Monday, July 2, 2018

Lymphadenitis

November 29, 2011

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 Lymphadenitis  Lymphadenitis   is an inflammation lymph nodes . It is a disease of the secondary type, it appears after the inflammation has arisen in a particular area of ​​the body. In rare occasions diagnosed primary purulent inflammation of lymph nodes . The agents of this disease are streptococci As well as a number of other pathogens. However, often there is a mixed flora. The disease occurs after organisms . Toxins , and decomposition products   fabrics come from lymph   lymph nodes. Infiltration may occur through the break in the skin, mucous membranes, and hematogenous route.

Lymphadenitis is usually divided into purulent . serous . Productive inflammation . If the process of inflammation spread to other tissues, the result may develop periadenit . For this state of the characteristic symptom is stiffness of nodes in which the inflammation extends, for example, if a person is diagnosed cervical lymphadenitis , Similar phenomena are observed in the neck area. Lymphadenitis may occur in acute or chronic. The course of acute lymphadenitis occurs in different ways. If suppurative focus to eliminate as soon as possible, the hyperemia   then disappear, there will be resolution exudate And after reducing nodes stop their pain.


At the beginning of suppurative lymphadenitis observed symptoms catarrhal-hyperplastic lymphadenitis Later formed purulent infiltration site and there are several foci. After their merger lymph node is melted. If purulent process involved his capsule and surrounding tissue, the result is developed phlegmonous adenitis . With the development of putrid lymphadenitis lymph nodes are affected sphacelism .

There is also a classification based on the division of the hearth of the inflammatory process ( bubonadenitis . cervical lymphadenitis ). One of the most common types of this disease is bubonadenitis.

Symptoms lymphadenitis

 Lymphadenitis  The patient feels lymphadenitis lymphadenitis following symptoms: severe pain, because of which he holds the limb in a forced position. Fever, swelling occurs. If lymphadenitis is superficial, it may be observed redness and increased temperature locally. At a late stage of the disease manifested fever, fluctuation . leukocytosis . Thus the primary site of infection is already irrelevant.

Lymphadenitis is like sharp And chronic , As distinguished specific   and nonspecific lymphadenitis . Nonspecific lymphadenitis usually provoke staphylococci More rarely pathogens are streptococci and other pyogenic bacteria . Foci of the disease may become purulent wound, carbuncle . boil , erysipelas, osteomyelitis . trophic ulcer   and other entities. Also, bacteria can enter the lymph node during his wounds. In such a situation is the primary disease lymphadenitis.

Inflammation in the lymph nodes is manifested and develops according to the general type. If progressing purulent lymphadenitis, inflammation can trigger destructive forms of the disease - abstsedirovanie   and necrosis And putrid infection can cause ihoroznym disintegration of the lymph nodes . Simple lymphadenitis   - This form of the disease in which inflammation, as a rule, does not come out within the lymph node. If there is a destructive form of lymphadenitis, the inflammation can spread to the tissues adjacent. Due to changes in the serosal tissue may serous inflammation or purulent inflammation with subsequent formation phlegmonous adenitis . Particularly severe symptoms lymphadenitis ihoroznym manifested in the form of the disease.

In acute non-specific form of the disease manifest the following symptoms of lymphadenitis. Swollen lymph nodes and sore appears periodically appears headache , Weakness, feeling of malaise, can increase the body temperature. Quite often in acute lymphadenitis manifested inflammation of the lymphatic vessels. Signs of acute lymphadenitis depends on the form of the disease and the nature of inflammation. Basically, the general condition of the patient at catarrhal lymphadenitis is not particularly disturbed. As symptoms can manifest pain in the area regional lymph nodes . At the same time there is an increase of lymph nodes, their pain during palpation.

If the disease process progresses and develops periadenit , The described symptoms may get worse. Soreness acquire the sharpness, the skin over the lymph nodes to become giperemirovanoy And node palpation the patient feels pain. Lymph nodes that previously it was possible to very accurately palpate now merge with each other and with the surrounding tissue, moreover, they become immobile.

Inflammatory processes   lymph nodes differ productive. In purulent form they pass on rare occasions. Among the manifestations of chronic nonspecific lymphadenitis are the following symptoms: increased and compacted lymph nodes, tenderness they felt weak, they are not soldered together. In this state, the lymph nodes stay long enough period of time later in the connective tissue grows and they decrease.

At tuberculous lymphadenitis   as a general disease manifests tuberculosis . Lymphadenitis in children may occur at a time of primary tuberculosis. Mycobacterium tuberculosis can cause tuberculosis of peripheral lymph nodes. The infection can be spread in many ways. Thus, it can penetrate through tonsils . Most often, the infection penetrates lymphohematogenous path extending from the affected lymph nodes.

If the disease begins acutely, the patient has been a sharp rise in temperature, symptoms of tuberculosis intoxication , Lymph nodes become more manifest in them inflammatory and necrotic changes . As a special feature of tuberculous lymphadenitis, which distinguishes it from other forms note the presence periadenita. Very rarely appear fistulas . The most common lesions occur on the neck, submandibular and axillary nodes. Chronic lymphadenitis in children sometimes develops in parallel with infectious diseases - sinusitis . tonsillitis . rhinitis . periodontitis . At the beginning of lymphadenitis in children manifests itself tumor   at the locations of the lymph nodes. When pressed on her child can feel pain. A few days later the inflammation goes to the next placed tissue. Lymph node becomes palpable hard, compacted tissue. In the presence of these symptoms should immediately contact the pediatrician.

Diagnosis lymphadenitis

 Lymphadenitis  To put appropriate diagnosis, the doctor is guided by the clinical picture, considering the medical history information. Surface lymphadenitis   ( inguinal . cervical lymphadenitis ), The doctor will determine quite easily. More difficult to diagnose lymphadenitis, which is a complication periadenit And is involved in the inflammatory process of the adipose tissue between the muscles, cellular spaces of the mediastinum and retroperitoneal space.

To install the differential diagnosis, it is important to know where the primary focus of purulent inflammation. It is important to differentiate chronic nonspecific lymphadenitis   with an increase in lymph nodes in other infectious and other diseases. In the process of recognition of the type of chronic lymphadenitis doctor evaluates a range of symptoms. If the diagnosis is difficult, it is necessary to carry out biopsy   lymph node, or remove it for subsequent histological examination. Such study material means a lot in the differential diagnosis of chronic lymphadenitis and detection metastases of malignant tumors .

Diagnosis " specific lymphadenitis "Established by the results of a comprehensive survey of the patient. This takes into account the patient's contact with patients Tuberculosis His reaction to tuberculin , Presence or absence of tuberculous lesions in the lungs and other organs.

It is also possible to establish the correct diagnosis by puncture of the affected lymph node. Using x-ray can determine the formation of the nodes calcifications Which can be seen on x-ray as a dense shadow on the soft tissues of the neck, under the jaw, in the area of ​​the armpits and groin. Important differentiation of tuberculous lymphadenitis with nonspecific purulent lymphadenitis, metastases of malignant tumors, limfagranulematozom .

If you suspect a bubonadenitis should conduct a thorough examination of the rectal area and genitals, determine which is the state of the pelvis and hips. It is important to establish the correct diagnosis, because in some cases, defined as bubonadenitis incarcerated hernia .

