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If you have interstitial pneumonia, you have to be hospitalized according to the doctor's requirements, and then use anti-inflammatory drugs, there are ways to cure you in your life, so you still have to listen to the doctor, don't just use other home remedies or the like.
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1. Pulmonary fibrosis can cause patients to have symptoms of dyspnea and respiratory failure, and the use of glucocorticoids can effectively alleviate such symptoms. After taking these drugs for about a week, you should check whether the fibrosis in your lungs has improved, and if necessary, you will need to use these drugs for about three months. If the patient's lung fibrosis is gradually reduced, and the symptoms are gradually reduced, the dosage needs to be appropriately reduced, and then the treatment course of six months to one year can effectively control the pulmonary fibrosis and the physical damage caused to the patient.
2. If the patient's pulmonary fibrosis is more severe, he or she needs to go to the hospital for routine blood lung function tests, as well as CT examinations of both lungs, including kidney function and bone mineral density level tests. The main thing is to prevent the use of hormonal drugs, which will aggravate the patient's condition. Therefore, after the patient has medium-term pulmonary fibrosis, he needs to follow the doctor's advice, adjust the **regimen and change the drugs used** at any time.
3. For advanced pulmonary fibrosis, it is recommended that the patient go to the hospital for hospitalization**, and can fully accept all the doctor's orders** and can be carried out as soon as possible**. At the same time of hospitalization, patients can also have a physical examination at any time, the uncomfortable symptoms caused by advanced pulmonary fibrosis to the patient's body, and can also observe whether the pulmonary fibrosis has been reduced and the symptoms have improved in real time.
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Hello, go to the hospital as soon as possible**, don't take it lightly, you must pay attention to any disease.
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What are the general measures for interstitial pneumonia?
Stay away from triggers.
Hypersensitivity pneumonitis can effectively stop the progression of inflammation and fibrosis by getting rid of known allergens as soon as possible, stopping suspected drugs immediately for drug-related interstitial pneumonia, and stopping smoking in time for smoking-associated interstitial pneumonia.
Anti-inflammatory**. Glucocorticoids are effective in reducing lung inflammation in interstitial pneumonia and can be combined with immunosuppressants** as appropriate.
Anti-fibrotic**.
In patients with idiopathic pulmonary fibrosis or progressive connective tissue disease Interstitial Pneumonia associated with systemic sclerosis, antipulmonary fibrosis drugs can partially delay the progression of pulmonary fibrosis.
Correction of hypoxemia
Oxygen therapy should be given to patients with significant hypoxemia at rest or after activity, either with a fixed home or portable mobile oxygen device, and for patients with stable interstitial pneumonia with hypoxemia Endotracheal intubation is not recommended**.
Antacid**. Patients with gastroesophageal reflux may be treated with antacids**.
Psychology**. Educate patients to strengthen their confidence, avoid pessimism and abandonment, and reduce their psychological anxiety and pain; Patients with end-stage qualitative lung disease should be given end-of-life care.
What medications are available for interstitial pneumonia**?
Due to individual differences, there is no absolute best, fastest and most effective medication, except for commonly used over-the-counter drugs, the most suitable drug should be selected under the guidance of a doctor in full combination with individual circumstances.
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Patients with interstitial pneumonia should pay attention to their diet, eat more light food, eat more fruits and vegetables, drink more water, eat less spicy and acidic food, and eat less fried food and aquatic products. Generally speaking, food should be diversified, rationalized, and nutritious.
The best principles of Western medicine.
It is to control alveolitis and find a way to reverse it and prevent the disease from getting worse. You may choose glucocorticoids or in combination with cytotoxic drugs, depending on the course and dose. Commonly used drugs are glucocorticoids, cyclophosphamide, azathioprine, etc.
It usually takes six months**. Because the disease of interstitial lung disease has not yet been fully identified and the effect of drugs is limited, only hormonal and cytotoxic drugs can be used to give a reasonable amount.
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If you have interstitial pneumonia, you need **! Interstitial pneumonia varies according to different **, severity, etc.**, mainly including drugs ** (cefradine anti-infection, methylprednisolone, cyclosporine, pirfenidone anti-fibrotic, etc.) and surgery**.
1.Drug**: Anti-infective**:
The disease can be caused by bacterial, viral and other infections, and drugs such as cefradine and erythromycin can be used to fight infection**. Glucocorticoids (methylprednisolone) in combination with immunosuppressants (cyclosporine) Antifibrotic drugs, such as pirfenidone and nintedanib, delay the decline in lung function and improve prognosis.
2.Surgery**: Lung transplantation is the only effective surgical modality for patients who meet the indications, but it is generally difficult to perform due to its high cost and limited donors.
The above drugs should be standardized and rationally used under the guidance of professional physicians and pharmacists.
