What is the right lung fiber if anyone can help me

Interstitial pneumonia is inflammation of the interstitial tissues of the lungs, and the inflammation mainly invades the bronchial wall, alveolar wall, especially the peribronchial blood vessels, the connective tissue between the surrounding lobules and the alveolar septum.

1. Make adequate preparations: Due to the characteristics of pulmonary fibrosis patients' own physical conditions, they should make adequate preparations when exercising, and make necessary preparations to adapt to the upcoming exercise. At the same time, at the beginning of the exercise, it is necessary to follow the principle of slow first and then fast, and do not rush to achieve results.

2. Choose the right sports: Pulmonary fibrosis patients can diversify their sports, among all sports, swimming is the most suitable for pulmonary fibrosis patients, followed by rowing, tai chi, practicing the eighteen methods, gymnastics, badminton, walking, cycling and jogging. By participating in some relaxing and entertaining sports competitions, patients can achieve the purpose of exercising in a pleasant mood.

However, when exercising, you should avoid being competitive and do not force yourself to do some sports that you are not capable of, which is not good for your body.

3. Avoid exercising in cold and dry places: due to the increase in the number of breaths after exercise, the loss of water and heat in the airway is aggravated, especially in cold and dry places, which can lead to an increase in the osmotic pressure of the airway mucosa, and the cooling of the airway induces bronchospasm, so you should try to exercise in a warm and humid environment.

4. Do not exercise too much: If the amount of exercise is too large, it is easy to cause excessive cardiopulmonary load, resulting in too fast heart rate and hyperventilation, which is easy to induce pulmonary fibrosis or aggravate hypoxia. If to.

The speed of the rate is used to measure whether the amount of exercise of pulmonary fibrosis patients is reasonable, so the more appropriate standard is that the heart rate during exercise is generally 60% to 70% of the maximum heart rate. When the patient adapts to a certain amount of exercise, gradually increase the amount of activity.

5. Exercise should not be done during the acute attack: the patient's body is already in a state of hypoxia during the acute attack, and then physical activity at this time is like "adding insult to injury", and active and full body breathing is the best way to alleviate hypoxia. Therefore, physical exercise for patients with pulmonary fibrosis is mainly carried out during remission, and as long as pulmonary fibrosis does not occur, they should continue to exercise daily from beginning to end.

6. Pre-exercise prophylactic medication: Patients with severe exercise pulmonary fibrosis should take preventive medication before exercise, and use it for 5 10 minutes before carrying out activities, which can avoid most of the episodes of exercise-induced pulmonary fibrosis.

It is necessary to have a calm mind, that is, a good mood, a reasonable diet, and exercise. It will definitely be relieved. If you have a heavy heart, you can easily have a nervous breakdown.

Patients with neurasthenia often have symptoms of neurasthenia after long-term sleep disorders caused by some mental and psychological factors. The patient's physique can be strengthened through exercise, but the neurasthenia must be a comprehensive one.

Neurasthenia is mainly caused by long-term mental stress, and appropriate and reasonable exercise can help relieve mental tension, so insisting on appropriate and reasonable exercise can alleviate neurasthenia.

In the exercise should be according to their age, physical condition to choose the appropriate way of exercise, to avoid long-term anaerobic exercise, so as not to lead to excessive physical consumption, the best way to exercise is walking, running, cycling, table tennis, yoga, etc., patients in addition to appropriate exercise, but also to maintain a good attitude, mental relaxation, do not have too high requirements for themselves.

At work, attention should be paid to the combination of work and rest, ensure sufficient sleep, a light and easily digestible diet, and eat more fruits and vegetables.

First of all, it is necessary to pay attention to the reception of oxygen** to avoid the occurrence of hypoxia, which may lead to serious damage to the body's functions. If the patient's condition is mild, it is recommended to take hormonal drugs under the guidance of a doctor**; If the final condition is severe, a lung transplant may be considered.

Pulmonary fibrosis is a very serious disease, when pulmonary fibrosis occurs, patients will have obvious cough, sputum symptoms, when the condition is severe, it will make patients have dyspnea, cyanosis, and even death, so once pulmonary fibrosis appears, we should pay attention to it in time, so, how is pulmonary fibrosis better?

1. The best method of pulmonary fibrosis.

1.Drugs**.

