Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
Stroke. 1998;29:2311-2317

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Pohjasvaara, T.
Right arrow Articles by Erkinjuntti, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Pohjasvaara, T.
Right arrow Articles by Erkinjuntti, T.
Right arrowPubmed/NCBI databases
Medline Plus Health Information
*Depression

(Stroke. 1998;29:2311-2317.)
© 1998 American Heart Association, Inc.


Original Contributions

Frequency and Clinical Determinants of Poststroke Depression

Tarja Pohjasvaara, MD; Antero Leppävuori, MD, PhD; Irina Siira, MD; Risto Vataja, MD; Markku Kaste, MD, PhD; Timo Erkinjuntti, MD, PhD

From the Memory Research and Stroke Unit, Department of Clinical Neuroscience, Helsinki University Central Hospital (T.P., R.V., M.K., T.E.), and the Psychiatric Consultation Unit, Department of Psychiatry, University of Helsinki (A.L., I.S.), Helsinki, Finland.

Correspondence to Dr T. Pohjasvaara, Sirkkalanmäki 52 H 31, 00760 Helsinki, Finland. E-mail Antero.Leppavuori{at}huch.fi.


*    Abstract
up arrowTop
*Abstract
down arrowIntroduction
down arrowSubjects and Methods
down arrowResults
down arrowDiscussion
down arrowReferences
 
Background and Purpose—Previous studies have shown a large variation concerning the frequency of poststroke depression. This variation is caused by differences in patient populations, psychiatric assessment methods, and diagnostic criteria. In this study, we evaluated the frequency and clinical correlates of poststroke depression in a large well-defined stroke cohort.

Methods—We studied a consecutive series of 486 patients with ischemic stroke aged from 55 to 85 years. Of these, 277 patients underwent a comprehensive psychiatric evaluation, including the Present State Examination, from 3 to 4 months after ischemic stroke. The criteria of the Diagnostic and Statistical Manual of Mental Disorders, edition 3, revised (DSM-III-R), were used for the diagnosis of depressive disorders.

Results—The frequency of any depressive disorder was 40.1% (n=111). Major depression was diagnosed in 26.0% (n=72) and minor depression in 14.1% (n=39). Major depression with no other explanatory factor besides stroke was diagnosed in 18.0% (n=49) of the patients. Comparing depressed and nondepressed patients, we found no statistically significant difference in sex, age, education, stroke type, stroke localization, stroke syndrome, history of previous cerebrovascular disease, or frequency of DSM-III-R dementia. According to the multiple logistic regression model, dependency in daily life correlated with the diagnosis of depression (odds ratio [OR], 1.8; 95% confidence interval [CI], 1.1 to 3.1) and with the diagnosis of major depression (OR, 2.9; 95% CI, 1.6 to 5.5). A history of previous depressive episodes also correlated with the diagnosis of depression (OR, 2.3; 95% CI, 1.3 to 4.4) and with the diagnosis of major depression (OR, 2.9; 95% CI, 1.6 to 5.5), whereas solely stroke-related major depression correlated only weakly with stroke severity as measured on the Scandinavian Stroke Scale (OR, 1.1; 95% CI, 1.0 to 1.1).

Conclusions—Clinically significant depression is frequent after ischemic stroke. We emphasize the importance of the psychiatric examination of poststroke patients, especially those with a significant disability and with a history of prior depressive episodes.


Key Words: cerebral ischemia • depression • diagnosis • Finland


*    Introduction
up arrowTop
up arrowAbstract
*Introduction
down arrowSubjects and Methods
down arrowResults
down arrowDiscussion
down arrowReferences
 
The reported frequency of poststroke depression (PSD) in previous studies ranges from 20% to 65%.1 This wide variation in results is due to different criteria for patient selection; earlier studies are concerned with depression after ischemic stroke only or both ischemic and hemorrhagic stroke.2 3 The results also depend on the time elapsed after stroke,4 5 6 7 and difficulties in estimating depression in stroke patients with a cognitive or physical handicap also cause inaccuracies.1

PSD is commonly unrecognized and untreated in clinical practice.1 5 According to Schubert et al,8 nonpsychiatric physicians fail to diagnose 50% to 80% of the actually existing depression. PSD has been related to physical handicap and the limitations in activities of daily living (ADL).4 9 10 11 12 13 However, PSD is most likely not solely a psychological reflection of a physical disability. Folstein et al14 demonstrated that stroke patients were significantly more commonly depressed than orthopedic patients with equal levels of functional disability. It has been claimed that PSD is related to specific locations of ischemic brain lesions,1 4 5 9 although this has also been denied.1 15

The aim of the present study was to evaluate the frequency and clinical correlates of PSD in an large well-defined stroke cohort from 3 to 4 months after ischemic stroke. The investigation makes use of a more versatile methodology than most of the previous studies. We used the Schedules for Clinical Assessment in Neuropsychiatry (SCAN)16 system to assess psychopathological symptoms. The criteria of the Diagnostic and Statistical Manual of Mental Disorders, edition 3, revised (DSM-III-R)17 and International Classification of Diseases, 10th Revision (ICD-10)18 were used in diagnosing depressive disorders.


