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Research draft

erectile dysfunction

vr.tr.erectile-dysfunction · INF.KNW

Enable an AI agent to recognise reported erectile dysfunction, assess its pattern and impact, and support appropriate evaluation and clinician-directed care while preserving uncertainty.

Thing Registry Information and virtual systems

Research draft, second pass

A second pass drafted this model: the structure a model of this thing needs, and what is known about it in the world. The line under this one says how the second half was obtained - researched against sources, or recalled without web access, in which case nothing here was read anywhere and every claim is a lead to verify. Unreviewed either way.

Researched by: Codex + Grok

Purpose and description

Enable an AI agent to recognise reported erectile dysfunction, assess its pattern and impact, and support appropriate evaluation and clinician-directed care while preserving uncertainty.

Erectile dysfunction is a male sexual dysfunction in which a man cannot repeatedly attain or keep a penile erection rigid and lasting enough for satisfactory sexual activity, generally diagnosed only after the problem has been present for at least three months.

It can be Elicit a private, consent-based account of erectile difficulty, its contexts, and the person's goals.; Summarise the symptom pattern and missing evidence for clinical evaluation without independently assigning a diagnosis.; Relate onset and fluctuations to documented conditions, medicines, procedures, and psychological circumstances.; Flag documented treatment contraindications and symptoms requiring urgent clinical assessment.; Support discussion of clinician-approved options against the person's preferences and practical constraints.; Track assisted and unaided outcomes separately and prepare an evidence-based reassessment summary..

Distinguishing features

Establish whether the reported limitation concerns erection attainment, rigidity, or maintenance; low desire alone does not establish ED. [NIDDK overview](https://www.niddk.nih.gov/health-information/urologic-diseases/erectile-dysfunction)

Ask separately about erection, ejaculation, and orgasm: a difficulty in one does not identify the state of the others. [NIDDK diagnosis](https://www.niddk.nih.gov/health-information/urologic-diseases/erectile-dysfunction/diagnosis)

Distinguish an isolated unsuccessful attempt from a recurring pattern by recording frequency, duration, and the diagnostic framework used.

Distinguish inadequate erection from sexual activity limited principally by penile pain or curvature; record coexistence without merging the conditions.

Distinguish current unaided function from function achieved using medicine, a vacuum device, or an implant; assisted success does not by itself establish unaided recovery.

Scope

+ Difficulty attaining, maintaining, or achieving sufficient rigidity of an erection

+ Onset, recurrence, situational variation, and change from the person's usual erectile function

+ Patient-reported impact, distress, and goals for erectile function

+ Evidence linking erectile difficulty to physical, psychological, medication-related, or contextual contributors

+ ED-specific evaluation, treatment suitability, treatment experience, and follow-up

- Sexual desire, arousal, orgasm, and ejaculation disorders as independent conditions

- Infertility, semen quality, and reproductive planning

- Primary models of cardiovascular, endocrine, neurological, or metabolic disease

- Penile curvature, injury, anatomical variation, and pain as independent conditions

- Priapism and other acute emergencies as independently managed conditions

- General relationship quality, sexual identity, and sexual orientation

Characteristics

Erectile-function limitation
attainment difficulty; insufficient rigidity; maintenance difficulty; combined; unclear Identifies the actual functional problem rather than treating every sexual complaint as ED.
Assessment state
reported concern; under evaluation; clinician-diagnosed; historical; clinician-assessed remission; uncertain Separates a person's report from a clinical determination.
Onset and duration
onset date or estimated interval; duration in days, months, or years; uncertainty recorded Supports assessment of persistence and temporal relationships to illness, injury, medication, or life events.
Difficulty frequency
attempts with difficulty / relevant attempts within a stated interval; unknown or no attempts permitted Avoids confusing lack of sexual opportunity with erectile failure.
Context dependence
generalised; situational; mixed; unassessed, with relevant contexts described Shows whether the limitation varies with activity, setting, or partner without assigning a cause automatically.
Spontaneous and self-stimulated erections
preserved; reduced; absent by report; variable; unknown, separately by context Adds contextual evidence without treating one observation as a definitive causal test.
Structured erectile-function assessment
instrument name, version, language, score, recall interval, and assistance status Makes repeated assessments interpretable without assuming different instruments are interchangeable.
Experienced impact
patient-described distress, avoidance, satisfaction, and interference with desired activities Keeps care goals grounded in the person's experience rather than a presumed sexual norm.
Suspected contributors
links to conditions, exposures, procedures, and contextual factors, each with evidence and confidence Supports multiple simultaneous explanations while distinguishing association from established causation.
Current treatment dependence
untreated; treatment attempted; effective with assistance; insufficient response; stopped; unknown Prevents successful treatment from being mistaken for resolution of the underlying difficulty.
Management suitability
not assessed; clinician review required; suitable for a specified option; contraindicated for a specified option; urgent assessment required Makes action boundaries specific to the proposed intervention and current clinical information.

