Late-presenter STEMI (>12 h after symptom onset)
Encounter flow
10/12 authoredCanonical 12-phase frame with authored status for this dossier.
Frame
Late-presenter STEMI = symptom onset >12 h ago. Decision axis: ongoing ischemia / shock / arrhythmia → emergent reperfusion (Class I); asymptomatic 12-72 h + viable myocardium → IIa delayed PCI; >72 h asymptomatic stable → OMT only per OAT
time-from-onset stratification documented
Patient inputs (9)
Elderly more likely to be late presenters; STREAM-2 half-dose TNK considerations
Contrast nephropathy risk for cath + DOAC dosing post-MI
Time-from-onset is the central decision axis: <12 h → emergent PCI; 12-72 h asymptomatic + viable → IIa PCI; >72 h asymptomatic stable → OMT only (OAT)
Persistent ST elevation vs evolved Q-waves drives reperfusion decision; rapidly evolving Q-waves → completed infarction with less viability
Trajectory (rising vs peaked-and-falling) helps localize where in the infarct timeline patient sits
Bedside echo: LVEF, regional wall motion, LV thrombus (more common in late presenters), aneurysm, mechanical complications
Persistent / recurrent chest pain or dynamic ECG → reperfusion still Class I regardless of time window
Hypotension / shock → emergent reperfusion regardless of time window (SCAI 2022)
Cardiac MRI with LGE / dobutamine stress echo / PET — for asymptomatic 12-72 h presenters to identify candidates for delayed PCI; viable myocardium >50% supplies revascularization benefit
* = hard-required. Engine cannot meaningfully run until these are filled.
Severity triggers (4)
- informationallife_threateninglate_stemi_with_shock_at_presentationLate-presenter STEMI + SBP <90 + lactate ≥2 + hypoperfusion — SCAI C+ at presentationTrigger could not be auto-evaluated — needs clinician judgement.
- informationallife_threateningmechanical_complication_in_late_presenterNew harsh holosystolic murmur OR pericardial effusion on echo OR sudden hemodynamic deterioration → free-wall rupture / VSR / papillary rupture (peak risk 3-7 d post-MI, more common in late presenters who never reperfused)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalseverelv_thrombus_in_late_presenter_on_echoLV thrombus on echo at 5-7 d post late STEMI — markedly higher rate in late presenters with anterior territory + EF <40 + apical akinesiaTrigger could not be auto-evaluated — needs clinician judgement.
- informationalsevereventricular_aneurysm_with_thrombusLate-presenter STEMI with developed ventricular aneurysm (typically anterior, apical) + mural thrombus on cardiac MRI / echoTrigger could not be auto-evaluated — needs clinician judgement.
Workflow calculators
Run this disease's risk and dosing calculators inline.
Recommended regimen
Late-presenter STEMI temporal phenotype — adds to parent cardio.stemi.core.v1 regimen if reperfusion indicated; otherwise OMT-only with secondary prevention bundle- aspirinfirst lineantiplatelet_cox1162-325 mg chewed • PO • load + 81 mg daily indefinitelytriggers: late_stemi_confirmedAHA 2025 ACS Class I — secondary prevention regardless of reperfusion decisionrxcui 243670
- ticagrelorfirst linep2y12_inhibitor180 mg load → 90 mg BID • PO • BID × 12 mo if PCI performedtriggers: late_stemi_pci_plannedPLATO PMID 19717846; only if PCI performedrxcui 1116632
- clopidogrelsecond linep2y12_inhibitor300 mg load → 75 mg daily • PO • daily × 12 mo if no PCI but late STEMI with persistent ECG changestriggers: late_stemi_no_pci_omt_only, ticagrelor_contraindicationOMT-only late STEMI: ASA + clopidogrel for secondary prevention per ACC/AHA 2025rxcui 309362
