Chronic coronary / ASCVD secondary prevention
Encounter flow
8/12 authoredCanonical 12-phase frame with authored status for this dossier.
Frame
Confirm chronic CCD/ASCVD scope; acute chest pain → cardio.stemi.core.v1 (ACC/AHA 2022)
patient is stable, secondary prevention focus
Patient inputs (12)
PREVENT calculator + drug tolerability (ACC/AHA 2022)
BP target <130/80 in CCD per 2025 HTN
Statin/DOAC dosing, COMPASS rivaroxaban renal cutoff (ACC/AHA 2022)
Target <55 very-high risk; <70 high risk per 2026 Lipid
DAPT duration + intensification post-ACS (ACC/AHA 2022)
DAPT timing, antiplatelet agent selection (ACC/AHA 2022)
COMPASS regimen rivaroxaban 2.5 BID + ASA (ACC/AHA 2022)
Existing statin/antiplatelet — escalation vs initiation (ACC/AHA 2022)
Glycemic control + SGLT2/GLP-1 in DM-ASCVD (ACC/AHA 2022)
2026 universal Lp(a) screening Class 1
Non-HDL/ApoB for residual risk (ACC/AHA 2022)
DAPT bleed risk + extended therapy decision (ACC/AHA 2022)
* = hard-required. Engine cannot meaningfully run until these are filled.
Severity triggers (8)
- informationalsevererecurrent_acsNew chest pain / ECG change / troponin rise in CCD patient (ACC/AHA 2022)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderateldl_above_55_very_high_riskLDL-C ≥55 mg/dL (or non-HDL-C ≥85) in established-ASCVD patient on max-tolerated statin + ezetimibe — residual-cholesterol phenotype (2026 ACC/AHA, PMID 41824590)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderateresidual_inflammatory_risk_hscrphsCRP ≥2 mg/L on optimised statin in established CCD/post-MI — residual-inflammatory phenotypeTrigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderatebp_above_130_80_ccdBP ≥130/80 in CCD patient at clinic visits and home BP (ACC/AHA 2022)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderatedm_a1c_above_7_with_ascvdA1c >7 with ASCVD (ACC/AHA 2022)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderatepad_leg_symptomsClaudication or rest pain with ABI <0.9 (ACC/AHA 2022)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderateaspirin_intolerant_or_high_bleedGI bleed on ASA / very high HAS-BLED (ACC/AHA 2022)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmildpost_mi_ef_preserved_bb_reassessmentPost-MI patient with LVEF ≥50% on a β-blocker without other indication (HF/angina/arrhythmia) — REDUCE-AMI reassessmentTrigger could not be auto-evaluated — needs clinician judgement.
Workflow calculators
Run this disease's risk and dosing calculators inline.
Recommended regimen
2023 AHA/ACC CCD + 2026 Dyslipidemia — secondary-prevention bundle (5 pillars, stepwise)- aspirinfirst lineantiplatelet_COX181 mg • PO • once dailytriggers: established_ASCVDSAPT cornerstone — irreversible COX-1/TxA2 platelet inhibition ~95%, steady-state 5–7 d; ATT secondary-prevention serious-vascular-event ↓~20%. Lifelong unless a defined DAPT/DPI window (2023 CCD Class I, PMID 37471501)rxcui 1191
