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Preoperative assessment enables the early diagnosis and successful treatment of lymphedema.

dc.contributor.authorStout Gergich, Nicole L.en_US
dc.contributor.authorPfalzer, Lucinda A.en_US
dc.contributor.authorMcGarvey, Charlesen_US
dc.contributor.authorSpringer, Barbaraen_US
dc.contributor.authorGerber, Lynn H.en_US
dc.contributor.authorSoballe, Peteren_US
dc.date.accessioned2008-07-01T14:06:47Z
dc.date.available2009-07-06T16:34:52Zen_US
dc.date.issued2008-06-15en_US
dc.identifier.citationStout Gergich, Nicole L.; Pfalzer, Lucinda A.; McGarvey, Charles; Springer, Barbara; Gerber, Lynn H.; Soballe, Peter (2008). "Preoperative assessment enables the early diagnosis and successful treatment of lymphedema." Cancer 112(12): 2809-2819. <http://hdl.handle.net/2027.42/60215>en_US
dc.identifier.issn0008-543Xen_US
dc.identifier.issn1097-0142en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/60215
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18428212&dopt=citationen_US
dc.description.abstractBACKGROUND The incidence of breast cancer (BC)-related lymphedema (LE) ranges from 7% to 47%. Successful management of LE relies on early diagnosis using sensitive measurement techniques. In the current study, the authors demonstrated the effectiveness of a surveillance program that included preoperative limb volume measurement and interval postoperative follow-up to detect and treat subclinical LE. METHODS LE was identified in 43 of 196 women who participated in a prospective BC morbidity trial. Limb volume was measured preoperatively and at 3-month intervals after surgery. If an increase >3% in upper limb (UL) volume developed compared with the preoperative volume, then a diagnosis of LE was made, and a compression garment intervention was prescribed for 4 weeks. Upon reduction of LE, garment wear was continued only during strenuous activity, with symptoms of heaviness, or with visible swelling. Women returned to the 3-month interval surveillance pathway. Statistical analysis was a repeated-measures analysis of variance by time and limb ( P ≤ .001) comparing the LE cohort with an age-matched control group. RESULTS The time to onset of LE averaged 6.9 months postoperatively. The mean (±standard deviation) affected limb volume increase was 83 mL (±119 mL; 6.5% ± 9.9%) at LE onset ( P = .005) compared with baseline. After the intervention, a statistically significant mean 48 mL (±103 mL; 4.1% ± 8.8%) volume decrease was realized ( P < .0001). The mean duration of the intervention was 4.4 weeks (±2.9 weeks). Volume reduction was maintained at an average follow-up of 4.8 months (±4.1 months) after the intervention. CONCLUSIONS A short trial of compression garments effectively treated subclinical LE. Cancer 2008. Published 2008 by the American Cancer Society.en_US
dc.format.extent425450 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCancer Research, Oncology and Pathologyen_US
dc.titlePreoperative assessment enables the early diagnosis and successful treatment of lymphedema.en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelOncology and Hematologyen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumPhysical Therapy Department, University of Michigan-Flint, Flint, Michiganen_US
dc.contributor.affiliationotherBreast Cancer Department, National Naval Medical Center, Bethesda, Maryland ; Fax: (301) 295-9076. ; CLT-LANA, National Naval Medical Center, 8901 Wisconsin Avenue, Building 10, Breast Care Center, fourth Floor West, Bethesda, MD 20889-5600en_US
dc.contributor.affiliationotherRehabilitation Medicine Department, National Institutes of Health, Bethesda, Marylanden_US
dc.contributor.affiliationotherPhysical Therapy Department, Walter Reed Army Medical Center, Bethesda, Marylanden_US
dc.contributor.affiliationotherCollege of Health and Human Services, George Mason University, Fairfax, Virginiaen_US
dc.contributor.affiliationotherBreast Cancer Department, National Naval Medical Center, Bethesda, Marylanden_US
dc.identifier.pmid18428212en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/60215/1/23494_ftp.pdf
dc.identifier.doihttp://dx.doi.org/10.1002/cncr.23494en_US
dc.identifier.sourceCanceren_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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