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Research article
Prevalence of depression and validation of the Beck Depression
Inventory-II and the Children’s Depression Inventory-Short
amongst HIV-positive adolescents in Malawi
Maria H Kim §, * ,1,2
, Alick C Mazenga* ,2 , Akash Devandra
1 , Saeed Ahmed
1 , Peter N Kazembe
2 , Xiaoying Yu
3 ,
Chi Nguyen 3 and Carla Sharp
4
§ Corresponding author: Maria H Kim, Baylor College of Medicine�Abbott Fund Children’s Clinical Center of Excellence, Private Bag B-397, Lilongwe 3, Malawi. Tel: �265 1 750 877. ([email protected]) *These authors contributed equally to the development of this manuscript.
Abstract
Introduction: There is a remarkable dearth of evidence on mental illness in adolescents living with HIV/AIDS, particularly in the
African setting. Furthermore, there are few studies in sub-Saharan Africa validating the psychometric properties of diagnostic
and screening tools for depression amongst adolescents. The primary aim of this cross-sectional study was to estimate the
prevalence of depression amongst a sample of HIV-positive adolescents in Malawi. The secondary aim was to develop culturally
adapted Chichewa versions of the Beck Depression Inventory-II (BDI-II) and Children’s Depression Inventory-II-Short (CDI-II-S)
and conduct a psychometric evaluation of these measures by evaluating their performance against a structured depression
assessment using the Children’s Rating Scale, Revised (CDRS-R).
Study design: Cross-sectional study.
Methods: We enrolled 562 adolescents, 12�18 years of age from two large public HIV clinics in central and southern Malawi. Participants completed two self-reports, the BDI-II and CDI-II-S, followed by administration of the CDRS-R by trained clinicians.
Sensitivity, specificity and positive and negative predictive values for various BDI-II and CDI-II-S cut-off scores were calculated
with receiver operating characteristics analysis. The area under the curve (AUC) was also calculated. Internal consistency was
measured by standardized Cronbach’s alpha coefficient, and correlation between self-reports and CDRS-R by Spearman’s
correlation.
Results: Prevalence of depression as measured by the CDRS-R was 18.9%. Suicidal ideation was expressed by 7.1% (40) using the
BDI-II. The AUC for the BDI-II was 0.82 (95% CI 0.78�0.89) and for the CDI-II-S was 0.75 (95% CI 0.70�0.80). A score of ]13 in BDI-II achieved sensitivity of �80%, and a score of ]17 had a specificity of �80%. The Cronbach’s alpha was 0.80 (BDI-II) and
0.66 (CDI-II-S). The correlation between the BDI-II and CDRS-R was 0.42 (pB0.001) and between the CDI-II-S and CDRS-R was
0.37 (pB0.001).
Conclusions: This study demonstrates that the BDI-II has sound psychometric properties in an outpatient setting among HIV-
positive adolescents in Malawi. The high prevalence of depression amongst HIV-positive Malawian adolescents noted in this
study underscores the need for the development of comprehensive services for HIV-positive adolescents.
Keywords: HIV; adolescents; depression; prevalence; BDI-II; CDI-II-Short.
Received 19 November 2013; Revised 2 May 2014; Accepted 20 May 2014; Published 30 July 2014
Copyright: – 2014 Kim MH et al; licensee International AIDS Society. This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported (CC BY 3.0) License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium,
provided the original work is properly cited.
Introduction In 2009, an estimated 5 million young people (aged 15�24) and 2 million adolescents (aged 10�19) were living with HIV, the vast majority in sub-Saharan Africa [1]. Nearly one in two
new HIV infections occurs in young people [1]. This, combined
with the successful scale-up of paediatric HIV services re-
sulting in improved survival into the teen years, has led to a
rising demand for comprehensive services focusing on the
special needs of adolescents [2].
Adolescence is a period of vulnerability for a host of well-
documented biological, behavioural, social and structural
reasons. Adolescents living with HIV/AIDS in sub-Saharan
Africa present unique challenges to health care providers
[3,4]. Furthermore, mental health in people living with HIV
and AIDS (PWLHA) is an area of scanty research, and there is
a dearth of evidence for adolescents, particularly in the
African setting.