If you have interstitial pneumonia, you should seek medical attention in time and carry out it under the guidance of a professional doctor**.
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Glucocorticoids: commonly used drugs are prednisone and methylprednisolone. During the period, attention should be paid to the *** of hormones, and the dose should be reduced slowly over a period of weeks to months, and at the same time, close follow-up should be followed up to prevent disease**.
Immunosuppressants: often used in combination with hormones, commonly used drugs are cyclophosphamide, azathioprine, methotrexate, mycophenolate mofetil, hydroxychloroquine, cyclosporine and sirolimus. During the period, you should pay attention to the hormones and pay attention to the prevention of infection.
Anti-fibrotic drugs: Pirfenidone pirfenidone has anti-inflammatory, antifibrotic and antioxidant properties, which can delay the decline of lung function and improve the survival of patients. Major adverse effects include photoallergy, rash, fatigue, stomach upset, and anorexia.
Nintedanib is a multi-targeted tyrosine kinase inhibitor that can block fibroblast proliferation, migration, and transformation, thereby inhibiting the occurrence of pulmonary fibrosis, and is indicated for patients with idiopathic pulmonary fibrosis, or interstitial pneumonia associated with systemic sclerosis of connective tissue disease. The main adverse reactions are diarrhea, nausea, and elevated liver enzymes, which are contraindicated in patients with moderate or severe liver damage. Antacids, including proton pump inhibitors (eg, omeprazole, pantoprazole) and H2 receptor antagonists (eg, cimetidine, famotidine), are used for gastroesophageal acid reflux and may reduce the risk of gastroesophageal reflux-related lung injury.
N-acetylcysteine is converted into glutathione precursor in vivo, which has antioxidant effects and can improve the patient's expectorant cough symptoms.
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Interstitial pneumonia is the inflammation of the interstitial tissue of the lungs, and the main part of the inflammation is the alveolar wall of the bronchial wall. Most patients will have symptoms such as shortness of breath, cough, sputum production, fever, malaise and depression after the onset of the disease, because the harm of interstitial pneumonia is greater, so it should be dealt with in time after the onset of the disease, and the following three treatment methods are introduced.
1. If interstitial pneumonia is suspected, it is necessary to conduct a detailed physical examination in order to deal with it in a timely manner, and the most commonly used examination methods are blood tests, lung biopsies and pulmonary function tests. Blood tests also include arterial blood gas analysis and bronchoalveolar perfusion. Lung biopsy is the best method for diagnosing this disease, which has the advantages of high safety, easy operation and easy reexamination.
Second, interstitial pneumonia is a disease that has been progressing, the course of this disease is about two to four years, **corticosteroids are preferred**, followed by traditional Chinese medicine and immune drugs, drugs ** need to follow the rules, comprehensive, correct and regular principles, and the dosage and time of medication should be controlled when taking drugs.
3. Patients with interstitial pneumonia also need to be treated in the first stage, the most common of which is nutritional support, the purpose of which is to provide patients with reasonable nutrition, maintain the metabolism of body cells, and promote. Patients with hypoxia should be treated with oxygen therapy and infection prevention.
After having interstitial pneumonia, you also need to strengthen care, be sure to pay close attention to the change in temperature, and never catch a cold. You can do proper physical exercise and try to do more aerobic exercises to enhance your physical fitness, including tai chi, swimming and badminton. It is very important to take a comprehensive nutritional supplement, eat more foods rich in vitamins and proteins, drink plenty of water, never smoke and drink alcohol, and maintain an optimistic attitude.
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Surgery**. Lung transplantation: The goal is to improve the quality of life and prolong survival. For patients with severe interstitial pneumonia, lung transplantation may be the last option.
Other**. Oxygen therapy: Oxygen therapy does not stop lung damage, but it can improve the patient's symptoms: it helps with breathing and movement; Prevent or reduce complications caused by low blood oxygen levels; Improvement of right heart blood pressure; Improves sleep and quality of life.
Lung**: Improves exercise tolerance, improves nutritional status, reduces dyspnea symptoms, increases walking distance, and improves quality of life [4].
What is the outcome of the disease development?
If the patient is not accepted in time**: If the patient is diagnosed late and extensive interstitial fibrosis has formed in the lungs, the normal respiratory function of the lungs will be greatly affected, causing obvious symptoms of dyspnea, seriously affecting the patient's quality of life, and if respiratory failure continues to develop, it may also be life-threatening.
If received in a timely manner**: If detected early and correctly diagnosed, giving a reasonable and effective ** can reduce symptoms, prevent or slow the formation of pulmonary fibrosis, alleviate and control the progression of the disease, and improve quality of life.
I also hope that you can adjust your mindset and be positive and optimistic about each day!
