Collateral Vessels on CT Angiography Predict Outcome in Acute Ischemic Stroke
Background and Purpose— Despite the abundance of emerging multimodal imaging techniques in the field of stroke, there is a paucity of data demonstrating a strong correlation between imaging findings and clinical outcome. This study explored how proximal arterial occlusions alter flow in collateral v...
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Published in | Stroke (1970) Vol. 40; no. 9; pp. 3001 - 3005 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hagerstown, MD
Lippincott Williams & Wilkins
01.09.2009
|
Subjects | |
Online Access | Get full text |
ISSN | 0039-2499 1524-4628 1524-4628 |
DOI | 10.1161/STROKEAHA.109.552513 |
Cover
Abstract | Background and Purpose—
Despite the abundance of emerging multimodal imaging techniques in the field of stroke, there is a paucity of data demonstrating a strong correlation between imaging findings and clinical outcome. This study explored how proximal arterial occlusions alter flow in collateral vessels and whether occlusion or extent of collaterals correlates with prehospital symptoms of fluctuation and worsening since onset or predict in-hospital worsening.
Methods—
Among 741 patients enrolled in a prospective cohort study involving CT angiographic imaging in acute stroke, 134 cases with proximal middle cerebral artery occlusion and 235 control subjects with no occlusions were identified. CT angiography was used to identify occlusions and grade the extent of collateral vessels in the sylvian fissure and leptomeningeal convexity. History of symptom fluctuation or progressive worsening was obtained on admission.
Results—
Prehospital symptoms were unrelated to occlusion or collateral status. In cases, 37.5% imaged within 1 hour were found to have diminished collaterals versus 12.1% imaged at 12 to 24 hours (
P
=0.047). No difference in worsening was seen between cases and control subjects with adequate collaterals, but cases with diminished sylvian and leptomeningeal collaterals experienced greater risk of worsening compared with control subjects measured either by admission to discharge National Institutes of Health Stroke Scale increase ≥1 (55.6% versus 16.6%,
P
=0.001) or ≥4 (44.4% versus 6.4%,
P
<0.001).
Conclusion—
Most patients with proximal middle cerebral artery occlusion rapidly recruit sufficient collaterals and follow a clinical course similar to patients with no occlusions, but a subset with diminished collaterals is at high risk for worsening. |
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AbstractList | Despite the abundance of emerging multimodal imaging techniques in the field of stroke, there is a paucity of data demonstrating a strong correlation between imaging findings and clinical outcome. This study explored how proximal arterial occlusions alter flow in collateral vessels and whether occlusion or extent of collaterals correlates with prehospital symptoms of fluctuation and worsening since onset or predict in-hospital worsening.
Among 741 patients enrolled in a prospective cohort study involving CT angiographic imaging in acute stroke, 134 cases with proximal middle cerebral artery occlusion and 235 control subjects with no occlusions were identified. CT angiography was used to identify occlusions and grade the extent of collateral vessels in the sylvian fissure and leptomeningeal convexity. History of symptom fluctuation or progressive worsening was obtained on admission.
Prehospital symptoms were unrelated to occlusion or collateral status. In cases, 37.5% imaged within 1 hour were found to have diminished collaterals versus 12.1% imaged at 12 to 24 hours (P=0.047). No difference in worsening was seen between cases and control subjects with adequate collaterals, but cases with diminished sylvian and leptomeningeal collaterals experienced greater risk of worsening compared with control subjects measured either by admission to discharge National Institutes of Health Stroke Scale increase > or =1 (55.6% versus 16.6%, P=0.001) or > or =4 (44.4% versus 6.4%, P<0.001).