- clopidogreladd onP2Y12_inhibitor75 mg • PO • once dailytriggers: recent_PCI, recent_ACS, aspirin_intolerantDAPT × 6–12 mo post-PCI; P2Y12 ~40–60% inhibition (CYP2C19-dependent), onset 2 h with 300–600 mg load. As SAPT monotherapy when ASA-intolerant: CAPRIE composite RRR 8.7% (95% CI 0.3–16.5) vs ASA (PMID 8918275)rxcui 32968
- ticagreloradd onP2Y12_inhibitor60 mg BID (extended DAPT) or 90 mg BID (≤1 y post-ACS) • PO • BIDtriggers: high_risk_post_MI, recent_ACSReversible P2Y12 ~80–90% inhibition, onset 30 min–2 h. PEGASUS-TIMI 54 60 mg BID beyond 1 y: CV death/MI/stroke HR 0.84 (0.74–0.95), TIMI major bleed 2.30 vs 1.06% (PMID 25773268)rxcui 1116632
- prasugreladd onP2Y12_inhibitor10 mg (5 mg if <60 kg or ≥75 y) • PO • once dailytriggers: post_PCI_ACS, no_prior_stroke_TIAIrreversible P2Y12 ~80% inhibition; post-PCI ACS DAPT. Contraindicated with prior stroke/TIA (net-harm signal)rxcui 613391
- rivaroxabanadd onDOAC_FXa_low_dose2.5 mg BID + ASA 81 mg • PO • BIDtriggers: stable_CAD_or_PAD, no_high_bleed_risk, CrCl_ge_15COMPASS dual-pathway (vascular dose): MI/stroke/CV death HR 0.74 (0.65–0.86), all-cause death HR 0.77 (0.65–0.90), major bleed HR 1.66 (1.37–2.03) vs ASA alone (PMID 29132879)rxcui 1114195
outpatient playbook — drug actions (6)
- 1. aspirin 81 mg81 mg • PO • dailytrigger: Established ASCVD (ACC/AHA 2022)Lifelong (ACC/AHA 2022)
- 2. high-intensity statin + ezetimibeAtorvastatin 80 + ezetimibe 10 • PO • dailytrigger: LDL >55 (ACC/AHA 2022)IMPROVE-IT (ACC/AHA 2022)
- 3. PCSK9i if LDL >55 on statin + ezetimibeEvolocumab 140 mg q2w • SC • q2wtrigger: LDL above goal (ACC/AHA 2022)FOURIER (ACC/AHA 2022)
- 4. ACEi/ARB + BB if EF <40 / recent MILisinopril 10-40 mg + metoprolol succinate 25-200 mg • PO • dailytrigger: LV dysfunction or post-MI (ACC/AHA 2022)HOPE / CAPRICORN (ACC/AHA 2022)
- 5. SGLT2i + GLP-1 in DMEmpagliflozin 10 mg + semaglutide 0.25 mg weekly titrated • PO + SC • daily / weeklytrigger: DM + ASCVD (ACC/AHA 2022)EMPA-REG / SELECT (ACC/AHA 2022)
- 6. COMPASS rivaroxaban 2.5 BID + ASA in stable CAD/PAD2.5 mg BID + ASA 81 • PO • BIDtrigger: Stable CAD or PAD with low bleed risk + CrCl >15 (ACC/AHA 2022)COMPASS (ACC/AHA 2022)
Auto-drafted A&P note
outpatientSubjective
- Possible entry pathways: Prior MI / PCI / CABG (ACC/AHA 2022); Stable angina / chronic coronary syndrome (ACC/AHA 2022); PAD or carotid disease (ASCVD broader) (ACC/AHA 2022).
Objective
- No vitals, labs, or imaging entered for this encounter.
Assessment
**Chronic coronary / ASCVD secondary prevention** (cardio.ascvd.chronic.v1). Scope: Confirm chronic CCD/ASCVD scope; acute chest pain → cardio.stemi.core.v1 (ACC/AHA 2022) No severity triggers fired against current inputs.
