Pediatric Breath Testing for SIBO & IMO from Commonwealth Diagnostics International

The $699 registered cost, $299 maximum out-of-pocket statement, insurance categories, Medicaid exclusion, financial assistance, and invalid-test billing terms are stated for the breath-test program. Refund or cancellation language and one consistent billing code are not available.

The 6 Tube Lactulose route captures serial hydrogen and methane over 90 minutes for the declared pediatric SIBO or IMO question. The current pediatric sources do not provide a complete report scope, additional gas coverage, or a pediatric-specific limitation map.

The product is explicitly labeled for pediatric SIBO and IMO evaluation and provides a pediatric lactulose hydrogen and methane route. CDI's own clinical-correlation and medical-advice limits mean the test supports, but does not independently establish, a diagnosis or treatment plan.

A CDI sample report explains values, CO2 correction, cutoffs, supported or not-supported outcomes, and clinical correlation, but it is an adult 10 specimen report. Pediatric report fields, pediatric cutoffs, and current family access are therefore unresolved.

The pediatric collection route, gas targets, sample timing, CO2 quality controls, and provider-reported GC characteristics are documented. Pediatric-specific validation evidence and a current active credential are not established because the displayed credential documents expired before review.

Provider ordering, shipment to the office or home, home collection, prepaid return shipping, provider result delivery, and one to two business-day reporting are described. Pediatric age eligibility, state availability, preparation burden, and conflicting sample-validity guidance remain material practical uncertainties.

The HIPAA notice provides meaningful PHI uses, rights, research conditions, business-associate rules, and breach obligations. The website policy allows broad site-data sharing and indefinite useful retention, while pediatric-specific retention, deletion, and portal controls are not stated.

The pediatric product page and IFU disclose scope, kit contents, timing, preparation, price, billing, and safety. Transparency is reduced by the missing pediatric report, expired displayed credentials, the Certificate of Compliance versus Certificate of Waiver mismatch, conflicting billing codes, and no refund term.