Depression is a major contributor to the burden of disease
worldwide and is estimated to be the leading cause of
disability as measured by Years Lost due to Disability (YLDs)
[5,6]. The prevalence of depression is estimated to be higher
in developing versus developed countries [7]. In PLWHA, the
Kim MH et al. Journal of the International AIDS Society 2014, 17:18965
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1
prevalence of depression has been documented to be as high
as double that of the general population [8]. In the few
studies in Africa, estimates of prevalence of depression in
PLWHA range between 12 and 60% [8�14]. Depression has been shown to worsen several HIV-related
health outcomes. It is associated with steeper declines in
CD4 counts, and more rapid progression to AIDS and death
[8,14�16]. Associations with suboptimal antiretroviral therapy (ART) adherence and discontinuation have been reported
with significant implications for long-term treatment efficacy
[17�19]. Depression in youth has also been correlated with high-risk behaviour including earlier sexual debut, low con-
dom use, substance abuse, more frequent sexual partners and
unplanned pregnancy [11,20]. However, most evidence comes
from high-income countries, and few associations have been
firmly established in sub-Saharan Africa, the epicentre of the
HIV epidemic. Other correlates more applicable to Africa and
the Malawian setting in particular, such as orphanhood,
poverty and urban migration, have been poorly described.
The lack of clinical data, limited awareness by healthcare
providers and patients and the scarcity of resources and
interventions, all act as obstacles in the provision of holistic
care to adolescents living with HIV. There is an urgency to
incorporate mental health into adolescent HIV care in Malawi
and sub-Saharan Africa to improve quality of life and health
outcomes.
Unfortunately, there are few studies in sub-Saharan Africa,
and virtually no published studies in Malawi validating the
psychometric properties of the commonly utilized diagnostic
and screening tools for depression amongst adolescents as
compared to adults [13,21�24]. Depression may manifest in a variety of ways across different cultural and age groups,
and research instruments need to be culturally appro-
priate [25]. Traditional instruments developed in the west
should, if used, undergo a careful process of translation,
back-translation and modification to ensure cross-cultural
equivalence [21,25].
The Beck Depression Inventory-II (BDI-II) and the Children’s
Depression Inventory-II-Short (CDI-II-S) were used as depres-
sion screening tools. The BDI-II is a 21-item tool that has been
extensively tested for validity and reliability since the 1960s
[26], including use in the paediatric population. One study in
Nigeria provided psychometric evidence in support of the
BDI-II in the African setting [22]. The CDI-II-S, a symptom-
oriented instrument, is a 12-item self-report tool used for
assessing depression in children aged 7�17 years. Psycho- metric evidence in support of the use of the long version
was provided in a study amongst children in Tanzania [13].
The CDI-II-S has been validated as being equally efficacious for
screening purposes as the long version [27�29]. Both tools can be completed in 5�10 minutes and, therefore, are ideal for use in typical high-volume clinical settings in Malawi. There
has been no assessment of either tool in Malawi to date.
Malawi, a land-locked country located in Southern Africa,
with an HIV prevalence of 11%, has successfully scaled up
access to HIV treatment services with 276,987 patients
retained alive on ART as of June 2011 [30]. However, there
are limited local options for diagnosis and treatment of
mental health problems. One previous survey of depression
in a cohort of orphaned children and adolescents (10�18 years) in the southern region reported a 53.2% prevalence
for clinical depression using the Center for Epidemiological
Studies Depression Scale Modified for Children (CES-DC) [31].
The primary aim of this cross-sectional study was to
estimate the prevalence of depression amongst a sample of
HIV-positive adolescents in Malawi. The secondary aim was
to develop culturally adapted Chichewa (the official and most
widely spoken language in Malawi) versions of the BDI-II and
CDI-II-S and conduct a psychometric evaluation of these
measures for use in HIV-positive adolescents by evaluating
their performance against a structured depression assess-
ment using the Children’s Depression Rating Scale, Revised
(CDRS-R).
Methods Study population
We recruited a convenience sample of adolescents aged
12�18 years from the Baylor College of Medicine Children’s Clinical Center of Excellence (COE) and Zomba ART Clinic. The
COE, the largest and first stand-alone paediatric HIV clinic in
Malawi, is located in Lilongwe, in central Malawi. It serves
both as an outpatient facility and as a national referral centre
for paediatric HIV care. Patients at both sites come from
urban and rural locations and are of various ethnic and socio-
economic backgrounds. As of March 2011, there were �420
(COE) and �200 (Zomba) patients 12�18 years of age active in care.
