sepsis 2015: you say you wanted a revolution
TRANSCRIPT
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Thomas Jefferson University Thomas Jefferson University
Jefferson Digital Commons Jefferson Digital Commons
Division of Pulmonary and Critical Care Medicine Presentations and Grand Rounds
Division of Pulmonary and Critical Care Medicine
6-10-2015
Sepsis 2015: You say you wanted a revolution Sepsis 2015: You say you wanted a revolution
R. Phillip Dellinger, MD, MCCM Professor and Chair, Department of Medicine Cooper Medical School of Rowan University Medical Director, Adult Health Institute Senior Attending, Critical Care Medicine Cooper University Health Care
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Recommended Citation Recommended Citation
Dellinger, MD, MCCM, R. Phillip, "Sepsis 2015: You say you wanted a revolution" (2015). Division
of Pulmonary and Critical Care Medicine Presentations and Grand Rounds. Presentation 122.
https://jdc.jefferson.edu/pulmcritcaregrandrounds/122
This Article is brought to you for free and open access by the Jefferson Digital Commons. The Jefferson Digital Commons is a service of Thomas Jefferson University's Center for Teaching and Learning (CTL). The Commons is a showcase for Jefferson books and journals, peer-reviewed scholarly publications, unique historical collections from the University archives, and teaching tools. The Jefferson Digital Commons allows researchers and interested readers anywhere in the world to learn about and keep up to date with Jefferson scholarship. This article has been accepted for inclusion in Division of Pulmonary and Critical Care Medicine Presentations and Grand Rounds by an authorized administrator of the Jefferson Digital Commons. For more information, please contact: [email protected].
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R. Phillip Dellinger MD, MSc, MCCM
Professor and Chair of Medicine
Cooper Medical School of Rowan University
Medical Director Adult Health Institute
Senior Critical Care Attending
Cooper University Hospital
Camden NJ USA
SEPSIS 2015: YOU SAY YOU WANT A REVOLUTION
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POTENTIAL CONFLICTS OF INTEREST
• Hold leadership position in Surviving Sepsis Campaign
• Cooper University Hospital receives consultant fees and research funding from Spectral Inc. for work with the EUPHRATES trial.
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Burden of Severe Sepsis
Sepsis Performance Improvement
Revolution
Research : New or Ongoing Clinical Trials
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Burden of Severe Sepsis
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SEVERE SEPSIS
• Severe Sepsis is the Leading Cause of Hospital Death
• Admissions with severe sepsis 8X > chance of death than other conditions
• Most expensive condition treated in the hospital (23 billion dollars per annum)
• Enormous economic burden that can be lessened with early identification and early appropriate evidence based medicine care
NCHS data brief #62, 2011
US National Lib Med, NIH, 2010
HCUP Statistical Brief #160
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Causes of death in New Jersey in 2011, according to the most recent data available.
New Jersey Department of Health posted January 8, 2015
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“HEALTHCARE, WE HAVE A PROBLEM.”
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CURRENTLY FUNDED WITH A GORDON AND BETTY MOORE FOUNDATION GRANT (INTEL FAMILY). NO DIRECT OR INDIRECT INDUSTRY SUPPORT FOR GUIDELINES REVISION
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R. Phillip Dellinger, Mitchell M. Levy, Andrew Rhodes, Djillali Annane, Herwig Gerlach, Steven M. Opal, Jonathan E. Sevransky, Charles L.
Sprung, Ivor S. Douglas, Roman Jaeschke, Tiffany M. Osborn, Mark E. Nunnally, Sean R. Townsend, Konrad Reinhart, Ruth M. Kleinpell, Derek
C. Angus, Clifford S. Deutschman, Flavia R. Machado,Gordon D. Rubenfeld, Steven A. Webb, Richard J. Beale, Jean-Louis Vincent, Rui Moreno, and the Surviving Sepsis Campaign Guidelines Committee
including the Pediatric Subgroup.
