Predicting the risk of chest radiograph abnormality 12-weeks post hospitalisation with SARS CoV-2 PCR confirmed

Tim Jm Wallis1, Benjamin Welham2, Alex Kong2

  • 1Department of Respiratory Medicine and Southampton NIHR Biomedical Research Centre, School of Clinical and Experimental Sciences, Faculty of Medicine, University Hospital Southampton, University of Southampton, Southampton, UK. timothy.wallis@soton.ac.uk.

Respiratory Research
|November 1, 2022
PubMed

Insights

A new SHADE-750 score accurately predicts persistent chest X-ray abnormalities in COVID-19 survivors. This tool helps identify patients who may not need routine radiological follow-up, reducing healthcare burdens.

Area of Science:

  • Pulmonary Medicine
  • Radiology
  • Infectious Diseases

Background:

  • Routine follow-up for COVID-19 survivors is resource-intensive.
  • Previous work identified a 5-point score for predicting persistent chest X-ray (CXR) abnormalities.
  • This study aimed to validate and refine this predictive score in an independent cohort.

Discussion:

  • The SHADE-750 score, incorporating smoking history, higher-level care, age ≥50, admission duration ≥15 days, and LDH ≥750U/L, demonstrates strong predictive accuracy.
  • The score showed robust performance across two independent cohorts and when combined.
  • A score of zero indicated complete CXR resolution at 12 weeks, suggesting its utility in de-escalating follow-up.

Key Insights:

  • Persistent CXR abnormalities were linked to older age, longer hospital stays, higher-level care, and smoking history.
  • The refined SHADE-750 score achieved an AUROC of 0.75 in a combined cohort.
  • The SHADE-750 score effectively identifies COVID-19 patients at low risk for persistent radiographic abnormalities.

Outlook:

  • The SHADE-750 score can guide clinical decisions regarding the necessity of radiological follow-up for COVID-19 survivors.
  • This tool has the potential to optimize healthcare resource allocation by identifying patients unlikely to benefit from routine monitoring.
  • Further validation in diverse populations could enhance the generalizability of the SHADE-750 score.
Abstract

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