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Post-stroke depression

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clinical evaluation and often requires the use of validated screening tools. One commonly used tool is the Beck Depression Inventory (BDI), which is a self-report questionnaire that assesses the severity of depression symptoms. The BDI is a reliable and valid tool for assessing depression in stroke patients. In addition to the BDI, the Hamilton Depression Rating Scale (HAM-D) is also commonly used to assess depression severity. Clinical evaluation for PSD typically includes a thorough medical history and physical examination to rule out other medical conditions that may be contributing to the patient's symptoms. It is important to consider that some symptoms of depression, such as fatigue, may overlap with other post-stroke complications, such as post-stroke fatigue. Neuroimaging studies, such as magnetic resonance imaging (MRI) or computed tomography (CT) scans, may also be used to evaluate the extent and location of brain damage caused by the stroke, which can help to understand the patient's clinical presentation and inform treatment decisions.
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Prevalence clearly varies over time with an apparent peak 3–6 months after stroke and subsequent decline in prevalence at one-year reaches about to 50% of initial rates. Robinson and colleagues characterized the natural course of major depression after stroke with spontaneous remission typically 1 to
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When diagnosing depression, doctors usually look for the presence of five or more symptoms that have persisted for at least two weeks. Post-stroke depression (PSD) is a common and debilitating complication of stroke, affecting up to one-third of stroke survivors. The diagnosis of PSD is based on
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Women were twice as likely to experience post-stroke depression than men. It is hypothesized, based on CT scanning, that of the two sexes experiencing post-stroke depression, women who had post-stroke depression had a higher rate of left hemisphere lesions than men. However, risk of post-stroke
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However, this model is far from being universally accepted and there are serious objections both to their model and findings showing the association between post-stroke depression and lesion sites. Depression-like behaviors are demonstrated in a mouse model of cortical intracerebral hemorrhage.
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The scientific community is divided into two “camps” supporting opposing views: some propose a primary biological mechanism with stroke affecting neural circuits involved in mood regulation which in turn causes post-stroke depression, while other researchers claim that post stroke depression is
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2 years after stroke. However, it was also noted that in few cases depression becomes chronic and may persist more than 3 years following stroke. On the other hand, minor depression appeared to be more variable, with both short term and long term depression occurring in these patients.
358:(ADL's), as a result of their stroke; the greater the limitation, the greater the severity. Risk of developing depression post-stroke in women is partly linked to a history of psychological disorders as well as limitations involving cognition as a result of their stroke. 150:
Despite this evidence, the association of post-stroke depression to specific brain lesions is still vague and needs replication from various independent groups. Furthermore, the cause of post stroke depression at a functional level is not clear.
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Miller, Jeffrey M.; Vorel, Stanislav R.; Tranguch, Anthony J.; Kenny, Edward T.; Mazzoni, Pietro; van Gorp, Wilfred G.; Kleber, Herbert D. (May 2006). "Anhedonia After a Selective Bilateral Lesion of the Globus Pallidus".
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Poynter, Brittany; Shuman, Mira; Diaz-Granados, Natalia; Kapral, Moira; Grace, Sherry L.; Stewart, Donna E. (November 2009). "Sex differences in the prevalence of post-stroke depression: A systematic review".
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It has also been postulated that the risk of developing post-stroke depression in male patients is partly linked to having a high level of limitations and disability in functioning, especially in performing
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Carson, Alan J.; MacHale, Siobhan; Allen, Kathryn; Lawrie, Stephen M.; Dennis, Martin; House, Allan; Sharpe, Michael (8 July 2000). "Depression after stroke and lesion location: a systematic review".
