Cardiogenic shock — SCAI Stage D (deteriorating)
Encounter flow
10/12 authoredCanonical 12-phase frame with authored status for this dossier.
Frame
SCAI D = classic CS not responding to initial therapy → escalating support, MCS active or imminent, deteriorating
D-stage criteria met
Patient inputs (6)
Persistent SBP <90 despite ≥2 hemodynamic agents defines deterioration
New AKI = D-stage organ marker; also drives MCS/contrast safety planning
LVEF + RV strain + valvular + tamponade exclusion before MCS device selection
Trend (not single value) defines deterioration vs response; lactate rise on therapy is a hard MCS trigger
MAP <65 despite NE + inotrope drives MCS escalation per DanGer Shock
Confirms reperfusion completeness; identifies salvageable myocardium pre-MCS
* = hard-required. Engine cannot meaningfully run until these are filled.
Severity triggers (5)
- informationallife_threateningpersistent_hypotension_on_ne_plus_dobutamineMAP <65 despite NE >0.5 mcg/kg/min + dobutamine ≥5 mcg/kg/min for ≥2h — D-stage hemodynamic floorTrigger could not be auto-evaluated — needs clinician judgement.
- informationallife_threateningrising_lactate_on_initial_therapyLactate rising or static ≥2 mmol/L for ≥6h despite resuscitation + first-line agentsTrigger could not be auto-evaluated — needs clinician judgement.
- informationallife_threateningmcs_failure_or_inadequateImpella CP deployed but persistent MAP <65 + lactate not clearing → escalate to VA-ECMOTrigger could not be auto-evaluated — needs clinician judgement.
- informationallife_threateningmulti_organ_failure_at_24_72hPersistent multi-organ failure (SOFA increasing) at 24-72h despite max MCS + pharmacology — futility thresholdTrigger could not be auto-evaluated — needs clinician judgement.
- informationalseverenew_aki_on_cs_therapyNew Cr rise ≥0.3 mg/dL or oliguria <0.5 mL/kg/h × 6h on CS therapy — multi-organ involvementTrigger could not be auto-evaluated — needs clinician judgement.
Workflow calculators
Run this disease's risk and dosing calculators inline.
Recommended regimen
SCAI D escalation regimen — adds MCS + second pressor to parent CS regimen- norepinephrinefirst linealpha_beta_agonist_pressor0.05 mcg/kg/min IV titrate to MAP ≥65 • IV • continuoustriggers: cs_with_map_below_65SOAP-II PMID 20200382 — NE preferred over dopamine in CS; first-line per ACC/AHA 2022 + SCAI 2022rxcui 7512
- dobutaminefirst linebeta1_agonist_inotrope2.5 mcg/kg/min IV titrate • IV • continuoustriggers: cs_with_low_ciFirst-line inotrope in CS per SCAI 2022; CI <2.2 + adequate filling pressurerxcui 3616
- vasopressinsecond linev1_agonist_pressor0.03 U/min IV (fixed-dose adjunct) • IV • continuoustriggers: scai_d_persistent_hypotension_on_ne, scai_d_high_ne_dose_above_0.5V1-mediated vasoconstriction spares pulmonary vasculature; adjunctive when NE >0.5 mcg/kg/min cannot maintain MAP — VANISH/VASST extrapolationrxcui 11149
- milrinonecomorbidity specificpde3_inhibitor_inotrope0.125-0.375 mcg/kg/min IV (no bolus in CS) • IV • continuoustriggers: scai_d_pulmonary_htn_predominant, scai_d_dobutamine_inadequatePDE3 inhibitor preferred when pulmonary HTN dominant; avoid bolus in CS (hypotension risk)rxcui 52769
- epoprostenol_inhaledcomorbidity specificpulmonary_vasodilator50 ng/kg/min nebulized • INH • continuoustriggers: scai_d_with_severe_pulm_htn, scai_d_rv_strain_on_echoInhaled pulmonary vasodilator if RV strain develops on Impella supportrxcui 8814
outpatient playbook — drug actions (1)
- 1. continue 4-pillar GDMTrxcui 593411ARNI + BB + MRA + SGLT2i at max tolerated • PO • as scheduledtrigger: Recovered HFrEFACC/AHA 2022 HF Class I (PMID 35363499)
Auto-drafted A&P note
outpatientSubjective
- Possible entry pathways: SBP <90 / MAP <65 despite norepinephrine + dobutamine — SCAI D; Lactate rising or static ≥2 mmol/L despite ≥6h initial therapy — failure to clear; New AKI + transaminitis + altered mentation on first-line therapy — D-stage progression.
Objective
- No vitals, labs, or imaging entered for this encounter.
Assessment
**Cardiogenic shock — SCAI Stage D (deteriorating)** (cardio.cardiogenic-shock.scai-d.v1). Scope: SCAI D = classic CS not responding to initial therapy → escalating support, MCS active or imminent, deteriorating No severity triggers fired against current inputs.
