Chest
Volume 159, Issue 1, January 2021, Pages 73-84
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Chest Infections: Original Research
Lung Histopathology in Coronavirus Disease 2019 as Compared With Severe Acute Respiratory Sydrome and H1N1 Influenza: A Systematic Review

https://doi.org/10.1016/j.chest.2020.09.259Get rights and content

Background

Patients with severe coronavirus disease 2019 (COVID-19) have respiratory failure with hypoxemia and acute bilateral pulmonary infiltrates, consistent with ARDS. Respiratory failure in COVID-19 might represent a novel pathologic entity.

Research Question

How does the lung histopathology described in COVID-19 compare with the lung histopathology described in SARS and H1N1 influenza?

Study Design and Methods

We conducted a systematic review to characterize the lung histopathologic features of COVID-19 and compare them against findings of other recent viral pandemics, H1N1 influenza and SARS. We systematically searched MEDLINE and PubMed for studies published up to June 24, 2020, using search terms for COVID-19, H1N1 influenza, and SARS with keywords for pathology, biopsy, and autopsy. Using PRISMA-Individual Participant Data guidelines, our systematic review analysis included 26 articles representing 171 COVID-19 patients; 20 articles representing 287 H1N1 patients; and eight articles representing 64 SARS patients.

Results

In COVID-19, acute-phase diffuse alveolar damage (DAD) was reported in 88% of patients, which was similar to the proportion of cases with DAD in both H1N1 (90%) and SARS (98%). Pulmonary microthrombi were reported in 57% of COVID-19 and 58% of SARS patients, as compared with 24% of H1N1 influenza patients.

Interpretation

DAD, the histologic correlate of ARDS, is the predominant histopathologic pattern identified in lung pathology from patients with COVID-19, H1N1 influenza, and SARS. Microthrombi were reported more frequently in both patients with COVID-19 and SARS as compared with H1N1 influenza. Future work is needed to validate this histopathologic finding and, if confirmed, elucidate the mechanistic underpinnings and characterize any associations with clinically important outcomes.

Key Words

acute respiratory distress syndrome
COVID-19
H1N1 influenza A
histopathology
SARS-CoV-2

Abbreviations

AFOP
acute fibrinous and organizing pneumonia
ALI
acute lung injury
COVID-19
coronavirus disease 2019
DAD
diffuse alveolar damage
EM
electron microscopy
OP
organizing pneumonia
PRISMA
preferred reporting items for a systematic review and meta-analysis
RT-PCR
real-time reverse-transcriptase polymerase chain reaction
SARS
severe acute respiratory syndrome
SARS-CoV-2
severe acute respiratory syndrome coronavirus 2

Cited by (0)

Drs Hariri and North contributed equally to this manuscript. Drs Stone and Mino-Kenudson also contributed equally to this manuscript.

FUNDING/SUPPORT: L. P. H. is supported by NIH K23HL132120 and R01HL152075. R. R. C. is supported by NIH T32HL116275 and the American Thoracic Society Foundation.

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