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Post-stroke depression is highly prevalent among both men and women. However, it appears that post-stroke depression is more common in women when prevalence is compared between the sexes.
308:(DSM) IV categorizes post-stroke depression as “mood disorder due to a general medical condition” (i.e. stroke) with the specifiers of depressive features, major depressive-like episodes, 113:
aspects of post stroke depression seems warranted, a number of studies clearly suggest that biological mechanisms play a major role in the development of post stroke depression.
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features, or mixed features. Utilizing patient data from acute hospital admission, community surveys, or out patient clinics previous studies have identified two types of
177:, where they arborize and send terminal projections into the superficial cortical layers. These norepinephrinergic and serotoninergic pathways are disrupted in 332:
or loss of interest and at least two but fewer than four symptoms of major depression. Minor depression occurs in up to 30% of patients following stroke.
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Gainotti, G; Azzoni, A; Marra, C (August 1999). "Frequency, phenomenology and anatomical-clinical correlates of major post-stroke depression".
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depression can not be determined effectively based on the location of the lesion in the brain and more research in this area is needed.
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Some studies reported an association between post-stroke mania and right orbital frontal, basotemporal, basal ganglia lesions.
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Gainotti, Guido; Marra, Camillo (February 2002). "Determinants and consequences of post stroke depression".
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The only biological model was proposed by Robinson and co-workers: They hypothesized that the depletion of
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Robinson, RG; Starksein, SE (Winter 1990). "Current research in affective disorders following stroke".
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Paradiso, Sergio; Robinson, Robert G. (Winter 1998). "Gender Differences in Poststroke Depression".
271: 30: 783: 231: 188:– sites that are shown to be associated with post stroke depression. Additionally, depletion in 410:
Zhu, Wei; Gao, Yufeng; Chang, Che-Feng; Wan, Jie-Ru; Zhu, Shan-Shan; Wang, Jian (15 May 2014).
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Robinson, Robert G.; Starr, Lyn Book; Kubos, Kenneth L.; Price, Thomas R. (September 1983).
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occurring after stroke play a role in post stroke-depression. They point out that
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caused by social and psychological stressors that emerge as a result of stroke.
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who are unaware of their disability still develop post stroke depression.
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https://itshealthilyeverafter.com/wp-admin/post.php?post=860&action
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Diagnostic and Statistical Manual of Mental Disorders: DSM-IV
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stroke patients show a higher rate of depression compared to
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and arc posteriorly, running through the deep layers of the
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Several studies proposed an association with specific
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Journal of Neuropsychiatry and Clinical Neurosciences
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Journal of Neuropsychiatry and Clinical Neurosciences
629: 121:patients with disabilities of comparable severity. 703: 770: 547: 409: 666: 324:, which occurs in up to 25% of patients; and 473:. Washington DC: American Psychiatric Press. 236:introducing citations to additional sources 136:) and occurrence of post stroke depression. 750: 519: 469:American Psychiatric Association (1994). 445: 435: 66:Learn how and when to remove this message 226:Relevant discussion may be found on the 29:This article includes a list of general 771: 543: 541: 539: 462: 142:It has been shown that patients with 203: 93:, functional recovery and survival. 15: 536: 13: 35:it lacks sufficient corresponding 14: 800: 306:Diagnostic and Statistical Manual 681:10.1097/00019052-200202000-00013 219:relies largely or entirely on a 208: 20: 169:nuclei send projections to the 576: 490: 477: 403: 377:American Journal of Psychiatry 367: 109:including both biological and 1: 632:British Journal of Psychiatry 597:10.1016/S0140-6736(00)02448-X 361: 337: 299: 132:lesions and lesions close to 669:Current Opinion in Neurology 437:10.1371/journal.pone.0097423 199: 96: 7: 10: 805: 622: 389:10.1176/ajp.2006.163.5.786 356:activities of daily living 779:Major depressive disorder 512:10.1176/appi.psy.50.6.563 316:associated with cerebral 247:"Post-stroke depression" 789:Complications of stroke 752:10.1161/01.str.14.5.736 107:bio-psycho-social model 50:more precise citations. 