Yu Mi Wi

Prof. Dr. Yu Mi Wi

Division of Infectious Diseases, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon 51353, Korea
orcid

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

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

Representative Publications

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1 January 2016 in Infection & Chemotherapy
Verified
Journal Article
Open access
PDF file
WCWon Suk Choi
Won Suk Choi
CKCheol-In Kang
Cheol-In Kang
YKYonjae Kim
Yonjae Kim
JCJae-Phil Choi
Jae-Phil Choi
JJJoon Sung Joh
Joon Sung Joh
TDThe Korean Society Of Infectious Diseases
The Korean Society Of Infectious Diseases
Choi WS, et al. Infect Chemother. 2016 Jun;48(2):118-126. https://doi.org/10.3947/ic.2016.48.2.118

1 December 2018 in Infectious Disease Clinics of North America
Verified
Journal Article
Closed access
YWYu Mi Wi
Yu Mi Wi
RPRobin Patel
Robin Patel

1 February 2023 in Radiology
Verified
Journal Article
Closed access
YJYeon Joo Jeong
Yeon Joo Jeong
YWYu Mi Wi
Yu Mi Wi
Hyunjin ParkHyunjin Park
Hyunjin Park
JLJong Eun Lee
Jong Eun Lee
SKSi-Ho Kim
Si-Ho Kim
KLKyung Soo Lee
Kyung Soo Lee
Advanced insights into the pathophysiology and imaging features of COVID-19 along with vaccine benefits have improved patient care, but emerging knowledge of post–COVID-19 condition (long COVID) al... COVID-19 has emerged as a pandemic leading to a global public health crisis of unprecedented morbidity. A comprehensive insight into the imaging of COVID-19 has enabled early diagnosis, stratificat...

1 February 2012 in Journal of Clinical Microbiology
Verified
Journal Article
Open access
PDF file
CKCheol-In Kang
Cheol-In Kang
YWYu Mi Wi
Yu Mi Wi
MLMi Young Lee
Mi Young Lee
Kwan Soo KoKwan Soo Ko
Kwan Soo Ko
DCDoo Ryeon Chung
Doo Ryeon Chung
JSJae-Hoon Song
Jae-Hoon Song
Limited clinical information is available regarding community onset infections caused by extended-spectrum β-lactamase (ESBL)-producing Escherichia coli . A case-control study was performed to evaluate the epidemiology and risk factors of these types of infections. A case patient was defined as a person whose clinical sample yielded ESBL-producing E. coli . For each case patient, one control was randomly chosen from a group of outpatients from whom non-ESBL-producing E. coli had been isolated and for whom a clinical sample had been sent to the same laboratory for culturing during the following week. Of 108 cases of ESBL-producing E. coli , 56 (51.9%) were classified as health care associated (HCA). Univariate analysis showed male gender, HCA infection, severe underlying illness, and a prior receipt of antibiotics to be associated with ESBL-producing E. coli . In the multivariate analysis, HCA infection (odds ratio [OR], 3.18; 95% confidence interval [CI], 1.67 to 6.06; P < 0.001) and previous use of antibiotics (OR, 4.88; 95% CI, 2.08 to 11.48; P < 0.001) were found to be significantly associated with the ESBL group. In a multivariate analysis that included each antibiotic, previous use of fluoroquinolone (OR, 7.32; 95% CI, 1.58 to 34.01; P = 0.011) was significantly associated with ESBL-producing E. coli . Of 101 isolates in which ESBLs and their molecular relationships were studied, all isolates produced ESBLs from the CTX-M family (CTX-M-14, 40 isolates; CTX-M-15, 39 isolates; and other members of the CTX-M family, 22 isolates). In conclusion, this study confirms that ESBL-producing E. coli strains are a notable cause of community onset infections in predisposed patients. HCA infection and previous use of fluoroquinolone were significant factors associated with ESBL-producing E. coli in community onset infections.

1 January 2019 in Infection & Chemotherapy
Verified
Journal Article
Open access
YWYu Mi Wi
Yu Mi Wi
Nontuberculous mycobacteria (NTM) diseases mainly manifest as pulmonary illnesses, but 20 -30% of NTM isolates originate from extrapulmonary diseases. These diseases cause a variety of clinical syndromes, including skin and soft-tissue infections, musculoskeletal infections, lymphadenitis, and disseminated disease. In skin and soft-tissue infections, musculoskeletal infections, prolonged treatment with combinations of antibiotics is effective in the treatment of NTM diseases, with surgery as an important complementary tool. The recommended duration of therapy for skin and soft-tissue infection is usually 2 - 4 months for mild disease and 6 months for severe disease, while treatment of musculoskeletal NTM disease usually requires at least 6 - 12 months. Management options of NTM lymphadenitis include surgical intervention, medical therapy, or observation. Treatment of disseminated NTM disease generally requires 6 to 12 months after immune restoration. However, despite a considerable increase in knowledge about NTM diseases, determining optimal treatment approaches remains a complex and challenging task.

1 January 2021 in Journal of Korean Medical Science
Verified
Journal Article
Open access
PDF file
SKSi-Ho Kim
Si-Ho Kim
YWYu Mi Wi
Yu Mi Wi
SYSu Yeon Yun
Su Yeon Yun
JRJeong Seon Ryu
Jeong Seon Ryu
JSJung Min Shin
Jung Min Shin
KPKyong Ran Peck
Kyong Ran Peck
Kim SH, et al. J Korean Med Sci. 2021 Apr;36(14):e107. https://doi.org/10.3346/jkms.2021.36.e107