Title of Assignment: Hematologic Disorder Concept Map Purpose of Assignment: The purpose of the assignment is to identify and analyze a hematologic disorder and process the possible manifestation of

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Hematological Disorder Concept Map.

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Student’s Name.

Institutional Affiliation(s).

Objective:

To investigate the presence of a defective mutation found in the blood for a possible cause of sickle cell anemia.

Focused assessment:

·         Identification of factors that might have led to previous causes.

·         Determining pain levels.

·         Observing the characteristics of pain.

·         Elevated acid phosphates.

·         Evaluation of kidney damage

·         Identifying abnormal hemoglobin types

Hematological Disorder Concept Map.

·         Past family history.

·         Race.

·         Protects against malaria development.

(Frédéric B. Pie, 2017)

Medical Condition: Sickle Cell Anemia.

A blood test to check the defective hemoglobin.

·         Pain easing medications.

·         L-glutamine Oral powder.

·         Blood transfusion.

·         Chemotherapy.

·         Vitamins.

(Quinn, 2017)

Assessment

Lab Tests

Subjective: It results through point mutation that results from a change in one nucleotide found in the gene in regards to hemoglobin.

Sample blood is drawn from the vein in the arm in adults and from a finger in children.

Subjective& Objective Data

Risk Factors

Diagnostic

Procedures

Safety Considerations

·         Avoidance of alcohol.

·         Avoid seeking care in multiple facilities.

·         Avoidance of cigarettes and smoking drugs.

Medications

Nursing

Interventions

Inter-disciplinary

Care

·         Monitor the rate of respiratory.

·         Monitor vital signs and make notes on cardiac rhythm.

Collaborative Care

Potential Complications/

·         Possible Eye damage.

·         Hypertension.

·         Blindness.

·         Ulcers in the leg.

·         Gallstones.

·         Possible stroke.

(Klings, 2016)

·         Drinking a lot of water.

·         Exercising regularly.

·         Keeping away from extreme temperatures.

Care After

Discharge/Education

Other interventions

Planning Client Outcomes

·         Ensuring that proper maintenance has been followed.

·         Make follow-ups with the client.

·         Performing regular blood tests.

·         Balanced bed rest and exercise.

·         Getting regular medical check-ups.

·         Taking prescribed medicines.

·         Staying hydrated.

·         Assess levels of consciousness.

·         Encourage continuous fluid intake.

·         Provide oxygen as required.

References

Frédéric B. Pie, M. H. (2017). Sickle Cell Disease. The New England Journal of Medicine, 1561-1567.

Klings, A. M. (2016). Chronic Pulmonary Complications of Sickle Cell Disease. CHEST Journal, 1313–1324.

Quinn, C. T. (2017). Glutamine for sickle cell anemia: more questions. Blood Journal Organization, 689-691.



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