
Thom
as et al., 2014 Self-report
Wom
en: C
ES-D ≥
19*
EPDS
8 37/48 (77%
) wom
en completed at least 80%
of the 6 sessions.
28/48 (58.3%)
attended at least one partner session
Note. B
oth = self-report + clinician-administered m
easures; BD
I/BD
I-II = Beck D
epression Inventory; GH
Q-D
= General H
ealth Questionnaire m
odified; EPDS = Edinburgh Postnatal D
epression Scale; SC
AN
ICD
-10 = Schedules for Clinical A
ssessment in N
europsychiatry using ICD
-10 criteria for depressive disorder; PSE = Present State Examination; C
CEI = C
rown C
risp Experiential Index; SR
Q = Self R
ating Questionnaire; C
IDI = C
omposite International D
iagnostic Interview; SA
DS-M
= Schedule for Affective D
isorders and Schizophrenia modified; PO
MS = Profile of M
ood States; LQ
= Leverton Questionnaire; PH
Q-9 = Patient H
ealth Questionnaire; SC
ID = Structured C
linical Interview for D
SM-IV
; DSM
-IV/D
SM-IV
-TR = D
SM-IV
/DSM
-IV-TR
depression criteria (D
iagnostic and Statistical Manual of M
ental Disorders, Fourth Edition/Text R
evision); DIS = D
iagnostic Interview Schedule; C
ES-D = C
enter for Epidemiological Studies D
epression Scale; DA
SS = D
epression Anxiety Stress Scales short form
; NIC
U = N
eonatal Intensive Care U
nit; NS = not specified.
* Measures adm
inistrated after the intervention completion but antenatally;
a Diagnosis of D
epression or Anxiety or A
djustment D
isorder with D
epressed Mood, A
nxiety, or Mixed A
nxiety and Depressed M
ood; b C
ouples attending the extra session in the Empathy (intervention) or B
aby Play (TAU
+) conditions, or the Control session in w
hich PPD w
as discussed. c Follow
-up data collection occurred at each of the session II through IV session interventions (2-4 days after the first session, 1-4 days before infant discharge from
the NIC
U, and 1 w
eek post–NIC
U
discharge, respectively), before the interventions.
!
10
Table 5 Assessm
ent characteristics of included studies assessing treatment interventions for PPD
(n =13)
Study
Treatm
ent inclusion M
ethod of outcome
assessment
Outcom
e measure
+ Cut-off/D
iagnostic criteria Post-intervention assessm
ent tim
ings (weeks)
Wom
en’s attendance Partner/C
ouple’s attendance
Brandon et
al., 2012 D
SM-IV
+ H
AM
-D ≥
16
Both
Wom
en: H
AM
-D > 9!
EPDS > 12
*
Partner: H
AM
-D > 9
EPDS-P
*
0 6-8
10/11 couples (100%
) a
Chen et al.,
2011
EPDS ≥
13 or ≥1 yes in
one of the 3 add questions (infanticide im
pulses, psychotic sym
ptoms)
Self-report W
omen:
EPDS!≥
13
24 weeks post-enrollm
ent or at discharge.
NS
NS
Danaher et
al., 2013
PHQ
-9 10-19 or EPD
S 12-20
Both
Wom
en: PH
Q-9!
HR
SD
12 and 24 weeks post-
enrollment.
46/53 (87%) w
omen com
pleted all 6 sessions.
18/53 (34%)
Hou et al.,
2014
DSM
-IV-TR
Self-report W
omen:
EPDS
0 6, 12, 18, 24 m
onths postpartum
.
NS
NS
Lane et al.,
2002 N
S Self-report
Wom
en: EPD
S 0
18/23 (78%) w
omen com
pleted the intervention.
NS
Meager &
M
ilgrom,
1996
EPDS >12 +
BD
I > 15 Self-report
Wom
en: EPD
S B
DI
POM
S
0 6/10 (40%
attrition) wom
en com
pleted the 10 sessions. N
S
Milgrom
et al., 2005
EPDS ≥12 +
DSM
-IV
Self-report W
omen:
BD
I!≥17
0 48 107/159 (67%
) wom
en allocated to the three psychological interventions attended the respective intervention.
NS
Milgrom
et al., 2015
EPDS ≥13 +
DSM
-IV
Self-report W
omen:
BD
I-II!≥13
12 and 24 weeks post-
enrollment.
