Wait a second!
More handpicked essays just for you.
More handpicked essays just for you.
Pediatric sickle cell anemia hesi answers
Pediatric sickle cell anemia hesi answers
Pediatric sickle cell anemia hesi answers
Don’t take our word for it - see why 10 million students trust us with their essay needs.
Recommended: Pediatric sickle cell anemia hesi answers
Interventions for Children with Sickle Cell Disease Children with Sickle Cell Disease According to the Centers for Disease Control and Prevention (CDC), sickle cell disease (SCD) affects millions of people worldwide and predominantly affects descendants from sub-Saharan Africa, South and Central America, the Caribbean, Saudi Arabia, India; and the Mediterranean. Sickle cell disease is a genetic disorder of the red blood cells where the red blood cells comprises of predominantly hemoglobin S, an abnormal type of hemoglobin (2011). Two most common types of sickle cell disease seen in the clinical setting are Sickle Cell Anemia (SS) and Sickle-Hemoglobin C Disease (SC) (Sickle Cell Disease Association of America, 2014, para.1). Sickle cell disease affects various body systems; but the introduction of mandatory child screening at birth, a comprehensive treatment plan, improvements in technology, up-to-date immunizations and increase research for better pain management and prophylactics to treat infections, the mortality rate and life expectancy of these children have improved immensely (Kavanagh et al., 2011, p.e1554). Children with sickle cell are at high risk for both bacterial and viral infection which can lead to death if not treated in a timely fashion. Dealing with sickle cell disease is a lifelong challenge for both children and parents; and both internal and external support for the family could help them better cope with the complications of sickle cell disease. Two of the intervention I would like to focus on to assist children with sickle cell disease at Jacobi Medical Center is related to infection control and peer-to-peer support. A CDC (2008) report on Sickle Cell Disease in New York shows that from 2004 to 2008 ... ... middle of paper ... ...educational programme on hospital-acquired infections in medical wards. Clinical Microbiology And Infection: The Official Publication Of The European Society Of Clinical Microbiology And Infectious Diseases, 18(12), 1215-1217. doi:10.1111/j.1469-0691.2011.03735.x Parent to Parent of New York State. (2011). Support. Retrieved from http://www.parentto parentnys.org/support/ Queens Sickle Cell Advocacy Network, Inc. (QSCAN). (2014). Programs & Services. Retrieved from http://www.qscan.org/programs-services/ Sickle Cell Disease Association of America (2014). Research and screening: About sickle cell disease (SCD) (para.1). Retrieved from http://www.sicklecelldisease.org/index.cfm? U.S. Department of Veterans Affairs (2013). Peer support proves effective in coping with chronic Disease. Retrieved from http://www.va.gov/health/NewsFeatures/20110505a.asp
...nt of patients with sickle cell anemia. However, the choice of interventions should be done carefully so as to realize the desired outcome otherwise it may not be successful. Key among the innervations listed here, is counseling. This may help the patients to have hope and this may aid in the quick recovery.
Clinical Infectious Diseases, 49(3), 438-443. Doi:10.1086/600391. See full address and map. Medicare.gov/Hospital Compare - The Official U.S. Government Site for Medicare (n.d).
What is Sickle cell disease? Sickle cell affects a disease; that disease is called which affects the hemoglobin when the red blood cells that send oxygen through the body are killed off and weakened. Sickle cells can be found in every 1 and 1000 African Americans, it is affecting about 70,000 to 80,000 Americans in the United States. Sickle cell is a death threatening disease, and the severity of symptoms can vary from person to person (Sickle cell disease (SCD), 2015). Some people have light conditions, but others can have severe conditions, which, mean they could be hospitalized. Characteristics of this disease are caused by a minimum of low blood cells, which is called anemia.
Healthcare-associates Infections (HAIs) are infections that patients acquire during the course of receiving healthcare treatment for other conditions and can be devastating or even deadly ("CDC - HAIs the Burden - HAI", 2013). An HAI was defined as a localized or systemic condition that (1) results from an adverse reaction to the pres¬ence of an infectious agent(s) or its toxin(s), (2) that occurs during a hospital admission, (3) for which there is no evidence the infection was present or incubating at admission, and (4) meets body site-specific criteria (Klevens et al., 2007, p.2).
