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Lung Histopathology in Coronavirus Disease 2019 as Compared With Severe Acute Respiratory Sydrome and H1N1 Influenza: A Systematic Review.
Hariri, Lida P; North, Crystal M; Shih, Angela R; Israel, Rebecca A; Maley, Jason H; Villalba, Julian A; Vinarsky, Vladimir; Rubin, Jonah; Okin, Daniel A; Sclafani, Alyssa; Alladina, Jehan W; Griffith, Jason W; Gillette, Michael A; Raz, Yuval; Richards, Christopher J; Wong, Alexandra K; Ly, Amy; Hung, Yin P; Chivukula, Raghu R; Petri, Camille R; Calhoun, Tiara F; Brenner, Laura N; Hibbert, Kathryn A; Medoff, Benjamin D; Hardin, C Corey; Stone, James R; Mino-Kenudson, Mari.
  • Hariri LP; Department of Pathology, Massachusetts General Hospital, Boston, MA; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • North CM; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Medical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Shih AR; Department of Pathology, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Israel RA; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Maley JH; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA.
  • Villalba JA; Department of Pathology, Massachusetts General Hospital, Boston, MA.
  • Vinarsky V; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA.
  • Rubin J; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Okin DA; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Sclafani A; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Alladina JW; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Griffith JW; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Gillette MA; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Raz Y; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Richards CJ; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Wong AK; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Ly A; Department of Pathology, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Hung YP; Department of Pathology, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Chivukula RR; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Whitehead Institute for Biomedical Research, Cambridge, MA; Harvard Medical School, Boston, MA.
  • Petri CR; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Calhoun TF; Department of Medicine, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Brenner LN; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Hibbert KA; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Medoff BD; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Hardin CC; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Stone JR; Department of Pathology, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
  • Mino-Kenudson M; Department of Pathology, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA.
Chest ; 159(1): 73-84, 2021 01.
Article in English | MEDLINE | ID: covidwho-996763
ABSTRACT

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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Distress Syndrome / Influenza, Human / Influenza A Virus, H1N1 Subtype / COVID-19 / Lung Type of study: Prognostic study / Reviews / Systematic review/Meta Analysis Limits: Humans Language: English Journal: Chest Year: 2021 Document Type: Article Affiliation country: J.chest.2020.09.259

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Distress Syndrome / Influenza, Human / Influenza A Virus, H1N1 Subtype / COVID-19 / Lung Type of study: Prognostic study / Reviews / Systematic review/Meta Analysis Limits: Humans Language: English Journal: Chest Year: 2021 Document Type: Article Affiliation country: J.chest.2020.09.259