*    Subjects and Methods
up arrowTop
up arrowAbstract
up arrowIntroduction
*Subjects and Methods
down arrowResults
down arrowDiscussion
down arrowReferences
 
The details of procedures in the Helsinki Stroke Aging Memory (SAM) Study have been reported.19 20 A group of 486 consecutive patients aged from 55 to 85 years were evaluated 3 months after ischemic stroke. The evaluation of each patient was based on (1) their structured medical and neurological history based on a review of all available hospital charts, (2) an interview with the subject and a knowledgeable informant, (3) a structured clinical and neurological examination, and (4) a clinical mental status examination conducted by a board-certified neurologist (T.P.).19 20 The cases were also reviewed by a senior neurologist (T.E.). The neurological examination emphasizes the factors and features that are related to dementia and stroke. The procedure is similar to the method of the Memory Research Unit, Department of Neurology, University of Helsinki,21 and the National Stroke Data Bank (United States).22

The clinical neurological examination included the Mini-Mental State Examination (MMSE),23 the Beck Depression Scale,24 and the Barthel Index.25 The presence of aphasia was assessed clinically and by using the Acute Aphasia Screening Protocol (AASP).26

The history of main vascular risk factors was completed for each patient.19 20 Types of ischemic stroke were classified according to the TOAST criteria into the following categories: large-artery arteriosclerosis, cardioembolism, small-vessel occlusion (lacunar), and stroke of undetermined etiology.27 The localization of the stroke was divided into right hemispheric, left hemispheric, and bilateral, as well as into anterior (carotid), posterior (vertebrobasilar), and anteroposterior circulation.28 29 30 31 32 33 34 The stroke syndromes assessed included major dominant and nondominant hemispheric, minor dominant and nondominant hemispheric, deep/lacunar, brain stem and cerebellar, and unknown.22 Stroke severity was assessed using the Scandinavian Stroke Scale (SSS).35

We applied the clinical criteria for dementia as presented by the DSM-III-R.17 Education level of the patients was divided into 2 categories of low and high education corresponding to periods of 0 to 6 years and of >6 years of formal education, respectively.

Dependence was defined on the basis of available history from the patient and a knowledgeable informant and the stroke, handicap, and ADL scales used. Patients who required daily assistance, home-attendant help, or admission to a nursing home were judged to be dependent. Our definition is in accordance with the study by Tatemichi et al.36

Clinical neurological and mental status examinations were conducted for 451 patients.19 The excluded patients comprised 32 with severe aphasia, 1 with a reduced level of consciousness, 1 with severe hearing impairment, and 1 who refused participation. This group (n=35) showed a higher ratio of stroke located in the left hemisphere (33 versus 2, P<0.001) and of more severe stroke as measured on the SSS35 (31.3 versus 54.0, P<0.001), but this group did not differ from the others in terms of main demographic and clinical features including age, sex, educational level, and living condition (alone or with someone else).

Both MRI37 of the head and a comprehensive psychiatric examination were conducted for 277 (61.4%) of the 451 patients.

The excluded patients (n=174) comprised 59 patients for whom MRI was not performed (contraindication in 27, refusal in 18, claustrophobia in 2, severe illness in 11, obesity in 1), 85 patients for whom the possibility of psychiatric evaluation could not be offered during the first 3 months of the study, and 30 who refused examination.

The 174 patients who did not undergo psychiatric examination were compared with the 277 who did. No substantial differences were found in the following demographic or clinical factors: age, sex, education, living condition (alone or with someone else), first versus later stroke, side and site of stroke, mean MMSE23 and AASP26 values, mean Beck Depression Scale24 scores, or the frequency of patients with DSM-III-R dementia.17 However, the patients who were not examined were more often dependent in daily life (51.7% versus 35.0%, P=0.0002), were more severely physically handicapped as measured on the Barthel Index25 (mean±SD 16.6±5.3 versus 18.3±3.6, P<0.0001), and had more severe stroke measured on the SSS35 (50.2±11.5 versus 53.9±8.6, P<0.0001).

Most of the patients (221 of the sample of 277; 80%) were examined at the psychiatrist's own place of work; 29 patients were seen in the hospital, 21 in the patient's home, and 6 in nursing homes. The clinical psychiatric examinations were conducted using the SCAN protocol.16 The majority of patients (n=222) were examined by a senior psychiatrist (A.L.) who had attended a WHO-designated SCAN training course. The senior psychiatrist also afterward supervised the data entry concerning patients examined by the resident psychiatrist (I.S., n=55). The main content of SCAN is the 10th version of the Present State Examination (PSE-1038). The PSE-10 procedure covers a wide range of affective and other psychiatric symptoms, signs, and behavior; its earlier version (PSE-9) has been widely used in research concerning elderly and physically ill patients.

The data from interviews (lasting from 1 to 2 hours) was put directly into a portable computer. The Gatego-5 computer program of SCAN first computes a total symptom score and derives syndromes from combinations of the rated symptoms; it then computes a measure of the severity of any psychopathology present, and finally it constructs a prediagnosis profile for the ICD-1018 and DSM-III-R17 categories.

The severity of depression was assessed using the Montgomery-Åsberg Rating Scale (MÅDRS39). A cutoff point of 6 or higher was applied to distinguish the patients with a depressive symptomatology in the clinical range from those with less severe symptoms. The reliability and validity of this scale have been demonstrated compared with other observer-rated scales.40 It emphasizes the psychological symptoms of depression, reducing the risk that depression-mimicking somatic symptoms may be erroneously interpreted as depression.

The patients completed the 21-item Beck Depression Inventory (BDI), the 20-item Zung's Self-Rating Depression Scale (SDS41), the 20-item Zung's Self-Rating Anxiety Scale (SAS42), and the Derogatis' Symptom Check List (SCL-90-R43). Whenever possible, the close informants of subjects were interviewed briefly in conjunction with the psychiatric evaluation. A Neuropsychiatric Inventory (University of California at Los Angeles44) was completed, assessing the frequency and severity of 10 neuropsychiatric symptoms or signs.

