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Original Article Short-Term Effects Of Dry Heat Treatment (Fluidotherapy) In The Management Of Breast Cancer Related Lymphedema: A Randomized Controlled Study Burcu Duyur Çakıt, 1 Seçil Pervane Vural 2 Abstract In this study, we aimed to investigate whether fluidotherapy added to complete decongestive therapy (CDT) would provide additional contribution to edema reduction in patients with breast cancer-related lymphedema (BCRL). CDT alone and CDT + fluidotherapy in combined manner performed daily for 3 weeks. Fluidotherapy added to CDT treatment provided more improvement in pain and edema severity compared to standard CDT in BCRL patients without any side effects. Background: To investigate whether fluidotherapy added to complete decongestive therapy (CDT) would provide additional contribution to edema reduction in patients with breast cancer related lymphedema (BCRL). Material and Methods: Thir thy-t wo patients with unilateral BCRL were randomly divided into 2 groups: standard treatment with CDT only (Group 1) and CDT + fluidotherapy (Group 2). All patients underwent phase 1 CDT, which included manual lymphatic drainage, multilayer bandaging, supervised exercises and skin care for a total of 15 sessions, 5 times a week for 3 weeks. Only Group 2 received a total of 15 sessions application of fluidotherapy. Before and after CDT, patients were evaluated for extremity volumes and excess volumes, according to circumferencial measurements of the extrem- ity. Arm pain was evaluated with Visual Analaogue Scale (VAS-Pain). Results: Seventeen patients in Group 1 and 15 patients in Group 2 completed the study. Patients’ demographic data and volume measurements were similar at the beginning of the treatment. Limb volumes of both groups were significantly reduced after treatment ( Pmonths had passed since the follow-up patients last received CDT. Patients had either breast-conserving surgery or mastectomy. Written informed consent was obtained from all patients and ethical approval was obtained from the local ethics committee before the study. The procedures followed were in accordance with the ethical standards Clinical Breast Cancer July 2024 of the national human experimentation committee and the princi- ples of the Helsinki Declaration of 1975, revised in 2008. Forty-five volunteer female patients who developed stage 2-3 upper extrem- ity lymphedema after breast cancer treatment were included in the study. Inclusion criteria were unilateral lymphedema following breast cancer treatment and a volume difference of more than 10% or a circumference difference of more than 2 cm between the 2 arms. Patients with the following characteristics were excluded: bilateral breast cancer, bilateral lymphedema, distant metastases, acute deep vein thrombosis, clinical or radiographic evidence of cancer, extrem- ity too large to be placed in the curing cabinet. Five patients did not meet the inclusion criteria. Using a random number table, 40 patients in the study were randomly divided into 2 groups: standard treatment with CDT only (Group 1) and CDT + fluidotherapy (Group 2). During the treatment of lymphedema, active infection was detected in 3 patients, 3 patients were dropped out due to social problems and 2 patients were dropped out for unknown reasons. Therefore, 8 patients were excluded from the analysis. As a result, a total of 32 patients were included in the final analysis ( Figure 1 ). Measurements The presence of lymphedema was assessed by inter-limb volume difference ( > 10%) based on the serial circumferential measurements in both affected and nonaffected extremities or a circumference difference of more than 2 cm between the 2 arms. 19 During the circumferential measurements, patients sat straight on a chair with their arms relaxed by their sides and elbows straight. Measurements were made in both arms at the beginning and at the end of the 3-week treatment. Circumferential measurements were performed by a standard 1-inch retractable tape, starting at the level of ulnar styloid, at 4 cm intervals along the arms and converted to an approx- imate arm volume to enable estimation of volume. 20 , 21 Extrem- ity volumes were calculated using the truncated cone formula. The excess percentage limb volume was expressed in a percentage reduc- tion in edema of the affected limb, which was calculated using standard methods. Excess limb volume represented the difference between both limbs and was expressed in mL. 21 Each patient was assessed by a single researcher who was blinded to the group allocation. The stages of lymphedema are determined according to Interna- tional Society of Lymphology (ISL). 