Obesity and smoking as risk factors for invasive mechanical ventilation in COVID-19: A retrospective, observational cohort study
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Abstract
To describe the trajectory of respiratory failure in COVID-19 and explore factors associated with risk of invasive mechanical ventilation (IMV).
Materials and methods
A retrospective, observational cohort study of 112 inpatient adults diagnosed with COVID-19 between March 12 and April 16, 2020. Data were manually extracted from electronic medical records. Multivariable and Univariable regression were used to evaluate association between baseline characteristics, initial serum markers and the outcome of IMV.
Results
Our cohort had median age of 61 (IQR 45–74) and was 66% male. In-hospital mortality was 6% (7/112). ICU mortality was 12.8% (6/47), and 18% (5/28) for those requiring IMV. Obesity (OR 5.82, CI 1.74–19.48), former (OR 8.06, CI 1.51–43.06) and current smoking status (OR 10.33, CI 1.43–74.67) were associated with IMV after adjusting for age, sex, and high prevalence comorbidities by multivariable analysis. Initial absolute lymphocyte count (OR 0.33, CI 0.11–0.96), procalcitonin (OR 1.27, CI 1.02–1.57), IL-6 (OR 1.17, CI 1.03–1.33), ferritin (OR 1.05, CI 1.005–1.11), LDH (OR 1.57, 95% CI 1.13–2.17) and CRP (OR 1.13, CI 1.06–1.21), were associated with IMV by univariate analysis.
Conclusions
Obesity, smoking history, and elevated inflammatory markers were associated with increased need for IMV in patients with COVID-19.
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SciScore for 10.1101/2020.08.12.20173849: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement IRB: Setting, Patient Population, and Study Design: This is a retrospective observational cohort study conducted from March 12 2020 and April 16 2020 approved by the UCLA (University of California, Los Angeles) institutional review board with waiver of informed consent.
Consent: Setting, Patient Population, and Study Design: This is a retrospective observational cohort study conducted from March 12 2020 and April 16 2020 approved by the UCLA (University of California, Los Angeles) institutional review board with waiver of informed consent.Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: …
SciScore for 10.1101/2020.08.12.20173849: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement IRB: Setting, Patient Population, and Study Design: This is a retrospective observational cohort study conducted from March 12 2020 and April 16 2020 approved by the UCLA (University of California, Los Angeles) institutional review board with waiver of informed consent.
Consent: Setting, Patient Population, and Study Design: This is a retrospective observational cohort study conducted from March 12 2020 and April 16 2020 approved by the UCLA (University of California, Los Angeles) institutional review board with waiver of informed consent.Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: Resources
No key resources detected.
Results from OddPub: We did not detect open data. We also did not detect open code. Researchers are encouraged to share open data when possible (see Nature blog).
Results from LimitationRecognizer: We detected the following sentences addressing limitations in the study:Study weaknesses included the single center nature and small sample size, which precluded more robust evaluation of risk factors associated with mortality. In addition, short follow up times precluded the assessment of disease sequela in our cohort. We also did not collect information on social determinants of health such as education level, insurance status or economic factors, all of which could have influenced observed outcomes. Finally, given its retrospective nature, we also cannot ascertain that any of our interventions directly affected patient outcomes. Nevertheless, our data identified potential risk factors for disease progression.
Results from TrialIdentifier: We found the following clinical trial numbers in your paper:
Identifier Status Title NCT04315298 Completed Evaluation of the Efficacy and Safety of Sarilumab in Hospit… NCT04280705 Completed Adaptive COVID-19 Treatment Trial (ACTT) NCT04347239 Recruiting Study to Evaluate the Efficacy and Safety of Leronlimab for … NCT04332991 Completed Outcomes Related to COVID-19 Treated With Hydroxychloroquine… Results from Barzooka: We did not find any issues relating to the usage of bar graphs.
Results from JetFighter: We did not find any issues relating to colormaps.
Results from rtransparent:- Thank you for including a conflict of interest statement. Authors are encouraged to include this statement when submitting to a journal.
- Thank you for including a funding statement. Authors are encouraged to include this statement when submitting to a journal.
- Thank you for including a protocol registration statement.
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