The diagnoses of depressive disorders 3 to 4 months after stroke were made on the basis of the DSM-III-R17 and ICD-1018 diagnostic criteria. The DSM-III criteria have been shown to be appropriate for the identification of depressive disorders in several studies, even for patients with acute stroke.45 46 Patients with DSM-III-R major depressive disorder (single or recurrent episode), bipolar disorder (depressed episodes), organic mood disorder (organic depressive disorder), or dementia with depressed mood (DSM-IV) were grouped as having "major depression." Patients with adjustment disorder (depressed or mixed anxiety and depressed mood), dysthymic disorder, or major depressive disorder in partial remission were grouped as having "minor depression." The patients with "major depression" and no other recent psychosocial stress factor except stroke were defined as having pure "stroke-related major depression." The grouping of poststroke depressive disorders into major and minor depression subgroups has been used in most earlier studies.47 48 We used it here to compare our results with those of other studies.

The study was approved by the ethics committee of the Department of Neurology, University of Helsinki. It was first fully explained to the patients, and if they agreed to participate, a written consent form was signed.

We compared the patients who did have depressive disorders to those who did not. The {chi}2 test was applied for categorical data and the pooled t test for continuous data. All the variables that significantly differentiated the 2 groups were put into a logistic regression model to work out the independent correlates of depression. The statistics were analyzed using the BMDP and SAS programs.49 50


*    Results
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowSubjects and Methods
*Results
down arrowDiscussion
down arrowReferences
 
Some depressive disorder was diagnosed in 111 of 277 patients (40.1%) according to both DSM-III-R and ICD-10 criteria: DSM-III-R major depression in 72 (26.0%), minor depression in 39 (14.1%), and pure stroke-related major depression in 49 (17.7%) patients (FigureDown). The Beck self-rating questionnaire (completed by 260 patients) identified depression in 98 or 48 patients (37.7% or 18.5%) when the cutoff point for depression was defined as being >=10 or >=14, respectively.



View larger version (17K):
[in this window]
[in a new window]
 
Figure 1. The distribution of patients into various depression classes in the SAM study.

On the basis of DSM-III-R and ICD-10 definitions, major depression was diagnosed in 72 and 78 patients (26.0% and 28.2%), and minor depression in 39 and 33 patients (14.1% and 11.9%), respectively. All the patients who were diagnosed as having major depression according to the DSM-III-R definition also fulfilled the ICD-10 criteria.

There were 49 patients (17.7%) who fulfilled the DSM-III-R criteria for dementia. Of these 49 demented patients, 30.6% (15 versus 34, P=0.4164) had major depression according to DSM-III-R criteria, 36.7% (18 versus 31, P=0.5991) had some depression, and 10.2% (5 versus 44, P=0.08764) had stroke-related depression. Comparing the depressed and nondepressed patients, there was no statistically significant difference with regard to sex, age, education, stroke type, stroke localization, stroke syndrome, history of previous CVD, AASP, or MMSE according to any definition. The statistics of stroke type and localizations in patients with and without any depression (major or minor) are shown in Table 1Down. There were no significant differences in these stroke characteristics in patients either with or without major depression or stroke-related depression.


View this table:
[in this window]
[in a new window]
 
Table 1. Type and Localization of Stroke in Patients With and Without Depression (Major or Minor) in the Helsinki Stroke Aging Memory Study Cohort (n=277)

The patients with depression were more severely physically handicapped (Barthel Index), had more physically disabling stroke (SSS), and were more often dependent (Table 2Down). Patients with some depression (26.1% versus 13.9%, P=0.0104) and DSM-III-R major depression (29.2% versus 15.1%, P=0.0087) more frequently had a history of prestroke depression compared with the nondepressed patients (Table 2Down). On the other hand, the patients with stroke-related major depression less often had a history of prestroke depression compared with the rest of the patients (8.2% versus 21.2%, P=0.0351) (Table 2Down). Of the patients with PSD, 38.7% (43 of 111) had received antidepressant treatment.


View this table:
[in this window]
[in a new window]
 
Table 2. Characteristics of Patients With Ischemic Stroke Classified According to Different Definitions of Depression in the SAM Cohort (n=277)

The variables that significantly differentiated the patients with and without depression were put into to a multiple logistic regression model (Table 3Down). Depression was related to dependence (odds ratio [OR], 1.8; 95% confidence interval [CI], 1.1 to 3.1) and to a history of prestroke depression (OR, 2.3; 95% CI, 1.3 to 4.4). DSM-III-R major depression was also related to dependence (OR, 2.9; 95% CI, 1.6 to 5.5) and to prestroke depression history (OR, 3.4; 95% CI, 1.7 to 6.7). However stroke-related major depression correlated only with stroke disability as measured on the SSS (OR, 1.1; 95% CI, 1.0 to 1.1).


