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Development and validation of a self-report lower-extremity lymphedema screening questionnaire in women.

Identifieur interne : 005488 ( Ncbi/Merge ); précédent : 005487; suivant : 005489

Development and validation of a self-report lower-extremity lymphedema screening questionnaire in women.

Auteurs : Kathleen J. Yost [États-Unis] ; Andrea L. Cheville ; Amy L. Weaver ; Mariam Al Hilli ; Sean C. Dowdy

Source :

RBID : pubmed:23288911

Descripteurs français

English descriptors

Abstract

Patient-reported signs and symptoms are often the first indication of clinically relevant lymphedema.

DOI: 10.2522/ptj.20120088
PubMed: 23288911

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pubmed:23288911

Le document en format XML

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<title xml:lang="en">Development and validation of a self-report lower-extremity lymphedema screening questionnaire in women.</title>
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<name sortKey="Yost, Kathleen J" sort="Yost, Kathleen J" uniqKey="Yost K" first="Kathleen J" last="Yost">Kathleen J. Yost</name>
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<nlm:affiliation>Department of Health Sciences Research, Mayo Clinic, 200 First St W, Rochester, MN 55905, USA. yost.kathleen@mayo.edu</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Health Sciences Research, Mayo Clinic, 200 First St W, Rochester, MN 55905</wicri:regionArea>
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<region type="state">Minnesota</region>
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<name sortKey="Cheville, Andrea L" sort="Cheville, Andrea L" uniqKey="Cheville A" first="Andrea L" last="Cheville">Andrea L. Cheville</name>
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<name sortKey="Weaver, Amy L" sort="Weaver, Amy L" uniqKey="Weaver A" first="Amy L" last="Weaver">Amy L. Weaver</name>
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<name sortKey="Al Hilli, Mariam" sort="Al Hilli, Mariam" uniqKey="Al Hilli M" first="Mariam" last="Al Hilli">Mariam Al Hilli</name>
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<name sortKey="Dowdy, Sean C" sort="Dowdy, Sean C" uniqKey="Dowdy S" first="Sean C" last="Dowdy">Sean C. Dowdy</name>
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<title xml:lang="en">Development and validation of a self-report lower-extremity lymphedema screening questionnaire in women.</title>
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<name sortKey="Yost, Kathleen J" sort="Yost, Kathleen J" uniqKey="Yost K" first="Kathleen J" last="Yost">Kathleen J. Yost</name>
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<term>Adult</term>
<term>Cross-Sectional Studies</term>
<term>Female</term>
<term>Humans</term>
<term>Lower Extremity</term>
<term>Lymph Node Excision (adverse effects)</term>
<term>Lymphedema (diagnosis)</term>
<term>Lymphedema (epidemiology)</term>
<term>Lymphedema (etiology)</term>
<term>Mass Screening (methods)</term>
<term>Obesity (epidemiology)</term>
<term>Self Report</term>
<term>Surveys and Questionnaires</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Adulte</term>
<term>Autorapport</term>
<term>Dépistage systématique ()</term>
<term>Enquêtes et questionnaires</term>
<term>Femelle</term>
<term>Humains</term>
<term>Lymphadénectomie (effets indésirables)</term>
<term>Lymphoedème (diagnostic)</term>
<term>Lymphoedème (épidémiologie)</term>
<term>Lymphoedème (étiologie)</term>
<term>Membre inférieur</term>
<term>Obésité (épidémiologie)</term>
<term>Études transversales</term>
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<keywords scheme="MESH" qualifier="adverse effects" xml:lang="en">
<term>Lymph Node Excision</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en">
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr">
<term>Lymphoedème</term>
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<keywords scheme="MESH" qualifier="effets indésirables" xml:lang="fr">
<term>Lymphadénectomie</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en">
<term>Lymphedema</term>
<term>Obesity</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en">
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>Mass Screening</term>
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<keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr">
<term>Lymphoedème</term>
<term>Obésité</term>
</keywords>
<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr">
<term>Lymphoedème</term>
</keywords>
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<term>Adult</term>
<term>Cross-Sectional Studies</term>
<term>Female</term>
<term>Humans</term>
<term>Lower Extremity</term>
<term>Self Report</term>
<term>Surveys and Questionnaires</term>
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<term>Autorapport</term>
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<term>Enquêtes et questionnaires</term>
<term>Femelle</term>
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<term>Membre inférieur</term>
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<div type="abstract" xml:lang="en">Patient-reported signs and symptoms are often the first indication of clinically relevant lymphedema.</div>
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<Month>05</Month>
<Day>02</Day>
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<DateCompleted>
<Year>2013</Year>
<Month>08</Month>
<Day>08</Day>
</DateCompleted>
<DateRevised>
<Year>2015</Year>
<Month>11</Month>
<Day>19</Day>
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<ISSN IssnType="Electronic">1538-6724</ISSN>
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<Volume>93</Volume>
<Issue>5</Issue>
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<Year>2013</Year>
<Month>May</Month>
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<Title>Physical therapy</Title>
<ISOAbbreviation>Phys Ther</ISOAbbreviation>
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<ArticleTitle>Development and validation of a self-report lower-extremity lymphedema screening questionnaire in women.</ArticleTitle>
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<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Patient-reported signs and symptoms are often the first indication of clinically relevant lymphedema.</AbstractText>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">The purpose of this study was to develop and assess the diagnostic accuracy of a screening questionnaire to detect lower-extremity lymphedema (LEL) among normal-weight women and women with obesity.</AbstractText>
<AbstractText Label="DESIGN" NlmCategory="METHODS">This was a cross-sectional survey study.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">The authors reviewed existing questionnaires assessing upper-extremity lymphedema (UEL) for potential questions and worked with content experts to generate new items. A draft questionnaire with 59 items was reviewed by 5 physicians and 5 physical therapists who specialized in lymphedema management and 5 female patients with clinically confirmed secondary LEL. A revised questionnaire with 45 items was administered by mail to 186 women with clinically confirmed LEL (n=116) or UEL (n=70). A total of 99 women (53.2% of 186) completed the mailed survey, and 28 women with lymphedema who were recruited directly in a lymphedema clinic waiting area also completed the survey. A parsimonious subset of items that best discriminated patients with and without LEL was identified using chi-square tests and logistic regression. Sensitivity and specificity for detecting LEL and positive and negative likelihood ratios (LR+, LR-) were estimated for the entire sample and for subsamples defined by obesity (body mass index ≥30 versus <30 kg/m(2)), which may confound the accurate diagnosis of LEL.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Questionnaires were completed by 127 women (LEL group, n=88; UEL group, n=39). A sum of 13 items (score range=0-52) was the most discriminating. Using a cutoff score of ≥5 points, the sensitivity and specificity for detecting LEL among all participants were 95.5% and 86.5%, respectively (LR+=7.1, LR-=0.05), and 94.8% and 76.5%, respectively (LR+=4.0, LR-=0.07), for participants who were obese.</AbstractText>
<AbstractText Label="LIMITATIONS" NlmCategory="CONCLUSIONS">By enumerating a sample with a high prevalence of LEL, a spectrum bias may have been introduced, which may have affected the accuracy of the screening questionnaire.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">The brief, 13-item self-report questionnaire is a sensitive and specific tool for detecting clinically relevant LEL among women, including those with a body mass index of ≥30 kg/m(2).</AbstractText>
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