Treatment lymphadenitis

 Lymphadenitis  Treatment lymphadenitis acute nonspecific form   is assigned depending on the stage at which it starts. If the presence of only the initial form of the disease, the treatment of lymphadenitis made using conservative methods. Thus, the affected body should remain at rest, as the treatment is applied Ultrahigh frequency therapy Therapy focus of infection (that is, an autopsy abscesses Autopsy purulent streaks ), Shall also be Antibiotic .

When purulent lymphadenitis used operative method of treatment: abscesses burst, the pus is removed from them, held drainage of wounds . All subsequent activities carried out are the same as in the treatment of purulent wounds.

In the treatment of chronic nonspecific lymphadenitis form must first eliminate the underlying disease, which was the source of this form of lymphadenitis. Lymphadenitis specific treatment is carried out depending on the nature of the lymph node, and in the presence of other bodies tuberculous changes. If a process is active, use first-line drugs: tubazid . streptomycin   in conjunction with PAS or Ethionamide . pyrazinamide . protionamid . ethambutol . The treatment process lasts from 8 to 15 months.

Also in the node with the defeat introduced streptomycin , It imposed tubazidovoy bandages, ointment tibonovoy and streptomycin. If purulent process is pronounced, it is used to treat antibiotics   broad spectrum of activity.

Complications lymphadenitis

The disease can cause a number of complications. The patient may manifest thrombophlebitis , Purulent process may spread to the cellular spaces, and the patient may receive the metastatic foci of purulent infection.

Prevention lymphadenitis

To prevent lymphadenitis to avoid injuries and wounds, rationally relates to the treatment of inflammatory diseases. In patients with axillary lymphadenitis may occur sepsis . subpektoralnaya abscess .

Abscess

September 13, 2011

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 Abscess  Abscess - A purulent inflammation of the tissue to form a cavity, which is surrounded by pyogenic membrane. Designated possible occurrence: bones . muscle . subcutaneous tissue As well as other organs.

The cause of the abscess may be a variety of diseases ( retropharyngeal abscess with angina, inflammation of pneumonia, trauma   etc.), are also known cases of independent origin.

The cause of the abscess are germs, infections occur more often through the damaged mucous membranes, skin, and with the introduction of the agent from the other chamber through the lymph and blood vessels. Thus, abscess formation using capsules exhibit protective functions, limiting uninfected tissue from infected areas.

Mixed flora with a predominance of staphylococci and streptococci is the causative agent, and abscesses phlegmons . Also, a significant role in their development play clostridia, Bacteroides and anaerobic. There may be a nonspecific abscess and current disease pathogens, such data were obtained by dissection of some inflammation. This explains the large number of atypical treatment.

Number of pus in the cavity depends on the pathogen, the type of tissue, as well as the overall clinical picture of inflammation, in some cases it can be up to a liter, while the most frequent abscesses with a few milliliters of pus.


Symptoms depend on the type of abscess, but basically it fever   (up to 41 degrees) general malaise . dizziness   and   loss of appetite . leukocytosis . The outcome of the abscess can be varied: the spontaneous breaking through the outside ( abscess, mastitis, an abscess subcutaneous tissue ), A breakthrough in the lumen of which are in communication with the external environment (bronchi, intestine), and a breakthrough in the closed system (the joint cavity, the abdominal cavity), this breakthrough is the most dangerous. Under favorable conditions, empty the cavity is reduced in size and undergoes scarring. Incomplete emptying can lead to chronic, resulting in the possible formation fistula .

There are several types of abscesses :

Scrofulous abscess   frequently observed in certain phases of currents actinomycosis or osteoarticular tuberculosis . It is characterized by accumulation of pus without general and local manifestations of inflammatory reactions that are characteristic of conventional abscess (fever, redness, pain).

NatŃ‘chny abscess   - It is an abscess, which is not accompanied by an acute inflammatory reaction usually occurs in bone and joint tuberculosis.

Subdiaphragmatic abscess   - A collection of pus, usually with a gas below the diaphragm (abdominal wall); is a complication of acute inflammatory diseases ( perforated ulcer of the stomach or duodenum, cholecystitis, appendicitis ).

Abscess care

Early diagnosis followed by treatment is a prerequisite for the successful disposal of purulent inflammation. The diagnosis of an abscess is the reason for the surgery, so in most cases for their treatment using surgical methods. First purulent cavity is opened, then emptied and drained. Getting rid of small abscesses subcutaneous fat is carried out ambulatnyh conditions and a simple operation under local anesthesia.

In case of suspicion of an abscess of an internal organ of the patient is usually admitted to the operating room. When abscesses produced some of puncture and aspiration of pus and antibiotics.

After opening of abscesses are treated in the same manner as sores. When antibiotics are taken into account sensitivity to them microflora. In the case where the suppurative inflammation occurs on a background Diabetes Necessary normalization of metabolism. Treatment of abscesses in most cases occurs successfully, without need for further surgery.

Intercostal neuralgia

December 4th, 2011

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 Intercostal neuralgia  Intercostal neuralgia - It is a manifestation of pain along the intercostal nerve. This condition occurs due to irritation or compression of the intercostal nerves. As a rule, the disease affects people in middle age, more often - the elderly, but children are not diagnosed with the disease almost.

Reasons intercostal neuralgia

This disease is a pain that has reflex origin. Typically, painful attacks of the disease occur in people who suffer from running osteochondrosis   by displacement due to the intercostal nerve roots intervertebral hernia . However, the causes of intercostal neuralgia symptoms are often other diseases - spondylitis . ankylosing spondylitis . Hormone spondylopathy Appearance neoplasms   in the spine, progressive kyphosis . Also neuralgia attacks often overwhelmed after colds . strong supercooling . Infectious Diseases . poisoning . stresses . injuries . Intercostal neuralgia can trigger very strong physical exertion, unusual for a person or made without proper preheat. Very often, a diagnosis "intercostal neuralgia" the expert concludes that the cause of this condition were herpetic lesions.


Also, the disease appears due to the pre-stimulation of the nerve trunks that have occurred as a result of pathological processes in organs and tissues, which are located nearby. Thus, intercostal neuralgia can trigger spinal surgery . pleurisy . d Reformation chest . tumor . aneurysm   thoracic aorta As well as other diseases. Sometimes neuralgia   It manifested as a result of changes in the spine, which develop due to hormonal imbalance in the period Menopause   women. Provoke the development of disease and the regular abuse of alcohol, diabetes Problems with the exchange of B vitamins latter phenomenon often occurs as a result of gastritis . colitis . hepatitis . peptic ulcer As stomach and duodenum, when nervous tissue deteriorates metabolism. Basically intercostal neuralgia progresses due to the influence of several factors at once.

The symptoms of intercostal neuralgia

The main symptom of this condition are pain in the intercostal spaces. Pain can manifest episodic. Basically it becomes stronger during the movement of the chest, when a person takes a deep breath, coughs, sneezes, speaks too loudly. The patient may be in antalgic posture when the body involuntarily bends in a healthy way. This state of a person suffering from the pain, trying to preserve. Basically localization of pain occurs in the fifth to the ninth rib. Also, the symptoms of intercostal neuralgia manifest feelings of pain in the shoulder blade area, or in his hand. During the palpation easily detected in terms of the pain. Such points are paravertebrally at the spine, as well as through the armpits - and the middle nerve at the edge of the sternum. In the process of pressing or feeling the pain becomes stronger.

