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Risk factors and outcomes associated with early airway dehiscence following lung transplantation [Meeting Abstract]

Ranganath, N; Malas, J; Phillips, K G; Bittle, G J; Lesko, M B; Angel, L F; Lonze, B E; Kon, Z N
Objective: Anastomotic complications occur in 77%-18% of lung transplants, but no large multi-institutional analyses to determine risk factors for airway dehiscence (AD) exist. Using national registry data, we compared pre-operative recipient/donor risk factors and post-operative outcomes in patients with and without AD.
Method(s): Data on adult lung transplants between 2007 and 2017 were provided by the Scientifc Registry of Transplant Recipients. Recipient/donor demographics were compared with regards to AD, and multivariable logistic regression identifed independent risk factors for AD. Kaplan-Meier curves and log-rank tests described mortality and graft survival.
Result(s): Two hundred and seventy-fve/18,122 recipients (1.5%) experienced AD. These recipients were more often male (71.6% vs. 59.6%, P < 0.001), obese (20.1% vs. 15.6%, P = 0.041), transplanted from intensive care unit (17.5% vs. 1 1 . 0 % , P = 0.001), and mechanically ventilated (11.6% vs. 6.9%, P = 0.002). AD was not associated with recipient steroid use (51.9% vs. 47.7%, P = 0.194) or lung disease diagnosis group. Donor diabetes (8.0% vs. 7.0%, P = 0.482) and donor smoking (7.4% vs. 9.0%, P = 0.449) were also not associated with AD. Patients with AD were more likely to have received bilateral lungs (78.5% vs. 68.3%, P < 0.001) and less likely to have received a single left lung (6.5% vs. 17.3%, P < 0.001). Cold ischemia time between 2 and 4 hours was less common in the AD group (17.2% vs. 23.7%, P = 0.013). Multivariable analysis revealed recipient obesity and donor gunshot death as independent predictive factors for AD, while donor age >40 and single left lung transplant were negative predictive factors (Table SA10-1). Mortality and graft failure were both signifcantly higher in the AD group (Fig. SA10-1).
Conclusion(s): We identifed independent risk factors for AD and confrmed poor post-operative outcomes. However, many known impediments to wound healing such as chronic steroid use, diabetes, and smoking did not appear to be associated with AD
EMBASE:632150686
ISSN: 1559-0879
CID: 4523902

Maintaining quality outcomes with a rapidly growing ECMO program [Meeting Abstract]

Toy, B; Angel, L; Beaulieu, T; Hill, F; Kon, Z; Moazami, N; Sullivan, B; Lubinsky, A; Smith, D
Introduction: Our institution's Adult ECMO Program started in 2015 and continues to see exponential growth with an average of 89% annual increase in volume. When demand for ECMO exceeds available resources, the multiple teams, resources and processes involved in the care of these patients are challenged to provide excellent outcomes. Our program made specific changes to accommodate increased volume while maintaining quality. Our growth directly impacted staff exposure and expertise, locations of ECMO care, emergent bedside cannulations, and utilization of equipment and supplies.
Result(s): Our team coordinated comprehensive training courses to increase the number of ECMO-credentialed physicians and advanced practice providers. We then focused on improving bedside cannulations. We provided cannulation didactic and simulation training for a cohort of critical care nurses, created a single ECMO Perfusion activation number, and increased available primed circuits. We also rebuilt our cannulation carts, using an exchange process for immediate replenishment of supplies. All carts were streamlined to one lay out and were expanded across the hospital in five different locations. We increased our equipment inventory from 9 to 15 consoles and introduced a more cost-effective ECMO system. Last, we implemented ECMO safety rounds, a biweekly bedside audit of existing safety measures that also allowed for real-time staff education.
Conclusion(s): Our patient outcomes continue to meet the national ELSO benchmarks for survival rates. As our growth continues, all areas require ongoing assessment and evaluation to maintain best practices. With proper planning and resources, quality patient outcomes can be maintained
EMBASE:631095447
ISSN: 1538-943x
CID: 4387242

A rare case of hermansky-pudlak syndrome involving bilateral lung: Histopathologic and electron microscopic findings [Meeting Abstract]

