Annotated Bibliography
Hodges, R. (2011). Sickle cell disease: acute complications and management. Journal Of Paramedic Practice, 3(11), 608-613.
In this article, Ross Hodges (2011) provides specific instructions to medical professionals working with the patients who have sickle cell disease (SCD). In particular, the author focuses on the tasks that should be done by prehospital clinicians. The scholar urges medical professionals to pay attention to such risk factors as dehydration, low oxygen levels, dehydration, or pregnancy because they can increase the likelihood of complications related to SCD (Hodges, 2011, p. 610). Additionally, the author shows that there are certain signs that should be recognized by medical workers, for example, pallor, hypotension, abdominal mass. They are the symptoms of splenic sequestration crisis which poses a significant threat to the life of a person (Hodges, 2011, p. 611). Additionally, the author speaks about specific actions that should be taken in order to mitigate the risks of SCD complications. Overall, Ross Hodges discusses a variety of issues that prehospital clinicians should address.
This article is a very useful source because it provides detailed instructions that should be taken by medical professionals in order to assist the patient. Moreover, these guidelines can eventually save a person suffering from complications. The instructions provided by the scholar are based on numerous clinical studies published in peer-reviewed journals. This is this source can be used by medical professionals.
Overall, this article can increase a person’s understanding of the complications that SCD can produce. This work can assist an individual who writes a paper about this illness from the perspective of a nurse. This source demonstrates that the effective management of SCD requires in-depth knowledge of risks to which a patient can be exposed. These are the main aspects that should be considered by the readers.
Lionnet, F., Hammoudi, N., Stojanovic, K., Avellino, V., Grateau, G., Girot, R., & Haymann, J. (2012). Hemoglobin sickle cell disease complications: a clinical study of 179 cases. Haematologica, 97(8), 1136-1141.
In this article, Francois Lionnet et al. (2012) examine the complications produced by hemoglobin sickle cell disease. The arguments of the authors are based on the clinical study that involved 179 cases (Lionnet et al., 2012, p. 1136). The authors note that the diagnosis of this disorder is often delayed. This is one of the reasons why its symptoms can become very acute. The authors focus on such side-effects as acute chest syndrome, priapism, and painful vaso-occlusive crisis (Lionnet et al., 2012, p. 1138). In turn, the most common treatment options are phlebotomy, cholecystectomy, or hydroxycarbanide (Lionnet et al., 2012, p. 1138). The scholars say that hemoglobin sickle cell disease requires the development of specific management guidelines.
This source is beneficial because it highlights the specific peculiarities of sickle cell disease. This article can help medical workers improve their services that they offer to the patients who have this disorder. As it has been said before, the authors’ claims are based on a clinical trial. Moreover, the scholars rely on other peer-reviewed studied; therefore, this information can be used by medical workers. The main distinction of this research article is that the authors do not simply rely on the ideas of other scholars. Their ideas are based on the original research and analysis of data.
This source is important since it highlights the idea that sickle cell disease has many variations. Therefore, this academic work should not be overlooked. It can help a student make a more balanced argument about the treatment of this disorder. Thus, this article can be used when it is necessary to conduct a secondary research.
Musumadi, L., Westerdale, N., & Appleby, H. (2012). An overview of the effects of sickle cell disease in adolescents. Nursing Standard, 26(26), 35-40.
This article, written by Musumadi, Westerdale, and Appleby is also aimed at examining the complications that can be caused by sickle cell disease. In particular, the authors focus on the way in which this disorder affects adolescents. When speaking about the effects brought by this disorder, researchers mention avascular necrosis, splenic sequestration, and hyposthenuria (Musumadi, Westerdale & Appleby, 2012, p. 37). In turn, teenagers may encounter specific problems that are peculiar to their age. For example, they can suffer from depression and alienation that can be explained by numerous admissions to hospitals or other medical institutions (Musumad et al., 2012, p. ). It is important to remember about the risks of vaso-occlusive crisis which can occur due to physical or emotional stressors that often affect teenagers (Musumadi, et al., 2012). Finally, the authors provide specific instructions for assessing an adolescent patient who has sickle cell disease.
This article can be of great use to medical professionals, especially those ones who work in schools. They should be aware of the risks to which students can be exposed. Overall, this source can be helpful for developing preventing measures that can minimize the impact SCD complications. This article incorporates up-to-date and relevant studies. Therefore, this information can be viewed as reliable; it can improve the work of medical professionals.
