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Sicle Cell Concept Map
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CONCEPT MAP Lucretia Shafer PLU SN 10/09/06 υ Pain r/t SCA AEB pt report, VS υInfection (pneumonia) r/t SC crisis AEB dec lung sounds, ele WBC, cough, sob, dec O2 sats, fever _ PCA, other pain meds _Incentive spirometer use _provide powerade (orange) _O2 while sleeping _ambulate as tolerated _assess vital signs q4h _provide smoking cessation info Severe deep, achy pain esp joints and hand and feet; fatigu;, jaundice (yellow sclerae); chronic anemia; cholelithiasis; pale mucous memb.; priapism, painful swelling of hands and feet is often the first symptom *Blood smear may show sickled cells *Electrophoresis of hemoglobin (shows presence of abnormal hemoglobin) *CBC --dec Hb/Hct, iron, --inc reticulocytes, bilirubin *Skeletal x-rays (bone and joint deformities and flattening) *DNA testing (costly) only needed once υRisk for altered tissue perfusion, peripheral r/t SC crisis AEB pain, swelling, dec cap refill, dusky, cool skin υIneffective mgt of therapeutic regimen r/t knowledge deficits, complexity of illness AEB frequency of episodes, smoking habit, “I don’t know why it happens” _ pt will rpt satisfaction with pain control measures _ infection will not spread during shift _ assess feet and hands for color, circulation, temp, pain, swelling _assess peripheral pulses _assess for pain _admin pain meds, SC meds _assess pt’s level of knowledge about disease(s) _provide printed materials about SC disease _discuss materials with pt _ listen to concerns, questions, fears _ No s/s of ineffective tissue perfusion during shift _Pt will list 5 facts about SC crisis by end of shift → Pneumonia—esp prone to infection because the spleen doesn’t phagocytize foreign substances. Pneumonia is the most common infection with SSA → Gilbert’s Syndrome—a benign, common mild liver disorder in which the liver lacks proper level of the enzyme that processes bilirubin- -can lead to jaundice. Affects 3% to 10% of US pop. → Arnold-Chiari Malformation—a rare malformation of the area where the brain and the spinal cord meet causing part of the cerebellum to protrude out through the foramen magnum into the spinal canal. This impedes the flow of CSF to and from the brain causing it to accumulate in the empty spaces of the brain and spinal cord. It may be present at birth but often it manifests itself at puberty or later. Symptoms include headaches, esp those c/b suddenly coughing, sneezing or straining; neck pain; unsteady gait; vomiting; swallowing difficulties and slurred speech. Dx is made by MRI. Tx is surgery if symptoms are worsening, to relieve the crowding of the cerebellum. ↔ Sickle Cell Crisis Incidence: 1:350 to 500 live births predominant in African Americans The abnormal RBCs sickle most commonly when triggered by low O2 in the blood (hypoxia)—bacterial infection, high altitude, stress, surgery, blood loss, dehydration, acidosis, low body temp. Male, mid-twenties, in for SC crisis, pneumonia, possible PE. Hospital day 11. Back pain, rt foot pain, general achy feeling. Fatigued, yellow sclerae, lungs clear, dim upper left, left sided weakness, numbness r/t Arnold-Chiari malformation. Quiet, no visitors during day. Slept for a good part of the day, ambulated off floor x1. Pain controlled with PCA dilaudid .4 q 8 min., methadone, benadryl, ibuprofin. Sickle cell anemia is the most severe form of an autosomal recessive disorder where the person has inherited HbS from each parent. SC crisis occurs when the RBCs change from a squished disc shape into a sickle shape. The misshapen cells get stuck in the capillaries, causing occlusion, vasospasm leading to tissue injury and hypoxia. Tissue ischemia, infarction and necrosis can eventually result as a result of lack of O2 and circulation. With repeated episodes of sickling, all body organs are impacted, esp spleen, lungs, kidneys, heart and brain leading to autosplenectomy, Pulmonary HT, pneumonia, hematuria, renal failure, CHF and CVA. ↔ Medical Diagnosis Patient’s Story Pathophysiology Diagnostic Workup Clinical Manifestation υ Nursing Diagnosis Etiology & Risk Factors _ Expected Outcome → Secondary Diagnosis _Nursing Interventions Patient’s Medications: Dilaudid Methadone Ibuprofen Folic Acid Benadryl Hydroxyurea Atenolol Discharge Planning: References: 1. Lewis, S. M., Heitkemper, M. M., & Dirksen, S. R. (2004). Medical- surgical nursing: Assessment and management of clinical problems (6th ed.). St. Louis: Mosby. 2. MayoClinic.com (2006). Chiari malformation. Retrieved October 9, 2006 from http://mayo clinic.com /health/chiari-malformation/ AN00506. 3. MayoClinic.com (2006). Gilbert’s syndrome. Retrieved October 9, 2006 from http://mayo clinic.com /health/gilberts-syndrome/ AN00506.
