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Featured researches published by Ina Jeong.


The New England Journal of Medicine | 2012

Linezolid for Treatment of Chronic Extensively Drug-Resistant Tuberculosis

Myungsun Lee; Jong Seok Lee; Matthew W. Carroll; Hongjo Choi; Seonyeong Min; Laura E. Via; Lisa C. Goldfeder; Eunhwa Kang; Boyoung Jin; Hyunchul Kim; Han-Seung Jeon; Ina Jeong; Joon Sung Joh; Ray Y. Chen; Kenneth N. Olivier; Pamela A. Shaw; Dean Follmann; Sun Dae Song; Jong-Koo Lee; Duk-Hyoung Lee; Cheon Tae Kim; Véronique Dartois; Seung-Kyu Park; Sang-Nae Cho; Clifton E. Barry

BACKGROUND Linezolid has antimycobacterial activity in vitro and is increasingly used for patients with highly drug-resistant tuberculosis. METHODS We enrolled 41 patients who had sputum-culture-positive extensively drug-resistant (XDR) tuberculosis and who had not had a response to any available chemotherapeutic option during the previous 6 months. Patients were randomly assigned to linezolid therapy that started immediately or after 2 months, at a dose of 600 mg per day, without a change in their background regimen. The primary end point was the time to sputum-culture conversion on solid medium, with data censored 4 months after study entry. After confirmed sputum-smear conversion or 4 months (whichever came first), patients underwent a second randomization to continued linezolid therapy at a dose of 600 mg per day or 300 mg per day for at least an additional 18 months, with careful toxicity monitoring. RESULTS By 4 months, 15 of the 19 patients (79%) in the immediate-start group and 7 of the 20 (35%) in the delayed-start group had culture conversion (P=0.001). Most patients (34 of 39 [87%]) had a negative sputum culture within 6 months after linezolid had been added to their drug regimen. Of the 38 patients with exposure to linezolid, 31 (82%) had clinically significant adverse events that were possibly or probably related to linezolid, including 3 patients who discontinued therapy. Patients who received 300 mg per day after the second randomization had fewer adverse events than those who continued taking 600 mg per day. Thirteen patients completed therapy and have not had a relapse. Four cases of acquired resistance to linezolid have been observed. CONCLUSIONS Linezolid is effective at achieving culture conversion among patients with treatment-refractory XDR pulmonary tuberculosis, but patients must be monitored carefully for adverse events. (Funded by the National Institute of Allergy and Infectious Diseases and the Ministry of Health and Welfare, South Korea; ClinicalTrials.gov number, NCT00727844.).


The New England Journal of Medicine | 2015

Linezolid for XDR-TB--Final Study Outcomes.

Myungsun Lee; Taeksun Song; Youngran Kim; Ina Jeong; Sang-Nae Cho; Clifton E. Barry

Treatment of extensively drug-resistant mycobacteria tuberculosis is a growing global challenge. In this report, the durability of linezolid as an adjunctive XDR-TB treatment is presented.


Emerging Infectious Diseases | 2016

Microevolution of Outbreak-Associated Middle East Respiratory Syndrome Coronavirus, South Korea, 2015.

Moon-Woo Seong; So Yeon Kim; Victor Max Corman; Taek Soo Kim; Sung Im Cho; Man Jin Kim; Seung-Jun Lee; Jee-Soo Lee; Soo Hyun Seo; Ji Soo Ahn; Byeong Su Yu; Nare Park; Myoung-don Oh; Wan Beom Park; Jiyeon Lee; Gayeon Kim; Joon Sung Joh; Ina Jeong; Eui Chong Kim; Christian Drosten; Sung Sup Park

During the 2015 Middle East respiratory syndrome coronavirus outbreak in South Korea, we sequenced full viral genomes of strains isolated from 4 patients early and late during infection. Patients represented at least 4 generations of transmission. We found no evidence of changes in the evolutionary rate and no reason to suspect adaptive changes in viral proteins.