19 ISL staging ranges from 0 to 3 and involves 2 criteria: the “softness” or “firmness” of the limb (reflecting fibrotic soft tissue changes) and the outcome after eleva- tion. Within stages 1 through 3, severity based upon volume differ- ences is determined as mild ( 40%). Patients were asked to report their ’average pain intensity in their affected arm over the previous week by using Visual Analog Scale (VAS-Pain) in which 0 indicates no pain, 10 indicates the worst pain. Complete Decongestive Therapy All patients were included in the intensive phase of the CDT protocol consisting of MLD, short stretch multilayer bandage, skin care and lymphedema exercises. Patients received a total of 15 sessions of treatment 5 days a week for 3 weeks. First, MLD Burcu Duyur Çakıt, Seçil Pervane Vural Figure 1 Flowchart of the study. was applied by the same physiotherapist according to the Vodder technique for 45-60 minutes. After MLD, a nonelastic, short- stretch, multilayer bandaging treatment was applied by the same experienced physiotherapist. Multilayer compression bandages were applied with the highest pressure to the distal regions and gradu- ally decreasing the pressure towards the proximal regions. 22 After bandaging, all patients underwent a 15-minute individualized active exercise program under the supervision of the same physiothera- pist. Exercises included neck and shoulder stretching, abdominal breathing exercise and strengthening of the arm muscles to facilitate lymphatic flow, increase strength, and range of motion. 23 Patients were asked to keep the compression bandage on the arm for 22-23 hours a day. Fluidotherapy Application Before the application, the patient washed her upper extremities and removed all jewelry. The patient was then positioned so that the area to be treated was comfortable and relaxed. The affected limb placed inside the sheath and closed tightly around the proximal arm ( Figure 2 ). Only the subjects Group 2 received a total of 15 sessions (5 sessions per week) application of fluidotherapy device (Fizyoflug by Fizyomed) which was used for fluidotherapy at a temperature of 42 °C for 20 minutes in continuous mode before the CDT program. Volumetric mesasurements and VAS-Pain evaluation were done before CDT and end of the 15 treatment sessions. Statistical Analysis Statistical analysis was performed using the IBM SPSS version 22.0 software (IBM Corp., Armonk, NY, USA). Descriptive data were presented in mean ± standard deviation (SD) or median (min-max) for continuous variables or in number and percentage for categorical variables. The chi-square or Fisher’s exact tests were used for the difference of categorical variables between the groups. The Kolmogorov-Smirnov and Levene’s tests were used to indicate normal distribution and homogeneity of the variance, respec- Clinical Breast Cancer July 2024 441 Term Effects Of Dry Heat Treatment (Fluidotherapy) In The Management Figure 2 Application of fluidotherapy. 442 tively. The differences between numerical variables of 2 indepen- dent groups were assessed by the independent samples t-test or MannWhitney U test. The Wilcoxon test was carried out to assess differences between before and after treatment. A P value of value of .05). Lymphedema stages, disease duration, type of surgery, adjunctive therapies, lymphedema volumes, and pretreatment pain levels were similar in both groups ( P > .05). Limb volumes of both groups were significantly reduced after treatment ( Pwe can say that fluidotherapy added to CDT treatment provided more improvement in pain and edema severity compared to standard CDT in BCRL patients. To the best of our knowledge, this is the first study in which fluidother- apy was used in addition to CDT in patients with BCRL. No worsening of lymphedema volume or side effects were detected in any of the patients. We observed that the addition of fluidother- apy, which can be easily applied to the upper extremity, to CDT in BCRL patients may provide additional benefit in pain and volume reduction. Heat is a powerful therapeutic agent. It increases blood flow, increases heart rate, reduces blood pressure, sedates, and provokes healing by accelerating biochemical reactions. There are studies using microwave as a thermotherapy modality in lymphedema. One of them is the study by Gan et al. 11 In 40 of 45 postmastectomy lymphedema patients, they found significant reduction in periph- eral edema and secondary acute erysipelas attacks after microwave therapy. They also reported improvement in skin elasticity. 