Informed consent
The National Health Sciences Research Committee (NHSRC) in
Malawi and Baylor College of Medicine Institutional Review
Board in USA approved the study protocol. The COE and
Zomba Central Hospital granted site approvals. All caregivers
and adolescents signed written informed consents/assents.
Measures
The CDI-II-S and the BDI-II were selected as the most appro-
priate tools to translate and evaluate for use in assessing
depression amongst Malawian adolescents living with HIV.
Both tools are widely used and validated self-report measures
of depression in youth.
The CDI-II-S is a 12-item self-report instrument used to
detect the presence and severity of depressive symptoms in
children aged 7�17 years [28,29]. The reading level is rated to be at the 2nd grade, and it can be completed in 5�10 minutes [28,29]. Each itemis scored: 0 for no symptom; 1 for a mild; and
2 for definite symptoms [13,29]. The CDI-II-Long [29,32�34] from which the CDI-II-S is derived has been validated in
a number of countries including Tanzania [13,35�37]. The CDI-II-S is reported to be a psychometrically comparable
screening instrument for depression [27�29]. Therefore, the CDI-II-S was selected as the measure most appropriate to
translate and examine for use in typical high-volume clinical
settings in Malawi.
The BDI-II is a 21-item self-report questionnaire that
assesses the presence and severity of depressive symptoms
in adolescents ]13 years [26,35,38]. Each question is scored:
0�symptom absent; 1�symptom present; 2�moderate symptom; and 3�severe symptom [35,39]. Total potential
Kim MH et al. Journal of the International AIDS Society 2014, 17:18965
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score is 63. The reading level is rated to be at the 6th grade,
and it can be completed in about 10 minutes. The tool has
been validated in other countries where English is not the
primary language [22,35,38].
To achieve accuracy in translation and cultural under-
standing, the tools underwent an adaptation process. The
process integrated input from multiple collaborators includ-
ing US, UK, Malawi-based researchers, linguistic experts
and Malawian adolescents. The tools were translated into
Chichewa by linguistic experts from Mzuzu University Centre
for Language Studies, back-translated, and edited. To help
ensure cultural validity in a Chichewa speaking culture, the
translated tools were checked by a Malawian Mental Health
Clinician, and pre-tested amongst a group of Malawian
adolescents. Translation of the English concepts to Chichewa
was straightforward for both tools. The process did identify
several items that needed clarification, for example, CDI-II-S
#12: in Chichewa ‘‘feeling’’ translated directly to ‘‘kumva’’
which could also mean ‘‘hearing.’’ Therefore, we opted to use
the word ‘‘kusungulumwa’’ meaning, ‘‘feeling alone.’’ BDI-II
#19: ‘‘weight loss’’ would translate to ‘‘decreasing weight’’ in
Chichewa, which would be too long and unclear. Therefore,
we used instead ‘‘kutsika kwa sikelo’’ meaning ‘‘decrease in
scale’’ since weight in Malawi is commonly referred to as
‘‘scale�sikelo.’’ CDRS-R is the most widely used rating tool for the as-
sessment of depressive symptoms in children and adoles-
cents, particularly in international research trials [40�42]. It is a clinician interview hand-rated instrument that covers
17 symptom areas of depression and can be used to both
diagnose and measure treatment response to depression
[36,38,43]. The CDRS-R was based on the adult Hamilton
Depression Rating Scale and can be administered in 15�20 minutes [39,43]. It rates 14 of 17 items from 1 to 7 while
the remaining three items are rated 1�5 [39]. The rating of the items is between 1 (�no difficulties) and 5, or 1 and 7 (7�clinically significant difficulties) summing up to a total potential raw score of 113 [41]. A child’s non-verbal
behaviour is rated by the observer for items 15�17 [39]. A raw score of ]30 with a T-score of ]55 has been
proposed to be indicative of depression [39].