View this table:
[in this window]
[in a new window]
 
Table 3. Correlates of Depression 3 Months After Ischemic Stroke Using Multiple Logistic Models in the SAM Cohort


*    Discussion
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowSubjects and Methods
up arrowResults
*Discussion
down arrowReferences
 
Our objective was to achieve a more precise and versatile evaluation of PSD. We therefore used various psychometric rating scales, a standardized clinical psychiatric interview (PSE-10),38 and the DSM-III-R and ICD-10 diagnostic criteria.17 18

Clinically significant depression was found to be common 3 to 4 months after stroke, affecting 40% (111 of 277) of the patients according to the DSM-III-R criteria17 for depression. Major depression was found in 26% and minor depression in 14% of the patients. The total frequency of depressive disorders as defined by the ICD-10 criteria18 was the same, and the rate of major depression was slightly higher (28.2%) than the corresponding values based on the DSM-III-R criteria.17 In studies of nonstroke patients, it has been shown that the frequencies obtained for depressive and bipolar disorders do not differ substantially between DSM-III-R and ICD-10 systems.51

In the previous studies based on self-report inventories, depressive symptoms were found in 20% to 50% of patients, from weeks to 1 year after stroke.15 52 53 54 55 In a previous study in Finland, it was shown using a population-based register that the frequency of depressive patients at 3 months from stroke onset was 44% (BDI cutoff point, >=14).52 In a recent large unselected stroke population, the corresponding figure was almost 50% (BDI cutoff point, >=10).53

The corresponding BDI values in the present study were 19% and 38%. Our BDI figures are comparable with those of the study of House et al,56 who found the prevalence of depression at 6 months after stroke to be 15% when using a BDI cutoff point of >=13 and 32% when using a cutoff point of >=10 for depression.

In 1983 and 1984, Robinson et al57 58 found that the rate of depression during the first 6 months of follow-up varied from 40% to 60%. This study was conducted using selected in-hospital population and modified rating scales. Robinson et al45 46 subsequently showed that the DSM-III criteria could be used to diagnose poststroke major depression without significant overdiagnosis or underdiagnosis.

In later studies, depression defined using DSM-III criteria was found to vary from 30% to 50%, major depression from 13% to 31%, and minor depression from 20% to 40%.4 58 59 60 Morris et al61 analyzed a sample of 99 patients at 2 months after stroke and diagnosed 18% and 14% as having minor and major depression, respectively. Åström et al4 found that the frequency of major depression in a population-based cohort of 80 patients with stroke was 25% at the acute stage and 31% at 3 months after stroke. Burvill et al62 reported that in a community-based study 4 months after stroke, the prevalence of depressive illness was 23% (15% major depression and 8% minor depression).

The only previous study to use a methodology similar to ours has been that of House et al.56 They reported that using an earlier version of PSE and DSM-III, the prevalence of major depression was 9% at 6 months after stroke. This is much lower than the percentage in the present study. The inclusion of organic mood disorder (5 patients) and dementia with depressed mood (13 patients) in the major depression group might explain the relatively high prevalence of major depression in our findings. As in the present study, the patients with minor depression fulfilled the diagnostic criteria of adjustment disorder (depressed or mixed anxious and depressed).56 In most other studies, minor depression was defined as DSM-III dysthymic disorder, without the 2-year symptom duration criteria.

The fourth version of the DSM63 categorizes PSD as "the mood disorder due to general medical condition (ie, stroke)" with 1 of the following subtypes: (1) depressive features, (2) major depressive-like episode, and (3) mixed (depression, mania) features. This classification requires that mood disorder is the direct physiological consequence of a general medical condition. This means a new starting point in the future classification of PSD.

It has been reported earlier that patients having ischemic stroke in the left hemisphere are more depressive than those having it in the right hemisphere.5 9 This is a controversial argument, and many studies disagree.10 15 52 53 64 65 66 This study showed no significant correlation between depression and stroke localization. Åström et al4 found that a left-sided hemispheric lesion was the most important predictor of immediate depression. When the lesion was located in the left anterior hemisphere, the rate of major depression was 3 times higher compared with a left posterior lesion, and as much as 10 times higher compared with a lesion in the right hemisphere. However, after 3 months, these intrahemispheric and interhemispheric differences were no longer significant. The latter finding is consistent with the results of this study at 3 months after stroke.

There was no significant difference between depressed and nondepressed patients in stroke type and stroke syndrome, history of previous cerebrovascular disease, age, sex, education, living condition (alone or with someone else), aphasia estimated by AASP battery, MMSE, or frequency of DSM-III-R dementia. Younger age has been found to be associated with depression.57 Living alone has been associated with depression in some studies4 but not in others.5 65 Cognitive impairment has been found to be associated with major depression in patients with left hemispheric lesions.61 However, this was not the case in the present study.

The depressed patients were more dependent in ADL functions, as measured by the Barthel Index, and were more severely handicapped, as measured on the SSS. According to multiple logistic regression analysis, dependence correlated with all depression and with DSM-III-R major depression; the severity of stroke, as estimated on the SSS, was the only weak correlate of stroke-related major depression. It also has been shown previously that depressive patients need more help in ADL and are more often in institutional care.4 11 13 53

A history of previous depression was more common among depressed patients and correlated to any depression and to major DSM-III-R depression, according to the logistic regression analysis. A prestroke history of depression has been found to be significant in some studies67 but not in others.4

Numerous emotional and behavioral disorders occur after cerebrovascular lesions. Depression is the most common of these, affecting up to 40% of patients47 (in the present study, 40.1%). Among similarly aged individuals in the community, the prevalence of depression has been estimated to be 15% and that of major depression 0.1% to 3.7%.68 We therefore agree with earlier studies5 9 53 that irrespective of the diagnostic methods of ascertaining depression, it is clearly underdiagnosed in clinical practice.8 Furthermore, the rate of psychiatric consultation in the case of stroke patients has been low (6.3%).69

Only 39% of patients with any depression in the present study were using antidepressive drugs at the time of psychiatric examination. This is the same level (39%) as reported by Morris et al61; however, it is much more than found in an unselected Finnish stroke population, in which only 17% of depressive patients were receiving antidepressive treatment.53

In conclusion, depressive patients were more often dependent and more often had a prestroke history of depression. They could have been more disabled because of retarded rehabilitation.13 There seemed to be a high percentage (17.7%) of major depression after stroke, for which no other explanatory factor besides stroke could be found. Altogether, 62 patients (22.4%) had minor or major depression along with other explanatory factors, the most significant of which was prestroke depression. We emphasize the importance of a thorough psychiatric evaluation of poststroke patients, particularly those who have a severe disability and a history of previous depressive episodes.