11 One of the largest and oldest studies investigating heat therapies for lymphedema is the study by Liu et al. 24 In this study, microwave and hot water immersion methods were used as heat modalities. Skin biopsies were performed before and after treatment in patients with lower extremity lymphedema and lymphoscintigraphy was also performed to evaluate lymphatic flow. At the end of the study, they found a decrease in limb circumference and volume, but no change Burcu Duyur Çakıt, Seçil Pervane Vural Table 1 The Demographic and Clinical Characteristics in Both Patient Groups Group 1 CDT N = 17 Group 2 CDT + Fluidoterapy N = 15 P Age (year) 59.23 ± 11.86 61.92 ± 12.41 > .05 BMI (kg/m2 ) 29.33 ± 3.67 28.96 ± 9.54 > .05 Type of surgery n(%) > .05 Mastectomy Lumpectomy 11 (64.7) 6 (35.3) 10 (66.6) 5 (33.4) Adjunctive Therapies n(%) > .05 Chemotherapy Radiotherapy Hormonal therapy 12 (70.5) 10 (58.8) 14 (82.3) 10 (66.6) 9 (60) 13 (86.6) Type of lymphedema n(%) > .05 Subclinic Reversible Spontaneous Irreversible 0 4(23.5) 13(76.4) 0 3(20) 12(80) Elephantiasis 0 0 Stage of lymphedema > .05 1 Mild 2 Moderate 3 Severe 3(17.6) 13(76.4) 1(5.8) 2(13.3) 12(80) 1(6.6) Lymphedema disease duration (months) 17.47 ± 14.51 17.68 ± 14.53 > .05 Lymphedema excess volume before treatment (ml) 3245.11 ± 826.34 3190.61 ± 812.90 > .05 Lymphedema excess percentage volume before treatment (%) 33.88 ± 28.31 39.69 ± 25.77 > .05 VAS-Pain before treatment 5.41 ±1.76 5.23 ± 1.64 > .05 VAS = Visual Analogue Scale, CDT = Complete decongestive therapy, BMI = Body mass index. Table 2 The Extremity Volumes, VAS-Pain Mean Values After Treatment and the Mean Change in Volume in Both Patient Groups Measurements and VAS-Pain Score Before and After Treatment Group 1 CDT N = 17 Group 2 CDT + Fluidoterapy N = 15 P 1 P 2 P 3 Lymphedema excess volume after treatment 2801.17 ± 831.37 2525.61 ± 709.12 > .05 .0001 .001 Lymphedema excess volume change 443.94 ± 235.62 665.00 ± 238.47 .028 Lymphedema excess percentage volume after treatment 21.80 ± 20.29 19.65 ± 19.97 > .05 .0001 .001 Lymphedema excess percentage volume change 12.07 ± 9.95 20.03 ± 7.93 .001 VAS-Pain after treatment 3.29 ± 1.79 1.84 ± 0.68 .039 .001 .001 VAS-Pain change 2.11 ± 1.26 3.38 ± 1.26 .020 P 1 : intergroup difference after treatment. P 2 : Group 1 P values before and after treatment. P 3 : Group 2 P values before and after treatment. VAS = Visual Analogue Scale, CDT = Complete decongestive therapy. in lymphatic flow evaluated by lymphoscintigraphy. Changes in skin biopsies were similar in microwave and hot water immersion groups. They showed that the most striking histopathologic changes after hyperthermic treatment were reduction of perivascular cell infiltra- tion, disappearance of free fluids (lymphatic lakes) in the tissues and dilatation of blood capillaries in the subcutis. Microwave derives from oscillating free charges or ions, rotating polar molecules, and the quantum effect of excitation of molecules in the living system. They hypothesized that these effects may alter large molecules and make it easier for them to be mobilized or produce internal macro- molecular rearrangement with denaturation and breakup. With heat, increased capillary infiltration of liquid may be greater than that of protein with an overall decrease in viscosity of tissue fluid. As a result, the polarized fragments of macromolecules and other wastes Clinical Breast Cancer July 2024 443 Term Effects Of Dry Heat Treatment (Fluidotherapy) In The Management 444 may more easily be transported into blood capilleries. They hypoth- esized that regional heating causes an altered immune response, changes in extracellular matrix protein composition, and greater elasticity of tissues leading to reduced edema. 