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Key Words
Disability HADS Mood disorders Poststroke
depression Stroke, prognosis
Abstract
Background: Poststroke depression (PSD) is one of the most
important long-term adverse psychosocial consequences in
stroke survivors. Our objective was to assess the prevalence
of PSD in Brazilian stroke patients and identify significant associated factors. Methods: A cross-sectional study of stroke
patients consecutively admitted for rehabilitation was conducted. The patients were evaluated by means of the NIH
Stroke Scale, Mini-Mental State Examination, Barthel Index,
Lawton Scale, modified Rankin Scale, Hospital Anxiety and
Depression Scale (HADS), Geriatric Depression Scale (GDS)
and MOS-Short Form 36. Patients with a HADS-depression
subscale score 611 and/or GDS score 68 were classified as
depressed. Results: Three hundred stroke survivors were assessed (mean age: 56.3 years; 51.7% males). Half (46.7%) of
the stroke patients had an m-RS score ^2. The proportion
of stroke patients who scored 611 points on the HADS-depression and HADS-anxiety subscales were 19.2 and 23.7%,
respectively. One third (29.7%) had a GDS mean score 68.
The GDS scores significantly correlated (p ! 0.0001) with the
HADS-depression (r = 0.51) and HADS-anxiety subscales (r =
0.54). The prevalence of mood disorders was significantly
higher in females than in males (24.8 vs. 14.2%; 2, p = 0.03).
PSD was significantly associated (p ! 0.0001) with work status (housewife), education level, lower social and cognitive
functioning, dependence in the instrumental activities of
daily living and presence of diabetes in the multivariable regression analysis (R adjusted = 0.32). Conclusions: PSD was
highly prevalent in the chronic phase of stroke. Early detection and recognition of associated risk factors is important
to treat and prevent PSD in a rehabilitation setting.
Copyright 2009 S. Karger AG, Basel
Introduction
Poststroke depression (PSD) is one of the most important long-term adverse psychosocial consequences in
stroke survivors. Depression commonly occurs after a
stroke, with an estimated prevalence as high as 30% in the
first year after the event [1]. PSD is associated with poor
functional and psychosocial outcome in chronic stroke
patients [2, 3]. It affects cognitive function, functional recovery, health-related quality of life and health care use
in stroke survivors [35]. Emotional factors also affect
the stroke survivors considered fully recovered. Patients
who are perceived functionally independent still experience social participation difficulties and depressive
symptoms [6]. This empirical evidence has provided support for a biopsychosocial model of PSD in chronic stroke
patients.
Francisco Javier Carod-Artal, MD, PhD
Neurology Department, Sarah Hospital
SMHS quadra 501 conjunto A
Brasilia DF 70330-150 (Brazil)
Tel. +55 61 3 319 1555, Fax +55 61 3 319 1538, E-Mail fjcarod-artal@hotmail.com
158
Carod-Artal/Ferreira Coral/Trizotto/
Menezes Moreira
(n = 300)
Age, years
Education, years
Mean time since stroke, months
Male gender
Marital status
Married
Single
Widower
Divorced
Occupation
Retired
Still working
Housewife
Unemployed
Previous stroke
Stroke subtype
Ischemic stroke
Hemorrhage
Vascular risk factors
Hypertension
Smoking
Hyperlipidemia
Diabetes
Atrial fibrillation
56.3814.3
8.285.5
22.5828.7
155 (51.7)
163 (54.3)
47 (15.7)
43 (14.3)
47 (15.7)
139 (46.3)
86 (28.7)
48 (16)
27 (9)
32 (10.7)
258 (86)
42 (14)
227 (75.6)
162 (54)
103 (34.3)
62 (20.7)
18 (6)
Results
Data Analysis
Mean scores of the HADS subscales, GDS and functional
stroke scales were calculated for the patients. The unpaired t test,
2 test and ANOVA were used for comparison between groups.
Three hundred and ninety stroke patients were consecutively admitted to the rehabilitation hospital during
the 1-year period of recruitment. On the basis of clinical
examination, 50 patients with severe aphasia and 32 with
vascular dementia were excluded; 5 patients refused to
participate in the study, and 3 were !18 years old. Three
hundred patients (mean age: 56.3 years; 51.7% males)
were included in the study. The demographic characteristics of the study population and vascular risk factors are
shown in table 1. One third (29.7%) of the patients were
665 years old. Females were slightly younger than males
(54.7 vs. 57.8 years; unpaired t test, p = 0.06), whereas the
mean time since stroke and level of education were similar. Most patients (87%) were living in their own home
and 13% with family members. A delay in stroke rehabilitation was observed and approximately two thirds
(57%) of the stroke patients started stroke rehabilitation
in the first 12 months following stroke.
