Libman–Sacks endocarditis
Enable an agent to recognise Libman-Sacks endocarditis, assess its valve and embolic consequences, and identify evidence needed for clinician-directed decisions.
Bundle → Layer → Finding → Questions Filled
6 bundles · 11 layers · 16 findings · 33 questions
Condition identity and attribution Define which autoimmune-associated valve condition the registry entry denotes and how a particular diagnosis is supported.
Terminological boundary
Preserve the distinction between Libman-Sacks endocarditis and neighbouring valve conditions.
Libman-Sacks concept boundary
Record the source's intended meaning and its relationship to the broader nonbacterial thrombotic endocarditis category.
- Does the diagnosing source use Libman-Sacks specifically for autoimmune-associated lesions or as a broader synonym? definition
- What evidence distinguishes this attribution from malignancy-associated or otherwise unexplained nonbacterial thrombotic endocarditis? boundary
Diagnostic assertion
Represent who made the diagnosis, its certainty, and the framework used.
Attribution evidence and version
Keep the diagnostic assertion distinct from the condition, its supporting observations, and the care encounter.
- Who attributed the lesions to Libman-Sacks endocarditis, when, and using which imaging, clinical, or pathological evidence? provenance
- If diagnostic criteria or a terminology code are recorded, what issuing body, edition, jurisdiction, and mapping source apply? provenance
- Is the assertion suspected, clinically supported, tissue-supported, disputed, or excluded, and what uncertainty remains? definition
Valve lesions and observation Describe individual lesions and the examinations that make them observable.
Lesion anatomy
Locate and characterise vegetations and associated leaflet changes.
Vegetation topography and morphology
Record valve, leaflet surface, attachment, shape, mobility, and dimensions as observations rather than diagnostic proof.
- Which valve, leaflet or cusp, and surface carry each lesion, and does it extend across the leaflet or coaptation region? measurement
- What dimensions, attachment breadth, mobility, and echogenicity were reported for each lesion? measurement
- What distinguishes the observed mass from isolated thickening, a strand, a tumour, or an artifact? boundary
Imaging and tissue provenance
Capture the technique and limitations behind positive or negative observations.
Examination detection confidence
TEE detected lesions more effectively than TTE in a comparative SLE study; an absent finding must therefore retain its examination context. [Comparative study](https://pubmed.ncbi.nlm.nih.gov/18085739/)
- Was the observation obtained using TTE, two-dimensional TEE, three-dimensional TEE, or tissue examination, and on what date? provenance
- Which image-quality or sampling limitations constrain interpretation of an absent or equivocal lesion? measurement
- Would additional imaging or review of existing tissue resolve a specific uncertainty sufficiently to justify clinician consideration? action
Autoimmune context and infection differential Connect the autoimmune setting to lesion attribution while preserving assessment of infection.
Autoimmune associations
Link independently assessed lupus and antiphospholipid findings to the valve condition.
Lupus and antiphospholipid evidence
Record associated diagnoses, antibody evidence, and their timing without converting an isolated antibody result into an antiphospholipid syndrome diagnosis.
- Is systemic lupus erythematosus or antiphospholipid syndrome independently established, suspected, or absent? boundary
- Which dated disease-activity assessments and antiphospholipid antibody results were available when the valve lesions were assessed? provenance
Infective alternative
Keep infective endocarditis, including unresolved culture-negative disease, visible in the differential.
Infection evidence and residual uncertainty
Represent the evidence used to judge infection unlikely or supported rather than inferring sterility solely from a negative culture.
- What blood cultures and other indicated microbiological investigations were obtained, and did antibiotic exposure precede sampling? provenance
- What clinical, imaging, or tissue evidence supports infection, argues against it, or leaves culture-negative infection unresolved? boundary
- Which new findings would trigger prompt reassessment for concurrent or alternative infective endocarditis? action
Valve and embolic consequences Assess functional valve effects and potentially related embolic injury.
Haemodynamic effect
Determine whether the valve lesion impairs function and how strongly it explains clinical findings.
Valve dysfunction attribution
Record regurgitation or stenosis severity, supporting measurements, and competing causes of dysfunction.
- What regurgitation or stenosis grade and quantitative measurements accompany each affected valve? measurement
- How strongly are symptoms or cardiac functional changes attributed to these lesions rather than another cardiac condition? boundary
Embolic consequences
Link neurological or systemic vascular events without assuming their source.
Event-to-valve attribution
An SLE study associated Libman-Sacks vegetations with cerebrovascular disease; individual event attribution still requires assessment of competing causes. [Embolic cerebrovascular study](https://pmc.ncbi.nlm.nih.gov/articles/PMC3941465/)
- Which suspected or established embolic events occurred, in what territories, and when relative to lesion detection? provenance
- What evidence supports a valvular embolic source rather than antiphospholipid-related in situ thrombosis or another source? boundary
- Do newly reported neurological or systemic ischaemic symptoms require urgent clinical assessment? action
Course and clinical review Track lesion evolution and the evidence underlying condition-specific management decisions.
