Cervical cancer screening (adult)
NEW preventive cervical-screening dossier authored 2026-05-16 (design-disease-first): child of the deepened prev.cancer-screening.core.v1; copies its screening-as-data structure exactly, narrowed to the cervix; authored to pulm.pe.core.v1 §5.5.2 Bayesian rigor. SCHEMA GAP: EngineDossier has NO first-class sensitivity/specificity/LR/PPV/pre-test-prevalence/ASCCP-risk-%/NNS field — the per-modality test-characteristic table, the age-band→modality matrix, and the ASCCP 2019 risk→action table are the authoritative payload in _briefs/prev.cervical-cancer-screening.v1.depth.md; encoded narratively here via severity_triggers, phase purpose/advance_when, calculator guideline_basis, and regimen rationale. SCHEMA GAP: RequiredCalculator.drives enum has no screening_eligibility/risk_table value — the ASCCP 2019 risk-table calculator uses drives:"risk_stratification". SCHEMA GAP: DossierDomain has no preventive_medicine value → general_internal_medicine (same workaround as parent). SCHEMA GAP: no dedicated cervical-cancer/colposcopy/CIN-treatment terminal engine exists on disk — the colposcopy/treatment pathway is encoded as differential-as-data (ASCCP risk table); branches_to only to grep-confirmed engine_ids (prev.cancer-screening.core.v1 parent, prev.adult-immunization.core.v1, gyn.pelvic-inflammatory-disease.core.v1). EVIDENCE: 12 PMIDs, all PubMed-verified 2026-05-16 (parent-engine PMIDs NOT blindly reused — cervical-specific set). ≥10 effect-size numbers: hrHPV sens 94.6% vs cytology 55.4% (Mayrand 17942871); spec 94.1% vs 96.8%; pooled invasive-ca RR 0.60 / 0.30 entry-negative (Ronco 24192252); ARTISTIC round-2 CIN3+ OR 0.53 (Kitchener 19540162); 10-y post-neg-HPV CIN3+ 0.31% ≈ 3-y post-cytology 0.30% (Gilham 31219027); Compass primary-HPV CIN2+ 1.0-1.2% vs 0.1% (28926579); self vs clinician sens ratio 0.99 + participation RR 2.33 (Arbyn 30518635); HPV-vaccination IRR 0.37 / 0.12 if <17y (Lei 32997908); ASCCP colpo threshold immediate CIN3+ ≥4%, 5-y return <0.15%, expedited treatment ≥60% (Perkins 32243307 / Egemen 32243308); deaths 2.8→2.3/100k 2000-2015 (USPSTF 30140884). See .depth.md for the full per-PMID table. GUIDELINE CURRENCY: USPSTF 2018 (PMID 30140884) is the binding FINAL floor. USPSTF posted a Dec-2024 DRAFT moving to primary-HPV-preferred-from-30 + patient/self-collected HPV (pooled CIN2+ sens 0.86 / spec 0.81) — NOT yet final, encoded as an emerging branch (self-collection axis entry, advance notes). ACS 2020 (PMID 32729638) already operationalizes start-25 + hrHPV-primary-preferred (transitional). Re-reconcile when the USPSTF 2024 draft finalizes. Special-population branches (≥4) encoded as triggers + contraindication_rules: age-21-29 cytology vs age-30-65 hrHPV/co-test/cytology, immunocompromised/HIV (more frequent, continue past 65), post-treatment-CIN surveillance (25-yr elevated-risk tail), STOP (>65 adequate-negative / post-benign-hysterectomy), HPV-vaccinated-cohort (prevalence shift, protocol unchanged), DES exposure, pregnancy (continue screening, defer low-grade colposcopy), self-collection (equity for under-screened). No hand-authored RxCUIs (screening engine — no pharmacotherapy). HPV-vaccination catch-up referenced only via the registry workup id workup.hpv as adjacent primary prevention (no CUI authored). Registry ids reused (confirmed resolve in clinical-tools-registry.ts PREVENTIVE_TOOLS): workup.cervical_screening_hpv_pap, panel.hpv_genotyping, workup.genetic_counseling, workup.hpv. No new registry ids invented; registry NOT edited. Cross-dossier engine_ids (real, grep-confirmed on disk 2026-05-16): prev.cancer-screening.core.v1, prev.adult-immunization.core.v1, gyn.pelvic-inflammatory-disease.core.v1 — wired via workups[].branches_to + 3 sibling_differentiation blocks. PROMOTED 2026-05-25 (PLANNED→INTEGRATED): dedicated seed manifest authored at prisma/seed/manifests/prev.cervical-cancer-screening.v1.ts (specialty_pack preventive_medicine; sourceWorkupIds [cervical_cancer_screening]; terminology projected 1:1 from this dossier — no new codes); all 12 PMIDs re-verified live vs PubMed E-utilities (every title matches its inline claim — zero fabricated citations); no RxCUIs to verify (screening engine, every regimen drug is non_pharm). manifest: pointer repointed off id.sepsis.core.v1.ts to the new file. NEXT STEPS: (1) build age-band modality + ASCCP-2019-risk-table atoms; (2) cytology/hrHPV/genotype result-interpretation atoms; (3) re-reconcile when USPSTF 2024 cervical draft finalizes.
