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						schemeid="dnet:result_subject" classid="keyword">DOAJ:Health Sciences
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						schemeid="dnet:result_subject" classid="keyword">Pathology</subject>
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						schemeid="dnet:result_subject" classid="keyword">DOAJ:Pathology</subject>
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						schemeid="dnet:result_subject" classid="keyword">DOAJ:Medicine (General)
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						schemeid="dnet:result_subject" classid="keyword">R</subject>
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						schemeid="dnet:result_subject" classid="keyword">Medicine</subject>
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						schemeid="dnet:result_subject" classid="keyword">Research Article</subject>
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						schemeid="dnet:result_subject" classid="keyword">RB1-214</subject>
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					<title schemename="dnet:dataCite_title" classname="main title"
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						schemeid="dnet:dataCite_title" classid="main title">Effects of EDTA and Sodium
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						Citrate on hormone measurements by fluorometric (FIA) and
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						immunofluorometric (IFMA) methods
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					</title>
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					<dateofacceptance>2002-05-23</dateofacceptance>
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					<publisher>BioMed Central</publisher>
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						classname="publication" schemeid="dnet:result_typologies" classid="publication" />
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					<language schemename="dnet:languages" classname="English"
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						schemeid="dnet:languages" classid="eng" />
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					<journal eissn="1472-6890" issn="1472-6890" lissn="">BMC
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						Clinical Pathology
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					</journal>
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					<description>
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						<p>Abstract</p>
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						<p>Background</p>
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						<p>Measurements of hormonal concentrations by immunoassays using
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							fluorescent tracer substance (Eu3+) are susceptible to the action
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							of chemical agents that may cause alterations in its original
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							structure. Our goal was to verify the effect of two types of
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							anticoagulants in the hormone assays performed by fluorometric
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							(FIA) or immunofluorometric (IFMA) methods.
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						</p>
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						<p>Methods</p>
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						<p>
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							Blood samples were obtained from 30 outpatients and were drawn in
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							EDTA, sodium citrate, and serum separation Vacutainer
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							<sup>®</sup>
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							Blood Collection Tubes. Samples were analyzed in automatized
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							equipment AutoDelfia™ (Perkin Elmer Brazil, Wallac, Finland) for
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							the following hormones: Luteinizing hormone (LH), Follicle
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							stimulating homone (FSH), prolactin (PRL), growth hormone (GH),
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							Sex hormone binding globulin (SHBG), thyroid stimulating hormone
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							(TSH), insulin, C peptide, total T3, total T4, free T4,
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							estradiol,
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							progesterone, testosterone, and cortisol. Statistical analysis was
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							carried out by Kruskal-Wallis method and Dunn's test.
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						</p>
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						<p>Results</p>
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						<p>No significant differences were seen between samples for LH,
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							FSH, PRL and free T4. Results from GH, TSH, insulin, C peptide,
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							SHBG, total T3, total T4, estradiol, testosterone, cortisol, and
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							progesterone were significant different between serum and
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							EDTA-treated samples groups. Differences were also identified
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							between serum and sodium citrate-treated samples in the analysis
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							for TSH, insulin, total T3, estradiol, testosterone and
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							progesterone.
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						</p>
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						<p>Conclusions</p>
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						<p>We conclude that the hormonal analysis carried through by FIA
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							or
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							IFMA are susceptible to the effects of anticoagulants in the
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							biological material collected that vary depending on the type of
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							assay.
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						</p>
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					</description>
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					<source>BMC Clinical Pathology, Vol 2, Iss 1, p 2 (2002)</source>
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						classid="doi">10.1186/1472-6890-2-2</pid>
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						classid="pmid">12033989</pid>
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							<ranking>4</ranking>
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							<fullname>Leme Cassia</fullname>
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							<ranking>5</ranking>
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							<fullname>Kohek Maria</fullname>
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							<fullname>Lando Valeria</fullname>
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							<fullname>Nakamura Izabel T</fullname>
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							<ranking>6</ranking>
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							<fullname>Mendonca Berenice B</fullname>
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							<ranking>2</ranking>
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							<fullname>de Oliveira Suzimara A</fullname>
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							<title schemename="dnet:dataCite_title" classname="main title"
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								schemeid="dnet:dataCite_title" classid="main title">Effects of EDTA and
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								Sodium
186
								Citrate on hormone measurements by fluorometric (FIA) and
187
								immunofluorometric (IFMA) methods
188
							</title>
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							<dateofacceptance>2002-05-01</dateofacceptance>
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							<publisher>BioMed Central</publisher>
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							<title schemename="dnet:dataCite_title" classname="main title"
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								schemeid="dnet:dataCite_title" classid="main title">Effects of EDTA and
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								Sodium
199
								Citrate on hormone measurements by fluorometric (FIA) and
200
								immunofluorometric (IFMA) methods
201
							</title>
202
							<dateofacceptance>2002-05-23</dateofacceptance>
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							<publisher>BioMed Central</publisher>
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								<url>http://www.biomedcentral.com/1472-6890/2/2</url>
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