Weight Approximation in Stroke Before Thrombolysis The WAIST-Study: A Prospective Observational Dose-Finding Study
Because of the narrow therapeutic range for thrombolysis in stroke, accurate weight-based dosing is essential for efficacy and safety. Stroke patients are frequently incapable to communicate their correct body weight (BW). Thus, dosing is often based on BW estimation, which may lead to dosing errors...
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Veröffentlicht in: | Stroke (1970) 2010-12, Vol.41 (12), p.2867-2871 |
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creator | BREUER, Lorenz NOWE, Tim HUTTNER, Hagen B BLINZLER, Christian KOLLMAR, Rainer SCHELLINGER, Peter D SCHWAB, Stefan KÖHRMANN, Martin |
description | Because of the narrow therapeutic range for thrombolysis in stroke, accurate weight-based dosing is essential for efficacy and safety. Stroke patients are frequently incapable to communicate their correct body weight (BW). Thus, dosing is often based on BW estimation, which may lead to dosing errors. The aim of our study was to evaluate availability of BW information, accuracy of estimations, and final dosing of Alteplase (tissue plasminogen activator [tPA]) in a routine clinical setting.
A total of 109 consecutive intravenous thrombolysis patients were prospectively included in the study. Recruitment concluded with 100 complete data sets. Before therapy, BW was estimated independently by 2 physicians, 2 emergency nurses, and a neuroradiological technical assistant. Patients were weighed, and anthropometric measurements for BW approximation were taken. Dosing errors were assessed. Clinical outcome was evaluated at 90 days.
Of 109 patients, 55 (50.5%) were unable to provide information on their BW. Of those, 11 (20%) were accompanied by relatives able to give BW information. For all patients, estimation errors rates ranged from 20.8% (patient's own estimation) up to 38.2% (treating physician) and 42.2% (emergency nurse). Finally, 29 patients received an Alteplase dosage diverging >10% from the optimal dose. Twelve were under- and 17 overdosed. Underdosage was an independent predictor for worse outcome in multivariate analysis.
Our study shows that reliable BW data are missing for a majority of intravenous thrombolysis patients. Measuring BW before administering Alteplase remains challenging. Given dosing errors in one-third of patients and the observed impact on outcome, standardized weighing before thrombolysis should be considered. Clinical Trial Registration-URL: http://www.clinicaltrials.gov. Unique identifier: NCT01006434. |
doi_str_mv | 10.1161/STROKEAHA.110.578062 |
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A total of 109 consecutive intravenous thrombolysis patients were prospectively included in the study. Recruitment concluded with 100 complete data sets. Before therapy, BW was estimated independently by 2 physicians, 2 emergency nurses, and a neuroradiological technical assistant. Patients were weighed, and anthropometric measurements for BW approximation were taken. Dosing errors were assessed. Clinical outcome was evaluated at 90 days.
Of 109 patients, 55 (50.5%) were unable to provide information on their BW. Of those, 11 (20%) were accompanied by relatives able to give BW information. For all patients, estimation errors rates ranged from 20.8% (patient's own estimation) up to 38.2% (treating physician) and 42.2% (emergency nurse). Finally, 29 patients received an Alteplase dosage diverging >10% from the optimal dose. Twelve were under- and 17 overdosed. Underdosage was an independent predictor for worse outcome in multivariate analysis.