Often the pain is accompanied by numbness . pricking . burning sensation . Features of intercostal neuralgia is such that pain can give under the shoulder blade, and even to the heart. Thus, a person suffering from this disease, there are suggestions of a heart attack when in fact there are symptoms of intercostal neuralgia. It is very important manifestation of pain under the left shoulder blade quickly make a cardiogram and a consultation with a specialist.

But in fact, the intercostal nerves have a lot of branches. To manually determine the nature of this pain, should take into account the differences: if the pain of intercostal neuralgia is constant, then at attacks angina   throbbing pain, increased sharply subsides. With heart pain has also been a violation heart rate, low or high blood pressure. At the same time, patients intercostal neuralgia and heart rate and blood pressure are in a normal state. Also neuralgia pain often gives in the back, giving the impression of symptoms of renal colic. In any case, the sudden onset of chest pain should immediately contact a qualified technician, who will be able to establish the correct diagnosis.

Treatment of intercostal neuralgia

 Intercostal neuralgia  It is important to begin treatment intercostal neuralgia when there were only the first signs of the disease. The main task that puts a specialist before starting treatment, it is relief and pain reduction. After achieving this goal are applied to drugs that may enhance trophic processes in affected tissues. If there is a primary lesion, you should pay attention to the use of reflex therapy. So, a good result gives acupuncture . Vacuum Therapy . pharmacopuncture . If the expert considers it appropriate to include in the total treatment therapy medical drugs, then the agent with anti-inflammatory effects, as well as vitamins of group "B".

During acute illness should apply strict bed rest for at least a few days. It is important that a patient lying on a firm and level the plane, which should be under the bed mattress to put a durable shield. The chest in the days of attacks is recommended to wrap a woolen scarf, and in the area near the spine can put mustard. Recommended massage and rubbing with analgesic ointments with anti-inflammatory effects. The patient should be remembered that the constant use of analgesics their effect after some time becomes ineffective. Therefore, before taking any pain medication, be sure to consult your doctor.

There are also many ways to facilitate people's status in the intercostal neuralgia. Thus, applied to the sore spot warm flax seeds in the bag fabric, lubricate sore spots horseradish and radish juice and apply it to the herb wormwood. It is also practiced by a special acupressure. If the patient is secondary to the disease, the treatment of intercostal neuralgia is carried out using symptomatic methods. It is important to clearly limit the physical activity during treatment with intercostal neuralgia, but sometimes patients received physiotherapy.

Prevention intercostal neuralgia

The most important point in the prevention of this disease is considered to avoid colds and severe hypothermia. If a person is diagnosed with inflammatory diseases of which are located near the intercostal spaces, you should immediately apply the appropriate therapy. For the treatment and prevention of intercostal neuralgia actively used the following methods. Effective are several courses of acupuncture, manual therapy Aimed at restoring the correct position of the spine, but it was his cervical and thoracic. Also used a special massage using ointments or creams with warming effect. It helps to relax muscles and reduce pain.

Friday, June 29, 2018

Dysplasia

April 22, 2012

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 Dysplasia  Dysplasia - A common name for a condition in which a person takes the wrong development of body parts, tissues, organs. When dysplasia in humans incorrectly formed some organs or tissues during fetal development, as well as after birth. For dysplasia is a characteristic change in shape, size, structure, cells, organs, tissues. As a rule, dysplasia is a congenital, but sometimes the disease occurs after birth and into adulthood. This term is taken to apply to various diseases, which becomes the basis for the anomaly of a cell, tissue or organ.

Cervical dysplasia

Cervical dysplasia   a precancerous condition: women with this diagnosis occurs many times the probability of cervical cancer . However, cervical dysplasia is not yet evidence of an absolute probability of such an outcome. In the development of cervical dysplasia occur in women hyperplasia   (ie, thickening) proliferation   (ie sprawl), and there is disruption of differentiation, maturation and aging and the subsequent rejection of the epithelial cells. Depending on how pronounced these pathological disorders, we can talk about three different degrees of cervical dysplasia: light . moderate   and heavy . To determine the current degree of the disease, it is taken into consideration the depth of penetration of the pathology.


 Dysplasia  Today, there are studies showing that the pathological processes of the cervix occur in every fourth woman.

Cervical dysplasia develops symptoms due to some reasons. This can be exogenous factors (I.e. derived from the external environment): herpes A number of diseases that are sexually transmitted infection human papilloma viruses . That human papillomaviruses play a leading role in the issue of provocation of cervical dysplasia.

As endogenous factors   (ie coming from the internal environment) determine the hormonal imbalance, reduced immunity . In addition, the development of dysplasia and provoke confounding factors.

To carry out a full diagnosis, it is necessary to apply a number of studies, appropriate in each individual case. In the process of diagnosis used colposcopy . This study involves a survey of cervical patient on the gynecological chair by a special device. During this inspection, the image is increased 10-30 times. During the colposcopy, a woman does not feel pain.

To obtain more accurate data used in the diagnosis extended colposcopy, in which the doctor examines the epithelium, as well as diagnostic tests applied. Holding control colposcopy accurately take tests to determine pockets of cervical dysplasia. Do not feel sick any discomfort and pap smears for Cytology . To do this with the help of special brushes are derived epithelial cells from the cervical canal and the surface of the cervix. Also, epithelial cells taken from an outbreak of dysplasia.

If the patient was detected cervical dysplasia, and there is a pattern of pathological cytology specialist assigns conduct Biopsy   cervix. Typically, this procedure is performed using a local anesthesia . During the colposcopy biopsy under the control of the altered tissue is removed from the source of the disease. After that the histological examination of the sample. This method of diagnosis accurately determine the appropriate approach to the treatment of the disease.

If cervical dysplasia was found in the cervical canal, sometimes carried out endocervical curettage and analysis of tissue that has been removed.

Treatment of cervical dysplasia

 Dysplasia  Method of treatment of cervical dysplasia, having a high effect is considered to be the destruction of the hearth dysplasia, laser photocoagulation, radio wave coagulation, cauterization by liquid nitrogen. If necessary, use one of these methods combined with antiviral treatment or therapy of diseases that are transmitted through sexual contact.

It is important for the treatment of cervical dysplasia women who did not give birth, conducted the most gentle methods. After the process of cauterization of the cervix may appear tripe Which subsequently can affect the course of delivery. Scar neck revealed a lot worse, so often in such a situation, recourse to   caesarean section .

Today is actively used for the treatment of cervical dysplasia fundamentally new techniques. Progressive methods considered argon-ablation   cervix. This method involves the action of the plasma, which generates an ionized argon. This tool does not touch the tissue, and the penetration depth is precisely controlled. A similar technique is used to treat both parous and nulliparous women.

