| Literature DB >> 32420073 |
Haoyue Guo1,2, Xiaoxia Chen1, Chunxia Su1, Yu Liu1,2, Hao Wang1,2, Chenglong Sun1,2, Peixin Chen1,2, Minlin Jiang1,2, Yi Xu1,2, Shengyu Wu1,2, Keyi Jia1,2, Sha Zhao1, Wei Li1, Bin Chen1, Lei Wang1, Jia Yu1, Anwen Xiong1, Guanghui Gao1, Fengying Wu1, Jiayu Li1, Lingyun Ye1, Bing Bo1, Shen Chen1, Shengxiang Ren1, Yayi He1, Caicun Zhou1.
Abstract
Since December, 2019, a 2019 novel coronavirus disease (COVID-19) infected by the severe acute respiratory syndrome corona virus 2 (SARS-CoV-2) emerged in Wuhan, Hubei province, and the epidemic situation has continued to spread globally. The epidemic spread of COVID-19 has brought great challenges to the clinical practice of thoracic oncology. Outpatient clinics need to strengthen the differential diagnosis of initial symptoms, pulmonary ground-glass opacity (GGO), consolidation, interstitial and/or interlobular septal thickening, and crazy paving appearance. In the routine of oncology, the differential diagnosis of adverse events from COVID-19 is also significant, including radiation pneumonitis, checkpoint inhibitor pneumonitis (CIP), neutropenic fever, and so on. During the epidemic, indications of transbronchial biopsy (TBB) and CT-guided percutaneous thoracic biopsy are strictly controlled. For patients who are planning to undergo biopsy operation, screening to exclude the possibility of COVID-19 should be carried out. For confirmed or suspected patients, three-level protection should be performed during the operation. Disinfection and isolation measures should be strictly carried out during the operation. At last, more attention to the protection of cancer patients and give priority to the treatment of infected cancer patients. 2020 Translational Lung Cancer Research. All rights reserved.Entities:
Keywords: 2019 novel coronavirus disease (COVID-19); severe acute respiratory syndrome corona virus 2 (SARS-CoV-2); thoracic oncology
Year: 2020 PMID: 32420073 PMCID: PMC7225133 DOI: 10.21037/tlcr.2020.02.10
Source DB: PubMed Journal: Transl Lung Cancer Res ISSN: 2218-6751
Characteristics of the main viruses involved in viral pneumonia
| Virus | Family | Subtype | Susceptible people | Seasonality | Incubation period (days) | Typical symptoms |
|---|---|---|---|---|---|---|
| Rhinovirus | Picornaviridae | – | All ages are susceptible, while the incidence is higher in children and decreases with age | Throughout the year, mainly in spring and autumn | 2–5 | Typical upper airway symptoms, including rhinorrhea, cough and nasal congestion |
| Syncytial respiratory virus (SRV) | Paramyxoviridae | 1 and 2 | Newborns and infants under 6 months | Throughout the year, mainly in autumn and winter | 4–5 | Moderate and severe cases present with more obvious dyspnea, wheezing, lips cyanosis, nasal fan, and three concave signs |
| Influenza virus (IV) | Orthomyxoviridae | A | All ages are susceptible | The northern hemisphere usually peaks in January and February, and the southern hemisphere peaks from May to September | 1–4 | Influenza-like syndrome including sudden fever, dizziness, headache, myalgia, mild systemic symptoms |
| B | Children <5 years (especially infants <2 years), the elderly >60, patients with chronic diseases (asthma, chronic obstructive pulmonary disease, diabetes, hypertension and so on) and healthcare personnel | |||||
| H1N1 (a special subtype of influenza A virus) | <65 years | Specific outbreaks in waves | 1–7 | General cases present with Influenza-like syndrome, while some cases present with vomiting and diarrhea | ||
| H5N1 (a special subtype of influenza A virus) | Contact with poultries | Outbreaks throughout the year | 2–17 | Common initial symptoms are high fever (> 38 °C) and cough | ||
| H7N9 (a special subtype of influenza A virus) | Contact with poultries and the elderly >60 | Autumn and winter | 1–10 | General cases present with Influenza-like syndrome, while sever cases can present with severe respiratory distress syndrome, mediastinal emphysema, sepsis, shock, disturbance of consciousness, and acute kidney injury | ||
| Parainfluenza virus (PIV) | Paramyxoviridae | 1, 2, 3 and 4 | Children, the elderly and in | Autumn (PIV1-2) Spring (PIV-3) | 3–7 | Laryngotracheobronchitis (children with PIV-1 or PIV-2), pneumonia and bronchiolitis (PIV-3) |
| Metapneumovirus | Paramyxoviridae | – | Infants under 3 years | End of winter and spring | 3–6 | Cough, wheezing, fever, and cyanosis |
| Coronavirus | Coronaviridae | 229E, NL63, OC43, KU1 | Geriatric care homes | Winter | 2–5 | Upper respiratory tract infection, acute gastroenteritis, and neurological symptoms |
| SARS | Contact with bats and civets, | End of winter and spring | 4–5 | Prone to respiratory distress syndrome | ||
| MERS | Contact with dromedaries, people aged between 50–59 years | Unknown | 2–14 | General cases present with severe acute respiratory disease, while severe cases can present with respiratory failure and renal failure in severe cases | ||
| SARS-COV-2 | All populations are susceptible | Unknown | 3–14 | Initial symptoms are fever, cough and shortness of breath, with muscle pain, headache, confusion, chest pain, and diarrhea | ||
| Adenovirus | Adenoviridae | 7, 14, 16 | Infants | All year | 4–5 | Acute febrile pharyngitis, conjunctivitis, diarrhea, and encephalitis |
| Bocavirus | Parvoviridae | – | Infants <2 years | End of autumn, beginning of winter | Unknown | Adults present with upper respiratory tract infections, while children present with pneumonia, rhinitis, laryngitis, bronchitis, bronchiolitis, asthma |
Adapted from Galván et al. (6).