For patients with phenylketonuria, what methods can be taken to treat the research plan, and what should be paid attention to in

First, choose the first dietary treatment plan for pku handbook phenylketonuria patients, how to carry out dietary treatment

1. Why you need to diet

For patients with phenylketonuria, if the diagnosis is made, a dietary treatment plan must be taken. Dietary treatment is mainly to maintain sufficient protein for patients, which can help patients improve protein synthesis. The diet is designed to make l-phenylalanine in patients with phenylketonuria Acid levels remained within the normal range. However, during dietary therapy, the phenylalanine level in the patient's blood must be monitored at all times, and supplementation should be provided to the patient according to the quality of the patient's daily protein requirements. In addition, it is necessary to pay attention to the phenylalanine level in the patient's blood and the level of l-phenylalanine that the patient can tolerate, depending on the patient's dietary preferences.

To carry out analysis, adjustment and treatment methods, because if Chinese food culture has no other interest in improving the life of patients, then according to patients in the process of dietary treatment will have a very important and difficult effect, especially for companies with their own patients. It is very difficult to develop an effective treatment method for infants and young children with phenylketonuria. In the process of dietary treatment, some more natural diets can be selected. The natural diet mainly includes breast milk, because breast milk contains phenylalanine The acid content is relatively high. But it only contains 1/3. If the patient is seriously ill, or suffers from phenylketonuria, older infants or children can use milk, porridge and eggs to supplement protein, but the patient must be the premise.

2. How to carry out diet therapy

So, how are you going to treat phenylketonuria? Because diet therapy can help patients relieve some relatively rare clinical symptoms, er diet therapy mainly adopts l-phenylalanine diet, and the content of l-phenylalanine in these diets is limited. It is also a relatively high requirement. For example, in the course of treatment, the patient should be treated according to the course and age of the patient. If a baby is found to have phenylketonuria in the first week of life, infant formula treatment should be given, the first choice is L-phenylalanine formula.

If the treatment is continued for 3 days or 5 days for 7 days, the blood phenylalanine level of the patient will decrease. Some natural milk, namely breast milk, can be added according to the patient's diet. In addition, some ordinary infant milk powder can also be selected. Or some supplementary food for processing, but the requirement of supplementary food is that the supplementary food that needs to process this alanine should be configured strictly according to the qualified configuration during the configuration process. Milk powder can make patients achieve curative effect.