Most patients with proximal middle cerebral artery occlusion rapidly recruit sufficient collaterals and follow a clinical course similar to patients with no occlusions, but a subset with diminished collaterals is at high risk for worsening. Despite the abundance of emerging multimodal imaging techniques in the field of stroke, there is a paucity of data demonstrating a strong correlation between imaging findings and clinical outcome. This study explored how proximal arterial occlusions alter flow in collateral vessels and whether occlusion or extent of collaterals correlates with prehospital symptoms of fluctuation and worsening since onset or predict in-hospital worsening.BACKGROUND AND PURPOSEDespite the abundance of emerging multimodal imaging techniques in the field of stroke, there is a paucity of data demonstrating a strong correlation between imaging findings and clinical outcome. This study explored how proximal arterial occlusions alter flow in collateral vessels and whether occlusion or extent of collaterals correlates with prehospital symptoms of fluctuation and worsening since onset or predict in-hospital worsening.Among 741 patients enrolled in a prospective cohort study involving CT angiographic imaging in acute stroke, 134 cases with proximal middle cerebral artery occlusion and 235 control subjects with no occlusions were identified. CT angiography was used to identify occlusions and grade the extent of collateral vessels in the sylvian fissure and leptomeningeal convexity. History of symptom fluctuation or progressive worsening was obtained on admission.METHODSAmong 741 patients enrolled in a prospective cohort study involving CT angiographic imaging in acute stroke, 134 cases with proximal middle cerebral artery occlusion and 235 control subjects with no occlusions were identified. CT angiography was used to identify occlusions and grade the extent of collateral vessels in the sylvian fissure and leptomeningeal convexity. History of symptom fluctuation or progressive worsening was obtained on admission.Prehospital symptoms were unrelated to occlusion or collateral status. In cases, 37.5% imaged within 1 hour were found to have diminished collaterals versus 12.1% imaged at 12 to 24 hours (P=0.047). No difference in worsening was seen between cases and control subjects with adequate collaterals, but cases with diminished sylvian and leptomeningeal collaterals experienced greater risk of worsening compared with control subjects measured either by admission to discharge National Institutes of Health Stroke Scale increase > or =1 (55.6% versus 16.6%, P=0.001) or > or =4 (44.4% versus 6.4%, P<0.001).RESULTSPrehospital symptoms were unrelated to occlusion or collateral status. In cases, 37.5% imaged within 1 hour were found to have diminished collaterals versus 12.1% imaged at 12 to 24 hours (P=0.047). No difference in worsening was seen between cases and control subjects with adequate collaterals, but cases with diminished sylvian and leptomeningeal collaterals experienced greater risk of worsening compared with control subjects measured either by admission to discharge National Institutes of Health Stroke Scale increase > or =1 (55.6% versus 16.6%, P=0.001) or > or =4 (44.4% versus 6.4%, P<0.001).Most patients with proximal middle cerebral artery occlusion rapidly recruit sufficient collaterals and follow a clinical course similar to patients with no occlusions, but a subset with diminished collaterals is at high risk for worsening.CONCLUSIONSMost patients with proximal middle cerebral artery occlusion rapidly recruit sufficient collaterals and follow a clinical course similar to patients with no occlusions, but a subset with diminished collaterals is at high risk for worsening. Background and Purpose— Despite the abundance of emerging multimodal imaging techniques in the field of stroke, there is a paucity of data demonstrating a strong correlation between imaging findings and clinical outcome. This study explored how proximal arterial occlusions alter flow in collateral vessels and whether occlusion or extent of collaterals correlates with prehospital symptoms of fluctuation and worsening since onset or predict in-hospital worsening. Methods— Among 741 patients enrolled in a prospective cohort study involving CT angiographic imaging in acute stroke, 134 cases with proximal middle cerebral artery occlusion and 235 control subjects with no occlusions were identified. CT angiography was used to identify occlusions and grade the extent of collateral vessels in the sylvian fissure and leptomeningeal convexity. History of symptom fluctuation or progressive worsening was obtained on admission. Results— Prehospital symptoms were unrelated to occlusion or collateral status. In cases, 37.5% imaged within 1 hour were found to have diminished collaterals versus 12.1% imaged at 12 to 24 hours ( P =0.047). No difference in worsening was seen between cases and control subjects with adequate collaterals, but cases with diminished sylvian and leptomeningeal collaterals experienced greater risk of worsening compared with control subjects measured either by admission to discharge National Institutes of Health Stroke Scale increase ≥1 (55.6% versus 16.6%, P =0.001) or ≥4 (44.4% versus 6.4%, P <0.001). Conclusion— Most patients with proximal middle cerebral artery occlusion rapidly recruit sufficient collaterals and follow a clinical course similar to patients with no occlusions, but a subset with diminished collaterals is at high risk for worsening. |
Author | Greer, David M. Singhal, Aneesh B. Lev, Michael H. Kemmling, André Maas, Matthew B. Harris, Gordon J. Furie, Karen L. Smith, Wade S. Ay, Hakan Koroshetz, Walter J. Halpern, Elkan |
