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QUESTION

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

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 the selected disorder.

Course Competency(s):

·         Compare pathophysiologic alterations that affect the hematologic disorder and cardiovascular systems.

Instructions:

Using the concept map, select a hematologic disorder and complete the fields included on the map.

1.       Include the pathophysiology of the hematologic disorder

2.       Explain the etiology of the hematologic disorder

3.       Describe the clinical manifestations of the hematologic disorder

4.       Provide the treatment for the hematologic disorder

Use two evidence-based articles from peer-reviewed journals or scholarly sources to support your findings. Be sure to cite your sources in-text and on a References page using APA format.

Resources:

You can find useful reference materials for this assignment in the School of Nursing guide:

https://guides.rasmussen.edu/nursing/referenceebooks

Have questions about APA? Visit the online APA guide: https://guides.rasmussen.edu/apa

Grading Rubric:

Levels of Achievement

Criteria

Emerging

Competence

Proficiency

Mastery

Pathophysiology

(15 pts)

Did not include discussion on the pathophysiology the hematologic disorder.

Failure to provide the pathophysiology will result in zero points for this criteria.

Briefly identified the pathophysiology of the hematologic disorder.

Clearly identified the pathophysiology of the hematologic disorder.

Thoroughly identified the pathophysiology of the hematologic disorder.

Points: 10

Points: 13

Points:  14

Points: 15

Etiology

(15 pts)

Did not include discussion on the etiology of hematologic disorder.

Failure to provide the etiology will result in zero points for this criteria.

Briefly discussed included etiology of the hematologic disorder.

Clearly discussed etiology of hematologic disorder.

Thoroughly discussed etiology of hematologic disorder.

Points: 10

Points: 13

Points: 14

Points: 15

Clinical Manifestation

(10 pts)

Did not provide examples of the clinical manifestations of the hematologic disorder.

Failure to provide clinical manifestations will result in zero points for this criteria.

Briefly provided clinical manifestations of hematologic disorder.

Clearly provided clinical manifestations of hematologic disorder. 

Thoroughly provided clinical manifestations of hematologic disorder.

Points: 6

Points: 8

Points:  9

Points: 10

Treatment

(5 pts)

Did not present treatment for the hematologic disorder.

Failure to provide treatment for hematologic disorder will result in zero points for this criteria.

Briefly provided treatment options for the hematologic disorder.

Clearly provided treatment options for the hematologic disorder.

Thoroughly provided detailed treatment for the hematologic disorder.

Points: 2

Points: 3

Points: 4

Points: 5

APA, Spelling and Grammar

 (5 pts)

Six or more APA, spelling or grammar errors.  Detracts from the readability of the submission. 

No more than five APA, spelling or grammar errors, minimally detracts from the readability of the submission. 

No more than three APA, spelling or grammar errors.  Does not detract from the readability of the submission. 

No APA, spelling or grammar errors.

Points: 2

Points: 3

Points: 4

Points: 5

Points:  30

Points:  40

Points:  45

Points:  50

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ANSWER

Hematological Disorder Concept Map.

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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