German Dental FHIR Profiles (R4)
0.41.6 - trial-use Germany

German Dental FHIR Profiles (R4) - Local Development build (v0.41.6) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions

Oral Appliances for Sleep-Related Care

Oral Appliances for Sleep-Related Care

PrimarySnoringCarePlanDE identifies the primary-snoring pathway explicitly. It references the clinical indication, available sleep-medicine assessment evidence, the supplied Device, and any recorded Consent or DocumentReference.

Primary snoring and OSAS care are not interchangeable. An OSAS pathway is identified separately as osas-medical-order and is based on a medical diagnosis or order. A screening result alone does not establish the absence of OSAS.

This clinical contract does not determine reimbursement, product eligibility, or legal compliance. Missing consent or disclosure documentation is not an automatic rejection rule.

Medically ordered OSAS pathway

OsasOralApplianceServiceRequestDE represents the medical order that initiates the dental pathway. OsasOralApplianceEligibilityObservationDE records the dental disposition and references the dental observations that informed it. The OSAS diagnosis remains a separate Condition.

OsasOralApplianceCarePlanDE requires:

  • one medical order;
  • one or more dental eligibility observations;
  • one identified OsasOralApplianceDeviceDE; and
  • one or more coded clinical activities.

The service-stage terminology maps to BEMA UP1 through UP6 only through a non-authoritative ConceptMap. A pathway stage does not establish billability.

Eligibility values intentionally contain no AHI thresholds, medical contraindication rules, or product brands. Those decisions remain with the responsible clinicians and current external guidance.

Complications are separate OsasOralApplianceComplicationObservationDE resources focused on the identified Device. This preserves the history of both the appliance and the observed clinical or technical issue.