Author_xml | – sequence: 1 givenname: Matthew B. surname: Maas fullname: Maas, Matthew B. organization: From the Departments of Neurology (M.B.M., A.B.S., D.M.G., K.L.F.) and Radiology (M.H.L., H.A., G.J.H., E.H., A.K.), Massachusetts General Hospital, Harvard Medical School, Boston, Mass; the Department of Neurology (W.S.S.), University of California, San Francisco, Calif; and the National Institute of Neurological Disorders and Stroke (W.J.K.), Bethesda, Md – sequence: 2 givenname: Michael H. surname: Lev fullname: Lev, Michael H. organization: From the Departments of Neurology (M.B.M., A.B.S., D.M.G., K.L.F.) and Radiology (M.H.L., H.A., G.J.H., E.H., A.K.), Massachusetts General Hospital, Harvard Medical School, Boston, Mass; the Department of Neurology (W.S.S.), University of California, San Francisco, Calif; and the National Institute of Neurological Disorders and Stroke (W.J.K.), Bethesda, Md – sequence: 3 givenname: Hakan surname: Ay fullname: Ay, Hakan organization: From the Departments of Neurology (M.B.M., A.B.S., D.M.G., K.L.F.) and Radiology (M.H.L., H.A., G.J.H., E.H., A.K.), Massachusetts General Hospital, Harvard Medical School, Boston, Mass; the Department of Neurology (W.S.S.), University of California, San Francisco, Calif; and the National Institute of Neurological Disorders and Stroke (W.J.K.), Bethesda, Md – sequence: 4 givenname: Aneesh B. surname: Singhal fullname: Singhal, Aneesh B. organization: From the Departments of Neurology (M.B.M., A.B.S., D.M.G., K.L.F.) and Radiology (M.H.L., H.A., G.J.H., E.H., A.K.), Massachusetts General Hospital, Harvard Medical School, Boston, Mass; the Department of Neurology (W.S.S.), University of California, San Francisco, Calif; and the National Institute of Neurological Disorders and Stroke (W.J.K.), Bethesda, Md – sequence: 5 givenname: David M. surname: Greer fullname: Greer, David M. organization: From the Departments of Neurology (M.B.M., A.B.S., D.M.G., K.L.F.) and Radiology (M.H.L., H.A., G.J.H., E.H., A.K.), Massachusetts General Hospital, Harvard Medical School, Boston, Mass; the Department of Neurology (W.S.S.), University of California, San Francisco, Calif; and the National Institute of Neurological Disorders and Stroke (W.J.K.), Bethesda, Md – sequence: 6 givenname: Wade S. surname: Smith fullname: Smith, Wade S. organization: From the Departments of Neurology (M.B.M., A.B.S., D.M.G., K.L.F.) and Radiology (M.H.L., H.A., G.J.H., E.H., A.K.), Massachusetts General Hospital, Harvard Medical School, Boston, Mass; the Department of Neurology (W.S.S.), University of California, San Francisco, Calif; and the National Institute of Neurological Disorders and Stroke (W.J.K.), Bethesda, Md – sequence: 7 givenname: Gordon J. surname: Harris fullname: Harris, Gordon J. organization: From the Departments of Neurology (M.B.M., A.B.S., D.M.G., K.L.F.) and Radiology (M.H.L., H.A., G.J.H., E.H., A.K.), Massachusetts General Hospital, Harvard Medical School, Boston, Mass; the Department of Neurology (W.S.S.), University of California, San Francisco, Calif; and the National Institute of Neurological Disorders and Stroke (W.J.K.), Bethesda, Md – sequence: 8 givenname: Elkan surname: Halpern fullname: Halpern, Elkan organization: From the Departments of Neurology (M.B.M., A.B.S., D.M.G., K.L.F.) and Radiology (M.H.L., H.A., G.J.H., E.H., A.K.), Massachusetts General Hospital, Harvard Medical School, Boston, Mass; the Department of Neurology (W.S.S.), University of California, San Francisco, Calif; and the National Institute of Neurological Disorders and Stroke (W.J.K.), Bethesda, Md – sequence: 9 givenname: André surname: Kemmling fullname: Kemmling, André organization: From the Departments of Neurology (M.B.M., A.B.S., D.M.G., K.L.F.) and Radiology (M.H.L., H.A., G.J.H., E.H., A.K.), Massachusetts General Hospital, Harvard Medical School, Boston, Mass; the Department of Neurology (W.S.S.), University of California, San Francisco, Calif; and the National Institute of Neurological Disorders and Stroke (W.J.K.), Bethesda, Md – sequence: 10 givenname: Walter J. surname: Koroshetz fullname: Koroshetz, Walter J. organization: From the Departments of Neurology (M.B.M., A.B.S., D.M.G., K.L.F.) and Radiology (M.H.L., H.A., G.J.H., E.H., A.K.), Massachusetts General Hospital, Harvard Medical School, Boston, Mass; the Department of Neurology (W.S.S.), University of California, San Francisco, Calif; and the National Institute of Neurological Disorders and Stroke (W.J.K.), Bethesda, Md – sequence: 11 givenname: Karen L. surname: Furie fullname: Furie, Karen L. organization: From the Departments of Neurology (M.B.M., A.B.S., D.M.G., K.L.F.) and Radiology (M.H.L., H.A., G.J.H., E.H., A.K.), Massachusetts General Hospital, Harvard Medical School, Boston, Mass; the Department of Neurology (W.S.S.), University of California, San Francisco, Calif; and the National Institute of Neurological Disorders and Stroke (W.J.K.), Bethesda, Md |
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CODEN | SJCCA7 |
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Cites_doi | 10.1161/strokeaha.107.488379 10.1161/01.str.0000032244.03134.37 10.1161/01.str.0000086465.41263.06 10.1161/01.str.0000016924.55448.43 10.1161/01.str.0000126043.83777.3a 10.1161/01.str.0000217418.29609.22 10.1212/01.wnl.0000173036.95976.46 10.3174/ajnr.A1153 10.1212/01.wnl.0000335929.06390.d3 10.1161/strokeaha.107.503482 10.1148/radiol.2442061028 10.1002/ana.21130 |
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SubjectTerms | Acute Disease Biological and medical sciences Cerebral Angiography - methods Cerebrovascular Circulation Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Humans Infarction, Middle Cerebral Artery - diagnostic imaging Medical sciences Nervous system (semeiology, syndromes) Neurology Predictive Value of Tests Prospective Studies Stroke - diagnostic imaging Time Factors Tomography, X-Ray Computed - methods Vascular diseases and vascular malformations of the nervous system |
Title | Collateral Vessels on CT Angiography Predict Outcome in Acute Ischemic Stroke |
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