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Patient handout

Cardiogenic shock — post-hematopoietic-stem-cell-transplant recipient

PRODUCTION

1. Your condition

This handout is for cardiogenic shock — post-hematopoietic-stem-cell-transplant recipient. Your care team identified this based on: recent high-dose cyclophosphamide conditioning (≥120 mg/kg) within past 1–10 d + acute hf + ↑ troponin → cyclophosphamide hemorrhagic myocarditis (goldberg jco 1986 pmid 3528404).

Other reasons your team may use this plan: hsct recipient (allogeneic or autologous) within past 100 d + acute biventricular dysfunction + shock physiology — multi-etiology cs workup; cmv pcr positive + acute lv dysfunction in post-hsct recipient (peak 30-100 d) → cmv myocarditis differential; sepsis physiology in neutropenic post-hsct recipient with cardiac dysfunction → mixed septic + cardiogenic shock.

2. Your medications

Take these medications exactly as prescribed. Do not stop or change a dose without talking to your provider.

MedicationStarting doseHowWhenWhat it does
norepinephrine0.05–0.5 µg/kg/min titrate MAP ≥65IVcontinuousSOAP-II PMID 20200382 — NE first-line in CS
dobutamine2.5 µg/kg/min cautious titrationIVcontinuousDOREMI PMID 33704937 — non-inferior to milrinone; CAUTION in inflamed myocardium given arrhythmia risk
methylprednisolone1000 mg IV daily × 3–5 days, then 1 mg/kg/d taperIVdailyGoldberg JCO 1986 PMID 3528404 — high-dose corticosteroids cornerstone for cyclophosphamide hemorrhagic myocarditis; AHA 2022 cardio-oncology + ESC 2022 (Lyon PMID 36017575)
ganciclovir5 mg/kg IV q12h induction × 14–21 d (renal-adjust); maintenance 5 mg/kg IV dailyIVq12h inductionASTCT CMV management guideline (PMID 20530287) — IV ganciclovir is first-line for CMV end-organ disease post-HSCT including myocarditis; renal dose adjustment essential
foscarnet60 mg/kg IV q8h × 14–21 d (renal-adjust)IVq8hASTCT CMV management — ganciclovir-resistant CMV; alternative if cytopenia limits ganciclovir; nephrotoxic — monitor closely
immune globulin (IVIG)500 mg/kg IV q48h × 5 doses (CMV myocarditis adjunct)IVq48hASTCT CMV management — IVIG adjunct in severe CMV pneumonitis / myocarditis post-HSCT; may also be considered for hypogammaglobulinemia + viral myocarditis context
ruxolitinib10 mg PO BID; titrate per platelet + ANCPOBIDREACH-2 NEJM 2020 — ruxolitinib for steroid-refractory acute GVHD; relevant when GVHD-related cardiac involvement contributes to CS
amiodarone150 mg IV bolus then 1 mg/min × 6 h then 0.5 mg/minIVcontinuousAHA 2020 ACLS Class IIb for refractory VT/VF
cefepime2 g IV q8h (renal-adjust)IVq8hIDSA neutropenic fever 2010 + ASTCT supportive-care guidelines — empirical broad-spectrum β-lactam for febrile neutropenia in HSCT recipient
AVOID nephrotoxic drugsAVOID aminoglycosides, NSAIDs, contrast unless essential; minimize loop diuretics if AKI; use nephrology-stewardship lensn/an/aCalcineurin inhibitors (cyclosporine / tacrolimus) on board for GVHD prophylaxis cause AKI; avoid stacking nephrotoxins per ASTCT supportive-care guidance

Plan: Post-HSCT cardiogenic shock — etiology-stratified support with nephrotoxin avoidance + sub-etiology-specific treatment + MDT-gated MCS bridge

3. When to call your provider

Contact your care team if any of the following happen:

  • Sustained VT / syncope → EP urgent consult
  • Persistent severe LV dysfunction → transplant evaluation if cancer-prognosis permits
  • CMV reactivation → ID urgent consult
  • Recurrent / new GVHD → transplant team

4. When to seek emergency care

Call 911 or go to the nearest emergency room right away if you have:

  • Refractory CS within 1–10 d of high-dose cyclophosphamide (≥120 mg/kg) conditioning with hemorrhagic CMR pattern (T2*/SWI signal) — high-mortality variant (Goldberg JCO 1986); demands pulse steroids + supportive + MCS bridge with MDT(life-threatening)
  • CMV PCR positive (whole blood) + cardiac dysfunction in post-allogeneic HSCT recipient (peak 30–100 d post-transplant) — emergent ganciclovir + IVIG + ID consult; consider EMB(life-threatening)
  • Sepsis physiology + cardiac dysfunction in profoundly neutropenic post-HSCT recipient (ANC <500) — mortality very high; SSC 2026 sepsis bundle + broad-spectrum + antifungal + G-CSF + early MCS evaluation with MDT(life-threatening)
  • Steroid-refractory acute GVHD with cardiac involvement (myocarditis or pericarditis pattern) and hemodynamic compromise — add ruxolitinib per REACH-2 + escalate systemic GVHD therapy
  • Sustained VT/VF or recurrent shocks within 24 h in post-HSCT recipient — high arrhythmia risk in inflamed myocardium; amiodarone + EP + escalate to MCS over higher inotropes; consider catheter ablation if refractory(life-threatening)

5. Follow-up

Repeat echo + CMR at 4-8 wks for recovery trajectory; cardiac rehab; long-term the four foundational heart-failure medications 4-pillar if persistent HFrEF; long-term cardio-oncology surveillance for late TBI / busulfan effects; coordination with transplant team for chronic GVHD + immunosuppression management; ICD eligibility per AHA 2017 VA/SCD with cancer-prognosis weighting

6. Sources

Guideline: Lyon et al ESC 2022 cardio-oncology guideline (PMID 36017575); AHA 2022 cardio-oncology scientific statement; Yeh & Bickford JACC 2009 cardiotoxicity in HSCT (PMID 19608050); Tichelli EBMT 2008 cardiac complications HSCT (PMID 18176622); ASTCT CMV management (PMID 20530287); REACH-2 NEJM 2020 (ruxolitinib for steroid-refractory acute GVHD)

  1. pubmed.ncbi.nlm.nih.gov/19608050
  2. pubmed.ncbi.nlm.nih.gov/18176622
  3. pubmed.ncbi.nlm.nih.gov/3528404