Facilitating Safe Discharge Through Predicting Disease Progression in Moderate Coronavirus Disease 2019 (COVID-19): A Prospective Cohort Study to Develop and Validate a Clinical Prediction Model in Resource-Limited Settings. (21st March 2022)
- Record Type:
- Journal Article
- Title:
- Facilitating Safe Discharge Through Predicting Disease Progression in Moderate Coronavirus Disease 2019 (COVID-19): A Prospective Cohort Study to Develop and Validate a Clinical Prediction Model in Resource-Limited Settings. (21st March 2022)
- Main Title:
- Facilitating Safe Discharge Through Predicting Disease Progression in Moderate Coronavirus Disease 2019 (COVID-19): A Prospective Cohort Study to Develop and Validate a Clinical Prediction Model in Resource-Limited Settings
- Authors:
- Chandna, Arjun
Mahajan, Raman
Gautam, Priyanka
Mwandigha, Lazaro
Gunasekaran, Karthik
Bhusan, Divendu
Cheung, Arthur T L
Day, Nicholas
Dittrich, Sabine
Dondorp, Arjen
Geevar, Tulasi
Ghattamaneni, Srinivasa R
Hussain, Samreen
Jimenez, Carolina
Karthikeyan, Rohini
Kumar, Sanjeev
Kumar, Shiril
Kumar, Vikash
Kundu, Debasree
Lakshmanan, Ankita
Manesh, Abi
Menggred, Chonticha
Moorthy, Mahesh
Osborn, Jennifer
Richard-Greenblatt, Melissa
Sharma, Sadhana
Singh, Veena K
Singh, Vikash K
Suri, Javvad
Suzuki, Shuichi
Tubprasert, Jaruwan
Turner, Paul
Villanueva, Annavi M G
Waithira, Naomi
Kumar, Pragya
Varghese, George M
Koshiaris, Constantinos
Lubell, Yoel
Burza, Sakib
… (more) - Abstract:
- Abstract: Background: In locations where few people have received coronavirus disease 2019 (COVID-19) vaccines, health systems remain vulnerable to surges in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections. Tools to identify patients suitable for community-based management are urgently needed. Methods: We prospectively recruited adults presenting to 2 hospitals in India with moderate symptoms of laboratory-confirmed COVID-19 to develop and validate a clinical prediction model to rule out progression to supplemental oxygen requirement. The primary outcome was defined as any of the following: SpO2 < 94%; respiratory rate > 30 BPM; SpO2 /FiO2 < 400; or death. We specified a priori that each model would contain three clinical parameters (age, sex, and SpO2 ) and 1 of 7 shortlisted biochemical biomarkers measurable using commercially available rapid tests (C-reactive protein [CRP], D-dimer, interleukin 6 [IL-6], neutrophil-to-lymphocyte ratio [NLR], procalcitonin [PCT], soluble triggering receptor expressed on myeloid cell-1 [sTREM-1], or soluble urokinase plasminogen activator receptor [suPAR]), to ensure the models would be suitable for resource-limited settings. We evaluated discrimination, calibration, and clinical utility of the models in a held-out temporal external validation cohort. Results: In total, 426 participants were recruited, of whom 89 (21.0%) met the primary outcome; 257 participants comprised the development cohort, and 166 comprisedAbstract: Background: In locations where few people have received coronavirus disease 2019 (COVID-19) vaccines, health systems remain vulnerable to surges in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections. Tools to identify patients suitable for community-based management are urgently needed. Methods: We prospectively recruited adults presenting to 2 hospitals in India with moderate symptoms of laboratory-confirmed COVID-19 to develop and validate a clinical prediction model to rule out progression to supplemental oxygen requirement. The primary outcome was defined as any of the following: SpO2 < 94%; respiratory rate > 30 BPM; SpO2 /FiO2 < 400; or death. We specified a priori that each model would contain three clinical parameters (age, sex, and SpO2 ) and 1 of 7 shortlisted biochemical biomarkers measurable using commercially available rapid tests (C-reactive protein [CRP], D-dimer, interleukin 6 [IL-6], neutrophil-to-lymphocyte ratio [NLR], procalcitonin [PCT], soluble triggering receptor expressed on myeloid cell-1 [sTREM-1], or soluble urokinase plasminogen activator receptor [suPAR]), to ensure the models would be suitable for resource-limited settings. We evaluated discrimination, calibration, and clinical utility of the models in a held-out temporal external validation cohort. Results: In total, 426 participants were recruited, of whom 89 (21.0%) met the primary outcome; 257 participants comprised the development cohort, and 166 comprised the validation cohort. The 3 models containing NLR, suPAR, or IL-6 demonstrated promising discrimination (c-statistics: 0.72–0.74) and calibration (calibration slopes: 1.01–1.05) in the validation cohort and provided greater utility than a model containing the clinical parameters alone. Conclusions: We present 3 clinical prediction models that could help clinicians identify patients with moderate COVID-19 suitable for community-based management. The models are readily implementable and of particular relevance for locations with limited resources. Abstract : We report 3 clinical prediction models to help identify which patients with moderate COVID-19 can be safely managed in the community. Each model contains 3 easily ascertained clinical parameters and 1 biochemical biomarker, measurable with a commercially available rapid test. … (more)
- Is Part Of:
- Clinical infectious diseases. Volume 75:Number 1(2022)
- Journal:
- Clinical infectious diseases
- Issue:
- Volume 75:Number 1(2022)
- Issue Display:
- Volume 75, Issue 1 (2022)
- Year:
- 2022
- Volume:
- 75
- Issue:
- 1
- Issue Sort Value:
- 2022-0075-0001-0000
- Page Start:
- e368
- Page End:
- e379
- Publication Date:
- 2022-03-21
- Subjects:
- COVID-19 -- prognostic model -- triage -- low- and middle-income country -- LMIC
Communicable diseases -- Periodicals
616.905 - Journal URLs:
- http://cid.oxfordjournals.org ↗
http://ukcatalogue.oup.com/ ↗
http://www.journals.uchicago.edu/CID/journal ↗
http://www.jstor.org/journals/10584838.html ↗ - DOI:
- 10.1093/cid/ciac224 ↗
- Languages:
- English
- ISSNs:
- 1058-4838
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.293860
British Library DSC - BLDSS-3PM
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