In sub-Saharan Africa, there is scarcity of research in child
mental health and likewise paucity of data concerning the
psychometric properties of the CDRS-R. However, the devel-
opers of the tool report internal consistency (Cronbach’s
alpha) of 0.85, inter-rater reliabilities of 0.92�0.96, test�retest reliability of 0.80 as well as evidence of extensive conver-
gent validity, moderate concurrent validity, discriminative
validity and predictive validity [43]. Many other studies in
Asia, Europe and America have demonstrated excellent
psychometric properties of the CDRS-R [36,39�41,43]. In Malawi, there is currently only one psychiatrist working
in the public sector. Therefore, although published studies
utilizing the CDRS-R in Malawi are lacking, given the strong
evidence supporting the use of CDRS-R internationally, in lieu
of a psychiatric interview to diagnose depression, we utilized
the validated English version of CDRS-R to help assess
convergent validity of the BDI-II and CDI-II-S. To help ensure
optimal administration, only clinicians with mental health
training and over two years of experience in adolescent
HIV care, were selected to undergo one week training in
the administration of the CDRS-R. The training involved
discussing and agreeing upon locally equivalent words for
terminology. The post training competency assessment in-
cluded observed administration of the CDRS-R to ensure
standardized administration and use of culturally accepted
vocabulary. Interviewers received on-going supervision by
a qualified mental health professional with expertise in
adolescent depression.
Procedure
Participants’ interviews were conducted between January
and August 2012. Consents/assents were obtained from
caregivers and adolescents. Adolescents first completed the
CDI-II-S and then the BDI-II in a private room. Finally, trained
clinicians, who were blinded to the results of the CDI-II-S and
BDI-II, administered the CDRS-R. All participants who were
determined as having depression were promptly referred to a
Mental Health Clinical Officer and Psychosocial Counsellor on
site for further assessment and expert management.
Data analysis
Descriptive statistics, such as mean and standard deviation
(SD) for continuous variables, and frequency and proportion
for categorical variables, were calculated. We used CDRS-R
T-score, BDI-II total raw score and CDI-II-S T-score in the
analysis. The CDRS-R was used as gold standard to classify
depression. The prevalence of depression was calculated by
the proportion of subjects with CDRS-R score ]55. Chi-
square test was used to compare the prevalence of depres-
sion between genders. Sensitivity, specificity, and positive
and negative predictive values for various cut-offs were
calculated to determine the optimal screening as well as dia-
gnostic threshold with receiver operating characteristics
(ROC) analysis.
Optimal cut-offs were determined first by identifying the
point that gave the smallest distance from the ROC curve to
the upper left corner of the graph. This point minimizes the
sum of squares of false negative (1-sensitvity) and false
positive (1-specificity). This cut-off gave the best discrimina-
tion between cases and non-cases. The second approach was
to find a point that maximizes both sensitivity and specificity
by determining the point at which sensitivity approximates
specificity. The area under the curve (AUC) was calculated to
determine the tools’ diagnostic ability; AUC of 1.00 indicating
perfect diagnostic ability. The SAS logistic procedure esti-
mated the AUC using the trapezoid rule and compared the
AUCs using the Chi-square test according to DeLong [44].
Since variances between items were widely spread,
internal consistency was measured by standardized Cron-
bach’s alpha coefficient. Measurements were not normally
distributed; therefore, the Spearman’s correlation coefficient
was used to measure the correlation between the two tools
and the clinical interview. For all statistical tests, a two sided
pB0.05 was considered significant. Data was analyzed using
SAS version 9.3 (SAS Institute, Cary, NC).
Kim MH et al. Journal of the International AIDS Society 2014, 17:18965
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Results The two clinics provided a list of 695 potential participants.
Of these, 102 could not be contacted due to death, loss to
follow-up, lack of contact information or transfer to another
facility. Of those contacted, 11 were unable to participate
due to disability. Of the 582 eligible participants, 97% (562)
consented/assented and enrolled in the study.
Descriptive characteristics
Table 1 describes the socio-demographic characteristics of
the adolescent study participants.
The mean scores (9SD) were 11.997.9 for BDI-II and
51.6910.2 for CDI-II-S. Females had significantly higher mean
BDI-II than males (12.898.1 vs. 10.997.5, p�0.005); CDI-II-S scores were similar between genders (p�0.56).
