| ARCHETYPE ID | openEHR-EHR-OBSERVATION.intraocular_pressure.v0 |
|---|---|
| Concept | Intraocular pressure test |
| Description | The measurement of intraocular pressure, most commonly using a tonometry device. |
| Use | Use to record one or more intraocular pressure measurements as part of a single assessment, including contextual factors. Measurements are recorded as separate events for each eye. Where test conditions differ, each measurement under a distinct set of conditions is recorded as an additional event. Where measurements are performed at different times within the same assessment, each time-point is also recorded as a separate event. For an IOP assessment, at least one of the following should be recorded: 'Pressure' or 'Palpation finding' or 'Inspection finding' or 'Examination not done'. Where the 'Corrected pressure' element is populated, the uncorrected 'Pressure' element should also be populated. Where a tonometry device is used, it is encouraged to populate the 'Device Name' element in the 'Tonometer details' SLOT. This is especially important for tonometry devices where the device name is considered clinically meaningful beyond the information included in the 'Tonometry Type' element. Examples include the ORA® or Corvis ST® devices. Where the intraocular pressure is measured by the patient themselves, the RM: provider attribute should be set to PARTY_SELF. The CLUSTER.exclusion_exam archetype can be nested within the 'Test not done' SLOT to optionally record that the intraocular pressure was not performed. |
| Purpose | To record one or more intraocular pressure measurements as part of a single assessment. |
| References | Glaucoma Procedure Data Set [Internet]. Royal College of Ophthalmologists, London. May 2024 [cited 2026 Jan 22]. Available from: https://www.rcophth.ac.uk/wp-content/uploads/2024/05/Glaucoma-Procedure-Data-Set.pdf Lamparter, J., & Hoffmann, E. M. (2009). Measuring intraocular pressure by different methods. Der Ophthalmologe, 106(8), 676-682. DOI 10.1007/s00347-009-1971-8 Pazos M, Traverso CE, Viswanathan A; European Glaucoma Society; Guidelines Task Force; Guidelines Writers, Authors and Contributors; Guidelines Internal Reviewers; Experts by Experience group (patients’ panel); Team of Clinica oculistica of the university of Genoa for medical editing and graphics; External Reviews; EGS Executive Committee; Board of The EGS Foundation. European Glaucoma Society - Terminology and guidelines for glaucoma, 6th Edition. Br J Ophthalmol. 2025 Sep 8;109(Suppl 1):1-212. doi: 10.1136/bjophthalmol-2025-egsguidelines. PMID: 41026937. |
| Copyright | © openEHR Foundation |
| Authors | Author name: Gustavo M Bacelar-Silva Organisation: Faculty of Medicine - University of Porto Email: mail@gustavobacelar.com Date originally authored: 2012-06-05 |
| Other Details Language | Author name: Gustavo M Bacelar-Silva Organisation: Faculty of Medicine - University of Porto Email: mail@gustavobacelar.com Date originally authored: 2012-06-05 |
| Other Details (Language Independent) |
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| Keywords | IOP, tonometry, glaucoma, eye, pressure, tension, ocular, GAT, intraocular, hypertension, hypotony, applanation, NCT |
| Lifecycle | in_development |
| UID | 1570d6f6-b0b7-4f28-b050-2dbff9d2d863 |
| Language used | en |
| Citeable Identifier | 1013.1.1369 |
| Revision Number | 0.0.1-alpha |
| events | |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| state | |
| Pupil state | Pupil state: Statement describing the condition of the individual's pupils during the measurement. The physical examination of the eye will be recorded using the CLUSTER.exam-eye family of archetypes. Use the 'Clinical evidence' archetype nested within the 'Additional details' SLOT to record structured details about relevant eye examination findings. Coding with a terminology is recommended. Free text entry should only be permitted if no appropriate coded value is available. Choice of:
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| Body position | Body position: Statement about the body position of the individual at the time of measurement. Coding with a terminology is recommended. Free text entry should only be permitted if no appropriate coded value is available. Choice of:
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| Anaesthesia state | Anaesthesia state: Statement about the use of anaesthesia during the measurement. Details of the anaesthesia procedure and the specific medications used should be recorded using separate archetypes. Coding with a terminology is recommended. Free text entry should only be permitted if no appropriate coded value is available. Choice of:
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| Confounding factors | Confounding factors: Description of any incidental factors related to the state of the subject which may affect clinical interpretation of the measurement. For example: 'blepharospasm', 'reduced cooperation', 'measurement interrupted', and 'difficulty holding lid open'. |
| Additional details | Additional details: Structured elements about specific factors related to the state of the subject which may affect clinical interpretation of the measurement. The scope of structured content appropriate for nesting within this SLOT includes, but is not limited to: Quality or reliability indicators generated by the device, such as the ORA Waveform Score, iCare measurement quality indicator, or Tono-Pen statistical confidence indicator; and clinical evidence relevant to interpretation of the pressure measurement, such as central corneal thickness or detailed physical examination findings relevant to the measurement, such as pupillary state at the time of measurement. Include: openEHR-EHR-CLUSTER.intraocular_ openEHR-EHR-CLUSTER.clinical_ |
| data | |
| Eye examined | Eye examined: Identification of the eye under examination.
