Can baby pulmonary hypertension be treated with traditional Chinese medicine?

Nowadays, there are many babies who are born and are not very well cared for, so they are prone to some diseases. In addition, the baby's resistance is very low, so it takes a long time to suffer from the disease, and the process is also very complicated. I believe that there are many babies who suffer from pulmonary hypertension not long after birth, and pulmonary hypertension should also be prioritized.

Traditional Chinese medicine can be used for **pulmonary hypertension, but the effect is not great, so it is not very recommended. <>

How is pulmonary hypertension caused in babies? In general, the biggest reason for pulmonary hypertension in babies is because the baby has congenital heart disease. In addition, if the ductus arteriosus is not closed or missing, these conditions will cause pulmonary hypertension in the baby.

Therefore, we must find out the baby's disease as soon as possible, and go to ** as soon as possible, and you may get a thorough **. If it is detected late, the results of the surgery will become very unsatisfactory. <>

What should I do if my baby has pulmonary hypertension**? In cases like this, you first need to go to the hospital to take oxygen**. The most effective** is to have surgery, but if it is only mild, it is not enough to have surgery.

If the baby has a rejection reaction to the drugs he usually takes, or if he has been taking ** drugs for a long time but no effect, he must undergo surgery**. Only after undergoing surgery** can it be possible to treat the disease**, and parents must go to a professional pediatric hospital to see a doctor for their baby. <>

How can I prevent pulmonary hypertension in my baby? First of all, if one of the parents has heart disease, it is not suitable to have children, and the chance of inheritance is very large. In addition, when the mother of the pregnant woman is pregnant, the pregnant woman herself and the father must quit their bad habits, such as drinking and smoking.

Pregnant women must do a good job of prenatal ** and go to the hospital regularly for prenatal checkups, just in case. It is necessary to pay attention to the serious illness and defects of both parents, which require everyone to be vigilant.

Of course, you can use traditional Chinese medicine**, but you must not use medicine indiscriminately, and you must go to a very professional and regular traditional Chinese medicine hospital for diagnosis and treatment, and then carry out **.

Yes, but you should consult a professional doctor before using Chinese medicine**, so that the doctor can give professional advice before proceeding**.

Yes, but at this time, don't blindly use medicine, be sure to go to a professional hospital system for examination, and then determine the corresponding method.

No. Because the baby's stomach and intestines have not yet developed well, drinking Chinese medicine will increase the burden on the stomach.

Analysis: Pulmonary hypertension can be treated.

Suggestion: The prognosis of patients with different types of pulmonary hypertension varies. Before the advent of targeted drugs for pulmonary hypertension, the natural history of patients with idiopathic pulmonary hypertension in PAH was the most clear, the median survival after diagnosis was only 2 3 years, and the prognosis of severe symptoms was worse, and targeted drugs** could significantly improve the 3-year survival rate, even so, due to the severe hemodynamic changes and functional impairment of most patients, the long-term clinical prognosis was poor.

Patients with both pulmonary hypertension and right ventricular dysfunction have a worse prognosis. Sudden elevation of pulmonary artery pressure and right ventricular dysfunction are also the most important causes of death in patients with pulmonary hypertension due to chronic lung disease. Patients with chronic thromboembolic pulmonary hypertension who are candidates for surgery have better long-term survival after pulmonary artery thromboendarterectomy than those who are medical** and lung transplanters.

Xu Weijie - Hebei Provincial People's Hospital.

Internal medicine. Physician.

Pulmonary hypertension**:

1.General measures.

** Exercise and exercise training, psychosocial support, contraception, vaccinations.

2.In the tank**.

Anticoagulants, diuretics, digitalis, oxygen.

3.Targeted drugs**.

At present, drugs that have been approved by the State Food and Drug Administration of China for targeting **pulmonary hypertension include:

1) Bosentan indications: for patients with class I pulmonary hypertension.

Precautions: Exacerbate sodium and water retention and edema. If there is a possibility of liver damage, liver function tests should be performed before taking the drug, and the liver function test should be checked once a month during the drug period.

It is contraindicated in pregnancy or in the process of becoming pregnant, and women who are likely to become pregnant should have a monthly pregnancy test. This drug can also affect the effectiveness of hormonal contraceptives, and other contraceptive methods should be used. Check the hemoglobin level before and after use, and every 3 months thereafter.

2) Ambrisentan indications: for patients with class I pulmonary hypertension.

Precautions: The risk of fetal malformations should be strictly contraceptive during the medication, and it is contraindicated for pregnant and lactating women. If there is a possibility of liver damage, liver function tests should be performed before taking the drug, and the liver function test should be checked once a month during the drug period.

Adverse reactions: fluid retention, heart failure, hypersensitivity, anemia, etc.

3) Iloprost indications: for patients with class I pulmonary hypertension.

Precautions: Adverse reactions: vasodilation, headache, cough, hypotension. Patients with abnormal liver function and renal failure should consider reducing the dose. It is forbidden for bleeding disorders, pregnant and lactating women, and pay attention to contraception.

4) Treprostinil indications: for patients with class I pulmonary hypertension.

Precautions: Adverse reactions include pain, diarrhea, jaw pain, edema, vasodilation, and nausea.

4.Intervention**.

Patients with chronic thromboembolic pulmonary hypertension and Takayasu's artery involvement: pulmonary vascular balloon dilation and stenting can be performed if indicated.

Balloon atrial septostomy: It is contraindicated in patients with pulmonary hypertension who have not responded to the best drug combination**, and in patients with terminal stage of MRAP > 20 mmHg and arterial oxygen saturation < 85% at rest.

5.Surgery**.

Pulmonary artery thromboendarterectomy: It is the first choice for chronic thromboembolic pulmonary hypertension, the indications are cardiac function, grade, pulmonary artery average pressure of more than 30mmHg, pulmonary vascular resistance of 300dyn·s cm, and thrombus located above the lung segment can be achieved by arterial surgery.

Hello pulmonary hypertension.

It is a group of clinicopathophysiological syndromes of pulmonary artery flat pressure of 25 mmHg measured by right heart catheterization in the resting state due to various causes.

Gene decoding studies have found that idiopathic pulmonary hypertension is caused by changes in gene sequences, which are commonly referred to as gene mutations. There are many causative genes that can cause idiopathic pulmonary hypertension.

For example, gene sequence changes associated with the coding of bone-forming protein type II receptor (BMPRII) are closely related to idiopathic pulmonary hypertension, and BM**2-mediated BMP signaling pathway plays an important role in the occurrence and development of pulmonary hypertension.

Pulmonary hypertension is a syndrome in which the pressure in the pulmonary arteries rises abnormally high due to known or unknown causes. It can be caused by the lesions of the pulmonary vessels themselves, or secondary to other cardiopulmonary diseases, which are widespread and have a high prevalence.

Whatever the cause, it often progresses and seriously affects the quality of life. After the discovery of pulmonary hypertension, it is necessary to actively look for the highest level of pulmonary hypertension, and the first satisfactory results are usually obtained.

As with high blood pressure, some types of pulmonary hypertension may require prolonged medication**. Echocardiography** can estimate pressure in the pulmonary arteries and can help determine the cause of pulmonary hypertension and assess cardiac function.