1.Treatment of Ulnar Olecranon Fracture Using Acutrak Screw.
Hyungchun KIM ; Kwangryul KIM ; Moonsup LIM ; Youngil PARK ; Inhwan HWANG ; Jihoon LEE
Journal of the Korean Fracture Society 2009;22(4):270-275
PURPOSE: To evaluate the clinical results of Acutrak screw fixation for ulnar olecranon fractures. MATERIALS AND METHODS: We reviewed 15 cases of ulnar olecranon fractures which were treated with Acutrak screws from February 2003 to September 2007. Follow-up period is from 12 months to 42 months. We used Mayo classification. Radiologic results were analyzed according to step-off, gap, reduction loss, and functional results were analyzed according to pain and ROM. We analyzed union time, operation time, incision size and complications. RESULTS: In functional results, there were 3 good cases out of 3 Mayo type IA, 8 good cases and 2 fair cases out of 10 type IIA, 1 fair case and 1 poor case out of 2 type IIB. In radiologic results, there was 1 case of reduction loss. Average union time was 9.4 weeks, average operation time was 24 minutes and average incision size was 1.8 cm. CONCLUSION: We conclude that Acutrak screw fixation can be a treatment option for olecranon fracture of Mayo type IA and IIA.
Follow-Up Studies
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Olecranon Process
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Ulna
2.Recombinant proteins of spike protein of SARS-CoV-2 with the Omicron receptor-binding domain induce production of highly Omicron-specific neutralizing antibodies
Hyangju KANG ; Daniel KIM ; Kyungmin MIN ; Minhee PARK ; Seok-Hyun KIM ; Eun-Ju SOHN ; Bo-Hwa CHOI ; Inhwan HWANG
Clinical and Experimental Vaccine Research 2022;11(3):285-289
Various vaccines have been developed to fight severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus responsible for the coronavirus disease 2019 pandemic.However, new variants of SARS-CoV-2 undermine the effort to fight SARS-CoV-2. Here, we produced S proteins harboring the receptor-binding domain (RBD) of the Omicron variant in plants. Plant-produced S proteins together with adjuvant CIA09A triggered strong immune responses in mice. Antibodies in serum inhibited interaction of recombinant human angiotensinconverting enzyme 2 with RBD of the Omicron variant, but not RBD of other variants. These results suggest that antibodies induced by RBD of the Omicron variant are highly specific for the Omicron RBD, but not for that of other variants.
3.Loffler Endocarditis Associated with Acute Lateral Medullary Infarction.
Hyung Jong PARK ; Young Seo KIM ; Yun Su HWANG ; Seon Jae IM ; Inhwan LIM ; In Sub YOO ; Dong Hee KIM ; Kyeong Ho YUN ; Hyun Young PARK
Journal of the Korean Neurological Association 2015;33(2):110-112
No abstract available.
Cerebral Infarction
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Endocarditis*
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Hypereosinophilic Syndrome
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Infarction*
4.Clinical Outcomes of Second-Line Chemotherapy after Progression on Nab-Paclitaxel Plus Gemcitabine in Patients with Metastatic Pancreatic Adenocarcinoma
Kyoungmin LEE ; Kyunghye BANG ; Changhoon YOO ; Inhwan HWANG ; Jae Ho JEONG ; Heung-Moon CHANG ; Dongwook OH ; Tae Jun SONG ; Do Hyun PARK ; Sang Soo LEE ; Sung Koo LEE ; Myung-Hwan KIM ; Jin-hong PARK ; Kyu-pyo KIM ; Baek-Yeol RYOO
Cancer Research and Treatment 2020;52(1):254-262
Purpose:
Since the introduction of nab-paclitaxel plus gemcitabine (nab-P+GEM) as first-line (1L) treatment for metastatic pancreatic adenocarcinoma (mPDAC), optimal second-line (2L) chemotherapy after progression is unclear. We assessed clinical outcomes of 2L chemotherapy for disease that progressed on 1L nab-P+GEM.
Materials and Methods:
Among the 203 patients previously treated with 1L nab-P+GEM for mPDAC at Asan Medical Center, between February and December 2016, records of 120 patients receiving 2L chemotherapy after progression on nab-P+GEM were retrospectively reviewed. The response rate and survival were evaluated along with analysis of prognostic factors.
Results:
Fluoropyrimidine-oxaliplatin doublets (FOLFOX or XELOX) were used in 78 patients (65.0%), fluoropyrimidine monotherapy in 37 (30.8%), and liposomal irinotecan plus fluorouracil in two (1.7%). The median progression-free survival (PFS) and overall survival (OS) were 3.29 months and 7.33 months from the start of 2L therapy. Fluoropyrimidine-oxaliplatin regimens and fluoropyrimidine monotherapy did not yield significantly different median PFS (2.89 months vs. 3.81 months, p=0.40) or OS (7.04 months vs. 7.43 months, p=0.86). A high neutrophil-lymphocyte ratio (> 2.2) and a short time to progression with 1L nab-P+GEM (< 6.4 months) were independent prognostic factors of poor OS with 2L therapy.
Conclusion
2L fluoropyrimidine-oxaliplatin doublets and fluoropyrimidine monotherapy after failure of 1L nab-P+GEM had modest efficacy, with no differences in treatment outcomes between them. Further investigation is warranted for the optimal 2L chemo-regimens and sequencing of systemic chemotherapy for patients with mPDAC.