Multimodality Approach to Lymphedema Surgery Achieves and Maintains Normal Limb Volumes: A Treatment Algorithm to Optimize Outcomes

Peter Deptula, Anna Zhou, Victoria Posternak, Hui He, Dung Nguyen, Peter Deptula, Anna Zhou, Victoria Posternak, Hui He, Dung Nguyen

Abstract

Surgical treatment of advanced lymphedema is challenging and outcomes are suboptimal. Physiologic procedures including lymphaticovenous anastomosis (LVA) and vascularized lymph node transfer (VLNT) improve lymphatic flow but cannot reverse fibrofatty tissue deposition, whereas liposuction removes fibrofatty tissue but cannot prevent disease progression. The adjunctive use of nanofibrillar collagen scaffolds (BioBridgeTM) can promote lymphangiogenesis. We report a treatment algorithm utilizing a multimodality approach to achieve sustained normal limb volumes in patients with stage II-III lymphedema. A retrospective review of late stage II-III lymphedema patients treated with liposuction, physiologic procedures, and BioBridgeTM from 2016 through 2019 was conducted. Treatment outcome in the form of excess volume reduction is reported. Total of 14 patients underwent surgical treatment of late stage II and III lymphedema according to our triple therapy algorithm. Patients had a baseline median volume excess of 29% (19.8, 43.3%). The median volume excess was improved to 0.5% (-4.3, 3.8%) at 14.4 months from the first stage surgery (p < 0.05) and further improved to -1.0% (-3.3, 1.3%) after triple therapy with BB placement at 24.6 months. A triple therapy surgical treatment algorithm can optimize outcomes and achieve sustained normalization of limb volume in late stage II-III lymphedema. The incorporation of nanofibrillar collagen scaffold technology allows for improved and sustained volume reduction.

Keywords: BioBridge; lymphangiogenesis; lymphaticovenous anastomosis; lymphedema; vascularized lymph node transfer.

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Treatment algorithm for Stage II-III lymphedema.
Figure 2
Figure 2
All patients combined demonstrated a median relative volume excess of 29% (19.8, 43.3%). Following liposuction and physiologic procedures, volume excess was 0.5% (−4.3, 3.8%, p < 0.0001). After BB placement and completion of triple therapy surgery, median volume excess was −1 (−3.3, 1.3%, p < 0.0001). Data are presented as median values and IQR. Signficiant values (p < 0.05) are indicated by (***).
Figure 3
Figure 3
Upper extremity excess volume of 24% reduced to 3% at 9 months following combined VLNT and liposuction. BB was implanted at 12 months post-op resulting in the stabilized volume excess of 4% at 21 months following triple therapy surgical management.
Figure 4
Figure 4
Lower extremity with 27% excess volume reduced to 6% at 12 months following VLNT and liposuction. BB placement at 1 year post-op resulted in volume excess improvement to −3% at 24 months following triple therapy surgical management.
Figure 5
Figure 5
Lower extremity with 9% volume excess reduced to −1% at 11 months following VLNT/LVA and liposuction. BB placement at 12 months post-op resulted in −3% volume excess at 23 months following triple therapy surgical management.
Figure 6
Figure 6
Subgroup analysis of patient median volume excess ratio at baseline, after liposuction and physiologic surgery, and after BB placement. Data are presented as median values and IQR. Statistically significant values (p < 0.05) are indicated by an asterisk (*).

