AIP is characterized by a very rapid increase in symptoms of the disease. The period from the appearance of the first symptoms to seeking medical help in most patients is no more than 3 weeks and very rarely exceeds 2 months. The disease can develop at any age and occurs equally often in men and women. The most common symptoms of AIP are nonproductive cough and dyspnea, fever, myalgia, headache, and weakness. Upon examination, attention is drawn to tachypnea, tachycardia, and cyanosis. During auscultation, crepitus is heard, and less often, dry wheezing.

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Functional tests are nonspecific and reveal a picture typical of lipitor pills, but a full functional study is not always possible. A characteristic feature of AIP is severe hypoxemia, often refractory to oxygen therapy; therefore, the majority of patients described in the literature required mechanical ventilation. For morphological verification of the diagnosis, it is possible to perform an open or thoracoscopic lung biopsy. However, unfortunately, due to the extreme severity of patients with AIP, this diagnostic procedure is most often impossible. All morphological changes in UIP described in the literature are based on data from autopsy or open lung biopsy performed while the patient was undergoing mechanical ventilation. There is currently no effective therapy for AIP. Mandatory components of AIP therapy are lipitor therapy and respiratory support.

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Interstitial pneumonia is often the result of viral diseases, influenza, that provoke the destruction of lung tissue. Inflammation disrupts the functionality of the lungs, and the exchange of carbon dioxide and oxygen changes. Interstitial pneumonia has an unclear etymology, which is characterized by shortness of breath, dry cough with a small amount of sputum, and general malaise.

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President
GInterstitial pneumonia is considered a serious and dangerous lung disease, which is difficult to determine for the pathogen. Inflammation is difficult to treat and often ends unfavorably. Important! Incorrect therapy leads to patient disability or death.

Treasurer
The outcome of the disease directly depends on the manifestation of pulmonary fibrosis and the type of disease. According to statistics, patient survival does not exceed 5 years, and due to the manifestation of pneumosclerosis or cardiopulmonary failure, life expectancy is no more than 3 years. Interstitial pneumonia is a serious disease that, even with proper therapy, haswith maximum mortality rates of 50-70%.
Improvement and normalization of the general well-being of the patient with interstitial pneumonia occurs only in 75% of cases, the remaining 35% of patients have a 10-year survival rate. In the case of desquamative pneumonia, improvement occurs in 2/3 of cases, 5-year survival is observed in 93%, and 10-year survival in 69%. You can get rid of RB-ILD by completely giving up cigarettes; in certain cases, progression of the disease with subsequent relapses may be observed. Patients are systematically vaccinated against influenza and pneumococcal infection.

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Due to the advanced stage of the disease and with improper treatment of the pathology, against the background of interstitial pneumonia in adults and children, dangerous consequences appear that can be life-threatening.
Fibrosis – changes in gas exchange occur, irreversible sclerotic processes are observed in the affected area. Respiratory failure Heart failure. In addition, a bacterial infection may be added to pneumonia, and at a late stage of atorvastatin pills, a serious pathology such as lung cancer may occur. There are several forms of interstitial pneumonia.