Basu, A; Seshan, S; Angel, L; Moreira, A; Zhou, F
Introduction: Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive hereditary disorder characterized by oculocutaneous albinism and bleeding diathesis. Transplantation is often conducted to treat lung fibrosis, which is the most fatal complication of this disease. While the literature discusses the diagnosis of HPS based on genetic testing, radiology, and electron microscopic (EM) findings of platelet granules, there is a paucity of images in the literature illustrating the pulmonary histopathologic and EM features of HPS. Case Report: Here we present striking histopathologic and EM images from a case of pulmonary fibrosis due to HPS in a 48-year-old female. The patient presented with restrictive lung disease and bilateral decreased breath sounds with diffuse crackles. She was clinically diagnosed with HPS and underwent bilateral lung transplant. On histopathology, both pneumonectomy specimens showed diffuse interstitial fibrosing and cellular pneumonitis with end-stage remodeling and type II pneumocyte (PC-II) hyperplasia. The PC-IIs had abundant foamy cytoplasm and compressed scalloped nuclei. Alveolar macrophages contained fine brown granules positive for PAS-D stain. EM analysis revealed that the PC-IIs contained numerous lamellated myelin bodies (so-called giant lamellar body degeneration) suggestive of surfactant admixed with lipid and luminal microvilli. The pigmented alveolar macrophages also contained lamellated myelin bodies, as well as clusters of single membrane-bound structures with varying size and electron density admixed with vacuolar and granular debris suggestive of ceroid deposits.
Conclusion(s): Based on light microscopy, histochemical analysis, EM, and clinical presentation, it was concluded that our findings were consistent with pulmonary changes as seen in HPS
EMBASE:631017734
ISSN: 1943-7722
CID: 4341802

Early airway dehiscence: Risk factors and outcomes with the rising incidence of extracorporeal membrane oxygenation as a bridge to lung transplantation

Malas, Jad; Ranganath, Neel K; Phillips, Katherine G; Bittle, Gregory J; Hisamoto, Kazuhiro; Smith, Deane E; Lesko, Melissa B; Angel, Luis F; Lonze, Bonnie E; Kon, Zachary N
BACKGROUND:Anastomotic complications occur in 7% to 18% of lung transplant recipients, among which airway dehiscence (AD) is particularly catastrophic. Using multi-institutional registry data, this study compared preoperative recipient/donor risk factors and outcomes in patients with and without AD and analyzed the effect of extracorporeal membrane oxygenation (ECMO) on the incidence of AD. METHODS:Data on adult lung transplants from 2007 to 2017 were provided by the Scientific Registry of Transplant Recipients. Patients receiving isolated lobar transplantation and patients with unknown AD status were excluded. Multivariable logistic regression identified independent risk factors for AD. Kaplan-Meier curves and log-rank tests describe mortality and graft survival. RESULTS:Of 18 122 lung transplants, 275 (1.5%) experienced AD. While the incidence of ECMO steadily increased from 0.7% to 5.9% over the study period, the incidence of AD remained relatively constant. Multivariable analysis revealed recipient male gender and prolonged ( > 48 hours) posttransplant mechanical ventilation as independent predictive factors for AD, while advanced donor age and single left lung transplant were protective factors. Recipient chronic steroid use, recipient diabetes, donor diabetes, and donor smoking history were not predictive of AD. Mortality and graft failure were significantly worse in the AD group. CONCLUSIONS:Despite increased ECMO utilization, the incidence of AD has remained stable. Multiple independent risk factors for AD were identified and poor postoperative outcomes confirmed. However, many known impediments to wound healing such as recipient chronic steroid use, recipient and donor diabetes, and donor smoking were not identified as risk factors for AD, reinforcing the critical role of technical performance.
PMID: 31334904
ISSN: 1540-8191
CID: 3986962

Impact of the Opioid Epidemic on Lung Transplantation: Donor, Recipient and Discard Characteristics

