Sickle Cell Care Plan 2025

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  1. Click ‘Get Form’ to open the Sickle Cell Care Plan in the editor.
  2. Begin by entering the student's name, date of birth, and grade in the designated fields. This information is crucial for identifying the student and ensuring proper care.
  3. Fill in the parent’s name and contact information, including phone and cell numbers. This allows for quick communication in case of emergencies.
  4. Complete the emergency contact section with a name and phone number. This ensures that someone can be reached if you are unavailable.
  5. In the Daily Medications section, list any medications prescribed along with dosage and timing. Include common side effects and special instructions as provided by the physician.
  6. Review the Maintenance Plan carefully. Ensure that all necessary accommodations for hydration, bathroom access, and signs of crisis are noted.
  7. Finally, have both parents sign and date the form, along with a certified school nurse's review signature to finalize the care plan.

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Management of sickle cell anemia is usually aimed at avoiding pain episodes, relieving symptoms and preventing complications. Treatments might include medicines and blood transfusions. For some children and teenagers, a stem cell transplant might cure the disease.
It can include special heating pads to help relieve excessive pain, Gatorade to replenish electrolytes and hydrate the patients body, thermometer, pain relieving topical medications, blanket, water bottles, hygiene packs, notebooks, pens, pencils, etc, and, Hospital Parking Assistance for two (2) weeks to the SCD
The UCP aims to improve healthcare outcomes for sickle cell patients by enabling patients to feel confident that healthcare professionals looking after them will have access to important information including individualised care plans, regardless of which hospital in London they attend.
Nursing Problem Priorities Prevent dehydration to help prevent vaso-occlusive crises and other complications. Ensure adequate oxygenation through supplemental oxygen therapy. Implement infection control measures to minimize the risk of infections, which can trigger sickle cell crises.
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