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X-ray and HRCT images show one or more foci of tissue compaction, thickening of cenforce pills and intralobular interstitial tissues, decreased transparency of the lung parenchyma (ground glass type, mainly observed in the lower lobes of the lungs). High-resolution computed tomography is the most informative research method for this disease. With its help, you can establish the prevalence of the pathological process, determine the stage and intensity of fibrosis progression. Pathology is differentiated from bacterial pneumonia, tuberculosis lesions, and other interstitial lung diseases. If the disease is diagnosed and treated in a timely manner, the prospects for the patient are favorable. The most dangerous is the acute form of the pathology, characterized by a rapid deterioration in respiratory function. The patient requires oxygen therapy and breathing support using artificial ventilation.
For other types of the disease, long courses of corticosteroids (Prednisolone) and cytostatic drugs (Cyclophosphamide) are prescribed to buy cenforce online the intensity of the inflammatory process, and immunosuppressive drugs (Azathioprine) to suppress the pathological activity of immune agents. To prevent the progression of the fibrotic process, medications such as D-penicillamine and Colchicine can be used. If the progression of the pathology has led to a decrease in the level of oxygen in the blood, then oxygen therapy methods are used. If the patient has pulmonary hypertension, then it is necessary to prescribe drugs to relax the smooth muscles of the vascularwalls In the most severe cases, a donor lung transplant may be required.
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If the cause of the development of inflammation of interstitial tissues is smoking, then the patient should treat pneumonia by completely abandoning this habit. Only following all the recommendations of your doctor will help cure this complex and dangerous disease. The prognosis for this pathology depends on the form in which it occurs, as well as on how pronounced the fibrous changes in the lung tissue are. On average, people live with this disease for about five years, but if it occurs in the form of idiopathic pulmonary fibrosis, complicated by sclerosis of lung tissue and insufficient function of the respiratory and cardiovascular systems, then the prospects worsen significantly, survival does not exceed three years.
Acute interstitial pneumonia is a serious and dangerous disease, which, even with early detection and adequate treatment, leads to death in more than half of the diagnosed cases. With nonspecific interstitial pneumonia, it is possible to achieve improvement in clinical parameters and stabilization of the patient’s condition in 70-75% of cases. In a third of cases, the life prognosis is estimated at 10 years. Desquamative interstitial pneumonia can be stabilized in 65% of patients, more than 90% live up to 10 years, 60% - five years. Sometimes, with the help of cenforce therapy, it is possible to achieve stable remission. With lymphoid and cryptogenic forms, the prognosis is usually favorable.