Our study shows that reliable BW data are missing for a majority of intravenous thrombolysis patients. Measuring BW before administering Alteplase remains challenging. Given dosing errors in one-third of patients and the observed impact on outcome, standardized weighing before thrombolysis should be considered. Clinical Trial Registration-URL: http://www.clinicaltrials.gov. Unique identifier: NCT01006434.</description><identifier>ISSN: 0039-2499</identifier><identifier>ISSN: 1524-4628</identifier><identifier>EISSN: 1524-4628</identifier><identifier>DOI: 10.1161/STROKEAHA.110.578062</identifier><identifier>PMID: 21071723</identifier><identifier>CODEN: SJCCA7</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Aged ; Analysis of Variance ; Anthropometry ; Biological and medical sciences ; Body Weight - physiology ; Cerebral Hemorrhage - chemically induced ; Cerebral Hemorrhage - epidemiology ; Data Interpretation, Statistical ; Dose-Response Relationship, Drug ; Female ; Fibrinolytic Agents - administration & dosage ; Fibrinolytic Agents - adverse effects ; Fibrinolytic Agents - therapeutic use ; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy ; Humans ; Injections, Intravenous ; Male ; Medical Errors ; Medical sciences ; Middle Aged ; Nervous system (semeiology, syndromes) ; Neurology ; Odds Ratio ; Prospective Studies ; Risk Factors ; Stroke - drug therapy ; Tissue Plasminogen Activator - administration & dosage ; Tissue Plasminogen Activator - adverse effects ; Tissue Plasminogen Activator - therapeutic use ; Treatment Outcome ; Vascular diseases and vascular malformations of the nervous system</subject><ispartof>Stroke (1970), 2010-12, Vol.41 (12), p.2867-2871</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c317t-eb85c7d7543cd197db1d09a46ecaaca9a5fff3e9179d19bf32a2559b2708d1af3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3687,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23652400$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21071723$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>BREUER, Lorenz</creatorcontrib><creatorcontrib>NOWE, Tim</creatorcontrib><creatorcontrib>HUTTNER, Hagen B</creatorcontrib><creatorcontrib>BLINZLER, Christian</creatorcontrib><creatorcontrib>KOLLMAR, Rainer</creatorcontrib><creatorcontrib>SCHELLINGER, Peter D</creatorcontrib><creatorcontrib>SCHWAB, Stefan</creatorcontrib><creatorcontrib>KÖHRMANN, Martin</creatorcontrib><title>Weight Approximation in Stroke Before Thrombolysis The WAIST-Study: A Prospective Observational Dose-Finding Study</title><title>Stroke (1970)</title><addtitle>Stroke</addtitle><description>Because of the narrow therapeutic range for thrombolysis in stroke, accurate weight-based dosing is essential for efficacy and safety. Stroke patients are frequently incapable to communicate their correct body weight (BW). Thus, dosing is often based on BW estimation, which may lead to dosing errors. The aim of our study was to evaluate availability of BW information, accuracy of estimations, and final dosing of Alteplase (tissue plasminogen activator [tPA]) in a routine clinical setting.
A total of 109 consecutive intravenous thrombolysis patients were prospectively included in the study. Recruitment concluded with 100 complete data sets. Before therapy, BW was estimated independently by 2 physicians, 2 emergency nurses, and a neuroradiological technical assistant. Patients were weighed, and anthropometric measurements for BW approximation were taken. Dosing errors were assessed. Clinical outcome was evaluated at 90 days.
Of 109 patients, 55 (50.5%) were unable to provide information on their BW. Of those, 11 (20%) were accompanied by relatives able to give BW information. For all patients, estimation errors rates ranged from 20.8% (patient's own estimation) up to 38.2% (treating physician) and 42.2% (emergency nurse). Finally, 29 patients received an Alteplase dosage diverging >10% from the optimal dose. Twelve were under- and 17 overdosed. Underdosage was an independent predictor for worse outcome in multivariate analysis.
