Cardiopulmonary Complications after Pulmonary Embolism in COVID-19.

Cardiopulmonary Complications after Pulmonary Embolism in COVID-19.

Publication date: Jul 02, 2024

Although pulmonary embolism (PE) is a frequent complication in COVID-19, its consequences remain unknown. We performed pulmonary function tests, echocardiography and computed tomography pulmonary angiography and identified blood biomarkers in a cohort of consecutive hospitalized COVID-19 patients with pneumonia to describe and compare medium-term outcomes according to the presence of PE, as well as to explore their potential predictors. A total of 141 patients (56 with PE) were followed up during a median of 6 months. Post-COVID-19 radiological lung abnormalities (PCRLA) and impaired diffusing capacity for carbon monoxide (DLCOc) were found in 55. 2% and 67. 6% cases, respectively. A total of 7. 3% had PE, and 6. 7% presented an intermediate-high probability of pulmonary hypertension. No significant difference was found between PE and non-PE patients. Univariate analysis showed that age > 65, some clinical severity factors, surfactant protein-D, baseline C-reactive protein, and both peak red cell distribution width and Interleukin (IL)-10 were associated with DLCOc < 80%. A score for PCRLA prediction including age > 65, minimum lymphocyte count, and IL-1β concentration on admission was constructed with excellent overall performance. In conclusion, reduced DLCOc and PCRLA were common in COVID-19 patients after hospital discharge, but PE did not increase the risk. A PCRLA predictive score was developed, which needs further validation.

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Concepts Keywords
Echocardiography Aged
Lymphocyte Biomarkers
Months Biomarkers
Performance cardiopulmonary complications
Pneumonia COVID-19
COVID-19
Echocardiography
Female
follow-up
Humans
Hypertension, Pulmonary
Lung
Male
Middle Aged
pneumonia
Pulmonary Embolism
pulmonary embolism
Respiratory Function Tests
SARS-CoV-2
SARS-CoV-2
thrombosis

Semantics

Type Source Name
disease MESH Complications
disease MESH Pulmonary Embolism
disease MESH COVID-19
disease IDO blood
disease MESH pneumonia
disease MESH abnormalities
drug DRUGBANK Carbon monoxide
disease MESH pulmonary hypertension
disease IDO cell
disease MESH thrombosis
disease IDO acute infection
drug DRUGBANK Coenzyme M
disease MESH comorbidity
disease MESH causality
disease MESH inflammation
disease MESH fibrosis
disease VO time
disease IDO host
disease VO population
drug DRUGBANK Oxygen
disease VO age
disease MESH Hypertension
disease MESH Diabetes mellitus
disease MESH Cardiovascular disease
disease MESH Cerebrovascular disease
disease MESH Chronic kidney disease
disease MESH COPD
disease MESH Asthma
pathway KEGG Asthma
drug DRUGBANK Azithromycin
drug DRUGBANK Hydroxychloroquine
drug DRUGBANK Lopinavir
drug DRUGBANK Ritonavir
drug DRUGBANK Tocilizumab
disease VO organization
disease IDO symptom
disease MESH arthralgias
drug DRUGBANK Albendazole
disease MESH pleural effusion
disease VO volume
drug DRUGBANK Activated charcoal
disease MESH left ventricular systolic dysfunction
drug DRUGBANK Phenindione
disease MESH tricuspid regurgitation
drug DRUGBANK Flunarizine
drug DRUGBANK Cholesterol
drug DRUGBANK Dextrose unspecified form
drug DRUGBANK Urea
drug DRUGBANK Creatinine
drug DRUGBANK Potassium
drug DRUGBANK Fibrinogen Human
disease VO leukocyte
drug DRUGBANK Nesiritide
drug DRUGBANK L-Alanine
disease VO Hormone
drug DRUGBANK Carbon dioxide
drug DRUGBANK Prothrombin
disease VO erythrocyte
disease MESH Interstitial Lung Disease
disease VO macrophage
drug DRUGBANK Saquinavir
drug DRUGBANK Sphingosine
drug DRUGBANK Phosphate ion

Original Article

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