Two hundred and fifty-eight subjects (86%) had an
ischemic stroke. The most common ischemic stroke subtypes were: cryptogenic stroke (25.6%), small-vessel infarction (25.2%), large artery occlusion (19.8%), cardioembolism (18.6%) and other causes (10.8%). Hypertension was significantly more common in males (81.3 vs.
69.7%; unpaired t test, p = 0.03).
Functional evaluation of stroke survivors is shown in
table 2. Forty-three percent of the stroke patients had an
NIHSS score ^5, 51% scored between 6 and 13, and 5.7%
had an NIHSS score 614. The median of BI score was 80
(interquartile range: 40), and the median of the m-RS was
3 (interquartile range: 2). Approximately half (46.7%) of
Poststroke Depression
mood and anhedonia [23]. The Brazilian version of the HADS was
used for the purpose of this study [20].
The GDS was developed as a screening test to detect depression in elderly individuals [17]. Subjects answer yes/no to questions about feelings, interests, activities and hopes. The focus of
the GDS items on affective rather than somatic components of
depression may increase its suitability for use among individuals
with stroke. The shortened 15-item Brazilian version was used.
The scores range from 0 to 15. A score of 66 indicates possible
depression and higher scores (cutoff value of 68) are associated
with clinically important depressive symptoms [21].
The SF-36 is a generic health-related quality of life measure
[18] that includes the following 8 domains: physical functioning,
role limitations due to physical problems, bodily pain, general
health perception, vitality, social functioning, role limitations
due to emotional problems and emotional well-being. The scores
for each domain range from 0 to 100, and higher values indicate
better function. Two summary scores of SF-36, the Physical Component Summary and the Mental Component Summary, can be
obtained.
159
NIHSS2
MMSE1
BI1
Lawton instrumental ADL scale1
HADS-depression subscale2
HADS-anxiety subscale2
HADS-total score2
GDS2
SF361
Physical functioning
Physical role
Bodily pain
Social functioning
Mental health
Emotional role
Vitality
General health
Physical component summary
Mental component summary
Sample
(n = 300)
Male
(n = 155)
Female
(n = 145)
6.883.8
25.983.4
72.7826.5
16.984.7
7.184.1
7.684.2
14.687.3
5.983.4
6.683.9
26.483.6
74.4825.9
17.084.8
6.583.6
7.284.1
13.786.7
5.783.5
7.083.7
25.483.8
70.8827.1
16.684.6
7.784.4
7.984.4
15.687.7
6.283.3
NS
0.04
NS
NS
<0.01
NS
0.02
NS
24.4826.8
15.1830.2
59.8829.3
51.0827.9
59.2823.8
37.9844.1
60.6821.8
63.6820.7
33.388.8
50.1811.2
27.9828.5
15.7831.2
66.5827.8
53.5827.3
62.5823.3
39.7845.2
63.4823.4
66.5820.7
33.989.4
50.5811.7
24.4826.1
14.6829.1
54.3829.7
48.6828.4
55.8824.0
35.8842.7
57.7821.9
60.5820.3
33.288.2
49.6811.2
NS
NS
<0.001
NS
0.01
NS
0.03
0.01
NS
NS
the stroke patients (140) had an m-RS score ^2; 71 patients (23.7%) were independent in the ADL and achieved
a BI score of 100.
No significant differences in neurological impairment
(as measured by NIHSS), disability (as measured by BI
and/or Lawton scale) or functional status (as measured by
m-RS) were observed between males and females. The
Lawton instrumental ADL scale significantly correlated
(p ! 0.0001) with BI (r = 0.82), m-RS (r = 0.78), NIHSS
(r = 0.68) and MMSE (r = 0.35). In addition, no significant differences were found in the mean scores of the
scales that evaluated stroke severity (NIHSS), cognition
(MMSE) and depression (HADS, GDS) between young
(!65 years) and elderly stroke patients. Young stroke survivors had higher levels of anxiety (p = 0.05) as measured
by the HADS-anxiety subscale and were more independent in the instrumental ADL (p = 0.03). The correlation
between age and mean number of comorbidities was
moderate (r = 0.31).