*    Acknowledgments
 
This work was supported by grants from the Medical Council of the Academy of Finland, Helsinki; the Clinical Research Institute, Helsinki University Central Hospital, Helsinki; and the Finnish Alzheimer Foundation for Research, Helsinki. We thank senior research officer Vesa Kuusela, Statistics Finland, Helsinki, for the statistical support and review. We also thank Megan Burton, BA, for linguistic assistance with the manuscript.


*    Footnotes
 
Reprint requests to Dr A. Leppävuori, Psychiatric Consultation Unit, Department of Psychiatry, University of Helsinki, PL 321, 00029 HYKS, Finland.

Received July 10, 1998; revision received August 25, 1998; accepted August 25, 1998.


*    References
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowSubjects and Methods
up arrowResults
up arrowDiscussion
*References
 

  1. Primeau F. Post-stroke depression: a critical review of the literature. Can J Psychiatry. 1988;33:757–765.[Medline] [Order article via Infotrieve]
  2. Sacco RL, Wolf PA, Kannel WB, McNamara PM. Survival and recurrence following stroke: the Framingham study. Stroke. 1982;13:290–295.[Abstract]
  3. Cummings JL, Benson DF. Dementia: a Clinical Approach. Boston, Mass: Butterworth Publishers; 1983:125–143.
  4. Åström M, Adolfsson R, Asplund K. Major depression in stroke patients: a 3-year longitudinal study. Stroke. 1993;24:976–982.[Abstract/Free Full Text]
  5. Robinson R, Price T. Post-stroke depressive disorders: a follow-up study of 103 patients. Stroke. 1982;13:635–640.[Abstract]
  6. Hamilton M. A rating scale for depression. J Neurol Neurosurg Psychiatry. 1960;23:56–62.
  7. Wing JK, Cooper JE, Sartorius N. Measurements and Classification of Psychiatric Symptoms. Cambridge, UK: Cambridge University Press; 1974.
  8. Schubert DS, Burns R, Paras W, Sioson E. Increase of medical hospital length of stay by depression in stroke and amputation patients: a pilot study. Psychother Psychosom. 1992;57:61–66.[Medline] [Order article via Infotrieve]
  9. Robinson RG, Szetela B. Mood change following left hemisphere brain injury. Ann Neurol. 1981;9:447–453.[Medline] [Order article via Infotrieve]
  10. Sinyor D, Amato P, Kaloupek DG, Becker R, Goldenberg M, Coopersmith H. Post-stroke depression: relationships to functional impairment, coping strategies, and rehabilitation outcome. Stroke. 1986;17:1102–1107.[Abstract/Free Full Text]
  11. Parikh RM, Lipsey JR, Robinson RG, Price TR. Two-year longitudinal study of post-stroke mood disorders: dynamic changes in correlates of depression at one and two years. Stroke. 1987;18:579–584.[Abstract/Free Full Text]
  12. Sharpe M, Hawton K, Seagroatt V, Bamford J, House A, Molyneux A, Sandercock P, Warlow C. Depressive disorders in long-term survivors of stroke: associations with demographic and social factors, functional status and brain lesion volume. Br J Psychiatry. 1994;164:380–386.[Abstract/Free Full Text]
  13. Parikh RM, Robinson RG, Lipsey JR, Starkstein SE, Fedoroff JP, Price TR. The impact of poststroke depression on recovery in activities of daily living over a 2-year follow-up. Arch Neurol. 1990;47:785–789.[Abstract]
  14. Folstein MF, Maiberger R, McHugh PR. Mood disorder as a specific complication of stroke. J Neurol Neurosurg Psychiatry. 1977;40:1018–1020.[Abstract]
  15. Burvill PW, Johnson GA, Chakera TMH, Stewart-Wynne EG, Anderson CS, Jamrozik KD. The place of site of lesion in the aetiology of post-stroke depression. Cerebrovasc Dis. 1996;6:208–215.
  16. Wing JK, Babor T, Brugha T, Burke J, Cooper JE, Giel R, Jablenski A, Regier D, Sartorius N. SCAN: Schedules for Clinical Assessment in Neuropsychiatry. Arch Gen Psychiatry. 1990;47:589–593.[Abstract]
  17. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, Revised. 3rd ed. Washington, DC: American Psychiatric Association; 1987.
  18. International Classification of Diseases, 10th Revision. Classification of Mental, and Behavioral Disorders: Clinical Definitions and Diagnostic Guidelines. Geneva, Switzerland: World Health Organization; 1989:25–31.
  19. Pohjasvaara T, Erkinjuntti T, Vataja R, Kaste M. Dementia three months after stroke: baseline frequency and effect of different definitions for dementia in the Helsinki Aging Memory Study (SAM) stroke cohort. Stroke. 1997;28:785–792.[Abstract/Free Full Text]