Entry points (5)
- historyRoutine preventive/wellness visit — age-appropriate cervical screening due (USPSTF 2018 Grade A PMID 30140884)routine_preventive_visit
- historyOverdue or never-screened person with a cervix identified at any encounter — equity recall (self-collection option; Arbyn BMJ 2018 PMID 30518635)overdue_or_never_screened
- historyFollow-up of a prior abnormal cytology/hrHPV/genotype result — apply ASCCP 2019 risk-table reasoning (Perkins PMID 32243307)abnormal_prior_result_followup
- historyPost-treatment CIN2/3 surveillance entry — 25-year elevated-risk tail, NOT routine interval (ASCCP 2019 PMID 32243307)post_treatment_cin_surveillance
- historyHPV-vaccinated-cohort review — prevalence sharply lower (Lei NEJM 2020 IRR 0.37 PMID 32997908) but protocol unchanged per USPSTF 2018 / ACS 2020hpv_vaccinated_cohort_review
Required inputs (14)
- agerequireddemographic • used at CONTEXTAge band IS the modality decision and sets the pre-test prevalence prior: <21 none (Grade D), 21-29 cytology q3y, 30-65 hrHPV/co-test/cytology, >65 stop if adequate-negative (USPSTF 2018 PMID 30140884)
- has_cervixrequireddemographic • used at FRAMEPerson must have a cervix — post-total-hysterectomy with cervix removed for benign indication and no CIN2+ history = no pretest target (USPSTF 2018 Grade D PMID 30140884)
- prior_screening_resultsrequiredhistory • used at CONTEXTPrior cytology/hrHPV/genotype dates + results set the CONDITIONAL post-test prior — a prior negative hrHPV greatly lowers current-abnormality CIN3+ risk (Egemen KPNC tables PMID 32243308)
- hysterectomy_statusrequiredhistory • used at CONTEXTTotal hysterectomy (cervix removed) for benign indication with no CIN2+ history = STOP screening (Grade D); supracervical/subtotal hysterectomy retains the cervix → continue (USPSTF 2018 PMID 30140884)
- immunocompromised_or_hivrequiredhistory • used at RISK_STRATIFICATIONHIV/immunocompromise = higher prior + faster CIN progression → start within 1 yr of sexual activity, screen more frequently, continue past 65 (special-population branch — not average-risk interval)
- hpv_vaccination_statushistory • used at CONTEXTQuadrivalent HPV vaccination lowers the prevalence prior substantially (IRR 0.37; 0.12 if <17 y — Lei NEJM 2020 PMID 32997908) but per USPSTF 2018 / ACS 2020 the screening protocol is unchanged (transitional)
- prior_cin_treatmenthistory • used at RISK_STRATIFICATIONPrior CIN2/3 treatment carries a ~25-year elevated CIN3+ risk tail — HPV-based surveillance, do NOT return to routine interval (ASCCP 2019 PMID 32243307)
- pregnancy_statushistory • used at CONTEXTPregnancy: continue age-appropriate screening but defer colposcopy/biopsy work-up of low-grade abnormalities per ASCCP — special-population branch
- des_exposurehistory • used at RISK_STRATIFICATIONIn-utero diethylstilbestrol exposure raises clear-cell adenocarcinoma prior → off-interval intensified screening (special-population branch)
- abnormal_vaginal_bleeding_or_visible_lesionsymptom • used at RED_FLAGSA visible cervical lesion or abnormal/post-coital bleeding is a DIAGNOSTIC indication (exit to diagnostic work-up), NOT average-risk screening (USPSTF 2018 scope)
- cytology_resultlab • used at BRANCHING_WORKUPCytology sens for CIN2/3 ~55.4% single-test (Mayrand NEJM 2007 PMID 17942871); NILM/ASC-US/LSIL/ASC-H/HSIL category is a likelihood input to the ASCCP risk table
- hrhpv_resultlab • used at BRANCHING_WORKUPPrimary hrHPV sens ~94.6% > cytology (Mayrand PMID 17942871); negative-hrHPV 10-y CIN3+ risk ≈ negative-cytology 3-y (Gilham ARTISTIC PMID 31219027) — drives the q5y interval
