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Novel Coronavirus Pneumonia Diagnosis and Treatment Plan (Provisional 7th Edition)Part 2IV. Clinical Characteristics(1) ...
03/23/2020

Novel Coronavirus Pneumonia Diagnosis and Treatment Plan (Provisional 7th Edition)

Part 2

IV. Clinical Characteristics

(1) Clinical presentation.

Based on the current epidemiological investigation, the incubation period is 1-14 days, and most often between 3-7 days.

The primary presentations are fever, dry cough, and fatigue. A minority of patients have symptoms such as nasal congestion, nasal discharge, sore throat, muscle pain, and diarrhea. Severe patients often suffer from dyspnea and/or hypoxemia one week after symptom onset, and severe patients can rapidly progress to acute respiratory distress syndrome, septic shock, difficult to correct metabolic acidosis, coagulation dysfunction and multiple organ failure. It is worth noting that severe and critical patients may have moderate to low fever or even no obvious fever during the course of the disease.

Some children and infants may present with atypical symptoms such as vomiting and diarrhea, or only with malaise and rapid breathing.

Patients with the mild form of the disease present only as low fever, slight fatigue, and so forth, with no lung inflammation.

Judging from the current cases, most patients have a good prognosis and a minority are in critical condition. The prognosis of the elderly and those with chronic underlying diseases is more poor. The clinical course of COVID-19 in pregnant patients is similar to that for patients of the same age. The symptoms of children are relatively mild.

(2) Laboratory examination.

1. General Examination

In the early stage of the disease, the total number of peripheral blood leukocytes is normal or reduced, and the lymphocyte count is reduced, and some patients may have elevated liver enzyme, lactate dehydrogenase (LDH), myoenzyme and myoglobin; some critically ill patients may have elevated troponin. C-reactive protein (CRP) and erythrocyte sedimentation rate increased in most patients, and procalcitonin was normal. In severe cases, D- dimer increased and peripheral blood lymphocytes progressively decreased. Inflammatory cytokines often increase in severe and critical patients.

2. Etiologic and serologic tests

(1) Etiologic testing: Use RT-PCR and/or NGS to detect 2019-nCoV nucleic acid in nasopharyngeal swabs, sputum and other lower respiratory tract secretions, blood, and stool samples. Testing done on lower respiratory tract samples (sputum or airway suction) is more accurate. After collection, samples should be sent for testing ASAP.

(2) Serologic testing: nCoV-specific IgM antibodies usually test positive 3-5 days after the onset of symptoms; the titre of IgG antibodies is elevated by 4 times or more in the recovery phase compared with the acute phase.

(3) Chest imaging

In the early stage, there are multiple small patches and interstitial changes, most notably in the outer lung. It further develops into multiple ground-glass opacity and infiltration shadows in both lungs; and in severe cases, consolidation of the lungs may occur, and pleural effusion is rare.

V. Diagnostic Criteria

(1) Suspected cases.

Comprehensively analyze combinations of the following epidemiological history and clinical presentations:

Epidemiological history
(1) Within 14 days prior to onset, had history of travel or residence in Wuhan or surrounding regions, or other communities reporting cases;

(2) Within 14 days prior to symptom onset, having had contact with patients infected with 2019-nCoV (positive nucleic acid test).

(3) Within 14 days prior to onset, had contact with patients who had a fever or respiratory tract symptoms that had come from Wuhan, its surrounding regions, or other communities reporting cases.

(4) Clustered onset (Within a span of 2 weeks, 2 or more cases with fever and/or respiratory symptoms appear in a small area, such as a family, an office, or a school class)

2. Clinical presentations

(1) Fever and/or respiratory tract symptoms;

(2) Having the imaging features of novel coronavirus pneumonia discussed above;

(3) During the early stages of the disease, white blood cell count is normal or reduced, while the lymphocyte count is normal or reduced.

Where there are any of the epidemiologic history items, and any 2 of the clinical presentions are met.

Where there is no clear epidemiological history, and at least 3 of the clinical presentations are met.

(2) Confirmed cases.

A 2019-nCoV diagnosis is confirmed if the suspected cases also have one of the following etiological or serological evidence.

Positive result in real-time fluorescence RT-PCR detection of novel coronavirus nucleic acid;
The sequence of the virus is highly homologues to that of 2019-nCoV.
Specific IgM and IgG antibodies against 2019-nCoV test positive in the serum; IgG antibodies specific to 2019-nCoV test positive after previous negative results, or increased by more than 4 times in the recovery phase compared to the acute phase.