Phillips, Katherine G; Ward, Alison F; Ranganath, Neel K; Malas, Jad; Lonze, Bonnie E; Moazami, Nader; Angel, Luis F; Kon, Zachary N
BACKGROUND:The national opioid epidemic may have expanded the donor pool for lung transplantation, but concerns remain regarding infectious risks and allograft function. This study compared donor/recipient characteristics, outcomes, and reasons for organ discard between overdose death donors (ODD) and all other mechanism-of-death donors. METHODS:Data on adult lung transplants from 2000-2017 were provided by the Scientific Registry of Transplant Recipients. Pulmonary allografts used in multiple organ transplantations were excluded. Donor/recipient demographics, outcomes, and organ discard were analyzed with regards to ODD since 2010. Discard analysis was limited to donors who had at least one organ transplanted but their pulmonary allografts discarded. RESULTS:From 2010-2017, 7.3% (962/13,196) of lung transplantations were from ODD, over a 3-fold increase from the 2.1% (164/7,969) in 2000-2007. ODD were younger but more likely to have a history of smoking, hepatitis C, or an abnormal bronchoscopy finding. Overall survival was similar between ODD and non-ODD groups. ODD of discarded pulmonary allografts were younger and more likely to be hepatitis C positive, but were less likely to have a history of smoking than their non-ODD counterparts. CONCLUSIONS:Rates of ODD utilization in lung transplantation have increased in accordance with the opioid epidemic, but there remains a significant pool of ODD pulmonary allografts with favorable characteristics that are discarded. With no significant difference in survival between ODD and non-ODD recipients, further expansion of this donor pool may be appropriate and pulmonary allografts should not be discarded based solely on ODD status.
PMID: 31323210
ISSN: 1552-6259
CID: 3978102

Single and Double Lung Transplantation Have Equivalent Functional Status Outcomes at One Year [Meeting Abstract]

Ranganath, N K; Geraci, T C; Malas, J; Phillips, K G; Smith, D E; Lonze, B E; Lesko, M B; Angel, L F; Kon, Z N
Purpose: Controversy remains over the mortality benefit of single (SLT) versus double lung transplantation (DLT) in idiopathic pulmonary fibrosis (IPF). Independent of this controversy, hesitancy to perform SLT in this population exists on the basis of unclear one year functional status. We compared functional status at one year between IPF patients listed for both who ultimately received SLT or DLT. Method(s): All consecutive adult lung transplants for IPF provided by the Scientific Registry of Transplant Recipients were retrospectively reviewed (2007-2017). Isolated lobar transplants (n=4), patients listed only for SLT (n=1834) or DLT (n=2372), and patients with missing functional status data (n=715) were excluded. Group stratification was based on the ultimate procedure (SLT or DLT). Group propensity matching was performed based on 25 recipient/donor characteristics. We compared 'good functional status' defined as >70%, at one year. Result(s): During the study period, 45% (660/1464) and 55% (804/1464) of patients listed for both procedures ultimately received SLT and DLT, respectively. After propensity matching, 341 matched patients remained in each group. Donor and recipient characteristics were similar (Table). There was no statistically significant difference in 'good functional status' at one year between SLT (77%, 264/341) and DLT (81%, 275/341) (p=0.301). The same trend is present for patients younger than 50 who receive SLT (82%, 23/28) versus DLT (94%, 34/36) (p=0.225), and patients between 50 and 60 who receive SLT (78%, 86/110) versus DLT (84%, 97/115) (p=0.305). The opposite trend is noted in patients older than 70 who receive SLT (72%, 13/18) versus DLT (61%, 11/18) (p=0.725). Conclusion(s): In this cohort of lung transplant recipients listed for both SLT and DLT, functional status was statistically similar between groups, even in younger recipients. This data suggests that SLT should not be precluded in IPF patients on the basis of expected functional status at one year.
EMBASE:2001696071
ISSN: 1557-3117
CID: 3790602

An international perspective on hospitalized patients with viral community-acquired pneumonia