24 In our study, we found that BCRL patients benefited more from heat therapy added to CDT than CDT alone. We think that the addition of heat thera- pies to CDT may potentialize the effects of CDT. Our results, in accordance with the literature, suggest that increased perfusion in tissues with the effect of heat does not increase lymphatic load, on the contrary, it may decrease it. Based on these theories, we suggest that fluidotherapy may similarly stimulate ion release by creating vibrational effects, which may lead to denaturation of macromolecules and degradation of proteins. Then, smaller pieces of macromolecules can be easily absorbed by tissues. This effect may provide an inflammation- reducing effect in the treatment of lymphedema, which in-turn may reduce the severity of lymphedema. However, further histopatho- logic studies are needed to prove these theories. Fluidotherapy is a heat modality consisting of finely divided solid particles suspended in a heated air providing a dry whirlpool system. Borrell et al. reported that hand fluidotherapy treatment at 46.2 °C resulted in a 6-fold increase in blood flow and a 4-fold increase in metabolic rates (measured by oxygen uptake) in a healthy young man. In their study, they compared the effect of fluidother- apy with other superficial heat modalities using in vivo temperature measurements. The greatest temperature increase was obtained with fluidotherapy (9 °C and 5.7 °C) compared with articular capsule and muscle temperature paraffin (7.5 °C and 4.5 °C) and hydrother- apy (6 °C and 4.3 °C), respectively. Dry whirlpool (fluidotherapy) provides much more heat than paraffin or hydrotherapy because higher temperatures can be tolerated in a dry environment. Data from the Borrell et al. study shows that surface heating methods are much more effective at generating high temperatures than ultra- sound therapy or diathermy at depths of up to 1.2 cm. 25 In the light of these informations, we chose fluidotherapy as a heat modality in BCRL patients because we think that it may be more effective in increasing blood flow and raising hand temperature in the treatment of lymphedema in the skin-subcutaneous area. We found that it is effective in the treatment of edema and pain when added to CDT in the treatment of BCRL. Patient compliance was very good and ease of use was among the advantages of fluidotherapy. Fluidotherapy not only increases tissue temperature but also provides tactile stimulus to the treated extremity. Thanks to this tactile stimulus, according to Melzack and Wall’s gate control theory, activation of large diameter cutaneous afferent nerve fibers by bombardment with synthetic cellulose fragments canreduce pain transmission to the brain. 26 Cellulose particles, which form a fluidized bed, are circulated around the extremities by hot air. Fluidotherapy provides 3 times more heat transfer than copper bars and heats muscle tissue 20%-50% more than warm water or wax baths. Patients’ tolerance of high temperatures in a fluidized bed (fluidotherapy) may be due to convective air movement and the high thermal conductivity of cellulose particles. Increased temper- ature tolerance occurs because cellulose particles over-stimulate skin thermoreceptors and mechanoreceptors, reducing pain sensitivity. Clinical Breast Cancer July 2024 Moreover dry heat reduces thermal irritation at high tempera- tures. 27 In our study, BCRL patients tolerated the high tempera- tures provided by fluidotherapy very well. When this dry heat was applied in addition to CDT treatment, BCRL patients experienced a decrease in limb volume rather than an increase in limb volume. Contrary to popular belief, we think that the increase in venous return by heat effect may not increase the lymphatic load; on the contrary, the increase in venous return may decrease the lymphatic load. Özcan et al. used fluidotherapy in patients with subacute poststroke complex regional pain syndrome. A total of 15 sessions, 40 °C 20 minutes in continuous mode, were used in addition to the conventional rehabilitation program. They evaluated limb volumes using a water displacement method. They reported a more signif- icant decrease in limb volumes in the group receiving fludother- apy compared to the group receiving only conventional treatment. 18 In a similar study, Han et al. evaluated the effect of fluidotherapy on activities of daily living, dexterity and edema in stroke patients. They reported that fluidotherapy causes a decrease in edema and this decrease can contribute to activities of daily living. 17 Neurogenic inflammation, nociceptive sensitization, vasomotor dysfunction has been blamed as the cause of edema in complex regional pain, but the pathophysiology has not been fully elucidated. 