Our study shows that reliable BW data are missing for a majority of intravenous thrombolysis patients. Measuring BW before administering Alteplase remains challenging. Given dosing errors in one-third of patients and the observed impact on outcome, standardized weighing before thrombolysis should be considered. Clinical Trial Registration-URL: http://www.clinicaltrials.gov. Unique identifier: NCT01006434.</description><subject>Aged</subject><subject>Analysis of Variance</subject><subject>Anthropometry</subject><subject>Biological and medical sciences</subject><subject>Body Weight - physiology</subject><subject>Cerebral Hemorrhage - chemically induced</subject><subject>Cerebral Hemorrhage - epidemiology</subject><subject>Data Interpretation, Statistical</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Fibrinolytic Agents - administration & dosage</subject><subject>Fibrinolytic Agents - adverse effects</subject><subject>Fibrinolytic Agents - therapeutic use</subject><subject>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</subject><subject>Humans</subject><subject>Injections, Intravenous</subject><subject>Male</subject><subject>Medical Errors</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neurology</subject><subject>Odds Ratio</subject><subject>Prospective Studies</subject><subject>Risk Factors</subject><subject>Stroke - drug therapy</subject><subject>Tissue Plasminogen Activator - administration & dosage</subject><subject>Tissue Plasminogen Activator - adverse effects</subject><subject>Tissue Plasminogen Activator - therapeutic use</subject><subject>Treatment Outcome</subject><subject>Vascular diseases and vascular malformations of the nervous system</subject><issn>0039-2499</issn><issn>1524-4628</issn><issn>1524-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1PGzEQhq2qqISPf1BVvlQ9LfhjvV5zWyApEUipSBDHldc7BpfNOrU3qPn3dZMUjj2NXs0zY40fhD5TckZpQc_ni_vZ7bi6qVIkZ0KWpGAf0IgKlmd5wcqPaEQIVxnLlTpERzH-JIQwXopP6JBRIqlkfITCI7in5wFXq1Xwv91SD8732PV4PgT_AvgSrA-AF8_BLxvfbaKLKQB-rKbzRTYf1u3mAlf4R_BxBWZwr4BnTYTwul2kO3ztI2QT17euf8Jb_gQdWN1FON3XY_QwGS-ubrK72ffpVXWXGU7lkEFTCiNbKXJuWqpk29CWKJ0XYLQ2WmlhreWgqFSp3VjONBNCNUySsqXa8mP0bbc3XfZrDXGoly4a6Drdg1_HWolcqEJJ-V-ypEIIXlCVyHxHmnRwDGDrVUifFjY1JfVfLfWblhRJvdOSxr7sH1g3S2jfhv55SMDXPaCj0Z0NujcuvnO8SFqTzj8znZeE</recordid><startdate>20101201</startdate><enddate>20101201</enddate><creator>BREUER, Lorenz</creator><creator>NOWE, Tim</creator><creator>HUTTNER, Hagen B</creator><creator>BLINZLER, Christian</creator><creator>KOLLMAR, Rainer</creator><creator>SCHELLINGER, Peter D</creator><creator>SCHWAB, Stefan</creator><creator>KÖHRMANN, Martin</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>20101201</creationdate><title>Weight Approximation in Stroke Before Thrombolysis The WAIST-Study: A Prospective Observational Dose-Finding Study</title><author>BREUER, Lorenz ; NOWE, Tim ; HUTTNER, Hagen B ; BLINZLER, Christian ; KOLLMAR, Rainer ; SCHELLINGER, Peter D ; SCHWAB, Stefan ; KÖHRMANN, Martin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c317t-eb85c7d7543cd197db1d09a46ecaaca9a5fff3e9179d19bf32a2559b2708d1af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Aged</topic><topic>Analysis of Variance</topic><topic>Anthropometry</topic><topic>Biological and medical sciences</topic><topic>Body Weight - physiology</topic><topic>Cerebral Hemorrhage - chemically induced</topic><topic>Cerebral Hemorrhage - epidemiology</topic><topic>Data Interpretation, Statistical</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Fibrinolytic Agents - administration & dosage</topic><topic>Fibrinolytic Agents - adverse effects</topic><topic>Fibrinolytic Agents - therapeutic use</topic><topic>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</topic><topic>Humans</topic><topic>Injections, Intravenous</topic><topic>Male</topic><topic>Medical Errors</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neurology</topic><topic>Odds Ratio</topic><topic>Prospective Studies</topic><topic>Risk Factors</topic><topic>Stroke - drug therapy</topic><topic>Tissue Plasminogen Activator - administration & dosage</topic><topic>Tissue Plasminogen Activator - adverse effects</topic><topic>Tissue Plasminogen Activator - therapeutic use</topic><topic>Treatment Outcome</topic><topic>Vascular diseases and vascular malformations of the nervous