Preview

Jaundice

Better Essays
Open Document
Open Document
1622 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Jaundice
Jaundice is defined as the yellow staining of the skin and sclerae that is caused by high levels in blood of the chemical bilirubin. The color of the skin and sclerae varies depending on how high or low the blood of the chemical bilirubin is. When the level is highly elevated, the skin or sclerae is yellowish; when the level is high the skin or sclerae is brown. Jaundice occurs when there is too much bilirubin being produced for the liver to remove from the blood. Jaundice also occurs when there is a defect in the liver that prevents bilirubin from being removed from the blood, converted to a conjugated acid or secreted in bile, or blockage of the bile ducts that decreases the flow of bile and bilirubin from the liver into the intestines. Jaundice in babies usually occurs because their immature livers are not efficient at removing bilirubin from the bloodstream. Jaundice can turn the skin and sclerae yellow. Stool also can become light in color, even clay-colored because of the absence of bilirubin that normally gives stool its brown color. With jaundice, urine may turn dark or brownish in color. Jaundice in newborns most commonly happens because their livers are not mature enough to remove bilirubin from the blood. A mother who has diabetes may cause a baby to develop neonatal jaundice. There are many signs and symptoms associated with Jaundice. The signs and symptoms that adults have when they have jaundice are yellow skin, yellow eyes, dark or reddish urine, bronze skin , loss of appetite , bitter taste in mouth , furry tongue, pale feces, foul-smelling feces, nausea, itching skin , lethargy, slow pulse, and confusion. The signs and symptoms that newborns have are ill appearance, fever, and poor feeding. Newborn babies will begin to appear jaundiced when they have more than 5 mg/dL of bilirubin in their blood.

There are several diagnostic tests to determine the diagnosis of Jaundice. These tests include blood tests , complete blood count , liver function

You May Also Find These Documents Helpful

  • Good Essays

    John Baker Case Summary

    • 1046 Words
    • 5 Pages

    A histamine blood test is also done to verify anaphylaxis and rule out Mastocytosis. An Immunoglobulin E (IgE) blood test is done to see if the immunoglobulin levels are elevated, and a complete blood count (CBC) is done to see if there are elevated levels of eosinophil white blood cell are elevated (2). Heart and lung disorders can be ruled out using an ECG and chest x-rays (1). The Tryptase blood test show elevated tryptase levels. The histamine blood test shows elevated levels of histamine.…

    • 1046 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Adl Case Study Essay

    • 488 Words
    • 2 Pages

    Derek is hypoglycaemic, having blood glucose below the normal levels. This has resulted him in experiencing paleness, agitation, diaphoresis and abdominal pain. This may have been caused by overmedication with insulin or antidiabetic pills. Even possibly due to any missed meals, a severe infection, and use of alcohol, kidney failure or liver failure.…

    • 488 Words
    • 2 Pages
    Good Essays
  • Good Essays

    Nicu Narrative Examples

    • 573 Words
    • 3 Pages

    This baby boy was born on 03/01/16 and after 2 days in the hospital it was ready to go home with his parents. The nurse did the last blood glucose test to make sure the baby was not hypoglycemic. The test result showed that the baby had very low blood glucose (34 L). Upon evaluation the baby needed to stay longer at the hospital to control his blood glucose levels. Simultaneously, the newborn presented jaundice with a bilirubin of (12.7).…

    • 573 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Lab tests such as CBC w/ diff, TSH, LFP, cholesterol, A1C, serum glucose, fasting glucose, U/A, CMP, B12, ECT……

    • 512 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Jaundice (yellow discoloration of the skin), upper abdominal pain, bowel sounds, and vomiting are symptoms seen in pancreatitis. It is an inflammation of the pancreas (located behind the stomach). Excessive alcohol drinking is most common cause of pancreatitis.…

    • 394 Words
    • 2 Pages
    Good Essays
  • Powerful Essays

    Symptoms of Addison’s disease are slow and progressive but if left untreated may become fatal. Worsening fatigue and muscle weakness, loss of appetite and weight loss are characteristic for this illness. In 50% of cases nausea, vomiting and diarrhoea are present. Skin changes are common – this is when certain areas of the skin (exposed or non-exposed) darken, most common on pressure points. Irritability and depression, salty food cravings, low blood sugar (usually in children) and irregular or no periods, for women, may occur.…

    • 1276 Words
    • 6 Pages
    Powerful Essays
  • Good Essays

    Blood tests may be ordered to check for the presence of antibodies that are common with this illness. The blood test will also be used for evidence of inflammatory conditions, this will show indications of problems with the liver and kidneys. A Schirmer tear test will be used to measure the dryness of the eyes. A slit lamp test may need to be performed by an ophthalmologist, this is a magnifying device where drops are placed in the eye that will make any damage to your cornea easier to see. Certain imaging test can check the function of your salivary glands. A sialogram is used to detect dye injected into the salivary glands located in front of the ears. This will show how much saliva flows into your mouth. A salivary scintigraphy uses an intravenous injection of radioactive isotope, which is track for an hour to show how quickly it arrives in the salivary glands. A lip biopsy may be needed to detect the presence of clusters of inflammatory…