- atorvastatinfirst linestatin_high_intensity80 mg • PO • daily indefinitelytriggers: late_stemi_confirmedPROVE-IT PMID 15007110; high-intensity statin regardless of reperfusionrxcui 83367
- carvedilolfirst linebeta_blocker_nonselective3.125 mg BID titrate • PO • BIDtriggers: late_stemi_with_lv_dysfunction, ef_below_40CAPRICORN PMID 11356436 — post-MI BB benefit independent of reperfusionrxcui 20352
- warfarincomorbidity specificvitamin_k_antagonist5 mg daily; INR 2-3 × 3 mo • PO • dailytriggers: lv_thrombus_on_echo, ventricular_aneurysm_with_thrombusLate presenters have higher LV thrombus / aneurysm rate; AHA 2022 Class IIa 3-mo ACrxcui 11289
- tenecteplaserescuethrombolytic_fibrin_specifichalf-dose if age ≥75 (STREAM-2); standard weight-based otherwise • IV • single bolustriggers: late_stemi_no_pci_capability_within_120_min, ongoing_ischemia_persistent_st_elevationSTREAM-2 (Armstrong 2020) — half-dose TNK in elderly; only when PCI not feasible AND ongoing ischemiarxcui 259280
outpatient playbook — drug actions (1)
- 1. continue secondary-prevention bundlerxcui 243670ASA 81 + P2Y12 × 12 mo + atorvastatin 80 + GDMT • PO • as scheduledtrigger: post-late-STEMIAHA 2025
Auto-drafted A&P note
outpatientSubjective
- Possible entry pathways: Ischemic chest pain with onset >12 h ago + persistent ST elevation; Persistent ST elevation + evolving Q waves on ECG (late STEMI); Delayed presentation (>12 h) with ongoing chest pain or hemodynamic instability — reperfusion still indicated.
Objective
- No vitals, labs, or imaging entered for this encounter.
Assessment
**Late-presenter STEMI (>12 h after symptom onset)** (cardio.stemi.late-presenter.v1). Scope: Late-presenter STEMI = symptom onset >12 h ago. Decision axis: ongoing ischemia / shock / arrhythmia → emergent reperfusion (Class I); asymptomatic 12-72 h + viable myocardium → IIa delayed PCI; >72 h asymptomatic stable → OMT only per OAT No severity triggers fired against current inputs.
Plan
Regimen axis: **Late-presenter STEMI temporal phenotype — adds to parent cardio.stemi.core.v1 regimen if reperfusion indicated; otherwise OMT-only with secondary prevention bundle**. 1. aspirin 162-325 mg chewed PO load + 81 mg daily indefinitely (antiplatelet_cox1, first line) — AHA 2025 ACS Class I — secondary prevention regardless of reperfusion decision 2. ticagrelor 180 mg load → 90 mg BID PO BID × 12 mo if PCI performed (p2y12_inhibitor, first line) — PLATO PMID 19717846; only if PCI performed 3. clopidogrel 300 mg load → 75 mg daily PO daily × 12 mo if no PCI but late STEMI with persistent ECG changes (p2y12_inhibitor, second line) — OMT-only late STEMI: ASA + clopidogrel for secondary prevention per ACC/AHA 2025 4. atorvastatin 80 mg PO daily indefinitely (statin_high_intensity, first line) — PROVE-IT PMID 15007110; high-intensity statin regardless of reperfusion 5. carvedilol 3.125 mg BID titrate PO BID (beta_blocker_nonselective, first line) — CAPRICORN PMID 11356436 — post-MI BB benefit independent of reperfusion 6. warfarin 5 mg daily; INR 2-3 × 3 mo PO daily (vitamin_k_antagonist, comorbidity specific) — Late presenters have higher LV thrombus / aneurysm rate; AHA 2022 Class IIa 3-mo AC 7. tenecteplase half-dose if age ≥75 (STREAM-2); standard weight-based otherwise IV single bolus (thrombolytic_fibrin_specific, rescue) — STREAM-2 (Armstrong 2020) — half-dose TNK in