The proportions of stroke patients who scored 611
points on the HADS-depression and HADS-anxiety subscales were 19.2 and 23.7%, respectively. A GDS score 66
160
Table 3. Depression and cognition scores of stroke survivors according to disability and functional status
Disability (BI)
HADS-depression
HADS-anxiety
HADS total score
GDS
MMSE
BI 60
(n = 99)
BI 6590
(n = 103)
BI 95
(n = 98)
8.183.9
8.284.1
16.286.9
6.783.4
24.984.1
7.483.9
7.684.6
15.287.5
5.982.9
25.784.4
5.283.8
6.983.9
12.486.9
5.283.7
27.182.7
p
<0.0001
NS
0.0005
0.01
<0.0001
Rankin 1
(n = 59)
Rankin 2
(n = 81)
Rankin 3
(n = 69)
Rankin 4
(n = 91)
5.583.7
6.983.9
13.386.9
4.782.8
27.282.5
6.783.9
7.184.2
13.887.2
6.083.7
26.883.0
7.883.9
8.484.8
16.387.5
6.683.3
24.684.7
7.884.1
7.683.8
15.686.9
6.283.3
25.083.9
0.001
0.1
0.006
0.01
0.001
to Trial of ORG 10172 in Acute Stroke Treatment classification. The HADS-depression mean scores (7.4 and 8.5;
ANOVA, p = 0.04) were significantly increased in moderate (NIHSS score: 613) and severely impaired stroke patients (NIHSS score 614), compared to patients with
mild impairment (NIHSS ^5), who scored 6.5.
Education, measured as the number of years of formal education, inversely correlated with the HADS-depression subscale (r = 0.25; p ! 0.0001). Patients who
were living alone scored significantly lower (worse) on
the HADS-depression subscale (5.6 8 3.9 vs. 7.3 8 3.9;
p = 0.01) and in the HADS total score (12.3 8 6.9 vs.
15.0 8 7.1; p = 0.02). No significant differences were observed in the GDS mean scores (5.3 8 3.6 vs. 6.2 8 3.3).
Depressed patients scored significantly worse (lower) in
the social function domain of the SF-36 (35.5 8 23.7 vs.
54.7 8 27.6, p ! 0.0001). Depressive symptoms were
more common in housewives (HADS-depression mean
score: 9.1) compared to retired and active workers
(HADS-depression mean score: 6.8 and 6.3, respectively; ANOVA, p = 0.001). Housewives who were married
scored significantly worse on the HADS-depression as
compared to those who were single (8.5 8 4.1 vs. 6.4 8
4.1; p = 0.04).
The depression and cognition scores broken down by
disability and functional status are shown in table 3. Disability and dependence in instrumental ADL were associated with PSD. Depressed patients had significantly
lower BI (65.9 vs. 74.2; unpaired t test, p = 0.03) and Lawton scores (14.8 vs. 17.2; p = 0.0003). Patients independent
in the ADL scored 5.2 on the HADS-depression subscale,
whereas severely disabled patients (BI ^60) scored 8.1
(p ! 0.0001). The Lawton mean score significantly (p !
0.001) correlated with the GDS mean score (r = 0.51),
HADS-depression subscale (r = 0.34) and HADS-anxiety subscale (r = 0.18). The HADS-depression subscale
scores significantly increased (ANOVA; p = 0.001) across
the m-RS stages. The HADS-depression mean score
ranged from 5.5 (m-RS 1) to 7.8 (m-RS 4).
Depressed stroke patients also scored worse in the
MMSE (25.4 vs. 26.4; p ! 0.0001). A significant association between cognition and dependence in the ADL was
also detected. Cognitive function, as measured by the
MMSE, significantly decreased as disability (measured
by the BI and/or Lawton scales) and functional status
(m-RS) worsened (ANOVA, p ! 0.0001).
Low scores were also observed in the Mental Component Summary (50.1 8 11.2) and the emotional role domain of the SF-36 (37.9 8 44.1). The HADS-depression
subscale significantly correlated with most domains of
the SF-36: physical functioning (r = 0.28), role limitations due to physical problems (r = 0.22), bodily pain
(r = 0.25), general health perception (r = 0.44), vitality (r = 0.49), social functioning (r = 0.40), role limitations due to emotional problems (r = 0.38) and emotional well being (r = 0.57). Significant correlations
(p ! 0.0001) were also observed between GDS scores and
SF-36 domains and ranged from 0.29 (physical functioning) to 0.59 (mental health). The SF-36 Mental
Component Summary significantly correlated (p !
0.0001) with HADS-depression (r = 0.37), HADS-anxiety (r = 0.40), HADS total score (r = 0.44) and GDS
(r = 0.34).