79:Post-stroke depression 644:10.1192/bjp.175.2.163 314:depressive disorders 232:improve this article 105:While an integrated 562:10.1176/jnp.10.1.41 428:2014PLoSO...997423Z 128:(left anterior and 163:norepinephrinergic 91:cognitive function 718:10.1176/jnp.2.1.1 591:(9224): 122–126. 297: 296: 282: 76: 75: 68: 796: 764: 754: 729: 700: 663: 617: 616: 580: 574: 573: 545: 534: 533: 523: 494: 488: 481: 475: 474: 466: 460: 459: 449: 439: 407: 401: 400: 371: 326:minor depression 322:major depression 292: 289: 283: 281: 240: 212: 204: 87:major depression 71: 64: 60: 57: 51: 46:this article by 37:inline citations 24: 23: 16: 804: 803: 799: 798: 797: 795: 794: 793: 769: 768: 767: 625: 620: 581: 577: 546: 537: 495: 491: 482: 478: 467: 463: 408: 404: 372: 368: 364: 340: 302: 293: 287: 284: 241: 239: 225: 213: 202: 99: 72: 61: 55: 52: 42:Please help to 41: 25: 21: 12: 11: 5: 802: 792: 791: 786: 784:Mood disorders 781: 766: 765: 745:(5): 736–744. 730: 701: 664: 638:(2): 163–167. 626: 624: 621: 619: 618: 575: 535: 506:(6): 563–569. 500:Psychosomatics 489: 476: 461: 402: 383:(5): 786–788. 365: 363: 360: 339: 336: 330:depressed mood 301: 298: 295: 294: 230:. Please help 216: 214: 207: 201: 198: 171:frontal cortex 148: 147: 140: 137: 122: 98: 95: 74: 73: 28: 26: 19: 9: 6: 4: 3: 2: 801: 790: 787: 785: 782: 780: 777: 776: 774: 762: 758: 753: 748: 744: 740: 736: 731: 727: 723: 719: 715: 711: 707: 702: 698: 694: 690: 686: 682: 678: 674: 670: 665: 661: 657: 653: 649: 645: 641: 637: 633: 628: 627: 614: 610: 606: 602: 598: 594: 590: 586: 579: 571: 567: 563: 559: 555: 551: 544: 542: 540: 531: 527: 522: 517: 513: 509: 505: 501: 493: 487: 480: 472: 465: 457: 453: 448: 443: 438: 433: 429: 425: 422:(5): e97423. 421: 417: 413: 406: 398: 394: 390: 386: 382: 378: 370: 366: 359: 357: 351: 347: 344: 335: 333: 331: 327: 323: 319: 315: 311: 307: 291: 280: 277: 273: 270: 266: 263: 259: 256: 252: 249: â€“  248: 244: 243:Find sources: 237: 233: 229: 223: 222: 221:single source 217:This section 215: 211: 206: 205: 197: 193: 191: 187: 184: 180: 179:basal ganglia 176: 172: 168: 164: 160: 157: 156:monoaminergic 152: 145: 141: 138: 135: 131: 130:basal ganglia 127: 123: 120: 116: 115: 114: 112: 108: 103: 94: 92: 88: 84: 80: 70: 67: 59: 49: 45: 39: 38: 32: 27: 18: 17: 742: 738: 709: 705: 675:(1): 85–89. 672: 668: 635: 631: 588: 584: 578: 556:(1): 41–47. 553: 549: 503: 499: 492: 479: 470: 464: 419: 415: 405: 380: 376: 369: 352: 348: 345: 341: 334: 303: 285: 275: 268: 261: 254: 242: 218: 194: 183:frontal lobe 167:serotonergic 153: 149: 134:frontal pole 111:psychosocial 104: 100: 78: 77: 62: 53: 34: 712:(1): 1–14. 521:10315/24309 144:anosognosia 48:introducing 773:Categories 585:The Lancet 362:References 338:Prevalence 300:Definition 258:newspapers 119:orthopedic 31:references 288:June 2020 228:talk page 200:Diagnosis 97:Mechanism 56:June 2020 697:15314498 689:11796955 652:10627800 613:24968663 605:10963248 530:19996226 456:24831292 416:PLOS ONE 397:16648316 318:ischemia 190:dopamine 761:6658957 726:2136055 660:9931981 623:Sources 570:9547465 447:4022524 424:Bibcode 272:scholar 186:lesions 126:lesions 44:improve 759:  739:Stroke 724:  695:  687:  658:  650:  611:  603:  568:  528:  454:  444:  395:  274:  267:  260:  253:  245:  175:cortex 159:amines 83:stroke 33:, but 693:S2CID 656:S2CID 609:S2CID 310:manic 279:JSTOR 265:books 757:PMID 722:PMID 685:PMID 648:PMID 601:PMID 566:PMID 526:PMID 452:PMID 393:PMID 304:The 251:news 181:and 165:and 747:doi 714:doi 677:doi 640:doi 636:175 593:doi 589:356 558:doi 516:hdl 508:doi 442:PMC 432:doi 385:doi 381:163 234:by 775:: 755:. 743:14 741:. 737:. 720:. 708:. 691:. 683:. 673:15 671:. 654:. 646:. 634:. 607:. 599:. 587:. 564:. 554:10 552:. 538:^ 524:. 514:. 504:50 502:. 450:. 440:. 430:. 418:. 414:. 391:. 379:. 320:: 763:. 749:: 728:. 716:: 710:2 699:. 679:: 662:. 642:: 615:. 595:: 572:. 560:: 532:. 518:: 510:: 458:. 434:: 426:: 420:9 399:. 387:: 290:) 286:( 276:· 269:· 262:· 255:· 238:. 224:. 69:) 63:( 58:) 54:( 40:.

Index

references
inline citations
improve
introducing
Learn how and when to remove this message
stroke
major depression
cognitive function
bio-psycho-social model
psychosocial
orthopedic
lesions
basal ganglia
frontal pole
anosognosia
monoaminergic
amines
norepinephrinergic
serotonergic
frontal cortex
cortex
basal ganglia
frontal lobe
lesions
dopamine

single source
talk page
improve this article
introducing citations to additional sources

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