hot topics in icm - pincer course 25th sept 2015
TRANSCRIPT
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Hot Topics in ICM
Steve Mathieu @stevemathieu75 @WessexICS
Consultant in Intensive Care Medicine Queen Alexandra Hospital, Portsmouth
15th September 2015
& some question spotting…
Examiners Report April/May 2014
http://www.ficm.ac.uk/sites/default/files/document-files/EXM-FFICM-Summary-ChairmanReport-April2014_0.pdf
Examiners Report Nov 2014
http://www.ficm.ac.uk/sites/default/files/Critical%20Eye%207%20-%20Winter%202015_0.pdf
‘some candidates appeared to consider that they should concentrate only on areas within their own experience rather than the breadth of the syllabus’
Examiners Report April 2015
http://www.ficm.ac.uk/sites/default/files/Critical%20Eye%208%20-%20Summer%202015%20FINAL%20WEBSITE2.pdf
“A doctor in training who is familiar with the syllabus and has done the necessary bookwork. They would clinically be at the level of a registrar who would be able to formulate a plan of care for a critically ill patient with appropriate consultant backup. Passing the exam is a requirement of progression to ST7 of the intensive care medicine training programme and the standard is set to reflect this”.
Hot Topics/Question spotting
• Examiners report • Syllabus • Review articles & key papers – JICS • Guidelines • Review FICM & ICS websites • Critical Eye • Other resources
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Any dodgy ones?
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Original Articles Reviews Case reports CAT reviews Others
August 2015 Psychological and neurocognitive consequences of critical illnessWeight calculationsScoring system for cirrhosis
NIV post oesophagecotmy. Safe?
Thyroid stormNAC
PARAMEDIC study (mechanical vs manual CPR)Damage control resuscitation
Prevention of VTEAnatomy of vessels relevant to central line placementNIV Defining deathStridor
May 2015 Tracheostomy careDepression following critical illnessConsultant cover and working practiceICU acquired weaknessPharmacokinetic considerations and dosing strategies of antibiotics
Strep toxic shock ProMISeCRISTAL Colloids vs crystalloids
Feeding patients with tracheostomiesAmitryptiline ODManaging acute central nervous system infections in the UK adult intensive care unit in the wake of UK encephalitis guidelines
Feb2015 Adult blunt chest traumaRRT in Scottish ICUsRehab after critical care
Troponin elevated in sepsis
DKA Monitoring-based antibiotic optimisation
VSE after IHCA
Rehab Improving qualityGPICSDoLS + DoLSEbolaTracheostomyAcute cardiomyopathy with amphetamine poisoning
October 2014 Minimising warm and cold ischaemic times liver transplantsDoLS +++Oral Feed and TracheostomyProphylactic IVC Filter
ECCO2R in NIVLimbic encephalitisEmphysematous pyelonephritisOndine’s Curse
Volume-Outcome Relationships for MV Adult Patients
Hyperglycaemic control on PICU
Evacuation of ICU due to a FireLetter about VAPHyperoxaemia in SAHElectrical Muscle Stimulation in ICU
July 2014 Echo in PEQuality (pressure ulcers)
DKAAcute mesenteric ischaemia
Epidural abscessJW GI haemorrhageMixed ODAcromegaly
Statin & VAPSEPSISPAMProtective ventilation in abdominal surgeryHeart rate control in septic shock
Delirium
April 2014 TracheostomyVAPImproving timeliness of time-critical transfers
HITHepatitis B & CSedationElectrical muscle stimulation in ICU (CIPN)
HD for dabigatran associated coagulopathyWernickesPatient with tetanus
TBIHope ICU (delirium)CSL or HESTTM
Prone ventilationCapnography
Jan 2014 COMET-UK (CO monitoring)Tracheostomy
Right heart failure Stabilisation and transport of critically ill child
ECG and traumaRhabdomyolysisPancreatitisMDMA toxicityHyperthyroidismPulmonary haemorrhage and AKI
TracMan AKIOrgan donationSurveillance for VAPPE supplement
Original Articles Reviews Case reports CAT reviews Others
October 2013
Echo NAVA ventilationPainBrainstem testing
Plasma exchange in HUSIntralipid in felodipine toxicityTracheostomy
Transfusion strategies for upper GI bleedProne TXA
Survey on rehab after critical illnessEcho in UKBlood transfusion in ICUBIS monitoringFaecal incontinence in ICU
July 2013 Noise level in ICU (delirium)
Serious Hazards of Transfusion (SHOT)Medical support for heart failurePCTNOCardiogenic shock
OTC deficiencyHyperkalaemia in HIV patient with ‘PCP’
ICP monitoringSedation
