Amniotic Membrane Transplantation for Symptomatic Bullous Keratopathy

OBJECTIVE To determine whether amniotic membrane transplantation can be used to treat symptomatic bullous keratopathy displaying poor visual potential. METHODS Amniotic membrane transplantation was performed at 5 centers on 50 consecutive eyes (50 patients) with symptomatic bullous keratopathy and p...

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Veröffentlicht in:Archives of ophthalmology (1960) 1999-10, Vol.117 (10), p.1291-1297
Hauptverfasser: Pires, Renato T. F, Tseng, Scheffer C. G, Prabhasawat, Pinnita, Puangsricharern, Vilavun, Maskin, Steven L, Kim, Jae Chan, Tan, Donald T. H
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Sprache:eng
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Zusammenfassung:OBJECTIVE To determine whether amniotic membrane transplantation can be used to treat symptomatic bullous keratopathy displaying poor visual potential. METHODS Amniotic membrane transplantation was performed at 5 centers on 50 consecutive eyes (50 patients) with symptomatic bullous keratopathy and poor visual potential. The underlying causes of bullous keratopathy included aphakia (9 eyes), pseudophakia (19 eyes), failed grafts (9 eyes), and others (13 eyes). RESULTS During the follow-up period of 33.8 weeks (3-96 weeks) after amniotic membrane transplantation, 43 (90%) of 48 eyes with intolerable pain preoperatively became pain free postoperatively. Among the 5 eyes with residual pain, 3 received repeated amniotic membrane transplantation, 1 required a conjunctival flap for pain relief, and 1 had reduced pain. Epithelial defects in 45 (90%) of 50 eyes created and covered by amniotic membrane healed rapidly within 3 weeks. Only 4 eyes (8%) showed recurrent surface breakdown. Epithelial edema or bullae recurred in a smaller area in 5 eyes (10%) and pseudopterygium developed in 1 eye. CONCLUSION Amniotic membrane transplantation can be considered as an alternative to conjunctival flaps in alleviating pain, promoting epithelial healing, and preserving cosmetic appearance in patients with symptomatic bullous keratopathy and poor visual potential.Arch Ophthalmol 1999;117:1291-1297-->
ISSN:0003-9950
2168-6165
1538-3601
2168-6173
DOI:10.1001/archopht.117.10.1291