28 Lymphatic stasis and edema may also be seen in CRPS due to disuse, primary pathol- ogy, or surgery for primary pathology. Therefore, the beneficial effects of fluidotherapy on CPRS edema made us think that it may produce similar improvement in lymphedema. In addition, the case report showing that MLD, the main component of CBT, is benefi- cial in the treatment of edema of the hand and upper extremity complex regional pain syndrome 29 and the benefit of post-traumatic edema from MLD 30 and fluidotherapy 31 suggest that similar treat- ments can be used in treatment and fluidotherapy may be beneficial in both edema. We used the dose and duration of fluidotherapy at the doses and durations used in the CPRS studies and obtained positive results in BCRL patients. Another treatment that has been tried in BCRL patients is far- infrared ray (FIR) therapy. It has been reported that FIR poten- tially reduces extremity fluid volume and extremity diameter, and also reduces dermatolymphangitis attacks. There were no differ- ences in cancer recurrence rates or tumor markers when BCRL patients who received FIR treatment were compared to controls after 1 year. Furthermore, the in vitro experiment indicated that FIR radiation does not affect viability, proliferation, cell cycle, and apoptosis of fibroblasts, human breast adenocarcinoma cells. 32 The conclusion we may draw from these studies is that heat treatments are oncologically safe, do not worsen lymphedema, on the contrary, they can reduce edema and make an additional contribution to CDT. Today, when lymphedema treatments do not provide a cure and medical and surgical modalities are insufficient, we think that thermal treatments may be promising modalities, and especially the use of fluidotherapy in this field may have the potential to make an additional contribution to neuropathic pain. We believe that it may provide significant clinical benefits, especially in patients with neuropathic complaints who cannot tolerate multilayer bandages and compression garments during CDT. Burcu Duyur Çakıt, Seçil Pervane Vural Limitations The main limitations of this study were the small number of the study group and the lack of long-term follow-up. We evaluated the patients before and after the 3-week CDT program, and we could not follow the patients due to the Covid 19 pandemic. Another important limitation was that majority of the patients had moder- ate (stage 2) lymphedema. Because we could not include extremi- ties that were too large to be placed in the cure cabin. So we could not generalize the outcome of our study to patients with all stage lymphedema. We also could not apply sham-fluidotherapy to the control group. Other limitations were the lack of an objective upper extremity function assessment method and ultrasonographic skin- subcutis measurements. Conclusion Fluidotheray added to CDT reduced pain and edema severity more than standard CDT in the patients with BCRL. As a noninva- sive, novel, and effective method, fluidotherapy may be promising treatment modality for the treatment of lymphedema. Therefore, thermotherapy modalities should not be considered contraindicated in the treatment of lymphedema and may have additional benefits with promising results. Further larger randomized controlled trials with long follow-up are needed to demonstrate the effects of fluidotherapy. Clinical Practice Points International guidelines recommend that patients with lymphedema take certain precautions to prevent treatment symptoms and complications. One of these precautions is to avoid temperature changes. It was believed that warming the extremity would increase venous return and increase lymphatic load. However, studies have reported improvement rather than increase in lymphedema with heat therapies, such as microwave, FIR, hot blanket, therapeutic ultrasound. Fludotherapy is a dry heat modality. It has been used in the of CRPS and has been reported to be beneficial in edema. In the light of this information, we applied it to our patients in addition to CDT treatment in BCRL patients. Compared to CDT treatment alone, the reduce in extremity volumes and pain of patients receiving CDT + Fluidotherapy was more significant. There was no increase in lymphedema or side effects. To our knowledge, our study is the first in which fluidotherapy was applied to BCRL patients. As a noninvasive, novel, and effective method, fluidotherapy may be promising treatment modality for the treatment of lymphedema. Therefore, thermotherapy modalities should not be considered contraindicated in the treatment of lymphedema and may have additional benefits with promising results. Funding This research did not receive any specific grant from funding agencies in the public, commercial or not-for-profit sectors. Disclosure No competing financial interest exists. CRediT authorship contribution statement Burcu Duyur Çakıt: Writing – review & editing, Methodology, Investigation, Formal analysis, Data curation, Conceptualization. Seçil Pervane Vural: Writing – original draft, Project administra- tion, Methodology, Investigation. Acknowledgments None. References 1. Liao SF, Li SH, Huang HY, et al. The efficacy of complex decongestive physiother- apy (CDP) and predictive factors of lymphedema severity and response to CDP in breast cancer-related lymphedema (BCRL). Breast . 