Question

In: Nursing

An African American young adult is admitted to the emergency department in sickle cell crisis with...

An African American young adult is admitted to the emergency department in sickle cell crisis with a report of 10/10 pain. The patient is known to several of the nurses and physicians in the department who have labeled the patient as a “drug seeker”.

Initial Discussion Post:

  • Identify one (1) intervention that can be taken by the RN to reduce the stigma and improve management of acute and chronic pain associated with sickle cell disease.
  • Does the intervention apply only to the patient? Does it apply only to the interprofessional team? Does it apply to both the patient and the members of the interprofessional team? Explain and support your answer.

Solutions

Expert Solution

The RN will have to raise awareness and sensitivity through case presentations or role plays in her ward to understand and empathize with the person with sickle cell disease. She will have to sensitize them about the intensity of pain the young adult is going through, to be observant to any complications and to treat the adult as a person needing our help and support rather than giving a label of a drug seeker. She will have to focus on improving the communication of the healthcare personnel with the patients.

This applies to the patient and the entire healthcare team who comes across patients needing our care and support. A well-educated nurse will set goals and outcomes and ensures the potential for reducing health-related stigmatization and improving the pain management experience for the patients. They will help them not only improve their self-esteem but also help them in building a coping mechanism.


Related Solutions

A patient is admitted to the hospital in sickle cell crisis. The orders from the physician...
A patient is admitted to the hospital in sickle cell crisis. The orders from the physician include: IV D5W/ ½ NS at 150 cc/hr Zofran 8 mg IV q8h Morphine sulfate 5 mg IV prn Calculate how many mg/day of Hydrea will be given PO to the patient weighing 125 lb.  
A patient is admitted to the hospital in sickle cell crisis. The orders from the physician...
A patient is admitted to the hospital in sickle cell crisis. The orders from the physician include: IV D5W/ ½ NS at 150 cc/hr Zofran 8 mg IV q8h Morphine sulfate 5 mg IV prn Hydrea 10 mg/kg/day PO Folic acid 0.5 mg daily PO Calculate cc/hr to set the IV pump to infuse Zofran 8 mg. Supply: Zofran 8 mg added to 50 cc D5W to infuse over 15 min.
Patient Profile G.N., a 65-year-old African American man, was admitted to the hospital emergency department with...
Patient Profile G.N., a 65-year-old African American man, was admitted to the hospital emergency department with partial-thickness burns that involved his face, neck, and upper trunk. He also had a lacerated right leg. His injuries occurred about 36 hours earlier when he fell out of a tree onto his gas grill (which was lit) while trimming tree branches. Subjective Data • Complains of slightly hoarse voice and irritated throat • States that he tried to treat himself because he does...
Neurology Assignment 4 A previously well 16-year-old African-American young man presented to the Emergency Department (ED)...
Neurology Assignment 4 A previously well 16-year-old African-American young man presented to the Emergency Department (ED) with persistent vomiting, severe headaches, and decreased energy of 5 weeks duration. Five weeks earlier, the patient had presented to his pediatrician with headache and vomiting. He was treated with oral amoxicillin for presumed streptococcal pharyngitis, but the group A Streptococcus antigen test was negative. Three weeks later, he presented to a local ED with worsening nausea, vomiting, dizziness, poor oral intake, worsening headaches,...
Tom Denton, a young adult male, is brought into the emergency department with a GI bleed....
Tom Denton, a young adult male, is brought into the emergency department with a GI bleed. He is vomiting blood, hypotensive, pale, and diaphoretic, and his pulse is weak and thready. He is alert enough to hear Sharon Hynes, the ED physician, order a type and cross for four units of blood. Mr. Denton interrupts and states that he does not want the blood transfusion because of personal beliefs. Dr. Hynes orders volume-expanding agents to be used instead. Mr. Denton’s...
I.T. is an 18-year-old African American male with sickle cell anemia who presents with a one-...
I.T. is an 18-year-old African American male with sickle cell anemia who presents with a one- day history of increasing pain localized to his arms and legs. His pain has not been relieved with 400-mg ibuprofen every 6 hours for the past 24 hours. He rates his current pain inten- sity level as 8 out of 10. He reports that he always seems to have some pain in his arms, legs, and back, but the pain intensified approximately 36 hours...
Describe the pathophysiology of sickle cell disease.•Discuss factors that can precipitate a sickle cell crisis.•Create a...
Describe the pathophysiology of sickle cell disease.•Discuss factors that can precipitate a sickle cell crisis.•Create a care plan for the patient presenting in sickle cell crisis.•Prioritize assessments and interventions for thepatient in sickle cell crisis.•Discuss the rationale for common medications and interventions used to treat sickle cell crisis.•Discuss pain management recommendations for the patient in sickle cell crisis.•Create an education plan for the patient being discharged following hospitalization for sickle cell crisis.•Describe common complications of sickle cell disease.•Discuss the rationale...
J.P. is a 15-year-old African American adolescent who was diagnosed with sickle cell disease 3 years...
J.P. is a 15-year-old African American adolescent who was diagnosed with sickle cell disease 3 years ago. J.P. presents to the emergency department with pain related to a sickle cell crisis. Subjective Data Pain level is an 8/10 location = bilateral legs, described as deep muscle pain A student in 10th grade, honor roll student On the track team Lives with mother and father Objective Data Vital signs: T 37 P 80 R 18 BP 140/68 Weight: 140 HT: 5...
J.P is a 15-year-old African American adolescent who was diagnosed with sickle cell disease 3 years...
J.P is a 15-year-old African American adolescent who was diagnosed with sickle cell disease 3 years ago. J.P. presents to the emergency department with pain related to sickle cell crisis. Subjective Data Pain level is an 8/10 location = bilateral legs, described as deep muscle pain Student in 10th grade, honor roll student On the track team Lives with mother and father Objective Data Vital signs: T 37 P 80 R 18 BP 140/68 Weight: 140 HT: 5 feet, 6...
If the proportion of an African population that are carriers of the Sickle Cell allele (HbS)...
If the proportion of an African population that are carriers of the Sickle Cell allele (HbS) is 0.409, what is the HbS allele frequency in the population? NOTE: You may get more than one solution for this question. If so, choose the smaller frequency. A. 0.652. B. 0.252. C. 0.060. D. 0.622. E. 0.287.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT