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      Fluid Shifts Induced by Physical Therapy in Lower Limb Lymphedema Patients

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          Abstract

          Complete decongestive therapy (CDT), a physical therapy including manual lymphatic drainage (MLD) and compression bandaging, is aimed at mobilizing fluid and reducing limb volume in lymphedema patients. Details of fluid shifts occurring in response to CDT are currently not well studied. Therefore, we investigated fluid shifts before, during and after CDT. Thirteen patients (3 males and 10 females, aged 57 ± 8.0 years, 167.2 ± 8.3 cm height, 91.0 ± 23.4 kg weight) diagnosed with stage II leg lymphedema participated. Leg volume, limb and whole-body fluid composition (total body water (limbTBW/%TBW), extracellular (limbECF/%ECF) and intracellular (limbICF/%ICF fluid), as well as ECF/ICF and limbECF/limbICF ratios were determined using perometry and bioelectrical impedance spectroscopy. Plasma volume, proteins, osmolality, oncotic pressure and electrolytes were assessed. Leg volume ( p < 0.001), limbECF ( p = 0.041), limbICF ( p = 0.005) and limbECF/limbICF decreased over CDT. Total leg volume and limbTBW were correlated (r = 0.635). %TBW ( p = 0.001) and %ECF ( p = 0.007) decreased over time. The maximum effects were seen within one week of CDT. LimbICF ( p = 0.017), %TBW ( p = 0.009) and %ICF ( p = 0.003) increased post-MLD, whereas ECF/ICF decreased due to MLD. Plasma volume increased by 1.5% post-MLD, as well as albumin and the albumin-to-globulin ratio ( p = 0.005 and p = 0.049, respectively). Our results indicate that physical therapy leads to fluid shifts in lymphedema patients, with the greatest effects occurring within one week of therapy. Fluid shifts due to physical therapy were also reflected in increased plasma volume and plasma protein concentrations. Perometry, in contrast to bioelectrical impedance analysis, does not seem to be sensitive enough to detect small fluid changes caused by manual lymphatic drainage.

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              Microvascular fluid exchange and the revised Starling principle.

              Microvascular fluid exchange (flow J(v)) underlies plasma/interstitial fluid (ISF) balance and oedematous swelling. The traditional form of Starling's principle has to be modified in light of insights into the role of ISF pressures and the recognition of the glycocalyx as the semipermeable layer of endothelium. Sum-of-forces evidence and direct observations show that microvascular absorption is transient in most tissues; slight filtration prevails in the steady state, even in venules. This is due in part to the inverse relation between filtration rate and ISF plasma protein concentration; ISF colloid osmotic pressure (COP) rises as J(v) falls. In some specialized regions (e.g. kidney, intestinal mucosa), fluid absorption is sustained by local epithelial secretions, which flush interstitial plasma proteins into the lymphatic system. The low rate of filtration and lymph formation in most tissues can be explained by standing plasma protein gradients within the intercellular cleft of continuous capillaries (glycocalyx model) and around fenestrations. Narrow breaks in the junctional strands of the cleft create high local outward fluid velocities, which cause a disequilibrium between the subglycocalyx space COP and ISF COP. Recent experiments confirm that the effect of ISF COP on J(v) is much less than predicted by the conventional Starling principle, in agreement with modern models. Using a two-pore system model, we also explore how relatively small increases in large pore numbers dramatically increase J(v) during acute inflammation.
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                Author and article information

                Journal
                J Clin Med
                J Clin Med
                jcm
                Journal of Clinical Medicine
                MDPI
                2077-0383
                16 November 2020
                November 2020
                : 9
                : 11
                : 3678
                Affiliations
                [1 ]Physiology Division, Otto Loewi Research Center, Gravitational Physiology and Medicine Research Unit, Medical University of Graz, 8036 Graz, Austria; bianca.brix@ 123456medunigraz.at (B.B.); andreas.roessler@ 123456medunigraz.at (A.R.); karin.schmid@ 123456medunigraz.at (K.S.-Z.); helmut.hinghofer@ 123456medunigraz.at (H.H.-S.)
                [2 ]Physical Medicine and General Rehabilitation Department, KABEG, Wolfsberg Site, 9400 Wolfsberg, Austria; gert.apich@ 123456kabeg.at
                [3 ]Wolfsberg Clinical Center for Lymphatic Disorders, Wolfsberg State Hospital, KABEG, 9400 Wolfsberg, Austria; christian.ure@ 123456kabeg.at
                Author notes
                [* ]Correspondence: nandu.goswami@ 123456medunigraz.at ; Tel.: +43-316-385-73852
                Author information
                https://orcid.org/0000-0002-7308-5450
                https://orcid.org/0000-0002-3422-0031
                Article
                jcm-09-03678
                10.3390/jcm9113678
                7697258
                33207688
                73a45f95-6e8e-4fa3-bcc9-83764f19a016
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 18 September 2020
                : 12 November 2020
                Categories
                Article

                lymph,lymphatic flow,complete decongestive therapy,lymphatic drainage

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