2021
Case Report: Freeze-Dried Human Amniotic Membrane Allograft for the Treatment of Chronic Wounds: Results of a Multicentre Observational Study
SCHMIEDOVA, Iveta, Zuzana OZANOVA, Elen STASTNA, Ludmila KISELAKOVA, Břetislav LIPOVÝ et. al.Základní údaje
Originální název
Case Report: Freeze-Dried Human Amniotic Membrane Allograft for the Treatment of Chronic Wounds: Results of a Multicentre Observational Study
Autoři
SCHMIEDOVA, Iveta (203 Česká republika), Zuzana OZANOVA (203 Česká republika), Elen STASTNA (203 Česká republika), Ludmila KISELAKOVA (203 Česká republika), Břetislav LIPOVÝ (203 Česká republika, domácí) a Serhij FOROSTYAK (203 Česká republika, garant)
Vydání
Frontiers in bioengineering and biotechnology, Laussane, Frontiers Media S.A. 2021, 2296-4185
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30401 Health-related biotechnology
Stát vydavatele
Švýcarsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 6.064
Kód RIV
RIV/00216224:14110/21:00121941
Organizační jednotka
Lékařská fakulta
UT WoS
000670555700001
Klíčová slova anglicky
biomaterials; amnion; clinical study; diabetes mellitus; wound management; biological dressing; regenerative medicine
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 6. 9. 2021 12:34, Mgr. Tereza Miškechová
Anotace
V originále
An inability of the human body to heal acute wounds under certain conditions results in the formation of chronic ulcers. Chronic wounds not only cause significant pain and discomfort for patients but also serve as an entry for microorganisms into the human body, which can result in serious life-threatening problems and become a significant burden for the patients and society. The current work present results of a multicentre prospective observational study demonstrating the use of a lyophilized amniotic membrane (AM) in the treatment of chronic wounds (various etiologies). Lyophilized AM produced under the commercial brand Amnioderm (R) was used as an allograft material for therapy of chronic wounds, in addition to chronic ulcer standard-of-care (SoC) protocols. The duration of wounds considered for the application of AM ranged between 2 months and 11 years. In total, 16 patients were enrolled to the study, of which eight were completely healed, six demonstrated a significantly reduced ulcer size, and two did not respond to the AM therapy. The current study unambiguously demonstrates an effective alternative to the standard of chronic wound care and confirms a significant effect of the AM application for chronic wound management as a new SoC.