ipl-logo

Eisenmenger Syndrome Research Paper

780 Words4 Pages

What is Eisenmenger Syndrome Heather A. Woods Stevens-Henager College – Boise Idaho Campus July 12, 2015 Author Note Heather A. Woods, Department, Stevens-Henager College, Boise, Idaho. Correspondence concerning this article should be addressed to Author Name, Department, Stevens-Henager College, 1444 S. Entertainment Avenue, Boise, ID 83702. E-mail: Heather.Woods@bo.steveanshenager.com Eisenmenger Syndrome is the combination of hypertension and left to right shunting of the blood within the heart. It is a rare heart condition that is progressive. It develops in patients that have structural malfunctions of the heart. Treatment includes surgical procedures as well as medications an suppliments. Eisenmenger Syndrome effects women …show more content…

Blood will flow from the left ventricle into the right ventricle with this particular defect. The defect causes increased blood flow into the lungs and can eventually result in pulmonary hypertension. Pulmonary hypertension will causes damage to the small blood vessels in lungs progressively through time. This is known as pulmonary vascular disease. As the damage progresses, pulmonary hypertension will increase and the small blood vessels become thickened and blocked affecting the flow of blood. Life threatening conditions can occur because of this. Symptoms of Eisenmenger syndrome can range by a case by case scenario. Signs and symptoms do not occur until approximately thirty years of age. It can however develop rapidly in some cases. Inadequate oxygen supply to the body cells, known as hypoxia, is part of the symptoms of Eisenmenger syndrome. The most recognizable symptom will include a bluish discoloration of the skin and mucous membranes; this is referred to as cyanosis. Patients with Eisenmenger syndrome can develop cyanosis in the lips, fingernails, and toes. Due to the inadequate oxygen to the blood supply the patient may also display high levels of red blood cells. Other signs can include broadening of the tips of the fingers and toes this is known as clubbing. …show more content…

Eisenmenger syndrome has decreased due to the prevention of prolonged pulmonary hypertension through early surgical correction of certain congenital defects. Approximately 8 percent of individuals with congenital heart disease will develop Eisenmenger syndrome. Pregnancy can result in cardiovascular changes that may increase the risk of potentially life-threatening complications in a woman with Eisenmenger syndrome as well as the fetus. The treatment of Eisenmenger syndrome is based off of specific symptoms of each patient and can vary. Patients are encouraged to seek help from a cardiologist, Doctors that specializes in the treatment of lung diseases, and a hematologist. Patients that have developed Eisenmenger syndrome are also recommended to take medications to help with symptoms, water retention, and iron supplements if they suffer from anemia, these would need to be monitored

Show More
Related

Poison Ivy Case Studies

663 Words | 3 Pages

In addition, he notices a little bit of swelling. He has a little bit in the upper arm on the left, but nothing on the right arm, a few areas on his chest wall and abdomen, as well. They do not seem to be as bad as his left arm. There has been no numbness or tingling in his arm. He has been trying to keep it covered as best he can.

Read More

C. M.'s Pneumonia Case Study

375 Words | 2 Pages

C.M. is an 85 year old patient. He is presenting to the hospital with shortness of breath and increased respiratory effect. He also was found to have rhonchi in the lungs and was using accessory muscles to breathe. He was then diagnosed with pneumonia. C.M. is a former smoker who would smoke half a pack a day.

Read More

Aarskog Syndrome Research Paper

479 Words | 2 Pages

Aarskog Syndrome Description Aarskog syndrome (also known as Aarskog–Scott syndrome, faciodigitogenital syndrome, shawl scrotum syndrome and faciogenital dysplasia) is a rare autosomal X-linked inherited disorder that affects a person 's height, muscles, skeleton, genitals, and appearance of the face. It mostly affects at birth and the symptoms usually become apparent by the age of 3years. Unfortunately, Aarskog syndrome is a lifelong condition without a cure. Some people with Aarskog syndrome are born with more serious abnormalities, such as heart defects or a cleft lip with or without an opening in the roof of the mouth (cleft palate). Most males with Aarskog syndrome have a shawl scrotum, in which the scrotum surrounds the penis.

Read More

Stevens Johnson Syndrome Research Paper

790 Words | 4 Pages

The common symptoms of Stevens-Johnson syndrome include: • Swelling of the face • Swelling of the tongue • Hives • Pain on the skin • Skin rash that looks red or purple and spreads within hours or days • Skin blisters, including mucous membranes of the mouth, eyes, nose, and genitals • Skin

Read More

Castleman's Disease Research Paper

670 Words | 3 Pages

The most common cytokine is IL-6, but in some cases the level of IL-6 is normal and is present with non-iron-deficient microcytic anemia. The release of IL-6 is caused by HIV-8, some studies suggest that cytokines are released by a mutation. HIV-8 is also capable in causing cancerous tumors in the blood vessels. Besides the circulatory system no other body system is affected bys Castleman’s disease. Castleman’s disease can affect anyone most diagnostics are around the age of thirty five.