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| Pressure | Pressure: The intraocular pressure of the identified eye, measured using the method specified by the 'Tonometry type' element. For devices that only output one pressure value per measurement, this element is used. For devices that output multiple pressure values per measurement, this element is used for the output that did not undergo a correction step or is correlated with an uncorrected method by design. Use the 'Corrected pressure' and 'Correction type' elements for outputs that have been corrected for factors such as corneal thickness or biomechanics. Where typical device output is based on integration of multiple measurement cycles, the final device output should be recorded in this data element. If not all cycles can be completed, this element can still be used to record the average of successful cycles, but note this as a confounding factor. Property: Pressure Units: 0.0..<1000.0 mmHg Limit decimal places: 1 |
| Tonometry type | Tonometry type: Type of tonometry used to measure the intraocular pressure. Coding with a terminology is recommended. Free text entry should only be permitted if no appropriate coded value is available. It is recommended to specify the device name and/or model in the 'Medical device' archetype nested in the 'Tonometer details' SLOT in this archetype. Note that 'Transpalpebral' refers to the use of a transpalpebral tonometer, not palpation through the eyelid. Choice of:
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| Tonometer details | Tonometer details: Structured details about the tonometry device used to measure the intraocular pressure. Include: openEHR-EHR-CLUSTER.device.v1 and specialisations |
| Corrected pressure | Corrected pressure: An adjusted intraocular pressure value derived from the measured 'Pressure' and using the method specified in 'Correction type', to more closely approximate the true pressure of the identified eye. Property: Pressure Units: 0.0..<1000.0 mmHg Limit decimal places: 1 |
| Correction type | Correction type: The type of correction applied to the measured 'Pressure' to calculate the 'Corrected pressure' value. Coding with a terminology is recommended. Free text entry should only be permitted if no appropriate coded value is available. Note that terms such as ccIOP and bIOP are based on the names of output variables, which may be shared by different devices that do not share identical methods. It is recommended to specify the device name and/or model in the 'Medical device' archetype nested in the 'Tonometer details' SLOT in this archetype. Choice of:
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| Palpation finding | Palpation finding: Semi-quantitative description of the softness or hardness of the eye based on palpation with the examiners fingers. Typically reserved for situations where measurement with a tonometer is not possible or reliable. Coding with a terminology is recommended. Free text entry should only be permitted if no appropriate coded value is available. Choice of:
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| Inspection finding | Inspection finding: Record of presence or absence of visible signs of a total lack of internal pressure of the examined eye. Typically reserved for rare situations where physical interaction with the globe is inadvisable, such as physically aggressive individuals or when an open globe injury is strongly suspected. Coding with a terminology is recommended. Free text entry should only be permitted if no appropriate coded value is available. Choice of:
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| Clinical interpretation | Clinical interpretation: Single word, phrase or brief description that represents the clinical meaning and significance of the findings. A single instance may be used to record a brief narrative summary of the findings. Alternatively, one or more instances may be used to represent coded interpretations. A combination of both approaches may also be used, with the narrative description recorded in one instance alongside one or more coded interpretations in separate instances. Examples: "Above target pressure", "elevated", "hypotonic". |
| Test not done | Test not done: Details to explicitly record that this test was not performed. Include: openEHR-EHR-CLUSTER.exclusion_ |
| Comment | Comment: Additional narrative about the measurement, not captured in other fields. |
| protocol | |
| Extension | Extension: Additional information required to extend the model with local content or to align with other reference models or formalisms. For example: local information requirements; or additional metadata to align with FHIR. Include: All not explicitly excluded archetypes |
| Other contributors | Luis Abegao Pinto, ULS Santa Maria, Portugal Vebjørn Arntzen, Oslo universitetssykehus HF, Norway Silje Ljosland Bakke, Helse Vest IKT AS, Norway (openEHR Norway Editor) Robert Bendau, Asklepios Eye Hospital North Hamburg, Germany Michael Boland, Mass Eye and Ear, United States Victoria de Juan, Alcon, Spain Christopher Dicke, DOG, Germany Aitor Eguzkitza, UPNA (Public University of Navarre) - CHN (Complejo Hospitalario de Navarra), Spain Corina Ehrne, INNOFORCE Est., Liechtenstein Manel Fernández Bonet, Consorci Sanitari Integral, Spain Tim Freisenich, University, Germany Lars Fuhrmann, German Society of Ophthalmology, Germany (openEHR Editor) Ciprian Gerstenberger, HN IKT, Norway Carsten Grohmann, University Medical Center Hamburg-Eppendorf, Germany Bettina Hohberger, Department of Ophthalmology, University of Erlangen, FAU, Germany Severin Kohler, Berlin Institute of Health, Germany Simon König, Augenklinik Unimedizin Mainz, Germany Stefan Lang, Universitätsklinikum Brandenburg an der Havel, Germany Heather Leslie, Atomica Informatics, Australia (openEHR Editor) Ramil Lising, University of the Philippines, Philippines Ian McNicoll, freshEHR Clinical Informatics, United Kingdom Olha Nikolaieva, University Hospital Basel, Switzerland Mona Nordvik, Haukeland Universitetssykehus, Norway Bjørn Næss, DIPS ASA, Norway Ariel Ong, Moorfields Eye Hospital, United Kingdom Marta Pazos, Hospital Clínic de Barcelona, Spain Rishi Ramessur, Moorfields Eye Hospital, United Kingdom Christian Richter, Dr. Richter & Dr. Richter PartG, Germany Ian Rodrigues, St Thomas' Hospital, United Kingdom Ruben Rognmo, Helse Nord IKT, Norway Marc Schargus, Asklepios Eye Hospital North Hamburg, Germany Wolfgang Schultz, MedicalCommunications GmbH, Germany Anne Stahl, adesso, Germany John Tore Valand, Helse Vest IKT, Norway Marte Vassli Gullesen, HNIKT, Norway Ines Žabkar, Better, Slovenia |
| Translators |