TY - JOUR
T1 - Applications of Human Amniotic Membrane Patching Assisted Vitrectomy in the Management of Postoperative PVR in Complex Retinal Detachments
AU - Caporossi, Tomaso
AU - Molle, Andrea
AU - Carla', Matteo Mario
AU - Picardi, Stefano Maria
AU - Gambini, Gloria
AU - Scampoli, Alessandra
AU - Governatori, Lorenzo
AU - Bernardinelli, Patrizio
AU - Rizzo, Stanislao
PY - 2023
Y1 - 2023
N2 - Human amniotic membranes (hAMs) are extraembryonic tissues currently employed in the treatment of many ocular and systemic diseases. Several reports indicate that hAMs can suppress the signaling pathway of tissue growth factor beta (TGF-β), a cytokine that plays a major role in the pathogenesis of proliferative vitreoretinopathy (PVR) through the induction of epithelial-mesenchymal transition (EMT) in exposed retinal pigmented epithelium (RPE) cells. The present study was conducted to evaluate the efficacy of a modified vitrectomy procedure (hAMP-V) involving the extensive coverage of exposed RPE with hAM patches to prevent postoperative PVR in a series of 15 cases of retinal detachment complicated by severe preoperatory PVR. The primary outcome was to assess the rate of successful retinal reattachment of a single hAMP-V procedure at 6 months from silicone oil removal. Secondary outcomes included the collection of intraoperative data concerning the quantity, size, and scope of hAM patches, and the assessment of postoperative improvements in mean LogMar BCVA at 3 and 6 months. Successful retinal reattachment was obtained in 14 out of 15 eyes (93.3%). Surgical failure due to major recurrence of PVR occurred in 1 out of 15 eyes (6.7%). Postoperative improvements in mean LogMar BCVA were statistically significant (p < 0.05, paired t-test). No intraoperative and postoperative adverse effects were reported. The study helped to refine the surgical technique while also offering cues for future improvements.
AB - Human amniotic membranes (hAMs) are extraembryonic tissues currently employed in the treatment of many ocular and systemic diseases. Several reports indicate that hAMs can suppress the signaling pathway of tissue growth factor beta (TGF-β), a cytokine that plays a major role in the pathogenesis of proliferative vitreoretinopathy (PVR) through the induction of epithelial-mesenchymal transition (EMT) in exposed retinal pigmented epithelium (RPE) cells. The present study was conducted to evaluate the efficacy of a modified vitrectomy procedure (hAMP-V) involving the extensive coverage of exposed RPE with hAM patches to prevent postoperative PVR in a series of 15 cases of retinal detachment complicated by severe preoperatory PVR. The primary outcome was to assess the rate of successful retinal reattachment of a single hAMP-V procedure at 6 months from silicone oil removal. Secondary outcomes included the collection of intraoperative data concerning the quantity, size, and scope of hAM patches, and the assessment of postoperative improvements in mean LogMar BCVA at 3 and 6 months. Successful retinal reattachment was obtained in 14 out of 15 eyes (93.3%). Surgical failure due to major recurrence of PVR occurred in 1 out of 15 eyes (6.7%). Postoperative improvements in mean LogMar BCVA were statistically significant (p < 0.05, paired t-test). No intraoperative and postoperative adverse effects were reported. The study helped to refine the surgical technique while also offering cues for future improvements.
KW - amniotic membrane
KW - epithelial mesenchymal transition
KW - new perspectives
KW - proliferative vitreoretinopathy
KW - retinal breaks
KW - retinal detachment
KW - retinectomy
KW - transforming growth factor beta
KW - vitrectomy
KW - vitreoretinal surgery
KW - amniotic membrane
KW - epithelial mesenchymal transition
KW - new perspectives
KW - proliferative vitreoretinopathy
KW - retinal breaks
KW - retinal detachment
KW - retinectomy
KW - transforming growth factor beta
KW - vitrectomy
KW - vitreoretinal surgery
UR - http://hdl.handle.net/10807/247605
U2 - 10.3390/jcm12031137
DO - 10.3390/jcm12031137
M3 - Article
SN - 2077-0383
VL - 12
SP - 1137
EP - 1149
JO - Journal of Clinical Medicine
JF - Journal of Clinical Medicine
ER -