Gentamycin & vancomycinAncillary tests in diagnosis of brainstem testingLCPScoring systems for CAPAtrial Fibrillation in ICU
Guidelines
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The Sepsis Studies
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Neuro
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
http://www.wessexics.com/WICS_Guidelines/
The SAH section definitely worth a read for the exam
NCEPOD 2014: Tracheostomy• Documentation & consent
– Indications, type, inner tube, reasons for failed extubation/why no trial of extubation
• Different types of tubes • Rapidly available difficult airway
trolley • Training programmes in blocked/
displaced tubes • Capnography • Discharge of patients with
tracheostomy • MDT – physio & SALT
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Capnography Airway equipment Back up planning Staffing Patient transfers Education/training Tracheostomy tube design Team working
Tracheostomy standards ICS• Indications for tracheostomy • Cautions and contraindications • Consent • Equipment • Ultrasound • Anaesthesia • Staffing • Types of tracheostomy tubes • Inner cannulae • Complication
– Early – Late – Airway emergencies
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HFNC non inferior to facemask and NIV in ALI
ARDS - lots of trials
Neuro
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
http://www.wessexics.com/WICS_Guidelines/
The SAH section definitely worth a read for the exam
ABLE Multicentre UK RBC transfusion (7d vs. 15-25d) NOAC
Transfusion triggers – TRICC, TRISS & Villaneuva, TITRe2 PROPPR: Plasma, Platelets & PRBC’s 1:1:1 vs. 1:1:2
Management of anaemia & RBC transfusion BCSH Guidelines 2012) Serious Hazards of Transfusion (SHOT) – JICS July 2013
Standards - quality• Staffing
– Consultant presence • 24/7 & within 30 minutes
– Consultant: patient 1:8 – 1:15; ICU resident/patient 1:8
– Designated CD – Ward rounds x2 daily – Training / FICM / Board Tutors – Nursing 1:1 (level 3); 1:2 (level 2) – MDT e.g. physio, pharmacy, dieticians
• Operational – Large ICUs divided into pods of 8-15 patients – Admit within 4 hrs of decision to admit – Avoid non-clinical transfers – Transfer to ward – clear and formalised – Out of hours transfers – Readmission within 48 hours bad – Assessment of rehab for each patient
• Equipment – Training
• Data Collection – ICNARC – Risk register
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Quality Indicators
SMR Scoring Systems
MCA & DoLSDoLS • 3 cases in 2014
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
MUST READ….
The landmark papers in Critical Care
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
NAP 4 - 2011• All NHS hospitals for 1 year ’08-’09 • 184 reports
133 anaesthesia 36 ICU 15 ED
• Inclusion criteria death, brain damage emergency surgical airway unanticipated ICU admission
– Prolongation ICU stay
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Summary of NAP 425% of major airway events in a hospital occur in ICU or the
ED
46% of ICU events and 53% of ED events occurred out of hours
50% of ICU events were due to tracheostomy related events
50% events in ICU and 27% events in ED resulted in death
61% events in ICU resulted in death or severe neurological harm
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Recommendations Capnography Airway equipment Back up planning Staffing Patient transfers Education/training Tracheostomy tube design Team working
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
TracMan - 2013
•Early tracheostomy (by d 4) or late (>10/7)
– 455 patients – Mortality the same 31% – LOS the same 13 d – Complications slightly higher in late group 6% vs. 5%
Young et al. JAMA 2013 May 22;309(20):2121-9
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
ARDS
ARDS - Incidence
• 1 yr prospective observational study; 255 patients
• Incidence 7.2/100,000/year (? US 75/100,000)
• Despite use of lung protective ventilation overall ICU mortality >40%
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
ARDS - lots of trials
OSCAR• 795 patients with moderate -
severe ARDS (<26.7kPa / 200mmHg)
• CMV vs. HFOV (MV <7 days) • No difference in
– 30/7 mortality (41%) – Duration antimicrobial agents (2/3
chest sepsis) – Vasoactive support duration – ICU LOS – Hospital LOS
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
OSCILLATE• 548 patients with moderate - severe
ARDS • HFOV vs low Vt/High PEEP CV (MV <
