Carlos K H Wong

Dr. Carlos K H Wong

orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

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

Representative Publications

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24 August 2022 in The Lancet Infectious Diseases
Verified
Journal Article
Closed access
CWCarlos K H Wong
Carlos K H Wong
IAIvan C H Au
Ivan C H Au
KLKristy T K Lau
Kristy T K Lau
ELEric H Y Lau
Eric H Y Lau
BCBenjamin Cowling
Benjamin Cowling
GLGabriel M Leung
Gabriel M Leung

13 January 2023 in Nature Medicine
Verified
Journal Article
Open access
PDF file
KLKathy Leung
Kathy Leung
ELEric H. Y. Lau
Eric H. Y. Lau
CWCarlos K H Wong
Carlos K H Wong
GLGabriel M. Leung
Gabriel M. Leung
JWJoseph T. Wu
Joseph T. Wu
We tracked the effective reproduction number Rt of the predominant SARS-CoV-2 variant Omicron BF.7 in Beijing in November – December 2022 by fitting a transmission dynamic model parameterized with real-time mobility data to (i) the daily number of new symptomatic cases on November 1–11 (when China’s zero-COVID interventions were still strictly enforced) and (ii) the proportion of individuals who participated in online polls on December 10–22 and self-reported to have been test-positive since November 1. After China’s announcement of ‘20 measures’ to transition from zero-COVID, we estimated that Rt increased to 3.44 (95% CrI: 2.82–4.14) on November 18 and the infection incidence peaked on December 11. We estimated that the cumulative infection attack rate (that is the proportion of population who have been infected since November 1) in Beijing was 75.7% (95% CrI: 60.7–84.4) on December 22, 2022, and 92.3% (95% CrI: 91.4–93.1) on January 31, 2023. Surveillance programmes should be rapidly set up to monitor the evolving epidemiology and evolution of SARS-CoV-2 across China.

16 August 2023 in eClinicalMedicine
Verified
Journal Article
Open access
KPKuan Peng
Kuan Peng
XLXue Li
Xue Li
DYDeliang Yang
Deliang Yang
SCShirley C.W. Chan
Shirley C.W. Chan
JZJiayi Zhou
Jiayi Zhou
IWIan Chi Kei Wong
Ian Chi Kei Wong
Case reports suggest that SARS-CoV-2 infection could lead to immune dysregulation and trigger autoimmunity while COVID-19 vaccination is effective against severe COVID-19 outcomes. We aim to examine the association between COVID-19 and development of autoimmune diseases (ADs), and the potential protective effect of COVID-19 vaccination on such an association. A retrospective cohort study was conducted in Hong Kong between 1 April 2020 and 15 November 2022. COVID-19 was confirmed by positive polymerase chain reaction or rapid antigen test. Cox proportional hazard regression with inverse probability of treatment weighting was applied to estimate the risk of incident ADs following COVID-19. COVID-19 vaccinated population was compared against COVID-19 unvaccinated population to examine the protective effect of COVID-19 vaccination on new ADs. The study included 1,028,721 COVID-19 and 3,168,467 non-COVID individuals. Compared with non-COVID controls, patients with COVID-19 presented an increased risk of developing pernicious anaemia [adjusted Hazard Ratio (aHR): 1.72; 95% Confidence Interval (CI): 1.12–2.64]; spondyloarthritis [aHR: 1.32 (95% CI: 1.03–1.69)]; rheumatoid arthritis [aHR: 1.29 (95% CI: 1.09–1.54)]; other autoimmune arthritis [aHR: 1.43 (95% CI: 1.33–1.54)]; psoriasis [aHR: 1.42 (95% CI: 1.13–1.78)]; pemphigoid [aHR: 2.39 (95% CI: 1.83–3.11)]; Graves' disease [aHR: 1.30 (95% CI: 1.10–1.54)]; anti-phospholipid antibody syndrome [aHR: 2.12 (95% CI: 1.47–3.05)]; immune mediated thrombocytopenia [aHR: 2.1 (95% CI: 1.82–2.43)]; multiple sclerosis [aHR: 2.66 (95% CI: 1.17–6.05)]; vasculitis [aHR: 1.46 (95% CI: 1.04–2.04)]. Among COVID-19 patients, completion of two doses of COVID-19 vaccine shows a decreased risk of pemphigoid, Graves' disease, anti-phospholipid antibody syndrome, immune-mediated thrombocytopenia, systemic lupus erythematosus and other autoimmune arthritis. Our findings suggested that COVID-19 is associated with an increased risk of developing various ADs and the risk could be attenuated by COVID-19 vaccination. Future studies investigating pathology and mechanisms would be valuable to interpreting our findings. Supported by RGC Collaborative Research Fund (C7154-20GF).