References

    1. Brazio P.S., Nguyen D.H. Combined Liposuction and Physiologic Treatment Achieves Durable Limb Volume Normalization in Class II–III Lymphedema: A Treatment Algorithm to Optimize Outcomes. Ann. Plast. Surg. 2021;86:S384–S389. doi: 10.1097/SAP.0000000000002695.
    1. Schaverien M.V., Coroneos C.J. Surgical treatment of lymphedema. Plast. Reconstr. Surg. 2019;144:738–758. doi: 10.1097/PRS.0000000000005993.
    1. Nguyen D.H., Zhou A., Posternak V., Rochlin D.H. Nanofibrillar Collagen Scaffold Enhances Edema Reduction and Formation of New Lymphatic Collectors after Lymphedema Surgery. Plast. Reconstr. Surg. 2021 doi: 10.1097/PRS.0000000000008590. Publish Ahead of Print.
    1. Rochlin D., Inchauste S., Zelones J., Nguyen D.H. The role of adjunct nanofibrillar collagen scaffold implantation in the surgical management of secondary lymphedema: Review of the literature and summary of initial pilot studies. J. Surg. Oncol. 2020;121:121–128. doi: 10.1002/jso.25576.
    1. Nguyen D., Zaitseva T.S., Zhou A., Rochlin D., Sue G., Deptula P., Tabada P., Wan D., Loening A., Paukshto M., et al. Lymphatic regeneration after implantation of aligned nanofibrillar collagen scaffolds: Preliminary preclinical and clinical results. J. Surg. Oncol. 2021;125:113–122. doi: 10.1002/jso.26679.
    1. Sitzia J. Volume measurement in lymphoedema treatment: Examination of formulae. Eur. J. Cancer Care. 1995;4:11–16. doi: 10.1111/j.1365-2354.1995.tb00047.x.
    1. Hadamitzky C., Zaitseva T.S., Bazalova Carter M., Paukshto M.V., Hou L., Strassberg Z., Ferguson J., Matsuura Y., Dash R., Yang P.C., et al. Aligned nanofibrillar collagen scaffolds—Guiding lymphangiogenesis for treatment of acquired lymphedema. Biomaterials. 2016;102:259–267. doi: 10.1016/j.biomaterials.2016.05.040.
    1. Karges J.R., Mark B.E., Stikeleather S.J., Worrell T.W. Concurrent validity of upper-extremity volume estimates: Comparison of calculated volume derived from girth measure- ments and water displacement volume. Phys. Ther. 2003;83:134–145. doi: 10.1093/ptj/83.2.134.
    1. Brorson H., Höijer P. Standardised measurements used to order compression gar- ments can be used to calculate arm volumes to evaluate lymphoedema treatment. J. Plast. Surg. Hand Surg. 2012;46:410–415. doi: 10.3109/2000656X.2012.714785.
    1. Szuba A., Rockson S.G. Lymphedema: Classification, diagnosis and therapy. Vasc. Med. 1998;3:145–156. doi: 10.1177/1358836X9800300209.
    1. Szuba A., Cooke J.P., Yousuf S., Rockson S.G. Decongestive lymphatic therapy for patients with cancer related or primary lymphedema. Am. J. Med. 2000;109:296–300. doi: 10.1016/S0002-9343(00)00503-9.
    1. Casley Smith J.R., Casley Smith J.R. Modern treatment of lymphoedema. I. Complex physical therapy: The first 200 Australian limbs. Australas. J. Dermatol. 1992;33:61–68. doi: 10.1111/j.1440-0960.1992.tb00081.x.
    1. McNeely M.L., Magee D.J., Lees A.W., Bagnall K.M., Haykowsky M., Hanson J. The addition of manual lymph drainage to compression therapy for breast cancer related lymphedema: A randomized controlled trial. Breast Cancer Res. Treat. 2004;86:95–106. doi: 10.1023/B:BREA.0000032978.67677.9f.
    1. Rockson S.G. Current concepts and future directions in the diagnosis and management of lymphatic vascular disease. Vasc. Med. 2010;15:223–231. doi: 10.1177/1358863X10364553.
