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<ui>ar3988</ui>
<ji>1478-6354</ji>
<fm>
<dochead>Meeting abstract</dochead>
<bibl>
<title><p>Poor methodological reporting in lupus clinical trials found in Cochrane reviews</p></title>
<aug>
<au ca="yes" id="A1"><snm>Goldsmith</snm><fnm>CH</fnm><insr iid="I1"/><insr iid="I2"/></au>
</aug>
<insg>
<ins id="I1"><p>Arthritis Research Centre of Canada, Vancouver, BC, Canada</p></ins>
<ins id="I2"><p>Simon Fraser University, Burnaby, BC, Canada</p></ins>
</insg>
<source>Arthritis Research &amp; Therapy</source>


<supplement><title><p>Lupus 2012: New targets, new approaches</p></title><editor>Peter E Lipsky, John M Esdaile, Matthew H Liang and Paul R Fortin</editor><note>Meeting abstracts</note></supplement><conference><title><p>Lupus 2012: New targets, new approaches</p></title><location>Whistler, Canada</location><date-range>27-30 September 2012</date-range></conference><issn>1478-6354</issn>
<pubdate>2012</pubdate>
<volume>14</volume>
<issue>Suppl 3</issue>
<fpage>A54</fpage>
<url>http://arthritis-research.com/content/14/S3/A54</url>
<xrefbib><pubid idtype="doi">10.1186/ar3988</pubid></xrefbib></bibl>
<history><pub><date><day>27</day><month>9</month><year>2012</year></date></pub></history>
<cpyrt><year>2012</year><collab>Goldsmith; licensee BioMed Central Ltd.</collab><note>This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</note></cpyrt>
</fm>
<bdy>
<sec><st><p>Background</p></st>
<p>Results of randomized clinical trials depend on the credibility of the methods reporting to support study findings.</p>
</sec>
<sec><st><p>Methods</p></st>
<p>We studied 24 trials from those in the Cochrane Database of Systematic Reviews with 'lupus' in the title and were printable. Each paper was scored by one reviewer using methodological criteria for design, allocation <abbrgrp><abbr bid="B1">1</abbr></abbrgrp>, blinding <abbrgrp><abbr bid="B2">2</abbr><abbr bid="B3">3</abbr><abbr bid="B4">4</abbr></abbrgrp>, reporting and imputation <abbrgrp><abbr bid="B5">5</abbr></abbrgrp>. Scores used yes, no, or ? when it was unclear. Yes <it>n </it>(integer %) for all 24 papers are reported for each criterion.</p>
</sec>
<sec><st><p>Results</p></st>
<sec><st><p>Design</p></st>
<p>Four (17%) papers had a sample size justification; 22 (92%) contained two groups and two (8%) contained three groups. Five (21%) stratified patients; yet two (8%) used stratification in the analysis.</p>
</sec>
<sec><st><p>Allocation</p></st>
<p>Six (25%) stated random numbers generated and three (12%) blocked the balance associated with the allocation ratio; yet zero (0%) used blocking in the analysis. Six (25%) used a randomization list concealed from the person deciding patient eligibility, zero (0%) provided an audit trail for randomization, one (4%) stated randomization integrity. Seven (29%) mentioned the randomization constructed with a computer program or random number table.</p>
</sec>
<sec><st><p>Blinding</p></st>
<p>Four (17%) stated the person deciding on the patient eligibility was blinded to block structure and eight (33%) claimed the study was double blinded, even though it was not clear who the two were; indeed one was really triple blinded! For three (12%) patient blinded, six (25%) therapy, four (17%) therapist, one (4%) other caregivers; two (8%) the outcome assessor; zero (0%) data analyst, zero (0%) manuscript writer.</p>
</sec>
<sec><st><p>Reporting/analysis</p></st>
<p>One (4%) checked statistical assumptions, 23 (96%) provided baseline data, not all for every patient randomized. Twenty-one (88%) provided <it>P </it>values for group comparisons, four (17%) provided confidence intervals and zero (0%) provided numbers needed to treat. One (4%) specified subgroups in advance <abbrgrp><abbr bid="B6">6</abbr></abbrgrp>, six (25%) adjusted for baseline differences as one of the reported analyses. Four (17%) stated statistical software, but not version, zero (0%) provided the computer used for analyses.</p>
</sec>
<sec><st><p>Imputation</p></st>
<p>Seventeen (71%) had missing data, yet one (4%) mentioned using last observation carried forward, zero (0%) used multiple imputation and zero (0%) mentioned impact on study conclusions <abbrgrp><abbr bid="B5">5</abbr></abbrgrp>. Two (8%) provided a flowchart as suggested by CONSORT <abbrgrp><abbr bid="B7">7</abbr><abbr bid="B8">8</abbr></abbrgrp>.</p>
</sec>
</sec>
<sec><st><p>Conclusion</p></st>
<p>Lupus trials did not report many of the methodological criteria that give papers credibility and validity to the study being reported. Reporting should be improved in future reports of studies of patients with lupus and related health problems. Possibly using the CONSORT checksheets would help make lupus papers more credible <abbrgrp><abbr bid="B7">7</abbr><abbr bid="B8">8</abbr></abbrgrp>.</p>
</sec>
</bdy>
<bm>
<ack><sec><st><p>Acknowledgements</p></st>
<p>CHG holds the Maureen and Milan Ilich/Merck Chair in Statistics for Arthritis and Musculoskeletal Diseases.</p>
</sec>
</ack>
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