Hemodynamic failure and graft dysfunction after lung transplant: A possible clinical continuum with immediate and long‐term consequences

Author:

Scaravilli Vittorio12ORCID,Guzzardella Amedeo3,Madotto Fabiana3,Morlacchi Letizia Corinna34,Bosone Marco3,Bonetti Claudia3,Musso Valeria3,Rossetti Valeria34,Russo Filippo Maria1,Sorbo Lorenzo Del5,Blasi Francesco34,Nosotti Mario36,Zanella Alberto13,Grasselli Giacomo13

Affiliation:

1. Department of Anesthesia, Critical Care and Emergency Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milan(MI) Italy

2. Department of Biomedical, Surgical and Dental Sciences University of Milan Milan(MI) Italy

3. Department of Pathophysiology and Transplantation University of Milan Milan(MI) Italy

4. Department of Internal Medicine Respiratory Unit and Cystic Fibrosis Center Fondazione IRCCS Ca' Granda – Ospedale Maggiore Policlinico Milan(MI) Italy

5. Interdepartmental Division of Critical Care Medicine Toronto General Hospital Toronto Ontario Canada

6. Department of Cardio‐thoraco‐vascular diseases Fondazione IRCCS Ca' Granda – Ospedale Maggiore Policlinico Milan(MI) Italy

Abstract

AbstractIntroductionThe postoperative hemodynamic management after lung transplant (LUTX) is guided by limited evidence. We aimed to describe and evaluate risk factors and outcomes of postoperative vasoactive support of LUTX recipients.MethodsIn a single‐center retrospective analysis of consecutive adult LUTX, two cohorts were identified: (1) patients needing prolonged vasoactive support (>12 h from ICU admission) (VASO+); (2) or not (VASO−). Postoperative hemodynamic characteristics were thoroughly analyzed. Risk factors and outcomes of VASO+ versus VASO− cohorts were assessed by multivariate logistic regression and propensity score matching.ResultsOne hundred and thirty‐eight patients were included (86 (62%) VASO+ versus 52 (38%) VASO−). Vasopressors (epinephrine, norepinephrine, dopamine) were used in the first postoperative days (vasoactive inotropic score at 12 h: 6 [4–12]), while inodilators (dobutamine, levosimendan) later. Length of vasoactive support was 3 [2–4] days. Independent predictors of vasoactive use were: LUTX indication different from cystic fibrosis (p = .003), higher Oto score (p = .020), longer cold ischemia time (p = .031), but not preoperative cardiac catheterization. VASO+ patients showed concomitant hemodynamic and graft impairment, with longer mechanical ventilation (p = .010), higher primary graft dysfunction (PGD) grade at 72 h (PGD grade > 0 65% vs. 31%, p = .004, OR 4.2 [1.54–11.2]), longer ICU (p < .001) and hospital stay (p = .013). Levosimendan as a second‐line inodilator appeared safe.ConclusionsVasoactive support is frequently necessary after LUTX, especially in recipients of grafts of lesser quality. Postoperative hemodynamic dysfunction requiring vasopressor support and graft dysfunction may represent a clinical continuum with immediate and long‐term consequences. Further studies may elucidate if this represents a possible treatable condition.

Publisher

Wiley

Subject

Transplantation

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