Crit Care Med 2013; 41:580-637
Intensive Care Medicine 2013; 39: 165-228
SURVIVING SEPSIS CAMPAIGN: INTERNATIONAL GUIDELINES FOR MANAGEMENT OF SEVERE SEPSIS
AND SEPTIC SHOCK: 2012
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CURRENT SURVIVING SEPSIS CAMPAIGN GUIDELINE SPONSORS
• American Association of Critical-Care Nurses
• American College of Chest Physicians
• American College of Emergency Physicians
• Australian and New Zealand Intensive Care Society
• Asia Pacific Association of Critical Care Medicine
• American Thoracic Society
• Brazilian Society of Critical Care(AIMB)
• Canadian Critical Care Society
• Chinese Society of Critical Care Medicine
• Emirates Intensive Care Society
• European Respiratory Society
• European Society of Clinical Microbiology and Infectious Diseases
• European Society of Intensive Care Medicine
• European Society of Pediatric and Neonatal Intensive Care
• Infectious Diseases Society of America
• Indian Society of Critical Care Medicine
• International Pan Arab Critical Care Medicine Society
• Japanese Association for Acute Medicine
• Japanese Society of Intensive Care Medicine
• Pediatric Acute Lung Injury and Sepsis Investigators
• Society Academic Emergency Medicine
• Society of Critical Care Medicine
• Society of Hospital Medicine
• Surgical Infection Society
• World Federation of Critical Care Nurses
• World Federation of Pediatric Intensive and Critical Care Societies
• World Federation of Societies of Intensive and Critical Care Medicine
Participation and endorsement:
German Sepsis Society
Latin American Sepsis Institute
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GUIDELINES ARE NOT ENOUGH
• Protocols
• Performance Improvement Programs
• Audit and Feedback
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Early Screening and a Hospital Based Performance
Improvement Program
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GUIDELINES TO BUNDLES
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CONVERTING GOALS TO MEASURABLE INDICATORS
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CHANGE IN COMPLIANCE OVER TIME
Levy MM, Dellinger, RP, Townsend SA et al.
CCM 38(2):367-374, February 2010.
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CHANGE IN MORTALITY OVER TIME
Levy MM, Dellinger, RP, Townsend SA et al.
CCM 38(2):367-374, February 2010.
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Levy, et al. Crit Care Med. 2015 Jan;43(1):3-12.
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SSC MORTALITY
Levy, et al. Crit Care Med. 2015 Jan;43(1):3-12.
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WHY?
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Levy, et al. Crit Care Med. 2015 Jan;43(1):3-12.
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INITIAL RESUSCITATION OF SEPSIS INDUCED TISSUE HYPOPERFUSION
Recommend
Insertion central venous catheter
Recommended goals :
• Central venous pressure: 8–12 mm Hg
• Higher with altered ventricular compliance or increased intrathoracic pressure
• ScvO2 saturation (SVC) 70%
Grade 1C
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STARLING PRINCIPLE RELATES TO VOLUME
The Starling principle relates to the fact that the more a myocardial fibril is stretched the greater the contraction.
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EXPECTED RESULT OF VOLUME EXPANSION
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CENTRAL VENOUS PRESSURE POORLY PREDICTS CARDIAC PRELOAD AND
VOLUME STATUS
Michard F, et al. Chest 2002; 121:2000–2008.
Kumar A, et al. Crit Care Med 2004; 32:691–699.
Shippy CR, et al. Crit Care Med 1984; 12:107–112.
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INTRAVASCULAR VOLUME STATUS AND PERFUSION PARAMETERS
• Limitation of pressure measurement to predict fluid responsiveness
• There are alternatives to CVP for judging fluid responsiveness that are in general more reliable
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ARTERIAL SYSTOLIC PRESSURE VARIATION
Parry-Jones, et al. Int J Respir Crit Care Med 2003;2:67
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EFFECT ON CARDIAC FILLING
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Part
A
t
EFFECT ON STROKE VOLUME
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EFFECT ON STROKE VOLUME
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Revolution
You say you want a revolution
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NATIONAL QUALITY FORUM 2012 NQF: SEPSIS 0500
TO BE COMPLETED WITHIN 3 HOURS OF TIME OF PRESENTATION :
1. Measure lactate level
2. Obtain blood cultures prior to administration of antibiotics
3. Administer broad spectrum antibiotics
4. Administer 30ml/kg crystalloid for hypotension or lactate ≥4mmol/L
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2012 NQF: SEPSIS 0500
TO BE COMPLETED WITHIN 6 HOURS OF TIME OF PRESENTATION:
5. Apply vasopressors (for hypotension that does not respond to initial fluid resuscitation to maintain a mean arterial pressure (MAP) ≥65mmHg)
6. In the event of persistent arterial hypotension despite volume resuscitation (septic shock) or initial lactate ≥4 mmol/L (36mg/dl): - Measure central venous pressure (CVP) - Measure central venous oxygen saturation (ScvO2)
7. Remeasure lactate if elevated.
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N Engl J Med. 2014 May 1;370(18):1683-93.
