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MONDAY • MAY 16 205<br />

CC2<br />

CLINICAL<br />

ADULT CLINICAL CORE CURRICULUM<br />

CME Credits Available: 1.5<br />

SLEEP MEDICINE CLINICAL CORE CURRICULUM I<br />

Adult Core Curriculum Working Group<br />

11:45 a.m. - 1:15 p.m. MOSCONE CENTER<br />

Gateway Ballroom 102-104 (South Building, Lower Level)<br />

Target Audience<br />

Internists and subspecialists in pulmonary, critical care, and sleep medicine<br />

who work in a clinical setting and are currently engaged in maintenance of<br />

certification.<br />

Objectives<br />

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

• remain current with medical knowledge relevant to their practice in<br />

pulmonary, critical care, and sleep medicine;<br />

• evaluate their understanding of key skills and content areas in pulmonary,<br />

critical care and sleep medicine, as well as receive feedback on their<br />

comprehension of a result of a pre-test/post-test comparison;<br />

• support clinicians who are engaged in maintenance of certification activities<br />

by providing updates on subjects included in recertification requirements.<br />

The ATS Clinical Core Curriculum Symposia focus on a 3-year content cycle of<br />

key medical content in the areas of pulmonary, critical care, and sleep medicine.<br />

The topics are also aligned with corresponding MOC Medical Knowledge<br />

modules. This symposium is intended to assist clinicians with staying current<br />

with the growth of information relevant to their medical practice, as well as<br />

provide an opportunity to evaluate individual knowledge and skills while earning<br />

MOC Medical Knowledge points.<br />

Chairing: J.S. Balachandran, MD, Chicago, IL<br />

T.S. Wang, MD, Los Angeles, CA<br />

11:45 Sleep Testing/Staging/Scoring: Staging and Scoring<br />

C. Lal, MD, Charleston, SC<br />

12:05 Sleep Testing/Staging/Scoring: In-Lab Diagnostics<br />

N.A. Shah, MD, MPH, New York, NY<br />

12:45 Sleep Testing/Staging/Scoring: Ambulatory Diagnostics<br />

K.F. Sarmiento, MD, MPH, La Jolla, CA<br />

L11<br />

CENTER FOR TOBACCO PRODUCTS,<br />

U.S. FOOD AND DRUG ADMINISTRATION<br />

FDA REGULATION OF TOBACCO PRODUCTS IN<br />

THE U.S.: 2016 UPDATE<br />

12:15 p.m. - 1:15 p.m. MOSCONE CENTER<br />

Room 3016/3018 (West Building, Level 3)<br />

Target Audience<br />

Any attendees interested in reducing tobacco related deaths.<br />

Objectives<br />

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

• understand the FDA’s Center for Tobacco Products’ (CTP) strategic<br />

priorities and CTP’s vision for the regulation of tobacco products to help<br />

reduce the death and disease toll caused by tobacco use;<br />

• discuss the Deeming Proposed Rule and how it will affect the way CTP<br />

evaluates the newly regulated products;<br />

• understand CTP’s research portfolio and how the Office of Science uses<br />

this information to inform tobacco product regulation.<br />

The 2009 Tobacco Control Act gave FDA regulatory authority over cigarettes,<br />

cigarette tobacco, roll-your-own tobacco, and smokeless tobacco. Newly<br />

“deemed” products in a proposed rule include electronic cigarettes, cigars, pipe<br />

tobacco, certain dissolvables that are not “smokeless tobacco,” gels, and<br />

waterpipe tobacco. Once the proposed rule becomes final, FDA will be able to<br />

use regulatory tools, such as age restrictions and rigorous scientific review of<br />

new tobacco products and claims to reduce tobacco-related disease and death.<br />

Youth use of certain unregulated tobacco products, such as e-cigarettes and<br />

cigars, is on the rise. FDA oversight of tobacco products can provide important<br />

information about proposed deemed tobacco products and help limit youth<br />

exposure to these products. Once final, the rule will also enable FDA to explore<br />

whether different products pose different levels of risk, and will help the Agency<br />

develop policies to improve public health. This session will help the medical,<br />

research, and public health communities understand the authority granted to the<br />

FDA to regulate tobacco and tobacco products and how science is used to<br />

make the most effective regulatory decisions.<br />

Chairing: P. Callahan-Lyon, MD, Silver Spring, MD<br />

12:15 FDA Regulation of Tobacco Products in the U.S.<br />

P. Callahan-Lyon, MD, Silver Spring, MD<br />

12:55 CTP Research Portfolio<br />

C. Dresler, MD, Silver Spring, MD<br />

L12<br />

NATIONAL AERONAUTICS AND<br />

SPACE ADMINISTRATION<br />

NASA’S SATELLITES AND MODELS TO STUDY<br />

THE ENVIRONMENT AND DISEASES<br />

12:15 p.m. - 1:15 p.m. MOSCONE CENTER<br />

Room 3010/3012 (West Building, Level 3)<br />

Target Audience<br />

Pulmonary health researchers and clinicians needing environmental data to<br />

study and understand the geographic, environmental, and meteorological<br />

differences in pulmonary disease. The researcher will hear from public health<br />

researchers new research and models that can be used to study the<br />

environment and related diseases.<br />

Objectives<br />

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

• inform clinicians and researchers about ongoing NASA projects related to lung<br />

performance and cardiac disease;<br />

• provide a synopsis of a project using observations of earth’s environment and public<br />

health applications that are of interest to pulmonary clinicians and researchers;<br />

• provide an overview of the NASA Health and Air Quality <strong>Program</strong> relating to public<br />

health applications that are of interest to pulmonary clinicians and researchers.<br />

MONDAY MID-DAY<br />

ATS 2016 • San Francisco

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