Complete Information on Esophageal Atresia

by Alicia Stock

Esophageal atresia is a condition in which a part of the oesophagus misses. Esophageal atresia is often associated another congenital anomalies, anomalies most generally cardiac. The disorder is a congenital defect, that the means it occurs before birth. There are several types of atresy oesophagienne. Esophageal atresia with the dent tracheoesophageal occurs in one from 3.000 to 5.000 births. This condition is frequently complicated by the saliva of breathing and secretions of infant in the lungs, causing pneumonia, obstruction, and probably dead. The disorder is usually detected little time after the birth when the food is tested.
Symptoms of esophageal atresia include bluish colouring with the skin with food tested, coughing, bâillonant, and obstructing with the food tested of food, radoter and poor. More one 30% people affected by this condition will also have another anomalies, such as disorders of heart or other digestive disorders of area. Roughly 50 % of children supported with the atresy oesophagienne have other associated problems which can be present. The atresy oesophagienne is considered a surgical urgency. Surgery to repair the oesophagus should be made quickly after the baby is stabilized so that the lungs are not damaged and the baby can be Fédéral.
Before the surgery, the baby is not fed by mouth. The care is taken to prevent the baby of secretions of breathing in the lungs. Mucus and saliva also without interruption will be removed by the intermediary of a catheter until the re-establishment occurred. When the surgery is carried out, the oesophagus is replugged and, if neccessary, is separated from the trachea. The therapy of oxygen is employed like necessary to maintain the saturation normal of oxygen. If one suspect the oral ea or TEF, all food are stopped and of the intravenous fluids are started.

The Basic Facts About Heart Disease - What Is It and What are the Risk Factors?

by Dee Braun

Heart diseases are also called cardiac diseases. Individuals of all ages can develop heart diseases. The most common form of heart disease in adults is coronary artery disease, which is the major cause of heart attacks and the most common form of heart disease in children, is congenital heart disease.
Heart disease can affect the heart muscle, the heart vessels, heart tissue or the heart valves. Heart disease can be caused by smoking, high blood pressure, high cholesterol, infection, and toxins or from a birth defect. Some people are born with heart disease and most develop heart disease over time.
There are certain factors that put certain people at risk for heart disease such as individuals who have a family history of heart disease, those who smoke, and those who have high blood pressure or high blood cholesterol. Individual who are obese or lead inactive lives are also at an increased risk for heart disease. Age increases your risk for heart disease. Some of the risk factors such as family history and age cannot be controlled.
Heart disease present at birth can usually not be controlled if it is heredity in nature. Factors such as smoking, blood pressure and blood cholesterol and controlling diseases such as diabetes that when uncontrolled can lead to heart disease. You can reduce your risk for heart disease by controlling your blood pressure and blood cholesterol, by not smoking, and by getting enough exercise and eating healthy foods.
If an individual suspects heart disease due to having symptoms such as chest pain or discomfort, nausea, vomiting, shortness of breath, dizziness or a feeling that something bad is going to happen they should contact their doctor for an exam and diagnosis. Doctors are trained and have the skills to make the diagnosis of heart disease. You will first be asked to fill out a medical history form that will list your general health, and your symptoms as well as any family history. During the examination your vital signs will be taken including your blood pressure, weight, height, pulse, respiratory rate and temperature.
The doctor will give you a complete examination to rule out any other diseases. You may be sent to a laboratory for blood tests and to the x-ray department for a chest x-ray. Your doctor will be evaluating your risk for heart disease and any sign of present heart disease. You may also be sent for an electrocardiogram (ECG or EKG), which will reveal any arrhythmias or irregular heart rhythms.
You may then be sent for special tests such as an exercise electrocardiogram, a fluoroscopy, phonocardiography, echocardiography, or an angiocardiography (cardiac catheterization). Your doctor will then put all the test results together and determine if you have heart disease or are at risk for heart disease.
Risk factors for heart disease are high blood pressure, high blood cholesterol, the presence of diabetes, and smoking. These are the highest risk factors. Other factors are age, family history, and being obese and having an inactive lifestyle as well as stress. These last factors are considered minor risk factors.
After your doctor review your test results and determines your heart health and your risk factors for heart disease the doctor will give you a diagnosis or tell you what you can do to decrease your risk for heart disease.

