Li-Chuan Weng
Mackay Memorial Hospital
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Featured researches published by Li-Chuan Weng.
PLOS ONE | 2014
Hsin Chi; Chyong-Hsin Hsu; Jui-Hsing Chang; Nan-Chang Chiu; Han-Yang Hung; Hsin-An Kao; Li-Chuan Weng; Fu-Yuan Huang; Yu-Ying Chiu; Luan-Yin Chang; Li-Min Huang
Background Respiratory syncytial virus (RSV) circulates year round in Taiwan. A novel six consecutive monthly doses of palivizumab for RSV prevention protocol has been approved for high risk preterm infants since December 2010. This study aimed to determine the clinical effectiveness and safety of this novel protocol for the prevention of RSV infection. Methods From April 2011 to March 2013, we enrolled infants born at ≤28 weeks gestation and infants born at ≤35 weeks gestation with chronic lung disease (CLD) who received palivizumab prophylaxis as study group and followed up for 12 months. Historic control, those who were born and followed up between July 2000 and June 2008, were retrieved for propensity score matching. Primary endpoint was RSV-related hospitalization, and secondary endpoints included the length of hospital stay and intensive care unit (ICU) care. Results We enrolled 127 infants (108 infants born at ≤28 weeks and 19 infants born at 29–35 weeks with CLD). They completed 6-dose palivizumab as scheduled. Among the study group, the RSV-related hospitalizations were 2 (1.6%) within 6 months and 5 (3.9%) within 12 months after discharge. We matched 127 infants in the control group with 127 infants in the study group by propensity score matching. The reduction of RSV-related hospitalization rates were 86% (10.2% vs 1.6%, p = 0.002) within 6 months after discharge and 78% (15.7% vs 3.9%, p = 0.004) within 12 months after discharge. Compared to the control group, the rate of ICU care significantly decreased from 7.1% to 0.8% (p = 0.024) within 6 months after discharge and from 7.9% to 0.8% (p = 0.014) within 12 months after discharge. Adverse events were recorded in 6.4% injections. Conclusions Six monthly intramuscular administration of palivizumab is effective for prevention of RSV hospitalization in regions with no single seasonal peak of RSV infection such as Taiwan.
PLOS ONE | 2013
Hsin Chi; Hsin-Fu Liu; Li-Chuan Weng; Nai-Yu Wang; Nan-Chang Chiu; Mei-Ju Lai; Yung Cheng Lin; Yu-Ying Chiu; Wen-Shyang Hsieh; Li-Min Huang
Background and Aims The glycoprotein (G protein) and fusion protein (F protein) of respiratory syncytial virus (RSV) both show genetic variability, but few studies have examined the F protein gene. This study aimed to characterize the molecular epidemiology and phylodynamics of the F protein gene in clinical RSV strains isolated in northern Taiwan from 2000–2011. Methods RSV isolates from children presenting with acute respiratory symptoms between July 2000 and June 2011 were typed based on F protein gene sequences. Phylogeny construction and evaluation were performed using the neighbor-joining (NJ) and maximum likelihood (ML) methods. Phylodynamic patterns in RSV F protein genes were analyzed using the Bayesian Markov Chain Monte Carlo framework. Selection pressure on the F protein gene was detected using the Datamonkey website interface. Results From a total of 325 clinical RSV strains studied, phylogenetic analysis showed that 83 subgroup A strains (RSV-A) could be further divided into three clusters, whereas 58 subgroup B strains (RSV-B) had no significant clustering. Three amino acids were observed to differ between RSV-A and -B (positions 111, 113, and 114) in CTL HLA-B*57- and HLA-A*01-restricted epitopes. One positive selection site was observed in RSV-B, while none was observed in RSV-A. The evolution rate of the virus had very little change before 2000, then slowed down between 2000 and 2005, and evolved significantly faster after 2005. The dominant subtypes of RSV-A in each epidemic were replaced by different subtypes in the subsequent epidemic. Conclusions Before 2004, RSV-A infections were involved in several small epidemics and only very limited numbers of strains evolved and re-emerged in subsequent years. After 2005, the circulating RSV-A strains were different from those of the previous years and continued evolving through 2010. Phylodynamic pattern showed the evolutionary divergence of RSV increased significantly in the recent 5 years in northern Taiwan.
Journal of Hospital Infection | 2004
C.-P. Liu; Nai-Yu Wang; Chun-Ming Lee; Li-Chuan Weng; Hsiang-Kuang Tseng; Chang-Pan Liu; Chuen-Sheue Chiang; Fu-Yuan Huang
Journal of Microbiology Immunology and Infection | 2011
Chi-Chun Sung; Hsin Chi; Nan-Chang Chiu; Daniel Tsung-Ning Huang; Li-Chuan Weng; Nai-Yu Wang; Fu-Yuan Huang
Journal of Infection | 2007
Chang-Pan Liu; Li-Chuan Weng; Hsiang-Kuang Tseng; Nai-Yu Wang; Chun-Ming Lee
Journal of Microbiology Immunology and Infection | 2008
Ching-Hsiang Leung; Nai-Yu Wang; Chang-Pan Liu; Li-Chuan Weng; Feng-Chih Hsieh; Chun-Ming Lee
Journal of Microbiology Immunology and Infection | 1999
Li-Chuan Weng; Liaw Gj; Nai-Yu Wang; Wang Sf; Lee Cm; Fu-Yuan Huang; Yang Di; Chiang Cs
Journal of Microbiology Immunology and Infection | 2017
Jia Lu Cheng; Chun-Chih Peng; Nan-Chang Chiu; Li-Chuan Weng; Yu-Ying Chiu; Lung Chang; Daniel Tsung-Ning Huang; Fu-Yuan Huang; Chang-Pan Liu; Hsin Chi
Journal of Microbiology Immunology and Infection | 1999
Nai-Yu Wang; Liaw Gj; Li-Chuan Weng; Yu-Ying Chiu; Fu-Yuan Huang; Yang Dl; Chiang Cs
Acta paediatrica Taiwanica | 1999
Wen-Chen Li; Chuen-Sheue Chiang; Nan-Chang Chiu; Li-Chuan Weng; Dine-Ie Yang; Ceng-Ping Cheng; Hung-Chang Lee; Chun-Yan Yeung; Fu-Yuan Huang