Seong Yeon Park

Dr. Seong Yeon Park

orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2017 in Infection & Chemotherapy
Verified
Journal Article
Open access
YKYee Gyung Kwak
Yee Gyung Kwak
Seong-Ho ChoiSeong-Ho Choi
Seong-Ho Choi
TKTark Kim
Tark Kim
SPSeong Yeon Park
Seong Yeon Park
SSSoo Hong Seo
Soo Hong Seo
SCSang Ho Choi
Sang Ho Choi
Skin and soft tissue infection (SSTI) is common and important infectious disease. This work represents an update to 2012 Korean guideline for SSTI. The present guideline was developed by the adaptation method. This clinical guideline provides recommendations for the diagnosis and management of SSTI, including impetigo/ecthyma, purulent skin and soft tissue infection, erysipelas and cellulitis, necrotizing fasciitis, pyomyositis, clostridial myonecrosis, and human/animal bite. This guideline targets community-acquired skin and soft tissue infection occurring among adult patients aged 16 years and older. Diabetic foot infection, surgery-related infection, and infections in immunocompromised patients were not included in this guideline.

14 November 2014 in BMC Infectious Diseases
Verified
Journal Article
Open access
PDF file
CKChung-Jong Kim
Chung-Jong Kim
HKHong Bin Kim
Hong Bin Kim
MOMyoung-Don Oh
Myoung-Don Oh
YKYunhee Kim
Yunhee Kim
AKArim Kim
Arim Kim
TGThe KIND Study group (Korea Infectious Diseases Study group)
The KIND Study group (Korea Infectious Diseases Study group)
We estimated the nationwide burden of nosocomial S. aureus bloodstream infection (SA-BSI), a major cause of nosocomial infection, in South Korea. To evaluate the nationwide incidence of nosocomial SA-BSI, cases of SA-BSI were prospectively collected from 22 hospitals with over 500 beds over 4?months. Data on patient-days were obtained from a national health insurance database containing the claims data for all healthcare facilities in South Korea. The additional cost of SA-BSI was estimated through a matched case?control study. The economic burden was calculated from the sum of the medical costs, the costs of caregiving and loss of productivity. Three hundred and thirty nine cases of nosocomial SA-BSI were included in the study: 254 cases of methicillin-resistant SA-BSI (MRSA-BSI) and 85 cases of methicillin-susceptible SA-BSI (MSSA-BSI). Death related to BSI occurred in 81 cases (31.9%) of MRSA-BSI and 12 cases (14.1%) of MSSA-BSI. The estimated incidence of nosocomial MRSA-BSI was 0.12/1,000 patient-days and that of nosocomial MSSA-BSI, 0.04/1,000 patient-days. The estimated annual cases of nosocomial BSI were 2,946 for MRSA and 986 for MSSA in South Korea. The additional economic burden per case of nosocomial SA-BSI was US $20,494 for MRSA-BSI and $6,914 for MSSA-BSI. Total additional annual cost of nosocomial SA-BSI was $67,192,559. In view of the burden of nosocomial SA-BSI, a national strategy for reducing nosocomial SA-BSI is urgently needed in South Korea.

