What tests are needed for pediatric convulsions?

Children with convulsions need to undergo routine blood tests, stool tests, urine tests, electrocardiograms, creatinine measurements, etc. It is recommended to observe the child's condition first and then tell the doctor. You can get an examination based on the doctor's advice and cooperate with the doctor for treatment after the diagnosis is confirmed. The treatment method needs to be selected based on the severity of the child's condition. Do not make decisions on your own.

Pediatric convulsions, commonly known as seizures, often occur in children aged 1-3 years. Although the onset is short, once it occurs frequently, it is easy to induce serious complications, which will have a negative impact on the physical and brain development of young children. When a child is found to have these conditions, it is necessary to check and confirm them as soon as possible. So how to check for pediatric convulsions? Let's take a closer look.
Convulsions are a common emergency in children, especially in infants and young children. They are caused by a variety of reasons that cause brain nerve dysfunction. The following tests are required to diagnose convulsions in children:
1. Routine blood test, examination method: blood biochemistry Routine blood test is the most common examination, which detects and analyzes the quantity and quality of the three systems of formed elements in the blood, namely red blood cells, white blood cells and platelets. Any pathological changes in the formed elements in the blood will affect the tissues and organs of the whole body; conversely, lesions in tissues or organs can cause changes in blood components, so hematological analysis and its results are very helpful in understanding the severity of the disease.
Routine stool examination, examination method: stool test Routine stool examination is the naked eye observation and microscopic examination of stool, which is a common examination for digestive tract diseases. It includes examination of stool shape, hardness, color, odor, presence of mucus, pus, blood, parasites, stones and foreign matter. The properties of stool are related to the disease, and its pathological changes often provide special clinical significance.
2. Urinalysis, examination method: Urine biochemistry Urinalysis is a preliminary examination that cannot be ignored in clinical practice. Many kidney diseases can show proteinuria or formed elements in urine sediment in the early stage. It is also of great reference value for the diagnosis of certain systemic diseases and diseases that affect urine changes in other organs of the body, such as diabetes, blood diseases, liver and gallbladder diseases, and epidemic hemorrhagic fever.
3. Electrocardiogram, examination method: imaging examination <br/>Electrocardiogram is the best way to measure and diagnose abnormal heart rhythm. It is used to diagnose abnormal heart rhythm when the electrical conduction tissue is damaged and changes in heart rhythm caused by electrolyte imbalance.
4. Creatinine determination, inspection method: blood biochemistry <br/>Creatinine is the final product of creatine metabolism and is excreted by the kidneys. Creatine in the human body comes partly from food and partly from body synthesis. The raw materials for synthesizing creatinine in the body are glycine, arginine and methionine. 98% of the creatine in the body exists in the muscles and combines with phosphoric acid to form creatine phosphate.