This article can be incorporated into an academic paper because it throws a new light on various aspects of sickle cell disease. It demonstrates that medical professionals should pay attention to the age of the patient who has this disorder. This source can help a person write a more comprehensive research paper. This is why this article should not be disregarded.
Ohara, D. G., Ruas, G., Castro, S. S., Martins, P. J., & Walsh, I. (2012). Musculoskeletal pain, profile and quality of life of individuals with sickle cell disease. Brazilian Journal Of Physical Therapy, 16(5), 431-438.
The article written by Daniela Ohara et al. (2012) is focused on the experiences of people who have sickle cell disease. This study involved the use of a structured interview, while the sample was 27 patients (Ohara et al., 2012, p. 431). The interviews conducted by researchers were related to various questions. For instance, one can speak about the regions of the body that are affected by this disease. It is necessary to focus on limbs, hips, lower back, and chest. Moreover, these patients normally struggle with musculoskeletal pain (Ohara et al., 2012, p. 431). Additionally, researchers note that these people can also be affected by mental problems such as emotional imbalance, depression or anxiety; this information should not be overlooked by medical professionals. (Ohara et al., 2012, p. 435). These are the main points that the authors examine in the work.
This source is relevant to the work of nurses and other medical workers because they should know what difficulties these patients encounter in their daily lives. It has to be admitted that the sample of this paper is not very large; however, the findings of the authors are backed up by other studies. Unlike, other articles included in this bibliography, this source is based on empirical research. Overall, this scholarly work should be considered by healthcare professionals.
This article is very informative because it helps medical workers to put themselves in the position of people with sickle cell disease. This information can extend the readers’ understanding of this disorder since it demonstrates that the patients with this disorder can struggle with various psychological problems. This is why this article can be incorporated into a research paper.
Thompson, L., Ceja, M., & Yang, S. (2012). Stem cell transplantation for treatment of sickle cell disease: bone marrow versus cord blood transplants. American Journal Of Health-System Pharmacy: AJHP: Official Journal Of The American Society Of Health-System Pharmacists, 69(15), 1295-1302.
In this article, the authors discuss various options for treating sickle cell disease (Thompson, Ceja, & Yang, 2012, p. 1295). In particular, the researchers focus on such methods as blood transplants, bone marrow transplants, and other methods that can help a patient. In this article, the scholars overview the advantages and disadvantages of such methods as cord blood or bone transplantation as well as the use of stem cells (Thompson et al.,2012). The scholars pay close attention to the clinical trials performed by other researchers. The main argument is that at this point, researchers should pay attention to such questions as the selection of stem cell source, or the type of GVHD that should be applied after transplantation (Thompson et al.,2012, p. 1295). These are the main aspects that the authors focus on; to a great extent, they strive to highlight the complications related to sickle cell disease.
This source is primarily intended for physicians who assist patients SCD patients. However, this article can also be of some use to nurses because these professionals also interact with patients who have undergone various forms of treatment. Overall, this source is based on the analysis of empirical studies. Therefore, this information can be considered by practitioners. It should also be ready by students who want to learn more about this disorder.
This article can be included into a research paper because it can extend the argument about sickle cell disease. By relying on this scholarly work, one can demonstrate that the most optimal treatment mode has not been fully developed. Moreover, various options that are not available require further investigation. This information can assist a person in making more informed arguments about sickle cell disease. This is why this source can be used.
Reference List
Hodges, R. (2011). Sickle cell disease: acute complications and management. Journal Of Paramedic Practice, 3(11), 608-613.
Lionnet, F., Hammoudi, N., Stojanovic, K., Avellino, V., Grateau, G., Girot, R., & Haymann, J. (2012). Hemoglobin sickle cell disease complications: a clinical study of 179 cases. Haematologica, 97(8), 1136-1141.
Musumadi, L., Westerdale, N., & Appleby, H. (2012). An overview of the effects of sickle cell disease in adolescents. Nursing Standard, 26(26), 35-40.
Ohara, D. G., Ruas, G., Castro, S. S., Martins, P. J., & Walsh, I. (2012). Musculoskeletal pain, profile and quality of life of individuals with sickle cell disease. Brazilian Journal Of Physical Therapy, 16(5), 431-438.
Thompson, L., Ceja, M., & Yang, S. (2012). Stem cell transplantation for treatment of sickle cell disease: bone marrow versus cord blood transplants. American Journal Of Health-System Pharmacy: AJHP: Official Journal Of The American Society Of Health-System Pharmacists, 69(15), 1295-1302.