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Li Jianjun, Shijiazhuang City: Hebei Yiling Hospital is the center of amyotrophy in Hebei Province, which has basically explored the law of amyotrophy through nearly 30 years of research in amyotrophic hospitals, and has applied the characteristic traditional Chinese medicine system to prolong the life span and improve the symptoms of many refractory amyotrophia. Especially for some types of amyotrophic diseases, with the deepening of research, the method is becoming more and more perfect, so as to achieve clinical practice.
For example, glycogen accumulation myopathy, lipid deposition myopathy, mitochondrial myopathy, etc., some types have targeted methods, which significantly improve the efficacy. Glycogen-accumulating myopathy type 2 (Pompe disease) has glycosidase replacement**; Glutaric aciduria in lipid-deposition myopathy can also be treated with vitamin B2 plus metabolic regulators**; Amyotrophic muscle weakness caused by primary carnitine deficiency can be supplemented with carnitine.
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At present, it is believed that patients with limb movement disorders caused by muscle atrophy can significantly reduce or alleviate the sequelae of paralysis after formal training, and some people regard ** as particularly simple, and even equate it with "exercise", rushing to achieve results, often half the effort, and lead to joint muscle damage, fractures, shoulder and hip pain, aggravated spasticity, abnormal spasm patterns and abnormal gait, as well as foot drop, inversion and other problems, that is, "misuse syndrome". Improper strength training can aggravate spasticity, and proper training can relieve this spasticity, so that limb movements tend to be coordinated. If the wrong training method is used, such as repeated practice of grasping vigorously with the hand on the affected side, the flexor muscle coordination of the upper limb on the affected side will be strengthened, and the spasm of the muscles responsible for joint flexion will be aggravated, resulting in elbow flexion, wrist flexion pronation, and finger flexion deformity, making it more difficult to recover hand function.
In fact, muscle atrophylimb movement disorder is not only a problem of muscle weakness, but also an important cause of muscle dysfunction. Therefore, it should not be mistaken that training is strength training. In the treatment of motor dysfunction in patients with muscular atrophy, the traditional concepts and methods only focus on restoring the patient's muscle strength, ignoring the coordination between the patient's range of motion, muscle tone and antagonism.
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Muscular wasting is a relatively common disease nowadays, and suffering from muscular wasting will have many impacts on the patient's daily life, and the patient may not be able to work or live normally. And muscle atrophy is a relatively difficult disease, and there are many ways to atrophy muscles, so what are the ways to atrophy muscles?
1. Acupuncture: According to the theory of syndrome differentiation and treatment of traditional Chinese medicine, appropriate laxative techniques are used to regulate the balance of yin and yang in the patient's body, dredge the meridians, open the brain, and promote the patient.
2. Tuina: The main function of Tuina is to dredge the meridians, activate blood and eliminate blood stasis through limb or acupuncture points and massage, so that the patient's limb function and other functional disorders can be restored.
3. Psychological plan: Psychological plan is formulated for the changes in different stages of psychology (such as denial, anger, depression, opposition to independence, adaptation, etc.), and various methods can be carried out individually, collectively, family, and behavioral.
4. Homework**: mainly daily life actions, occupational labor actions, craft labor actions (such as weaving, etc.), so that patients can adapt to the needs of personal life, family life, social life and labor after discharge.
The above content introduces you to what are the methods that can lead to muscle atrophy, and now patients should know about these methods of muscle atrophy. After suffering from muscle atrophy, the patient must not delay, should go to a regular hospital for diagnosis in time, and take scientific methods.
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Whether muscle atrophy can be related to **, long-term inactivity can lead to muscle atrophy, and muscle atrophy can be caused by impaired nerve function, **can only control the condition, difficult**.
Whether muscle atrophy depends on the specifics. If muscle atrophy is caused by long-term inactivity, it can be exercised through **function. Due to damage to the spinal cord and cranial nerves, it is difficult and the prognosis is poor, which can only control the condition and delay the rate of muscle atrophy.
Muscular dystrophy should be targeted at the primary disease. In the case of inflammatory muscle atrophy, glucocorticoids, immunosuppressants, etc.** can be used, and dystrophic muscle atrophy can be given to nutritional muscle drugs**. Caused by cervical spine disease, lumbar disc herniation, etc., it can be operated**.
