More handpicked essays just for you.
Flashcard on congenital heart disease
Flashcard on congenital heart disease
Flashcard on congenital heart disease
Don’t take our word for it - see why 10 million students trust us with their essay needs.
All parents hope to have a healthy child. However, there are cases where a child may have a congenital heart defect. A child diagnosed with this devastating cardiovascular disease must be one of the worst news parents could ever get. With the advancement of science, early detections and interventions are in place to manage the disease. Proper management and treatment should be taken into consideration to avoid any complications. If left untreated, a congenital heart defect could lead to another disease called Eisenmenger Syndrome.
Eisenmenger Syndrome in Children
According to Freeborn and Holloway (2016), Eisenmenger Syndrome (ES) is an advanced form of pulmonary artery hypertension (PAH) that is associated with congenital heart defect. Congenital heart defects such as ventricular septal defect (VSD), patent ductus arteriosus (PDA),
Lowering pulmonary hypertension, bringing more oxygen to the lung tissues and ease the cyanosis are the primary treatment focus for patient with ES (Freeborn & Holloway, 2016). Treatments include medicine, oxygen, and phlebotomy. According to Baffa (2014), heart and lung transplant are the only available treatment for a severe ES once the condition develops. A child will be given with great caution medications such as calcium channel blockers, prostacyclin, and endothelin receptor antagonists to dilate blood vessels and lower pulmonary hypertension. The provider may also prescribe diuretics to decrease the blood volume in case heart failure develops. According to Stanford Children’s Health (2015), removing some blood (phlebotomy) twice a year could also be ordered by a provider to reduce the number of red blood cells when the symptoms are so severe, and the hematocrit is extremely high. According to El-Chami and Willis (2014), a child could get oxygen therapy while sleeping or resting, or
Ehlers Danlos Syndrome Ehlers-Danlos syndrome (EDS) is a rare inherited group of connective tissue disorders characterized by defects of the major structural protein in the body (collagen). Collagen is a tough fibrous protein that plays an essential role in binding, holding together, strengthening, and providing elasticity to bodily cells and tissues. There are six major types of EDS that I will discuss, however I will only go into a detailed discussion on two of the six types of EDS. The two major types of EDS are Classical EDS and Hypermobile EDS. These two types make up 90% of all EDS cases.
“Hypoplastic left heart syndrome accounts for 9% of all critically ill newborns with congenital cardiac disease, causing the largest number of cardiac deaths in the first year of life.(2) ” HLHS is a severe heart defect that is present at birth. HLHS combines different defects that result in an underdeveloped left side of the heart. This syndrome is one of the most challenging and difficult to manage of all of the congenital heart defects. Multiple portions on the left side of the heart are affected including the left ventricle, the mitral and aortic valve, and the ascending aorta. These structures are greatly reduced in size, or completely nonexistent causing the functionality of the left heart to be reduced, or non-functional all together.
During my second pediatric residency at Woodhull hospital I did two-month rotations in pediatric cardiology in which I was directly involved in taking care of wide variety of congenital heart disease and to attend diagnostic and interventional cardiac catheterization cases, my interest in pediatric cardiology was further strengthened. My experience to pediatric cardiology field back home as well as in USA further intensify my insistence to pursue training in pediatric cardiology and eventually in interventional congenital cardiology. Being able to treat complicated lesions via transcatheter approach, sparing patients from having major cardiac surgery is indeed a revolution in patient care which I
According to Batshaw, Roizen, and Lotrecchiano (2013), patent ductus arteriosus (PDA) is “the persistence of a fetal passage permitting blood to bypass the lungs” (p. 745). This is an inherited heart condition in which the ductus, a small pathway between the pulmonary and the aortic, valves remain open. This cardiovascular problem usually occurs in low birth weight infants. The blood vessels usually naturally closes after birth (Batshaw et al., 2013, p. 96). It becomes atypical if it remains open after the neonatal period. The structure usually closes in typical developing newborns around the initial 24 hours, and anatomical closure is supposed to follow several weeks later (Stanford Children’s Health, 2015). At the point when the ductus arteriosus stays open, the blood from the oxygen-rich aorta blends with the oxygen-poor pulmonary artery causing the higher chance of blood pressure in the lung pathways (U. S. Department of Health and Human Services, 2011). Certain children who have patent ductus arteriosus may be given medication, relying upon the circumstance to standardize the blood and oxygen levels until surgery is performed. Doctor can treat this condition by providing pharmaceutical medicine, catheter-based procedures, and surgery (U. S. Department of Health and Human Services, 2011).
Sudden infant death syndrome ( SIDS) is the greatest cause of infant deaths ranging from ages one month to one year. Most of these deaths occur before the age of six months. Normally, any unexplainable infant death is considered to be due to SIDS. Numerous attempts have been made to discover the exact cause of this syndrome. However,the only known pathology is that SIDS is due to a dysfunction or abnormality in the cardiac and/or respiratory systems. To this point, an exact and definite cause has not been named. This paper will attempt to present several of the proposed and hypothesized causes of SIDS.
According to “Heart Disease and Marfan Syndrome” (n.d.) Marfan syndrome is caused by a change in the gene that controls how the body makes fibrillin, a part of connective tissue that contributes to its elasticity and strength. It is also stated that Marfan syndrome is mostly inherited from a parent, but 1 in 4 cases occurs when the patient has no known family history of the disease. To add, the condition occurs
Cardiofaciocutaneous syndrome may be generated through various genetic mutations. As mentioned before, there are four genes that can cause this condition to be brought about in an individual. The most frequent mutation of these is the BRAF gene, because it is responsible for approximately 75 to 80 percent of each case of the syndrome. The two genes, MEK1 and MEK2, are very much alike and together are the result of 10 to 15 percent of ...
