J 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

Štítky

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.