Clinical correlates of memory complaints during AED treatment

Objectives To investigate clinical correlates of memory complaints (MC) during anti‐epileptic drug (AEDs) treatment in adults with epilepsy with special attention to the role of depression, using user‐friendly standardized clinical instruments which can be adopted in any outpatient setting. Material...

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Veröffentlicht in:Acta neurologica Scandinavica 2016-11, Vol.134 (5), p.368-373
Hauptverfasser: Mula, M., von Oertzen, T. J., Cock, H. R., Lozsadi, D. A., Agrawal, N.
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container_end_page 373
container_issue 5
container_start_page 368
container_title Acta neurologica Scandinavica
container_volume 134
creator Mula, M.
von Oertzen, T. J.
Cock, H. R.
Lozsadi, D. A.
Agrawal, N.
description Objectives To investigate clinical correlates of memory complaints (MC) during anti‐epileptic drug (AEDs) treatment in adults with epilepsy with special attention to the role of depression, using user‐friendly standardized clinical instruments which can be adopted in any outpatient setting. Materials & methods Data from a consecutive sample of adult outpatients with epilepsy assessed with the Neurological Disorder Depression Inventory for Epilepsy (NDDIE), the Adverse Event Profile (AEP) and the Emotional Thermometer (ET) were analysed. Results From a total sample of 443 patients, 28.4% reported MC as ‘always’ a problem. These patients were less likely to be seizure free (18.3% vs 34.3%; P < 0.001), had a high number of previous AED trials (4 vs 3; P < 0.001) and high AEP total scores (49 vs 34.2; P < 0.001). There was no correlation with specific AED type or combination. Depression was the major determinant with a 2‐fold increased risk (95%CI 1.15–3.86; P = 0.016). When depression was already known and under treatment, patients with MC were less likely to be in remission from depression despite antidepressant treatment (11.9% vs 1.6% P < 0.001). Among patients without depression, those reporting MC presented with significantly high scores for depression (3.3 vs 2; t = 3.07; P = 0.003), anxiety (4.5 vs 2.7; t = 4.43; P < 0.001), anger (3 vs 2; t = 2.623; P = 0.009) and distress (3.8 vs 2.2; t = 4.027; P < 0.001) than those without MC. Conclusions Depression has to be appropriately treated and full remission from depression should represent the ultimate goal as subthreshold or residual mood and anxiety symptoms can contribute to MC.
doi_str_mv 10.1111/ane.12553
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J. ; Cock, H. R. ; Lozsadi, D. A. ; Agrawal, N.</creator><creatorcontrib>Mula, M. ; von Oertzen, T. J. ; Cock, H. R. ; Lozsadi, D. A. ; Agrawal, N.</creatorcontrib><description><![CDATA[Objectives To investigate clinical correlates of memory complaints (MC) during anti‐epileptic drug (AEDs) treatment in adults with epilepsy with special attention to the role of depression, using user‐friendly standardized clinical instruments which can be adopted in any outpatient setting. Materials & methods Data from a consecutive sample of adult outpatients with epilepsy assessed with the Neurological Disorder Depression Inventory for Epilepsy (NDDIE), the Adverse Event Profile (AEP) and the Emotional Thermometer (ET) were analysed. Results From a total sample of 443 patients, 28.4% reported MC as ‘always’ a problem. These patients were less likely to be seizure free (18.3% vs 34.3%; P < 0.001), had a high number of previous AED trials (4 vs 3; P < 0.001) and high AEP total scores (49 vs 34.2; P < 0.001). There was no correlation with specific AED type or combination. Depression was the major determinant with a 2‐fold increased risk (95%CI 1.15–3.86; P = 0.016). When depression was already known and under treatment, patients with MC were less likely to be in remission from depression despite antidepressant treatment (11.9% vs 1.6% P < 0.001). Among patients without depression, those reporting MC presented with significantly high scores for depression (3.3 vs 2; t = 3.07; P = 0.003), anxiety (4.5 vs 2.7; t = 4.43; P < 0.001), anger (3 vs 2; t = 2.623; P = 0.009) and distress (3.8 vs 2.2; t = 4.027; P < 0.001) than those without MC. Conclusions Depression has to be appropriately treated and full remission from depression should represent the ultimate goal as subthreshold or residual mood and anxiety symptoms can contribute to MC.]]