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The document provides information on managing sickle cell anemia including:
- Nursing assessments would include family history, reports of pain/crisis and monitoring vital signs, pain levels, and lab results.
- Vaso-occlusive crises present with severe pain and other acute symptoms while chronic complications include organ damage.
- Nursing care focuses on pain management, oxygen therapy, hydration, infection prevention, and monitoring for complications.
- Client education covers signs of crisis, importance of rest/nutrition, medication management, and genetic counseling.
The document provides information on managing sickle cell anemia including:
- Nursing assessments would include family history, reports of pain/crisis and monitoring vital signs, pain levels, and lab results.
- Vaso-occlusive crises present with severe pain and other acute symptoms while chronic complications include organ damage.
- Nursing care focuses on pain management, oxygen therapy, hydration, infection prevention, and monitoring for complications.
- Client education covers signs of crisis, importance of rest/nutrition, medication management, and genetic counseling.
The document provides information on managing sickle cell anemia including:
- Nursing assessments would include family history, reports of pain/crisis and monitoring vital signs, pain levels, and lab results.
- Vaso-occlusive crises present with severe pain and other acute symptoms while chronic complications include organ damage.
- Nursing care focuses on pain management, oxygen therapy, hydration, infection prevention, and monitoring for complications.
- Client education covers signs of crisis, importance of rest/nutrition, medication management, and genetic counseling.
List 3 Things for Which the Nurse Would Assess/Monitor Care After Discharge - List 3 Teaching/Reinforcement Items to be Instructed
Vaso-Occlusive Crisis Nursing Care
List 3 Manifestations for Each, Acute and Chronic Conditions List 3 Nursing Actions Acute Conditions Chronic Conditions
Pain Management Laboratory Tests
List the Medications That List the 3 Labs Tests That Will be Done Should be Used for Pain
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Concept Map: Sickle Cell Anemia Management Subjective and Objective Data Client Education List 3 Things for Which the Nurse Would Assess/Monitor Care After Discharge - List 3 Teaching/Reinforcement • Impaired healing, • Family history of sickle cell • Lethargy, irritability, and • Systolic heart murmur Items to be Instructed loss of skin anemia or sickle cell trait muscle weakness and heart failure elasticity, and • Reports of pain, crisis, and • Abdominal pain, nausea, • Shortness of thinning of hair management vomiting, and loss of appetite breath/fatigue • Provide emotional support, • Tachycardia • Pallor or jaundice • Nail bed deformities and refer to social services • Low-grade fever if appropriate. • Instruct in signs and Vaso-Occlusive Crisis Nursing Care symptoms of crisis and List 3 Manifestations for Each, Acute and Chronic Conditions List 3 Nursing Actions infection. • Advise the family of the Acute Conditions Chronic Conditions • Promote rest to importance of promoting • Severe pain, • Swollen joints, • Increased risk of • Systolic murmurs decrease oxygen rest and adequate nutrition usually in hands, and feet respiratory • Renal failure and consumption of the for the child. bones, joints, • Hematuria infections and/or enuresis tissue • Encourage the child and and abdomen • Obstructive osteomyelitis • Liver failure • Administer oxygen as family to maintain good • Anorexia, jaundice • Retinal • Seizures prescribed if hypoxia hand hygiene and avoid vomiting, and • Visual detachment and • Deformities of is present individuals with fever disturbances blindness the skeleton • Maintain fluid and colds/infection/viruses. electrolyte balance • Give specific directions Pain Management Laboratory Tests • Administer/monitor regarding fluid intake List the Medications That List the 3 Labs Tests That Will be Done blood products (RBCs) requirements, such as how Should be Used for Pain • Observe for signs of many bottles or glasses of • CBC to detect anemia hypervolemia and fluid should be consumed • Treat mild to moderate pain with • Hgb electrophoresis – Separates the transfusion reaction daily. acetaminophen or ibuprofen various forms of Hgb and is the • Treat and prevent • Provide information about • Manage severe pain with opioid definitive diagnosis of sickle cell anemia infection genetic counseling. analgesics; Administer orally or • Sickledex (sickle solubility test) – A • Monitor and report • Encourage maintenance of by IV route screening tool that will detect the laboratory results up-to-date immunizations. • Apply comfort measures, such as presence of HbS but will not • Encourage passive • Advise the child to wear a warm packs to painful joints differentiate the trait from the disease. range –of – motion medical identification exercises to prevent wristband or medical venous stasis identification tags.