Plan
Regimen axis: **2023 AHA/ACC CCD + 2026 Dyslipidemia — secondary-prevention bundle (5 pillars, stepwise)** — step "Step 1 — Antiplatelet / antithrombotic". 1. aspirin 81 mg PO once daily (antiplatelet_COX1, first line) — SAPT cornerstone — irreversible COX-1/TxA2 platelet inhibition ~95%, steady-state 5–7 d; ATT secondary-prevention serious-vascular-event ↓~20%. Lifelong unless a defined DAPT/DPI window (2023 CCD Class I, PMID 37471501) 2. clopidogrel 75 mg PO once daily (P2Y12_inhibitor, add on) — DAPT × 6–12 mo post-PCI; P2Y12 ~40–60% inhibition (CYP2C19-dependent), onset 2 h with 300–600 mg load. As SAPT monotherapy when ASA-intolerant: CAPRIE composite RRR 8.7% (95% CI 0.3–16.5) vs ASA (PMID 8918275) 3. ticagrelor 60 mg BID (extended DAPT) or 90 mg BID (≤1 y post-ACS) PO BID (P2Y12_inhibitor, add on) — Reversible P2Y12 ~80–90% inhibition, onset 30 min–2 h. PEGASUS-TIMI 54 60 mg BID beyond 1 y: CV death/MI/stroke HR 0.84 (0.74–0.95), TIMI major bleed 2.30 vs 1.06% (PMID 25773268) 4. prasugrel 10 mg (5 mg if <60 kg or ≥75 y) PO once daily (P2Y12_inhibitor, add on) — Irreversible P2Y12 ~80% inhibition; post-PCI ACS DAPT. Contraindicated with prior stroke/TIA (net-harm signal) 5. rivaroxaban 2.5 mg BID + ASA 81 mg PO BID (DOAC_FXa_low_dose, add on) — COMPASS dual-pathway (vascular dose): MI/stroke/CV death HR 0.74 (0.65–0.86), all-cause death HR 0.77 (0.65–0.90), major bleed HR 1.66 (1.37–2.03) vs ASA alone (PMID 29132879) Setting playbook (outpatient) — Maintain all 5 secondary-prevention pillars at goal; identify gaps annually; integrate cardiometabolic comorbidity therapies (DM/HF) (ACC/AHA 2022) 6. aspirin 81 mg 81 mg PO daily — Established ASCVD (ACC/AHA 2022) (Lifelong (ACC/AHA 2022)) 7. high-intensity statin + ezetimibe Atorvastatin 80 + ezetimibe 10 PO daily — LDL >55 (ACC/AHA 2022) (IMPROVE-IT (ACC/AHA 2022)) 8. PCSK9i if LDL >55 on statin + ezetimibe Evolocumab 140 mg q2w SC q2w — LDL above goal (ACC/AHA 2022) (FOURIER (ACC/AHA 2022)) 9. ACEi/ARB + BB if EF <40 / recent MI Lisinopril 10-40 mg + metoprolol succinate 25-200 mg PO daily — LV dysfunction or post-MI (ACC/AHA 2022) (HOPE / CAPRICORN (ACC/AHA 2022)) 10. SGLT2i + GLP-1 in DM Empagliflozin 10 mg + semaglutide 0.25 mg weekly titrated PO + SC daily / weekly — DM + ASCVD (ACC/AHA 2022) (EMPA-REG / SELECT (ACC/AHA 2022)) 11. COMPASS rivaroxaban 2.5 BID + ASA in stable CAD/PAD 2.5 mg BID + ASA 81 PO BID — Stable CAD or PAD with low bleed risk + CrCl >15 (ACC/AHA 2022) (COMPASS (ACC/AHA 2022)) Non-pharmacologic actions: - Cardiac rehabilitation (Class I) - Mediterranean / DASH diet (ACC/AHA 2022) - 150 min/week aerobic + resistance (ACC/AHA 2022) - Smoking cessation pharmacotherapy (ACC/AHA 2022) - Annual flu + pneumococcal + COVID + RSV (ACC/AHA 2022) - AAA screening if eligible (ACC/AHA 2022) - Sleep apnoea screen (ACC/AHA 2022) AVOID / contraindication checks: - DAPT_avoid_high_bleed_risk — 2023 CCD (PMID 37471501) - DPI_rivaroxaban_avoid_high_bleed_or_CrCl_below_15 — COMPASS exclusion (PMID 29132879) - Prasugrel_avoid_prior_stroke_TIA — net harm signal - ACEi_ARB_avoid_pregnancy — 2023 CCD Class III - Beta_blocker_avoid_decompensated_HF_or_high_grade_AV_block — 2023 CCD - Beta_blocker_deescalate_if_post_MI_EF_preserved — REDUCE AMI (PMID 38587241) - Colchicine_avoid_eGFR_below_30_or_strong_CYP3A4_Pgp_inhibitor — COLCOT/LoDoCo2 dosing - Icosapent_caution_AF_and_bleeding — REDUCE IT (PMID 30415628) - GLP1_avoid_personal_family_MTC_MEN2 — label - SGLT2_hold_periprocedural_NPO_DKA_risk — 2023 CCD
