[Mercury pressotherapy in the treatment of lymphedema].
Identifieur interne : 005E71 ( PubMed/Curation ); précédent : 005E70; suivant : 005E72[Mercury pressotherapy in the treatment of lymphedema].
Auteurs : C J CartierSource :
- Journal des maladies vasculaires [ 0398-0499 ] ; 1990.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical : Mercury.
- therapy : Lymphedema, Vascular Diseases.
- Arm, Clinical Protocols, Equipment Design, Gravity Suits, Humans, Leg, Methods.
Abstract
Increasingly growing pressure gradients impressed upon a limb maintained vertically positioned in mercury (metal) have been used as an individually-adjusted compressive, evacuating and atraumatic mould in lymphatic or venolymphatic disease of the limbs. We studied this new so-called mercury pressure-therapy applied to 100 cases of lymphedema of the upper extremity, 100 cases of lymphedema of the lower extremity, 150 cases of inflammatory hypodermitis of the leg and 50 refractory venous ulcers. During the first trials, the patients were treated with a prototype, then with a model of the latest version of the Gradient-1000 device (fig. 1), allowing for mercury displacement along the limb controllable by 6 parameters. During experimentation, we used the following methodology: 1) Each patient's treatment consisted in 3 to 4 compression sessions at 3 to 8 day intervals. Later, the patient was followed up for 3 to 6 months and received 1 to 2 additional pressure treatments, as deemed necessary. 2) Each session comprised 30 minutes of actual compression by several rising mercury waves falling back to the zero level each time, using the following criteria: slow velocities (1 to 2 cm/second), progressively higher rising levels (45 to 70, even 80 cm), each level upheld for 3 to 5 minutes, few repeated up and down phases (6 to 10, depending upon the duration of each phase). 3) In between the compression sessions, the patient wore a compressive elastic bandage permanently. 4) The first 3 to 4 compression sessions constituted the initial treatment; the patient was then fit with a removable elastic bandage to be worn 12/24 hours.(ABSTRACT TRUNCATED AT 250 WORDS)
PubMed: 2212872
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C J Cartier<affiliation><nlm:affiliation>Cabinet Médical, Châtearoux.</nlm:affiliation><wicri:noCountry code="subField">Châtearoux</wicri:noCountry></affiliation>Le document en format XML
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We studied this new so-called mercury pressure-therapy applied to 100 cases of lymphedema of the upper extremity, 100 cases of lymphedema of the lower extremity, 150 cases of inflammatory hypodermitis of the leg and 50 refractory venous ulcers. During the first trials, the patients were treated with a prototype, then with a model of the latest version of the Gradient-1000 device (fig. 1), allowing for mercury displacement along the limb controllable by 6 parameters. During experimentation, we used the following methodology: 1) Each patient's treatment consisted in 3 to 4 compression sessions at 3 to 8 day intervals. Later, the patient was followed up for 3 to 6 months and received 1 to 2 additional pressure treatments, as deemed necessary. 2) Each session comprised 30 minutes of actual compression by several rising mercury waves falling back to the zero level each time, using the following criteria: slow velocities (1 to 2 cm/second), progressively higher rising levels (45 to 70, even 80 cm), each level upheld for 3 to 5 minutes, few repeated up and down phases (6 to 10, depending upon the duration of each phase). 3) In between the compression sessions, the patient wore a compressive elastic bandage permanently. 4) The first 3 to 4 compression sessions constituted the initial treatment; the patient was then fit with a removable elastic bandage to be worn 12/24 hours.(ABSTRACT TRUNCATED AT 250 WORDS)</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">2212872</PMID><DateCreated><Year>1990</Year><Month>11</Month><Day>21</Day></DateCreated><DateCompleted><Year>1990</Year><Month>11</Month><Day>21</Day></DateCompleted><DateRevised><Year>2013</Year><Month>11</Month><Day>21</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0398-0499</ISSN><JournalIssue CitedMedium="Print"><Volume>15</Volume><Issue>3</Issue><PubDate><Year>1990</Year></PubDate></JournalIssue><Title>Journal des maladies vasculaires</Title><ISOAbbreviation>J Mal Vasc</ISOAbbreviation></Journal><ArticleTitle>[Mercury pressotherapy in the treatment of lymphedema].</ArticleTitle><Pagination><MedlinePgn>277-81</MedlinePgn></Pagination><Abstract><AbstractText>Increasingly growing pressure gradients impressed upon a limb maintained vertically positioned in mercury (metal) have been used as an individually-adjusted compressive, evacuating and atraumatic mould in lymphatic or venolymphatic disease of the limbs. We studied this new so-called mercury pressure-therapy applied to 100 cases of lymphedema of the upper extremity, 100 cases of lymphedema of the lower extremity, 150 cases of inflammatory hypodermitis of the leg and 50 refractory venous ulcers. During the first trials, the patients were treated with a prototype, then with a model of the latest version of the Gradient-1000 device (fig. 1), allowing for mercury displacement along the limb controllable by 6 parameters. During experimentation, we used the following methodology: 1) Each patient's treatment consisted in 3 to 4 compression sessions at 3 to 8 day intervals. Later, the patient was followed up for 3 to 6 months and received 1 to 2 additional pressure treatments, as deemed necessary. 2) Each session comprised 30 minutes of actual compression by several rising mercury waves falling back to the zero level each time, using the following criteria: slow velocities (1 to 2 cm/second), progressively higher rising levels (45 to 70, even 80 cm), each level upheld for 3 to 5 minutes, few repeated up and down phases (6 to 10, depending upon the duration of each phase). 3) In between the compression sessions, the patient wore a compressive elastic bandage permanently. 4) The first 3 to 4 compression sessions constituted the initial treatment; the patient was then fit with a removable elastic bandage to be worn 12/24 hours.(ABSTRACT TRUNCATED AT 250 WORDS)</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Cartier</LastName><ForeName>C J</ForeName><Initials>CJ</Initials><AffiliationInfo><Affiliation>Cabinet Médical, Châtearoux.</Affiliation></AffiliationInfo></Author></AuthorList><Language>fre</Language><PublicationTypeList><PublicationType UI="D004740">English Abstract</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><VernacularTitle>Pressothérapie au mercure dans le traitement du lymphoedème.</VernacularTitle></Article><MedlineJournalInfo><Country>France</Country><MedlineTA>J Mal Vasc</MedlineTA><NlmUniqueID>7707965</NlmUniqueID><ISSNLinking>0398-0499</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>FXS1BY2PGL</RegistryNumber><NameOfSubstance UI="D008628">Mercury</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D001132" MajorTopicYN="Y">Arm</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002985" MajorTopicYN="N">Clinical Protocols</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004867" MajorTopicYN="N">Equipment Design</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005676" MajorTopicYN="Y">Gravity Suits</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007866" MajorTopicYN="Y">Leg</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName><QualifierName UI="Q000628" MajorTopicYN="Y">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008628" MajorTopicYN="N">Mercury</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008722" MajorTopicYN="N">Methods</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014652" MajorTopicYN="N">Vascular Diseases</DescriptorName><QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1990</Year><Month>1</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1990</Year><Month>1</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1990</Year><Month>1</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">2212872</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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