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136 MONDAY • MAY 16<br />

Target Audience<br />

Pulmonologists, post graduate fellows and trainees, advanced practice nurses.<br />

Objectives<br />

At the conclusion of this session, the participant will be able to:<br />

• identify clinical features from a patient’s history that can help distinguish<br />

among the non-IPF ILDs in a patients with newly recognized ILD;<br />

• identify radiographic features from a patient’s HCRT that can help<br />

distinguish among the non-IPF ILDs in a patients with newly recognized<br />

ILD;<br />

• identify pathologic features from a patient’s biopsy that can help distinguish<br />

among the non-IPF ILDs in patients with newly recognized ILD.<br />

Distinguishing among the non-IPF interstitial lung diseases can be very<br />

challenging for the clinician. This symposium will seek to review the evidence<br />

for the best discriminating clinical, pathologic and radiologic features that can be<br />

used to differentiate among the non IPF ILDs. Following a review of these<br />

characteristics, 3 ILD clinicians will discuss real life cases that they will have<br />

been given ahead of time (without the diagnosis) to demonstrate how best to<br />

work thorough these challenging cases.<br />

Chairing: M. Kreider, MD, Philadelphia, PA<br />

G. Tino, MD, Philadelphia, PA<br />

A. Olson, MD, MSPH, Denver, CO<br />

9:00 Introduction<br />

G. Tino, MD, Philadelphia, PA<br />

9:10 Top 5 Clinical Features to Differentiate Among Non-IPF ILD<br />

K.K. Brown, MD, Denver, CO<br />

9:30 Top 5 Radiographic Features to Differentiate Among Non-IPF ILD<br />

D. Hansell, MD, London, United Kingdom<br />

9:45 Top 5 Pathologic Features to Differentiate Among Non-IPF ILD<br />

W.D. Travis, MD, New York, NY<br />

10:00 Case I<br />

T.M. Maher, MD, MSc, PhD, London, United Kingdom<br />

A. Olson, MD, MSPH, Denver, CO<br />

10:15 Case II<br />

C.D. Fell, MD, MSc, Calgary, Canada<br />

M. Kreider, MD, Philadelphia, PA<br />

10:30 Case III<br />

G. Tino, MD, Philadelphia, PA<br />

J.S. Lee, MD, Aurora, CO<br />

10:45 Questions and Answers<br />

M. Kreider, MD, Philadelphia, PA<br />

This session and the International Conference are supported by an educational grant from<br />

Boehringer Ingelheim Pharmaceuticals, Inc.<br />

All CME sessions have been planned and implemented in accordance with the Essential<br />

Areas and Policies of the Accreditation Council for Continuing Medical Education (ACCME)<br />

and are free of the control of commercial interests.<br />

B4<br />

BASIC • CLINICAL • TRANSLATIONAL<br />

CRITICAL CARE TRACK<br />

CME Credits Available: 2.0<br />

MECHANISMS OF ORGAN FAILURE IN SEPSIS<br />

Assemblies on Critical Care; Respiratory Cell and Molecular Biology;<br />

Respiratory Structure and Function<br />

9:00 a.m. - 11:00 a.m. MOSCONE CENTER<br />

Room 3000/3002/3004 (West Building, Level 3)<br />

Target Audience<br />

Pulmonary and critical care researchers (undergraduates, graduates, post<br />

graduates and postdoctoral), clinicians (adults and peds), and trainees interested<br />

in understanding the athophysiology and pathogenesis of organ failure in sepsis.<br />

Objectives<br />

At the conclusion of this session, the participant will be able to:<br />

• learn new paradigms about sepsis-induced organ failure;<br />

• recognize risk and development of sepsis-induced organ failure;<br />

• translate new advancements in basic research with current and future clinical<br />

practice.<br />

This session will review seminal concepts in sepsis-induced organ failure as well<br />

as present novel and cutting edge research in the field. The aim is to translate<br />

cutting-edge advancements in molecular physiology and functional genomics of<br />

organ failure in the septic patient to a broad clinical and translational audience.<br />

The session will engage/stimulate and enhanced understanding of the leading<br />

concepts regarding the relative contributions of over-inflammation,<br />

immunosuppression, the microbiome, epithelium and endothelium as critical<br />

target(s) of organ failure that ultimately determine (lung, kidney, liver, heart,<br />

muscle, gut and brain) dysfunction and clinical outcomes in the critically ill. The<br />

session will have broad appeal to physicians and scientists at any level of training<br />

who work on diverse problems in the critically ill, and it will draw a diverse<br />

international audience because of the generalizability of the topics.<br />

Chairing: C.C. Dos Santos, MD, Toronto, Canada<br />

I.S. Douglas, MD, Denver, CO<br />

J. Chiche, MD, PhD, Paris, France<br />

9:00 Mechanisms of Organ Failure in Sepsis<br />

R. Hotchkiss, MD, St. Louis, MO<br />

9:15 Innate Immune Training in Sepsis?<br />

M. Netea, MD, PhD, Nijmegen, Netherlands<br />

9:30 Liver Dysfunction in Sepsis<br />

M. Bauer, MD, Jena, Germany<br />

9:45 Is the Microbiome an “Organ” that Fails in Septic Patients?<br />

J. Alverdy, MD, Chicago, IL<br />

10:00 Is All Organ Failure Created Equal?<br />

C.C. Dos Santos, MD, Toronto, Canada<br />

10:15 Sepsis Induced Immunosuppression Shift in Therapeutic<br />

Paradigm<br />

J. Chiche, MD, PhD, Paris, France<br />

ATS 2016 • San Francisco

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