As methods for preventing cervical dysplasia and recurrence of the disease is important to ensure adequate nutrition, which includes foods high in selenium, vitamin A , B vitamins and other trace elements and vitamins. Women are advised to give up smoking completely, mandatory use barrier contraception during casual sexual contacts, and at least once a year to visit the gynecologist.

Hip dysplasia

The disease is currently diagnosed frequently. It is characterized by incorrect placement of elements of the hip joint. All tissues of the hip joint are underdeveloped, resulting in pathology such acetabulum, the femoral head and the surrounding ligaments and muscles located correctly. In young children hip dysplasia   called congenital predvyvih . subluxation . dislocation . immature hip joint .

The cause of this disease is considered to delay the development of the hip joint during the prenatal period as a consequence of a bad heredity, infections in the mother, her older toxemia , Breech presentation, and a number of other factors.

 Dysplasia  In this case, extremely important as early as possible to diagnose the problem, because a newborn baby continues to be formed joint. Therefore, the use of the correct approach to the treatment after the timely diagnosis allows to restore the correct ratio in the hip before the age of three children. At the same time, in the absence of treatment the patient's condition worsens child each month.

Congenital dislocation of the hip diagnosed even in the maternity hospital. Then he re-examines the orthopedic baby in the first weeks of life and in the age of three months. The most common hip dysplasia detected due to the presence of some characteristic symptoms.

In a sick child from the defeat of a limitation of passive hip abduction in varying degrees depending on the particular pathology. With time limit diversion becomes more pronounced.

Also, your child has a so-called symptom "click" : During the abduction reduce a dislocated leg and arm at the same time feel a click. If the baby legs lead to the middle line, the dislocation of the femoral head occurs again, and again hear a click. This symptom generally disappears within a week after the birth of the baby, but sometimes with muscle hypotonia it lasts longer.

A child with dysplasia asymmetrical folds of skin on the thighs. On the side, where a dysplasia, there is more of the folds. They are located deeper and higher.

When the baby sleeps, his leg is set to external rotation, that is, there is a rotation of the foot. Lower limb dysplasia can be shortened. Such symptoms may also appear in combination, or separately. It is important to contact a podiatrist at the slightest suspicion.

Early diagnosis of the disease can be carried out through the use of ultrasound. This method does not harm the child and allows you to monitor its status over time.

At the time of diagnosis of hip dysplasia in newborns is actively used radiological methods. X-ray is performed for children who have turned three months. X-ray shows the degree of dislocation that allows you to assign the correct therapy.

If hip dysplasia is assigned a complex treatment that involves the use of multiple therapies. First of all, the treatment position requires broad and imposing swaddling baby buses . Carrying out of therapeutic massage Which comprises from ten to fifteen sessions, while necessary to repeat the course of about a month. Also good effect physiotherapy, which is carried out several times a day, doing all the exercise ten times. The method of treatment of the disease is selected depending on the severity of disease and the age of the sick child. Ideally, treatment of hip dysplasia should start even in the maternity hospital.

To cure a congenital predvyvih practiced the use of special diverting tires Vilna. To be in the bus the child must continuously for four months. There are many other buses, which are also often used in the treatment process on doctor.

If the child's treatment was started early, it can be put on the legs at the age of 8-11 months. Yet conservative method of treatment does not always give the desired result. Sometimes the child is shown holding a surgery. A similar operation is carried out when the child is a year, and it is applied at the irreducible dislocation, reduction in complications of early dislocations.

When the child grows up, it is recommended to ride a bicycle, legs wide apart, doing gymnastics in warm water, to swim, to carry out regular exercises therapeutic exercises.

Connective tissue dysplasia

 Dysplasia  Connective tissue dysplasia   develops in children, both in utero and after birth. Thus the development of connective tissue is broken. The tissue cells comprise fibers and extracellular matrix. It is widespread in humans and equipped in the skin, bone, cartilage, vascular wall and in the blood. The most important role in the structure of the fiber fabrics play. It collagen Which is responsible for maintaining the shape and elastin Who is responsible for the ability to relax and reduce.

Connective tissue dysplasia is a genetically determined disease, because the basis for the development of the disease is mutation of genes that are responsible for the synthesis of fibers. These mutations occur in different genes, and as a result holds malformation chains of collagen and elastin. Those structures were formed under their influence, they can not withstand strong mechanical loads.

Connective tissue disease hereditary nature are usually subdivided into differentiated   and undifferentiated .

As a rule, people with connective tissue dysplasia, tall, thin and stooped, they are the scapula and clavicle. However, patients may have a small stature and very fragile body composition.

Connective tissue dysplasia appears very diverse symptoms while patients tend to have a lot of different complaints. Accordingly, the diagnosis is not always easy.

However, in most cases, people are turning to specialists with complaints of cardiac nature. They also present vegetative symptoms : Can manifest hypotension . feeling of general weakness . headache   etc. Moreover, in patients with connective tissue dysplasia often occur various dyspeptic symptoms . constipation . flatulence , Abdominal pain uncertain.

Also, patients with this disease may develop respiratory problems - namely, repetitive bronchitis . pneumonia That causes congenital weakness of the walls of the alveoli and bronchi. In addition, a history of such patients tend to appear Hernia . flatfoot . weakness . hypomyotonia . kyphoscoliosis . poor appetite . Doctors are the following warning signs that a person has developed connective tissue dysplasia too low body weight, the presence of chest deformation, the presence of various pathologies of the spine (this can be scoliosis . hyperkyphosis . hyperlordosis ). In addition, evidence of this illness dolichostenomelia (too long limbs, hands and feet, which generally makes the body asymmetrical), hypermobility of joints, deformed limbs, skin, through which lurks vascular grid, the ears are very soft.

To properly diagnose, requires a very thorough examination of the patient and further study. For the examination of the patient he carried ultrasound and analysis dysbiosis . In the process of examination of the patient is also necessary to check the status of view, the presence of ENT pathologies.

People with connective tissue dysplasia is very important to take seriously the issue of family planning, because this pathology parents with children are born with the same disease. Parents must realize that the most difficult task is to fight the already established dysplasia, so the treatment of dysplasia of the baby have to deal with immediately after diagnosis. With early treatment may prevent its progression.

In the treatment of connective tissue dysplasia integrated approach, which uses both non-drug and medication therapies.

For the treatment of necessary medication used drugs that stimulate the production of collagen in the body. In this case, the treatment is applied ascorbic acid . drugs mucopolysaccharide nature , Reception B vitamins   and trace elements ( zinc . copper . magnesium ).

As a non-drug therapy is used the correction mode of the day, psychological support, massage, physiotherapy, acupuncture , Physical therapy exercises. People who suffer from connective tissue dysplasia, can not play sports, implying severe stress. So in this case it is a therapeutic exercise. It is also important to adjust the power of the patient, so that he gets enough proteins . amino acids   and microelements .

It is important to take into account that the positive effect of the treatment is possible only in case of an early diagnosis and a comprehensive approach to therapy.

Rickets in children and adults

March 9, 2013

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 Rickets in children and adults  Rickets   - A disease that mainly develops in a person's childhood and infancy. This disease is known to mankind for a long time. Thus, the mention of this illness have been found in the manuscripts of the ancient physicians. The first clear symptoms of rickets were described in the seventeenth century in England. By the way, British doctors call this disease " misty disease ", As rickets is most often seen in children of working people who constantly live in the smog, it arises from the smoking factories. Yet the real cause of the disease has been identified only 1980s .