3d) • Trial stopped early as harm with HFOV • HFOV
– Hospital mortality 47% vs 35% – More sedation – More NMBA’s – More vasopressors
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
PROSEVA• 466 patients with severe ARDS • Prone position vs supine position • Prone position was associated
with – Improved mortality
• 28 day: 16% vs 33% • 90 day: 24% vs 41%
– Less cardiac arrests – No difference in
complications
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
PROSEVA
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HARP 2 - 2014
• 540 patients ARDS; 40 UK ICUs • ARDSnet +/- statin for 28 days (80mg od simvastatin) • Primary outcome
– No difference in ventilator free days at 28d
• Secondary outcome – No difference in SOFA, oxygenation – Elevated CK or ALT/AST > in statin
group
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Statins in ARDS
• Multicentre, RCT • Rosuvastatin vs. placebo in ARDS • Statin may modulate inflammatory response • 745 patients (trial stopped early because of
futility) • Primary outcome:
• 60d mortality: 28.5% vs. 24.9% (statin vs. placebo) • Ventilator free days: 15.1 vs. 15.1
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Statin & VAP• 300 patients with suspected VAP
(CPIS ≥ 5) • Simvastatin 60mg vs placebo • No difference in
– 28d survival – ICU or hospital mortality – Duration MV – Delta SOFA
• Increased mortality in statin naieve
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
BALTI - 2012
• 162 patients; 46 UK ICU’s • ARDS & MV
- salbutamol 15mcg/kg/hr or placebo - Treatment for up to 7 d
• Mortality greater in those given salbutamol 34% vs 23% at 28d
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Steroids in ARDS
• 9 studies (4 RCT’s & 5 cohort) • 648 patients • Trend to reduced mortality but only ss when result pooled • Trials vary ++ 1.Dose 2.Initiation of treatment 3.Course length 4.Not all studies report adverse events
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Nitric oxide – just say No• Potent pulmonary vasodilator which when inhaled =
selective vasodilation in well ventilated lung units • Improved V/Q mismatch and PVR & PAP • Also anti-inflammatory effects • Systematic review of 12 trials with 1200 patients =
improved oxygenation d1, no improvement in mortality
• ⇧AKI and methaemaglobinaemia ⇧intracranial bleeding in children
Afshari Cochrane review 2007 - adults Barrington Cochrane review 2010 – children Afshari – systematic review 2011
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Magnesium in asthma
• 1200 patients 2008-2012 • Neb vs. IV Mg vs. placebo • No role for neb Mg • Limited role at best for IV
Mg • Not life threatening
asthma
Intravenous or nebulised magnesium sulphate versus standard therapy for severe acute asthma (3Mg trial): a double-blind, randomised controlled trial Goodacre et al Lancet 2013 Vol 1 (4) 293-300
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
VAP
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
What is VAP?
What are the common organisms (early
vs. late?
Scoring systems e.g. CPIS, HELICS
What antibiotics would you use?
How can you reduce incidence
Open Access!#FOAMcc
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HFNC non inferior to facemask and NIV in ALI
FLORALI
• 12 French ICU’s; 310 patients • ‘ALI’ • NRB vs HFNC vs NIV • Primary outcome: Proportion of patients who required
endotracheal intubation within 28 days after randomisation:
• High-Flow oxygen: 40 patients (38%) • Non-invasive ventilation: 55 patients (50%) • Standard oxygen: 44 patients (47%) • p = 0.18
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
PREOXYFLOW
• 6 French ICUs. 119 patients • Acute hypoxaemia • Primary outcome: Lowest SpO2 during the
endotracheal intubation (ETI) procedure • ETI = the beginning of laryngoscopy to
patient connection to the mechanical ventilator
• HFNC 91.5 [80-96] vs HFFM 89.5% [81–95] p = 0.44.
• HFNC without discontinuation during an apnoeic period, was not any more effective than using a high FiO2 facemask at 15 l/min for preventing desaturation during RSI
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
CO Monitoring – COMET-UK• Survey to all UK ICUs • Respondents
– Majority used CO monitoring • Oesophageal doppler 57% • LiDCO 43% • PiCCO 42%
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
How does doppler work? Thermodilution?
Pulse contour analysis ?