Transcript of Sicle Cell Concept Map
CONCEPT MAP Lucretia Shafer PLU SN 10/09/06
υ Pain r/t SCA AEB pt report, VS
υInfection (pneumonia) r/t SC crisis AEB dec lungsounds, ele WBC, cough, sob, dec O2 sats, fever
_ PCA, other pain meds_Incentive spirometer use_provide powerade (orange)_O2 while sleeping_ambulate as tolerated_assess vital signs q4h_provide smoking cessation info
Severe deep, achy pain esp jointsand hand and feet; fatigu;, jaundice(yellow sclerae); chronic anemia;cholelithiasis; pale mucous memb.;priapism, painful swelling of handsand feet is often the first symptom
*Blood smear may show sickled cells *Electrophoresis of hemoglobin (showspresence of abnormal hemoglobin) *CBC --dec Hb/Hct, iron, --inc reticulocytes, bilirubin *Skeletal x-rays (bone and joint deformitiesand flattening) *DNA testing (costly) only needed once
υRisk for altered tissue perfusion, peripheral r/t SC crisisAEB pain, swelling, dec cap refill, dusky, cool skinυIneffective mgt of therapeutic regimen r/t knowledgedeficits, complexity of illness AEB frequency of episodes,smoking habit, “I don’t know why it happens”
_ pt will rpt satisfaction with pain control measures_ infection will not spread during shift
_ assess feet and hands for color, circulation, temp, pain, swelling_assess peripheral pulses_assess for pain_admin pain meds, SC meds_assess pt’s level of knowledge about disease(s)_provide printed materials about SC disease_discuss materials with pt_ listen to concerns, questions, fears
_ No s/s of ineffective tissue perfusion during shift_Pt will list 5 facts about SC crisis by end of shift
→ Pneumonia—esp prone to infection because the spleen doesn’tphagocytize foreign substances. Pneumonia is the most commoninfection with SSA→ Gilbert’s Syndrome—a benign, common mild liver disorder inwhich the liver lacks proper level of the enzyme that processes bilirubin--can lead to jaundice. Affects 3% to 10% of US pop.→ Arnold-Chiari Malformation—a rare malformation of thearea where the brain and the spinal cord meet causing part of thecerebellum to protrude out through the foramen magnum into thespinal canal. This impedes the flow of CSF to and from the braincausing it to accumulate in the empty spaces of the brain and spinalcord. It may be present at birth but often it manifests itself at pubertyor later. Symptoms include headaches, esp those c/b suddenly coughing,sneezing or straining; neck pain; unsteady gait; vomiting; swallowingdifficulties and slurred speech. Dx is made by MRI. Tx is surgery ifsymptoms are worsening, to relieve the crowding of the cerebellum.
↔ Sickle Cell Crisis
Incidence: 1:350 to 500 live births predominantin African Americans
The abnormal RBCs sickle mostcommonly when triggered by low O2 inthe blood (hypoxia)—bacterialinfection, high altitude, stress, surgery,blood loss, dehydration, acidosis, lowbody temp.
Male, mid-twenties, in for SC crisis,pneumonia, possible PE. Hospital day 11.Back pain, rt foot pain, general achy feeling.Fatigued, yellow sclerae, lungs clear, dimupper left, left sided weakness, numbness r/tArnold-Chiari malformation. Quiet, novisitors during day. Slept for a good part ofthe day, ambulated off floor x1. Paincontrolled with PCA dilaudid .4 q 8 min.,methadone, benadryl, ibuprofin.
Sickle cell anemia is the most severe form of anautosomal recessive disorder where the person hasinherited HbS from each parent. SC crisis occurs whenthe RBCs change from a squished disc shape into a sickleshape. The misshapen cells get stuck in the capillaries,causing occlusion, vasospasm leading to tissue injury andhypoxia. Tissue ischemia, infarction and necrosis caneventually result as a result of lack of O2 and circulation.With repeated episodes of sickling, all body organs areimpacted, esp spleen, lungs, kidneys, heart and brainleading to autosplenectomy, Pulmonary HT, pneumonia,hematuria, renal failure, CHF and CVA.
↔ Medical Diagnosis Patient’s Story
Pathophysiology Diagnostic Workup
Clinical Manifestation υ Nursing Diagnosis
Etiology & Risk Factors _ Expected Outcome
→ Secondary Diagnosis _Nursing Interventions
Patient’s Medications:DilaudidMethadoneIbuprofenFolic AcidBenadrylHydroxyureaAtenolol
Discharge Planning:
References:1. Lewis, S. M., Heitkemper, M. M., &
Dirksen, S. R. (2004). Medical-surgical nursing: Assessment andmanagement of clinical problems(6th ed.). St. Louis: Mosby.
2. MayoClinic.com (2006). Chiari malformation. Retrieved October 9, 2006 from http://mayo clinic.com/health/chiari-malformation/AN00506.
3. MayoClinic.com (2006). Gilbert’s syndrome. Retrieved October 9, 2006 from http://mayo clinic.com/health/gilberts-syndrome/AN00506.
