File Download
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.ijid.2020.09.022
- Scopus: eid_2-s2.0-85093667923
- PMID: 32947055
- WOS: WOS:000596075200019
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Development and Validation of Risk Prediction Models for COVID-19 Positivity in a Hospital Setting
Title | Development and Validation of Risk Prediction Models for COVID-19 Positivity in a Hospital Setting |
---|---|
Authors | |
Keywords | COVID-19 Prediction model Nomogram White cell count Chest x-ray |
Issue Date | 2020 |
Publisher | Elsevier - Open Access. The Journal's web site is located at http://www.elsevier.com/locate/ijid |
Citation | International Journal of Infectious Diseases, 2020, v. 101, p. 74-82 How to Cite? |
Abstract | Objectives:
To develop: (1) two validated risk prediction models for coronavirus disease-2019 (COVID-19) positivity using readily available parameters in a general hospital setting; (2) nomograms and probabilities to allow clinical utilisation.
Methods:
Patients with and without COVID-19 were included from 4 Hong Kong hospitals. The database was randomly split into 2:1: for model development database (n = 895) and validation database (n = 435). Multivariable logistic regression was utilised for model creation and validated with the Hosmer–Lemeshow (H–L) test and calibration plot. Nomograms and probabilities set at 0.1, 0.2, 0.4 and 0.6 were calculated to determine sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV).
Results:
A total of 1330 patients (mean age 58.2 ± 24.5 years; 50.7% males; 296 COVID-19 positive) were recruited. The first prediction model developed had age, total white blood cell count, chest x-ray appearances and contact history as significant predictors (AUC = 0.911 [CI = 0.880−0.941]). The second model developed has the same variables except contact history (AUC = 0.880 [CI = 0.844−0.916]). Both were externally validated on the H–L test (p = 0.781 and 0.155, respectively) and calibration plot. Models were converted to nomograms. Lower probabilities give higher sensitivity and NPV; higher probabilities give higher specificity and PPV.
Conclusion:
Two simple-to-use validated nomograms were developed with excellent AUCs based on readily available parameters and can be considered for clinical utilisation. |
Persistent Identifier | http://hdl.handle.net/10722/287273 |
ISSN | 2023 Impact Factor: 4.8 2023 SCImago Journal Rankings: 1.435 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ng, MY | - |
dc.contributor.author | Wan, EYF | - |
dc.contributor.author | Wong, HYF | - |
dc.contributor.author | Leung, ST | - |
dc.contributor.author | Lee, JCY | - |
dc.contributor.author | Chin, TWY | - |
dc.contributor.author | Lo, CSY | - |
dc.contributor.author | Lui, MMS | - |
dc.contributor.author | Chan, EHT | - |
dc.contributor.author | Fong, AHT | - |
dc.contributor.author | Fung, SY | - |
dc.contributor.author | Ching, OH | - |
dc.contributor.author | Chiu, KWH | - |
dc.contributor.author | Chung, TWH | - |
dc.contributor.author | Vardhanabhuti, V | - |
dc.contributor.author | Lam, HYS | - |
dc.contributor.author | To, KKW | - |
dc.contributor.author | Chiu, JLF | - |
dc.contributor.author | Lam, TPW | - |
dc.contributor.author | Khong, PL | - |
dc.contributor.author | Liu, RWT | - |
dc.contributor.author | Chan, JWM | - |
dc.contributor.author | Wu, KLA | - |
dc.contributor.author | Lung, KC | - |
dc.contributor.author | Hung, IFN | - |
dc.contributor.author | Lau, CS | - |
dc.contributor.author | Kuo, MD | - |
dc.contributor.author | Ip, MSM | - |
dc.date.accessioned | 2020-09-22T02:58:28Z | - |
dc.date.available | 2020-09-22T02:58:28Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | International Journal of Infectious Diseases, 2020, v. 101, p. 74-82 | - |
