ARCHETYPE Intraocular pressure test (openEHR-EHR-OBSERVATION.intraocular_pressure.v0)

ARCHETYPE IDopenEHR-EHR-OBSERVATION.intraocular_pressure.v0
ConceptIntraocular pressure test
DescriptionThe measurement of intraocular pressure, most commonly using a tonometry device.
UseUse 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.
PurposeTo record one or more intraocular pressure measurements as part of a single assessment.
ReferencesGlaucoma 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
AuthorsAuthor name: Gustavo M Bacelar-Silva
Organisation: Faculty of Medicine - University of Porto
Email: mail@gustavobacelar.com
Date originally authored: 2012-06-05
Other Details LanguageAuthor 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)
  • Licence: This work is licensed under the Creative Commons Attribution-ShareAlike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-sa/4.0/.
  • Custodian Organisation: openEHR Foundation
  • 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.
  • Current Contact: Lars Fuhrmann, lars.fuhrmann@dog.org
  • Original Namespace: org.openehr
  • Original Publisher: openEHR Foundation
  • Custodian Namespace: org.openehr
  • MD5-CAM-1.0.1: A864D0C1C8D397A42B4338EA5111667B
  • Build Uid: a408cb26-1d76-4e57-8842-27d94a248791
  • Ip Acknowledgements: This artefact includes content from SNOMED Clinical Terms® (SNOMED CT®) which is copyrighted material of the International Health Terminology Standards Development Organisation (IHTSDO). Where an implementation of this artefact makes use of SNOMED CT content, the implementer must have the appropriate SNOMED CT Affiliate license - for more information contact https://www.snomed.org/snomed-ct/get-snomed or info@snomed.org.
  • Revision: 0.0.1-alpha
KeywordsIOP, tonometry, glaucoma, eye, pressure, tension, ocular, GAT, intraocular, hypertension, hypotony, applanation, NCT
Lifecyclein_development
UID1570d6f6-b0b7-4f28-b050-2dbff9d2d863
Language useden
Citeable Identifier1013.1.1369
Revision Number0.0.1-alpha
events
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
state
Pupil statePupil 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:
  •  Coded Text
    • Normal [The pupil is in its natural physiological state without pharmacological intervention or pathological changes.]
    • Medically induced mydriasis [The pupil was dilated due to prior administration of mydriatic agents.]
    • Medically induced miosis [The pupil was constricted due to prior administration of miotic agents.]
    • Pathological pupil state [The pupil was in an unphysiological state due to disease, trauma, or structural abnormalities.]
  •  Text
Body positionBody 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:
Anaesthesia stateAnaesthesia 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:
  •  Coded Text
    • No anaesthesia [The patient was not under anaesthesia during the measurement.]
    • Sedation [The patient was under sedation during the measurement.]
      [SNOMED-CT::17971005 | Sedated]
    • General anaesthesia [The patient was under general anaesthesia during the measurement.]
      [SNOMED-CT::420653000 | Under general anaesthesia]
    • Topical anaesthesia [The patient's eye was anaesthetised by a topical agent during the measurement.]
    • Periocular injection [The patient's eye was anaesthetised by a periocular injection during the measurement.]
  •  Text
Confounding factorsConfounding 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 detailsAdditional 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_pressure_test_reliability_indicator.v0 or
openEHR-EHR-CLUSTER.clinical_evidence.v1
data
Eye examinedEye examined: Identification of the eye under examination.
PressurePressure: 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 typeTonometry 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:
Tonometer detailsTonometer details: Structured details about the tonometry device used to measure the intraocular pressure.
Include:
openEHR-EHR-CLUSTER.device.v1 and specialisations
Corrected pressureCorrected 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 typeCorrection 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:
  •  Coded Text
    • Corneal compensated intraocular pressure (IOPcc) [The pressure result was compensated for corneal parameters. Produced by devices such as the Reichert ORA® or 7CR® tonometers.]
    • Biomechanically corrected intraocular pressure (bIOP) [The pressure was corrected for parameters of corneal biomechanics. Produced by devices such as the Corvis ST® tonometer.]
    • Corrected for central corneal thickness [The pressure was corrected for central corneal thickness (CCT).]
  •  Text
Palpation findingPalpation 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:
  •  Coded Text
    • Unpressurized [The eyeball appears to lack any internal pressure.]
    • Softer than normal [The pressure is approximated to be below the normal range, but some pressure is present.]
    • Normal [The pressure is approximated to be within the normal range (10-21mmHg).]
    • Harder than normal [The pressure is approximated to be above the normal range, but not very hard or rock-hard.]
    • Very hard [The pressure appears to be extremely elevated, sometimes referred to as a rock-hard eye.]
  •  Text
Inspection findingInspection 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:
  •  Coded Text
    • The eye shows signs of being unpressurized. [Based on visual examination, there are signs of a total loss of intraocular pressure. For instance, the eye may have lost its round shape in the setting of significant trauma.]
    • The eye shows no signs of being unpressurized. [Based on visual examination, there are no signs of a total loss of intraocular pressure.]
    • Uncertain [Based on visual examination, it is uncertain if there are signs of a total loss of intraocular pressure.]
  •  Text
Clinical interpretationClinical 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 doneTest not done: Details to explicitly record that this test was not performed.
Include:
openEHR-EHR-CLUSTER.exclusion_exam.v1 and specialisations
CommentComment: Additional narrative about the measurement, not captured in other fields.
protocol
ExtensionExtension: 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 contributorsLuis 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
  • Norwegian Bokmål: Silje Ljosland Bakke, Liv Laugen, Helse Vest IKT AS, ​Oslo University Hospital, Norway, silje.ljosland.bakke@helse-vest-ikt.no, liv.laugen@ous-hf.no