**During the period, you should actively carry out muscle strength training and pay attention to adequate nutritional intake.
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Muscular atrophy is a clinical manifestation caused by a variety of diseases, and some diseases can be cured at the same time as muscle atrophy.
Muscular atrophy is a clinical manifestation that can be caused by a variety of diseases and can be broadly divided into neurogenic and myogenic and disuse atrophy. Some of these muscle atrophy can be recovered through functional exercises, such as atrophy caused by reduced local muscle activity due to stroke, fracture, etc., and can be gradually recovered after the disease is relieved by ** exercise, or even reach normal. However, there is no effective method for muscle atrophy caused by diseases such as muscular dystrophy and amyotrophic lateral sclerosis.
If muscle atrophy occurs, you should go to the hospital in time, clarify**, follow the doctor's guidance**, strive to be as soon as possible**, or delay the rate of disease progression.
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Maintain optimism Increases muscle strength and muscle growth, high in protein, rich in vitamins, phospholipids and trace elements in the early stages.
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Muscle atrophy is the primary disease that causes muscle wasting in the first place. If it is caused by muscle disease, caused by muscular dystrophy and muscle inflammation, hormones** and ion channel drugs are needed to improve muscle wasting symptoms. If it is caused by myasthenia gravis, hormones, immunosuppressants, pyridostigmine bromide, etc., can be given to improve myasthenia gravis and improve muscle atrophy.
If it is diabetes and peripheral neuropathy that cause muscle atrophy, it is good for diabetes to retrove nerves. If autoimmune is caused, immunoglobulin is given, and then the nerves are nourished. For muscle atrophy caused by spinal cord lesions and cerebral central lesions, it is necessary to actively have cerebral infarction, cerebral hemorrhage or spinal cord lesions, and then train to improve symptoms.
There are also disuse reasons, because fractures are caused by long-term bed rest, and muscle atrophy should be improved through active exercise and nutrition.
Muscle atrophy can cause weakness in walking, inability to stand, inability to squat, inability to step, etc., and muscle weakness in the hand can cause abnormalities in some hand movements, such as not being able to clench fists, not being able to do some fine movements, etc., and at the same time there is significant weight loss. It can also lead to some accompanying symptoms due to common causes, such as neurogenic muscle atrophy, in addition to muscle atrophy in the corresponding innervated area, there will also be paresthesias, such as decreased sensation, weakness, ant crawling sensation, etc
Common causes of neurogenic muscular atrophy are disuse, dystrophy, ischemia, and toxicity. Anterior horn lesions, nerve roots, plexus, peripheral nerve lesions, etc. can cause conduction disorders of nerve excitatory impulses, so that some muscle fibers are disused, resulting in disuse amyotrophy. On the other hand, after any part of the motor neuron is damaged, the release of acetylcholine from its terminal part decreases, and the sympathetic nerve nutrition is weakened, resulting in muscle atrophy. >>>More
Charoneal muscular atrophy is mainly manifested by motor, sensory, and autonomic symptoms, and motor symptoms are mainly manifested by muscle atrophy, which is characterized by muscle atrophy at the distal end of the limbs; The second is that it only affects the extensor muscles in the early stage and starts from the legs; third, the atrophy of the upper limbs does not involve the elbow joint and the upper third of the thigh; Fourth, cavus feet, scoliosis or clubfoot are often present; Sensory impairment is mainly sensory impairment of peripheral nerves, and autonomic nerve symptoms are mainly manifested as local ** bruising, swelling, and ulceration.
Muscle atrophy is a relatively harmful disease in life, with a high incidence and serious harm to the health of patients. Disuse muscle atrophy: Disuse muscle atrophy is the most common type, usually caused by infection by other diseases, or long-term lack of labor. >>>More
Brain atrophy refers to the phenomenon of atrophy caused by organic lesions in the brain tissue itself due to various reasons. Physiologically, the volume of brain tissue is reduced, the number of cells is reduced, and the ventricles and subarachnoid space are enlarged. The disease mostly occurs in people over 50 years old, the course of the disease can reach several years to decades, more men than women, can be divided into diffuse brain atrophy (including cortical atrophy, cerebellar atrophy and cortex, cerebellum, brainstem atrophy) and localized brain atrophy (more common after localized brain organic lesions such as trauma, vascular disease, intracranial localized ** infection, etc.). >>>More