2018
Organization model for allotransplantations of cryopreserved vascular grafts in Czech Republic
ŠPAČEK, Miroslav, Pavel SMĚŘIČKA, Libor JANOUŠEK, Petr ŠTÁDLER, Miloš ADAMEC et. al.Základní údaje
Originální název
Organization model for allotransplantations of cryopreserved vascular grafts in Czech Republic
Autoři
ŠPAČEK, Miroslav (203 Česká republika, garant), Pavel SMĚŘIČKA (203 Česká republika), Libor JANOUŠEK (203 Česká republika), Petr ŠTÁDLER (203 Česká republika), Miloš ADAMEC (203 Česká republika), Robert VLACHOVSKÝ (203 Česká republika, domácí), Igor GUŇKA (203 Česká republika), Pavel NAVRÁTIL (203 Česká republika), Filip THIEME (203 Česká republika), Petr MITÁŠ (203 Česká republika), Rudolf ŠPUNDA (203 Česká republika), Jaroslav ŠPATENKA (203 Česká republika), Robert STAFFA (203 Česká republika, domácí), Petr NĚMEC (203 Česká republika) a Jaroslav LINDNER (203 Česká republika)
Vydání
Cell and Tissue Banking, Dordrecht, Springer, 2018, 1389-9333
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10601 Cell biology
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 1.939
Kód RIV
RIV/00216224:14110/18:00104200
Organizační jednotka
Lékařská fakulta
UT WoS
000442599400018
Klíčová slova anglicky
Vascular allograft; Cryopreservation; Tissue transplantation; Organization model
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 10. 2. 2019 17:08, Soňa Böhmová
Anotace
V originále
The transplantation of fresh or cryopreserved vascular allografts in patients with a prosthetic graft infection or critical limb ischemia is necessary for their limb salvage and, in many cases, represents a lifesaving procedure. While transplantation of fresh allografts has a long history in the Czech Republic, the standard use of cryopreserved vascular allografts was introduced into the clinical practice in 2011 as a result of the implementation of EU Directive 2004/23/EC into national legislation (Human Cell and Tissue Act No. 296/2008 Coll.). The authors present an organizational model based on cooperation between the majority of Czech Transplant Centers with a tissue establishment licensed by the national competent authority. In various points, we are addressing individual aspects of experimental and clinical studies which affect clinical practice. Based on experimental and clinical work, the first validation of cryopreserved arterial and venous grafts for clinical use was performed between 2011 and 2013. The growing number of centers participating in this programme led to a growing number of patients who underwent transplantation of vascular allografts. In 2015 the numbers of transplanted fresh versus cryopreserved allografts in the Czech Republic were almost equal. Cooperation of the participating centers in the Czech Republic with the licensed Tissue Establishment made it possible to achieve a full compliance with the European Union Directives, and harmonized national legal norms and assured a high quality of cryopreserved vascular allografts.