Novel Coronavirus Pneumonia Diagnosis and Treatment Plan (Provisional 7th Edition in China)Part 1Since December 2019, ma...
03/20/2020

Novel Coronavirus Pneumonia Diagnosis and Treatment Plan (Provisional 7th Edition in China)

Part 1

Since December 2019, many cases of novel coronavirus pneumonia have been found in Wuhan City, Hubei Province, and with the spread of the epidemic, such cases have also been found in other regions of China and overseas. As an acute respiratory infectious disease, the disease has been listed as a Class B infectious disease as provided by the "Law of the People's Republic of China on Prevention and Control of Infectious Diseases", and is managed as a Class A infectious disease. By employing a series of measures for prevention, control, and treatment, the upward trend of the epidemic in our nation has been contained to a certain degree, and the epidemic has eased in most provinces, but the number of cases outside China is on the rise. With thorough understanding of the clinical manifestations and pathology of the disease and the accumulation of experience in its diagnosis and treatment, we have revised the "Novel Coronavirus Diagnosis and Treatment Plan (Provisional Version 6)" to form the "New Coronavirus Pneumonia Diagnosis and Treatment Plan (Trial Version 7)", in order to further strengthen the early diagnosis and treatment of the disease, to improve the cure rate, to reduce the mortality rate, and to avoid hospital infection to the greatest extent possible, and at the same time to give a reminder to pay attention to the transmission and spread caused by imported cases.

I. Pathogenic Characteristics

The Novel Coronavirus belonging to the genus of betacoronavirus. The enveloped viral particles may appear spherical or oblong, with a diameter of 60-140nm. Its genetic characteristics are significantly different from SARS-CoV and MERS-CoV. Current research shows that it has more than 85% homology with bat SARS-like coronavirus (bat-SL-CoVZC45). When isolated and cultured in vitro, the new coronavirus can be found in human respiratory epithelial cells in about 96 hours, while it takes about 6 days to isolate and culture in Vero E6 and Huh-7 cell lines.

Most of the understanding of the physicochemical properties of coronavirus comes from the research of SARS-CoV and MERS-CoV. The virus is sensitive to ultraviolet rays and heat, exposure to 56 °C for 30 minutes, ether solvents, 75% ethanol, chlorine-containing disinfectants, peracetic acid, and chloroform can effectively inactivate the virus. Chlorhexidine cannot effectively inactivate the virus.

II. Epidemiological Characteristics

(1) Source of infection.

At present, the source of infection is mainly patients infected by the novel coronavirus. Those who are asymptomatic but infected may also become a source of infection.

(2) Route of transmission.

The main route of transmission is respiratory droplets and close contact. There is the possibility of aerosol transmission when exposed to high concentration aerosol for a long time in a relatively closed environment. As new coronaviruses can be isolated in f***s and urine, attention should be paid to aerosol or contact transmission of f***l and urine to environmental pollution.

(3) Susceptible populations.

The population is generally susceptible.

III. Pathological Changes

The pathological observations from autopsies and biopsies are summarized below.

(1) Lungs

Pulmonary consolidation of varying degrees. Intra-alveolar serous fluids, fibrinous exude and hyaline-membrane formation are present. Exudate consists mainly of mononuclear macrophages. Multinucleated giant cells are common. Significant hyperplasia of type II pneumocyte. Some desquamation is present.

Inclusion bodies can be seen inside type II pneumocyte and macrophages. Alveolar congestion and edema can be seen. Infiltration of monocytes and lymphocytes, as well as the formation of hyaline thrombus in blood vessels, are evident. Focal pulmonary hemorrhage and necrosis. Hemorrhagic infarction can be seen. Exudate organization and pulmonary interstitial fibrosis are present in some alveoli.

Desquamation of bronchial mucosal epithelium is present. Intra-cavity mucus and mucus plugs can be seen. Overinflation, alveolar septa fracture and cyst formation are present in some alveoli.

Coronavirus particles can be seen in the cytoplasm of tracheal mucosal epithelial cells and type II pneumocytes under an electron microscope. A portion of the alveolar epithelium and macrophages contain the 2019-nCoV antigen as shown by IHC. Sample tests positive for the nucleic acid of 2019-nCoV with RT-PCR.

(2) Spleen, hilar lymph nodes and bone marrow

The size of the spleen is significantly reduced. Lymphocyte count is significantly reduced. Focal hemorrhage and necrosis are present. Macrophage hyperplasia and phagocytosis can be observed in the spleen. In the lymph nodes, the number of lymphocytes is reduced; some necrosis can be seen. A reduction of CD4+ T cells and CD8+ T cells can be detected in both the spleen and the lymph nodes by IHC. Trilineage hematopoiesis is reduced in the bone marrow.

(3) Heart and blood vessels

Degeneration and necrosis can be seen in cardiomyocytes. Interstitial infiltration of a small number of monocytes, lymphocytes and/or neutrophils can be seen. Desquamation of vascular endothelium, endothelial inflammation and thrombus formation are observed in some vessels.

(4) Liver and gallbladder

The liver appears enlarged and dark red in colour. Hepatocyte degeneration and focal necrosis are accompanied by neutrophil infiltration; hepatic sinusoidal congestion, infiltration of lymphocytes and monocytes in the hepatic portal area can be seen. Microthrombi are formed. The gallbladder appears highly filled.

(5) Kidneys

Proteinaceous exudate can be seen inside the glomerular capsule. Degeneration and desquamation of renal tubular epithelium are present. Hyaline casts can be seen. Interstitial congestion, microthrombi and focal fibrosis can be seen.

(6) Other organs. Cerebral hyperemia, edema, and degeneration of some neurons. Focal necrosis in the adrenal glands.

Varying degrees of degeneration, necrosis or desquamation of the esophageal, gastric and intestinal mucosal epithelium.

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