Read More

Wernicke Korsakoff Syndrome Research Paper

762 Words | 4 Pages

It could easily happen to anybody. Wernicke Korsakoff Syndrome goes by the names of Wet Brain, Korsakoff 's Phychosis, and Alcoholic Encephalopathy. This disease is a result of a Vitamin B deficiency, which causes brain damage, and is fairly common in people who have an alcohol addiction, and are between the ages of 40-80. WKS is a carrier of plenty of side

Read More

Chronic Obstructive Pulmonary Disease: A Case Study

440 Words | 2 Pages

Chronic obstructive pulmonary disease (COPD) has been identified as the fourth most common cause of death worldwide.1 This disease is treatable and can be prevented if the appropriate measures are taken. Its functional limitation is characterized by restricted airflow that cannot be fully reversed.2 The restricted airflow is commonly progressive and is associated with an abnormal inflammatory response of the lungs.3

Read More

Sturge-Weber Syndrome Research Paper

440 Words | 2 Pages

• Seizures. • Muscle weakness.

Read More

Angelman Syndrome Research Paper

708 Words | 3 Pages

A Rare Disorder called Angelman Syndrome This research paper will discuss a specific disability called Angelman Syndrome. (AS) This Syndrome is a disorder, and can be diagnosed at an early age. AS don’t have a cure, but there are ways to treat this disorder.

Read More

Meconium Aspiration Syndrome

601 Words | 3 Pages

Another effect of meconium aspiration is an inflammatory response called chemical pneumonitis; the inflammation results in mucosal edema, decreasing lung compliance, and further impairment of gas exchange (Whitaker, 2001). Persistent pulmonary hypertension may result from asphyxiation in utero, these patients’ arterial blood gases may worsen, and blood flow continues to follow fetal pathways. Other effects of meconium aspiration include cyanosis without response to oxygen therapy, tachypnea, and pulmonary infection. Auscultation often reveals pulmonic systolic ejection clicks and a loud second heart sound (Whitaker,

Read More

Informative Speech On Ischemia Heart Disease

568 Words | 3 Pages

Right Coronary Artery. When these arteries are narrowed, the blood flow and oxygen circulation is forced to stop causing your body to have less movement. This is a very dangerous disease due to the fact that when the blood clot occurs in the body, your heart may stop pumping blood and inhaling/exhaling oxygen which leads to certain heart attacks and/or death.

Read More

Turner Syndrome

2422 Words | 10 Pages

Ullrich- Turner Syndrome can affect proper development of several body systems. There are a number of expected complications that will occur including heart problems, cardiovascular disease, hearing loss, kidney problems, immune disorders, dental problems, visual impairments, skeletal problems, pregnancy issues and thyroid issues. Defects in the main blood vessel leading out of the heart (aorta) increase the risk of a tear in the inner layer of the aorta (aortic dissection). A defect in the valve between the heart and the aorta may also increase the risk of a narrowing of the valve that cause heart problems.

Read More

Cannabinoid Hyperemesis Syndrome Case Report

1201 Words | 5 Pages

It provides a clear description of what CHS is and how it affects someone with the syndrome. Brewerton and Anderson take the reader through the full process of someone with CHS. They start by presenting the reported symptoms, the diagnosis, and the treatments for the syndrome. The authors also discuss the pathophysiology and the different theories of CHS. The purpose of this case report is to provide the facts on CHS and what causes the syndrome.

Read More

Neurological Syndrome Case Study

4987 Words | 20 Pages

RARE NEUROLOGICAL SYNDROMES: An Overview INTRODUCTION: Syndrome is a clinical guide to symptoms and diagnosis, propose a brief useful resources for knowing a subset of neurological clinical features depict a disease or disorder whereas disorder is an abnormal physical or mental condition.[1] Rare neurological syndromes is one of the challenges to public health. Careful analysis of the signs and symptoms can compare with other neurological diseases.

Read More

Zellweger Syndrome Research Paper

1017 Words | 5 Pages

Abstract: Zellweger syndrome is an autosomal and recessive disease. It is part of one a 4 disease of disorders known as peroxisomal biogenesis disorders. It is caused by absence of peroxisomes, which remove the body of toxic substances in the liver, brain, and kidneys. The most common features the zellweger syndrome patients include swell liver, high levels of copper and iron in the blood, and vision disturbances. This disorder results from the inheritance by 2 mutations genes for one of the receptors (PXR1) needed to import proteins into the peroxisome.

Read More

More about Eisenmenger Syndrome Research Paper

Open Document