TY - JOUR
T1 - Prognostic Value of Electrocardiographic QRS Diminution in Patients Hospitalized With COVID-19 or Influenza
AU - Lampert, Joshua
AU - Miller, Michael
AU - Halperin, Jonathan Lee
AU - Oates, Connor
AU - Giustino, Gennaro
AU - Nelson, Kyle
AU - Feinman, Jason
AU - Kocovic, Nikola
AU - Pulaski, Matthew
AU - Musikantow, Daniel
AU - Turagam, Mohit Kiran
AU - Sofi, Aamir
AU - Choudry, Subbarao
AU - Langan, Marie Noelle
AU - Koruth, Jacob Sam
AU - Whang, William
AU - Miller, Marc Andrew
AU - Dukkipati, Srinivas Rao
AU - Bassily-Marcus, Adel
AU - Kohli-Seth, Roopa
AU - Goldman, Martin Elliot
AU - Reddy, Vivek Yerrapu
N1 - Funding Information:
Funding: This manuscript was internally funded.
Publisher Copyright:
© 2021 Elsevier Inc.
PY - 2021/11/15
Y1 - 2021/11/15
N2 - During the clinical care of hospitalized patients with COVID-19, diminished QRS amplitude on the surface electrocardiogram (ECG) was observed to precede clinical decompensation, culminating in death. This prompted investigation into the prognostic utility and specificity of low QRS complex amplitude (LoQRS) in COVID-19. We retrospectively analyzed consecutive adults admitted to a telemetry service with SARS-CoV-2 (n = 140) or influenza (n = 281) infection with a final disposition—death or discharge. LoQRS was defined as a composite of QRS amplitude <5 mm or <10 mm in the limb or precordial leads, respectively, or a ≥50% decrease in QRS amplitude on follow-up ECG during hospitalization. LoQRS was more prevalent in patients with COVID-19 than influenza (24.3% vs 11.7%, p = 0.001), and in patients who died than survived with either COVID-19 (48.1% vs 10.2%, p <0.001) or influenza (38.9% vs 9.9%, p <0.001). LoQRS was independently associated with mortality in patients with COVID-19 when adjusted for baseline clinical variables (odds ratio [OR] 11.5, 95% confidence interval [CI] 3.9 to 33.8, p <0.001), presenting and peak troponin, D-dimer, C-reactive protein, albumin, intubation, and vasopressor requirement (OR 13.8, 95% CI 1.3 to 145.5, p = 0.029). The median time to death in COVID-19 from the first ECG with LoQRS was 52 hours (interquartile range 18 to 130). Dynamic QRS amplitude diminution is a strong independent predictor of death over not only the course of COVID-19 infection, but also influenza infection. In conclusion, this finding may serve as a pragmatic prognostication tool reflecting evolving clinical changes during hospitalization, over a potentially actionable time interval for clinical reassessment.
AB - During the clinical care of hospitalized patients with COVID-19, diminished QRS amplitude on the surface electrocardiogram (ECG) was observed to precede clinical decompensation, culminating in death. This prompted investigation into the prognostic utility and specificity of low QRS complex amplitude (LoQRS) in COVID-19. We retrospectively analyzed consecutive adults admitted to a telemetry service with SARS-CoV-2 (n = 140) or influenza (n = 281) infection with a final disposition—death or discharge. LoQRS was defined as a composite of QRS amplitude <5 mm or <10 mm in the limb or precordial leads, respectively, or a ≥50% decrease in QRS amplitude on follow-up ECG during hospitalization. LoQRS was more prevalent in patients with COVID-19 than influenza (24.3% vs 11.7%, p = 0.001), and in patients who died than survived with either COVID-19 (48.1% vs 10.2%, p <0.001) or influenza (38.9% vs 9.9%, p <0.001). LoQRS was independently associated with mortality in patients with COVID-19 when adjusted for baseline clinical variables (odds ratio [OR] 11.5, 95% confidence interval [CI] 3.9 to 33.8, p <0.001), presenting and peak troponin, D-dimer, C-reactive protein, albumin, intubation, and vasopressor requirement (OR 13.8, 95% CI 1.3 to 145.5, p = 0.029). The median time to death in COVID-19 from the first ECG with LoQRS was 52 hours (interquartile range 18 to 130). Dynamic QRS amplitude diminution is a strong independent predictor of death over not only the course of COVID-19 infection, but also influenza infection. In conclusion, this finding may serve as a pragmatic prognostication tool reflecting evolving clinical changes during hospitalization, over a potentially actionable time interval for clinical reassessment.
UR - http://www.scopus.com/inward/record.url?scp=85117140034&partnerID=8YFLogxK
U2 - 10.1016/j.amjcard.2021.07.048
DO - 10.1016/j.amjcard.2021.07.048
M3 - Article
C2 - 34579830
AN - SCOPUS:85117140034
VL - 159
SP - 129
EP - 137
JO - American Journal of Cardiology
JF - American Journal of Cardiology
SN - 0002-9149
ER -