  20. Pohjasvaara T, Erkinjuntti T, Vataja R, Kaste M. Comparison of stroke features and disability in daily life in patients with ischemic stroke aged 55 to 70 and 71 to 85 years. Stroke. 1997;28:729–735.[Abstract/Free Full Text]
  21. Erkinjuntti T, Sulkava R, Kovanen J, Palo J. Suspected dementia: evaluation of 323 consecutive referrals. Acta Neurol Scand. 1987;76:359–364.[Medline] [Order article via Infotrieve]
  22. Foulkes MA, Wolf PA, Price TR, Mohr JP, Hier DB. The Stroke Data Bank: design, methods, and baseline characteristics. Stroke. 1988;19:547–554.[Abstract/Free Full Text]
  23. Folstein MF, Folstein SE, McHugh PR. "Mini-mental state": a practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975;12:189–198.[Medline] [Order article via Infotrieve]
  24. Beck AT, Beck RW. Screening depressed patients in family practice. Postgrad Med. 1972;11:561–579.
  25. Mahoney FI, Barthel DW. Functional evaluation: the Barthel Index. Md State Med J. 1965;14:61–65.[Medline] [Order article via Infotrieve]
  26. Crary MA, Haak NJ, Malinsky AE. Preliminary psychometric evaluation of an acute aphasia screening protocol. Aphasiology. 1989;3:611–618.
  27. Adams HP, Bendixen BH, Kappelle LJ, Biller J, Love BB, Gordon DL, Marsh EE, for the TOAST Investigators. Classification of subtype of acute ischemic stroke: definitions for use in a multicenter clinical trial. Stroke. 1993;24:35–41.[Abstract/Free Full Text]
  28. World Health Organization. Stroke–1989. Recommendations on stroke prevention, diagnosis, and therapy: report of the WHO Task Force on Stroke and other Cerebrovascular Disorders. Stroke. 1989;20:1407–1431.[Free Full Text]
  29. Walker AE, Robins M, Weinfeld FD. Clinical findings: report on the National Survey of Stroke. Stroke. 1981;12(suppl I):I-32–I-35.
  30. Gent M, Blakely JA, Easton JD, Ellis DJ, Hachinski VC, Harbison JW, Panake E, Roberts RS, Tech M, Sicurella J, Turpier AG, for the CATS Group. The Canadian American Ticlopidine Study (CATS) in thromboembolic stroke: design, organization, and baseline results. Stroke. 1988;19:1203–1210.[Abstract/Free Full Text]
  31. National Institute of Neurological Disorders and Stroke. Special report from the National Institute of Neurological Disorders and Stroke: classification of cerebrovascular diseases III. Stroke. 1990;21:637–676.[Free Full Text]
  32. Bamford J, Sandercock P, Dennis M, Burn J, Warlow C. Classification and natural history of clinically identifiable subtypes of cerebral infarction. Lancet. 1991;337:1521–1526.[Medline] [Order article via Infotrieve]
  33. North American Symptomatic Carotid Endarterectomy Trial (NASCET) Steering Committee. North American Symptomatic Carotid Endarterectomy Trial: methods, patient characteristics, and progress. Stroke. 1991;22:711–720.[Abstract/Free Full Text]
  34. Caplan LR. Stroke: A Clinical Approach. 2nd ed. Boston, Mass: Butterworth-Heinemann; 1993.
  35. Scandinavian Stroke Study Group. Multicenter trial of hemodilution in ischemic stroke: background and study protocol. Stroke. 1985;16:885–890.[Free Full Text]
  36. Tatemichi TK, Desmond DW, Stern Y, Paik M, Sano M, Bagiella E. Cognitive impairment after stroke: frequency, patterns and relationship to functional abilities. J Neurol Neurosurg Psychiatry. 1994;57:202–207.[Abstract]
  37. Mäntylä R, Erkinjuntti T, Salonen O, Aronen HJ, Peltonen T, Pohjasvaara T, Standerstskjöld-Nordenstam C-G. Variable agreement between visual rating scales for white matter hyperintensities on MRI: comparison of 13 rating scales in a poststroke cohort. Stroke. 1997;28:1614–1623.[Abstract/Free Full Text]
  38. Wing JK, Cooper JE, Sartorius N. Measurement and Classification of Psychiatric Symptoms: Instruction Manual for the PSE. London, UK: Cambridge University Press; 1974.
  39. Montgomery SA, Åsberg M. A new depression scale designed to be sensitive to change. Br J Psychiatry. 1979;134:382–389.[Abstract/Free Full Text]
  40. Korrer A, Nielsen BM, Escher F, Mobler-Madsen S, Sfendert A, Christensen EM, Aggernaes H, Kastrup M, Larsen JK. Quantifying depressive symptomatology: inter-rater reliability and inter-item correlations. J Affect Disord. 1990;20:143–149.[Medline] [Order article via Infotrieve]
  41. Zung WWK. A self-rating scale for depression. Arch Gen Psychiatry. 1965;12:63–70.
  42. Zung WWK. A rating instrument for anxiety disorders. Psychosomatics. 1971;12:271–279.
  43. Parloff MB, Kelman HC, Frank JD. Comfort, effectiveness and self-awareness as criteria of improvement in psychotherapy. Am J Psychiatry. 1954;111:343–351.[Abstract/Free Full Text]
