Estimating the Pain Rate in a Patient with Sickle Cell Disease Using the Equation of Platt et al

Purpose: To estimate a patient's "pain rate" using 4 clinical findings and the equation of Platt et al.

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Evaluation

Are you evaluating a patient with sickle cell disease?

Yes

Age of the patient

years

Gender of the patient

Male

Female

Fetal hemoglobin (enter from 0 to 100)

percent

Hematocrit (enter from 0 to 100)

percent

Results

Please fill out required fields.

Results Interpretation and Description References Next Steps

Data complete?

Evaluation appropriate?

Value for X

Estimated pain rate

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Interpretation and Description

References

Next Steps in Evaluation

Diagnosis

Risk Factors
Clinical Diagnosis, Including Family History For Genetics
- Severity Index of Wali et al for a Child with Sickle Cell Disease (SCD)
- Index of van den Tweel et al for Severity of Sickle Cell Disease (SCD) in a Pediatric Patient
Laboratory Tests
- Model of Miller et al for Predicting the Risk of Severe Complications in a Child with Sickle Cell Disease
Criteria For Diagnosis
- Index of van den Tweel et al for Severity of Sickle Cell Disease (SCD) in a Pediatric Patient
Severity, Prognosis, Stage
Complications

Societal Concerns

Economic Cost
- Factors for Hospital Readmission in Adult with Acute Sickle Cell Pain

Specialty

Hematology Oncology
Clinical Laboratory
Genetics

Objective

risk factors
severity
prognosis
stage
complications

ICD-10

D57 - Sickle-cell disorders

Info

Purpose: To estimate a patient's "pain rate" using 4 clinical findings and the equation of Platt et al.

Specialty: Hematology Oncology, Clinical Laboratory, Genetics

Objective: risk factors, severity, prognosis, stage, complications

ICD-10: D57,

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