Radovanovic, Dejan; Sotgiu, Giovanni; Jankovic, Mateja; Mahesh, Padukudru Anand; Marcos, Pedro Jorge; Abdalla, Mohamed I; Di Pasquale, Marta Francesca; Gramegna, Andrea; Terraneo, Silvia; Blasi, Francesco; Santus, Pierachille; Aliberti, Stefano; Reyes, Luis F; Restrepo, Marcos I; Aruj, Patricia Karina; Attorri, Silvia; Barimboim, Enrique; Caeiro, Juan Pablo; Garzón, María I; Cambursano, Victor Hugo; Ceccato, Adrian; Chertcoff, Julio; Cordon Díaz, Ariel; de Vedia, Lautaro; Ganaha, Maria Cristina; Lambert, Sandra; Lopardo, Gustavo; Luna, Carlos M; Malberti, Alessio Gerardo; Morcillo, Nora; Tartara, Silvina; Pensotti, Claudia; Pereyra, Betiana; Scapellato, Pablo Gustavo; Stagnaro, Juan Pablo; Shah, Sonali; Lötsch, Felix; Thalhammer, Florian; Anseeuw, Kurt; Francois, Camille A; Van Braeckel, Eva; Vincent, Jean Louis; Djimon, Marcel Zannou; Aranha Nouér, Simone; Chipev, Peter; Encheva, Milena; Miteva, Darina; Petkova, Diana; Balkissou, Adamou Dodo; Pefura Yone, Eric Walter; Mbatchou Ngahane, Bertrand Hugo; Shen, Ning; Xu, Jin-Fu; Bustamante Rico, Carlos Andres; Buitrago, Ricardo; Pereira Paternina, Fernando Jose; Kayembe Ntumba, Jean-Marie; Vladic-Carevic, Vesna; Jakopovic, Marko; Matkovic, Zinka; Mitrecic, Ivan; Bouchy Jacobsson, Marie-Laure; Bro Christensen, Anette; Heitmann Bødtger, Uffe Christian; Meyer, Christian Niels; Vestergaard Jensen, Andreas; El-Said Abd El-Wahhab, Ibrahim; Elsayed Morsy, Nesreen; Shafiek, Hanaa; Sobh, Eman; Abdulsemed, Kedir Abdella; Bertrand, Fabrice; Brun-Buisson, Christian; de Montmollin, Etienne; Fartoukh, Muriel; Messika, Jonathan; Tattevin, Pierre; Khoury, Abdo; Ebruke, Bernard; Dreher, Michael; Kolditz, Martin; Meisinger, Matthias; Pletz, Mathias W; Hagel, Stefan; Rupp, Jan; Schaberg, Tom; Spielmanns, Marc; Creutz, Petra; Suttorp, Norton; Siaw-Lartey, Beatrice; Dimakou, Katerina; Papapetrou, Dimosthenis; Tsigou, Evdoxia; Ampazis, Dimitrios; Kaimakamis, Evangelos; Bhatia, Mohit; Dhar, Raja; D'Souza, George; Garg, Rajiv; Koul, Parvaiz A; Jayaraj, B S; Narayan, Kiran Vishnu; Udnur, Hirennappa B; Krishnamurthy, Shashi Bhaskara; Kant, Surya; Swarnakar, Rajesh; Salvi, Sundeep; Limaye, Sneha; Golshani, Keihan; Keatings, Vera M; Martin-Loeches, Ignacio; Maor, Yasmin; Strahilevitz, Jacob; Battaglia, Salvatore; Carrabba, Maria; Ceriana, Piero; Confalonieri, Marco; d'Arminio Monforte, Antonella; Del Prato, Bruno; De Rosa, Marino; Fantini, Riccardo; Fiorentino, Giuseppe; Gammino, Maria Antonia; Menzella, Francesco; Milani, Giuseppe; Nava, Stefano; Palmiero, Gerardo; Petrino, Roberta; Gabrielli, Barbra; Rossi, Paolo; Sorino, Claudio; Steinhilber, Gundi; Zanforlin, Alessandro; Franzetti, Fabio; Carone, Mauro; Patella, Vincenzo; Scarlata, Simone; Comel, Andrea; Kurahashi, Kiyoyasu; Aoun Bacha, Zeina; Barajas Ugalde, Daniel; Ceballos Zuñiga, Omar; Villegas, José F; Medenica, Milic; van de Garde, E M W; Raj Mihsra, Deebya; Shrestha, Poojan; Ridgeon, Elliott; Ishola Awokola, Babatunde; Nwankwo, Ogonna N O; Olufunlola, Adefuye Bolanle; Olumide, Segaolu; Ukwaja, Kingsley N; Irfan, Muhammad; Minarowski, Lukasz; Szymon, SkoczyÅ„ski; Froes, Felipe; Leuschner, Pedro; Meireles, Mariana; Ferrão, Cláudia; Leuschner, Pedro; Neves, João; Ravara, Sofia B; Brocovschii, Victoria; Ion, Chesov; Rusu, Doina; Toma, Cristina; Chirita, Daniela; Dorobat, Carmen