The term " rickets "Comes from the Greek word" spine ". The disease is relatively common among children. When rickets broken bone formation. This is due to the deficiency in the body calcium-phosphorus metabolism . Signs of rickets in children are found in all countries of the world. However, most developing rickets in infants in the Nordic countries, where very little sunlight. Some modern scholars argue that rickets varying severity sick more than half of the children. In most cases the disease is diagnosed in infants who were born in the fall and winter.

In countries with well-developed medicine, being clear prevention of this disease, and children receive adequate treatment as soon as the first signs of rickets. However, after a radiographic examination in children may reveal the hidden signs of rickets, which is difficult to notice during the inspection or on the photo.


If a person suffered rickets in infancy, the consequences of the disease remain for life. Rickets had been ill person remains   incorrect posture . flatfoot Present deformation of the pelvic bones . myopia . Also in adulthood develop dental disease, in particular, caries . But if a person has a child there was only mild rickets, that such effects are not observed.

Causes of rickets

 Rickets in children and adults  It means a lot in the formation of bone tissue Vitamin D Since without it the body can not absorb calcium. Accordingly, the mineral, which is the main material for the structure of the bone tissue does not enter the bone. Consequently, a lack of vitamin D in the body is considered the main cause of rickets. But recently, it has become possible to determine the concentration of vitamin D metabolites in the blood. As a consequence, it was found that vitamin D deficiency is just one of the causes of rickets. Today experts say that the main reason is the lack of rickets Phosphates   and calcium While priority is hypophosphatemia .

In infants and children at an early age is determined by a number of reasons for which the body can be observed a lack of calcium and phosphate. First of all, the birth of a baby is premature, as the phosphorus and calcium most active is delivered to the child is in the last trimester pregnancy .

After the birth of a lack of calcium and phosphorus in the body can occur due to improper feeding baby. Due to the fact that rickets considered a disease organism that grows higher need for minerals is, when there is a period of intense growth of the child.

The reason for shortage of these minerals are also sometimes becomes a violation of their transport in the kidney, liver, gastrointestinal tract, bones. This is due to either of these diseases because of the immaturity of enzyme systems. In addition, the cause of rickets could be a bad environmental situation, disruptions to the endocrine system and the genetic predisposition to the disease. Rickets smuglokozhih often ill children, those with blood group II (A), rickets diagnosed in boys more often than girls.

Symptoms of rickets

Symptoms of rickets first become noticeable in children aged two to three months. If the parents are closely watching the baby, they can disturb the fact that the child began to show anxiety, afraid of bright lights and loud noises. Rickets in infants manifest sleep disturbance: a baby is sleeping very anxious and restless. There is a constant sweating: the child's head is sweating face. This pot has a distinct sour smell. Rickets in children under one year is shown by the fact that at the head of the child gradually appears bald, because baby constantly rubbing against the neck pillow. This is an important feature, which can be determined by inspection and even a photo.

In the development of the disease symptoms of rickets in infants become more varied and severe. The kid is poor appetite, muscle tone decreases. The edges of a large fontanelle, which remains open in newborns, become soft. On the edges of infants suffering from rickets, observed thickening. Parents important not to miss this period and to consult with your doctor about how to treat rickets. Typically, an expert assigns the necessary preparations. Otherwise, a six-month age the disease progresses to a more serious degree. Then it is already marked neuromuscular disorders show signs of delays in physical and mental development. The bones of the skull in a sick child are softened and flattened back of the head.

Sometimes the bone grows in the forehead and crown appear bumps and wrists and ribs appear noticeable thickening. Severe cases of rickets in infants expresses the change in the chest: it is deformed and pressed or bulges. There is bending the legs, narrow pelvis.

Rickets in adults as in children has multiple periods. It is also determined by three degrees of severity of rickets - hidden . the average degree . severe degree . By the nature of the disease stands sharp . subacute   and palindromic   rickets.

Diagnosis of rickets

 Rickets in children and adults  To diagnose rickets expert can after detailed examination with a clinical picture of the disease. Furthermore, blood tests to determine the levels of calcium, phosphorus, and alkaline phosphatase activity. If the activity is increased, then this is the earliest sign of the disease. Moreover, it can be detected before symptoms manifest visible disease. Also sometimes it appointed a urine test to determine the concentration of calcium in it. The study also assigned to conduct X-ray examination of bones of the child.

Treatment of rickets

To effectively cure the disease, action should be taken immediately after diagnosis. The most important point is the saturation of the body of a sick child or adult fluorine . calcium   and Vitamin D . Since the treatment of rickets in children, parents should be aware that one of the important points of therapy is to stay regular kid on the street, when the sun is high. Note, however, that if there are signs of rickets in a child who is not yet one year old, in the summer this kid can not be exposed to direct sunlight. Artificial ultraviolet irradiation is also contraindicated. But the child after a year, you can occasionally take a sun bath, but only a limited amount of time. During the summer, to get a sufficient dose of vitamin child enough to walk on the street about 20 minutes to dress with short sleeves. But in the autumn and winter babies can be taken out into the street for an indefinite period.

Parents who note signs of rickets in children, should be taken very carefully to the organization of the diet. Foods rich in the vitamin D, is cod liver, halibut. Calcium is contained in a variety of dairy products, green vegetables.

Every day, the child should receive Vitamin D   dose 400 IU . Without sufficient amounts of this vitamin, calcium is not absorbed in the intestine. Therefore, treatment and prevention of rickets provides its reception. In the treatment of the disease, experts recommend taking preparations containing Vitamin D3 , so how vitamin D2   digested worse. The aqueous solution of vitamin D3 - is a medical drug " Akvadetrim ". It is given to children who have attained 3-4 weeks. Take the drug 1-2 drops per day. However, finding the symptoms of rickets in children whose parents do not have to make a decision about taking the drug with vitamin D, since an overdose can have negative consequences for the organism. To determine how to treat rickets, in each case it can only be a specialist after diagnosis and examination of the child. Neither the stories of parents or photo to pinpoint features of the disease is impossible.

An important part of treatment is a non-specific treatment. First of all, breast feeding the baby, the correct mode of the day, a massage, gymnastics, hardening, etc. If the treatment of rickets started on time and at the same time carried out correctly, the symptoms gradually disappear, and the consequences of the disease do not manifest themselves later.

Prevention of rickets

 Rickets in children and adults  The fact that the baby can get sick rickets, the expectant mother should think about it during pregnancy. Therefore, prevention of rickets begins during fetal development. A pregnant woman should have a balanced diet. Every day you need to eat vegetables, meat, dairy products. For a pregnant woman is important the correct mode of the day, gymnastics, treatment toxemia Anemia. Throughout the period of gestation of the child must take vitamin complexes, which picks up a doctor. Expectant mother should do everything to ensure that the fetus develops harmoniously.

Young mother must continue to take vitamins, but choose them only after consulting your doctor. It is important that, at least up to six months old child received breast milk, as trace elements that it contains, are well absorbed. Breastfeeding fully satisfies the need of the child in trace elements and vitamins. Sometimes, if necessary, the pediatrician may prescribe reception Multivitamins   directly to the kid.

