Generated Narrative: CodeSystem kps-data-elements This case-sensitive code system https://nshr-uat.sha.go.ke/fhir/CodeSystem/kps-data-elements provides a fragment that includes following codes: Code Display Definition KPS.A.DE.1 Identifier Government-issued identifier used to distinguish individuals, e.g., National ID (adults) or Birth Certificate number (under 18) KPS.A.DE.2 Name Given Client's first name KPS.A.DE.3 Name Family Client's family name or last name KPS.A.DE.4 Date of Birth Client's date of birth, if known KPS.A.DE.5 Sex Sex of the client assigned at birth KPS.A.DE.8 Address Country Name of country of affiliation KPS.A.DE.9 Address County County where the client resides KPS.A.DE.10 Address Subcounty Subcounty of residence KPS.A.DE.11 Address Ward Ward where the client lives KPS.A.DE.12 Address Village Village or estate of residence KPS.A.DE.13 Address Postal Address Mailing address including P.O. Box, street or building details KPS.A.DE.14 Telecom Phone Phone number (mobile or landline) KPS.A.DE.15 Telecom Email Email address KPS.A.DE.16 Contact Person Role Role: legal guardian, next of kin, or other KPS.A.DE.20 Contact Person Relationship Relationship to the client (e.g., father, spouse, daughter) KPS.A.DE.21 Contact Person Name Given First name of contact person KPS.A.DE.22 Contact Person Name Family Surname of contact person KPS.A.DE.23 Contact Person Phone Phone number of contact person KPS.A.DE.24 Contact Person Email Email of contact person KPS.A.DE.26 Insurance Number Health insurance ID assigned to the client KPS.B.DE.1 Allergy Allergen Substance or agent triggering the reaction KPS.B.DE.25 Allergy Propensity Type Allergy, intolerance, or unknown KPS.B.DE.29 Allergy Description Text description of the allergy or intolerance KPS.B.DE.66 Allergy Severity Severity of the clinical manifestation of the allergic reaction. KPS.B.DE.70 Allergy Criticality Risk of future life-threatening adverse reactions KPS.B.DE.71 Allergy Onset Date Date the allergy was observed KPS.B.DE.72 Allergy Onset Age Age at onset of the allergy KPS.B.DE.73 Allergy End Date Date of resolution of the allergy KPS.B.DE.74 Allergy Status Current status of the allergy KPS.B.DE.78 Allergy Certainty Certainty about the reaction's presence KPS.B.DE.83 Medical Alert Description Description of the alert KPS.B.DE.84 Medical Alert Code Priority level KPS.B.DE.88 Medical Alert Status Alert status (active/inactive/etc) KPS.B.DE.93 Resolved Problem Description Problem or diagnosis KPS.B.DE.94 Resolved Problem Onset Date Date of problem onset KPS.B.DE.96 Resolved Problem End Date Resolution date KPS.B.DE.97 Resolved Problem Resolution Circumstances How the problem was resolved KPS.B.DE.98 Medical History Narrative or synthesized summary of the client's medical background KPS.B.DE.99 Current Problem Condition Problem or diagnosis KPS.B.DE.102 Current Problem Clinical Status Clinical state (active, recurrence, relapse) KPS.B.DE.106 Current Problem Verification Status Certainty of diagnosis (confirmed, differential) KPS.B.DE.110 Current Problem Condition Category Problem list or encounter diagnosis KPS.B.DE.111 Current Problem Condition Encounter Encounter when the condition was first recorded KPS.B.DE.113 Current Problem Severity Clinical severity KPS.B.DE.117 Current Problem Body Site Anatomical location KPS.B.DE.118 Current Problem Onset Date Date of onset KPS.B.DE.119 Current Problem Onset Age Age at onset KPS.B.DE.120 Current Problem Assertion Status Assertion about diagnosis certainty KPS.B.DE.121 Social History Observation Social history observation KPS.B.DE.122 Social History Reference Period Time period of observation KPS.B.DE.123 Pregnancy Status Pregnancy status KPS.B.DE.127 Pregnancy Status Observation Date Date of pregnancy observation KPS.B.DE.128 Pregnancy Status Expected Delivery Date Estimated due date KPS.B.DE.129 Previous Pregnancy Status Has the client been pregnant before? KPS.B.DE.133 Previous Pregnancy Outcome Pregnancy outcome KPS.B.DE.144 Previous Pregnancy Outcome Date Date of pregnancy outcome KPS.B.DE.145 Previous Pregnancy Number of Children Number of children/fetuses in the pregnancy KPS.B.DE.146 Travel History Destination Destination of travel KPS.B.DE.147 Travel History Period Period of travel (entry and departure dates) KPS.C.DE.1 Category Diagnostics Category - clinical discipline, department, or diagnostic service KPS.C.DE.2 Diagnostic Name Exact name or code of the diagnostic request/report (e.g. Lipid Profile) KPS.C.DE.3 Request Date Date and time of the diagnostic request KPS.C.DE.4 Justification Reason for diagnostic request, including relevant clinical notes KPS.C.DE.5 Status Status of the diagnostic request KPS.C.DE.13 Specimen Type Type of material collected for analysis KPS.C.DE.14 Specimen Availability Status Specimen availability status KPS.C.DE.18 Imaging Study Type Type of imaging study requested (e.g. XR Lumbar spine) KPS.C.DE.19 Imaging Date Date when imaging was performed KPS.C.DE.20 Imaging Body Site Body part observed KPS.C.DE.21 Imaging Images References or links to image series from imaging KPS.C.DE.22 Results Date Date and time of result availability KPS.C.DE.23 Performer Name or code of diagnostics performer (originator of result) KPS.C.DE.24 Interpreter Interpreter of result or validator KPS.C.DE.25 Diagnostic Results Results from the analysis, e.g. numeric value, boolean, or description KPS.C.DE.26 Interpretation Interpretation of diagnostic results (e.g. normal, high, low) KPS.C.DE.27 