  44. Cummings JL, Mega M, Gracy K, Rosenberg-Thompson S, Carzusi DA, Gorrbein J. The Neuropsychiatric Inventory: comprehensive assessment of psychopathology in dementia. Neurology. 1994;44:2308–2314.[Abstract/Free Full Text]
  45. Lipsey JR, Spencer WC, Robins PV, Robinson RG. Phenomenological comparison of poststroke depression and functional depression. Am J Psychiatry. 1986;143:527–529.[Abstract/Free Full Text]
  46. Fedoroff JP, Starkstein SE, Parikh RM, Price TR, Robinson RG. Are depressive symptoms nonspecific in patients with acute stroke. Am J Psychiatry. 1991;148:1172–1176.[Abstract/Free Full Text]
  47. Robinson RG. Neuropsychiatric consequences of stroke. Annu Rev Med. 1997;48:217–229.[Medline] [Order article via Infotrieve]
  48. Starkstein SE, Robinson RG. Affective disorders and cerebral vascular disease. Br J Psychiatry. 1989;154:170–182.[Abstract/Free Full Text]
  49. BMDP. New System for Windows. Los Angeles, Calif: BMDP; 1994.
  50. SAS Inc. SAS Procedures Guide, Version 6. 3rd ed. Gary, NC: SAS Institute Inc; 1990.
  51. Hiller W, Dichtl G, Hecht H, Hundt W, von Zerssen D. An empirical comparison of diagnoses and reliabilities in ICD-10 and DSM-III-R. Eur Arch Psychiatry Clin Neurosci. 1993;242:209–217.[Medline] [Order article via Infotrieve]
  52. Kotila M, Waltimo O, Niemi ML, Laaksonen R, Lempinen M. The profile of recovery from stroke and factors influencing outcome. Stroke. 1984;15:1039–1044.[Abstract/Free Full Text]
  53. Kotila M, Numminen H, Waltimo O, Kaste M. Depression after stroke: results of the FINNSTROKE study. Stroke. 1998;29:368–372.[Abstract/Free Full Text]
  54. Ebrahim S, Barer D, Nouri F. Affective illness after stroke. Br J Psychiatry. 1987;151:52–56.[Abstract/Free Full Text]
  55. Wade DT, Smith LJ, Hewer RA. Depressed mood after stroke: a community study of its frequency. Br J Psychiatry. 1987;151:200–205.[Abstract/Free Full Text]
  56. House A, Dennis M, Mogridge L, Warlow C, Hawton K, Jones L. Mood disorders in the year after first stroke. Br J Psychiatry. 1991;158:83–92.[Abstract/Free Full Text]
  57. Robinson RG, Starr LB, Kubos KL, Price TR. A Two-year longitudinal study of post-stroke mood disorders: findings during the initial evaluation. Stroke. 1983;14:736–741.[Abstract]
  58. Robinson RG, Starr LB, Lipsey JR, Rao K, Price TR. A two-year longitudinal study of post-stroke mood disorders: dynamic changes in associated variables over the first six months of follow-up. Stroke. 1984;15:510–517.[Abstract/Free Full Text]
  59. Eastwood MR, Rifat SL, Nobbs H, Ruderman J. Mood disorder following cerebrovascular accident. Br J Psychiatry. 1989;154:195–200.[Abstract/Free Full Text]
  60. Dam H, Pedersen HE, Ahlgren P. Depression among patients with stroke. Acta Psychiatry Scand. 1989;80:118–124.[Medline] [Order article via Infotrieve]
  61. Morris PLP, Robinson RG. Prevalence and course of depressive disorders in hospitalized stroke patients. Int J Psychiatry Med. 1990;20:349–364.[Medline] [Order article via Infotrieve]
  62. Burvill PW, Johnson GA, Jamrozik KD, Anderson CS, Stewart-Wynne EG, Chakera TM. Prevalence of depression after stroke: the Perth Community Stroke Study. Br J Psychiatry. 1995;166:320–327.[Abstract/Free Full Text]
  63. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV). Washington, DC: American Psychiatric Association; 1994.
  64. House A, Dennis M, Warlow C, Hawton K, Jones L. Mood disorders after stroke and their relation to lesion location: a CT scan study. Brain. 1990;113:1113–1129.[Abstract/Free Full Text]
  65. Feibel JH, Springer CJ. Depression and failure to resume social activities after stroke. Arch Phys Med Rehabil. 1982;63:276–278.[Medline] [Order article via Infotrieve]
  66. Collin SJ, Tinson D, Lincoln NB. Depression after stroke. Clin Rehabil. 1987;1:27–31.
  67. Andersen G, Vestergaard K, Ingemann-Nielsen M, Lauritzen L. Risk factors for post-stroke depression. Acta Psychiatry Scand. 1995;92:193–198.[Medline] [Order article via Infotrieve]
  68. Fujikawa T, Yamawaki S, Touhouda Y. Incidence of silent cerebral infarction in patients with major depression. Stroke. 1993;24:1631–1634.[Abstract/Free Full Text]
  69. Rosse RB, Ciolino CP. Effects of cortical lesion location on psychiatric consultation referral for depressed stroke inpatients. Int J Psychiatry Med. 1985;15:311–320.[Medline] [Order article via Infotrieve]