Also called

vasculogenic impotencecondom-associated erection problem

Where this came from

wikidata · CC0 1.0

Drafted structure

Bundle to layer to finding to question, as the second pass will find it: 6 bundles · 11 layers · 18 findings · 28 questions.

Erectile difficulty recognition Identify the erectile limitation and establish the evidential status of the ED label.

An agent must distinguish a specific erectile complaint from other sexual difficulties and from an established diagnosis.

Functional complaint

Describe what the erection does not permit in the person's intended activity.

Attainment, rigidity, and maintenance

Record each erectile limitation separately, including the person's meaning of sufficient function.

  1. Is the difficulty obtaining an erection, achieving sufficient firmness, maintaining it, or a combination? definition
  2. Which desired activities are limited, and is erection inadequacy the limiting factor rather than desire, pain, ejaculation, or orgasm? boundary

Diagnostic standing

Keep reported symptoms, assessment findings, and diagnostic conclusions distinguishable.

Label and criteria

Retain who applied the ED label, when, and under which criteria; leave unresolved criteria explicit.

  1. Is ED self-reported, suspected during evaluation, or diagnosed by a clinician, and what record supports that status? provenance
  2. Which diagnostic framework, if any, supplies the persistence, frequency, or distress requirements used for this assessment? definition
Erection pattern and burden Describe recurrence, context, severity, and lived consequences.

The same complaint can represent substantially different patterns and care priorities.

Temporal and situational pattern

Place erectile difficulty against baseline function, time, and relevant sexual contexts.

Onset, recurrence, and variation

Record lifelong or acquired presentation, sudden or gradual onset, and context-dependent differences without inferring their cause.

  1. When did the difficulty begin, how did it differ from prior function, and how often has it occurred within a specified interval? measurement
  2. How does function differ during partnered activity, self-stimulation, and spontaneous or waking erections, and which observations are unknown? measurement

Severity and personal impact

Pair structured assessment with the person's experience and desired outcomes.

Interpretable severity and goals

Record instrument context, opportunities for sexual activity, treatment assistance, and personally meaningful improvement.

  1. What assessment or description captures severity, over which interval, and were responses affected by assistance or lack of sexual opportunity? measurement
  2. What distress or activity limitation does the person report, and what change would they consider worthwhile? action
Contributors and evaluation Organise causal hypotheses and the evidence needed to assess them.

An agent must accommodate interacting contributors and avoid converting a plausible explanation into a confirmed cause.

Contributor hypotheses

Link erectile difficulty to relevant health, exposure, and psychosexual information.

Multifactorial explanation

Maintain separate hypotheses for vascular, neurological, hormonal, anatomical, medication-related, and psychological contributions. Clinical history and examination inform evaluation. [NIDDK diagnosis](https://www.niddk.nih.gov/health-information/urologic-diseases/erectile-dysfunction/diagnosis)

  1. Which conditions, medicines, substances, procedures, injuries, or psychological circumstances preceded or accompany the erectile change? provenance
  2. What supports or weakens each proposed contribution, and which explanations remain possible together? boundary

Targeted assessment

Capture completed evaluation and the decision each additional assessment would inform.

Evaluation evidence and gaps

Record relevant examination and test results with dates, interpretation, and limitations; specialised testing is not treated as a universal prerequisite.

  1. What relevant history, examination, laboratory, or specialised erectile-function testing has been completed, and who interpreted it? provenance
  2. Which unresolved clinical decision would further assessment change, and has a clinician recommended that assessment? action
Treatment suitability and safety Represent the clinical constraints that govern ED management and escalation.

A treatment suggestion is incomplete without information about interactions, health status, and urgent complications.

Option-specific eligibility

Attach suitability assessments to particular treatments and current clinical circumstances.