During a short break of solitude from studying, I explored and came across that the environment in which most African Americans reside in has a high occurrence of malaria virus. The malaria virus disease is contagious and when it contaminates someone with sickle cell traits, it cannot survive on the external part of the human body so therefore the individual doesn’t develop the deadly malaria virus. While looking further into our class textbook on Human Genetics 11th Edition by Ricki Lewis, and this issue of sickle-cell among the African Americans, I
Sickle cell anemia is a hereditary disorder that mostly affects people of African ancestry, but also occurs in other ethnic groups, including people who are of Mediterranean and Middle Eastern descent. More than 70,000 Americans have sickle cell anemia. And about 2 million Americans - and one in 12 African Americans - have sickle cell trait (this means they carry one gene for the disease, but do not have the disease itself).
“In the United States, it's estimated that sickle cell anemia affects 70,000–100,000 people, mainly African Americans” (NHLBI, NIH, Who is at risk for sickle cell anemia). SCD is a disease that is a serious disorder in which the body can make normal blood cells and sickle shape cells. Sickle shape cells can block the blood flow in your vessels and cause pain or organ damage also put you in risk for infections. SCD has no cure available but there are many treatments out there to deal with the complications of it. From over years treatments did get better from way back in the day doctors have learned. Sickle cell disease has lack of attention and funding because it’s only affecting African American the most.
Sickle cell anemia is an inherited disease of red blood cells. Normally red blood cells contain a protein called hemoglobin A, which carries oxygen to all the organs in the body. With sickle cell anemia, however, the body makes a different kind of protein, called hemoglobin S.
Hospital-acquired infections (HAI) are preventable and pose a threat to hospitals and patients; increasing the cost, nominally and physically, for both. Pneumonia makes up approximately 15% of all HAI and is the leading cause of nosocomial deaths. Pneumonia is most frequently caused by bacterial microorganisms reaching the lungs by way of aspiration, inhalation or the hematogenous spread of a primary infection. There are two categories of Hospital-Acquired Pneumonia (HAP); Health-Care Associated Pneumonia (HCAP) and Ventilator-associated pneumonia (VAP).
Sickle cell anemia is a disease that has to be inherited from both parents. Both parents have sickle cell trait, which means each parent has sickle hemoglobin and normal hemoglobin. So people with the sickle cell trait can pass the sickle cell gene to their children. Most families that come from Africa, South Central, and Central America are more common with sickle cell anemia. According to National Heart, Lung and Blood, it’s estimated that the sickle cell disease has affected 70,000-100,000 people mainly African Americans (National Institute of Health, 2012). Hispanic Americans also are common to having sickle cell anemia. According to National heart, Lung, and Blood Institute, statistics shows sickle cell anemia occurs in about 1 out of every 500 African American births and 1 out of 36,000 Hispanic American births (National Institute of Health, 2012). Signs of sickle cell anemia don’t show until after 4 months of age. Sickle cell anemia begins from ...
Sickle Cell Anemia is a disease found right here in America, but in low levels compared to some areas of the world. The rate for this disease is around five times greater in certain places in Africa. That is because the potentially fatal disease Sickle Cell Anemia can also work as a sort of vaccination for another disease called malaria. First the mechanics of Sickle Cell Anemia will be discussed, then its possible benefits.
Holmes, A., Castro-Sanchez, E., & Ahmad, R. (2015). Guidelines in infection prevention: Current challenges and limitations. British Journal Of Healthcare Management, 21(6), 275-277 3p.
Secondary:Curtis, L. (2008). Prevention of hospital-acquired infections: review of non-pharmacological interventions. Journal of Hospital Infection, 69(3), 204-219. Revised 01/20
Infection control is very important in the health care profession. Health care professionals, who do not practice proper infection control, allow themselves to become susceptible to a number of infections. Among the most dreaded of these infections are: hepatitis B (HBV), hepatitis C (HCV), and human immunodeficiency virus (HIV). Another infection which has more recently increased in prevalence is methicillin-resistant Staphylococcus aureus (MRSA). These infections are all treated differently. Each infection has its own symptoms, classifications, and incubation periods. These infections are transmitted in very similar fashions, but they do not all target the same population.
B1.1 Where do you think you’ll find that the most villagers are dying from sickle-cell anemia? Explain.