Mihaela; Birkun, Alexei; Kaluzhenina, Anna; Almotairi, Abdullah; Bukhary, Zakeya Abdulbaqi Ali; Edathodu, Jameela; Fathy, Amal; Mushira Abdulaziz Enani, Abdullah; Eltayeb Mohamed, Nazik; Ulhadi Memon, Jawed; Bella, Abdelhaleem; Bogdanović, Nada; Milenkovic, Branislava; Pesut, Dragica; Borderìas, Luis; Bordon Garcia, Noel Manuel; Cabello Alarcón, Hugo; Cilloniz, Catia; Torres, Antoni; Diaz-Brito, Vicens; Casas, Xavier; Encabo González, Alicia; Fernández-Almira, Maria Luisa; Gallego, Miguel; Gaspar-GarcÍa, Inmaculada; González Del Castillo, Juan; Javaloyes Victoria, Patricia; Laserna Martínez, Elena; Malo de Molina, Rosa; Menéndez, Rosario; Pando-Sandoval, Ana; Prat Aymerich, Cristina; Lacoma de la Torre, Alicia; García-Olivé, Ignasi; Rello, Jordi; Moyano, Silvia; Sanz, Francisco; Sibila, Oriol; Rodrigo-Troyano, Ana; Solé-Violán, Jordi; Uranga, Ane; van Boven, Job F M; Vendrell Torra, Ester; Pujol, Jordi Almirall; Feldman, Charles; Kee Yum, Ho; Fiogbe, Arnauld Attannon; Yangui, Ferdaous; Bilaceroglu, Semra; Dalar, Levent; Yilmaz, Ufuk; Bogomolov, Artemii; Elahi, Naheed; Dhasmana, Devesh J; Feneley, Andrew; Hancock, Carole; Hill, Adam T; Rudran, Banu; Ruiz-Buitrago, Silvia; Campbell, Marion; Whitaker, Paul; Youzguin, Alexander; Singanayagam, Anika; Allen, Karen S; Brito, Veronica; Dietz, Jessica; Dysart, Claire E; Kellie, Susan M; Franco-Sadud, Ricardo A; Meier, Garnet; Gaga, Mina; Holland, Thomas L; Bergin, Stephen P; Kheir, Fayez; Landmeier, Mark; Lois, Manuel; Nair, Girish B; Patel, Hemali; Reyes, Katherine; Rodriguez-Cintron, William; Saito, Shigeki; Soni, Nilam J; Noda, Julio; Hinojosa, Cecilia I; Levine, Stephanie M; Angel, Luis F; Anzueto, Antonio; Scott Whitlow, K; Hipskind, John; Sukhija, Kunal; Totten, Vicken; Wunderink, Richard G; Shah, Ray D; Mateyo, Kondwelani John; Carugati, Manuela; Morosi, Manuela; Monge, Elisa
BACKGROUND:Who should be tested for viruses in patients with community acquired pneumonia (CAP), prevalence and risk factors for viral CAP are still debated. We evaluated the frequency of viral testing, virus prevalence, risk factors and treatment coverage with oseltamivir in patients admitted for CAP. METHODS:Secondary analysis of GLIMP, an international, multicenter, point-prevalence study of hospitalized adults with CAP. Testing frequency, prevalence of viral CAP and treatment with oseltamivir were assessed among patients who underwent a viral swab. Univariate and multivariate analysis was used to evaluate risk factors. RESULTS:553 (14.9%) patients with CAP underwent nasal swab. Viral CAP was diagnosed in 157 (28.4%) patients. Influenza virus was isolated in 80.9% of cases. Testing frequency and viral CAP prevalence were inhomogeneous across the participating centers. Obesity (OR 1.59, 95%CI: 1.01-2.48; p = 0.043) and need for invasive mechanical ventilation (OR 1.62, 95%CI: 1.02-2.56; p = 0.040) were independently associated with viral CAP. Prevalence of empirical treatment with oseltamivir was 5.1%. CONCLUSION/CONCLUSIONS:In an international scenario, testing frequency for viruses in CAP is very low. The most common cause of viral CAP is Influenza virus. Obesity and need for invasive ventilation represent independent risk factors for viral CAP. Adherence to recommendations for treatment with oseltamivir is poor.
PMID: 30401576
ISSN: 1879-0828
CID: 3455932