Monitoring
Regimen monitoring: - lipid panel 4-12wk post-change then q3-12 months (2026 ACC/AHA PMID 41824590) - BMP q3-6 months (2023 CCD PMID 37471501) - A1c q3-6 months in DM (ADA SoC 2026) - BP at each visit target below 130 80 (2025 HBP PMID 40811516) - CK/LFT with statin only if symptomatic (2026 ACC/AHA) - cardiac rehab completion (Cochrane CR PMID 34741536) Setting (outpatient) monitoring: - Lipid + BP + A1c + BMP cadence per pillars (ACC/AHA 2022) - Adherence assessment (ACC/AHA 2022) - Symptom-driven workup if recurrent angina (ACC/AHA 2022) Follow-up plan: Cardiac rehab referral, vaccination (flu/pneumococcal/COVID), lifestyle, AAA screening if eligible (ACC/AHA 2022) - Close-out criterion: follow-up + adjunctive prevention plan in place Monitoring phase: Lipid 4–12 wks post-change then q3–12 mo; LFT/CK with statin only if symptomatic; A1c q3–6 mo; BP at each visit (ACC/AHA 2022)
Disposition
Current setting: outpatient — Maintain all 5 secondary-prevention pillars at goal; identify gaps annually; integrate cardiometabolic comorbidity therapies (DM/HF) (ACC/AHA 2022) Disposition criteria: - At goal across pillars → q6–12 month visits (ACC/AHA 2022) - Gaps → q3 month visits until optimised (ACC/AHA 2022) Escalation triggers (move to higher acuity): - Recurrent angina / equivalent → calc.heart triage; consider repeat angiography (ACC/AHA 2022) - Acute chest pain → ED + STEMI engine (ACC/AHA 2022) - New HF symptoms → echo + HF engine (ACC/AHA 2022)
Earlier-Return Triggers
Return-precaution thresholds (watch for): - [SEVERE] New chest pain / ECG change / troponin rise in CCD patient (ACC/AHA 2022) - [MODERATE] LDL-C ≥55 mg/dL (or non-HDL-C ≥85) in established-ASCVD patient on max-tolerated statin + ezetimibe — residual-cholesterol phenotype (2026 ACC/AHA, PMID 41824590) - [MODERATE] hsCRP ≥2 mg/L on optimised statin in established CCD/post-MI — residual-inflammatory phenotype
Citations
- 2023 AHA/ACC/ACCP/ASPC/NLA/PCNA Chronic Coronary Disease Guideline (PMID 37471501, DOI 10.1161/CIR.0000000000001168) + 2026 ACC/AHA Multisociety Dyslipidemia Guideline (PMID 41824590/41824552) + 2019 AHA/ACC Primary Prevention (PMID 31613350) + 2025 AHA/ACC HBP + ADA SoC 2026 [PMID:37471501](https://pubmed.ncbi.nlm.nih.gov/37471501/) - Cited evidence (PMID 41824590) [PMID:41824590](https://pubmed.ncbi.nlm.nih.gov/41824590/) - Cited evidence (PMID 41824552) [PMID:41824552](https://pubmed.ncbi.nlm.nih.gov/41824552/) - Cited evidence (PMID 8918275) [PMID:8918275](https://pubmed.ncbi.nlm.nih.gov/8918275/) - Cited evidence (PMID 25773268) [PMID:25773268](https://pubmed.ncbi.nlm.nih.gov/25773268/) Last reconciled with current guidelines: 2026-05-26.
- 2023 AHA/ACC/ACCP/ASPC/NLA/PCNA Chronic Coronary Disease Guideline (PMID 37471501, DOI 10.1161/CIR.0000000000001168) + 2026 ACC/AHA Multisociety Dyslipidemia Guideline (PMID 41824590/41824552) + 2019 AHA/ACC Primary Prevention (PMID 31613350) + 2025 AHA/ACC HBP + ADA SoC 2026 — PMID:37471501
- Cited evidence (PMID 41824590) — PMID:41824590
- Cited evidence (PMID 41824552) — PMID:41824552
- Cited evidence (PMID 8918275) — PMID:8918275
- Cited evidence (PMID 25773268) — PMID:25773268