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Validation of the Edinburgh Postnatal Depression
Scale (EPDS) as a screening tool for postnatal depression in Samoan and Tongan
women living in New Zealand
Alec J Ekeroma, Bettina Ikenasio-Thorpe, Sara Weeks, Jesse
Kokaua, Kasalanaita Puniani, Peter Stone, Siale A Foliaki
Postnatal depression (PND) is a serious public health issue
and more so in women of Pacific ethnicity in New Zealand
(NZ).1,2 Pacific women have a higher fertility
rate, most are untreated in the community; and depression is higher in NZ-born
women than those born in the Islands.3–5
PND causes major maternal morbidity resulting in
dysfunctional relationships and with effects that continue to affect the
woman’s children—deficits in social, psychological, and cognitive
domains and an increased risk of suffering from child
abuse.6,7
The prevalence of PND from an aggregation of worldwide
studies averages 13% (of all pregnancies)8 but
the only study specifically on Pacific women found a prevalence of
16.4%.1 The study cohort of 1376 Pacific women,
in the Pacific Island Family Study (PIF study), found a statistically
significantly difference in prevalence rates of 30.9% in Tongan women and 7.6%
in Samoan women.
The PIF study used the Edinburgh Postnatal Depression Scale
(EPDS), a 10-item self-report questionnaire that was developed in
1987,9 and has been translated into many
languages and used in many prevalence studies. Even though the EPDS had also
been used in two other NZ studies,10,11 it had
not been validated in Pacific or NZ populations. The PIF study administered the
EPDS as an interview and “a score above 12 is widely used to indicate the
presence of probable depressive
disorder”.1
The EPDS has been validated in more than 25 different ethnic
groups and populations.12–14 A review of
37 validation studies of the EPDS had showed a highly variable sensitivity from
34%–100% and a specificity of
44%–100%,12 therefore supporting several
recommendations that validation precede clinical use in culturally diverse
populations.9,15
The purpose of this study was to validate the EPDS in Samoan
and Tongan women as a pre-requisite to repeating a prevalence study. These two
population groups make up 65% of all Pacific women residing in New
Zealand.16
Materials and MethodsBackground—This prospective
cohort study was approved by the Northern “X” Ethics Committee and
was conducted at Middlemore Hospital in Auckland, New Zealand. It is the
referral hospital of the Counties Manukau District Health Board (CMDHB) with a
catchment population of 500,000 that includes about 36% of all 250,000 people of
Pacific ethnicity in NZ.
Questionnaire—The EPDS is a
commonly used screening tool and rates each of the 10 items on a four-point
scale (0-3), giving a maximum score of 30. A score of ≥13 has been used in
previous prevalence studies signifying serious PND whereas women with scores of
10 to 12 were considered to have mild depression. A woman with a score of 0 to 9
was considered not depressed. The EPDS has been found to be acceptable to
women17 and a useful tool in cross-cultural
research on depression.18
The EPDS was translated into the Samoan and Tongan
languages and then independently back-translated, by a professional translation
service. The translated versions were checked by clinical researchers AE (fluent
in Samoan) and SF (fluent in Tongan) for appropriateness of language and
meaning. Agreement between depression resulting from the English and translated
versions were also tested using a Kappa Statistic. Each translated and English
version was then piloted by five Samoan and five Tongan women who were fluent in
their language.
Sample and data collection—The
sample size was determined from published validation methodology for the
EPDS.19,20 Names and contact details of Samoan
and Tongan women scheduled to deliver the following month were communicated to
the research team comprising both a Samoan and Tongan researcher. Excluded from
the study were women who were critically ill, had a stillbirth, serious
complications in pregnancy or delivery and who were unable to provide informed
consent.
Women were initially contacted by posted information
followed by a phone call. Interested women were recruited in a clinic or at
their home. The women could choose to complete the EPDS in English or in their
own language and were not offered any assistance in completing the
questionnaire. The questionnaires were completed between 4 and 7 weeks after
delivery.
An interview was then arranged with one of two
psychiatrists who were blind to the EPDS scores and who had received accredited
training in the use of the World Health Organization Composite International
Diagnostic Interview (WHO-CIDI v3). The interview was completed within 4 weeks
of completing the EPDS. Psychiatrist SF who was fluent in the Tongan language
interviewed Tongan women and SW who was semi-fluent in Samoan interviewed the
Samoan women. Interpreters were provided where requested. Women who were
diagnosed with serious depression were referred to the Maternal Mental Health
Service.
Statistical analysis—The raw
data was entered into an Excel Spreadsheet (Microsoft Corporation), then
analysed using Stata v8.0 software (Stata Corporation, Texas, USA). SAS v9.1
software was used to analyse the CIDI data and diagnoses. Cronbach's coefficient
alpha was calculated to estimate the reliability of the EPDS by determining its
internal consistency or the average correlation of items within the EPDS. A
value of 0.70 is considered an acceptable level for
consistency.21
Kappa statistics was used to measure the level of
agreement between the EPDS and CIDI standard. A Kappa of >0.6 is an
indication of substantial agreement and >0.8 is an indication of an almost
perfect agreement.22 The sensitivity,
specificity, positive predictive value (PPV), negative predictive value (NPV) as
well as the receiver operating characteristics (ROC) were used to determine the
global performance of the EPDS against the CIDI and the best cut-off points in
predicting PND.
