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Single Versus Bilateral Lung Transplantation for Idiopathic Pulmonary Fibrosis in the Lung Allocation Score Era.
Spratt, John R; Tomic, Rade; Brown, Roland Z; Rudser, Kyle; Loor, Gabriel; Hertz, Marshall; Shumway, Sara; Kelly, Rosemary F.
Afiliación
  • Spratt JR; Department of Surgery, University of Minnesota, Minneapolis, Minnesota. Electronic address: sprat020@umn.edu.
  • Tomic R; Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, Department of Medicine, University of Minnesota, Minneapolis, Minnesota.
  • Brown RZ; Division of Biostatistics, University of Minnesota, Minneapolis, Minnesota.
  • Rudser K; Division of Biostatistics, University of Minnesota, Minneapolis, Minnesota.
  • Loor G; Division of Cardiothoracic Surgery, Department of Surgery, University of Minnesota, Minneapolis, Minnesota.
  • Hertz M; Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, Department of Medicine, University of Minnesota, Minneapolis, Minnesota.
  • Shumway S; Division of Cardiothoracic Surgery, Department of Surgery, University of Minnesota, Minneapolis, Minnesota.
  • Kelly RF; Division of Cardiothoracic Surgery, Department of Surgery, University of Minnesota, Minneapolis, Minnesota.
J Surg Res ; 234: 84-95, 2019 02.
Article en En | MEDLINE | ID: mdl-30527505
ABSTRACT

BACKGROUND:

Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal disease. Lung transplantation is the only therapy associated with prolonged survival. The ideal transplant procedure for IPF is unclear. Outcomes after single transplantation (SLTx) versus bilateral lung transplantation (BLTx) in IPF patients after introduction of the Lung Allocation Score were examined.

METHODS:

Records of patients undergoing lung transplantation for IPF at our institution between May 2005 and March 2017 were reviewed to examine the effect of transplant laterality. Primary outcomes were overall, rejection-free, and bronchiolitis obliterans (BOS)-free survival at 1 and 5 years post-transplant.

RESULTS:

Lung transplantation was performed in 151 IPF patients post-Lung Allocation Score. Most recipients were male with average age 59 ± 8 years. SLTx was performed in 94 patients (62%). In the overall cohort, comparative survival between SLTx and BLTx was similar at 1 and 5 years before and after adjusting for age and pulmonary hypertension (PH). SLTx was associated with shorter ventilator time and intensive care unit stay and trended toward improved survival over BLTx in patients without PH.

CONCLUSIONS:

The use of SLTx versus BLTx in IPF did not correspond to significantly different survival adjusting for age and PH. BLTx was associated with prolonged postoperative ventilation and length of stay compared with SLTx. Patients without PH, all older patients, and patients with PH and advanced disease should be considered for SLTx for IPF.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trasplante de Pulmón / Fibrosis Pulmonar Idiopática Tipo de estudio: Etiology_studies / Observational_studies Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: J Surg Res Año: 2019 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trasplante de Pulmón / Fibrosis Pulmonar Idiopática Tipo de estudio: Etiology_studies / Observational_studies Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: J Surg Res Año: 2019 Tipo del documento: Article