elderly; only when PCI not feasible AND ongoing ischemia Setting playbook (outpatient) — Long-term cardiology surveillance: 40-90d LVEF re-echo for ICD eligibility decision; cardiac rehab completion; secondary prevention bundle maintenance; mental health follow-up 8. continue secondary-prevention bundle ASA 81 + P2Y12 × 12 mo + atorvastatin 80 + GDMT PO as scheduled — post-late-STEMI (AHA 2025) Non-pharmacologic actions: - ICD/WCD adherence - Cardiac rehab maintenance phase - Driving restriction per state law if VF arrest AVOID / contraindication checks: - Tenecteplase_avoid_recent_stroke_or_intracranial_hemorrhage (FDA label) - Tenecteplase_avoid_active_bleeding (FDA label) - Warfarin_avoid_active_bleeding (AHA 2022) - No_thrombolytic_after_24h_from_symptom_onset (no benefit per LATE/EMERAS trials)
Monitoring
Regimen monitoring: - echo at 5-7d for lv thrombus screen (peak thrombus formation period; higher rate in late presenters) - echo at 40d for lvef reassessment for icd eligibility (MADIT-II) - INR q week during warfarin initiation - cardiac MRI at 6-12 weeks for viability quantification if delayed revasc considered Setting (outpatient) monitoring: - Quarterly + annual EF + lipid Follow-up plan: Cardiology + EP follow-up; LVEF re-echo at 40-90 d for ICD eligibility (MADIT-II EF ≤30); cardiac rehab; secondary prevention bundle maintenance - Close-out criterion: ICD/WCD pathway + cardiac rehab booked Monitoring phase: Telemetry, daily exam for new murmur (mechanical complications), echo at 5-7 d for LV thrombus screen, echo at 40 d for LVEF reassessment + ICD eligibility
Disposition
Current setting: outpatient — Long-term cardiology surveillance: 40-90d LVEF re-echo for ICD eligibility decision; cardiac rehab completion; secondary prevention bundle maintenance; mental health follow-up Disposition criteria: - Long-term continuation; cross-link to cardio.hf.core.v1 if HFrEF persists Escalation triggers (move to higher acuity): - ICD therapy delivered → urgent EP - EF declining despite GDMT → advanced HF eval
Earlier-Return Triggers
Return-precaution thresholds (watch for): - [LIFE_THREATENING] Late-presenter STEMI + SBP <90 + lactate ≥2 + hypoperfusion — SCAI C+ at presentation - [LIFE_THREATENING] New harsh holosystolic murmur OR pericardial effusion on echo OR sudden hemodynamic deterioration → free-wall rupture / VSR / papillary rupture (peak risk 3-7 d post-MI, more common in late presenters who never reperfused) - [SEVERE] LV thrombus on echo at 5-7 d post late STEMI — markedly higher rate in late presenters with anterior territory + EF <40 + apical akinesia
Citations
- 2025 ACC/AHA ACS Guideline + ESC 2023 ACS + OAT trial framework for late presenters [PMID:17112106](https://pubmed.ncbi.nlm.nih.gov/17112106/) - Cited evidence (PMID 37622670) [PMID:37622670](https://pubmed.ncbi.nlm.nih.gov/37622670/) - Cited evidence (PMID 35718438) [PMID:35718438](https://pubmed.ncbi.nlm.nih.gov/35718438/) - Cited evidence (PMID 38587234) [PMID:38587234](https://pubmed.ncbi.nlm.nih.gov/38587234/) - Cited evidence (PMID 11907286) [PMID:11907286](https://pubmed.ncbi.nlm.nih.gov/11907286/) Last reconciled with current guidelines: 2026-05-15.
- 2025 ACC/AHA ACS Guideline + ESC 2023 ACS + OAT trial framework for late presenters — PMID:17112106
- Cited evidence (PMID 37622670) — PMID:37622670
- Cited evidence (PMID 35718438) — PMID:35718438
- Cited evidence (PMID 38587234) — PMID:38587234
- Cited evidence (PMID 11907286) — PMID:11907286