TY - JOUR
T1 - Global Consensus on the Management of Limbal Stem Cell Deficiency
AU - International Limbal Stem Cell Deficiency Working Group
AU - Deng, Sophie X.
AU - Kruse, Friedrich
AU - Gomes, José A.P.
AU - Chan, Clara C.
AU - Daya, Sheraz
AU - Dana, Reza
AU - Figueiredo, Francisco C.
AU - Kinoshita, Shigeru
AU - Rama, Paolo
AU - Sangwan, Virender
AU - Slomovic, Allan R.
AU - Tan, Donald
AU - Borderie, Vincent
AU - Cursiefen, Claus
AU - Djalilian, Ali
AU - Epstein, Dan
AU - Frueh, Beatrice
AU - Hjortdal, Jesper
AU - Holland, Edward
AU - Kaufman, Stephen
AU - Lee, Barry
AU - Mannis, Mark
AU - Merayo, Jesus
AU - Pellegrini, Graziella
AU - Perez, Victor
AU - Shimmura, Shigeto
AU - Shortt, Alex
AU - Solomon, Avi
AU - Tsai, Ray
AU - Tseng, Scheffer
AU - Tu, Elmer
N1 - Funding Information:
S. X. Deng receives funding from the National Eye Institute (2R01EY021797) and California Institute for Regenerative Medicine (CLIN1-08686; CLIN2-11650) and is a consultant for F-Prime Capital, W. L. Gore & Associates, Inc, Kowa Research Institute, Inc, and Domp? US. F. Kruse is a consultant for Kowa Research Institute, Inc. C. C. Chan received honoraria previously from Alcon Labs Inc, Allergan, Bausch & Lomb, Santen, Shire, Thea, Labtician and Zeiss, and received previous research funding from Allergan, Bausch & Lomb, Shire, Tearlab. R. Dana receives funding from the National Eye Institute (R01 EY012963, R01 EY020889, R21 EY029387, UG1 EY026508-01) and the Department of Defense (VR170189), holds equity in Aramis Biosciences and Claris Biotherapeutics, and is a consultant to Domp? US, GSK, Kala, Aldeyra, and Santen. F. C. Figueiredo is a consultant and has received research grants from Chiesi Farmaceutici S.P.A. and Domp?. P. Rama received consultant fees from Chiesi Company Parma (Italy) and consultant fees and research support from Domp? Italy. The other authors have no conflicts of interest to disclose.
Funding Information:
Supported by the Cornea Society. Editorial support was provided by Julia C. Jones, PharmD, PhD, MWC, ELS, and Alis Balayan, BS.
Publisher Copyright:
Copyright © 2020 Wolters Kluwer Health, Inc.
PY - 2020
Y1 - 2020
N2 - Purpose: In recent decades, the medical and surgical treatment of limbal stem cell deficiency (LSCD) has evolved significantly through the incorporation of innovative pharmacological strategies, surgical techniques, bioengineering, and cell therapy. With such a wide variety of options, there is a need to establish a global consensus on the preferred approaches for the medical and surgical treatment of LSCD. Methods: An international LSCD Working Group was established by the Cornea Society in 2012 and divided into subcommittees. Four face-to-face meetings, frequent email discussions, and teleconferences were conducted since then to reach agreement on a strategic plan and methods after a comprehensive literature search. A writing group drafted the current study. Results: A consensus in the medical and surgical management of LSCD was reached by the Working Group. Optimization of the ocular surface by eyelid and conjunctival reconstruction, antiinflammatory therapy, dry eye and meibomian gland dysfunction treatment, minimization of ocular surface toxicity from medications, topical medications that promote epithelialization, and use of a scleral lens is considered essential before surgical treatment of LSCD. Depending on the laterality, cause, and stage of LSCD, surgical strategies including conjunctival epitheliectomy, amniotic membrane transplantation, transplantation of limbal stem cells using different techniques and sources (allogeneic vs. autologous vs. ex vivo-cultivated), transplantation of oral mucosal epithelium, and keratoprosthesis can be performed as treatment. A stepwise flowchart for use in treatment decision-making was established. Conclusions: This global consensus provides an up-to-date and comprehensive framework for the management of LSCD.
AB - Purpose: In recent decades, the medical and surgical treatment of limbal stem cell deficiency (LSCD) has evolved significantly through the incorporation of innovative pharmacological strategies, surgical techniques, bioengineering, and cell therapy. With such a wide variety of options, there is a need to establish a global consensus on the preferred approaches for the medical and surgical treatment of LSCD. Methods: An international LSCD Working Group was established by the Cornea Society in 2012 and divided into subcommittees. Four face-to-face meetings, frequent email discussions, and teleconferences were conducted since then to reach agreement on a strategic plan and methods after a comprehensive literature search. A writing group drafted the current study. Results: A consensus in the medical and surgical management of LSCD was reached by the Working Group. Optimization of the ocular surface by eyelid and conjunctival reconstruction, antiinflammatory therapy, dry eye and meibomian gland dysfunction treatment, minimization of ocular surface toxicity from medications, topical medications that promote epithelialization, and use of a scleral lens is considered essential before surgical treatment of LSCD. Depending on the laterality, cause, and stage of LSCD, surgical strategies including conjunctival epitheliectomy, amniotic membrane transplantation, transplantation of limbal stem cells using different techniques and sources (allogeneic vs. autologous vs. ex vivo-cultivated), transplantation of oral mucosal epithelium, and keratoprosthesis can be performed as treatment. A stepwise flowchart for use in treatment decision-making was established. Conclusions: This global consensus provides an up-to-date and comprehensive framework for the management of LSCD.
KW - Conjunctiva
KW - Cornea
KW - Limbal stem cell deficiency
KW - Limbal stem cells
KW - Stem cells
KW - Treatment
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U2 - 10.1097/ICO.0000000000002358
DO - 10.1097/ICO.0000000000002358
M3 - Article
C2 - 32639314
AN - SCOPUS:85090510767
SN - 0277-3740
VL - 39
SP - 1291
EP - 1302
JO - Cornea
JF - Cornea
IS - 10
ER -