Sequential pneumatic compression for lymphedema. A controlled trial.
Identifieur interne : 006738 ( PubMed/Corpus ); précédent : 006737; suivant : 006739Sequential pneumatic compression for lymphedema. A controlled trial.
Auteurs : D M Richmand ; T F O'Donnell ; A. ZelikovskiSource :
- Archives of surgery (Chicago, Ill. : 1960) [ 0004-0010 ] ; 1985.
English descriptors
- KwdEn :
- Aspartate Aminotransferases (blood), Creatine Kinase (blood), Evaluation Studies as Topic, Extremities (anatomy & histology), Female, Fructose-Bisphosphate Aldolase (blood), Gravity Suits, Humans, Lymphedema (enzymology), Lymphedema (etiology), Lymphedema (therapy), Male, Methods, Muscles (enzymology), Prospective Studies.
- MESH :
- chemical , blood : Aspartate Aminotransferases, Creatine Kinase, Fructose-Bisphosphate Aldolase.
- anatomy & histology : Extremities.
- enzymology : Lymphedema, Muscles.
- etiology : Lymphedema.
- therapy : Lymphedema.
- Evaluation Studies as Topic, Female, Gravity Suits, Humans, Male, Methods, Prospective Studies.
Abstract
We examined prospectively the effect of a new compression device for lymphedema, which utilizes a short duration and high-pressure cycle, that provides a sequential milking pattern to the limb through multiple compartments. Twenty-five patients (seven patients for upper-extremity and 18 for lower-extremity problems) underwent 24 hours of treatment. All extremities showed a decrease in circumferential measurements with the maximal reduction occurring at the wrist (45%) for the upper extremities and at the mid-calf (47%) for the lower extremities. Lower-extremity leg volume was reduced by 45%. Despite the high pressures no elevation in serum muscle enzyme levels was noted. This device reduced lymphedematous limbs rapidly and safely.
PubMed: 4038053
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pubmed:4038053Le document en format XML
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Zelikovski</name></author></analytic><series><title level="j">Archives of surgery (Chicago, Ill. : 1960)</title><idno type="ISSN">0004-0010</idno><imprint><date when="1985" type="published">1985</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aspartate Aminotransferases (blood)</term><term>Creatine Kinase (blood)</term><term>Evaluation Studies as Topic</term><term>Extremities (anatomy & histology)</term><term>Female</term><term>Fructose-Bisphosphate Aldolase (blood)</term><term>Gravity Suits</term><term>Humans</term><term>Lymphedema (enzymology)</term><term>Lymphedema (etiology)</term><term>Lymphedema (therapy)</term><term>Male</term><term>Methods</term><term>Muscles (enzymology)</term><term>Prospective Studies</term></keywords><keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en"><term>Aspartate Aminotransferases</term><term>Creatine Kinase</term><term>Fructose-Bisphosphate Aldolase</term></keywords><keywords scheme="MESH" qualifier="anatomy & histology" xml:lang="en"><term>Extremities</term></keywords><keywords scheme="MESH" qualifier="enzymology" xml:lang="en"><term>Lymphedema</term><term>Muscles</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Evaluation Studies as Topic</term><term>Female</term><term>Gravity Suits</term><term>Humans</term><term>Male</term><term>Methods</term><term>Prospective Studies</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We examined prospectively the effect of a new compression device for lymphedema, which utilizes a short duration and high-pressure cycle, that provides a sequential milking pattern to the limb through multiple compartments. Twenty-five patients (seven patients for upper-extremity and 18 for lower-extremity problems) underwent 24 hours of treatment. All extremities showed a decrease in circumferential measurements with the maximal reduction occurring at the wrist (45%) for the upper extremities and at the mid-calf (47%) for the lower extremities. Lower-extremity leg volume was reduced by 45%. Despite the high pressures no elevation in serum muscle enzyme levels was noted. This device reduced lymphedematous limbs rapidly and safely.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">4038053</PMID><DateCreated><Year>1985</Year><Month>10</Month><Day>16</Day></DateCreated><DateCompleted><Year>1985</Year><Month>10</Month><Day>16</Day></DateCompleted><DateRevised><Year>2007</Year><Month>11</Month><Day>15</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0004-0010</ISSN><JournalIssue CitedMedium="Print"><Volume>120</Volume><Issue>10</Issue><PubDate><Year>1985</Year><Month>Oct</Month></PubDate></JournalIssue><Title>Archives of surgery (Chicago, Ill. : 1960)</Title><ISOAbbreviation>Arch Surg</ISOAbbreviation></Journal><ArticleTitle>Sequential pneumatic compression for lymphedema. A controlled trial.</ArticleTitle><Pagination><MedlinePgn>1116-9</MedlinePgn></Pagination><Abstract><AbstractText>We examined prospectively the effect of a new compression device for lymphedema, which utilizes a short duration and high-pressure cycle, that provides a sequential milking pattern to the limb through multiple compartments. Twenty-five patients (seven patients for upper-extremity and 18 for lower-extremity problems) underwent 24 hours of treatment. All extremities showed a decrease in circumferential measurements with the maximal reduction occurring at the wrist (45%) for the upper extremities and at the mid-calf (47%) for the lower extremities. Lower-extremity leg volume was reduced by 45%. Despite the high pressures no elevation in serum muscle enzyme levels was noted. This device reduced lymphedematous limbs rapidly and safely.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Richmand</LastName><ForeName>D M</ForeName><Initials>DM</Initials></Author><Author ValidYN="Y"><LastName>O'Donnell</LastName><ForeName>T F</ForeName><Initials>TF</Initials><Suffix>Jr</Suffix></Author><Author ValidYN="Y"><LastName>Zelikovski</LastName><ForeName>A</ForeName><Initials>A</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Arch Surg</MedlineTA><NlmUniqueID>9716528</NlmUniqueID><ISSNLinking>0004-0010</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>EC 2.6.1.1</RegistryNumber><NameOfSubstance UI="D001219">Aspartate Aminotransferases</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 2.7.3.2</RegistryNumber><NameOfSubstance UI="D003402">Creatine Kinase</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 4.1.2.13</RegistryNumber><NameOfSubstance UI="D005634">Fructose-Bisphosphate Aldolase</NameOfSubstance></Chemical></ChemicalList><CitationSubset>AIM</CitationSubset><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D001219" MajorTopicYN="N">Aspartate Aminotransferases</DescriptorName><QualifierName UI="Q000097" MajorTopicYN="N">blood</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003402" MajorTopicYN="N">Creatine Kinase</DescriptorName><QualifierName UI="Q000097" MajorTopicYN="N">blood</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005069" MajorTopicYN="N">Evaluation Studies as Topic</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005121" MajorTopicYN="N">Extremities</DescriptorName><QualifierName UI="Q000033" MajorTopicYN="N">anatomy & histology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005634" MajorTopicYN="N">Fructose-Bisphosphate Aldolase</DescriptorName><QualifierName UI="Q000097" MajorTopicYN="N">blood</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005676" MajorTopicYN="Y">Gravity Suits</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName><QualifierName UI="Q000201" MajorTopicYN="N">enzymology</QualifierName><QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName><QualifierName UI="Q000628" MajorTopicYN="Y">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008722" MajorTopicYN="N">Methods</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009132" MajorTopicYN="N">Muscles</DescriptorName><QualifierName UI="Q000201" MajorTopicYN="N">enzymology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011446" MajorTopicYN="N">Prospective Studies</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1985</Year><Month>10</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2001</Year><Month>3</Month><Day>28</Day><Hour>10</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1985</Year><Month>10</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">4038053</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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