If the symptoms of pulmonary fibrosis are not too severe, drugs can be used under the guidance of a doctor**, the more commonly used drugs include pirfenidone, nintedanib, glucocorticoids, immunosuppressants, etc., which can not only reduce the patient's lung function index, but also greatly reduce the risk of death.

2.Oxygen**.

Because the patient will have symptoms such as dyspnea, when suffering from this disease, the patient can be moderately inhaled, such as continuous low-flow oxygen inhalation, or oxygen concentrator can be used at home to inhale oxygen, which can relieve the symptoms of dyspnea.

3.Lungs** training.

When the patient has difficulty breathing, the patient can insist on abdominal breathing, fist breathing and other methods to relieve the symptoms, and if necessary, the ball breathing trainer can also be used for breathing training to improve the function of the lungs and alleviate the condition.

4.Surgery**.

If the patient's condition is particularly severe, pulmonary fibrosis has reached an advanced stage, or even symptoms of liver failure, kidney transplantation can only be selected to prolong the patient's survival.

Pulmonary fibrosis is common in patients with chronic pneumonia, pneumoconiosis, and interstitial pneumonia.

The ** of the above patients is mainly ****:

1. For example, pneumoconiosis, it is necessary to avoid dust environments and use some anti-pulmonary fibrosis drugs at home.

2. For pulmonary interstitial lesions, first of all, the underlying diseases, such as rheumatic connective tissue disease, can be added with glucocorticoids if necessary, and anti-pulmonary fibrosis drugs can be used.

3. When patients have pulmonary fibrosis, it can cause some changes in respiratory function, such as restrictive ventilatory dysfunction, and some patients can also be combined with obstructive pulmonary function decline, and some nebulized glucocorticoids and bronchodilators can be added.

Patients with pulmonary fibrosis need to be seen by a respiratory medicine specialist for a detailed evaluation to determine the cause of pulmonary fibrosis. Then give a targeted **. Some pulmonary fibrosis can be carried out**, and through these ** measures, it is helpful to alleviate the patient's condition and delay the progression of the disease.

For example, pulmonary fibrosis secondary to connective tissue disease or vasculitis, through the application of glucocorticoids and even immunosuppressants and other drugs, can reduce the patient's chest tightness and other related conditions, improve the condition of pulmonary fibrosis, and delay the progression of the disease. In addition, for the type of cryptogenic organizing pneumonia, the application of glucocorticoids can often achieve good curative effects, and even achieve clinical **.

Go to the hospital**, you can drink Chinese medicine to recuperate.

The most effective drugs are pirfenidone and nintedanib, which are currently available as direct anti-fibrotic drugs. Other antioxidants**, such as acetylcysteine, can also be used. When pulmonary fibrosis is acutely exacerbated, it will lead to inflammation and exudation of the lungs, and hormones can be added at this time, but hormones ** are inflammation and cannot fight fibrosis.

The whole replacement is irreversible, you may go to a doctor and ask.

The best methods of pulmonary fibrosis are:

1. Anticoagulants**.

Anticoagulant intervention is beneficial in patients with pulmonary interstitial fibrosis**. The commonly used drugs are low-molecular-weight hepatic hand earlyin, pyrine, pyrine, and vignone, which are mainly used in patients with pulmonary fibrosis. Although the preliminary results show good prospects and are encouraging, its efficacy, safety and route of administration have yet to be further confirmed before it can be recommended for widespread clinical use.

2. Glucocorticoids**.

Due to various factors such as the severity of the disease, age, and weight, the dosage of hormones may vary greatly. That is, the ** of hormones should follow the principle of individualization. The condition of patients with pulmonary fibrosis has not changed much in the short term, and the condition is now stable.

3. Oxygen**.

By giving oxygen to patients with pulmonary fibrosis, the drop in blood oxygen can be improved, which belongs to the category of inhalation**. It can increase the partial pressure of oxygen in arteries, improve tissue hypoxia caused by blood oxygen drop, and maintain the function of important organs such as brain, heart, and kidneys; It can also reduce the increased burden of heart and lung work due to increased heart rate and breathing during hypoxia. It has a good effect on hypoxia caused by the decrease in arterial oxygen partial pressure for respiratory diseases, and can only partially improve the hypoxia condition for patients with poor circulatory function or anemia.