OPTIMISE• RCT, multicentre, 17 UK ICUs • 734 patients • > 50y undergoing GI surgery with one or more ‘high risk’ risk factors • Algorithm-directed care dictating colloid and dopexamine
administration using vs. clinician directed care without use of CO monitoring
• Primary outcome: composite of 30d mortality and mod/major complications
– Intervention: 36.6% – Control arm: 43.4%
• No SS difference in secondary outcomes – POMS, infectious complications, critical care free days at 30d, mortality
at 30d and 180d, hospital LOS
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
IVOIRE Study
• Randomised, open study • 18 ICU’s in France, Belgium and
Netherlands 2005-2010 • 140 pts with septic shock & AKI • HVHF 70mls/kg/hr v 35mls/kg/hr • Slow recruitment • No difference in mortality = 40%
28/7 • HVHF not recommended
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
TTM• 950 unconscious adults; 36 ICU’s • 33°C (n=473) with 36°C (n=466) • No difference in
– All cause mortality 33°C (50%) with 36°C (48%) – poor neurological function
at 180 days 33°C (54%) with 36°C (52%)
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Cognitive function post TTM• 652 cardiac arrest survivors from TTM • Survival until 180 days 52% - invited to follow up - about half had psychometric testing - compared with a control group
(STEMI but no cardiac arrest) • About 50% had cognitive impairment • 33 vs. 36 vs. control group similar
• Attention & mental speed more affected in cardiac arrest patients
• Memory & executive functioning similar
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Pre-hospital hypothermia• Prehospital cooling vs. standard care • 2L of cold normal saline once ROSC • 1,359 OOHCA patients • Cooling effective (reduced temp) • No difference
– Survival to hospital discharge • VF 63% vs 64% • nonVF 19% vs 16%
– Good neurological recovery • VF 57% vs 62% • nonVF 14% vs 13%
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
IABP – SHOCK II• 600 patients with cardiogenic shock
secondary to AMI • IABP vs no IABP • All received early revascularisation
and best medical therapy • No difference
– 30/7 mortality (40%) – ICU LOS, catecholamine, bleeding
• Lancet 2013 Sept – 12/12 results = no difference in mortality or reinfarction rate
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
VSE in cardiac arrest• 268 patients in hospital cardiac arrest • Vasopressin(20IU/CPR cycle) +
epinephrine (1mg/CPR cycle) + methylprednisilone (40mg) vs placebo + epinephrine (1mg/CPR cycle)
• VSE group – ROSC at 20 mins higher 84% vs 66% – Improved survival to hospital discharge with
CPC 1 or 2 – Improved haemodynamics & cvSpO2 – Less organ dysfunction
• and
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Therapeutic Hypothermia after OOH CA in ChildrenIn children suffering an out-of-hospital cardiac arrest, does hypothermia (33)
compared to normothermia increase survival with a good neurobehavioural outcome?
38 sites in US & Canada; 260 patients
There was no statistically significant difference in survival to 12 months with good neurobehavioural outcome (age-corrected standard score of 70 or higher on the Vineland Adaptive Behaviour Scale 2nd ed. [VABS-II])
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Therapeutic Hypothermia in Deceased Organ Donors and Kidney-Graft Function
• 394 donors with BSD • Mild hypothermia (34-35) vs
normothermia • Primary outcome: Delayed graft function
(the recipient's requirement for dialysis during the 1st week post-transplantation) - significantly lower in hypothermia group
• 28.2% vs 39.2%, P=0.008
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Monitor: Protocolised fluid therapy in brain-dead donors
• US • BSD 508 • Protocolised LiDCO vs routine • Primary outcome: Number of organs transplanted per donor – no
difference
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
CHEER• Refractory cardiac arrest treated
with mechanical CPR, hypothermia, ECMO and early reperfusion
• 26 patients (11 OHCA; 15 IHCA) • Primary outcome
– Survival with good neurological recovery (CPC 1-2) 14/26 (54%)
• Secondary outcomes – ROSC achieved in 25/26 (92%) of patients – Survival to hospital discharge 14/26 (54%)
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
The oxygenator in veno-venous ECMO
Study type Year pub
N (ECMO)
N (non
ECMO)
% H1N1
ECMO mortality
Non-ECMO mortality
p
RCT 2009 90 90 0 37% 50% 0.07
RCT 1994 21 19 0 67% 58% 0.8
RCT 1979 48 42 0 90% 92% 0.84
Cohort 2006 32 118 0 47% 29% 0.06
Cohort 2000 62 183 0 45% 39% NS
Cohort 1997 49 73 0 45% 11% <0.001
Case series
2009 68 133 100% 23% 13% 0.06
Case series
2011 69 11 100% 27.5% ?52% ***
ECMO for H1N1• 2009-2010 • 80 patients referred for
ECMO • 69 received ECMO • 22 of these died (27.5%) • Matching cohort = 52% • For patients with H1N1
related ARDS, mortality reduced with ECMO
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Passive Leg Raise
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
• Meta-analysis • 16 trials inc PEITHO, MAPPETT,
MOPETT, TOPCOT • Thrombolysis + anticoagulation
vs. anticoagulation alone • All cause mortality less in
thrombolysis group but major bleeding & ICH higher
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
SEPSIS
The Sepsis Studies
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
ARISE• Randomised, controlled,
multicentre, • 51 hospitals 1,600 patients with
septic shock • EGDT vs. Usual Care • No difference in:
