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Sickle Cell Disease with Pain Clinical Pathway – Emergency Department and Inpatient – History and Physical

Sickle Cell Disease with Pain Clinical Pathway – Emergency Department and Inpatient

History and Physical

Carefully assess for other causes of pain as well as complications that can be associated with vaso-occlusive event (VOE).

Consider Stroke Protocol:

  • Severe or typical HA
  • Altered mental status
  • Focal neurologic findings
  • New seizure
History
  • Pain Assessment
    • Time of onset
    • Pain characteristics typical of previous VOE?
    • Location, quality, duration, intensity
  • Analgesics
    • Medications used
    • Frequency, dose, time of last dose
    • Usual pain regimen
    • Medications that work best for individual child
    • Non-pharmacologic interventions that help
      • Heat, blankets, distractions
    • Chronicity
      • Pain most days?
  • Complications of Sickle Cell Disease
    • Acute chest syndrome
    • Aplastic crisis (parvovirus Infection)
    • Documented bacteremia
    • Stroke, transient ischemic attack
    • Splenic sequestration
    • Gall bladder disease
    • Osteomyelitis, septic arthritis
    • Pulmonary embolism
    • Priapism
  • Past Medical History
    • Baseline pulse oximetry reading
    • Previous admissions, ICU admissions
    • Transfusion history
    • Vaccination history, including Prevnar
  • Medications
    • Penicillin prophylaxis
    • Hydroxyurea
    • Folic acid
    • Chronic pain medications
    • L-glutamine
    • Voxelotor
    • Crizanlizumab
  • Allergies
Physical
  • VS, pulse oximetry reading
  • General appearance, jaundice, pallor
  • Pain assessment
  • Respiratory, circulatory, neurologic status
  • Evidence of focal infection
  • Spleen size
  • Presence of rash or petechiae
  • Neurologic signs
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