When it comes to foods, as the introduction of new products periodically to give the child meals with foods that contain large amounts of vitamin D. This eggs . fish . butter . greens . From about 7 months, the child can be given cheese, meat. A month later, it can be gradually introduced into the diet of fish. It is particularly important to ensure a sufficient amount of vitamin D and trace children who reside on the artificial and mixed feeding. We should pay careful attention to the selection of compounds for feeding. It is important that they contained a delivery and a balanced amount of calcium, phosphorus and vitamin D. With the right approach to the prevention of the disease can be avoided.

Dysbacteriosis children

May 4, 2012

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 Dysbacteriosis children  Dysbacteriosis kishechnika- is a condition in which a child is a violation of the ratio of Representatives gut Which should be observable in a normal state. If guided by the criteria of the World Health Organization, the goiter do not carry disease. For example, many scientists believe that dysbiosis - a consequence of the presence in humans of other pathologies. However, goiter in children yavletsya a serious problem and a threat to health.

For the normal functioning of the body as a whole it is very important the role of the human intestinal microflora. It is responsible for the normal microflora in the intestines of gas exchange, synthesize vitamins, stimulates cell regeneration of the intestinal mucosa, cleanses the body of harmful toxins   etc.

The kid is born, with a sterile intestine, and the microorganisms colonize it immediately after birth. In the first hours and days of the life of the body and adapted microflora, thus there is a formation of the body of the ecosystem, which becomes unsuitable for colonization with new microorganisms. Children who are fed breast milk and artificial, in every case, there are particular microflora. If the child remains in full-fed breast milk, then he has more in the intestine bifidobacteria Which actively proliferate under the action of substance present in breast milk.

Stages of dysbiosis in children

Dysbacteriosis children manifested by changing the number and composition of microorganisms in the intestine, at which drastically reduced the amount of beneficial bacteria, thus increasing the number of harmful microorganisms.


The symptoms of dysbiosis manifest more or less depending on what stage of the disorder occurs in a child. The first stage of dysbiosis in infants can be determined only after an analysis of feces child. This pronounced signs of dysbiosis of the child at this stage do not appear. But the results of microbiological studies of feces indicate that the number of bifidobacteria decreased. There may also be a reduced number of lactobacilli   and normal coli bacteria .

In the second stage symptoms manifest constant dysbiosis constipation . This occurs due to the increase in the infant gut of opportunistic pathogens, which include Candida . Proteus   and others. At the same time continuing to cut the beneficial bacteria.

Typically, if the baby is healthy, aged 0 to 6 months of its stool frequency equals the number of feeding and up to seven times a day. If the child suffers constipation, the frequency of his chair, usually decreases, but even this does not always happen.

 Dysbacteriosis children  The signs of dysbiosis have a baby is often denser stool consistency, reducing the number of feces, difficult process of bowel movement. In this case, the child may cry, make an effort, be a strong concern. He may occasionally occur as small abdominal distention . However, these signs may be evidence of other ailments, so the child necessarily need to show the doctor. In the second stage of dysbiosis may also occur at times unstable chair. For this phenomenon is characterized by periodic diarrhea, has an unpleasant smell and some admixture of green. In the third stage of dysbiosis in children, which is called decompensation , Increasing the quantity and variety of pathogenic bacteria in the gut of the baby. This stage is characterized particularly severe symptoms of dysbiosis. Sick child turns pale, he was constantly lethargic, has a poor appetite and thus lose weight. Disbkterioz in infants less than one year of age, can occur atopic dermatitis   ( diathesis ). At the third stage of the disease and unhealthy baby chair: odorous, liquid consistency, it may contain particles of food that is not digested. Similar phenomena - the result of failure enzymes Which manifests itself at this stage. If the child has signs of dysbiosis manifested described, then he may need treatment in a hospital, because such a state shortfall threatens the infant needed nutrients.

The fourth step becomes a manifestation of dysbiosis acute intestinal infections Which require immediate hospitalization or intensive care unit.

Causes of dysbiosis in children

Dysbacteriosis in children occurs due to several different reasons. It can provoke the development of applications antibiotics Too late newborn attachment to the mother's breast, early weaning and transfer to artificial mixture. Furthermore, dysbacteriosis may develop as a result of acute and chronic diseases of the gastrointestinal tract, exposure to environmental factors (pesticides, industrial toxins, radiation, heavy metals), treatment   radiation therapy   and immunosuppressants . Negative impact on the child in this case, and frequent stresses , Regular expression cold, passive smoking, unhealthy diet.

The symptoms of dysbiosis in children

 Dysbacteriosis children  Dysbacteriosis infants manifested frequent regurgitation, recurrent vomiting, the presence of bad breath, sleep disorders. In addition, symptoms of dysbiosis is often a decrease in the rate of increase of weight, constant anxiety nursing infant. The character of stool dysbacteriosis is different, but always unhealthy: it can be a liquid or pasty, frothy, sometimes it contains lumps of white, greenish impurity. The smell of feces putrid or sour.

The child suffers from pain that has the character attacks. It usually appears within a few hours after eating, with distended abdomen, it heard rumbling, you may experience the urge to defecate.

If the child is disturbed intestinal absorption, in this case, the symptoms of dysbiosis manifested diarrhea putrid fermentation, flatulence . Reduced weight baby, symptoms of polyhypovitaminosis . As a result, the child may develop toxic-degenerative condition. Gradually, in the pathological process is activated pancreas and hepatobiliary system. As a result, in the body there is a lack of enzymes and bile acids. Violated the metabolic processes in the body is an accumulation of macromolecules is not fully digested food, provokes the development of allergic .

Dysbacteriosis have older children provokes persistent constipation , The occurrence of intestinal colic . unstable chair . dyskinesia   intestines. The child sometimes complains of constant belching, feeling of fullness in the stomach strong. The appetite gradually decreases. If intestinal dysbiosis is continuing a long period, the child is suffering from total intoxication   and body asthenoneurotic syndrome . However, the variant of the disease, when clinical symptoms of disorders of intestinal microflora can not be detected.

The hardest hit among children occurs common disbakterio s In which pathogenic microorganisms from the intestines fall into other organs. This could trigger the development of inflammatory processes in the different organs of the body. But even if for dysbiosis passes without visible signs, yet your child has a low appetite and thus less weight than that of its peers. The child is often sick other ailments. In this case, we are talking about dormant during dysbiosis.

Diagnosis of dysbiosis in children

To determine whether a child dysbiosis, applied microbiological examination of stool (the so-called bacterial culture). The analysis on a dysbacteriosis held for about one week after for its full implementation requires that the colonies of fecal microorganisms grown in a special medium. When the colonies grow, the specialist can determine the ratio of their quantity and quality. It is important that the collected feces was taken for analysis on a dysbacteriosis not later than three hours after collection. This method allows to determine only the content of microorganisms in the final part of the colon, although food is digested predominantly in the small intestine. Therefore, it should be noted that the microorganisms that are in feces, and microorganisms from the intestines are not identical.

In addition, the results of which allows you to get analysis on dysbiosis will not be stable. After all, each laboratory can be estimated only about a dozen species of bacteria in the gut and may be about a hundred of their species.