Cardiovascular and interaction review

Record cardiovascular review and medication reconciliation. Concomitant organic nitrates or nitric oxide donors, including poppers, contraindicate PDE5 inhibitors. [EAU guideline](https://uroweb.org/guidelines/sexual-and-reproductive-health/chapter/management-of-erectile-dysfunction)

  1. Has a clinician assessed cardiovascular suitability for sexual activity and the proposed ED treatment, and what remains unresolved? action
  2. Does the current medicine and substance history include nitrates, nitric oxide donors, or other contraindications or interactions relevant to the proposed option? boundary

Acute complication routing

Separate routine erectile difficulty from urgent symptoms arising during treatment.

Urgent treatment-associated symptoms

An erection lasting longer than four hours or vision or hearing loss following oral ED medicine requires prompt medical attention. Record symptoms and route to urgent care. [NIDDK treatment](https://www.niddk.nih.gov/health-information/urologic-diseases/erectile-dysfunction/treatment)

  1. Is there a prolonged erection, new vision or hearing loss, or another acute symptom, and when did it begin relative to treatment? measurement
  2. What immediate clinical escalation is indicated by the reported symptom and applicable care pathway? action
Management experience and response Connect patient preferences, treatment experience, and observed change in erectile function.

An agent must distinguish unsuitable treatment, an inadequately assessed trial, effective assistance, and improvement without assistance.

Shared management choice

Document options discussed, preferences, and the agreed clinical plan.

Acceptable treatment plan

Record the person's priorities concerning medication, devices, counselling, contributing conditions, and procedural options, including a preference to defer treatment.

  1. Which clinician-discussed options fit the person's goals, preferences about spontaneity and invasiveness, access, and willingness to involve a partner? action
  2. What plan was agreed, including any prescribed treatment, use instructions, training, and review point? provenance

Response and reassessment

Interpret outcomes against actual treatment exposure and the original goals.

Assisted outcome and trial adequacy

Keep erectile response, satisfaction, adverse effects, and adherence distinct; avoid declaring treatment failure without assessing how it was used.

  1. What changed in attainment, rigidity, maintenance, and satisfaction, under what assistance and use conditions, and with which adverse effects? measurement
  2. Does the clinician consider the trial adequate, and does the evidence support continuation, instruction review, another option, or renewed evaluation? action
Evidence and external alignment What the world already says about this thing, gathered so the model can be checked against it.

A model that cannot be lined up against existing standards, identifiers and practice cannot be adopted by anyone who already uses them.

Reported evidence

Findings from the breadth pass, kept separate from the structural claims.

Kinds and varieties

Reported by the breadth pass; each item needs checking against its source before it becomes normative.

  • Vasculogenic (arteriogenic inflow failure or veno-occlusive/cavernosal leak)
  • Neurogenic (central, spinal, or peripheral, including after pelvic surgery or neuropathy)
  • Endocrinological (hypogonadism, hyperprolactinaemia, thyroid disease)
  • Anatomical or structural (Peyronie's plaque, cavernosal fibrosis, congenital deformity)
  • Drug-induced or iatrogenic (antihypertensives, SSRIs, anti-androgens, pelvic radiation)
  • Psychogenic
  • Mixed organic and psychogenic (the majority of clinic presentations)
  • Situational versus generalised (partner-specific or context-limited versus present in all settings)
  1. Which of these kinds and varieties hold for the sense of erectile dysfunction this model covers, and on what evidence? provenance

Identifiers and schemes

Reported by the breadth pass; each item needs checking against its source before it becomes normative.

  • ICD-10 - N52 (N52.0-N52.9) - WHO/ICD-10-CM Male erectile dysfunction, with cause-specific subcodes (e.g. drug-induced, post-procedural).
  • ICD-11 - HA01.1 - WHO ICD-11 Male erectile dysfunction, under sexual arousal dysfunctions.
  • DSM-5 / DSM-5-TR - 302.72 (F52.21) - Erectile Disorder in the mental-disorders classification; not a synonym for all organic ED.
  • SNOMED CT - 397803000 - Erectile dysfunction (disorder).
  • MeSH - D007172 - Erectile Dysfunction; older heading Impotence redirects here.
  • Wikidata - Q837551 - Item for the medical condition erectile dysfunction.
  • UMLS CUI - C0242350 - Unified Medical Language System concept for erectile dysfunction.
  1. Which of these identifiers and schemes hold for the sense of erectile dysfunction this model covers, and on what evidence? provenance

Standards and regulation

Reported by the breadth pass; each item needs checking against its source before it becomes normative.