- hpv_16_18_genotypelab • used at BRANCHING_WORKUPHPV-16/18 partial genotyping is a high-LR+ stratifier → immediate colposcopy; other-hrHPV → reflex cytology triage (ASCCP 2019 PMID 32243307)
- self_collected_hrhpvlab • used at INITIAL_WORKUPFDA-approved 2024 self-collection: PCR-based self vs clinician hrHPV sens ratio 0.99 (Arbyn BMJ 2018 PMID 30518635); pooled absolute CIN2+ sens 0.86 / spec 0.81 (USPSTF 2024 draft) — equity tool for under-screened
12-phase flow (12)
- 1FRAMEConfirm cervical-screening scope: asymptomatic person WITH A CERVIX, age 21-65. Excludes <21 (Grade D — transient HPV/regressive CIN, overdiagnosis dominates), >65 with adequate prior negatives (Grade D), post-total-hysterectomy for benign indication with no CIN2+ history (Grade D — no pretest target), and any visible lesion/abnormal bleeding (→ diagnostic work-up, not screening) (USPSTF 2018 PMID 30140884)inputs: age, has_cervixadvance: Asymptomatic, has cervix, age 21-65, not in a Grade-D stop category
- 2ENTRYTrigger: routine wellness visit, overdue/never-screened recall (equity — self-collection option), prior-abnormal-result follow-up, post-treatment-CIN surveillance entry, or HPV-vaccinated-cohort review (USPSTF 2018; ACS 2020 PMID 32729638)advance: Entry trigger captured
- 3CONTEXTSet the pre-test prevalence prior: age band, prior cytology/hrHPV/genotype results (CONDITIONAL prior — prior-negative-hrHPV greatly lowers current-abnormality risk, Egemen PMID 32243308), hysterectomy status + indication, HIV/immunocompromise, HPV-vaccination status (Lei NEJM 2020 IRR 0.37 PMID 32997908 — prior shifts, protocol unchanged), pregnancy, DES exposure. This phase SETS the Bayesian prior — modality choice flows from itinputs: age, prior_screening_results, hysterectomy_status, hpv_vaccination_status, pregnancy_statusadvance: Pre-test prevalence tier + age band assignable
- 4RED_FLAGSA visible cervical lesion, abnormal/post-coital bleeding, or new symptoms = DIAGNOSTIC indication → exit average-risk screening to diagnostic colposcopy/work-up. HIV/immunocompromise → off-interval more-frequent screening (not average-risk). Rare hereditary look-alike (e.g., Peutz-Jeghers cervical adenoma malignum) → genetics referral (NCCN). Symptomatic cervicitis/PID is a gyn look-alike — route to gyn.pelvic-inflammatory-disease.core.v1, do NOT process as screeninginputs: abnormal_vaginal_bleeding_or_visible_lesion, immunocompromised_or_hivactions: workup.genetic_counselingadvance: Diagnostic/look-alike indications excluded or routed; average-risk eligibility confirmed
- 5INITIAL_WORKUPOrder the age-band-appropriate screen — the test with its fixed characteristics: 21-29 cytology q3y (sens ~55.4% single-test, Mayrand PMID 17942871); 30-65 primary hrHPV q5y (sens ~94.6%, PREFERRED per ACS 2020 / USPSTF-2024-draft) OR co-test q5y OR cytology q3y (USPSTF 2018 Grade A PMID 30140884). Self-collected hrHPV (PCR-based, sens ratio 0.99 vs clinician — Arbyn PMID 30518635) offered to under-screened. Each order is the "treatment"inputs: age, self_collected_hrhpvactions: workup.cervical_screening_hpv_pap, panel.hpv_genotypingadvance: Age-band-appropriate screen ordered (modality documented; self-collection offered to under-screened)
- 6BRANCHING_WORKUPGenotype/cytology triage of the positive screen — the second conditional likelihood layer: HPV-16/18+ (high LR+) → immediate colposcopy; other-hrHPV+ → reflex cytology (NILM → 1-yr surveillance vs ASC-US+/abnormal → colposcopy per ASCCP risk %); co-test discordance resolved by the ASCCP risk table. Feeds the structured result into RISK_STRATIFICATION (ASCCP 2019 PMID 32243307; Egemen PMID 32243308)inputs: cytology_result, hrhpv_result, hpv_16_18_genotypeactions: panel.hpv_genotypingadvance: Every positive screen has a genotype/cytology-triaged ASCCP-risk-table input assembled