– All cause mortality at 90d (18%) – ICU & Hospital LOS
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
ProCESS• RCT 31 ICUs in US • 03/2008 – 05/2013 • 1351 patients with septic shock • 3 groups
– EGDT – Protocol based standard therapy – Usual care – No difference in 60 d mortality between
groups
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
ProMISe• RCT 56 ICUs in UK • 02/2011 – 07/2014 • 1260 patients with septic shock • EGDT vs Usual care
– All cause mortality at 90 days in EGDT group vs. usual care group
– 29.5% vs. 29.2% p=0.9
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Ferrer: Empiric antibiotics in sepsis
• Retrospective observational cohort study • 165 ICUs – Europe, US & S America • Jan 2005- Feb 2010 • 18,000 patients with septic shock • Delay in antibiotics administration over first 6 hours after
identification of SS or septic shock -> increased mortality • < 1 hr 24.6%; 1-2h 25.9% > 6h 33%
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
SEPSISPAM• RCT, multicentre, 29 French ICUs • March 2010 – Dec 2011 • Septic shock • Target MAP 80-85 vs. 65-70 • No difference in
– 28 day mortality (high MAP 36.6% vs. 34%) • New AF 6.7% in higher MAP group vs. 2.8% P=0.02 • In chronic hypertension group, worsening creatinine and need for RRT
was lower in higher MAP group
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
PROWESS SHOCK• Randomised, controlled,
multicentre, parallel group study • 1,697 patients with septic shock • No difference in
– 28 day mortality (APC 26.4% vs 24.2%)
– 90 day mortality (34.1% vs 32.7%) • No subgroup effect seen in protein C
deficient group • Serious bleeding n = 10 APC vs 8
placebo
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
B blockers in septic shock• Open label, single unit • Septic shock + HR ≥ 95 + NADR • 77 patients – esmolol infusion (HR
80-94) vs 77 patients standard treatment
• Esmolol group – 28d Mortality 50% vs 81% in placebo – Improved SV index, LVSWI, lactate – Less NADR requirement – Less fluid requirement
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Esmolol in refractory VF• Single centre, non randomised • 25 patients with refractory (>3 defib
attempts) VF or pulseless VT • Esmolol vs. placebo • Primary outcome
– Survival with good neurological recovery – 50% esmolol vs 11% control group – No difference in rates of ROSC or survival
to hospital discharge
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Steroids in Sepsis
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
The evidence…..let’s give it
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
8 trials published before ’89 - No mortality benefit (some worse) - Decreased time for shock resolution - More secondary infections - Higher doses and for shorter periods
19 ICU’s 300 patients - 50mg hydrocortisone + fludrocorisone vs. placebo by 8hrs of onset of septic shock. - ‘Non responders’ (adrenal suppression) better ICU (53% vs. 63%) and hospital mortality (61% vs. 72%). - Increase secondary bacterial infections - NNT = 7 (Annane JAMA 2002)
The evidence…..perhaps don’t give
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
CORTICUS
- 52 ICU’s, 499 patients
- 50mg hydrocortisone QDS vs. placebo 6/7 - 28/7 mortality no different between groups and subset of non- responders
Quicker shock resolution, catecholamine sparing, more secondary infections Sprung et al. NEJM 2008: 358; 111-24
- Etomidate used in 1/5th of patients - Only 35% power to detect a 20% mortality reduction - High variability between laboratories in cortisol assays
Hang on….
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Post hoc analysis of patients in VASST
Review of patients with noradrenaline (293) and steroids and vasopressin (295) and steroids 28 day mortality difference 44.7% versus 35.9% (p=0.03) ? Increased responsiveness to catecholamines ? Increased vasopressin levels ? Decreased inflammation Russell J, et al, Interaction of vasopressin infusion, corticosteroid treatment, and mortality of septic shock, Crit Care Med 2009 Vol. 37, 811-8
VANISH – second arm includes steroids. Eagerly await results
VASST
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
- RCT 778 pts with septic shock
- Noradrenaline vs. Norad & Vaso (0.03 units/min)
- No mortality benefit
- Higher doses associated with ischaemia
“Possible use if other vasopressors failed”
Less severe shock associated with reduced mortality when vasopressin used
Russell et al. NEJM 2008: 358: 877-87
VANISH
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Vasopressin & corticosteroids in Septic Shock. A Pilot Study – Gordon A, 2014 Hydrocortisone - vasopressin sparing - reduced duration vasopressin - reduced dose vasopressin - no effect on vasopressin levels
ABLE• RCT 64 ICUs in Canada & Europe • 2510 patients administered RBC
transfusion up to seven days post ICU-admission & anticipated length of MV of at least 48 hours
• "fresh" RBC's (stored for 8 days or less) compared with standard issue RBCs (stored 2-42 days)
• Primary outcome: – 90 day mortality – 448 patients (37%) vs. 430 patients
(35%) (Absolute Risk Difference 1.7%; 95% CI -2.1-5.5)
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
TITRe2• RCT 17 cardiac ICUs in UK • In adults undergoing cardiac surgery,
does a restrictive transfusion strategy (Hb > 75 g/l) compared to a liberal transfusion strategy (Hb > 90 g/l) lead to fewer infections and ischaemic events within 3 months?