Prevalence of depression
The prevalence of depression as measured by the CDRS-R
was 18.9% (106/562): 21.6% (68/315) in females and 15.4%
(38/247) in males. Although this finding approached sig-
nificance (p�0.06), the difference in mean CDRS-R scores was significant, 48.797.2 (females) and 47.296.7 (males),
p�0.013. Using the CDRS-R (score of �2 on question #13), suicidal ideation was expressed by 3.0% (17), and using BDI-II
(score of �0 on question #9) by 7.1% (40) (pB0.001).
Psychometric evaluation of the BDI-II and CDI-II-S
Diagnostic accuracy
Figure 1 demonstrates the ROC curves for the two tools as
compared to the CDRS-R. The AUC of the BDI-II 0.82 (95%
CI 0.77�0.87) was significantly greater than the AUC of the CDI-II-S 0.75 (95% CI 0.70�0.80) (p�0.003). By gender, the AUCs for the BDI-II were 0.88 (males) and 0.78 (females),
and for CDI-II-S were 0.85 (males) and 0.69 (females). The
difference between the scales was significant among females
(p�0.007) but not among males (p�0.35). The sensitivity, specificity, positive predictive value, and
negative predictive value at various cut-off scores for both
tools are shown in Tables 2 and 3 and Figures 2 and 3.
For the BDI-II, a cut-off of 15 gives both the shortest distance
from the ROC curve to the upper left corner of the graph as
well as the point where specificity approximates sensitivity.
This cut-off remains consistent for both genders. A score of
]13 achieved sensitivity of �80% and, therefore, may be
ideal to screen for cases, whereas a score of ]17 had a
specificity of �80%, making it appropriate for identifying non-
cases (diagnosis).
For the CDI-II-S, a cut-off of 53 gives both the shortest
distance from the ROC curve to the upper left corner of the
graph as well as the point where specificity approximates
sensitivity. Cut-offs differ slightly by gender: 52�53 (females) and 54�57 (males). Specificity approximates sensitivity at 52 (females) and 56 (males). The shortest distance from ROC
curve to the upper left corner of the graph was 53 (females)
and 57 (males). Overall, a score of ]48 achieved sensitivity
of �80% and, therefore, may be ideal as a screening cut-off,
Table 1. Socio-demographic characteristics of the study
participants
Variable
n (%)
N�562
Age (mean9SD) 14.592.0
Sex
Female 315 (56.1)
Male 247 (44.0)
Residential location
Urban 369 (65.7)
Peri-urban 93 (16.5)
Rural 100 (17.8)
Education status
Primary School 402 (71.5)
Secondary School 153 (27.2)
Post-Secondary School 4 (0.7)
Not at School 3 (0.5)
Figure 1. Receiver operating characteristic (ROC) curve for the
BDI-II and CDI-II-S as compared to the CDRS-R.
Table 2. Psychometric properties of the BDI-II in screening for
depression in HIV-positive Malawian adolescents
Cut-off BDI-II
(raw score) Specificity Sensitivity PPV NPV
11 0.588 0.849 0.324 0.944
12 0.638 0.830 0.348 0.942
13 0.686 0.811 0.376 0.940
14 0.739 0.774 0.408 0.934
15 0.774 0.745 0.434 0.929
16 0.794 0.679 0.434 0.914
17 0.829 0.623 0.458 0.904
18 0.866 0.575 0.500 0.898
19 0.906 0.557 0.578 0.898
20 0.930 0.500 0.624 0.889
Kim MH et al. Journal of the International AIDS Society 2014, 17:18965
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whereas a score of ]58 had a specificity of �90%, making
it appropriate for diagnostic use.
Internal consistency and validity
The Cronbach’s alpha for the BDI-II was 0.80 indicating strong
internal consistency. The Cronbach’s alpha for the CDI-II-S
was 0.66. The convergent validity between the BDI-II and
CDI-II-S as calculated by the Spearman correlation was 0.54
(pB0.001). The correlation between the BDI-II and CDRS-R
was 0.42 (pB0.001). The correlation between the CDI-II-S
and CDRS-R was 0.37 (pB0.001). Similar internal consistency
(BDI-II: 0.80 vs. 0.80; CDI-II-S: 0.65 vs. 0.66) and medium
correlation (BDI-II and CDRS-R: 0.38 vs. 0.45; CDI-II-S and
CDRS-R: 0.31 vs. 0.44) were found by female vs. male gender.