  • American Urological Association - Erectile Dysfunction guideline (evaluation, cardiovascular risk, and treatment sequencing).
  • European Association of Urology - Guidelines on Sexual and Reproductive Health (diagnostic criteria, imaging, and therapy).
  • American Psychiatric Association - DSM-5-TR diagnostic criteria for Erectile Disorder.
  • World Health Organization - ICD-10 N52 and ICD-11 HA01.1 as the statistical classification of the condition.
  • U.S. Food and Drug Administration / EMA / national medicines regulators - marketing authorisation and labelling of PDE5 inhibitors, alprostadil, and penile prostheses; boxed contraindication with nitrates.
  • Sexual Medicine Society of North America / International Society for Sexual Medicine - clinical guidance on specialised testing and third-line therapies.
  • Princeton Consensus (I-III) - joint sexual-medicine and cardiology recommendations on ED as a cardiovascular-risk marker.
  1. Which of these standards and regulation hold for the sense of erectile dysfunction this model covers, and on what evidence? provenance

Real-world use

Reported by the breadth pass; each item needs checking against its source before it becomes normative.

  • Presents in general practice and urology as difficulty getting or keeping an erection, often first disclosed while requesting a PDE5 inhibitor.
  • Used as a sentinel symptom of atherosclerotic and endothelial disease; new ED in a middle-aged man commonly triggers cardiovascular risk review rather than sexual counselling alone.
  • Graded with IIEF-5/SHIM or EHS to decide watchful waiting, oral PDE5 inhibitors, vacuum devices, intraurethral or intracavernosal alprostadil, or penile prosthesis.
  • Recorded after pelvic surgery, radiotherapy, diabetes, or antidepressant treatment as an expected iatrogenic outcome.
  • Serves as the primary efficacy endpoint in drug and device trials (IIEF erectile-function domain, successful-penetration diaries).
  • Encountered in online and unregulated markets as counterfeit sildenafil/tadalafil sold as 'herbal' sexual enhancers.
  1. Which of these real-world use hold for the sense of erectile dysfunction this model covers, and on what evidence? provenance

Typical measurements

Reported by the breadth pass; each item needs checking against its source before it becomes normative.

  • IIEF-5 (SHIM) total score - 5-7 severe, 8-11 moderate, 12-16 mild-moderate, 17-21 mild, 22-25 no ED - points
  • IIEF erectile-function domain - 6-10 severe, 11-16 moderate, 17-21 mild-moderate, 22-25 mild, 26-30 no ED - points
  • Erection Hardness Score - 0 (none) to 4 (fully rigid); 3 is the usual minimum for penetrative sex - score (0-4)
  • Symptom duration before diagnosis - ≥3 months in EAU practice; DSM-5 requires about 6 months for Erectile Disorder - months
  • Penile duplex peak systolic velocity (after pharmacologic stimulation) - <25 suggests arterial insufficiency; 25-30 borderline; >30 generally adequate inflow - cm/s
  • Penile duplex end-diastolic velocity - >5 with resistive index <0.75 suggests veno-occlusive dysfunction - cm/s
  • Morning total testosterone (ED work-up) - Adult male roughly 8-35 nmol/L (about 230-1000 ng/dL); many guidelines repeat and investigate below about 10.4 nmol/L (300 ng/dL) - nmol/L or ng/dL
  1. Which of these typical measurements hold for the sense of erectile dysfunction this model covers, and on what evidence? provenance

Failure modes and hazards

Reported by the breadth pass; each item needs checking against its source before it becomes normative.

  • Combining a PDE5 inhibitor with organic nitrates or riociguat can cause profound hypotension, syncope, or coronary events.
  • Intracavernosal or intraurethral alprostadil can cause priapism and, with repeated injection, cavernosal fibrosis.
  • Inflatable or malleable penile implants can become infected, erode, or fail mechanically and then require explant.
  • Treating ED as an isolated sexual complaint can miss occult coronary or peripheral arterial disease.
  • Counterfeit or undeclared PDE5 inhibitors in 'herbal' products cause uncontrolled dosing and drug interactions.
  • Chronic untreated ED is associated with anxiety, depression, relationship breakdown, and avoidance of medical care.
  • Rare reported association of PDE5 inhibitors with non-arteritic anterior ischaemic optic neuropathy remains a labelled caution.
  1. Which of these failure modes and hazards hold for the sense of erectile dysfunction this model covers, and on what evidence? provenance

Regional variation

Reported by the breadth pass; each item needs checking against its source before it becomes normative.

