Which diagnostics fit an integrative or functional practice?
WAVi brain assessment, TM-Flow autonomic and vascular testing, Max Pulse pulse wave screening, and provider-ordered genetic panels through PreCheckHealth. WAVi is FDA 510(k) cleared (K213900) to aid in diagnosis, not to diagnose any condition on its own, and runs in about twenty minutes; TM-Flow is built on three FDA 510(k)-cleared modules and runs chairside in about ten minutes. Each is ordered when clinically indicated, never on a schedule.
Is integrative testing covered?
Coverage for WAVi and TM-Flow is decided by your payer on the documented indication, so confirm every code with your own certified coder before you bill. TITN recommends no code for TM-Flow; your contractor and plan decide. Max Pulse and the Hue Light BAHI suite are cash pay. PreCheckHealth bills the genetic panels directly, including insurance billing where a panel is covered.
Is nutrigenomic or genetic panel testing scientifically validated?
It is mixed, and worth saying plainly. Federal reviewers have described gene-diet science as promising but not ready for prime time, and published work has found a lack of definite gene-diet-disease associations for many commonly tested genes. Multi-gene panels typically mix genes with established clinical utility and genes with limited evidence, so read a given result for its own evidence base rather than treating the whole panel as equally actionable.
How do pharmacogenomic results compare with CPIC guidance?
Published comparisons have found real discordance between commercial laboratory interpretations and CPIC's peer-reviewed gene-drug guidance in a meaningful share of cases. Cross-reference CPIC directly before you act on a PharmacoCheck+ result for a specific gene-drug pair, and treat the panel as one input the prescriber weighs alongside the clinical picture, not a final answer.
Is autonomic or HRV testing useful for chronic fatigue and stress evaluations?
Heart rate variability has documented value in describing autonomic function, and TM-Flow captures it as a measured index alongside sudomotor and vascular data. The honest limits: HRV measurement carries real standardization variability across studies and settings, and it is not a validated root-cause diagnostic for chronic fatigue. Use it as a baseline you can retest on the same protocol, interpreted by the clinician.
Are hyperbaric and light therapy suites evidence-based treatments?
The four Hue Light BAHI devices, the PBM bed, H-2000 hydrogen, H-Bot hyperbaric, and Wave Motion vibration, are positioned under the FDA General Wellness policy for low-risk products. They are not FDA cleared, they are cash pay, and they are not for the diagnosis, treatment, cure, or prevention of any disease. Blood circulation, antioxidant, hormonal balance, and immunity are the manufacturer's framing, not TITN claims.
Who reads and signs the reports?
Board-certified neurologists at BMTG read WAVi and TM-Flow autonomic data and return one interpreted report through TITN's HIPAA-compliant portal, so your practice does not need an in-house reader. A board-certified neurologist signs the conclusion. The Cognitive Function Report documents measured data a clinician interprets; it does not diagnose mild cognitive impairment or any other condition.
How much staff training does this add?
A trained technician runs both scans, not the physician, and TITN provides the onboarding on device operation, software, and workflow. Consistent placement and protocol are what make a retest a real comparison, so the training is mostly about running the same protocol the same way every visit. Adequate patient volume and room space are the usual gating factors for any in-office testing program.