Discussion To our knowledge, this is the first study to estimate the
prevalence of depression amongst HIV-positive Malawian
youth as well as the first study to evaluate the psychometric
properties of the BDI-II and CDI-II-S for depression screening
in this population. Our findings suggest that the prevalence
of depression is high and that the BDI-II can be used to
screen for depression amongst this population. The internal
consistency of the CDI-II-S as measured by Cronbach’s alpha
was lower than the 0.73�0.91 established in American samples across all versions of the CDI-II [29]. However, the
internal consistency is similar to what was reported in
Tanzania amongst orphans (0.67) [13]. The relatively lower
internal consistency estimates suggest that additional mod-
ifications may need to be made to the CDI-II-S for use in this
population. In all, the BDI-II had superior internal consistency
and AUC, as well as better concordance with the clinical
interview. Furthermore, our study suggests a score of ]13
in BDI would be appropriate as a screening cut-off score,
whereas a score of ]17 would be more appropriate for
diagnostic use.
Due to the paucity of studies in HIV-positive adolescents,
different age ranges and diverse measures, it is difficult to
make prevalence comparisons. However, our prevalence of
18.9% using the CDRS-R was similar to the 17.8% prevalence
found amongst HIV-positive children, 6�18 years of age in Kenya using the Mini International Neuropsychiatric Inter-
view for Major Depressive Episode (MINI-kid) [14], and 18.3%
found in Malaysia (Diagnostic and Statistical Manual of
Mental Disorders, Fourth Edition and MINI-kid) [37]. Since
the CDRS-R, unlike the MINI-kid, was not designed to identify
other mental disorders such as bipolar and anxiety disorders,
we were unable to report on other potentially co-morbid
mental health conditions. Studies in both HIV-positive and
uninfected adolescents and adults have demonstrated that
females show higher rates of depression compared to males
[22,23,45,46]. In our study, the difference in prevalence of
depression between genders appeared to be considerable,
and we found a statistically significant difference in mean
CDRS-R scores between genders. Interestingly, suicidal idea-
tion as expressed by the BDI-II was higher than that found by
the CDRS-R.
Table 3. Psychometric properties of the CDI-II-S in screening
for depression in HIV-positive Malawian adolescents
Cut-off CDI-II-S
(T-score) Specificity Sensitivity PPV NPV
47 0.456 0.868 0.271 0.937
48 0.474 0.868 0.277 0.939
50 0.553 0.792 0.292 0.920
52 0.662 0.689 0.322 0.901
53 0.667 0.689 0.324 0.902
54 0.735 0.594 0.342 0.886
56 0.750 0.594 0.356 0.888
57 0.785 0.509 0.355 0.873
58 0.831 0.472 0.394 0.871
Figure 2. Sensitivity and specificity of the BDI-II.
Kim MH et al. Journal of the International AIDS Society 2014, 17:18965
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5
It is possible that having a more highly trained and
sympathetic interviewer could encourage a participant to be
more forthcoming in reporting symptoms. However, typically,
there is higher endorsement of all psychopathology on self-
report screening measures like the BDI-II versus interview-
based measures [38]. The youth in this study may have felt
more comfortable answering certain questions by self-report
versus interview.
There were several limitations to the study. Given the
extremely limited number of qualified psychiatrists in
Malawi, we opted for assessment of convergent validity
with the CDRS-R, in lieu of the gold standard diagnosis of
depression via psychiatric interview. Results demonstrated a
medium correlation between the BDI-II and the CDRS-R
probably reflecting a method effect (self-report vs. interview-
based). More research using interview-based tools alongside
self-report measures is needed to clarify these results. In
addition, we cannot definitively conclude that our prevalence
estimate is representative of all HIV-positive adolescents in
Malawi. However, the Baylor COE is the largest referral centre
for paediatric HIV in Malawi, with patients coming from
a wide geographic area. Zomba Central Hospital ART Clinic in
southern Malawi is one of two referral centres for patients
from the southern region. Therefore, sampling from these
centres should provide a fairly reliable estimate of prevalence
of depression amongst HIV-positive Malawian youth.