- 7DIFFERENTIALAverage-risk vs special-population (HIV/immunocompromised, post-treatment-CIN, DES, pregnancy), AND true-positive (CIN3+/AIS/invasive) vs false-positive (transient HPV, reactive/inflammatory cytology, regressive CIN overdiagnosis). The false-positive cascade + over-screening overdiagnosis are encoded as harm DATA, not prose; screen-negative returns to interval (USPSTF 2018; ASCCP 2019)advance: Each result classified as average/special-pop and true/false-positive likelihood assigned
- 8RISK_STRATIFICATIONASCCP 2019 risk-based management — the post-test decision engine: the current+recent-past result combination maps to an immediate & 5-year CIN3+ risk percentage → one of six actions: 5-y return to routine (5-y CIN3+ risk <0.15%), 3-y surveillance (~0.15-0.54%), 1-y surveillance (~0.55-3.9%), colposcopy/biopsy (immediate CIN3+ risk ≥4%), or expedited treatment (immediate ≥60%, e.g., HPV-16+ HSIL). Risk is CONDITIONAL on screening history (Perkins PMID 32243307; Egemen KPNC 1.5M PMID 32243308)inputs: prior_screening_results, immunocompromised_or_hiv, prior_cin_treatment, des_exposureactions: calc.asccp_risk_based_managementadvance: ASCCP risk % computed and the corresponding 1-of-6 action threshold assigned
- 9TREATMENTThe screen IS the intervention; document modality + shared decision (hrHPV-primary preferred 30-65 per ACS 2020 PMID 32729638). Adjacent primary prevention: HPV-vaccination catch-up through age 26 (ACIP) — does NOT change the screening interval (USPSTF 2018) but reduces future prevalence (Lei NEJM 2020 IRR 0.37 PMID 32997908). No pharmacotherapy in this engineactions: workup.hpvadvance: Screen completed, modality + shared decision documented, HPV-vaccination status addressed
- 10DISPOSITIONAll screening is ambulatory. ASCCP immediate CIN3+ risk ≥4% → colposcopy referral; CIN3+/AIS/invasive → gynecologic oncology (differential-as-data — no dedicated colposcopy/CIN terminal engine on disk). Symptomatic gyn look-alike → gyn.pelvic-inflammatory-disease.core.v1; HPV-vaccination need → prev.adult-immunization.core.v1; broader multi-cancer screening context → parent prev.cancer-screening.core.v1 (ASCCP 2019; USPSTF 2018)advance: Disposition + referral route documented per ASCCP risk tier
- 11MONITORINGInterval + recall by age band AND ASCCP risk tier: cytology q3y 21-29; hrHPV q5y or co-test q5y or cytology q3y 30-65 (hrHPV-primary preferred per ACS 2020 / USPSTF-2024-draft); negative-hrHPV safe ≥5y (10-y CIN3+ risk 0.31% ≈ 3-y post-cytology — Gilham ARTISTIC PMID 31219027); 1-yr/3-yr surveillance per ASCCP risk %; post-treatment-CIN HPV-based surveillance with a 25-yr elevated-risk tail; immunocompromised/HIV more frequent and beyond 65 (USPSTF 2018; ASCCP 2019)advance: Next-screen date set by age band + ASCCP risk tier; recall scheduled
- 12FOLLOWUPSTOP-screening / over-screening-harm logic (the deprescribing-equivalent): discontinue at >65 with adequate prior negatives (≥3 consecutive negative cytology OR ≥2 negative hrHPV/co-test in 10 y, most recent within 5 y) and no CIN2+ in 25 y; discontinue after total hysterectomy for benign indication with no CIN2+ history (USPSTF 2018 Grade D PMID 30140884). Patient education: over-screening harms (colposcopy/biopsy of regressive CIN, overtreatment), the value of NOT screening <21 / >65 / post-benign-hysterectomy, and that HPV vaccination does not change the interval (transitional — ACS 2020)inputs: age, hysterectomy_statusadvance: Stop-screening decision OR continued-interval education delivered and documented