Question

In: Nursing

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 feet, 6 inches

Questions

  1. What other assessments should be included for this patient? Explain your answers.
  2. Discuss the various types of pain that a patient can experience. Explain your answers.
  3. What type of pain does this patient describe? Explain your answers.
  4. What standards of assessing pain will be applied to this patient’s plan of care? Explain your answers.
  5. Discuss three (3) patient education/teachings that should the nurse consider from the problems list. Explain your answer.
  6. Provide four (4) interventions that should be included in the plan of care for this patient. Explain your answers.

Solutions

Expert Solution

Nightingale answered 1 year ago
Next > < Previous

Related Solutions

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...
O.P is a 15 years old African American adolescent JP is a 16 years old African...
O.P is a 15 years old African American adolescent JP is a 16 years 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; T37, P 80,R 18, BP...
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...
A 13-year-old adolescent with sickle cell disease is being admitted for RBC transfusion therapy. Explain potential...
A 13-year-old adolescent with sickle cell disease is being admitted for RBC transfusion therapy. Explain potential complications from transfusion therapy and the nurse’s role in prevention.
A 13-year-old adolescent with sickle cell disease is being admitted for RBC transfusion therapy. Explain potential...
A 13-year-old adolescent with sickle cell disease is being admitted for RBC transfusion therapy. Explain potential complications from transfusion therapy and the nurse’s role in prevention.
M.Y, an 80 year old asian, american man was diagnosed with Alzheimer’s disease (AD) 3 years...
M.Y, an 80 year old asian, american man was diagnosed with Alzheimer’s disease (AD) 3 years ago. Today his wife brings him to the emergency department because he wandered from his home, fell, and injured his left hip. Subjective data: Can state his name Confused as to place and time Denies memory of wandering or falling Agitated, trying to get up Denies pain Objective Data: Physical examination Left leg shorter than right leg Tense and anxious What precipitating factors may...
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...
Searches related to Ms. Jackson is a 51-year-old African-American patient who has recently been diagnosed with...
Searches related to Ms. Jackson is a 51-year-old African-American patient who has recently been diagnosed with type 2 diabetes mellitus. While the nurse is providing patient teaching about foot care, Ms. Jackson questions why she should be concerned about her feet, and how this relates to type 2 diabetes mellitus. 1. What point should the nurse focus on regarding the importance of foot care for patients with type 2 diabetes mellitus? After 6 months, Ms. Jackson has routine laboratory testing...
S.B. is a 57-year-old African American man with newly diagnosed late-stage small-cell lung cancer. He has...
S.B. is a 57-year-old African American man with newly diagnosed late-stage small-cell lung cancer. He has undergone radiation therapy to the brain for his metastases and is to start chemotherapy next week. His past medical history includes hypertension. He has no known drug allergies. A combination chemotherapy regimen has been chosen: cisplatin 100 mg/m2 for one dose on the first day and etoposide 100 mg/m2 IV every day for 3 days. He has experienced nausea and vomiting. List the specific...
A 32-year-old female patient was diagnosed with sickle cell anemia had complicated recurrent hospital admissions with...
A 32-year-old female patient was diagnosed with sickle cell anemia had complicated recurrent hospital admissions with vaso-occlusive crises and chest syndrome. Lab findings showed normochromic, normocytic mild to moderate anemia. Genetic investigations showed lysine was substituted for glutamine acid at position 6 on some chains and valine instead of glutamine at position 6 on other chains.  What anemia does she have and what are the two genetic (base to base changes) point mutations that cause her disease?
ADVERTISEMENT
Subjects
ADVERTISEMENT
Latest Questions
ADVERTISEMENT