Advancing Health Equity in North Carolina

Page 53

Additional Considerations

Adjustment of PHP contracts to cover RBC molecular antigen testing is a short-term investment. NC Medicaid can look to Blue Cross NC’s medical policy for language regarding the scope of coverage. Blue Cross NC recommends two FDA-approved panel test systems— BLOODchip® ID CORE XT™ by Grifols Diagnostic Solutions Inc. and PreciseType® HEA Test by Immuncor, Inc.—that are appropriate for patients with SCD who require frequent transfusions.265

3.4 Transcranial Doppler Ultrasonography NC Medicaid should facilitate annual transcranial doppler ultrasonography (TCD) screening for children with SCD aged 2 to 16. Implementation: • NC Medicaid should remove prior authorization requirements for TCD. • NC Medicaid should reimburse PHPs to coordinate care between radiologists and SCD clinics and training of SCD clinical staff to perform TCD screening. Background

Annual TCD screening is standard for children with SCD aged 2 to 16. TCD identifies those individuals who need transfusions, which in turn reduces their risk of stroke.266 If left untreated, approximately 11 percent of children with SCD will experience a stroke by age 20, a rate 250 times higher than the child population at large.267 Nationally, TCD screening rates among Medicaid patients are under 40 percent.268 Patient-related barriers to annual TCD screenings include inadequate transportation, duration of clinic visits, missed appointments, lack of awareness of the need for annual screenings, and mistrust of the procedure.269 Provider-related barriers include lack of awareness that TCD should begin at age 2, expectations that children will be uncooperative, lack of motivation, and poor coordination.270 North Carolina Context

As of February 2021, NC Medicaid covers TCD screening, however, the screening requires prior authorization, even for children.271 This prior authorization requirement results in an unnecessary barrier and burden to care. In many clinics, TCD screenings are managed

Part II. Sickle Cell Disease Recommendations 53


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5. Administrative Burden

5min
pages 77-80

Endnotes

52min
pages 84-104

Appendix: Implementation Considerations

1min
pages 82-83

2.2 Group Prenatal Care

4min
pages 70-71

4. Quality Measures

2min
page 76

3.2 Screening of Perinatal Mental Health Conditions

3min
pages 74-75

3.3 Red Blood Cell Molecular Testing

2min
page 52

5.2 Subscription-Based Payment Models

5min
pages 60-62

3.4 Transcranial Doppler Ultrasonography

3min
pages 53-54

3.2 Pain Management

4min
pages 50-51

4.2 Quality Measures

4min
pages 56-57

1.2 Postpartum Continuity of Care

4min
pages 65-66

2.2 Sickle Cell Day Hospitals

6min
pages 46-48

1.3 DPH Existing Programs

2min
page 43

5. Data Gaps

3min
pages 36-37

Executive Summary

1min
page 9

2. Transportation

5min
pages 30-31

3. Provider Bias Training

4min
pages 32-33

Introduction

2min
page 12

4. Non-Medical Drivers of Health

4min
pages 34-35

1.2 Primary and Specialty Care Coordination

3min
pages 41-42

Summary of Recommendations

3min
pages 10-11
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