"Sickle cell anemia nursing care plan" Essays and Research Papers

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    Nursing Care Plan

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    ASSOCIATE DEGREE NURSING NURSING PROCESS FORM: PART I – ASSESSMENT Student: Date of Care: 3/4/13 Client’s Initial: WB Room # 1011 Occupation: Teacher Age: 59 Sex: F Race: Black Religion: Christian Admission Date: 3/1/13 Primary Language: English Role in family: Widowed from husband Stage in Life Cycle: Generativity vs. Stagnation Surgery date(s) this admission: N/A Chief complaint: Brain Dysfunction/Traumatic‚ closed injury Admission Diagnosis:

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    Cues Nursing Problem Scientific Reasoning Planning Implementation Evaluation Subjective: >”Nay‚ kelan po tayo uuwi?” as verbalized by the patient >”Nag-aaya na nga syang umuwi.” as verbalized by the caretaker Objective: >Patient is silent when hospital staff is around >Patient does not have eye contact with the hospital staff Fear related to hospitalization as manifested by alteration in behavior. Hospitalization is usually perceived as a threat that is consciously

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    NURSING DIAGNOSIS GOAL INTERVENTIONS RATIONALE EVALUATION impaired Gas Exchange R/T STG: 3/17/2014 throughout shift 1. Auscultate breath sounds 1. Abnormal breathing STG: PT O2 saturation on admission abnormal breathing AEB PT will maintain O2 saturation noting areas of decreased sounds are indicative was 87%. Measured at 1602 with a Objective: use of wall oxygen of 95 or higher AEB breathing sounds of numerous problems reading of

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    Sickle-Cell Disease Greatly affecting the body’s oxygen levels due to mutated red blood cellssickle-cell disease‚ influences an individual’s childhood in multiple ways: cognitive‚ social‚ emotional‚ and physical development. Sickle-cell disease (SCD) refers to an inherited disorder where abnormal hemoglobin is present in one’s red blood cells. Hemoglobin is the protein in red blood cells responsible for carrying oxygen throughout the body. The deformed sickle hemoglobin in people with SCD can form

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    Sickle-cell disease‚ also known as sickle-cell anaemia‚ is a hereditary blood disorder‚ caused by an abnormality in the oxygen-carrying protein hemoglobin found in red blood cells. This leads to a propensity for the cells to assume an abnormal‚ rigid‚ sickle-like shape under certain circumstances. Sickle-cell disease is associated with a number of acute and chronic health problems‚ such as severe infections‚ attacks of severe pain‚ stroke‚ and an increased risk of death. Sickle-cell disease occurs

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    2011‚ “Cephalosporins are semisynthetic antibiotics widely used in clinical practice. They are structurally and pharmacologically related to the penicillins. Like penicillins‚ cephalosporins are bactericidal and work by interfering with bacterial cell wall synthesis. They also bind to the same penicillin-binding proteins inside bacteria” (p.594). Medication Trade Name: Ancef Generic Name: cefazolin Indications and Usage: Upper‚ lower respiratory tract‚ urinary tract‚ skin infections;

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    N.C.P 1 Nursing Care Plan Catherine Traylor F.H. January 31‚2007 Karen Ruffin Mercer County Community College 2 Abstract F.H. is an 83 year old male‚ whom was cared for on January 31‚2007 by the writer. He was admitted to Capital Health System at the Mercer Campus with diagnoses of an

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    A payment status of IN PROCESS means your payment is still being processed. A payment status other than PAID indicates that the Department of State has not received your payment. If you receive a notice that your case has entered termination do not attempt to pay any fees. You must contact the NVC immediately to resume processing of your petition. NVC contact information can be found at http://travel.state.gov/visa/immigrants/info/info_3177.html. Next Steps 1. When the IV fee payment status is

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    Case Study 97 1. Sickle cell disease is a group of disorders that affects hemoglobin‚ the molecule in red blood cells that delivers oxygen to cells throughout the body. People with this disorder have atypical hemoglobin molecules called hemoglobin S‚ which can distort red blood cells into a sickle‚ or crescent‚ shape. SCD affects millions of people worldwide‚ particularly those with African‚ Spanish‚ Mediterranean‚ and Indian ancestry. Some 120‚000 infants are born with SCD every year worldwide

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    CDC‚ sickle cell disease is a hereditary disease where the red blood cells have an unusual shape that prevents them from moving easily through the blood vessels and satisfying their metabolic needs causing them to die faster. People with sickle cell disease often experience pain due to the sickle cell blocking the small blood vessels‚ anemia due to the low healthy blood cell count‚ and infections. Although it is impossible to obtain accurate information about everyone that has the sickle cell disease

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