Longitudinal comparison
Compare lesions and consequences across compatible examinations.
Lesion evolution and residual damage
Track vegetation visibility and valve function separately, retaining uncertainty from changes in modality or image quality.
- Are the same anatomical lesions being compared using sufficiently comparable imaging techniques and measurement methods? measurement
- Have vegetation burden, valve dysfunction, and embolic events changed in the same or different directions? measurement
- Does a no-longer-visualised lesion represent convincing regression, limited detection, or an unresolved change? boundary
Management decision evidence
Represent clinician decisions and their indications without embedding an unsupported universal treatment algorithm.
Intervention rationale and follow-up
Link autoimmune treatment, antithrombotic treatment, valve intervention, and surveillance decisions to the specific problem they address.
- Which documented indication supports each treatment decision: autoimmune activity, an embolic event, independently established antiphospholipid syndrome, or valve dysfunction? action
- Which patient-specific constraints and unresolved infection questions materially affect the proposed intervention? action
- What clinician-defined follow-up interval, outcome measures, and escalation triggers apply, and what evidence supports them? provenance
Evidence and external alignment What the world already says about this thing, gathered so the model can be checked against it.
Reported evidence
Findings from the breadth pass, kept separate from the structural claims.
Check these first
Recalled without web access and unsourced; every item is a lead to verify.
- Which of these check these first hold for the sense of Libman-Sacks endocarditis this model covers, and on what evidence? provenance
Identifiers and schemes
Recalled without web access and unsourced; every item is a lead to verify.
- Which of these identifiers and schemes hold for the sense of Libman-Sacks endocarditis this model covers, and on what evidence? provenance
Real-world use
Recalled without web access and unsourced; every item is a lead to verify.
- Which of these real-world use hold for the sense of Libman-Sacks endocarditis this model covers, and on what evidence? provenance
Failure modes and hazards
Recalled without web access and unsourced; every item is a lead to verify.
- Which of these failure modes and hazards hold for the sense of Libman-Sacks endocarditis this model covers, and on what evidence? provenance
Regional variation
Recalled without web access and unsourced; every item is a lead to verify.
- Which of these regional variation hold for the sense of Libman-Sacks endocarditis this model covers, and on what evidence? provenance
Neighbouring kinds and how to tell them apart
Recalled without web access and unsourced; every item is a lead to verify.
- Which of these neighbouring kinds and how to tell them apart hold for the sense of Libman-Sacks endocarditis this model covers, and on what evidence? provenance
Classifiers Filled
- Family
- Thing Registry
- Category
- Information and virtual systems
- Entry kind
- thing
- Plane
- INF
- Domain
- INF.KNW
What it is Filled
Libman-Sacks endocarditis is a form of noninfective endocarditis characterized by sterile verrucous vegetations, predominantly on the mitral and aortic valves, associated especially with systemic lupus erythematosus and antiphospholipid syndrome.
In scope
- Noninfective valvular lesions attributed to Libman-Sacks endocarditis and the certainty of that attribution.
- Lesion location, morphology, imaging provenance, and available tissue evidence.
- Relationships to systemic lupus erythematosus and antiphospholipid syndrome.
- Assessment of competing diagnoses, especially infective endocarditis and other nonbacterial thrombotic endocarditis.
- Valve dysfunction, suspected embolic consequences, and changes during follow-up.
- Condition-specific evidence supporting monitoring and treatment review.
Out of scope
- The patient's identity and complete medical history.
- Full diagnostic and management models for systemic lupus erythematosus or antiphospholipid syndrome.
- Infective endocarditis and malignancy-associated nonbacterial thrombotic endocarditis as independent conditions.
- Independent stroke, heart failure, or systemic embolism models.
- Encounter administration, procedure execution, and medication prescribing.
Why it exists Filled
Enable an agent to recognise Libman-Sacks endocarditis, assess its valve and embolic consequences, and identify evidence needed for clinician-directed decisions.
Distinguishing features Filled
- Establish whether noninfective valve lesions occur in a relevant autoimmune context; systemic lupus erythematosus or antiphospholipid syndrome alone does not establish Libman-Sacks endocarditis. [Diagnostic TEE study](https://pubmed.ncbi.nlm.nih.gov/19763069/)
- Assess for sessile, nodular or coalescent vegetations at leaflet coaptation, potentially extending across leaflet surfaces; these are supportive imaging patterns rather than definitive identifiers. [Three-dimensional TEE study](https://pmc.ncbi.nlm.nih.gov/articles/PMC4592775/)
- Distinguish a supported noninfective attribution from unresolved infective endocarditis through microbiology, clinical evidence, and serial imaging; negative cultures alone should not determine the label. [Diagnostic case study](https://pmc.ncbi.nlm.nih.gov/articles/PMC2517866/)
- Distinguish this autoimmune-associated condition from other causes of nonbacterial thrombotic endocarditis by recording the underlying attribution and the terminology used by the diagnosing source.