International Journal of Chronic Obstructive Pulmonary Disease | 2015

Association of blood eosinophils and plasma periostin with FEV1 response after 3-month inhaled corticosteroid and long-acting beta2-agonist treatment in stable COPD patients

Hye Yun Park; Hyun Moo Lee; Won-Jung Koh; Seonwoo Kim; Ina Jeong; Hyeon-Kyoung Koo; Tae-Hyung Kim; Jinwoo Kim; Woo Jin Kim; Yeon-Mok Oh; Don D. Sin; Seong Yong Lim; Sang-Do Lee

Background COPD patients with increased airway eosinophilic inflammation show a favorable response to inhaled corticosteroids (ICS) in combination with a long-acting bronchodilator. Recent studies have demonstrated a significant correlation of sputum eosinophilia with blood eosinophils and periostin. We investigated whether high blood eosinophils and plasma periostin were associated with an improvement in forced expiratory volume in 1 second (FEV1) after 3-month treatment with ICS/long-acting beta2-agonist (LABA) in stable COPD patients. Patients and methods Blood eosinophils and plasma periostin levels were measured in 130 stable COPD subjects selected from the Korean Obstructive Lung Disease cohort. Subjects began a 3-month ICS/LABA treatment after washout period. Results High blood eosinophils (>260/µL, adjusted odds ratio =3.52, P=0.009) and high plasma periostin (>23 ng/mL, adjusted odds ratio =3.52, P=0.013) were significantly associated with FEV1 responders (>12% and 200 mL increase in FEV1 from baseline after treatment). Moreover, the addition of high blood eosinophils to age, baseline positive bronchodilator response, and FEV1 <50% of the predicted value significantly increased the area under the curve for prediction of FEV1 responders (from 0.700 to 0.771; P=0.045). Conclusion High blood eosinophils and high plasma periostin were associated with improved lung function after 3-month ICS/LABA treatment. In particular, high blood eosinophils, in combination with age and baseline lung function parameters, might be a possible biomarker for identification of COPD patients with favorable FEV1 improvement in response to ICS/LABA treatment.


Respirology | 2012

Vitamin D deficiency and changes in serum vitamin D levels with treatment among tuberculosis patients in South Korea

Hyeon-Kyoung Koo; Ji Sun Lee; Yun Jeong Jeong; Sun Mi Choi; Hyo Jae Kang; Hyo-Jeong Lim; Ina Jeong; Jong Sun Park; Sang Min Lee; Seok-Chul Yang; Chul-Gyu Yoo; Young Whan Kim; Sung-Koo Han; Jae-Joon Yim

Background and objective:  Vitamin D deficiency has been reported to be associated with the development of active tuberculosis (TB), but many discrepancies exist among studies. The aims of this study were to compare the frequency of vitamin D deficiency in a Korean population of TB patients and control subjects, and to monitor the changes in vitamin D levels during TB treatment.


American Journal of Infection Control | 2010

Mild form of 2009 H1N1 influenza infection detected by active surveillance: Implications for infection control

Ina Jeong; Chang-Hoon Lee; Deog Kyeom Kim; Hee Soon Chung; Sang Won Park

BACKGROUND Screening patients with suspected influenza is a key step for infection control within communities and institutions. By analyzing the clinical characteristics of mild 2009 H1N1 influenza cases detected by active surveillance, we assessed the utility of the commonly used influenza case definition. METHODS We retrospectively reviewed medical records of 44 patients who were hospitalized and quarantined and who tested positive for the 2009 H1N1 virus using real-time reverse-transcriptase polymerase chain reaction between May 29 and July 28, 2009. RESULTS Patient median age was 17 years (range, 8-79 years), and 37 patients were male (84%). Common symptoms included cough (34/44; 77.3%), subjective fever (23/44; 52.3%), rhinorrhea or nasal congestion (22/44; 50%), sore throat (19/44; 43.2%), and diarrhea (7/44; 15.9%). All patients were treated with oseltamivir after the onset of initial symptoms (mean, 2.6 days). Common laboratory test results included leucopenia (23/44; 52.3%) and mildly elevated C-reactive protein (26/44; 59.1%). CONCLUSION There were many mild afebrile cases of the 2009 pandemic H1N1 influenza. Cough, mild leukopenia, and mildly elevated C-reactive protein were relatively common clinical manifestations. Thus, case-based surveillance for the index cluster of 2009 pandemic influenza is not an effective method for infection control in communities or hospital settings.