system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BREUER, Lorenz</creatorcontrib><creatorcontrib>NOWE, Tim</creatorcontrib><creatorcontrib>HUTTNER, Hagen B</creatorcontrib><creatorcontrib>BLINZLER, Christian</creatorcontrib><creatorcontrib>KOLLMAR, Rainer</creatorcontrib><creatorcontrib>SCHELLINGER, Peter D</creatorcontrib><creatorcontrib>SCHWAB, Stefan</creatorcontrib><creatorcontrib>KÖHRMANN, Martin</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Stroke (1970)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BREUER, Lorenz</au><au>NOWE, Tim</au><au>HUTTNER, Hagen B</au><au>BLINZLER, Christian</au><au>KOLLMAR, Rainer</au><au>SCHELLINGER, Peter D</au><au>SCHWAB, Stefan</au><au>KÖHRMANN, Martin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Weight Approximation in Stroke Before Thrombolysis The WAIST-Study: A Prospective Observational Dose-Finding Study</atitle><jtitle>Stroke (1970)</jtitle><addtitle>Stroke</addtitle><date>2010-12-01</date><risdate>2010</risdate><volume>41</volume><issue>12</issue><spage>2867</spage><epage>2871</epage><pages>2867-2871</pages><issn>0039-2499</issn><issn>1524-4628</issn><eissn>1524-4628</eissn><coden>SJCCA7</coden><abstract>Because of the narrow therapeutic range for thrombolysis in stroke, accurate weight-based dosing is essential for efficacy and safety. Stroke patients are frequently incapable to communicate their correct body weight (BW). Thus, dosing is often based on BW estimation, which may lead to dosing errors. The aim of our study was to evaluate availability of BW information, accuracy of estimations, and final dosing of Alteplase (tissue plasminogen activator [tPA]) in a routine clinical setting.
A total of 109 consecutive intravenous thrombolysis patients were prospectively included in the study. Recruitment concluded with 100 complete data sets. Before therapy, BW was estimated independently by 2 physicians, 2 emergency nurses, and a neuroradiological technical assistant. Patients were weighed, and anthropometric measurements for BW approximation were taken. Dosing errors were assessed. Clinical outcome was evaluated at 90 days.
Of 109 patients, 55 (50.5%) were unable to provide information on their BW. Of those, 11 (20%) were accompanied by relatives able to give BW information. For all patients, estimation errors rates ranged from 20.8% (patient's own estimation) up to 38.2% (treating physician) and 42.2% (emergency nurse). Finally, 29 patients received an Alteplase dosage diverging >10% from the optimal dose. Twelve were under- and 17 overdosed. Underdosage was an independent predictor for worse outcome in multivariate analysis.
Our study shows that reliable BW data are missing for a majority of intravenous thrombolysis patients. Measuring BW before administering Alteplase remains challenging. Given dosing errors in one-third of patients and the observed impact on outcome, standardized weighing before thrombolysis should be considered. Clinical Trial Registration-URL: http://www.clinicaltrials.gov. Unique identifier: NCT01006434.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>21071723</pmid><doi>10.1161/STROKEAHA.110.578062</doi><tpages>5</tpages></addata></record> |
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source | MEDLINE; American Heart Association Journals; Journals@Ovid Complete; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Aged Analysis of Variance Anthropometry Biological and medical sciences Body Weight - physiology Cerebral Hemorrhage - chemically induced Cerebral Hemorrhage - epidemiology Data Interpretation, Statistical Dose-Response Relationship, Drug Female Fibrinolytic Agents - administration & dosage Fibrinolytic Agents - adverse effects Fibrinolytic Agents - therapeutic use Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Humans Injections, Intravenous Male Medical Errors Medical sciences Middle Aged Nervous system (semeiology, syndromes) Neurology Odds Ratio Prospective Studies Risk Factors Stroke - drug therapy Tissue Plasminogen Activator - administration & dosage Tissue Plasminogen Activator - adverse effects Tissue Plasminogen Activator - therapeutic use Treatment Outcome Vascular diseases and vascular malformations of the nervous system |
title | Weight Approximation in Stroke Before Thrombolysis The WAIST-Study: A Prospective Observational Dose-Finding Study |
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