Treatment of dysbiosis in children

 Dysbacteriosis children  First of all, the treatment of dysbiosis in children involves the creation of the necessary conditions of life for the child. It is proved that dysbiosis often affects children who are in conditions of constant stress and overstrain , Rarely in the open center.

It is equally important to correct the child's eating habits. It is the quality of its supply depends is whether to develop the normal microflora in the gut. If we are talking about a baby, thanks breastfeeds, which contains lactose In the intestine formed a sufficient number of bifidobacteria. They are processed lactose, and eventually produce lactic acid, lowers the pH of the intestine. Therefore, children who are breast-fed, ill dysbiosis less. At the same time the children are fed artificial mixtures multiplication of bifidobacteria either not occur at all, or they are in the intestine only in small quantities. Therefore, if you can not feed the child breast-feeding should select special infant formula, which include vitamins . probiotics . minerals . Supplements . enzymes . It is important that the choice of the mixture for feeding baby endorsed pediatrician. This is especially important if your child is sick or in the use of certain mixtures of manifest health problems.

If it is an older child, it is necessary to take care of the diet, which will include all the vitamins necessary for the growth and harmonious development of the child.

Dining at dysbacteriosis should not include those products that provoke the development of pathogenic microflora in the intestines. It is the product of high-grade flour, sweets, fats   animal preserves, ice cream.

Correction Power can achieve good results in the initial stages of the process of correction of dysbiosis.

To overcome the more serious forms of dysbiosis, applied substitution therapy. In this case, we are talking about the treatment of dysbiosis by administering to the patient a child missing component to it.

When dysbacteriosis used those drugs that contain live bacteria that restore normal levels of microflora - the so-called probiotics. These drugs are not a cure, but rather a functional food. Today, there are a lot of different foods, which contain culture bifidobacteria and lactobacilli. There are also preparations of bacteria ( Linex . Subtitle . bifidoform . laktobakterin   et al.), which help to restore normal intestinal microflora. These preparations contain live bacteria resistant to antibiotics. Therefore, goiter, provoked by antibiotics, such treatment is appropriate.

The duration of treatment with these drugs by a doctor. Generally, administration of drugs may last a few weeks or several months. If the treatment of dysbiosis started on time and carried out correctly, the result is possible to prevent the occurrence of a number of diseases of the digestive tract, and diseases that occur due to malnutrition. Most important to the proper treatment of dysbiosis in young children, because this condition can adversely affect the child's development in general.

It is important that the treatment of dysbiosis doctor practicing individual approach, paying attention to all the features of the child's body.

There are some treatments dysbiosis folk remedies that are sometimes recommended to be used in parallel with conventional treatment. So, at a dysbacteriosis in older children it is recommended to drink a third cup three times a day infusion of herbs yarrow, sage, St. John's wort, chamomile. You can also use the infusion of the roots of dandelion and burdock. Children are encouraged to use a decoction of crushed fennel seeds and fennel. Reproduction of artichoke stimulates beneficial bacteria - it can be given to children in small portions.

Prevention of dysbiosis in children

 Dysbacteriosis children  Even during pregnancy   the woman should take care of the future baby's intestinal health and take as little medication as possible, avoiding antibiotic treatment. It is also proper nutrition of the pregnant woman: it is strongly recommended to use fruit, berries and juices. The food that is difficult to digest, from the diet is better to exclude.

To prevent the occurrence of disbkterioza children practiced early attachment of the child to the mother's breast. This is important for an hour after delivery. An equally important measure of prevention of dysbiosis is also prolonged feeding with breast milk (for up to one and a half years).

In the future, parents need to teach a child to a healthy life. Kid important to a lot of walking in the fresh air, do exercises, water procedures. The gradual hardening will help improve the body's defenses, which is the main measure of prevention of dysbiosis.

To prevent problems with the intestines, you should pay special attention to the right approach to feeding the baby. Every day its menu must be available vegetables, fruits, cereals, porridge. Vegetable oils are also useful product. When it comes to nutrition at dysbacteriosis, in this case it will be useful stew of vegetables, berry jelly, broth hips.

Dining at dysbacteriosis must necessarily include milk products, which significantly stimulate the bowels. Cottage cheese, yogurt, yogurt should be included in the diet of the child, which is already one year old. Until that time should not rush with the introduction of similar products. After all, the most appropriate food for infants at a dysbacteriosis - a mother's milk, with the impossibility of breastfeeding substitutes artificial milk mixture.

Enuresis

March 18, 2012

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 Enuresis  Enuresis   - A condition in which children older than five years, night or day comes involuntary urination . Enuresis in children spread widely enough, this disease is very often turn to experts. What signs of enuresis clearly expressed, and diagnosis is easy, sometimes gives the impression that the disease can be quickly and easily cured. But in fact such a violation requires an individual approach to treatment, because in each case the disease can trigger other reasons. Therefore, parents and children should be aware that the treatment of enuresis continues sufficiently long period, and for its successful completion requires a lot of effort and patience from all family members. Attempts unsystematic treatment are often unsuccessful.

Types of enuresis

To date, to distinguish between enuresis primary   and secondary , and daily   and night . Primary enuresis   - A condition in which a child born there urinary incontinence . Consequently, if such symptoms occur only during the day, we are talking about the daily primary enuresis. If bedwetting should talk about the night primary enuresis. These states can be combined.

Secondary enuresis   It is diagnosed when a child in a certain period, which shall not be less than six months, was "dry", after which he again began to suffer from urinary incontinence. As in the first case of secondary enuresis in boys and girls is day, night or two of these forms are combined.


At daytime enuresis   become a cause of urinary disturbances in the functioning of the bladder muscles. If these muscles are extremely excited, then the child is determined giperreflektorny   or neurogenic urinary bladder . If the excitation of the muscles is insufficient, then we are talking about giporeflektornom bladder .

At nocturnal enuresis   urinary incontinence during the night is due to delay ripening of certain brain centers that are responsible for control of bladder function. To date, more common among children it is nocturnal enuresis. In the case of primary nocturnal enuresis often occurs spontaneously self-treatment.

Features enuresis

This disease has described Avicenna   in his work " The Canon of Medicine ". Today the disease is quite common: according to statistics, about 15-20% of children under the age of five, about 10% in seven years, a decade of 5% of children and 3% of twelve can not supervise the work of the bladder. Besides enuresis occurs in adults: by different data, the disease suffers from 1% to 3% of adults. Enuresis in boys occurs in about two times more often than girls.

If a child is developing normally, then he gradually acquires the ability to control their bladder, and in 2-3 years, children learn to consciously control urination. However, many children this process may be delayed, which is considered a normal variant. Therefore, parents may not sound the alarm before the child's fifth birthday. However, if the sixth year of the life of a child can not control this process, in this case, you have to visit a doctor.

Causes of enuresis

 Enuresis  All of the above types of enuresis in children is caused by the different reasons. The most important factor which affects the appearance and fluorescent secondary enuresis considered emotional stress . At the same time the manifestation of primary nocturnal enuresis, usually occurs due to delay ripening centers of the brain or shortage vasopressin .