Journal of Korean Medical Science | 2015

Renal Complications and Their Prognosis in Korean Patients with Middle East Respiratory Syndrome-Coronavirus from the Central MERS-CoV Designated Hospital

Ran Hui Cha; Joon Sung Joh; Ina Jeong; Ji Yeon Lee; Hyoung-Shik Shin; Gayeon Kim; Yeonjae Kim

Some cases of Middle East Respiratory Syndrome-Coronavirus (MERS-CoV) infection presented renal function impairment after the first MERS-CoV patient died of progressive respiratory and renal failure. Thus, MERS-CoV may include kidney tropism. However, reports about the natural courses of MERS-CoV infection in terms of renal complications are scarce. We examined 30 MERS-CoV patients admitted to National Medical Center, Korea. We conducted a retrospective analysis of the serum creatinine (SCr), estimated glomerular filtration rate (eGFR), urine dipstick tests, urinary protein quantitation (ACR or PCR), and other clinical parameters in all patients. Two consecutive results of more than trace (or 1+) of albumin and blood on dipstick test occurred in 18 (60%) (12 [40%]) and 22 (73.3%) (19 [63.3%]) patients, respectively. Fifteen (50.0%) patients showed a random urine ACR or PCR more than 100 mg/g Cr. Eight (26.7%) patients showed acute kidney injury (AKI), and the mean and median durations to the occurrence of AKI from symptom onset were 18 and 16 days, respectively. Old age was associated with a higher occurrence of AKI in the univariate analysis (HR [95% CI]: 1.069 [1.013-1.128], P = 0.016) and remained a significant predictor of the occurrence of AKI after adjustment for comorbidities and the application of a mechanical ventilator. Diabetes, AKI, and the application of a continuous renal replacement therapy (CRRT) were risk factors for mortality in the univariate analysis (HR [95% CI]: diabetes; 10.133 [1.692-60.697], AKI; 12.744 [1.418-114.565], CRRT; 10.254 [1.626-64.666], respectively). Here, we report renal complications and their prognosis in 30 Korean patients with MERS-CoV.


Tuberculosis and Respiratory Diseases | 2016

The Korean Cough Guideline: Recommendation and Summary Statement.

Chin Kook Rhee; Ji Ye Jung; Sei Won Lee; Joo-Hee Kim; So Young Park; Kwang Ha Yoo; Dong Ah Park; Hyeon Kyoung Koo; Yee Hyung Kim; Ina Jeong; Je Hyeong Kim; Deog Kyeom Kim; Sung Kyoung Kim; Yong Hyun Kim; Jinkyeong Park; Eun Young Choi; Ki Suck Jung; Hui Jung Kim

Cough is one of the most common symptom of many respiratory diseases. The Korean Academy of Tuberculosis and Respiratory Diseases organized cough guideline committee and cough guideline was developed by this committee. The purpose of this guideline is to help clinicians to diagnose correctly and treat efficiently patients with cough. In this article, we have stated recommendation and summary of Korean cough guideline. We also provided algorithm for acute, subacute, and chronic cough. For chronic cough, upper airway cough syndrome (UACS), cough variant asthma (CVA), and gastroesophageal reflux disease (GERD) should be considered. If UACS is suspicious, first generation anti-histamine and nasal decongestant can be used empirically. In CVA, inhaled corticosteroid is recommended in order to improve cough. In GERD, proton pump inhibitor is recommended in order to improve cough. Chronic bronchitis, bronchiectasis, bronchiolitis, lung cancer, aspiration, angiotensin converting enzyme inhibitor, habit, psychogenic cough, interstitial lung disease, environmental and occupational factor, tuberculosis, obstructive sleep apnea, peritoneal dialysis, and idiopathic cough can be also considered as cause of chronic cough. Level of evidence for treatment is mostly low. Thus, in this guideline, many recommendations are based on expert opinion. Further study regarding treatment for cough is mandatory.