Wom
en completed an average of 10.6
sessions and all completed at least
half of the sessions (CB
T condition)
NS
Misri et al.,
2000 D
SM-IV
+ EPD
S ≥12
Both
Wom
en: EPD
S 0 4
29/29 (100%) w
omen attended all
sessions. N
S
!
11
M
INI (D
SM-IV
) SQ
Partner: G
HQ
Morgan et al.,
1997
EPDS ≥
13
Self-report W
omen:
GH
Q
EPDS ≥
13 Partner: G
HQ
≥7/8
b
0 24 weeks (only for the last 4
groups) c
Only one w
oman dropped-out;
attendance at the sessions was at a
level of 90%.
21/29d
(72%)
Puckering et al., 2010
EPDS > 10
Self-report W
omen:
EPDS
0 11/12 w
omen attended the
intervention group.
NS
Reay et al.,
2006
EPDS ≥13 +
DSM
-IV
Both
Wom
en: EPD
S B
DI
HA
M-D!≥
8
0 12
17/18 (94%) w
omen attended the
intervention. 14/18 (78%
)
Mulcahy et al.,
2010 D
SM-IV
+ H
AM
-D ≥
14
Both
Wom
en: EPD
S ≥13
BD
I-II H
AM
-D!≥ 8
0 12
22/29 (76%) w
omen attended the
intervention.
NS
Reay et al.,
2012 (follow-
up)
Self-report
EPDS ≥
13 B
DI-II
2-year post-intervention.
Note. D
SM-IV
/DSM
-IV-TR
= DSM
-IV/D
SM-IV
-TR depression criteria (D
iagnostic and Statistical Manual of M
ental Disorders, Fourth Edition/Text R
evision); HA
M-D
/HR
SD = H
amilton R
ating Scale for D
epression; EPDS = Edinburgh Postnatal D
epression Scale; EPDS-P = Edinburgh Postnatal D
epression Scale – Partner; PHQ
-9 = Patient Health Q
uestionnaire; NS = not specified;
BD
I/BD
I-II = Beck D
epression Inventory; Both = self-report + clinician-adm
inistered measures; PO
MS = Profile of M
ood States; MIN
I = MIN
I-International Neuropsychiatric Interview
; SQ =
(Kellner) Sym
ptom Q
uestionnaire; GH
Q = G
eneral Health Q
uestionnaire; Y = efficacious; N
= Not efficacious.
* Measures adm
inistrated during the intervention before each session; a C
ouples attending all the sessions (one couple excluded because of the presence of partner violence; attendance 100%);
b Partners assessed “in the last three joint sessions” at week 6;
c 48 weeks (12 m
onths) follow-up for the first group and 36 w
eeks (9 months) for the second group;
d Because couple’s session w
as run from the second group onw
ards (of a total of six groups), only 21 out of 29 partners attended the session.
!
12
Table 6 Intervention outcom
es of preventive interventions for PPD (n =
13) Study
Efficacy of the intervention on w
omen’s depressive sym
ptoms
Relevant inform
ation about partner (for this review
) B
ernard et al., 2011
Wom
en in the intervention group tended to report marginally significant low
er levels of depressive sym
ptoms at follow
-up in comparison w
ith those in the CG
(p = 0.06).
Since few partners choose to participate in the study, only data on m
others were presented.
No objective inform
ation was given about partner’s attendance.
B
rugha et al., 2000
No significant differences in the percentage of w
omen w
ith clinically significant depressive sym
ptoms betw
een intervention group and CG
at 12 weeks postpartum
.
Buist et al.,
1999
No significant differences in depressive sym
ptoms betw
een intervention group and CG
at both assessm
ent time points. N
o significant change over time w
ithin groups.
Elliott et al.,
2000
First-time m
others in the intervention group reported significantly lower levels of
depressive symptom
s in comparison w
ith those in the CG
at 12-weeks postpartum
(effects no longer present at 48 w
eeks postpartum). A
significantly lower percentage
of first-time m
others in the intervention group experienced clinically significant depressive sym
ptoms during the first 2 m
onths postpartum.
Fisher et al., 2010
Wom
en without psychiatric history in the intervention group w
ere significantly less likely to experience the onset of D
epression or Anxiety or A
djustment D
isorder in com
parison with those in the C
G at 24 w
eeks postpartum.