></description><identifier>ISSN: 0001-6314</identifier><identifier>EISSN: 1600-0404</identifier><identifier>DOI: 10.1111/ane.12553</identifier><identifier>PMID: 26756805</identifier><identifier>CODEN: ANRSAS</identifier><language>eng</language><publisher>Denmark: Blackwell Publishing Ltd</publisher><subject>Adult ; adverse events ; anti-epileptic drugs ; Anticonvulsants - adverse effects ; antidepressant drugs ; Antidepressive Agents - therapeutic use ; Complaints ; depression ; Depression - psychology ; Epilepsy ; Epilepsy - drug therapy ; Epilepsy - psychology ; Female ; Humans ; Male ; memory ; Memory Disorders - chemically induced ; Memory Disorders - etiology ; Middle Aged</subject><ispartof>Acta neurologica Scandinavica, 2016-11, Vol.134 (5), p.368-373</ispartof><rights>2016 John Wiley &amp; Sons A/S. 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Published by John Wiley &amp; Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5293-fe7a05e366a1ab6985264180035fe7fe103a2aa1f944d0631f970f26e67ce8c53</citedby><cites>FETCH-LOGICAL-c5293-fe7a05e366a1ab6985264180035fe7fe103a2aa1f944d0631f970f26e67ce8c53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fane.12553$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fane.12553$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26756805$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mula, M.</creatorcontrib><creatorcontrib>von Oertzen, T. J.</creatorcontrib><creatorcontrib>Cock, H. R.</creatorcontrib><creatorcontrib>Lozsadi, D. A.</creatorcontrib><creatorcontrib>Agrawal, N.</creatorcontrib><title>Clinical correlates of memory complaints during AED treatment</title><title>Acta neurologica Scandinavica</title><addtitle>Acta Neurol Scand</addtitle><description><![CDATA[Objectives To investigate clinical correlates of memory complaints (MC) during anti‐epileptic drug (AEDs) treatment in adults with epilepsy with special attention to the role of depression, using user‐friendly standardized clinical instruments which can be adopted in any outpatient setting. Materials & methods Data from a consecutive sample of adult outpatients with epilepsy assessed with the Neurological Disorder Depression Inventory for Epilepsy (NDDIE), the Adverse Event Profile (AEP) and the Emotional Thermometer (ET) were analysed. Results From a total sample of 443 patients, 28.4% reported MC as ‘always’ a problem. These patients were less likely to be seizure free (18.3% vs 34.3%; P < 0.001), had a high number of previous AED trials (4 vs 3; P < 0.001) and high AEP total scores (49 vs 34.2; P < 0.001). There was no correlation with specific AED type or combination. Depression was the major determinant with a 2‐fold increased risk (95%CI 1.15–3.86; P = 0.016). When depression was already known and under treatment, patients with MC were less likely to be in remission from depression despite antidepressant treatment (11.9% vs 1.6% P < 0.001). Among patients without depression, those reporting MC presented with significantly high scores for depression (3.3 vs 2; t = 3.07; P = 0.003), anxiety (4.5 vs 2.7; t = 4.43; P < 0.001), anger (3 vs 2; t = 2.623; P = 0.009) and distress (3.8 vs 2.2; t = 4.027; P < 0.001) than those without MC. Conclusions Depression has to be appropriately treated and full remission from depression should represent the ultimate goal as subthreshold or residual mood and anxiety symptoms can contribute to MC.]]></description><subject>Adult</subject><subject>adverse events</subject><subject>anti-epileptic drugs</subject><subject>Anticonvulsants - adverse effects</subject><subject>antidepressant drugs</subject><subject>Antidepressive Agents - therapeutic use</subject><subject>Complaints</subject><subject>depression</subject><subject>Depression - psychology</subject><subject>Epilepsy</subject><subject>Epilepsy - drug therapy</subject><subject>Epilepsy - psychology</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>memory</subject><subject>Memory Disorders - chemically induced</subject><subject>Memory Disorders - etiology</subject><subject>Middle Aged</subject><issn>0001-6314</issn><issn>1600-0404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMlOwzAQhi0EomU58AIoEhc4hNrxmgOHqrSFqsCF5Wi56QSlZCl2IujbY0jbAxISvozs-eaT50fohOBL4k_PlHBJIs7pDuoSgXGIGWa7qIsxJqGghHXQgXMLf4skY_uoEwnJhcK8i64GeVZmicmDpLIWclODC6o0KKCo7Mo_FsvcZGXtgnljs_I16A-vg9qCqQso6yO0l5rcwfG6HqKn0fBxcBNOH8a3g_40THgU0zAFaTAHKoQhZiZixSPBiMKYct9KgWBqImNIGjM2x_7DaSxxGgkQMgGVcHqIzlvv0lbvDbhaF5lLIM_95lXjNFGRVIpJ9S9UCB8PFx49-4UuqsaWfpFvihPOFWGeumipxFbOWUj10maFsStNsP6OX3uz_onfs6drYzMrYL4lN3l7oNcCH1kOq79Nun8_3CjDdiJzNXxuJ4x900JSyfXL_VhP7uLR82TKNKFf4Q2aqg</recordid><startdate>201611</startdate><enddate>201611</enddate><creator>Mula, M.