- Separate characteristic vegetations from isolated nonspecific valve thickening and from imaging artifacts; record modality limitations when lesions are absent or equivocal. [TTE versus TEE study](https://pubmed.ncbi.nlm.nih.gov/18085739/)
What robots and AI may and may not do Filled
Must not
- Diagnose the condition from symptoms or a report.
- Advise starting or stopping anticoagulants or immune treatment.
- Confuse it with infective endocarditis in a way that changes care.
- Share a person's diagnosis or test results without consent.
Only with a human decision
- Any clinical decision about a person's heart valves or blood thinning.
May
- Explain Libman-Sacks endocarditis and its links to lupus and antiphospholipid syndrome, citing medical sources.
- Advise a person with lupus and new heart symptoms to contact their clinician.
Moral aspects Filled
- It can cause strokes; wrong advice on blood thinners can be fatal.
- People with lupus often face disbelief about their symptoms.
Who is affected
- People with lupus
- People with antiphospholipid syndrome
- Clinicians
Owners Filled
Steward
Nobody owns the condition; clinicians answer for each patient's care.
Links to other meta-models Filled
parent
- Q4826340 - registry parent class
- Q73518 - registry parent class
What else AI and robots need to interact with it Filled
Identity and identifiers required Filled
- Vercy registry: vr.tr.libman-sacks-endocarditis
- Wikidata: Q1532243 (https://www.wikidata.org/wiki/Q1532243)
Direct properties not applicable Not applicable
- Diagnostic attribution: suspected | clinically supported | tissue-supported | disputed | excluded; assessor, date, and supporting evidence required
- Associated autoimmune condition: Links to systemic lupus erythematosus and antiphospholipid syndrome assessments, including certainty and date
- Valve and lesion distribution: Valve, leaflet or cusp, surface, attachment site, and number of lesions; unknown permitted
- Vegetation dimensions: mm for reported dimensions; mm² for area if measured; examination date, modality, and measurement plane required
- Lesion morphology: Reported shape, attachment breadth, mobility, echogenicity, and leaflet thickening
- Infection assessment: not assessed | unresolved | infection considered unlikely | infection supported; microbiology and antibiotic exposure linked
- Valve functional effect: Regurgitation and stenosis grades with grading standard, version, examination date, and quantitative support
- Embolic event attribution: Linked event, territory, date, competing causes, and clinician-assessed attribution certainty
- Longitudinal lesion state: newly detected | persistent | increased | decreased | no longer visualised | indeterminate; comparator examination required
Plane INF: no invented physical properties.
Recognition not applicable Not applicable
Not applicable
This internal disease has no reliable external visual signature and requires clinical assessment supported by diagnostic evidence.
Capabilities and actions required Filled
- Assemble a traceable evidence summary supporting or challenging the Libman-Sacks attribution.
- Identify missing infection assessments or imaging limitations that require clinical review.
- Compare matched valve lesions across dated examinations.
- Connect valve dysfunction and embolic events to their evidence and alternative explanations.
- Prepare clinician review of monitoring, antithrombotic treatment, autoimmune treatment, or valve intervention using recorded indications and constraints.
Hazards and failure modes required Filled
- Material from valve vegetations can embolize and cause stroke or injury to other organs.
- Valve dysfunction can contribute to heart failure.
- Confusion with infective endocarditis can delay appropriate clinical management.
Standards and interfaces required Filled
- The International Classification of Diseases, issued by the World Health Organization, provides the official framework for coding this condition and its associated systemic disease.
Context of use required Filled
- This condition is encountered in clinical assessment of sterile heart valve lesions, particularly in people with systemic lupus erythematosus or antiphospholipid syndrome.
- Its identification informs evaluation of valve function, embolic complications and possible alternative causes of endocarditis.
Sources Filled
- Wikidata item Q1532243: Libman–Sacks endocarditis - identity and sense of the item
- Wikipedia: Libman–Sacks endocarditis - general description of the item
Open questions
- Which authoritative definition should govern this registry entry when sources differ over whether Libman-Sacks includes primary antiphospholipid syndrome-associated lesions or broader nonbacterial thrombotic endocarditis?
- Is there a validated, generally accepted Libman-Sacks-specific diagnostic framework, and how should imaging-supported and tissue-supported diagnoses be distinguished without inventing criteria?
- What are the verified ICD-10, jurisdiction-specific ICD-10 modification, ICD-11, and SNOMED CT mappings in named releases, and which require associated-disease coding?
- What prevalence estimates are defensible by population, study year, age group, autoimmune diagnosis, and imaging or autopsy ascertainment method?
- What evidence supports surveillance intervals and thresholds for antithrombotic treatment or valve intervention, particularly in asymptomatic patients without previous embolism?
Machine files
Provenance
thing registry research (pass 2) · unreviewed
Built from: models/things/publications/thing-q1532243/spec.json