• No difference
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
TRISS• 32 general ICUs in Scandinavia • 998 patients with septic shock & Hb <9 • Transfusion threshold <7 vs. <9 • Excluded patients with ACS • Primary outcome:
– No difference in death at 90 days • Secondary outcomes: No difference in
• Vasoactive drugs • Ventilation • RRT • % of days alive & out of hospital • Ischaemic events
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Acute UGI Bleed• Randomised, parallel group study • 921 pts with severe upper GI bleeding • Compared restrictive (Hb <7g/dL) vs liberal
transfusion strategy (Hb<9g/dL) • Restrictive strategy associated with
– Reduced number of pts receiving transfusion (15% vs 51%)
– Increased probability survival (HR 0.55) – Less rebleeding (10% vs 16%) – Less adverse events (40% vs 48%)
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
PROPPR
• RCT in 12 N. American Level 1 trauma centres • 680 patients • Transfusion of plasma:plts:PRBCs • 1:1:1 vs. 1:1:2 • Primary outcome:
- 24 hour and 30d mortality no different • Secondary outcomes: No difference
Time of haemostasis; Any of 23 pre-defined complications; Hospital, ventilator & ICU free days • Post- hoc analysis:
- Death by exasanguination in 1st 24 hrs much less in 1:1:1 group
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
PROPPR
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
TXACRASH - 2 Lancet 2010
• tranexamic acid in reducing transfusion requirements and death from significant haemorrhage following injury
• 20,000 patients
• Risk of haemorrhage reduced by 0.8% • No reduction in transfusion usage • Only 50% received blood and average only 3 (? ‘significant haemorrhage’)
CRASH - 2 subanalysis Lancet 2011 • Mortality directly related to haemorrhage Tranexamic acid only effective if within first 3 hours. Beyond
this time mortality increases
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
TXACRASH – 2 Does TXA reduce the risk of
intracranial bleeding in patients with TBI? BMJ 2011
• 250 of the 20,000 patients eligible. • Brain haemorrhage growth 5mm vs. 8mm (TXA vs. placebo) • Not SS • No mention of extent of extracranial injuries in either group
making mortality comparisons difficult • Not well matched as there were more pts with SAH (61% vs
43%) • No increase is focal cerebral ischaemia • Conclusion “it is probable that benefits of tranexamic acid
outweigh risks’
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Trauma Haemorrhage
1. Coagulation monitoring and measures to support coagulation should be implemented early
2. Damage control surgery 3. Physiological targets, suggested use & dosing of
fluids, blood products and TXA 4. Patients on antiplatelet agents and/or oral
anticoagulants require special attention 5. Mutlidisciplinary approach & evidence based
protocols adapted to local circumstances need to be developed and implemented
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Fluids• Don’t give too much • Don’t give too little • Make sure you give the right
amount • Starches bad…very bad Association of HES administration with mortality and AKI
in critically ill patients requiring volume resuscitation. Meta-analysis. JAMA 2013 vol 309 (7)
• Albumin back in? SAFE subgroup analysis 1200 pts with severe sepsis - 28/7
mortality lower in albumin group (30% vs. 35% OR 0.87) Finfer S et al 2011 Intensive Care Med 37:86–96 Delayney metaanalysis. Role of albumin as a
resuscitation fluid for patients with sepsis. 17 studies, 1977 patients. Crit Care Med 2011
Albios Study – Gattinoni (video ion ESICM website)
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
“lets talk about fluid responsiveness”
NO!
ESICM statement on colloids
1. Recommend not to use HES with mw ≥ 200kDa in patients with severe sepsis or risk of AKI
2. Suggest avoid 6% HES or gelatin in these groups 3. Recommend not to use colloids in patients with head
injury and not to administer gelatins and HES in orhan donors
4. Suggest avoid hyperoncotic solutions for fluid resuscitation
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
ALBIOS• RCT, 100 ICUs in Italy • Aug 2008 – Feb 2012 • 1818 patients with severe sepsis • 300mls 20% HAS daily to maintain serum albumin at 30g/dl + CSL vs.