    1. Brorson H., Svensson H. Complete reduction of lymphoedema of the arm by lipo- suction after breast cancer. Scand. J. Plast. Reconstr. Surg. Hand Surg. 1997;31:137–143. doi: 10.3109/02844319709085480.
    1. Frick A., Hoffmann J.N., Baumeister R.G., Putz R. Liposuctiontechnique and lymphatic lesions in lower legs: Anatomic study to reduce risks. Plast. Reconstr. Surg. 1999;103:1868–1873. doi: 10.1097/00006534-199906000-00009.
    1. Hoffmann J.N., Fertmann J.P., Baumeister R.G., Putz R., Frick A. Tumescent and dry liposuc- tion of lower extremities: Differences in lymph vessel injury. Plast. Reconstr. Surg. 2004;113:718–724, 725–726. doi: 10.1097/01.PRS.0000101506.84361.C9.
    1. Campisi C.C., Ryan M., Boccardo F., Campisi C. Fibro-lipo-lymph-aspiration with a lymph vessel sparing procedure to treat advanced lymphedema after multiple lymphatic-venous anastomoses: The complete treatment protocol. Ann. Plast. Surg. 2017;78:184–190. doi: 10.1097/SAP.0000000000000853.
    1. Liu N.F., Lu Q., Jiang Z.H., Wang C.G., Zhou J.G. Anatomic and functional evaluation of the lym- phatics and lymph nodes in diagnosis of lymphatic circulation disorders with con- trast magnetic resonance lymphangiography. J. Vasc. Surg. 2009;49:980–987. doi: 10.1016/j.jvs.2008.11.029.
    1. O'Brien B., Khazanchi R.K., Kumar P.V., Dvir E., Pederson W. Liposuction in the treatment of lymphoedema; a preliminary report. Br. J. Plast. Surg. 1989;42:530–533. doi: 10.1016/0007-1226(89)90039-8.
    1. Hoffner M., Ohlin K., Svensson B., Manjer J., Hansson E., Troëng T., Brorson H. Liposuction gives complete reduction of arm lymphedema following breast cancer treatment—A 5-year prospective study in 105 patients without recurrence. [(accessed on 7 April 2020)];Plast. Reconstr. Surg. Glob. Open. 2018 6:e1912. doi: 10.1097/GOX.0000000000001912. Available online:
    1. Brorson H. Liposuction normalizes lymphedema induced adipose tissue hypertro- phy in elephantiasis of the leg—A prospective study with a ten-year follow-up. Plast. Reconstr. Surg. 2015;136:133–134. doi: 10.1097/01.prs.0000472449.93355.4a.
    1. Brorson H., Svensson H., Norrgren K., Thorsson O. Liposuctionreducesarmlymphedema without significantly altering the already impaired lymph transport. Lymphology. 1998;31:156–172.
    1. Becker C., Assouad J., Riquet M., Hidden G. Postmastectomy lymphedema: Long-term re- sults following microsurgical lymph node transplantation. Ann. Surg. 2006;243:313–315. doi: 10.1097/01.sla.0000201258.10304.16.
    1. Nicoli F., Constantinides J., Ciudad P., Sapountzis S., Kiranantawat K., Lazzeri D., Lim S.Y., Nicoli M., Chen P.-Y., Yeo M.S.-W., et al. Free lymph node flap transfer and laser-assisted liposuction: A combined technique for the treatment of moderate up- per limb lymphedema. Lasers Med. Sci. 2015;30:1377–1385. doi: 10.1007/s10103-015-1736-3.
    1. Agko M., Ciudad P., Chen H.-C. Staged surgical treatment of extremity lymph- edema with dual gastroepiploic vascularized lymph node transfers followed by suction-assisted lipectomy—A prospective study. J. Surg. Oncol. 2018;117:1148–1156. doi: 10.1002/jso.24969.
    1. Di Taranto G., Bolletta A., Chen S.H. A prospective study on combined lymphedema surgery: Gastroepiploic vascularized lymph nodes transfer and lymphaticovenous anastomosis followed by suction lipectomy. Microsurgery. 2021;41:34–43. doi: 10.1002/micr.30641.

Source: PubMed

3
Suscribir