</creator><creator>von Oertzen, T. 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A. ; Agrawal, N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5293-fe7a05e366a1ab6985264180035fe7fe103a2aa1f944d0631f970f26e67ce8c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>adverse events</topic><topic>anti-epileptic drugs</topic><topic>Anticonvulsants - adverse effects</topic><topic>antidepressant drugs</topic><topic>Antidepressive Agents - therapeutic use</topic><topic>Complaints</topic><topic>depression</topic><topic>Depression - psychology</topic><topic>Epilepsy</topic><topic>Epilepsy - drug therapy</topic><topic>Epilepsy - psychology</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>memory</topic><topic>Memory Disorders - chemically induced</topic><topic>Memory Disorders - etiology</topic><topic>Middle Aged</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mula, M.</creatorcontrib><creatorcontrib>von Oertzen, T. J.</creatorcontrib><creatorcontrib>Cock, H. R.</creatorcontrib><creatorcontrib>Lozsadi, D. A.</creatorcontrib><creatorcontrib>Agrawal, N.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Acta neurologica Scandinavica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mula, M.</au><au>von Oertzen, T. J.</au><au>Cock, H. R.</au><au>Lozsadi, D. A.</au><au>Agrawal, N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical correlates of memory complaints during AED treatment</atitle><jtitle>Acta neurologica Scandinavica</jtitle><addtitle>Acta Neurol Scand</addtitle><date>2016-11</date><risdate>2016</risdate><volume>134</volume><issue>5</issue><spage>368</spage><epage>373</epage><pages>368-373</pages><issn>0001-6314</issn><eissn>1600-0404</eissn><coden>ANRSAS</coden><abstract><![CDATA[Objectives To investigate clinical correlates of memory complaints (MC) during anti‐epileptic drug (AEDs) treatment in adults with epilepsy with special attention to the role of depression, using user‐friendly standardized clinical instruments which can be adopted in any outpatient setting. Materials & methods Data from a consecutive sample of adult outpatients with epilepsy assessed with the Neurological Disorder Depression Inventory for Epilepsy (NDDIE), the Adverse Event Profile (AEP) and the Emotional Thermometer (ET) were analysed. Results From a total sample of 443 patients, 28.4% reported MC as ‘always’ a problem. These patients were less likely to be seizure free (18.3% vs 34.3%; P < 0.001), had a high number of previous AED trials (4 vs 3; P < 0.001) and high AEP total scores (49 vs 34.2; P < 0.001). There was no correlation with specific AED type or combination. Depression was the major determinant with a 2‐fold increased risk (95%CI 1.15–3.86; P = 0.016). When depression was already known and under treatment, patients with MC were less likely to be in remission from depression despite antidepressant treatment (11.9% vs 1.6% P < 0.001). Among patients without depression, those reporting MC presented with significantly high scores for depression (3.3 vs 2; t = 3.07; P = 0.003), anxiety (4.5 vs 2.7; t = 4.43; P < 0.001), anger (3 vs 2; t = 2.623; P = 0.009) and distress (3.8 vs 2.2; t = 4.027; P < 0.001) than those without MC. Conclusions Depression has to be appropriately treated and full remission from depression should represent the ultimate goal as subthreshold or residual mood and anxiety symptoms can contribute to MC.]]></abstract><cop>Denmark</cop><pub>Blackwell Publishing Ltd</pub><pmid>26756805</pmid><doi>10.1111/ane.12553</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
adverse events
anti-epileptic drugs
Anticonvulsants - adverse effects
antidepressant drugs
Antidepressive Agents - therapeutic use
Complaints
depression
Depression - psychology
Epilepsy
Epilepsy - drug therapy
Epilepsy - psychology
Female
Humans
Male
memory
Memory Disorders - chemically induced
Memory Disorders - etiology
Middle Aged
title Clinical correlates of memory complaints during AED treatment
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