中华结核和呼吸杂志
2018年 · 第41卷第07期
中华结核和呼吸杂志
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This journal published the "Guidelines for the Diagnosis and Treatment of Hospital-Acquired Pneumonia (HAP) and Ventilator-Associated Pneumonia (VAP) in Adults in China (2018 Edition) (referred to as the Guidelines) in Volume 41, Issue 4, 2018, which was pushed on the WeChat platform of this journal at the same time. As of June 25, 2018, the Guidelines have been clicked 43,610 times on the WeChat platform and have received wide attention. In the essay column of the editor-in-chief of this issue, Professor Liu Youning put forward his own views on the content of the Guidelines in the article" Can Mechanical Ventilation-Associated Pneumonia be Completely Separated from Hospital-Acquired Pneumonia "," Although the guidelines jointly formulated by the American Association of Infectious Diseases/Thoracic Society in 2016 emphasize that HAP and VAP in the narrow sense are completely different groups, with great differences in clinical manifestations and treatment methods, and believe that they should be treated as different diseases ", the author believes that" HAP in the broad sense corresponds to community-acquired pneumonia (CAP), emphasizing that the places of acquired pneumonia are different. In this case, there is no reason why pneumonia, including VAP, that occurs in hospitals does not fall under the category of HAP. Combined with the actual situation in China, the guideline believes that 'VAP is a special type of HAP', that is, VAP is still included in the definition of macro HAP, but it also adopts' independent definition of HAP/VAP with different meanings', which is in line with China's national conditions ".
In 2016, the guidelines jointly developed by the American Association of Infectious Diseases (IDSA) /Thoracic Society (ATS) emphasized that hospital-acquired pneumonia (HAP) and mechanical ventilation-associated pneumonia (VAP) in the narrow sense are completely different groups, and their clinical manifestations and treatment methods are quite different, and they are believed to be treated as different diseases. Countries around the world have not responded to this view according to the "leading" opinion of IDSA/ATS. Chinese Journal of Tuberculosis and Respiration published "Guidelines for the Diagnosis and Treatment of Hospital-Acquired Pneumonia and Ventilator-Associated Pneumonia in Adults in China (2018 Edition)" in Volume 41, Issue 4, 2018[
eosinophilic granulomatosis with polyangiitis (EGPA) is a rare autoimmune disease that can involve multiple systems in the whole body. It is mainly manifested by increased eosinophilia in peripheral blood and tissues, infiltration and necrotizing granulomatous inflammation of small and medium blood vessels. It belongs to anti-neutrophil cytoplasmic antibodies (ANCA) -related systemic vasculitis. The literature reported that nearly 50% of patients tested positive for ANCA[
mycobacterium genus includes mycobacterium tuberculosis complex, mycobacterium leprae complex and non-tuberculosis mycobacterium. By the end of 2017, the number of mycobacterium species and subspecies reported has reached 194 (http: / /www.bacterio.net/mycobacterium.html), but only 119 mycobacteria have corresponding Chinese names. Other mycobacteria have no corresponding Chinese translations, so their Latin names can only be used in official domestic journals. Moreover, due to the lack of uniform Chinese translation principle of mycobacterial species in China, even the Chinese translation of mycobacterial species has irregular translation[
chronic thromboembolic pulmonary hypertension (CTEPH) is the fourth largest type of pulmonary hypertension caused by repeated pulmonary thromboembolism causing pulmonary artery stenosis or occlusion, pulmonary arteriolar remodeling, resulting in increased pulmonary artery resistance and increased right ventricular afterload, and finally leading to right ventricular decompensation or even death. The 3-year survival rate of untreated patients with poor prognosis of CTEPH was only 10%, and the median survival time was 2.8 years[
obstructive fibrinous tracheal pseudomembrane (OFTP) is one of the rare complications caused by tracheal intubation. It is characterized by the formation of thick tubular pseudomembrane on the tracheal wall. After the tracheal intubation is removed, different degrees of tracheal obstruction are formed, which leads to dyspnea, wheezing, acute respiratory failure or death from asphyxia[
plastic bronchitis (PB), also known as fibrotic bronchitis, Hofman's bronchitis, tubular bronchitis, pseudomembranous bronchitis, or fibrinous bronchitis, is a rare and fatal lung disease characterized by the formation and adhesion of gelatinous bronchial tree-like tubes to fill the airways[
Mechanical ventilation is the primary means of life support in critically ill patients, which can buy time for other treatments, but also has numerous potential comorbidities, even affecting distant organs[
The pathogenesis of obstructive sleep apnea (OSA) is involved by many factors, and the PALM theory, which consists of critical closing pressure (Pcrit), low arousal threshold, high loop gain and dilator muscle function of the upper airway, has attracted widespread attention[
The 2017 global initiative for chronic obstructive lung disease (GOLD)[
The vast majority of bacteria in the human digestive tract are concentrated in the colon, and the amount of bacteria carried by the colon of standard weight adult men is about 3.9×1013(Uncertainty 24%, variation rate 52%)[
endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) is a new examination technique in recent years. It is mainly used for the diagnosis of mediastinal and hilar lesions and staging of lung malignant lesions[
Bronchial asthma (asthma) as a chronic airway inflammatory disease[
Bronchial occlusion is an effective treatment for refractory pneumothorax. Locating the bronchus leading to the pleural rupture, i.e. draining the bronchus, is a key step. Balloon exploration is the most commonly used localization method. However, when there is multi-lobar pleural fistula or obvious collateral ventilation, balloon exploration is difficult to succeed. This study attempted to establish the transbronchoscopic end-expiratory carbon dioxide (EtCO2) Methodology for detecting and locating refractory pneumothorax drainage bronchus. Twenty-eight pneumothorax patients with persistent air leakage>7 d through intercostal drainage from July 2012 to September 2015 were included, all male, aged (65 ± 13) years. Underlying diseases include chronic obstructive pulmonary disease, silicosis, old pulmonary tuberculosis, lung cancer, segmental resection and idiopathic pneumothorax, etc.
I was fortunate to read the Chinese Journal of Tuberculosis and Respiration, Volume 40, Issue 8, 2017, and gained a lot. Among them, the article "Clinical Manifestations, Pathological Characteristics and Gene Mutations of Patients with Lung Involvement in Erdheim-Chester Disease" written by Lu Tao and others has been read carefully. With a rigorous attitude, I have the following three feelings, which are specially put forward for discussion: (1) Example 3 of the article uses "methotrexate 1.8 g intravenous continuous drip for 24 hours, 1 day of medication, and 1 course of chemotherapy". The dose of methotrexate is obviously too large. Is the dose wrong? (2) Case 3 of the article "No obvious abnormalities were found in CT pulmonary angiography in June 2016, and interferon was adjusted to 10 mU, once every other day + prednisone 30 mg, and chemotherapy once a day (days 1 to 5)". Because the patient was admitted to the hospital on May 21, 2015, spanning 1 year, the application of interferon was not explained before the article, and the dose was adjusted directly, resulting in poor connection before and after the article and difficulty in understanding; In addition, is the abnormality of pulmonary angiography necessarily related to interferon adjustment? It may be more appropriate to give an explanation if any.
At 4: 21 pm on February 10, 2018, Professor Yu Runjiang, a famous domestic respiratory scientist, finished his difficult and magnificent life and drove to the west at the age of 93.
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