    • 830 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Anemia Case Study Essay

    • 393 Words
    • 2 Pages

    These values are compared to accepted reference ranges to find abnormal values. According to JJ’s lab values, her RBC’s, Hgb and Hct are below the lower end of the reference ranges for all three values. These objective data provide evidence that JJ is anemic. To further classify the anemia and help determine the underlying cause, the MCV can be calculated by using the Hct and RBC values. It is determined that JJ’s MCV is 85 fL/cell, which is within the reference range of normocytic anemia (81-99 fL/cell). As mentioned above, one of the causes of normocytic anemia is acute blood loss. Since her PMH does not mention chronic disease or any other condition that would result in blood loss, the evidence suggests that JJ’s anemic condition is possibly due to acute blood loss during her…

    • 393 Words
    • 2 Pages
    Good Essays
  • Good Essays

    This makes the disease hard to diagnose. There are only a handful of laboratories able to test for celiac and some doctors don't even know about the disease. Recent researchers have found that people with celiac disease have high levels of certain antibodies to gluten such as antigliadin, anti-endomysium, and antireticulum. Doctors test for celiac by testing the levels of these antibodies. If the test shows they have the disease doctors must perform a biopsy testing intestine tissue for damage to the villi. The only definite test for celiac is a gluten-free…

    • 671 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Paper On Crohn's Disease

    • 901 Words
    • 4 Pages

    “People who have experience chronic abdominal pain, diarrhea, fever, weight loss, and anemia may be examined for signs of Crohn’s disease” (Sanford 3). Docter also looks at other aspects such as “medical history and physical examinations, diagnostic procedures for Crohn's disease may include: blood tests, stool culture, endoscopy. Colonoscopy, biopsy, upper GI, or a barium enema” (Sandford 3). Another person that can be of help is called a pediatric gastroenterologist. They can perform a variety of tests that include “complete blood count (CBC), erythrocyte sedimentation rate (ESR), C-reactive protein (CRP)” (Riley Children’s Health 1) which are blood tests. “Hemoccult, calprotectin, culture, clostridium difficult (C.diff)” (Riley Children’s Health 1) which are stool tests. “Small bowel barium x-ray, ultrasound, computed tomography (CT) scan, magnetic resonance imaging (MRI) which are a variety of imaging studies (Riley Children’s Health…

    • 901 Words
    • 4 Pages
    Good Essays
  • Better Essays

    Nicu Rotation Paper

    • 1538 Words
    • 7 Pages

    My patients was exhibiting some respiratory distress symptoms, such as flaring of the nares and tachypnea. She was also exhibiting a sign of hypoglycemia, which is a sign of hypothermia. This was more likely due to the minimal or no fat stores of a preterm infant, which then results in the infant burning more calories and glucose in order to conserve heat, as a result the infant becomes hypoglycemic due to the low level of glucose in the bloodstream. My patient was also showing signs of physiological jaundice, it is common among preterm babies due to an immature liver and inability to conjugate bilirubin. In preterm infants, jaundice…

    • 1538 Words
    • 7 Pages
    Better Essays
  • Good Essays

    Miss

    • 1210 Words
    • 5 Pages

    • Liver disease (possibly presenting as yellowing of the eyes and/or skin), liver failure (very rare),…

    • 1210 Words
    • 5 Pages
    Good Essays
  • Better Essays

    Anemia

    • 1601 Words
    • 7 Pages

    The purpose of this paper is to briefly describe the initial core diagnostic questioning and core set of diagnostic testing related to the patient presenting with anemia. Subjective information and recommended testing are written with consideration of the scope of practice of the family nurse practitioner. In addition, three specific case studies are examined.…

    • 1601 Words
    • 7 Pages
    Better Essays
  • Better Essays

    Sickle Cell

    • 1572 Words
    • 7 Pages

    Sickle Cell Anemia is a hereditary disease that changes the smallest and most important components of the body. A gene causes the bone marrow in the body to make sickled shapes, when this happens; it causes the red blood cell to die faster. This is what causes Hemolytic Anemia. Older children and adults with sickle cell disease may experience a few complications, or have a pattern of ongoing problems that shorten their lives. The most common and serious complications of sickle cell disease are anemia, pain, fatigue, and organ failure. Today there are many alternatives and opportunities that a sickle cell patient may consider. One outlined in this paper is the Hydroxyurea method.…

    • 1572 Words
    • 7 Pages
    Better Essays
  • Better Essays

    Thalassemia Disorders

    • 1913 Words
    • 8 Pages

    Thalassemia is a group of related blood disorders that cause abnormal hemoglobin production. It is a genetic disorder that is recessive; therefore both parents must be carriers to pass on the disorder in its major form. Thalassemia is categorized into two types, major and minor. Individuals suffering from the major form, tend to need frequent blood transfusions in order to survive. (Garrison & Peterson ) Other names for Thalassemia disorders are: Mediterranean Anemia, Sickle Cell Anemia, and Cooley’s anemia (named after the first…

    • 1913 Words
    • 8 Pages
    Better Essays

Related Topics