Clinical Risk Factors for Primary Graft Dysfunction after Lung Transplantation

被引:522
作者
Diamond, Joshua M. [1 ]
Lee, James C. [1 ]
Kawut, Steven M. [1 ,2 ,3 ]
Shah, Rupal J. [1 ]
Localio, A. Russell [2 ]
Bellamy, Scarlett L. [2 ]
Lederer, David. J. [6 ]
Cantu, Edward [4 ]
Kohl, Benjamin A. [5 ]
Lama, Vibha N. [8 ]
Bhorade, Sangeeta M. [9 ]
Crespo, Maria [10 ]
Demissie, Ejigayehu [1 ,2 ]
Sonett, Joshua
Wille, Keith [11 ]
Orens, Jonathan [7 ,12 ]
Shah, Ashish S. [13 ]
Weinacker, Ann [14 ]
Arcasoy, Selim [6 ]
Shah, Pali D. [12 ]
Wilkes, David S. [15 ]
Ware, Lorraine B. [16 ,17 ]
Palmer, Scott M. [18 ]
Christie, Jason D. [1 ,2 ,3 ]
机构
[1] Univ Penn, Perelman Sch Med, Pulm Allergy & Crit Care Div, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Penn Cardiovasc Inst, Philadelphia, PA 19104 USA
[4] Univ Penn, Perelman Sch Med, Div Cardiovasc Surg, Philadelphia, PA 19104 USA
[5] Univ Penn, Perelman Sch Med, Dept Anesthesiol & Crit Care, Philadelphia, PA 19104 USA
[6] Columbia Univ Coll Phys & Surg, Div Pulm Allergy & Crit Care Med, New York, NY 10032 USA
[7] Columbia Univ Coll Phys & Surg, Dept Surg, New York, NY 10032 USA
[8] Univ Michigan, Div Pulm Allergy & Crit Care Med, Ann Arbor, MI 48109 USA
[9] Univ Chicago, Div Pulm & Crit Care Med, Chicago, IL 60637 USA
[10] Univ Pittsburgh, Div Pulm Allergy & Critical Care, Pittsburgh, PA USA
[11] Univ Alabama Birmingham, Div Pulm & Crit Care Med, Birmingham, AL USA
[12] Johns Hopkins Univ Hosp, Dept Med, Div Pulm Allergy & Crit Care Med, Baltimore, MD 21205 USA
[13] Johns Hopkins Univ Hosp, Dept Surg, Baltimore, MD 21205 USA
[14] Stanford Univ, Div Pulm & Crit Care Med, Palo Alto, CA 94304 USA
[15] Indiana Univ Sch Med, Div Pulm Allergy Crit Care & Occupat Med, Indianapolis, IN USA
[16] Vanderbilt Univ, Dept Med, Nashville, TN USA
[17] Vanderbilt Univ, Dept Pathol Microbiol & Immunol, Nashville, TN USA
[18] Duke Univ, Div Pulm Allergy & Crit Care Med, Raleigh, NC USA
关键词
lung transplantation; clinical risk factors; primary graft dysfunction; ISHLT WORKING GROUP; INTERNATIONAL-SOCIETY; ALLOGRAFT DYSFUNCTION; POTENTIAL REFINEMENTS; HEART; OUTCOMES; INJURY; VENTILATION; SURVIVAL; IMPACT;
D O I
10.1164/rccm.201210-1865OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Primary graft dysfunction (PGD) is the main cause of early morbidity and mortality after lung transplantation. Previous studies have yielded conflicting results for PGD risk factors. Objectives: We sought to identify donor, recipient, and perioperative risk factors for PGD. Methods: We performed a 10-center prospective cohort study enrolled between March 2002 and December 2010 (the Lung Transplant Outcomes Group). The primary outcome was International Society for Heart and Lung Transplantation grade 3 PGD at 48 or 72 hours post-transplant. The association of potential risk factors with PGD was analyzed using multivariable conditional logistic regression. Measurements and Main Results: A total of 1,255 patients from 10 centers were enrolled; 211 subjects (16.8%) developed grade 3 PGD. In multivariable models, independent risk factors for PGD were any history of donor smoking (odds ratio [OR], 1.8; 95% confidence interval [CI], 1.2-2.6; P = 0.002); F-IO2 during allograft reperfusion (OR, 1.1 per 10% increase in Fro; 95% CI, 1.0-1.2; P = 0.01); single lung transplant (OR, 2; 95% CI, 1.2-3.3; P = 0.008); use of cardiopulmonary bypass (OR, 3.4; 95% CI, 2.2-5.3; P < 0.001); overweight (OR, 1.8; 95% Cl, 1.2-2.7; P = 0.01) and obese (OR, 2.3; 95% CI, 1.3-3.9; P = 0.004) recipient body mass index; preoperative sarcoidosis (OR, 2.5; 95% Cl, 1.1-5.6; P = 0.03) or pulmonary arterial hypertension (OR, 3.5; 95% CI, 1.6-7.7; P = 0.002); and mean pulmonary artery pressure (OR, 1.3 per 10 mm Hg increase; 95% Cl, 1.1-1.5; P < 0.001). PGD was significantly associated with 90-day (relative risk, 4.8; absolute risk increase, 18%; P < 0.001) and 1-year (relative risk, 3; absolute risk increase, 23%; P < 0.001) mortality. Conclusions: We identified grade 3 PGD risk factors, several of which are potentially modifiable and should be prioritized for future research aimed at preventative strategies. Clinical trial registered with www.clinicaltrials.gov (NCT 00552357).
引用
收藏
页码:527 / 534
页数:8
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