N Engl J Med. 2014 Oct 16;371(16):1496-506.
1600 Patients
Over 1500 Patients
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Both the ProCESS and ARISE trials demonstrated the lack of necessity of using central venous oxygen saturation and central venous pressure monitoring as resuscitation targets when compared to the usual care group.
EARLY GOAL DIRECTED THERAPY (EGDT)
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Revolution
You say you got a real solution Well, you know We’d all love to see the plan
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You ask me for a contribution Well, you know We’re all doing what we can
Revolution
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Revolution
You tell me it’s (for) the institution
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N Engl J Med. 2014 May 1;370(18):1683-93.
N Engl J Med. 2014 Oct 16;371(16):1496-506.
1600 Patients
Over 1500 Patients
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ProCESS ARISE
Enrollment <2 hours from detection of shock
2.8 hours (median) from presentation to
ED
Antibiotics 75% received prior to enrollment
70 minutes (median) from presentation to
ED
Fluids >2 liters prior ot enrollment
2515ml (mean) prior to enrollment
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• SSC 2006 six hour bundle
• SSC 2012 three hour bundle
• NQF 0500
• ProCESS/ARISE/PROMISE
• NQF 0500 (revised)
• CMS SEP 1
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TO SAVE LIVES.....
Early fluid resuscitation
Early antibiotics
Early identification
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IMPORTANCE OF REASSESSMENT
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• Sepsis is a big problem
• Logic of indicators is good
• Benchmarked performance
CMS SEP-1
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Revolution
Don’t you know it’s gonna be alright, alright, alright
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Research / New or Ongoing Clinical
Trials
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SELEPRESSIN
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Koshimizu, et al. Physiol Rev. 2012 Oct;92(4):1813-64.
V1A Receptor
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LB1148
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Gut Integrity in Shock
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“SSAIL” TRIAL (TREATMENT OF SEPTIC SHOCK BY INHIBITING AUTODIGESTION AND PRESERVING GUT INTEGRITY WITH ENTERIC LB1148)
• LB1148 – broad-spectrum serine protease inhibitor delivered enterally to gut
• Inhibit the intraluminal pancreatic proteolytic enzymes (proteases) that leak due to loss of gut integrity
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SOLUBLE THROMBOMODULIN
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ANGIOTENSIN II
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Chawla, et al. Crit Care. 2014 Oct 6;18(5):534.
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POLYMYXIN B HEMOPERFUSION
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Endotoxemia
SOURCES OF ENDOTOXIN
Endotoxin translocation
from GI Tract
Every human has 25-30 grams
of Endotoxin in their GI tract
Less than 0.001 grams of Endotoxin
is enough to kill a person
Endotoxin shed from local
bacterial infection
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Opal SM, et al. Infect Dis, 1999
SEPSIS AND ENDOTOXIN
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INTERVENTION DIRECT HEMOPERFUSION WITH ADSORBENT COLUMN USING
POLYMYXIN B IMMOBILIZED FIBER
ANTICOAGULANT
Heparin (3000 U in bolus followed by a
continuous infusion of 20 U/kg/h)
FEMORAL or IJ VEIN
FEMORAL or IJ VEIN
BLOOD TUBE
P
BLOOD PUMP
Perfusion rate 80-120 ml/min
Duration: 2 hours
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HEMODYNAMIC EFFECTS OF PMX
Cruz D. et al. Critical Care 2007; 11:R47
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JAMA. 2009;301(23):2445-2452
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JAMA. 2009;301(23):2445-2452
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ENDOTOXIN ACTIVITY ASSAY EAA™
The only FDA cleared test for detection of Endotoxin
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