10 December 2013 in BMC Infectious Diseases
Verified
Journal Article
Open access
PDF file
KSKyoung-Ho Song
Kyoung-Ho Song
EKEu Suk Kim
Eu Suk Kim
HSHye-Yun Sin
Hye-Yun Sin
KPKyung-Hwa Park
Kyung-Hwa Park
SJSook-In Jung
Sook-In Jung
KGKorea INfectious Diseases (KIND) study group
Korea INfectious Diseases (KIND) study group
Despite the importance of invasive Staphylococcus aureus (ISA) infection, its overall burden in non-selected populations has only been defined in a small number of studies in Europe and North America. To define the characteristics of ISA infections in Korea, we conducted a multi-center cohort study to estimate population-based incidence rates. We conducted a multicenter prospective cohort study at nine university-affiliated active-surveillance core centers (ASCs) in three regions of Korea. To cover all available clinical microbiologic laboratories, we classified the laboratories in these regions into three groups according to their clinical environment as: 1) Nine ASCs, 2) Five major commercial laboratories and 3) Forty-four acute-care hospital-affiliated microbiology laboratories. We requested all the laboratories to report prospectively their numbers of cases of S. aureus isolated from normally sterile sites. Detailed clinical information was collected about the cases in the nine ASCs. From 1 July 2009 to 30 June 2011, a total of 1,198 cases of ISA infection were identified at the nine ASCs, including 748 (62%) methicillin-resistant S. aureus (MRSA) infections. Most (81%) ISA infections were healthcare-associated (HCA): 653 (55%) hospital-onset and 322 (27%) community-onset. 223 (19%) were community-associated infections. The most common primary diagnosis was catheter-associated infection (225 cases, 19%). Respiratory tract infection (160, 13%), skin & soft tissue (152, 13%) and bone & joint infections (120, 10%) were also common. 30-day and 12-week mortality rates were 25.6% (262/1,024) and 36.5% (314/860), respectively. Complications, including metastatic infection within 12 weeks, occurred in 17.8% of ISA infections. The most common site of metastatic infection was the lung (9.8%, 84/860). Based on the total of 2,806 observed cases of ISA infection, estimated annual rates of ISA and invasive MRSA infections were 43.3 and 27.7 per 100,000 populations, respectively. Our data provide important information about the clinical characteristics of ISA infections. We estimate that over 21,000 ISA infections and 13,000 invasive MRSA infections occurred in Korea in 2010.

1 June 2015 in International Journal of Antimicrobial Agents
Verified
Journal Article
Closed access
KKKi Hwan Kwon
Ki Hwan Kwon
JOJin Young Oh
Jin Young Oh
YYYoung-Soon Yoon
Young-Soon Yoon
YJYun-Jeong Jeong
Yun-Jeong Jeong
KKKyung Soo Kim
Kyung Soo Kim
SPSeong Yeon Park
Seong Yeon Park

23 November 2021 in Viruses
Verified
Journal Article
Open access
PDF file
JKJi-Soo Kwon
Ji-Soo Kwon
SJSol Jin
Sol Jin
JKJi-Yeun Kim
Ji-Yeun Kim
SRSang-Hyun Ra
Sang-Hyun Ra
TKTaeeun Kim
Taeeun Kim
SKSung-Han Kim
Sung-Han Kim
Significant progress has been made on the molecular biology of the severe fever with thrombopenia virus (SFTSV); however, many parts of the pathophysiological mechanisms of mortality in SFTS remain unclear. In this study, we investigated virologic and immunologic factors for fatal outcomes of patients with SFTS. We prospectively enrolled SFTS patients admitted from July 2015 to October 2020. Plasma samples were subjected to SFTSV RNA RT-PCR, multiplex microbead immunoassay for 17 cytokines, and IFA assay. A total of 44 SFTS patients were enrolled, including 37 (84.1%) survivors and 7 (15.9%) non-survivors. Non-survivors had a 2.5 times higher plasma SFTSV load than survivors at admission (p < 0.001), and the viral load in non-survivors increased progressively during hospitalization. In addition, non-survivors did not develop adequate anti-SFTSV IgG, whereas survivors exhibited anti-SFTSV IgG during hospitalization. IFN-α, IL-10, IP-10, IFN-γ, IL-6, IL-8, MCP-1, MIP-1α, and G-CSF were significantly elevated in non-survivors compared to survivors and did not revert to normal ranges during hospitalization (p < 0.05). Severe signs of inflammation such as a high plasma concentration of IFN-α, IL-10, IP-10, IFN-γ, IL-6, IL-8, MCP-1, MIP-1α, and G-CSF, poor viral control, and inadequate antibody response during the disease course were associated with mortality in SFTS patients.

1 January 2021 in Journal of Korean Medical Science
Verified
Journal Article
Open access
PDF file
SPSeong Yeon Park
Seong Yeon Park
KLKwang-Hoon Lee
Kwang-Hoon Lee
Park SY, et al. J Korean Med Sci. 2021 Dec;36(50):e344. https://doi.org/10.3346/jkms.2021.36.e344