In real life, the occurrence of pulmonary fibrosis is undoubtedly a serious health damage for patients, bringing serious harm to the patient's physical health, resulting in the patient's inability to work and live normally. So, what about pulmonary fibrosis? Let's find out!

In general, pulmonary fibrosis can be divided into two types: idiopathic pulmonary fibrosis and secondary pulmonary fibrosis

The symptoms of secondary pulmonary fibrosis are relatively mild, and most patients do not need to receive special **. The reason is that the adverse effects of such adverse symptoms on the human body are often very mild, and generally do not cause damage to the human lung function.

1. Secondary pulmonary fibrosis.

Patients with more severe pulmonary fibrosis may have some adverse symptoms such as chest tightness and wheezing, as well as coughing up mucus and thick sputum, and at the same time, there may also be weight loss and fatigue, as well as anorexia and limb joint pain and other systemic adverse symptoms, which usually need to be carried out with the help of hormones and immunosuppressants**, it is recommended that it is best to go to the hospital as soon as possible to receive regular**.

2. Idiopathic pulmonary fibrosis.

However, in the case of idiopathic pulmonary fibrosis, the situation is much more complicated. The reason for this is idiopathic pulmonary fibrosis, which is still a world-class problem at present, and it is a very difficult disease. The reason is that this adverse symptom usually appears in the alveoli and pulmonary interstitium, and the adverse symptoms of inflammatory alveolitis are generally taken as the main adverse manifestation, because at present, ** is still unclear, so ** aspect is undoubtedly very tricky.

For idiopathic **, the current method of anti-fibrosis with the help of glucocorticoids and immunosuppressants is usually the main method. At the same time, it is necessary to prevent and avoid infection, and if necessary, appropriate oxygen**. If the patient's condition is severe, a lung transplant may need to be considered.

1. Oral anti-infective drugs: pulmonary fibrosis is a phenomenon caused by lung inflammation and infection, and oral drugs or intravenous antibiotic drugs can be selected for **, more common drugs include cephalosporin, penicillin, azithromycin and other drugs, which have certain anti-inflammatory and anti-infective effects, and have a good effect on lung fibrosis or lung inflammation.

2. Glucocorticoid drugs: oral glucocorticoid drugs can improve shortness of breath and shortness of breath, and the more common drugs include methylprednisolone, prednisone, etc. It is best to use the drug rationally under the advice of a doctor to avoid undermedication or excessive medication, which will have a serious impact on the patient's health.

3. Nebulization**: Pulmonary fibrosis will cause symptoms of dry cough, if the cough is not ideal through conventional drugs to relieve cough, you can choose nebulization** to alleviate the condition, with cough and phlegm and anti-inflammatory effects. **During the illness, it is also necessary to maintain a good daily routine and work and rest routine, eat more light food, and go to the hospital for regular check-ups.

Hello, this pulmonary interstitial fibrosis is irreversible, this is mainly anti-inflammatory, keep the condition stable, avoid **, maintain the physical state is to increase the body's nutrients, improve the resistance.

There are many causes of pulmonary fibrosis, which may be related to interstitial lung disease, tuberculosis, lung infection, etc. Its ** methods mainly include: 1. Drugs**:

Antioxidant drugs**, such as pirfenidone, can alleviate and improve the condition and delay the progression of pulmonary fibrosis, but cannot reach the clinical level**; 2. Oxygen inhalation: patients with advanced pulmonary fibrosis are mostly combined with hypoxemia, and oxygen inhalation should be given in time; 3. Anti-infection**: anti-infection when co-infection**; 4. Lung transplantation.

Mild fibrosis is found in the lungs and the need for it should be considered based on the patient's cause**. If the inflammation of the lungs** is not complete, the slight fibrosis caused by ** does not need to be done. If fibrosis is caused by an immune-related disorder, antifibrosis is indicated**.

Inflammation of the lungs causes the destruction of lung tissue, inflammation is not complete, and replacement by fibroblasts and extracellular matrix is a physiological repair process that does not cause severe symptoms and further damage, so mild fibrosis is not required.

Immune-related diseases such as idiopathic non-specific interstitial pneumonia and pulmonary sarcoidosis are generally the terminal stage of the disease. Antioxidant and antifibrotic drugs such as pirfenidone, nintedanib, etc., need to be actively administered, which can delay the progression of pulmonary fibrosis and prevent further decline in lung function and cause serious consequences such as respiratory failure.