A comparative evaluation of the efficacy of complete decongestive therapy in the treatment of unilateral breast cancer–related lymphedema with and without metabolic syndrome
Supportive Care in Cancer, ISSN: 1433-7339, Vol: 32, Issue: 7, Page: 473
2024
- 1Citations
- 15Captures
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Metrics Details
- Citations1
- Citation Indexes1
- Captures15
- Readers15
- 15
Article Description
Aim: This study aimed to investigate the effect of the presence of metabolic syndrome (MetS) on the limb volume and quality of life (QoL) of patients who underwent complex decongestive therapy (CDT) due to unilateral breast cancer-related lymphedema (BCRL). Methods: Forty female patients with unilateral BCRL, of whom 20 had MetS (MetS group) and 20 did not have MetS (control group), were included in the study. The participants received CDT 5 days a week for 3 weeks. The participants’ limb volume (percentage of excess volume (PEV) and percentage reduction of excess volume (PREV) was determined using a tape measure, and their QoL was assessed using the Lymphedema Quality of Life questionnaire (LYMQoL) before and after treatment. Results: After the treatment, the PEV and PREV values and LYMQoL-symptoms scores of the patients improved (p < 0.05); however, the LYMQoL-function, appearance/body image, mood/emotions, and overall QoL scores did not change in the MetS group (p > 0.05). In the control group, the PEV and PREV values and the LYMQoL-appearance/body image, mood/emotions, and overall QoL scores improved (p < 0.05), but the LYMQoL-symptoms and LYMQoL-function scores did not change (p > 0.05). There was a greater increase in the post-treatment PEV and PREV values of the control group compared to the MetS group (p < 0.001). Conclusion: The study yielded that CDT was an effective treatment in BCRL with and without MetS; however, the improvement was greater in BCRL cases without MetS than in those with MetS. Therefore, the presence of MetS should be taken into account in the treatment of lymphedema in patients who develop BCRL. Trial registration: ClinicalTrials.gov, identifier: NCT05426993. Registered 2022–06-16. https://clinicaltrials.gov/search?cond=NCT05426993.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85197577865&origin=inward; http://dx.doi.org/10.1007/s00520-024-08676-z; https://clinicaltrials.gov/ct2/show/NCT05426993; http://www.ncbi.nlm.nih.gov/pubmed/38949715; https://link.springer.com/10.1007/s00520-024-08676-z; https://dx.doi.org/10.1007/s00520-024-08676-z; https://link.springer.com/article/10.1007/s00520-024-08676-z
Springer Science and Business Media LLC
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