ResultsDuring the study period, February 2009 to June 2010, a total
of 170 women (85 Tongan and 85 Samoan) completed the study and their
characteristics are compared in Table 1.
There was no significant difference between the Samoan and
Tongan women with regards to age, parity, country of birth and mode of delivery.
However, 51% of Tongan women completed the Tongan (rather than the English)
questionnaire compared to 28% of Samoan women completing the Samoan
questionnaire.
Table 1. Characteristics of the Samoan (n=85)
and Tongan (n=85) women participants
df=degrees of freedom;
χ2=Chi squared.
Are the items of the EPDS internally
consistent?—The Cronbach’s alpha for all of the EPDS
language versions and English version reached acceptable levels of reliability
with adjusted overall alpha values of 0.86. The English version was consistent
and there was little difference observed between Tongan and Samoan women.
The EPDS scores—About 1 in 5 (19%) of
both Tongan and Samoan women had an EPDS score of 10–12. Using the cut-off
points as recommended in the original EPDS developed by Cox JL et
al9 the prevalence of serious depression (EPDS
score ≥13) in this study would be 16.6% and for all depression (EPDS score
≥10) would be at 35.9%.
Serious depression was observed in 19% of Samoan and 13% of
Tongan women with an EPDS score of 13 or more. The average EPDS score was 8.4
(SD of 5.2), Samoan average was 8.7 (SD 5.1) and Tongan was 8.1 (SD 5.1).
The CIDI findings—Of the 170 women
interviewed, 36 (21.2%) had a positive CIDI, of which there was an equal number
of Samoan and Tongan women. Of those women, 29 (17.1%) women had serious
depression by interview (15 Samoan and 14 Tongan).
How well does the EPDS compare with the CIDI
diagnoses?—The range of EPDS scores for women identified with a
serious depressive disorder ranged from 5 to 24 with a median of 15 for both
groups. A clear pattern of higher EPDS scores for those with diagnosed disorders
was shown. The EPDS median for those with no depression and mild depression was
similar in the Tongan women whereas for the Samoan group, the EPDS median was
similar for serious depression. 62% of women with serious depression diagnosed
by CIDI were identified by the EPDS.
If only serious depression was considered, the EPDS compared
to the CIDI yielded a Kappa of 0.57, which indicates mild agreement. The
prevalence of any diagnosed depression resulted in mild agreement (Kappa
>0.5) for Tongan, Samoan and the combined results. A comparison between
serious depression identified by the EPDS with the CIDI for serious depression
resulted in mild agreement for both Tongan (Kappa = 0.58) and Samoan women
(Kappa = 0.56).
The area under the ROC was equal to 0.8948 and 0.8308 for
Samoan and Tongan women respectively (Figure 1). The
probability that a randomly selected Samoan or Tongan woman with depression has
a higher EPDS score than one selected without depression is more than 80%.
The EPDS score that gave the highest sensitivity (79%) and
specificity (76%) for the Tongan women was ≥10. The best score for the
Samoan women was ≥11, where both the sensitivity and specificity was 80%
(Table 2).
An EPDS score of ≥10 gave a PPV of 46% and NPV of 93%
for the combined EPDS in all three languages. However, an EPDS score at ≥
16 gave a higher PPV (82%) and NPV (86%). An EPDS score of ≥16 for Tongan
women gave the highest PPV and NPV whereas an EPDS score ≥17 for Samoan
women resulted in an optimal PPV and NPV combination.
Figure 1: Receiver operator characteristics by
ethnicity
Samoan
![]() Tongan
![]() Table 2. Sensitivity and specificity for
depression assigned by different cut-off levels for Edinburgh Postnatal
Depression Scale (EPDS) compared to diagnosed depressive disorder by
ethnicity
DiscussionPrevious validation studies had not found any issues with
translating the EPDS into many languages and that was also our experience. The
women found the EPDS in English and the translated versions easy to complete,
confirmed by the Kappa Statistic of 0.85, which showed agreement between the
English and Samoan or Tongan versions.
A significantly higher number of Tongan women preferred to
complete the questionnaire in their language compared to Samoan women
(p<0.003) which may mean that more Tongan women were more recent migrants.