Hayes &
M
uller, 2004
No significant differences in changes in depressive sym
ptoms from
pre- to postpartum
assessment tim
e points between intervention group and C
G.
Hayes et al.,
2001
Significant improvem
ents in depressive symptom
s from pre- to postpartum
assessment
time points w
ithin both groups, but no significant differences in improvem
ent were
found between intervention group and C
G.
Kozinszky et
al., 2012
Wom
en in the intervention group reported significantly lower levels of depressive
symptom
s, and were less likely to experience PPD
, in comparison w
ith those in the C
G at 6-8 w
eeks postpartum.
Mao et al., 2012
W
omen in the intervention group reported significantly low
er levels of depressive sym
ptoms, and w
ere less likely to experience PPD, in com
parison with those in the
CG
at 6-weeks postpartum
.
!
13
Matthey et al.,
2004 W
omen w
ith low self-esteem
in the intervention group (empathy condition) reported
significantly lower levels of depressive sym
ptoms at 6 w
eeks postpartum in
comparison w
ith those in the two C
G (effects no longer present at 24 w
eeks postpartum
). There were no significant differences in the percentage of low
self-esteem
wom
en with clinically significant depressive sym
ptoms betw
een conditions at both assessm
ent time points.
The results of these wom
en were related to their partners’ increased aw
areness of what the
wom
en were experiencing. These w
omen also reported, at 6 w
eeks postpartum, a higher
satisfaction with the sharing of baby and hom
e-related tasks. No significant im
pact of the intervention on partner’s depressive sym
ptoms w
as found.
Melnyk et al.,
2006 W
omen in the intervention group reported significantly low
er levels of depressive sym
ptoms in com
parison with those in the C
G at 8 w
eeks’ corrected infant age.
No significant differences in depressive sym
ptoms betw
een partners/significant others in the intervention group and those in the C
G.
Milgrom
et al., 2011
Wom
en in the intervention group reported significantly lower levels of depressive
symptom
s in comparison w
ith those in the CG
at 12-weeks postpartum
. A
significantly lower percentage of w
omen in the intervention group experienced
clinically significant depressive symptom
s following intervention.
Most partners (intervention: n = 16, C
G: n = 8) did not com
plete follow-up assessm
ent and 14%
wom
en were single. A
lthough partners in the intervention group scored lower in
postpartum depressive sym
ptoms in com
parison to those in the CG
, no significant differences w
ere found between the groups.
Stam
p et al., 1995
No significant differences in the percentage of w
omen w
ith clinically significant depressive sym
ptoms betw
een intervention group and CG
at all assessment tim
e points.
Thom
as et al., 2014
Significant improvem
ents in depressive symptom
s among w
omen from
pre- to post-intervention (antenatal period), and up to 2-m
onths postpartum.
The feedback reported by 21 partners (75%) about their participation w
as highly positive, underscoring a better understanding of parental m
ental health issues and resources available to their fam
ily. 67% said they w
ould recomm
end the program to other fathers. The authors
intended to assess the benefits perceived by wom
en from partner’s attendance but no data
were reported in the article.
Note. C
G = control group.
!
14
Table 7 Intervention outcom
es of treatment interventions for PPD
(n =13)
Study E
fficacy of the intervention on wom
en’s depressive symptom
s R
elevant information about partner
(for this review)
Brandon et al.,
2012 Significant im
provements in depressive sym
ptoms from
pre- to post-intervention, w
hich were m
aintained at 6/8-weeks follow
-up. By the end of the intervention, 90%
(9/10) of the w
omen m
eet criteria for clinical response (HA
M-D
= 9), and at 6/8-weeks
follow-up 8 of these 9 w
omen m
et criteria for symptom
atic recovery.
Partner’s depressive symptom
s remained low
from intake to the end of the intervention
(except in one partner). One of the tw
o partners that met criteria for past episodes of M
ajor D
epressive Disorder experienced sym
ptom recurrence over the course of the acute phase.
Wom
en and their partners reported some benefits from
participating in the intervention, and the authors observed a better recognition of w
omen’s depressive sym
ptoms by their partners
at the end of the intervention.
Chen et al.,
2011
Significant improvem
ents in depressive symptom
s from pre- to post-enrollm
ent assessm
ent in 78% (32/41) of w
omen (EPD
S < 13).
