TY - JOUR
T1 - Long-term changes in endothelial cell counts after early phacoemulsification versus laser peripheral iridotomy using sequential argon:YAG laser technique in acute primary angle closure
AU - Park, Hae Young Lopilly
AU - Lee, Na Young
AU - Park, Chan Kee
AU - Kim, Man Soo
PY - 2012/11
Y1 - 2012/11
N2 - Objective To compare the change in endothelial cell counts (ECC) after early phacoemulsification and laser peripheral iridotomy (LPI) using sequential argon:yttrium-aluminum-garnet (YAG) laser technique for the treatment of acute primary angle closure (APAC). Methods: This was a retrospective chart review, case-control study; 86 APAC patients were enrolled. Sixteen patients who underwent early phacoemulsification with intraocular lens implantation and 32 patients who underwent LPI were matched by propensity score analysis. All subjects underwent a complete ophthalmic examination, including intraocular pressure (IOP)measurements, optic disc examinations, and gonioscopy. ECC were acquired at the center of the cornea with a noncontact specular microscope before treatment, and at 1, 6, 12, and 24 months following phacoemulsification or LPI. Results: The mean follow-up was 26.1±4.7 months in the phacoemulsification group and 26.3±4.5 months in the LPI group. After intervention, the changes in anterior chamber depth and Shaffer grading by gonioscopy were significantly different between groups. ECC were not different before treatment; however, after phacoemulsification or LPI at 12 months (2280±320 vs 1993±380 cells/mm2) and 24 months (2113±333 vs 1880±422 cells/mm2), there was a significant difference between the two groups (P=0.040 and P=0.032 respectively). Regression analysis showed that anterior chamber depth at baseline (P=0.041) and intervention modality (phacoemulsification vs LPI; P<0.001) were significantly related to the change in ECC. Conclusions: Early phacoemulsification showed lower endothelial cell loss than did LPI in the treatment of APAC after a 2-year follow-up. In terms of ECC, early phacoemulsification could be a better intervention modality for APAC.
AB - Objective To compare the change in endothelial cell counts (ECC) after early phacoemulsification and laser peripheral iridotomy (LPI) using sequential argon:yttrium-aluminum-garnet (YAG) laser technique for the treatment of acute primary angle closure (APAC). Methods: This was a retrospective chart review, case-control study; 86 APAC patients were enrolled. Sixteen patients who underwent early phacoemulsification with intraocular lens implantation and 32 patients who underwent LPI were matched by propensity score analysis. All subjects underwent a complete ophthalmic examination, including intraocular pressure (IOP)measurements, optic disc examinations, and gonioscopy. ECC were acquired at the center of the cornea with a noncontact specular microscope before treatment, and at 1, 6, 12, and 24 months following phacoemulsification or LPI. Results: The mean follow-up was 26.1±4.7 months in the phacoemulsification group and 26.3±4.5 months in the LPI group. After intervention, the changes in anterior chamber depth and Shaffer grading by gonioscopy were significantly different between groups. ECC were not different before treatment; however, after phacoemulsification or LPI at 12 months (2280±320 vs 1993±380 cells/mm2) and 24 months (2113±333 vs 1880±422 cells/mm2), there was a significant difference between the two groups (P=0.040 and P=0.032 respectively). Regression analysis showed that anterior chamber depth at baseline (P=0.041) and intervention modality (phacoemulsification vs LPI; P<0.001) were significantly related to the change in ECC. Conclusions: Early phacoemulsification showed lower endothelial cell loss than did LPI in the treatment of APAC after a 2-year follow-up. In terms of ECC, early phacoemulsification could be a better intervention modality for APAC.
KW - Acute primary angle closure
KW - Corneal endothelial cell
KW - Laser peripheral iridotomy
KW - Phacoemulsification
UR - http://www.scopus.com/inward/record.url?scp=84871424588&partnerID=8YFLogxK
U2 - 10.1007/s00417-012-1998-4
DO - 10.1007/s00417-012-1998-4
M3 - Article
C2 - 22437486
AN - SCOPUS:84871424588
SN - 0721-832X
VL - 250
SP - 1673
EP - 1680
JO - Graefe's Archive for Clinical and Experimental Ophthalmology
JF - Graefe's Archive for Clinical and Experimental Ophthalmology
IS - 11
ER -