Several models of multivariate regression analysis
were tested for HADS-depression subscale and GDS (table 4), due to the alternative introduction of disability
(BI vs. Lawton scale) and functional impairment (m-RS
vs. NIHSS) scales. Dependence in instrumental ADL
Poststroke Depression
161
Measure
HADS-depression
Diabetes
Housewife
SF-36 social
Education
Lawton scale
MMSE
GDS
SF-36 social
Lawton
Coefficient
Standard error
95% CI
R2 adjusted
0.32
1.76
1.80
0.05
0.11
0.16
0.21
0.54
0.71
0.01
0.05
0.07
0.06
0.001
0.01
<0.0001
0.01
0.02
0.002
2.800.69
2.711.12
0.06 to 0.03
0.20 to 0.02
0.29 to 0.02
0.33 to 0.08
0.05
0.19
0.01
0.61
<0.0001
0.002
0.06 to 0.03
0.31 to 0.07
0.23
and lower social functioning showed to have an independent effect in chronic stroke patients in both models.
In addition, PSD was significantly associated with
housewives, lower education level, decreased cognitive
functioning (as measured by the MMSE) and presence
of diabetes in the HADS-depression model (R adjusted = 0.32).
Discussion
Poststroke Depression
163
References
1 Hackett ML, Yapa C, Parag V, Anderson CS:
Frequency of depression after stroke: a systematic review of observational studies.
Stroke 2005; 36:13301340.
2 Berg A, Palomki H, Lehtihalmes M, Lnnqvist J, Kaste M: Poststroke depression: an
18-month follow-up. Stroke 2003; 34: 138
143.
3 Pohjasvaara T, Vataja R, Leppavuori A, Kaste
M, Erkinjuntti T: Depression is an independent predictor of poor long-term functional
outcome post-stroke. Eur J Neurol 2001; 8:
315319.
4 Carod-Artal J, Egido JA, Gonzlez JL, Varela
de Seijas E: Quality of life among stroke survivors evaluated 1 year after stroke: experience of a stroke unit. Stroke 2000; 31: 2995
3000.
5 Carota A, Berney A, Aybek S, Iaria G, Staub
F, Ghika-Schmid F, Annable L, Guex P, Bogousslavsky J: A prospective study of predictors of poststroke depression. Neurology
2005;64:428433.
6 Lai SM, Studenski S, Duncan P, Perera S: Persisting consequences of stroke measured by
the Stroke Impact Scale. Stroke 2002; 33:
18401844.
7 Edwards DF, Hahn G, Baum CM, Perlmutter
MS, Sheedy C, Dromerick AW: Screening patients with stroke for rehabilitation needs:
validation of the post-stroke rehabilitation
guidelines. Neurorehabil Neural Repair
2006;20:4248.
8 De Padua Mansur A, de Ftima Marinho do
Souza M, Favarato D, Avakian SD, Machado
Csar LA, Mendes Aldrigui J, Franchini
Ramires JA: Stroke and ischemic heart disease mortality trends in Brazil from 1979 to
1996. Neuroepidemiology 2003;22:179183.
9 Foulkes MA, Wolf PA, Price TR, Mohr JP,
Hier DB: The Stroke Data Bank: design,
methods, and baseline characteristics. Stroke
1988;19:547554.
10 Adams HP Jr, Bendixen BH, Kappelle LJ,
Biller J, Love BB, Gordon DL, Marsh EE 3rd:
Classification of subtype of acute ischemic
stroke: definitions for use in a multicenter
clinical trial. Stroke 1993; 24:3541.
11 Brott T, Adams HP Jr, Olinger CP, Marler JR,
Barsan WG, Biller J, Spilker J, Holleran J,
Eberle R, Hertzberg V: Measurements of
acute cerebral infarction: a clinical examination scale. Stroke 1989; 20:864870.
164
Carod-Artal/Ferreira Coral/Trizotto/
Menezes Moreira
Poststroke Depression
47 Joubert J, Joubert L, Reid C, Barton D, Cumming T, Mitchell P, House M, Heng R, Meadows G, Walterfang M, Pantelis C, Ames D,
Davis S: The positive effect of integrated care
on depressive symptoms in stroke survivors.
Cerebrovasc Dis 2008;26:199205.
48 Laska AC, Martensson B, Kahan T, von Arbin M, Murray V: Recognition of depression
in aphasic stroke patients. Cerebrovasc Dis
2007;24:7479.
49 Starkstein SE, Fedoroff JP, Price TR, Leiguarda R, Robinson RG: Apathy following
cerebrovascular lesions. Stroke 1993; 24:
16251630.
50 Quaranta D, Marra C, Gainotti G: Mood disorders after stroke: diagnostic validation of
the poststroke depression rating scale. Cerebrovasc Dis 2008;26:237243.
165
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