Danaher et al.,
2013
Significant improvem
ents in depressive symptom
s from pre- to 12 w
eeks post-enrollm
ent and to 24-weeks follow
-up. 90% (26) of the 29 w
omen w
ho met PH
Q-9
criteria for minor or m
ajor depression at baseline did not report these criteria anymore
at 12 weeks post-enrollm
ent.
Hou et al.,
2014
Wom
en in the intervention group reported significantly lower levels of postpartum
depressive sym
ptoms in com
parison with those in the C
G follow
ing intervention. O
bserved improvem
ents in depressive symptom
s from pre- to different post-
intervention time points in both groups, but significantly greater am
ong wom
en in the intervention group.
Lane et al.,
2002 Significant im
provements in depressive sym
ptoms from
pre- to post-intervention.
The authors mentioned higher partner attendance w
ithout reporting objective information.
Partners reported benefits (not specified) from participating in the intervention.
M
eager &
Milgrom
, 1996
Significant improvem
ents in depressive symptom
s among w
omen in the intervention
group from pre- to post-intervention, w
ith these wom
en reporting significantly lower
levels of depressive symptom
s in comparison w
ith those in the CG
following
intervention.
Milgrom
et al., 2005
Wom
en who received psychological interventions (C
BT and counseling) reported
significantly lower levels of postpartum
depressive symptom
s in comparison w
ith those in the standard care group follow
ing intervention. More than 50%
of these w
omen (vs. 29%
in the standard care group) reported minim
al levels of depression (B
DI-II < 17). Follow
-up data were too scarce to adequate analyses.
Milgrom
et al., 2015
CB
T mono-therapy and sertraline m
ono-therapy were found to be superior at 12 w
eeks post-enrollm
ent to combination therapy in reducing depressive sym
ptoms. W
ithin the
!
15
CB
T mono-therapy group, the percentage of w
omen reporting m
inimal levels of
depression (BD
I-II < 13) was significantly higher at 24 w
eeks follow-up com
pared to pre-intervention.
Misri et al.,
2000 W
omen in the support group (partners involved) reported significantly low
er levels of postpartum
depressive symptom
s in comparison w
ith those in the CG
(partners not involved) at 1 m
onth post-intervention. 81% (13) of the 16 w
omen in the support group
who m
et MIN
I criteria for major depression at baseline did not report these criteria
anymore at 1 m
onth post-intervention (vs. 39% in the C
G).
Higher data com
pletion at assessment tim
e points from partners. Partner’s general m
ental health w
as higher among those involved in treatm
ent than those who did not (C
G) at both
assessment tim
e points. Wom
en in the support group reported significantly higher levels of dyadic adjustm
ent in comparison w
ith those in the CG
following intervention.
M
organ et al., 1997
Significant improvem
ents in depressive symptom
s from pre- to post-intervention. A
ny w
omen scored above the cut-off score on the EPD
S at follow-up.
There were no significant differences in w
omen’s outcom
es based on the partner’s participation in the couple’s session. 8/14 m
en scored in the GH
Q distressed range, and 6 of
them had a partner w
ho scored above the EPDS cut-off score.
Wom
en and their partners reported some benefits from
participating in the joint session.
Puckering et al., 2010
Significant improvem
ents in depressive symptom
s among w
omen in the intervention
group from pre- to post-intervention, w
ith these wom
en reporting significantly lower
levels of depressive symptom
s in comparison w
ith those in the CG
following
intervention.
The authors mentioned higher partner attendance w
ithout reporting objective information.
Reay et al.,
2006
Significant improvem
ents in depressive symptom
s from pre- to post-intervention,
which w
ere maintained at 12-w
eeks follow-up. B
y the end of the intervention, 50% of
the wom
en fully remitted (H
AM
-D!< 8).
Mulcahy et al.,
2010
Significant improvem
ents in depressive symptom
s from pre- to post-intervention in
both groups, but significantly greater among w
omen in the intervention group, w
ho reported significantly low
er levels of postpartum depressive sym
ptoms com
pared to those in the C
G (differences betw
een groups persisted at 12-weeks follow
-up). A
significantly higher percentage of wom
en in the intervention group met criteria for
recovery following intervention (EPD
S < 13 and HA
M-D!<
8).
Reay et al.,
2012 (follow-
up)
Mothers w
ho received IPT-G w
ere less likely to develop persistent depressive sym