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Interstitial pneumonia tends to cause some damage to the lungs. Moreover, the symptoms of patients are mainly active dyspnea, ventilation disorders and other symptoms, and are easily accompanied by systemic symptoms such as weight loss, fatigue, and anorexia. In order to better ** this disease, the patient's ** timing is important.
****。There are many factors that cause interstitial pneumonia, so patients can take the best results. Interstitial pneumonia caused by rheumatic immune diseases can be predominantly rheumatic immune diseases.
For lesions caused by idiopathic pulmonary interstitial fibrosis, glucocorticoids are usually the main measure. However, this kind of ** measure will cause many adverse reactions in the body, and everyone needs to control the occurrence of hypertension, diabetes, stress ulcers and other diseases. Drugs**.
At present, the development of drugs to play the role of interstitial pneumonia is relatively rare, and the common effective drugs mainly include nintedanib, pyrenidone and other drugs are very targeted. Since this disease can easily lead to fibrosis in the lungs, taking these two drugs can be a good way to alleviate the appearance of fibrosis. The impact of interstitial pneumonia is relatively large.
Although the best measures taken have a certain effect, they need to be used for a long time. Since there is no specific method for interstitial pneumonia, we need to carry out a variety of methods to cooperate. If you want to give better play to the best effect of interstitial pneumonia, the time of diagnosis and treatment should be controlled three months before the disease.
The condition is more stubborn for more than three months, and it is not the best time for this disease. In daily life, patients should adjust their mentality. Appropriate physical exercise can effectively improve one's immune resistance and prevent interstitial pneumonia.
Although the best method for interstitial pneumonia introduced above is relatively ordinary, it requires systematic cooperation to be truly implemented. In particular, the best time to take action is within three months of the onset of the disease.
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Interstitial pneumonia is a type of pneumonia and is a relatively common disease. This disease is more troublesome, and it is still a worldwide problem. In fact, there are some home remedies that can play a good role in relieving the symptoms of interstitial pneumonia, so in addition to actively taking drugs according to the doctor's instructions**, patients with interstitial pneumonia can choose some home remedies**.
1. Green onion white porridge: 3 green onions, appropriate amount of rice, 2 slices of ginger. Add the above ingredients to an appropriate amount of water, cook porridge together, and give it to the patient while it is hot.
2. Almond porridge: appropriate amount of almonds, peel the tip, add water to grind, filter and extract juice, a little rice. Add an appropriate amount of water to the above ingredients, cook porridge together, and give it to the patient.
3. 100 ginger juice: 100 appropriate amounts, appropriate amount of ginger, a little honey. Add an appropriate amount of water to 100 parts and ginger, decoction to extract the juice, add honey, and give it to the patient when it is warm. Children under 1 year old should not consume honey, and can be flavored with a little sugar.
4. Pear porridge: Wash 3 pears, chop them, add an appropriate amount of water and cook them for 30 minutes, remove the pear pomace, then add an appropriate amount of washed rice, cook them into porridge and eat them hot. It is used for pediatric pneumonia, fever, cough.
Pork lung porridge: Wash the pork lungs, add an appropriate amount of water, cook for seven years, remove them, and cut them into cubes for later use. Take coix seeds, japonica rice, a little diced pork lungs, an appropriate amount of pork lung soup, cook porridge, add green onions, ginger, and five-flavor seasonings.
Treatment of lung deficiency, cough, hemoptysis, etc.
This article talks about several very good home remedies for interstitial pneumonia, which can promote interstitial pneumonia, so if you are unfortunate enough to suffer from interstitial pneumonia, you can follow these small home remedies mentioned in this article to treat interstitial pneumonia.
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1. Western medicine for interstitial pneumonia**.
1.Glucocorticoids: Patients with interstitial pneumonia can generally take prednisone for **, the specific dosage is 30-40 mg daily, and can be taken in 3-4 doses. If the condition is more severe, intravenous methylprednisolone is required. >>>More
First Drug**.
Drugs ** The key to pulmonary interstitial pneumonia is that patients with interstitial pneumonia and cough require a combination of hormones and immunosuppressants in the early stages**. Sputum cultures are examined to identify flora, and appropriate antibiotics are used symptomatically, such as penicillins and cephalosporins. Patients with interstitial pneumonia with alveolar and irreversible interstitial lesions require a combination of glucocorticoids and immunosuppressants**, and the dose is tapered after the patient is stable. >>>More
Interstitial pneumonia (LID) is a general term for a group of heterogeneous non-neoplastic and non-infectious lung diseases with varying forms and degrees of inflammation and fibrosis in the lung interstitium, alveolar wall, and alveolar cavity as the main pathological changes. The main symptoms are dyspnea, cough, and a few have hemoptysis, chest pain, stridor, and pneumothorax, and it is recommended to go to the hospital for relevant examinations.
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