This study found the EPDS had strong internal consistency by
language and by ethnicity. It had greater consistency in those using the English
version (alpha 0.85) than the Samoan version (alpha 0.75) and Tongan version
(alpha 0.81). Questions 5, 8 and 9 had poor internal consistency in the Samoan
EPDS and it was these three items that reduced the overall consistency of the
Samoan version. The level of consistency however compares favourably with other
validation studies with high Cronbach
alphas,23,24 and is similar to the alphas found
in the PIF study for Samoan and Tongan women.1
The overall serious PND prevalence rate by CIDI was 17.1%
and there was no statistically significant difference between the rates of
Samoan (19%) and Tongan (13%) women. The serious PND prevalence rate of 17.1%
found in our study was similar to the 16.4% prevalence found in the PIF
study.1
The difference in PND prevalence between Samoan and Tongan
in the PIF study1 cannot however be explained
by our findings. Methodological differences such as the administration of the
EPDS by interview and by different interviewers in the PIF
study1 may not give a full explanation. The
significantly higher number of Tongan women preferring the Tongan questionnaire
suggests a higher number of them may be recent migrants and lower acculturation
rates have been associated with a higher rate of
depression.25
The difference in the EPDS cut-off points for depression
between Samoan (≥11) and Tongan (≥10) women suggests that
more Tongan women will have positive EPDS screening for depression given they
have a lower EPDS cut-off than Samoan. Whether this difference will make a
difference in PND depression prevalence between the Samoan and Tongan women will
be difficult to say. The variation in cut-off scores between the different
validation studies may be a reflection of the differing ethnic populations and
sample characteristics of the various studied groups.
In our study, the best cut-off points for the scale were
≥10 (71%, 79%) for Tongan and ≥11 (80%, 80%) for Samoan women that
gave the best sensitivity and specificity for those with postnatal depression.
However, using these cut-off points gave a poor positive predictive value (PPV)
and this was also found in other studies.26
Differences in PPV differ with the prevalence of depression which can vary
between and within populations. Populations or groups with high rates of PND
have better PPVs with the EPDS than those with lower prevalence of PND.
We have taken into account the prevalence rate of all PND
and using the best positive and negative predictive values, alternative EPDS
cut-off scores were determined. We found that the best cut-off scores were
≥16 for the English and Tongan versions (PPV 82% and 88%; NPV 86% and 88%
respectively) whilst the Samoan version was ≥17 (PPV 84%, NPV 83%)
for any depressive disorder.
A few validation studies have differentiated an EPDS score
cut-off based solely on the sensitivity and specificity of the test or solely
based on its PPV and NPV. In a systematic review of 37 validation studies, a
cut-off score on the EPDS at 12/13 yielded a PPV of
17–100%.12 We feel that the two cut-off
scores can be used simultaneously with the first being used for prevalence
studies and the latter being used for clinical
screening.26 The higher EPDS cut-off score
ensures the screening test has the best performance by identifying most cases so
that a diagnostic or/and therapeutic intervention could be offered.
The limitations of our study include the differing time
points of administering the EPDS which was between 4 to 7 weeks postpartum and
prevalence of PND by EPDS has been shown to change at different time
points.27 The gap of up to 4 weeks between the
EPDS completion and CIDI interview could have been shorter but the prevalence of
diagnosed depression by CIDI should not differ as the instrument was designed to
ascertain an episode of depression over a stated period.
The NZ Ministry of Health (MOH) has decided against a formal
screening programme for PND following a decision of the British National Health
Service citing evidence that the condition does not satisfy screening
criteria.28 The MOH has decided instead to
adopt the National Institute for Health and Clinical Excellence (NICE)
guideline’s advice for the use of more focussed questioning in primary
care, in the form of three questions.29 The
routine use of the first three questions of the Patient Health Questionnaire
(PHQ-3) has been promoted during the Well Child/Tamariki Ora
programme,30 even though this tool had not been
validated for PND screening in NZ and has had limited validation elsewhere.
Despite the recent recommendations by the NZ MOH, we propose
that the EPDS is a valid and reliable tool for PND screening in Samoan and
Tongan women and that its use should be continued in both primary and secondary
care settings. Our findings suggest a cut-off score of ≥10 for Tongan and
≥11 for Samoan women was appropriate for screening whereas a cut-off of
≥16 for Tongan and ≥17 for Samoan was more appropriate where
predictive value was important.
Competing interests: None
declared.
Author information: Alec J Ekeroma, Head,
Pacific Women's Health Research & Development Unit, Department of Obstetrics
& Gynaecology, Middlemore Hospital, University of Auckland; Bettina
Ikenasio-Thorpe, Researcher, Pacific Women's Health Research & Development
Unit, Auckland; Sara Weeks, Psychiatrist, Lotofale Pacific Mental Health
Service, Auckland District Health Board, Auckland; Jesse Kokaua, Statistician,
Ministry of Health, Dunedin; Kasalanaita Puniani, Researcher, Pacific Women's
Health Research & Development Unit, Auckland; Peter Stone, Head, Department
of Obstetrics & Gynaecology, University of Auckland; Siale A Foliaki,
Psychiatrist, Department of Psychiatry, Middlemore Hospital, Counties Manukau
District Health Board (CMDHB), South Auckland
Acknowledgement: This study was supported
by Mr Manu Sione (General Manager, Pacific Division of the CMDHB).
Correspondence: Alec Ekeroma, Pacific
Women's Health Research & Development Unit, Department of Obstetrics &
Gynaecology, University of Auckland, Middlemore Hospital, PB 93311, Auckland,
New Zealand.Fax:+64 (0)9 5235253; email: aekeroma@middlemore.co.nz
References:
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