CSL • Primary outcome: mortality at 28d
– HAS + CSL: 31.8% – CSL: 32%
• Secondary outcomes: 90 d mortality – No difference
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
6S Study• 804 ICU pts with severe sepsis • Compared fluid resuscitation
– 130/0.4 hydroxyethyl starch (tetraspan) vs Ringer's acetate
• HES associated with – Increased 90 day mortality 51% vs 43% – Increased RRT requirement 22% vs 16% – Trend for increased bleeding 10% vs 6%
-
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
CHEST Study• 7000 ICU pts • Fluid resuscitation with 6% HES
130/0.4 (Voluven) or 0.9% saline • No differences in
– Mortality (HES 18% vs 17%) – LOS – ICU / Hospital
• HES associated with increased – RRT (7% vs 5.8%; RR 1.21) – Pruritus / Rash / Hepatic failure
-
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
CRISTAL Study• 2857 sequential ICU patients 2003-2012 57
ICU’s • Colloids vs CSL for all fluid interventions
other than maintenance • Colloids
– Reduced mortality at 28d & 90d (25% vs 27% & 30% vs 34%) – More days alive without MV – More days alive without vasopressors – Less RRT
-
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Gastrointestinal
Need a nice summary?
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Open Access!#FOAMcc
CALORIES• Open, multicentre, RCT • 2400 patients in 33 ICUs in UK • PN vs. EN within 36 hours for 5/7 • Primary outcome:
– All cause mortality 33.1% (PN) vs. 34% (EN)
• Secondary outcome: – Vomiting more in EN – No difference on other 16 outcomes including
‘serious’ hypoglycaemia
– NB daily calorific targets achieved in <40% in both groups
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
The SuDDICU studySDD
12 meta-analyses of 28 RCT’s. 10 show reduced pneumonia rate; 6 show morality benefit
• Why have clinicians avoided implementing it in UK?
• What are the barriers?
• What further evidence is required before full scale clinical implementation
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
VITdAL-ICU• RCT, Single Centre with 5 ICUs in
Austria, 475 patients • Vit D or placebo • Primary outcome:
– Hospital LOS no different
• Secondary outcome. No difference: – ICU LOS – ICU-, 28d- , hospital- & 6 month- mortality
• Subgroup analysis – If severe vit D def and given Vit D3 -> improvement
in 28d- hospital- and 6 month- mortality
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Systematic review: CCM 2010 In those patients
receiving enteral nutrition, stress ulcer prophylaxis may not be required and may actually increase VAP
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
H2R antagonists vs PPI
• Cohort Study of 35,000 pts
• MV > 24 hours and either H2R antagonist or PPI
• H2R antagonist group had – Less GI haemorrhage 2.1
vs 5.9%
– Pneumonia 27% vs 39%
– C.Diff 2.2% vs 3.8%
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Hepatology
• ALD Alcohol related illness costs NHS £1.7 billion/year
Systematic review of 21 articles
Overall ICU mortality 40-50%
Mackle study only one to provide data on GI haemorrhage - mortality 48%, 62%, 67%,68% for unit, hospital, 6/12 and one yr - if get out of hospital most will survive
Organ support - 3 papers (ventilation, vasoactive drugs, RRT)
Mackle - - if MV and vasoactive drugs hospital mortality 86%
- If MV, vasoactive drugs and RRT > 90%
- If just MV 31%
Saliba RRT 90%
Rye 100% mortality if require RRT
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
STOPAH• RCT, 65 UK Hospitals • 1103 patients with alcoholic hepatitis • Primary outcome: mortality at 28 days was not
statistically different between any individual group – p-value for drug interaction was 0.41
• Prednisolone + placebo: 14.3% • Pentoxifylline + placebo: 19.4% • Prednisolone + pentoxifylline: 13.5% • Placebo: 16.7%
• Secondary outcome. No difference: – ICU LOS – ICU-, 28d- , hospital- & 6 month- mortality
• Subgroup analysis – If severe vit D def and given Vit D3 -> improvement in 28d- hospital-
and 6 month- mortality
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Neuro
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
http://www.wessexics.com/WICS_Guidelines/
The SAH section definitely worth a read for the exam
DESTINY II• RCT 13 hospitals in Germany • MCA infarct with NIHHS > 14 • Decompressive craniotomy vs standard ICU treatment • Primary outcome: score of 0-4 on Modified Rankin Scale
at 6 months • 20/49 in hemicraniectomy group vs. 10/63 in control
group • Bias-corrected, adjusted for the sequential nature of the