Immune Checkpoint Ligand PD-L1 is Upregulated in Pulmonary Lymphangioleiomyomatosis (LAM)

Maisel, Katharina; Merrilees, Mervyn J; Atochina-Vasserman, Elena N; Lian, Lurong; Obraztsova, Kseniya; Rue, Ryan; Vasserman, Alexander N; Zuo, Ning; Angel, Luis F; Gow, Andrew J; Kang, Inkyung; Wight, Thomas N; Eruslanov, Evgeniy; Swartz, Melody A; Krymskaya, Vera P
Pulmonary Iymphangioleiomyomatosis (LAM) is a slow-progressing metastatic disease that is driven by mutations in the tumor suppressor tuberous sclerosis complex 1/2 (TSC1/2). Rapamycin inhibits LAM cell proliferation and is the only approved treatment, yet it can only stabilize the disease but not cause regression of existing lesions. However, in other cancers, immunotherapies such as checkpoint blockade against PD-1 and its ligand PD-L1 have shown promise in causing tumor regression and even curing some patients. Thus, we asked whether PD-L1 has a role in LAM progression. In vitro, PD-L1 expression in murine Tsc2-null cells is unaffected by mTOR inhibition with torin, but can be upregulated by IFN--γ. Using immunohistochemistry and single cell flow cytometry, we report increased PD-L1 expression in both human lung tissue from LAM patients as well as in Tsc2-null lesions in a murine model of LAM. In this model, PD-L1 is highly expressed in the lung by antigen-presenting and stromal cells, and activated T cells expressing PD-1 infiltrate the affected lung. In vivo treatment with anti-PD-1 antibody significantly prolongs mouse survival in the model of LAM. Together, these data demonstrate that PD-1-/PD-L1-mediated immunosuppression may occur in LAM and suggest new opportunities for therapeutic targeting that provide benefits beyond those of rapamycin.
PMID: 30095976
ISSN: 1535-4989
CID: 3226772

Pulmonary Lymphangioleiomyomatosis (lam): Inflammatory Cell Infiltration In Human Lam Lung [Meeting Abstract]

Atochina-Vasserman, EN; Angel, LF; Eruslanov, E; Krymskaya, VP
ISI:000390749601593
ISSN: 1535-4970
CID: 2577632

Management of the Potential Organ Donor in the ICU: Society of Critical Care Medicine/American College of Chest Physicians/Association of Organ Procurement Organizations Consensus Statement

Kotloff, Robert M; Blosser, Sandralee; Fulda, Gerard J; Malinoski, Darren; Ahya, Vivek N; Angel, Luis; Byrnes, Matthew C; DeVita, Michael A; Grissom, Thomas E; Halpern, Scott D; Nakagawa, Thomas A; Stock, Peter G; Sudan, Debra L; Wood, Kenneth E; Anillo, Sergio J; Bleck, Thomas P; Eidbo, Elling E; Fowler, Richard A; Glazier, Alexandra K; Gries, Cynthia; Hasz, Richard; Herr, Dan; Khan, Akhtar; Landsberg, David; Lebovitz, Daniel J; Levine, Deborah Jo; Mathur, Mudit; Naik, Priyumvada; Niemann, Claus U; Nunley, David R; O'Connor, Kevin J; Pelletier, Shawn J; Rahman, Omar; Ranjan, Dinesh; Salim, Ali; Sawyer, Robert G; Shafer, Teresa; Sonneti, David; Spiro, Peter; Valapour, Maryam; Vikraman-Sushama, Deepak; Whelan, Timothy P M
This document was developed through the collaborative efforts of the Society of Critical Care Medicine, the American College of Chest Physicians, and the Association of Organ Procurement Organizations. Under the auspices of these societies, a multidisciplinary, multi-institutional task force was convened, incorporating expertise in critical care medicine, organ donor management, and transplantation. Members of the task force were divided into 13 subcommittees, each focused on one of the following general or organ-specific areas: death determination using neurologic criteria, donation after circulatory death determination, authorization process, general contraindications to donation, hemodynamic management, endocrine dysfunction and hormone replacement therapy, pediatric donor management, cardiac donation, lung donation, liver donation, kidney donation, small bowel donation, and pancreas donation. Subcommittees were charged with generating a series of management-related questions related to their topic. For each question, subcommittees provided a summary of relevant literature and specific recommendations. The specific recommendations were approved by all members of the task force and then assembled into a complete document. Because the available literature was overwhelmingly comprised of observational studies and case series, representing low-quality evidence, a decision was made that the document would assume the form of a consensus statement rather than a formally graded guideline. The goal of this document is to provide critical care practitioners with essential information and practical recommendations related to management of the potential organ donor, based on the available literature and expert consensus.
PMID: 25978154
ISSN: 1530-0293
CID: 2576472