2013;22:703–706 . 2. Eyigör S, Cinar E, Caramat I, Unlu BK. Factors influencing response to lymphedema treatment in patients with breast cancer-related lymphedema. Support Care Cancer . 2015;23:2705–2710 . 3. Sezgin Ozcan D, Dalyan M, Unsal Delialioglu S, Duzlu U, Polat CS, Koseoglu BF. Complex decongestivetherapy enhances upper limb functions in patients with breast cancer-related lymphedema. Lymphat Res Biol . 2018;16(5):446–452. doi: 10. 1089/lrb.2017.0061 . 4. Borman P, Yaman A, Yasrebi S, Pınar İnanlı A, Arıkan Dönmez A. Combined complete decongestive therapy reduces volume and improves quality of life and functional status in patients with breast cancer-related lymphedema. Clin Breast Cancer . 2022;22(3):e270–e277. doi: 10.1016/j.clbc.2021.08.005 . 5. Stuiver MM, Ten Tusscher MR, Agasi-idenburg CS, et al. Conservative inter- ventions for preventing clinically detectable upper-limb lymphoedema in patients who are at risk of developing lymphoedema after breast cancer therapy. Cochrane Database Syst Rev . 2015(2):CD009765 . 6. Moffatt CD D, Morgan P. international Consensus . Best practice for the manage- ment of lymphoedema. London: Framework, l. ltd M.; 2006 . 7. National lymphedema Network. Risk Reduction Practices . New York: National lymphedema Network; 2022 . Available from: https://lymphnet. org/risk- reduction- practices 8. Dell DD, Doll C. Caring for a patient with lymphedema. Nursing (Lond) . 2006;36(6):49–51. doi: 10.1097/00152193- 200606000- 00041 . 9. Cemal Y, Pusic A, Mehrara BJ. Preventative measures for lymphedema: separating fact from fiction. J Am coll Surg . 2011;213(4):543–551 . 10. Hill JE, Whitaker JC, Sharafi N, et al. The effectiveness and safety of heat/cold therapy in adults with lymphoedema: systematic review. Disabil Rehabil . 2023;10:1–12 . 11. Gan JL, Li SL, Cai RX, Chang TS. Microwave heating in the management of postmastectomy upper limb lymphedema. Ann Plast Surg . 1996;36(6):576–580 discussion 580–1 . 12. Li K, Liu NF, Zhang YX. Therapeutic effects of far-infrared ray in treating chronic lower extremity lymphedema with dermatolymphangioadenitis. J Shanghai Jiaotong Univ (Med Sci) . 2018;38(9):1059–1065 . 13. Balzarini A, Pirovano C, Diazzi G, et al. Ultrasound therapy of chronic arm lymphedema after surgical treatment of breast cancer. Lymphology . 1993;26(3):128–134 . 14. Campisi C, Boccardo F, Tacchella M. Use of thermotherapy in management of lymphedema: clinical observations. Int J Angiol . 1999;8(1):73–75 . 15. Cameron MH. Thermal agents: physical principles, cold and superficial heat. In: Cameron MH, ed. Physical Agents in Rehabilitation: from Research to Practice . Philadelphia, PA: W.B. Saunders; 1999:163–164 . 16. Herrick RT, Herrick S. Fluidotherapy. Clinical applications and techniques. Ala Med . 1992;61(12):20–25 . 17. Han SW, Lee MS. The effect of fluidotherapy on hand dexterity and activ- ities of daily living in patients with edema on stroke. J Phys Ther Sci . 2017;29(12):2180–2183 . 18. Sezgin Ozcan D, Tatli HU, Polat CS, Oken O, Koseoglu BF. The effectiveness of fluidotherapy in poststroke complex regional pain syndrome: a randomized controlled study. J Stroke Cerebrovasc Dis . 2019;28(6):1578–1585 . 19. Executive Committee of the International Society of LymphologyThe diagnosis and treatment of peripheral lymphedema: 2020 Consensus Document of the Inter- national Society of Lymphology. Lymphology . 2020;53(1):3–19 . 20. Ancukiewicz M, Russell TA, Otoole J, et al. Standardized method for quantifica- tion of developing lymphedema in patients treated for breast cancer. Int J Radiat Oncol Biol Phys . 2011;79(5):1436–1443. doi: 10.1016/j.ijrobp.2010.01.001 . 21. Karges JR, Mark BE, Stikeleather SJ, Worrell TW. Concurrent validity of upper-ex- tremity volume estimates: comparison of calculated volume derived from girth measurements and water displacement volume. Phys Ther . 