Trials | 2017

Substitution of ethambutol with linezolid during the intensive phase of treatment of pulmonary tuberculosis: study protocol for a prospective, multicenter, randomized, open-label, phase II trial

Jiyeon Lee; Deog Kyeom Kim; Jung-Kyu Lee; Ho Il Yoon; Ina Jeong; Eunyoung Heo; Young Sik Park; Jae Ho Lee; Sung Soo Park; Sang Min Lee; Chang-Hoon Lee; Jinwoo Lee; Sun Mi Choi; Jong Sun Park; Joon-Sung Joh; Young-Jae Cho; Yeon Joo Lee; Se Joong Kim; Young Ran Hwang; Hyeonjeong Kim; Jongeun Ki; Hyungsook Choi; J.K. Han; Heejung Ahn; Seokyung Hahn; Jae-Joon Yim

BackgroundLinezolid, an oxazolidinone, substantially improves treatment outcomes of multidrug-resistant tuberculosis and extensively drug-resistant tuberculosis. We started a trial to test whether the use of linezolid instead of ethambutol could increase the rate of sputum culture conversion as of 8 weeks of treatment in patients with drug-susceptible tuberculosis.Methods/designThis is a phase II, multicenter, randomized study with three arms. We are enrolling patients with pulmonary tuberculosis without rifampicin resistance screened by the Xpert MTB/RIF® assay. The standard treatment arm uses isoniazid (6 months), rifampicin (6 months), pyrazinamide (2 months), and ethambutol (2 months). Experimental arm 1 uses linezolid (600 mg/day) for 4 weeks instead of ethambutol. Experimental arm 2 uses linezolid (600 mg/day) for 2 weeks instead of ethambutol. The primary outcome is the sputum culture conversion rate on liquid media after 2 months of treatment. Secondary outcomes include the sputum culture conversion rate on solid media after 2 months of treatment, time to sputum culture conversion on liquid and solid media, cure rate, and treatment success rate. The frequencies of total adverse events (AEs) and serious AEs will be described and documented. Based on an α = 0.05 level of significance, a power of 85%, a 15% difference in the culture conversion rate after 2 months between the control arm and experimental arm 1 (75% vs. 90%), a 10% default (loss to follow-up) rate, and a 10% culture failure, the required number per arm was calculated to be 143 (429 in total).DiscussionThis trial will reveal the effectiveness and safety of 2 or 4 weeks of use of linezolid instead of ethambutol for patients with drug-susceptible pulmonary tuberculosis. If a new regimen including linezolid shows a higher culture conversion rate by week 8, and is safe, it could be tested as a 4-month antituberculosis treatment regimen in the future.Trial registrationClincalTrials.gov, NCT01994460. Registered on 13 November 2013.


American Journal of Infection Control | 2017

A Middle East respiratory syndrome screening clinic for health care personnel during the 2015 Middle East respiratory syndrome outbreak in South Korea: A single-center experience

Jiyeon Lee; Gayeon Kim; Dong-Gyun Lim; Hyeon-Gun Jee; Yunyoung Jang; Joon-Sung Joh; Ina Jeong; Yeonjae Kim; Eunhee Kim; Bum Sik Chin

Background: Transmission of Middle East respiratory syndrome (MERS) to health care personnel (HCP) is a major concern. This study aimed to review cases of MERS‐related events, such as development of MERS‐like symptoms or exposure to patients. Methods: A MERS screening clinic (MSC) for HCP was setup in the National Medical Center during the MERS outbreak in 2015. Clinical and laboratory data from HCP who visited the MSC were retrospectively reviewed. Additionally, these data were compared with the results of postoutbreak questionnaire surveys and interviews about MERS‐related symptoms and risk‐related events. Results: Of the 333 HCP who participated in MERS patient care, 35 HCP (10.5%) visited the MSC for MERS‐like symptoms. No one was infected with MERS, and the most common symptom was fever (68.6%) followed by cough (34.3%). However, 106 of 285 postoutbreak survey participants experienced at least 1 MERS‐related symptom and 26 reported exposure to patients without appropriate personal protective equipment, whereas only 4 HCP visited the MSC to report exposure events. Conclusions: Although a considerable number of HCP experienced MERS‐related symptoms or unprotected exposure during MERS patient care, some did not take appropriate action. These findings imply that for infection control strategy to be properly performed, education should be strengthened so that HCP can accurately recognize the risk situation and properly notify the infection control officer.

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Jiyeon Lee

Seoul National University

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Deog Kyeom Kim

Seoul Metropolitan Government

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Gayeon Kim

Seoul National University

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Chang-Hoon Lee

Seoul Metropolitan Government

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Myungsun Lee

National Institutes of Health

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Chin Kook Rhee

Catholic University of Korea

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