25 January 2022 in Annals of Internal Medicine
Verified
Journal Article
Open access
FLFrancisco Lai
Francisco Lai
XLXue Li
Xue Li
KPKuan Peng
Kuan Peng
LHLei Huang
Lei Huang
PIPatrick Ip
Patrick Ip
IWIan Chi Kei Wong
Ian Chi Kei Wong
This case–control study from Hong Kong examined the association between COVID-19 vaccination with an mRNA vaccine or an inactivated virus vaccine and subsequent risk for carditis. The results could... Visual Carditis Risk After Messenger RNA and Inactivated Virus Vaccination. This case–control study from Hong Kong examined the association between COVID-19 vaccination with an mRNA vaccin... Background: Case reports of carditis after BNT162b2 vaccination are accruing worldwide. Objective: To examine the association of BNT162b2 and CoronaVac (Sinovac) vaccination with carditis. Design: ...

14 November 2017 in Diabetes Care
Verified
Journal Article
Open access
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EWEric Yuk Fai Wan
Eric Yuk Fai Wan
CFColman Siu Cheung Fung
Colman Siu Cheung Fung
FJFang Fang Jiao
Fang Fang Jiao
EYEsther Yee Tak Yu
Esther Yee Tak Yu
WCWeng Yee Chin
Weng Yee Chin
CLCindy Lo Kuen Lam
Cindy Lo Kuen Lam
OBJECTIVE: To evaluate the 5-year effectiveness of a multidisciplinary Risk Assessment and Management Programme–Diabetes Mellitus (RAMP-DM) in primary care patients with type 2 diabetes. RESEARCH DESIGN AND METHODS: A 5-year prospective cohort study was conducted with 121,584 Chinese primary care patients with type 2 DM who were recruited between August 2009 and June 2011. Missing data were dealt with multiple imputations. After excluding patients with prior diabetes mellitus (DM)-related complications and one-to-one propensity score matching on all patient characteristics, 26,718 RAMP-DM participants and 26,718 matched usual care patients were followed up for a median time of 4.5 years. The effect of RAMP-DM on nine DM-related complications and all-cause mortality were evaluated using Cox regressions. The first incidence for each event was used for all models. Health service use was analyzed using negative binomial regressions. Subgroup analyses on different patient characteristics were performed. RESULTS: The cumulative incidence of all events (DM-related complications and all-cause mortality) was 23.2% in the RAMP-DM group and 43.6% in the usual care group. RAMP-DM led to significantly greater reductions in cardiovascular disease (CVD) risk by 56.6% (95% CI 54.5, 58.6), microvascular complications by 11.9% (95% CI 7.0, 16.6), mortality by 66.1% (95% CI 64.3, 67.9), specialist attendance by 35.0% (95% CI 33.6, 36.4), emergency attendance by 41.2% (95% CI 39.8, 42.5), and hospitalizations by 58.5% (95% CI 57.2, 59.7). Patients with low baseline CVD risks benefitted the most from RAMP-DM, which decreased CVD and mortality risk by 60.4% (95% CI 51.8, 67.5) and 83.6% (95% CI 79.3, 87.0), respectively. CONCLUSIONS: This naturalistic study highlighted the importance of early optimal DM control and risk factor management by risk stratification and multidisciplinary, protocol-driven, chronic disease model care to delay disease progression and prevent complications.