2003;83(2):134–145 . 22. Zuther JE. Treatment sequences. In: Zuther JE, Norton S, eds. Lymphedema Management. The Comprehensive Guide for Practitioners . New York: Thieme; 2018:311–312 . Clinical Breast Cancer July 2024 445 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0001 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0002 https://doi.org/10.1089/lrb.2017.0061 https://doi.org/10.1016/j.clbc.2021.08.005 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0005 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0006 https://lymphnet.org/risk-reduction-practices https://doi.org/10.1097/00152193-200606000-00041 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0009 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0010 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0011 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0012 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0013 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0014 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0015 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0016 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0017 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0018 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0019 https://doi.org/10.1016/j.ijrobp.2010.01.001 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0021 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0022 Term Effects Of Dry Heat Treatment (Fluidotherapy) In The Management 446 23. Zhang L, Fan A, Yan J, et al. Combining manual lymph drainage with physi- cal exercise after modified radical mastectomy effectively prevents upper limb lymphedema. Lymphat Res Biol . 2016;14(2):104–108. doi: 10.1089/lrb.2015.0036 . 24. Liu NF, Olszewski W. The influence of local hyperthermia on lymphedema and lymphedematous skin of the human leg. Lymphology . 1993;26(1):28–37 . 25. Borrell RM, Parker R, Henley EJ, Masley D, Repinecz M. Comparison of in vivo temperatures produced by hydrotherapy, paraffin wax treatment, and fluidother- apy. Phys Ther . 1980;60(10):1273–1276 . 26. Kelly R, Beehn C, Hansford A, Westphal KA, Halle JS, Greathouse DG. Effect of fluidotherapy on superficial radial nerve conduction and skin temperature. J Orthop Sports Phys Ther . 2005;35(1):16–23. doi: 10.2519/jospt.2005.35.1.16 . 27. Kumar P, McDonald GK, Chitkara R, Steinman AM, Gardiner PF, Giesbrecht GG. Comparison of distal limb warming with fluidotherapy and warm water immersion for mild hypothermia rewarming. Wilderness Environ Med . 2015;26(3):406–411. doi: 10.1016/j.wem.2015.02.005 . Clinical Breast Cancer July 2024 28. Marinus J, Moseley GL, Birklein F, et al. Clinical features and pathophysiology of complex regional pain syndrome. Lancet Neurol . 2011;10(7):637–648. doi: 10. 1016/S1474- 4422(11)70106- 5 . 29. Safaz I, Tok F, Taş kaynatan MA, Ozgul A. Manual lymphatic drainage in management of edema in a case with CRPS: why the(y) wait? Rheumatol Int . 2011;31(3):387–390. doi: 10.1007/s00296- 009- 1187- x . 30. Iannello C, Biller MK. Management of edema using simple manual lymphatic drainage techniques for hand and upper extremity patients. J Hand Ther . 2020;33(4):616–619. doi: 10.1016/j.jht.2018.09.013 . 31. Dorf E, Blue C, Smith BP, Koman LA. Therapy after injury to the hand. J Am Acad Orthop Surg . 2010;18(8):464–473. doi: 10.5435/00124635- 201008000- 00003 . 32. Li K, Xia L, Liu NF, et al. Far infrared ray (FIR) therapy: an effective and oncolog- ical safe treatment modality for breast cancer related lymphedema. J Photochem Photobiol B . 2017;172:95–101 . https://doi.org/10.1089/lrb.2015.0036 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0024 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0025 https://doi.org/10.2519/jospt.2005.35.1.16 https://doi.org/10.1016/j.wem.2015.02.005 https://doi.org/10.1016/S1474-4422(11)70106-5 https://doi.org/10.1007/s00296-009-1187-x https://doi.org/10.1016/j.jht.2018.09.013 https://doi.org/10.5435/00124635-201008000-00003 http://refhub.elsevier.com/S1526-8209(24)00056-9/sbref0032 Short-Term Effects Of Dry Heat Treatment (Fluidotherapy) In The Management Of Breast Cancer Related Lymphedema: A Randomized Controlled Study Introduction Material and Methods Patients Measurements Complete Decongestive Therapy Fluidotherapy ApplicationStatistical Analysis Results Discussion Limitations Conclusion Clinical Practice Points Funding Disclosure CRediT authorship contribution statement Acknowledgments References