  • Coding: ICD-10-CM N52.x in the United States versus ICD-11 HA01.1 where that revision is in force; older charts still say 'impotence'.
  • Access: PDE5 inhibitors are prescription-only in the United States; several European systems allow pharmacy supply of sildenafil under protocol; some health systems historically rationed NHS/public reimbursement by cause or severity.
  • The everyday word remains 'impotence' or local equivalents (impotencia, impuissance) in many languages and older statutes, while clinics use erectile dysfunction.
  • Reporting is strongly shaped by stigma: under-ascertainment is common where sexual difficulty is not a legitimate medical complaint, and traditional frames (e.g. kidney-yang deficiency, semen-loss) still organise help-seeking.
  • Unregulated markets for PDE5-adulterated sexual enhancers are a larger share of real-world exposure in parts of Asia, Africa, and online trade than in tightly regulated clinic pathways.
  1. Which of these regional variation hold for the sense of erectile dysfunction this model covers, and on what evidence? provenance

Neighbouring kinds and how to tell them apart

Reported by the breadth pass; each item needs checking against its source before it becomes normative.

  • Premature ejaculation - Ejaculation latency and perceived control are impaired while erection rigidity is adequate; separate with IELT/PEDT versus IIEF erectile-function items.
  • Hypoactive sexual desire / male hypoactive sexual desire disorder - The primary deficit is lack of desire, not inability to become rigid when desire and stimulation are present; IIEF desire domain and history of morning or masturbatory erections separate the two (they often coexist).
  • Peyronie's disease - Pain, palpable plaque, and curvature or hinge deformity on erection, with or without secondary ED; physical exam and stretched-penile or erect photography separate deformity from primary erectile failure.
  • Hypogonadism - Low morning testosterone with compatible symptoms may cause or worsen ED but is a hormonal diagnosis; repeat total (and free) testosterone plus LH/FSH, not erection scores alone, establishes it.
  • Delayed ejaculation or anejaculation - Orgasm or emission fails despite a usable erection; sexual history of rigidity versus climax, not Doppler, is the discriminator.
  • Age-related slowing of erection without dysfunction - More stimulation or time is needed but rigidity remains sufficient for satisfactory sex; IIEF-5 ≥22 and patient/partner satisfaction mark the boundary with ED.
  • Priapism - A prolonged unwanted erection, ischaemic or otherwise, is the opposite problem; duration >4 hours and pain/rigidity at rest separate it from ED.
  • Female sexual arousal disorder - Different anatomy and diagnostic criteria; the shared word 'arousal' does not make the conditions interchangeable.
  1. Which of these neighbouring kinds and how to tell them apart hold for the sense of erectile dysfunction this model covers, and on what evidence? provenance

Sources

  1. Impotence: NIH Consensus Development Panel on Impotence - The still-cited specialist definition that replaced the older term impotence: inability to attain and/or maintain erection sufficient for satisfactory sexual performance.
  2. Erectile Dysfunction: AUA Guideline - Practice classification, work-up (including cardiovascular risk), IIEF-based severity, and treatment pathway used in North American urology.
  3. EAU Guidelines on Sexual and Reproductive Health - European diagnostic threshold of about three months, organic versus psychogenic work-up, Doppler criteria, and first- to third-line therapy.
  4. ICD-10 code N52 Male erectile dysfunction; ICD-11 code HA01.1 Male erectile dysfunction - The coding identifiers used in health systems to name the condition.
  5. Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision: Erectile Disorder - Psychiatric diagnostic criteria, duration, and situational versus generalised specifiers.
  6. Impotence and its medical and psychosocial correlates: results of the Massachusetts Male Aging Study - Age-associated prevalence and the mixed organic-psychogenic picture seen in community practice.
  7. The international index of erectile function (IIEF): a multidimensional scale for assessment of erectile dysfunction - The IIEF and later IIEF-5/SHIM scores used to grade severity in clinic and trials.
  8. The Princeton III Consensus recommendations for the management of erectile dysfunction and cardiovascular disease - Use of ED as a cardiovascular-risk sentinel and the nitrate contraindication for PDE5 inhibitors.

What the second pass must settle

  • Which clinical diagnostic frameworks should this registry support, and how should their differing persistence, frequency, and distress requirements be represented without conflation?
  • Which erectile-function instruments and interpretations are validated for the intended languages, sexual practices, anatomical contexts, and levels of sexual opportunity?
  • What evidence is sufficient to assign confidence to individual causal contributors when physical and psychological factors coexist?
  • Which jurisdiction-specific cardiovascular assessment, prescribing, interaction-checking, and urgent referral pathways should govern agent-supported actions?
  • How should adequate treatment trials, meaningful improvement, and unaided remission be defined consistently across medicines, devices, counselling, and procedures?