1.Short-term Efficacy and Safety of Faricimab Switching in Neovascular Age-related Macular Degeneration Previously Treated with Anti-vascular Endothelial Growth Factor
Jun Sung LEE ; Chang Ryong KIM ; Sun Taek LIM ; Yung-Hwi KIM
Journal of Retina 2025;10(1):20-30
Purpose:
To evaluate the short-term efficacy and safety of intravitreal faricimab injection (IFI) in patients with neovascular age-related macular degeneration (nAMD) previously treated with another anti-vascular endothelial growth factor (anti-VEGF).
Methods:
We retrospectively reviewed the medical records of patients with nAMD refractory to previous anti-VEGF treatment who were switched to faricimab from June 2023 to July 2024. A good responder was defined as a case with complete absence of subretinal fluid (SRF) or intraretinal fluid (IRF) 8 weeks after IFI, whereas a poor responder was defined as having residual SRF or IRF 8 weeks after IFI. We evaluated best-corrected visual acuity (BCVA), central subfield retinal thickness (CST), sub-foveal choroidal thickness (SFCT), maximum height of pigment epithelial detachment (PED) and the presence of SRF or IRF, and the presence of optical coherence tomography parameters of nAMD at baseline (before the injection of faricimab) and 8 weeks and 16 weeks after faricimab switching. All adverse events following faricimab injection were analyzed.
Results:
Seventy-two eyes of 69 patients were included. There was no significant BCVA change after IFI. CST, SFCT and maximum PED height were significantly decreased 8 weeks and 16 weeks after faricimab switching compared to baseline (all p < 0.05). A fluid-free state was reached in 39% at 16 weeks. The poor responder group had a higher number of brolucizumab injections before switching compared to the good responder group (1.1 ± 1.9 vs. 2.4 ± 3.3, p = 0.04). The good responder group had more cases without SRF before switching and lower baseline CST than the poor responder group (all p < 0.05). There were no severe adverse events after IFI.
Conclusions
Faricimab was safe and anatomically effective, though it did not produce functional improvements. IFI could serve as another option in the treatment of patients with nAMD treated with previous anti-VEGF.
2.Rhabdomyolysis following Frostbite.
Jun Hwi CHO ; Sung Whan KIM ; Chan Woo PARK ; Hae Hyeuk CHEONG ; Sun Sook HSN ; Jae Bong CHUNG ; Ji Hoon BAE ; Jeong Yeul SEO ; Yung Mi CHOI ; Hee Cheol AHN ; Moo Eob AHN ; Ki Cheol YOU ; Kang Hyun LEE
Journal of the Korean Society of Emergency Medicine 2003;14(1):129-131
No abstract available.
Acute Kidney Injury
;
Frostbite*
;
Renal Dialysis
;
Rhabdomyolysis*
3.Transurethral Resection of Prostate under Local Anesthesia in Patients with Benign Prostatic Hyperplasia.
Yung Hwi LEE ; Kyung Jun OH ; Kyu Hwan KIM
Korean Journal of Urology 1996;37(1):85-87
This study was performed for the patients with benign prostatic hyperplasia who had underlying diseases which increase the risk of spinal or general anesthesia. Standard transurethral resections of prostate were done on patients with prostatic hyperplasia under local anesthesia. The selection criteria were urinary retention or below 10 ml/sec of maximum flow rate, coexist with medical problems which increase the risk of spinal and general anesthesia. Local infiltrations of 1% lidocaine were done at penoscrotal junction on each side of the corpus spongiosum, the lateral portion of the prostate and the bladder neck. This anesthesia was supplemented usually by modest dose of intravenous tranquilizers and analgesics under the continuous monitoring by an anesthesiologist. The Visual Pain Analogue Scale(VAS) was used for the evaluation of intraoperative and postoperative pain. The mean operating time, amount of the resected tissues and intraoperative and postoperative visual analogue scale were 50.2 min, 16 grams. 2.7 and 2.0. We thought that this type of anesthesia was a safe, simple and effective procedure.
Analgesics
;
Anesthesia
;
Anesthesia, General
;
Anesthesia, Local*
;
Humans
;
Lidocaine
;
Neck
;
Pain, Postoperative
;
Patient Selection
;
Prostate
;
Prostatic Hyperplasia*
;
Transurethral Resection of Prostate*
;
Urinary Bladder
;
Urinary Retention
4.A Case of Incidental Testicular Teratoma Found during Hydrocelectomy.
Seong Soo AN ; Chul Bo PARK ; Yung Hwi LEE ; Yang Il JANG ; Kyung Jun OH ; Kyu Kwan KIM
Korean Journal of Urology 1996;37(5):603-605
Testicular teratoma contains more than one germ cell layer in various stages of maturation and differentiation. The teratoma occurs at all ages but is most common in the 25-30 year age group. It is relatively infrequently seen in childhood and infancy. In these age group, teratoma is a benign tumor. Recently, we experienced one case of incidental testicular teratoma during hydrocelectomy in 22 month-old child, The hydrocele is frequently associated with teratoma under age 4 years and is the most common misdiagnosis. So we report this one case of testicular teratoma with review of related literatures.
Child
;
Diagnostic Errors
;
Germ Cells
;
Humans
;
Infant
;
Teratoma*
;
Testis
5.A Case of Urethral Diverticulum Combined with Giant Stone.
Yung Hwi LEE ; Chul Bo PARK ; Sung Soo AN ; Yang Il JANG ; Kyung Jun OH ; Kyu Hwan KIM
Korean Journal of Urology 1995;36(10):1165-1167
A case of one of the largest stone in a giant penile urethral diverticulum which disturbed voiding and ejaculation was responded with review of some literatures.
Diverticulum*
;
Ejaculation
;
Male
;
Urethra
6.A Case of 47XYY Syndrome with Azoospermia.
Jun Yong LEE ; Chul Bo PARK ; Yung Hwi LEE ; Kyung Jun OH ; Kyu Hwan KIM
Korean Journal of Urology 1994;35(2):208-210
The XYY syndrome is a rare entity, which is a phenotypic man with a 47 XYY It was first reported by Sandberg and associates in 1961. The XYY individual is seldom detected during childhood or even in adult because the features of XYY syndrome are often subtle and not overtly suggestive of a chromosomal abnormalities. We have reported a case of XYY syndrome associated with absence of pubic and axillary hair, no voice mutation and azoospermia. Clinical, endocrinologic and genetic studies were presented and theories regarding the etiology of the XYY syndrome were discussed with review of the literature.
Adult
;
Azoospermia*
;
Chromosome Aberrations
;
Hair
;
Humans
;
Voice

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