This article has been cited by other articles:


Home page
J. Neuropsychiatry Clin. Neurosi.Home page
R. G. Robinson, R. E. Jorge, and K. Clarence-Smith
Double-Blind Randomized Treatment of Poststroke Depression Using Nefiracetam
J Neuropsychiatry Clin Neurosci, May 1, 2008; 20(2): 178 - 184.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
S. A. Thomas and N. B. Lincoln
Predictors of Emotional Distress After Stroke
Stroke, April 1, 2008; 39(4): 1240 - 1245.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
E. Townend, M. Brady, and K. McLaughlan
A Systematic Evaluation of the Adaptation of Depression Diagnostic Methods for Stroke Survivors Who Have Aphasia
Stroke, November 1, 2007; 38(11): 3076 - 3083.
[Abstract] [Full Text] [PDF]


Home page
Clin RehabilHome page
T. K. Tihanyi, M. Horvath, G. Fazekas, T. Hortobagyi, and J. Tihanyi
One session of whole body vibration increases voluntary muscle strength transiently in patients with stroke
Clinical Rehabilitation, September 1, 2007; 21(9): 782 - 793.
[Abstract] [PDF]


Home page
AJGPHome page
H. Brodaty, A. Withall, A. Altendorf, and P. S. Sachdev
Rates of Depression at 3 and 15 Months Poststroke and Their Relationship With Cognitive Decline: the Sydney Stroke Study
Am J Geriatr Psychiatry, June 1, 2007; 15(6): 477 - 486.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
T. Linden, C. Blomstrand, and I. Skoog
Depressive Disorders After 20 Months in Elderly Stroke Patients: A Case-Control Study
Stroke, June 1, 2007; 38(6): 1860 - 1863.
[Abstract] [Full Text] [PDF]


Home page
RadiologyHome page
W. Mlekusch, I. Mlekusch, E. Minar, M. Haumer, C. W. Kopp, R. Ahmadi, J. Lehrner, and M. Schillinger
Is There Improvement of "Vascular Depression" after Carotid Artery Stent Placement?
Radiology, August 1, 2006; 240(2): 508 - 514.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
H. Naess, U. Waje-Andreassen, L. Thomassen, H. Nyland, and K.-M. Myhr
Health-Related Quality of Life Among Young Adults With Ischemic Stroke on Long-Term Follow-Up
Stroke, May 1, 2006; 37(5): 1232 - 1236.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
I. G.L. van de Port, G. Kwakkel, I. van Wijk, and E. Lindeman
Susceptibility to Deterioration of Mobility Long-Term After Stroke: A Prospective Cohort Study
Stroke, January 1, 2006; 37(1): 167 - 171.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
M. L. Hackett and C. S. Anderson
Predictors of Depression after Stroke: A Systematic Review of Observational Studies
Stroke, October 1, 2005; 36(10): 2296 - 2301.
[Abstract] [Full Text] [PDF]


Home page
Arch Intern MedHome page
D. Polsky, J. A. Doshi, S. Marcus, D. Oslin, A. Rothbard, N. Thomas, and C. L. Thompson
Long-term Risk for Depressive Symptoms After a Medical Diagnosis
Arch Intern Med, June 13, 2005; 165(11): 1260 - 1266.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
M. L. Hackett, C. Yapa, V. Parag, and C. S. Anderson
Frequency of Depression After Stroke: A Systematic Review of Observational Studies
Stroke, June 1, 2005; 36(6): 1330 - 1340.
[Abstract] [Full Text] [PDF]


Home page
J Geriatr Psychiatry NeurolHome page
W. K. Tang, S. S. M. Chan, H. F. K. Chiu, G. S. Ungvari, K. S. Wong, T. C. Y. Kwok, V. Mok, K. T. Wong, P. S. Richards, and A. T. Ahuja
Poststroke Depression in Chinese Patients: Frequency, Psychosocial, Clinical, and Radiological Determinants
J Geriatr Psychiatry Neurol, March 1, 2005; 18(1): 45 - 51.
[Abstract] [PDF]


Home page
NeurologyHome page
A. Carota, A. Berney, S. Aybek, G. Iaria, F. Staub, F. Ghika-Schmid, L. Annable, P. Guex, and J. Bogousslavsky
A prospective study of predictors of poststroke depression
Neurology, February 8, 2005; 64(3): 428 - 433.
[Abstract] [Full Text] [PDF]


Home page
AJGPHome page
R. Vataja, T. Pohjasvaara, R. Mantyla, R. Ylikoski, M. Leskela, H. Kalska, M. Hietanen, H. Juhani Aronen, O. Salonen, M. Kaste, et al.
Depression-Executive Dysfunction Syndrome in Stroke Patients
Am J Geriatr Psychiatry, February 1, 2005; 13(2): 99 - 107.
[Abstract] [Full Text] [PDF]


Home page
J. Neuropsychiatry Clin. Neurosi.Home page
R. Vataja, A. Leppavuori, T. Pohjasvaara, R. Mantyla, H. J. Aronen, O. Salonen, M. Kaste, and T. Erkinjuntti
Poststroke Depression and Lesion Location Revisited
J Neuropsychiatry Clin Neurosci, May 1, 2004; 16(2): 156 - 162.
[Abstract] [Full Text] [PDF]


Home page
AJGPHome page
J. Cervilla, M. Prince, S. Joels, C. Russ, and S. Lovestone
Genes Related to Vascular Disease (APOE, VLDL-R, DCP-1) and Other Vascular Factors in Late-Life Depression
Am J Geriatr Psychiatry, April 1, 2004; 12(2): 202 - 210.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
A. Verdelho, H. Henon, F. Lebert, F. Pasquier, and D. Leys
Depressive symptoms after stroke and relationship with dementia: A three-year follow-up study
Neurology, March 23, 2004; 62(6): 905 - 911.
[Abstract] [Full Text] [PDF]