Clinical Impression Working diagnosis or clinical hypothesis based on diagnostics KPS.D.DE.1 Medication Reason Reason for prescribing or using the medication. May link to past/current conditions. KPS.D.DE.2 Intended Use Indication for use: prevention, treatment, diagnostic, anaesthesia, equipment care. KPS.D.DE.3 Medication Code Medication that was or is to be administered (coded). KPS.D.DE.4 Active Ingredient Active substance in the medication (e.g. paracetamol). KPS.D.DE.5 Strength Content of active ingredient per dosage unit (e.g. 500 mg/tablet). KPS.D.DE.7 Dosage Regimen Dosage instructions: quantity, frequency, and duration (e.g. 1 tab every 24h for 10 days). KPS.D.DE.8 Route of Administration Path of administration (e.g. oral, intravenous). KPS.D.DE.9 Treatment Start Date Date to start the treatment or medication. KPS.D.DE.10 Plan of Care Therapeutic recommendations excluding medication: diet, surgery, exercise, etc. KPS.D.DE.11 External Reference External reference to guidelines or other clinical knowledge. KPS.D.DE.12 Related With Link to related entries in the Patient Summary (e.g. rare disease). KPS.E.DE.1 Target Disease Disease or agent that the vaccination provides protection against KPS.E.DE.1.1 Status Current status of immunization against the disease KPS.E.DE.2 Vaccine Prophylaxis Generic description of the vaccine/prophylaxis or its component(s) KPS.E.DE.3 Vaccine Brand Brand name of the vaccine medicinal product KPS.E.DE.4 Vaccine Identifier Identifier for the vaccine medicinal product (e.g. MPID, EMA PMS ID, or national ID) KPS.E.DE.5 Marketing Authorisation Holder Organization or individual authorized to market the vaccine KPS.E.DE.6 Dose Number Order in the vaccination course KPS.E.DE.7 Lot Number Specific identifier of the vaccine batch KPS.E.DE.8 Vaccination Date Date when the vaccination was administered KPS.E.DE.8.1 Age at Vaccination Age at which the vaccination was administered KPS.E.DE.9 Administering Centre Name or code of the administering centre or health authority KPS.E.DE.10 Health Professional Name or code of the health professional who administered the vaccine KPS.E.DE.12 Next Vaccination Date Date of the planned next vaccination (e.g. next dose)
Digital Health Agency of Kenya – Interoperability Team
Kenya Patient Summary logical data element identifiers referenced by the logical models published in this implementation guide. This fragment intentionally includes the subset of identifiers used in the IG so generated definitional-code links resolve to concrete concepts.
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Government-issued identifier used to distinguish individuals, e.g., National ID (adults) or Birth Certificate number (under 18)
Mailing address including P.O. Box, street or building details
Role: legal guardian, next of kin, or other
Relationship to the client (e.g., father, spouse, daughter)
Health insurance ID assigned to the client
Substance or agent triggering the reaction
Text description of the allergy or intolerance
Severity of the clinical manifestation of the allergic reaction.
Risk of future life-threatening adverse reactions
Resolved Problem Resolution Circumstances
Narrative or synthesized summary of the client's medical background
Clinical state (active, recurrence, relapse)
Certainty of diagnosis (confirmed, differential)
Encounter when the condition was first recorded
Number of children/fetuses in the pregnancy
Period of travel (entry and departure dates)
Diagnostics Category - clinical discipline, department, or diagnostic service
Exact name or code of the diagnostic request/report (e.g. Lipid Profile)
Reason for diagnostic request, including relevant clinical notes
Type of imaging study requested (e.g. XR Lumbar spine)
References or links to image series from imaging
Name or code of diagnostics performer (originator of result)
Results from the analysis, e.g. numeric value, boolean, or description
Interpretation of diagnostic results (e.g. normal, high, low)
Working diagnosis or clinical hypothesis based on diagnostics
Reason for prescribing or using the medication. May link to past/current conditions.
Indication for use: prevention, treatment, diagnostic, anaesthesia, equipment care.
Medication that was or is to be administered (coded).
Active substance in the medication (e.g. paracetamol).
Content of active ingredient per dosage unit (e.g. 500 mg/tablet).
Dosage instructions: quantity, frequency, and duration (e.g. 1 tab every 24h for 10 days).
Path of administration (e.g. oral, intravenous).
Date to start the treatment or medication.
Therapeutic recommendations excluding medication: diet, surgery, exercise, etc.
External reference to guidelines or other clinical knowledge.
Link to related entries in the Patient Summary (e.g. rare disease).
Disease or agent that the vaccination provides protection against
Current status of immunization against the disease
Generic description of the vaccine/prophylaxis or its component(s)
Brand name of the vaccine medicinal product
Identifier for the vaccine medicinal product (e.g. MPID, EMA PMS ID, or national ID)
Organization or individual authorized to market the vaccine
Specific identifier of the vaccine batch
Date when the vaccination was administered
Age at which the vaccination was administered
Name or code of the administering centre or health authority
Name or code of the health professional who administered the vaccine
Date of the planned next vaccination (e.g. next dose)