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Team-based approach to identify cardiac toxicity in critically ill hematopoietic stem cell transplant recipients.
Dandoy, Christopher E; Jodele, Sonata; Paff, Zachary; Hirsch, Russel; Ryan, Thomas D; Jefferies, John L; Cash, Michelle; Rotz, Seth; Pate, Abigail; Taylor, Michael D; El-Bietar, Javier; Myers, Kasiani C; Wallace, Gregory; Nelson, Adam; Grimley, Michael; Pfeiffer, Thomas; Lane, Adam; Davies, Stella M; Chima, Ranjit S.
Afiliación
  • Dandoy CE; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Jodele S; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Paff Z; Division of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Hirsch R; Division of Cardiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Ryan TD; Division of Cardiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Jefferies JL; Division of Cardiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Cash M; Division of Cardiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Rotz S; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Pate A; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Taylor MD; Division of Cardiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • El-Bietar J; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Myers KC; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Wallace G; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Nelson A; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Grimley M; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Pfeiffer T; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Lane A; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Davies SM; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Chima RS; Division of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Pediatr Blood Cancer ; 64(10)2017 Oct.
Article en En | MEDLINE | ID: mdl-28271596
ABSTRACT

INTRODUCTION:

We observed pulmonary hypertension (PH), pericardial effusions, and left ventricular systolic dysfunction (LVSD) in multiple critically ill hematopoietic stem cell transplant (HSCT) recipients. We implemented routine structured echocardiography screening for HSCT recipients admitted to the pediatric intensive care unit (PICU) using a standardized multidisciplinary process.

METHODS:

HSCT recipients admitted to the PICU with respiratory distress, hypoxia, shock, and complications related to transplant-associated thrombotic microangiopathy were screened on admission and every 1-2 weeks thereafter. Echocardiography findings requiring intervention and/or further screening included elevated right ventricular pressure, LVSD, and moderate to large pericardial effusions. All echocardiograms were compared to the patient's routine pretransplant echocardiogram.

RESULTS:

Seventy HSCT recipients required echocardiography screening over a 3-year period. Echo abnormalities requiring intervention and/or further screening were found in 35 (50%) patients. Twenty-four (34%) patients were noted to have elevated right ventricular pressure; 14 (20%) were at risk for PH, while 10 (14%) had PH. All patients with PH were treated with pulmonary vasodilators. LVSD was noted in 22 (31%) patients; 15/22 (68%) received inotropic support. Moderate to large pericardial effusions were present in nine (13%) patients, with six needing pericardial drain placement.

DISCUSSION:

Echocardiographic abnormalities are common in critically ill HSCT recipients. Utilization of echocardiogram screening may allow for early detection and timely intervention for cardiac complications in this high-risk cohort.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Derrame Pericárdico / Disfunción Ventricular Izquierda / Trasplante de Células Madre Hematopoyéticas / Hipertensión Pulmonar Tipo de estudio: Etiology_studies / Prognostic_studies / Qualitative_research / Screening_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Pediatr Blood Cancer Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Derrame Pericárdico / Disfunción Ventricular Izquierda / Trasplante de Células Madre Hematopoyéticas / Hipertensión Pulmonar Tipo de estudio: Etiology_studies / Prognostic_studies / Qualitative_research / Screening_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Pediatr Blood Cancer Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2017 Tipo del documento: Article