Skip to main content

First Treatment If You Have Cystic Fibrosis

Cystic fibrosis or better known as cystic fibrosis is a congenital disorder that causes severe damage to the lungs, digestive system, and other organs in the body. It affects cells that produce mucus, sweat, and digestive juices.

Mucus is a fluid that serves to lubricate and protect the mucous membranes. Normally mucus in the body is liquid and slippery. But in people with cystic fibrosis, the mucus is thicker and sticky, clogging various channels in the body, especially the respiratory and digestive tract.

People with cystic fibrosis require intensive care to improve their quality of life. Through the development of increasingly sophisticated health technology, people with this condition usually can still perform daily activities such as school and work.

Symptoms of Cystic Fibrosis

Symptoms of cystic fibrosis may vary depending on the severity of the disease. Symptoms can appear after birth or just appear when someone has grown up.

Airway obstruction may occur in people with cystic fibrosis. This will cause some symptoms like :

Prolonged cough
Shortness of breath.
Diarrhea.
Gag
Shortness of breath or difficulty breathing
Mengi (bitch).
Airways widen due to inflammation (bronchiectasis).
In addition to the above symptoms, lung infections are also susceptible to cystic fibrosis sufferers because the mucus becomes a suitable place for bacterial proliferation.

The same conditions can also occur in the digestive system, where the pancreas ducts can be clogged by sticky mucus. As a result, the digestive enzymes produced by the pancreas can not reach the small intestine, to help digest food. This condition often causes symptoms such as:

Weight loss or even stunted growth due to undigested food so that people with nutritional deficiencies or malnutrition.
Fecesy, oily, and strong-smelling stool texture.
Severe constipation.
Interruption of early sewage (meconium) process on the first or second day after birth, due to blockage. This condition is called meconium ileum.
Baby's skin color turns yellow (jaundice).

First Cystic Fibrosis Treatment

If it is confirmed that a person has cystic fibrosis, other tests need to be done to find out the extent of the disease and to identify possible problems caused by the condition. Some examples are:

Pulmonary function test - check the health of the lungs
Sputum culture - examines the types of bacteria that may be present in a person's body
CT scan - checks the health of the lungs, pancreas, and other parts of the body
Chest X-rays - check the heart and lungs
Blood tests - check blood sugar levels and check whether the liver is functioning properly
Fecal analysis - checks whether the patient digests the nutrients well
Arterial blood gas analysis - compares the levels of oxygen and carbon dioxide to determine the health of the lungs.
Because of the different symptoms in each patient, the treatment for cystic fibrosis is also adjusted, depending on the patient's age, health, and symptoms. Most of the treatment will focus on eliminating certain health problems caused by this disease. Following a treatment plan and working with a doctor will help patients live long and healthy despite these conditions. This means that you should make regular visits to the doctor for examination and monitoring.

Comments

Post a Comment

Popular posts from this blog

What is Three Parts of Nucleotide ?

What is Three Parts of Nucleotide ? Nucleotides are biological molecules that form the building blocks of nucleic acids (DNA and RNA) and serve to carry packets of energy within the cell (ATP). In the form of the nucleoside triphosphates (ATP, GTP, CTP and UTP), nucleotides play central roles in metabolism.  In addition, nucleotides participate in cell signaling (cGMP and cAMP), and are incorporated into important cofactors of enzymatic reactions (e.g. coenzyme A, FAD, FMN, NAD, and NADP+). A nucleotide is composed of a nucleobase (nitrogenous base), a five-carbon sugar (either ribose or 2-deoxyribose), and one or more phosphate groups. Three parts of nucleotide image  That are three parts of nucleotide, Nucleotides can be synthesized by a variety of means both in vitro and in vivo. There a 4 different nucleotides ATP,GTP (purines) TTP,CTP (pyrimidines) which differ in the chemical structure of the base. They are generally referred by a single letter A, G, T,C. UTP
Post a Comment
Read more

The Noonan Syndrome Characteristics You Must Know

Noonan Syndrome is a genetic disorder that impedes normal development in various parts of the body. A child can be stricken with Noonan syndrome in a variety of ways: unusual facial characteristics, short stature heart defect, other physical problems, and sometimes mental retardation. Noonan syndrome is caused by a genetic mutation and are obtained when a child inherits a copy of the affected genes from the parents. It can also occur as a spontaneous mutation in children, which means there is no family history involved. The characteristics of children with Noonan Syndrome, among others: 1. Characteristics of the face -Early childhood. An infant with age less than 1 month seems lowly ears, short neck and at the back of the head low hairline -Childhood. Children have eyes stand out with the slope down and the nose is wide and round. Often seen the lack of facial expression. -Teens. At adolescence, her face is wide, usually the facial features become sharper and less promine
Post a Comment
Read more

Why Patau Syndrome or Known as Trisomy 13

Trisomy 13 or Patau Syndrome  is the most severe viable trisomy caused by an additional copy of chromosome 13 that usually causes a host of developmental problems and physical deformities in a newborn. Patau syndrome is generally recognized at birth by the presence of structural birth defects and poor neurologic performance. Additional structural anomalies are common, particularly facial anomalies (midline clefts, hypotelorism, microphthalmia, and anophthalmia) arising from structural anomalies of the brain, frequently microcephaly and holoprosencephaly. Other associated anomalies include cardiac, renal, and intestinal (diaphragmatic hernia) anomalies. Characteristic features include low set ears, post-axial polydactyly, flexion contractures, rocker bottom feet, scalp defects, and haemangiomas. What is the cause of Patau Syndrome ? The exact incidence of Patau syndrome is not known, although it appears to affect females more than males, most likely because male fetuses do not
Post a Comment
Read more