Left vs. Right Bundle Branch Block in COVID-19 Patients: Distinct Clinical Presentations and Prognostic Implications
Elena Ciurariu1, Mara Amalia Balteanu2, Marius Georgescu1,3
1Department of Functional Sciences, Physiology Discipline, Faculty of Medicine, "Victor Babeș" University of Medicine and Pharmacy Timișoara, Eftimie Murgu Square No. 2, 300041 Timişoara, Romania.
Insights
COVID-19 patients with left bundle branch block (LBBB) show a more severe clinical profile than those with right bundle branch block (RBBB). This distinction in cardiac and inflammatory markers suggests bundle branch block type influences COVID-19 progression and risk stratification.
Area of Science:
- Cardiology
- Infectious Diseases
- Internal Medicine
Background:
- COVID-19 is linked to systemic effects, including cardiovascular complications.
- The interaction between COVID-19 and cardiac conduction abnormalities like bundle branch block (BBB) is not well understood.
- Comparing clinical profiles of COVID-19 patients with pre-existing left bundle branch block (LBBB) versus right bundle branch block (RBBB) is crucial.
Purpose of the Study:
- To compare the clinical characteristics of COVID-19 patients with LBBB versus RBBB at hospital admission.
- To identify predictors that differentiate COVID-19 patients with LBBB from those with RBBB.
- To explore the influence of BBB type on disease presentation and potential risk stratification in COVID-19.
Main Methods:
- A cohort of 100 COVID-19 patients with antecedent BBB (50 LBBB, 50 RBBB) was studied.
- Key cardiometabolic, renal, hematological, and inflammatory markers were assessed.
- Logistic regression and Spearman's correlations were employed for data analysis.
Main Results:
- LBBB patients exhibited lower systolic blood pressure but larger left atrial size, left ventricular diameter, and interventricular septal thickness compared to RBBB patients.
- Significant differences in hematological and inflammatory markers were observed, with LBBB patients showing higher red cell distribution width, lymphocyte count, neutrophil count, and C-reactive protein.
- Absolute lymphocyte count, C-reactive protein, and left ventricular diameter were key predictors distinguishing LBBB from RBBB.
Conclusions:
- COVID-19 patients with LBBB and RBBB present distinct clinical profiles upon hospital admission.
- The LBBB group demonstrated a more adverse baseline profile, particularly regarding cardiac and inflammatory markers.
- Pre-existing BBB type may impact COVID-19 disease progression, aiding in risk stratification.
Abstract:
Background/Objectives: COVID-19 is associated with multiple systemic effects, including cardiovascular complications. However, its interplay with cardiac conduction abnormalities remains underexplored. We compared the clinical profile of COVID-19 patients with pre-existing left bundle branch block (LBBB) or right bundle branch block (RBBB) at hospital admission. Methods: This study included 100 COVID-19 patients with antecedent BBB (50 LBBB, 50 RBBB). Critical cardiometabolic, renal, hematological, and inflammatory markers were measured. Logistic regression was used to identify key predictors differentiating COVID-19 patients with LBBB and RBBB. Spearman's correlations were applied to assess intra-strata associations for these variables. Results: COVID-19 patients with LBBB patients were significantly more likely to display lower systolic blood pressure (p = 0.012) but greater left atrial size (p = 0.008), left ventricular diameter (p = 0.001), and interventricular septal thickness (p = 0.023). Hematological and inflammatory markers differed, with LBBB patients being prone to exhibit higher red cell distribution width (p = 0.005), lymphocyte count (p < 0.001), neutrophil count (p = 0.045), and C-reactive protein (p < 0.001). This group also tended to show lower erythrocyte sedimentation rate (p = 0.013) and glycated hemoglobin (p = 0.045) but higher random glucose (p = 0.014). Absolute lymphocyte count, C-reactive protein, and left ventricular diameter were the most robust predictors distinguishing LBBB from RBBB. Significant associations were found exclusively for LBBB, all of them being weak. These predominantly negative relationships indicated an inflammatory origin, and most of them occurred for lymphocyte count. Conclusions: COVID-19 patients with LBBB and RBBB present distinct clinical profiles at hospital admission. The former group demonstrates a more adverse baseline clinical profile, particularly in terms of cardiac and inflammatory markers. These findings suggest that pre-existing BBB type may influence disease progression, potentially helping in risk stratification for COVID-19 patients.
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