Also note that the common factor in the emergence of all kinds of enuresis, is a genetic factor. About seventy percent of patients with this disease have relatives who also suffered from enuresis.

Daytime enuresis and secondary nocturnal enuresis in boys and girls seen as a consequence of specific deregulation of the nervous system. The disease develops under the influence of emotional stress: initially child imbalance in the nervous system, because of which there is a disorder of bladder functioning. There are many things that can be a source for the child severe stress: it is the death of loved ones, and parents' divorce, and the appearance in the family another baby.

Another cause of daytime enuresis experts believe the wrong approach to a child accustomed to the pot. In some cases, this process begins in the family too early may parents show excessive severity or inconsistent approach to the issue.

In addition, the causes of these types of enuresis may be the child's behavioral problems, as well as a small bladder capacity (inherent problem).

Primary nocturnal enuresis in children is manifested as a consequence of the delay in the maturation centers in the brain that are responsible for overseeing the functioning of the bladder. Because of this delay in the child there is a very deep sleep disorders and the ability to wake up to urinate on their own. Before the brain of a sick child not getting impulses from the bladder. As a consequence, the wake up signal does not occur.

Another reason for nocturnal enuresis - insufficient production of vasopressin in the body of the child. Urine is produced in the body all the time, around the clock. To the night the person did not appear the need to get up to the toilet several times, the body produces the hormone of the posterior lobe pituitary   - Vasopressin. Under its influence the production of urine during the night suspended. In children with enuresis sometimes this hormone is not produced in the right quantities. As a consequence, during the night they have to empty the bladder at the same rate as during the day. Most often enuresis in children occurs as a consequence of the presence of several factors.

In more rare cases, the presence of enuresis may indicate the development of a child in the body of organic disease. This can be defects of the lumbar vertebrae . congenital or   acquired lesions of the lower spinal cord . sleep apnea . epilepsy . sugar or   diabetes insipidus . In order to eliminate these diseases, it is necessary to visit a specialist, who will appoint necessary in case of inspection. Find out the cause of enuresis, your doctor will prescribe the correct and effective treatment of the disease.

In addition, the cause of urinary incontinence are sometimes urological disorders character of the disease, and abnormalities in the structure of the urinary system.

Diagnosis enuresis

 Enuresis  In the case of nocturnal enuresis diagnosis is mainly guided by the patient's complaints, as well as carried out the study of history, both individual and family. To date, there are studies showing that if the bedwetting episodes occurred in the father or mother, then the risk of developing the disease in a child increases by about three times.

The process of collecting medical history is necessary to understand how to raise children is conducted and how he passes the formation of skills of neatness. In this case, the doctor takes into account what the incidence of urinary incontinence, what type of enuresis, clarifies the nature of urination, checks whether the child moved a urinary tract infection, not whether there is a encopresis   or constipation . Furthermore, it is important to determine the presence or absence of sleep apnea, epilepsy, food allergies or drug, hives . asthma . Allergic rhinitis . All of these diseases affect the condition of the bladder, making it more excitable.

Some medications, mostly tranquilizers   and anticonvulsants May have the side effect of urinary incontinence, so it is important to find out whether their child received before.

It is also in the process of diagnosing doctor conducts a physical examination, paying attention to the structure of the abdominal organs, endocrine glands, urogenital system. It is important to assess the adequacy of the physical development of the child and his psycho-neurological status.

To eliminate the pathology of the genitourinary system conducted laboratory tests of urine, ultrasound of the bladder and kidneys. In some cases, the doctor prescribes any additional investigation.

There are also a number of states, which differentiate enuresis in children. This epileptic seizures, some types of allergies, some endocrine disease, sleep apnea, as a result of side effects of medication.

Enuresis Treatment

 Enuresis  To date, the treatment of enuresis is conducted by doctors who work in different fields of medicine. A versatile approach to the treatment of the disease is important in order to effectively eliminate all the causes that lead to enuresis in children

As the day therapies and secondary enuresis usually used methods to exercise the muscles of the bladder, as well as psychological help. Sometimes children prescribed reception preparatov- holinoblokatorov .

For the treatment of nocturnal enuresis is used as a psychologist, and the impact of the special unit "Night Service", which stimulates the brain to wake up to train at night. As of drugs prescribed desmopressin , More rarely used tricyclic antidepressants .

Medications are also versatile effects. Holinoblokatory   lower the tone of the bladder, while the frequency of urination is reduced. Tricyclic antidepressants   have a different effect: they relax the muscles of the bladder and make sleep less deep. Imipramine   should be taken at night, he starts to work after a week. This drug is used for three months, and the amount gradually decreased. But very often after receiving this drug appears enuresis in a child again. In addition, imipramine may negatively affect the state of the child's heart. Therefore, it is important to constantly monitor his condition, conducting an electrocardiogram.

Desmopressin   take those children who have nocturnal enuresis occurs as a result of shortage in the body of vasopressin. This drug is a synthetic analogue. The drug affects about thirty minutes, the action lasts about 8-12 hours. After receiving means the disease is often renewed.

Thus, therapy with medication is often only temporarily removes the symptoms of the disease, it does not lead to complete recovery. Medications recommended situationally, for example, in the days of long-distance travel, and others.

However, very often the doctors, taking into account the large number of cases of arbitrary cure enuresis in children, it is advised never to treat those children who perceive the problem peacefully. To treat nocturnal enuresis is necessary when children are very experienced because of this problem. The treatment of enuresis usually lasts from two to six months, and repeated twice.

Training methods for patients with enuresis are used to train the child to control their bladder. Special exercises that teach longer hold urine, urinating interrupt via Kegel exercises Gradually helping to show the child how to influence this process.

In addition, doctors often recommend a special method to try nighttime awakenings. Throughout the week, the child should wake up at night in the same time - after midnight every hour. Later, the child's need to wake up repeatedly during the night at a certain time, trying to pick up the watch so that the child does not have time to wet oneself. Then if there are repeated cases of enuresis, the course is carried out again.

In addition, some experts prescribing practices of other treatments related to unconventional therapies. This can be acupuncture . magnetotherapy . music therapy   and etc.

 Enuresis  In the treatment of the parents should pay attention to the features diet   child. It is important to significantly limit the amount of liquid as well as those products which promote frequent urination. After dinner, before bedtime fluid intake must be limited to the maximum. Also, special attention should be paid to monitoring the use of products that contain caffeine   - They have a diuretic effect.

In addition, it is important to follow some general rules that will help to quickly deal with the problem. Parents and other family members have the most relaxed and tolerant of a sick child. You can not punish children for the failures, it is important to constantly impress upon them the belief that they will be able to cope with the problem.

A child with enuresis should not experience severe stress and situations that exciting from an emotional point of view. No need to avoid strong supercooling child. Before going to bed, the child must go to the toilet.

Prevention of enuresis in children

There are some preventive measures designed to prevent nocturnal enuresis in children. Experts advise in time to give up diapers as reusable and disposable. Usually, the best time to reject the diaper - a two-year age of the child. Given the time of year and the air temperature, the parents need to monitor how much fluid a child consumes. In addition, parents are required to pay special attention to sanitary and hygienic education of children, teaching them the rules of the care of the external genital organs and other.