The purpose of this paper is to establish an understanding of the rare heart disease Tetralogy of Fallot. Tetralogy of Fallot is a congenital heart defect that is present at birth, with the structure of the heart being problematic. It changes the normal flow of blood through the heart. The aspects of it being explained are the overall disease and symptoms of it. Secondly, the long term and short term effects corresponding to the particular disease. Lastly, the causes, prevention, and statistics of the disease. This research will provide an insight to the disease and all aspects and forms. It will allow a better understanding on how to cope with such disease or better prepare us in a case where this disease may be present and have to be dealt with.
Marfan syndrome (MFS) is a fairly common inherited connective-tissue disorder. The syndrome can be found in 1 in every 5000 births worldwide (Giarelli, Bernhardt, & Pyeritz, 2010). MFS has been recognized for more than 100 years, in fact it was speculated that Abraham Lincoln had the disorder (Amado & Thomas, 2002). There is still no current cure, but early recognition and intervention can play a key role in the prevention of the sudden cardiac complications (Midla, 2008). For those Marfan patients diagnosed the life expectancy is close to normal, yet tends to be under diagnosed (Pyrietz, 2000). The nurse should have a broader understanding of MFS since recognition is essential for the diagnosis. Since MFS is primarily an inherited disorder, it of equal importance that the nurse understands that a referral to a geneticist is an imperative n...
Shaun White is an Olympic medalist and daredevil. “White was born with four heart abnormalities causing him to go through two open-heart surgeries before he was a year old” (Good Housekeeping). This condition is termed “tetralogy of Fallot – a term that describes a combination of heart defects including a hole between the pumping chambers of the heart and an abnormally narrowed valve and surrounding structures that link the right side of the heart to the lungs” (Learn). “The causes of tetralogy of Fallot among babies are unknown. Heart defects such as tetralogy of Fallot are thought to be caused by a combination of genes and other risk factors including the environment the mother comes in contact with” (CDC). The pulmonary circuit of the respiratory system is affected. In this circuit the oxygenated blood is moved from the lungs to the right side of the heart. In the early medicine era, “doctors created a shunt by disconnecting an artery leading to the arm, reconnecting it to the lungs” (Learn). Surgery is needed in order to correct the defects. “White had surgery as a baby and says he’s grateful to his doctors. Even after successful surgery, patients with tetralogy of Fallot face a greater risk of serious heart problems. [White must] get regular checkups to monitor his heart throughout his lifetime” (Mayberry). “During su...
Hypertrophic cardiomyopathy is an inherited disease that affects the cardiac muscle of the heart, causing the walls of the heart to thicken and become stiff. [1] On a cellular level, the sarcomere increase in size. As a result, the cardiac muscles become abnormally thick, making it difficult for the cells to contract and the heart to pump. A genetic mutation causes the myocytes to form chaotic intersecting bundles. A pathognomonic abnormality called myocardial fiber disarray. [2,12] How the hypertrophy is distributed throughout the heart is varied. Though, in most cases, the left ventricle is always affected. [3] The heart muscle can thicken in four different patterns. The most common being asymmetrical septal hypertrophy without obstruction. Here the intraventricular septum becomes thick, but the mitral valve is not affected. Asymmetrical septal hypertrophy with obstruction causes the mitral valve to touch the septal wall during contraction. (Left ventricle outflow tract obstruction.) The obstruction of the mitral valve allows for blood to slowly flow from the left ventricle back into the left atrium (Mitral regurgitation). Symmetrical hypertrophy is the thickening of the entire left ven...
Hinkle, Janice, and Kerry Cheever. “Management of Patients with Chronic Pulmonary Disease." Textbook of Medical-Surgical Nursing, 13th Ed. Philadelphia: Lisa McAllister, 2013. 619-630. Print.
Angelman Syndrome is a rare genetic disorder characterized by neurological and developmental issues. Dr. Harry Angelman discovered the syndrome in 1965. It was formerly called “Happy Puppet Syndrome” due to the clinical features possessed by those affected. Dr. Angelman observed those affected as appearing normal upon birth but eventually showing signs of development disabilities. Angelman Syndrome mainly targets the nervous system and can be detected in infants as early as six months. Typically, the first noticeable sign is usually feeding problems or a delay in development. It is caused by a deletion or mutation, such as translocation, in Chromosome 15, long arm q, band 12. Some references note the affected region as bands 11.2-13. This area encodes for the UBE3A gene. Usually, the body uses information from both copies of a gene. The activity of each gene copy is dependent on whether it was passed from your mother or from your father. This parent-specific gene activity is called imprinting. In a few instances, only one copy of a gene pair is active. For the UBE3A gene, only the maternal copy is active in the brain. This is an example of genomic imprinting in which the body only recognizes or requires one copy to be active. In Angelman Syndrome, the body only recognizes the maternal copy of chromosome 15. However, there have been a few rare incidences in which uniparental disomy was the cause of acquiring the syndrome. This occurs when both copies of chromosome 15 were inherited from the paternal side.
Cardiovascular System: He does not experience any chest pain or palpitation. He does not have dyspnea or leg swelling.
...ey may require aggressive treatment, such as continuous fluid drainage and use of mechanical ventilation to help the patient to breathe. Whatever the severity of it, it is important to get medical care as quickly as possible to have the best chance of full recovery.