Early Attention Is Required With Children With Down Syndrome

by Mike Selvon

Parents of children with Down syndrome are flooded with a barrage of emotions. They may experience disappointment, anger, grief, frustration, fear and anxiety. Mothers over the age 35, who have a higher chance of having a baby with Down syndrome, may experience guilt or self-blame.
These feelings naturally come up, which is why establishing a support network is important for new parents. Talking with others who've been through the same challenges will offer inspiration and ensure the best possible upbringing for the developmentally disabled child.
Children with this chromosomal disorder will have tribulations early on. Parents should be aware of the special-care needs for babies with Down syndrome as early as possible, to prepare themselves for the challenges that lie ahead. Some babies require medication to address a heart defect, while others require physical therapy sessions to help develop better muscle tone and coordination.
Some syndrome babies have a difficult time learning to breastfeed at first, which is sometimes related to stomach or intestinal blockages. Eye, ear, nose, throat and thyroid problems are not uncommon, as is late teething. The main thing to keep in mind is that the baby will eventually get there, but patience and offering loving support are critical to the child's development.
The educational needs for children with Down syndrome vary, depending on the degree of mental retardation. Early intervention and skill assessment is the key to relating to the child on terms he or she can relate with. For example, often concrete concepts are more easily understood than abstract ideas.
Step-by-step teaching and providing consistent feedback are two techniques that can help the developmentally disabled. In the past, Down syndrome children went to separate schools or were home-schooled.
Now, the mainstreaming of these children is proving effective at decreasing the emotional gap between children with this chromosomal disorder and those without. In countries like Denmark or Germany, a two-teacher approach allows these kids to observe and be exposed to others, while focusing on their special needs.
There are certain health risks for children with Down syndrome. About half of all Down syndrome babies are born with congenital heart defects and 60% suffer an eye disease, including cataracts (15%) and the need for corrective glasses or contact lenses (50%). Nearly 75% suffer hearing loss, sleep apnea and persistent ear infections.
Other problems include thyroid disease (15%), gastrointestinal atresias (12%) and acquired hip dislocation (6%). Less than 1% of all cases report leukemia or Hirschsprung disease. Over time, adults with Down syndrome may suffer respiratory infections, heart disease, surgery for bowel obstruction or cataracts, hearing loss, epilepsy and osteoarthritis.

What Vitamin and Mineral Supplements do Healthy People Need?

by Tony Johns

Why should healthy people take vitamin and mineral supplements?
Many people eating the typical American diet are not getting adequate quantities of all the necessary vitamins and nutrients that their bodies need. Supplementing with larger quantities of nutrients may offer protection from certain diseases.
Most Americans do not get enough calcium, magnesium, iron, and zinc in their diet. People that are on diets to lose weight are at risk of vitamin and mineral deficiencies. Another group of people who are especially at risk of dietary deficiencies are the elderly. Older adults often have deficiencies of vitamin D, Vitamin A, vitamin E, calcium, zinc, and vitamins B1 and B2.
What is the importance of taking... Vitamin A- important for the function of the immune system. Vitamin D- not getting enough of this vitamin is associated with bone loss and fractures in older adults and post menopausal women. Vitamin E- associated with lowered risk of heart a disease. Calcium- most people get less than the desired amount of calcium in their diet. Calcium is essential for preventing bone loss. Magnesium- also helps prevent bone loss. Zinc- has been shown to increase immune function in healthy people.
Supplementing with Folic acid is important, about 11% of healthy people in the United Stated are deficient in Folic acid. A diet low in folic acid has been associated with a higher than normal risk of pre-cancerous polyps in the colon. Women who are pregnant and who take a multivitamin with folic acid in it reduce their risk of giving birth to babies having birth defects and other congenital malformations.
I think anybody who is not eating a optimal diet, and who is, should do as I do, and take a high quality multivitamin. Look for one that has all of the above listed vitamins and minerals in its ingredients.