As the study did not include a control group and national
statistics on depression prevalence in Malawian adolescents
are lacking, we were unable to conclude whether our pre-
valence estimate is higher than that of non-HIV-positive adoles-
cents in Malawi. In addition, caution should be exercised in
generalizing the results, including use of the tools to ado-
lescents without HIV infection. However, the high prevalence
of depression amongst Malawian adolescents living with
HIV highlights a significant mental health need, and raises a
concern regarding how these needs will be met in a resource-
limited setting.
The strength of our study is that it is the first epidemio-
logical study to assess the prevalence of depression in HIV-
positive youth in Malawi, and the first to use two self-report
measures and a semi-structured diagnostic instrument. In
addition, to our knowledge, this is the largest mental health
prevalence study done in HIV-positive youth in Africa.
Conclusions Despite the limitations, this study has demonstrated that the
BDI-II has sound psychometric properties in an outpatient
setting among HIV-positive adolescents in Malawi. Our study
also supports the use of the BDI-II as a viable measure for
identifying possible cases of depression amongst this popula-
tion and, in fact, may be easier to administer as compared to
an interview-based tool for assessing depression. The CDI-II-S
can be used to screen for depressive symptoms. However, the
low internal consistency estimates suggest that modifications
may need to be made. Importantly, our study demonstrates a
high prevalence of depression amongst HIV-positive Malawian
youth and underscores the need for the development of
comprehensive services for HIV-positive adolescents. Further
research is needed to explore factors contributing to and
protective of depression in adolescents living with HIV/AIDS.
Interventional studies are also needed to determine the most
efficacious treatments.
Authors’ affiliations 1 Baylor College of Medicine International Paediatric AIDS Initiative, Texas
Children’s Hospital, Houston, TX, USA; 2 Baylor College of Medicine�Abbott
Fund Children’s Clinical Centre of Excellence, Lilongwe, Malawi; 3 Department
of Paediatrics, Epidemiology Center, Baylor College of Medicine, Houston, TX,
USA; 4 Department of Psychology, University of Houston, Houston, TX, USA
Competing interests
The authors have no competing interests to declare.
Authors’ contributions
MHK and ACM conceived and designed the study, were responsible for study
coordination and data management, helped analyze data, interpreted findings
Figure 3. Sensitivity and specificity of the CDI-II-S.
Kim MH et al. Journal of the International AIDS Society 2014, 17:18965
http://www.jiasociety.org/index.php/jias/article/view/18965 | http://dx.doi.org/10.7448/IAS.17.1.18965
6
and wrote the manuscript. AD assisted in reviewing the protocol and study
coordination in the field, contributed to data management and reviewed the
manuscript. PNK and SA reviewed the study protocol, provided guidance on
the conduct of the study and critically reviewed the manuscript for important
intellectual content. CN, XY and CS assisted in statistical analysis, interpretation
and manuscript writing. All authors have read and approved the final
manuscript.
Acknowledgements
We thank the Malawi Ministry of Health for their partnership in this endeavour.
We thank the Baylor College of Medicine Children’s Foundation Malawi data
team, clinicians and nurses who participated in data collection including Menard
Bvumbwe, William Kamuyango, Mphatso Machika, and Adamson Munthali.
Special thanks to Joseph Mhango for creation of the study database. We extend
our gratitude to Chrissie Gondwe and Edson Mwinjiwa of Diginitas International
for facilitating and helping us with recruitment of study participants at Zomba
Central Hospital ART Clinic. We are grateful to all the adolescents living with HIV
and their caregivers who participated in this study.This study was made possible
by support from the Texas Children’s Global Health Stimulus Grant and USAID
cooperative agreement number 674-A-00-10-00093-00. MHK was supported
by the Fogarty International Center of the National Institutes of Health under
award number K01 TW009644. Data analysis was provided by the Design and
Analysis Core of the Baylor-UT Houston Center for AIDS Research, an NIH funded
program numbered P30-AI36211.
Disclaimer
The contents are the responsibility of the authors and do not necessarily reflect
the views of the funders, including the National Institutes of Health, USAID and
the United States Government.
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/ENU <FEFF00530065007400740069006e0067007300200066006f00720020007400680065002000520061006d007000610067006500200077006f0072006b0066006c006f0077002e> >> >> setdistillerparams << /HWResolution [2400 2400] /PageSize [612.000 792.000] >> setpagedevice