Treatments for Cystic fibrosis
Although there is no cure for cystic fibrosis, there are a number of procedures to alleviate symptoms and reduce complications in order to enhance life quality. The management of this disease is complex and necessitates evaluation and therapy at a centre staffed by a competent group of physicians and medical experts.
The primary aims include
Providing sufficient nourishment
Elimination of phlegm from the lungs
Treating and preventing intestinal and other tube blockages
Controlling the lung infection that will develop
Medical treatments
Several medications are administered to patients, including those that target gene mutation. Recently, a new medication consisting of three medicines for the treatment of the genetic mutation causing cystic fibrosis (CF) has proven to be effective and a significant advance in the treatment.
drugs that target specific genes
Due to the fact that the disease is caused by gene mutations, physicians prescribe Cystic fibrosis transmembrane conductance regulator (CTFR). The newly developed medications enhance the function of the defective CFTR protein, which can play a role in enhancing lung function and decreasing sweat salt levels. These medications have been approved for individuals with at least one CFTR gene mutation.
A new medicine combination containing lumacaftor, ivacaftor, and ivacaftor has been approved for patients 12 years and older. The medication has produced remarkable results.
Ivacaftor alone is permitted for infants older than 6 months.
Before prescribing these medications, however, liver function tests and an eye exam are required, and regular testing is necessary to detect adverse effects such as liver function abnormalities and cataracts.
