Aurora Burlington Charges $785 for Cytogenetics Breakage Syndrome Procedure

Cost Breakdown

• Chromosome analysis laboratory work
• Specimen collection and preparation
• Professional interpretation and reporting

The $785 fee generally includes the above components. Additional costs may arise if further genetic counseling, follow-up tests, or physician consultations are needed.

Associated Costs

• Initial physician consultation (not always included in procedure fee)
• Follow-up appointments to discuss results
• Genetic counseling services
• Additional laboratory tests, if recommended

Insurance & Payment Advice

• Check with your insurance provider to determine if the Cytogenetics Breakage Syndrome Procedure is covered and whether pre-authorization is required.
• Ask the hospital for an itemized estimate and clarification of any separate billing for physician or facility services.
• Inquire about financial assistance or payment plans if you are uninsured or have a high deductible.

Recovery Tips & Considerations

• The procedure itself involves a simple blood sample or tissue collection and does not require recovery time.
• Discuss any concerns about the procedure, such as discomfort from blood draws, with your provider.
• Plan for a follow-up visit to review results and discuss next steps based on the findings.

Frequently Asked Questions

• What is included in the $785 charge?
  The fee usually covers laboratory processing, chromosome analysis, and the interpretation/reporting of results. Consultation and follow-up costs may be billed separately.
• Will my insurance cover the Cytogenetics Breakage Syndrome Procedure?
  Coverage varies by plan. Contact your insurer to confirm benefits, requirements for pre-authorization, and any out-of-pocket responsibilities.
• Are there additional costs I should expect?
  Yes, you may incur charges for initial consultations, follow-up appointments, genetic counseling, or further testing if recommended.
• How is the procedure performed?
  Typically, a blood sample or tissue specimen is collected and sent to a specialized lab for chromosomal analysis.
• What conditions can be diagnosed with this test?
  Genetic syndromes associated with increased chromosome breakage, such as Fanconi anemia and others, can be identified through this procedure.
• How long does it take to receive results?
  Results may take several days to a few weeks, depending on the complexity of the analysis and laboratory workload.
• Is the procedure painful?
  The procedure generally involves only minor discomfort, similar to a routine blood draw.
• Do I need to prepare in advance for the test?
  No special preparation is usually required, but follow any instructions provided by your healthcare team.
• Can I get financial assistance for this procedure?
  Many hospitals offer financial assistance or payment plans. Inquire with the billing department if you are uninsured or concerned about costs.
• Who interprets the test results?
  A specialist in genetics or pathology will analyze and interpret the findings, providing a detailed report to your referring physician.
• What should I do after I receive the results?
  Schedule a follow-up appointment with your doctor or genetic counselor to discuss the implications of the findings and plan any necessary next steps.