| dc.contributor | Camino Bravo, Ivonne Aracely | |
| dc.creator | Eras Ajila, Alexandra Patricia | |
| dc.date | 2023-05-30T16:34:23Z | |
| dc.date | 2023-05-30T16:34:23Z | |
| dc.date | 2023 | |
| dc.date.accessioned | 2023-08-08T17:37:15Z | |
| dc.date.available | 2023-08-08T17:37:15Z | |
| dc.identifier | http://dspace.utb.edu.ec/handle/49000/14086 | |
| dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/8053611 | |
| dc.description | The present clinical case is about an 18-year-old male patient diagnosed with sickle cell anemia, with a clinical picture of pain in the right iliac fossa with a decline in his general condition, agitation, nausea and greenish vomiting, tests are performed. Sickle cell anemia is a hereditary disease also known as sickle cell disease, it originates when two mutant hemoglobin genes are inherited, one from each parent, causing a hemoglobin disorder (hemoglobinopathy). Sickle cell disease primarily affects individuals of African descent. The frequency of the sickle cell gene in certain areas results in high birth rates for newborns affected by the disease. Worldwide, an estimated 300,000 children were born with sickle cell disease in 2010, of whom more than 200,000 are black. The clinical manifestations depend on the genotype and age. In the most severe forms, it can start in the first months of life and produce a high mortality. Thanks to the evaluation by the functional models of Maryori Gordon, it was possible to determine the altered models, which allowed, with the NANDA, NOC, NIC taxonomies, to determine the nursing actions, favorably improving the clinical manifestations. | |
| dc.description | The present clinical case is about an 18-year-old male patient diagnosed with sickle cell anemia, with a clinical picture of pain in the right iliac fossa with a decline in his general condition, agitation, nausea and greenish vomiting, tests are performed. Sickle cell anemia is a hereditary disease also known as sickle cell disease, it originates when two mutant hemoglobin genes are inherited, one from each parent, causing a hemoglobin disorder (hemoglobinopathy). Sickle cell disease primarily affects individuals of African descent. The frequency of the sickle cell gene in certain areas results in high birth rates for newborns affected by the disease. Worldwide, an estimated 300,000 children were born with sickle cell disease in 2010, of whom more than 200,000 are black. The clinical manifestations depend on the genotype and age. In the most severe forms, it can start in the first months of life and produce a high mortality. Thanks to the evaluation by the functional models of Maryori Gordon, it was possible to determine the altered models, which allowed, with the NANDA, NOC, NIC taxonomies, to determine the nursing actions, favorably improving the clinical manifestations. | |
| dc.description | El presente caso clínico se trata de un paciente masculino de 18 años con diagnóstico de anemia falciforme, con un cuadro clínico de dolor en región costal inferior tipo punzadas que posteriormente evoluciona a dolor abdominal tipo cólico y difuso, con cuadro de nauseas+ vómitos en abundante cantidad de coloración verdosa/amarillo. La anemia de células falciformes es una enfermedad de tipo hereditaria conocida también como drepanocitosis, se origina cuando se hereda dos genes mutantes de la hemoglobina, uno de cada progenitor, causando un trastorno de la hemoglobina (hemoglobinopatía). La anemia de células falciformes afecta primordialmente a individuos afrodescendientes. La frecuencia del gen de la drepanocitosis en ciertas áreas da lugar a elevadas tasas de natalidad de recién nacidos afectados por esta enfermedad. Se estima que, en 2010, en todo el mundo, 300.000 niños nacieron con anemia falciforme, de los cuales más de 200.000 son de raza negra. Las manifestaciones clínicas dependen del genotipo y de la edad. En las formas más graves puede iniciarse en los primeros meses de vida y producir una elevada mortalidad. Gracias a la evaluación por los modelos funcionales de Maryori Gordon fue posible determinar los modelos alterados, lo que permitió, con las taxonomías NANDA, NOC, NIC, determinar las acciones de enfermería, mejorando favorablemente las manifestaciones clínicas. | |
| dc.format | 34 p. | |
| dc.format | application/pdf | |
| dc.language | es | |
| dc.publisher | Babahoyo: UTB-FCS, 2023 | |
| dc.rights | Atribución-NoComercial-SinDerivadas 3.0 Ecuador | |
| dc.rights | http://creativecommons.org/licenses/by-nc-nd/3.0/ec/ | |
| dc.subject | Drepanocitosis | |
| dc.subject | Células falciformes | |
| dc.subject | Complicaciones | |
| dc.subject | Hemoglobina | |
| dc.subject | Taxonomías | |
| dc.title | Proceso de atención de enfermería en paciente de 18 años con anemia falciforme. | |
| dc.type | bachelorThesis | |