dc.identifier.issn | 1201-9712 | - |
dc.identifier.uri | http://hdl.handle.net/10722/287273 | - |
dc.description.abstract | Objectives: To develop: (1) two validated risk prediction models for coronavirus disease-2019 (COVID-19) positivity using readily available parameters in a general hospital setting; (2) nomograms and probabilities to allow clinical utilisation. Methods: Patients with and without COVID-19 were included from 4 Hong Kong hospitals. The database was randomly split into 2:1: for model development database (n = 895) and validation database (n = 435). Multivariable logistic regression was utilised for model creation and validated with the Hosmer–Lemeshow (H–L) test and calibration plot. Nomograms and probabilities set at 0.1, 0.2, 0.4 and 0.6 were calculated to determine sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV). Results: A total of 1330 patients (mean age 58.2 ± 24.5 years; 50.7% males; 296 COVID-19 positive) were recruited. The first prediction model developed had age, total white blood cell count, chest x-ray appearances and contact history as significant predictors (AUC = 0.911 [CI = 0.880−0.941]). The second model developed has the same variables except contact history (AUC = 0.880 [CI = 0.844−0.916]). Both were externally validated on the H–L test (p = 0.781 and 0.155, respectively) and calibration plot. Models were converted to nomograms. Lower probabilities give higher sensitivity and NPV; higher probabilities give higher specificity and PPV. Conclusion: Two simple-to-use validated nomograms were developed with excellent AUCs based on readily available parameters and can be considered for clinical utilisation. | - |
dc.language | eng | - |
dc.publisher | Elsevier - Open Access. The Journal's web site is located at http://www.elsevier.com/locate/ijid | - |
dc.relation.ispartof | International Journal of Infectious Diseases | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | COVID-19 | - |
dc.subject | Prediction model | - |
dc.subject | Nomogram | - |
dc.subject | White cell count | - |
dc.subject | Chest x-ray | - |
dc.title | Development and Validation of Risk Prediction Models for COVID-19 Positivity in a Hospital Setting | - |
dc.type | Article | - |
dc.identifier.email | Ng, MY: myng2@hku.hk | - |
dc.identifier.email | Wan, EYF: yfwan@hku.hk | - |
dc.identifier.email | Fong, AHT: ahtfong@hku.hk | - |
dc.identifier.email | Chiu, KWH: kwhchiu@hku.hk | - |
dc.identifier.email | Vardhanabhuti, V: varv@hku.hk | - |
dc.identifier.email | To, KKW: kelvinto@hku.hk | - |
dc.identifier.email | Khong, PL: plkhong@hku.hk | - |
dc.identifier.email | Hung, IFN: ivanhung@hkucc.hku.hk | - |
dc.identifier.email | Lau, CS: cslau@hku.hk | - |
dc.identifier.email | Ip, MSM: msmip@hku.hk | - |
dc.identifier.authority | Ng, MY=rp01976 | - |
dc.identifier.authority | Wan, EYF=rp02518 | - |
dc.identifier.authority | Chiu, KWH=rp02074 | - |
dc.identifier.authority | Vardhanabhuti, V=rp01900 | - |
dc.identifier.authority | To, KKW=rp01384 | - |
dc.identifier.authority | Khong, PL=rp00467 | - |
dc.identifier.authority | Hung, IFN=rp00508 | - |
dc.identifier.authority | Lau, CS=rp01348 | - |
dc.identifier.authority | Ip, MSM=rp00347 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1016/j.ijid.2020.09.022 | - |
dc.identifier.pmid | 32947055 | - |
dc.identifier.pmcid | PMC7491462 | - |
dc.identifier.scopus | eid_2-s2.0-85093667923 | - |
dc.identifier.hkuros | 314561 | - |
dc.identifier.volume | 101 | - |
dc.identifier.spage | 74 | - |
dc.identifier.epage | 82 | - |
dc.identifier.isi | WOS:000596075200019 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.issnl | 1201-9712 | - |