Plan
Regimen axis: **SCAI D escalation regimen — adds MCS + second pressor to parent CS regimen**. 1. norepinephrine 0.05 mcg/kg/min IV titrate to MAP ≥65 IV continuous (alpha_beta_agonist_pressor, first line) — SOAP-II PMID 20200382 — NE preferred over dopamine in CS; first-line per ACC/AHA 2022 + SCAI 2022 2. dobutamine 2.5 mcg/kg/min IV titrate IV continuous (beta1_agonist_inotrope, first line) — First-line inotrope in CS per SCAI 2022; CI <2.2 + adequate filling pressure 3. vasopressin 0.03 U/min IV (fixed-dose adjunct) IV continuous (v1_agonist_pressor, second line) — V1-mediated vasoconstriction spares pulmonary vasculature; adjunctive when NE >0.5 mcg/kg/min cannot maintain MAP — VANISH/VASST extrapolation 4. milrinone 0.125-0.375 mcg/kg/min IV (no bolus in CS) IV continuous (pde3_inhibitor_inotrope, comorbidity specific) — PDE3 inhibitor preferred when pulmonary HTN dominant; avoid bolus in CS (hypotension risk) 5. epoprostenol_inhaled 50 ng/kg/min nebulized INH continuous (pulmonary_vasodilator, comorbidity specific) — Inhaled pulmonary vasodilator if RV strain develops on Impella support Setting playbook (outpatient) — Long-term advanced HF follow-up: GDMT maintenance, transplant listing if appropriate, end-of-life planning if not eligible 6. continue 4-pillar GDMT ARNI + BB + MRA + SGLT2i at max tolerated PO as scheduled — Recovered HFrEF (ACC/AHA 2022 HF Class I (PMID 35363499)) Non-pharmacologic actions: - Transplant listing maintenance - Advance care planning if not transplant candidate AVOID / contraindication checks: - Vasopressin_avoid_severe_peripheral_ischemia (drug label) - Milrinone_avoid_severe_aortic_stenosis (vasodilator effect) - Impella_relative_contraindication_severe_aortic_regurg (device label) - Impella_avoid_lv_thrombus (embolic risk — DanGer Shock 2024 exclusion)
Monitoring
Regimen monitoring: - pa catheter continuous for ci pcwp rv stroke work (D-stage standard) - lactate q1h x 6h then q4h (D-stage clearance benchmark) - echo daily for lv recovery and device position (Impella position migration risk) - limb perfusion assessment q2h if femoral access (ischemic complication monitoring) Setting (outpatient) monitoring: - Quarterly NT-proBNP + BMP - Annual echo Follow-up plan: If recovery: MCS wean, GDMT initiation, advanced HF clinic; if no recovery → SCAI E pathway - Close-out criterion: recovery vs E-stage decision made Monitoring phase: Continuous PA catheter; q1h lactate × 6h then q4h; daily echo; SOFA score q12h
Disposition
Current setting: outpatient — Long-term advanced HF follow-up: GDMT maintenance, transplant listing if appropriate, end-of-life planning if not eligible Disposition criteria: - Long-term continuation; cross-link to cardio.hf.core.v1 Escalation triggers (move to higher acuity): - Recurrent CS → readmit + escalate to chronic engine or hospice
Earlier-Return Triggers
Return-precaution thresholds (watch for): - [LIFE_THREATENING] MAP <65 despite NE >0.5 mcg/kg/min + dobutamine ≥5 mcg/kg/min for ≥2h — D-stage hemodynamic floor - [LIFE_THREATENING] Lactate rising or static ≥2 mmol/L for ≥6h despite resuscitation + first-line agents - [LIFE_THREATENING] Impella CP deployed but persistent MAP <65 + lactate not clearing → escalate to VA-ECMO
Citations
- SCAI 2022 CS staging + 2025 ACC/AHA ACS + 2022 ACC/AHA HF (with 2023 Focused Update) [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 26333869) [PMID:26333869](https://pubmed.ncbi.nlm.nih.gov/26333869/) - Cited evidence (PMID 20200382) [PMID:20200382](https://pubmed.ncbi.nlm.nih.gov/20200382/) - Cited evidence (PMID 37634145) [PMID:37634145](https://pubmed.ncbi.nlm.nih.gov/37634145/) Last reconciled with current guidelines: 2026-05-14.
- SCAI 2022 CS staging + 2025 ACC/AHA ACS + 2022 ACC/AHA HF (with 2023 Focused Update) — PMID:35718438
- Cited evidence (PMID 38587234) — PMID:38587234
- Cited evidence (PMID 26333869) — PMID:26333869
- Cited evidence (PMID 20200382) — PMID:20200382
- Cited evidence (PMID 37634145) — PMID:37634145