trial • 38% vs. 18%, OR 2.91 (95% C.I. 1.06-7.49, P=0.04) • Early hemicraniectomy significantly increased probability
of survival in patients >60 years of age with malignant MCA infarction, but most survivors had substantial disability
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Neuro-ICU
ICP Monitoring• Multicentre RCT of 324
patients Bolivia and Ecuador
• Intraparenchymal ICP monitoring vs. clinical & imaging
• No difference in mortality or neuropsycholoigcal status at 6/12
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
A Trial of Intracranial-Pressure Monitoring in Traumatic Brain Injury Randall M. Chesnut et al N Engl J Med 2012; 367:2471-2481
CATIS• 4,071 patients • Within 48 hrs ischaemic stroke • nonthrombolysed and ↑BP • Hypertension therapy vs no BP Rx • BP control effective • No difference
– death and major disability • 14 days / hospital discharge • 3 months
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
INTERACT 2
• 2,839 pts with early spontaneous intracerebral haemorrhage & ↑SBP
• Compared SBP <140 mmHg vs <180 • Aggressive BP control associated
with – Trend for less adverse events
(p=0.06) – Lower modified Rankin scores
• No difference in mortality
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Magnesium for aneurysmal SAH (MASH-2): a randomised placebo-controlled trial Mees S et al. 2012 The Lancet. Vol 380 9834:44-49
• 8 ICU’s in Europe and S America • 1204 patients • The question: does Mg reduce poor
outcome by reducing vasospasm and delayed cerebral ischaemia (DCI)
• Magnesium 64mmol/day for 20/7 or placebo
• Primary outcome of poor outcomes as defined by score 4-5 on modified Rankin Scale at 3/12, or death
• NO DIFFERENCEAcademic Department of Critical Care
Queen Alexandra Hospital Portsmouth
Delirium
HOPE ICU• 142 patients with delirium • CAM-ICU assessment • Double blinded • Haloperidol vs. placebo • No change in duration of
delirium in critically ill patients • Haloperidol should be reserved
for short term management on acute agitation
Effect of intravenous haloperidol on the duration of delirium and coma in critically ill patients (Hope-ICU): a randomised, double-blind, placebo-controlled trial Valeirie Page. The Lancet Respiratory Medicine, Volume 1, Issue 7, Pages 515 - 523, September 2013
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Treating Delirium
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
101 MV patients RCT haloperidol vs. ziprasidone vs placebo 21/7 study period No difference in any of the groups!
The beginning; Kress NEJM 2000 Reduction in LOS
Girard Lancet 2008 Decreased ICU stay, time on ventilator and mortality
Strom Lancet 2010 Reduction in LOS and ventilator days No sedation group - boluses of morphine, well established in institution, more agitated delerium in no sedation group
Jacob JAMA 2012 PRODEX/MIDEX No better than midaz or propofol at maintaining light to mod sedation and more adverse effects. Increased patient interactions. Less vent days than midazolam
Ryker JAMA 2009 Reduction in ventilator days and delirium
Mehta 2013 For MV patients managed with protocolised sedation, the additon of daily sedation interruption did not reduce duration MV or ICU LOS
The beginning; Kress NEJM 2000 Reduction in LOS
Girard Lancet 2008 Decreased ICU stay, time on ventilator and mortality
Strom Lancet 2010 Reduction in LOS and ventilator days No sedation group - boluses of morphine, well established in institution, more agitated delerium in no sedation group
Jacob JAMA 2012 PRODEX/MIDEX No better than midaz or propofol at maintaining light to mod sedation and more adverse effects. Increased patient interactions. Less vent days than midazolam
Ryker JAMA 2009 Reduction in ventilator days and delirium
Mehta 2013 For MV patients managed with protocolised sedation, the additon of daily sedation interruption did not reduce duration MV or ICU LOS
Don’t forget the simple things….
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
• Small RCT 136 patients • Used NEECHAM score • Delirium (20%) similar
but less mild confusion with ear plugs and good night sleep <50% vs. 25%
Guidelines for managing delirium
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Functional disability 5 years after ARDS
109 survivors from ’98 - ’01 Interview, PFT’s, 6 min walk test, resting & exercise oximetry, chest imaging, QOL survey PFT’s normalish BUT 6 min walk test 76% predicted, physical/psychological problems
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Microbiology
• 96 ICU’s • Data from 60,000 admissions ’09-’11 • Invasive fungal disease defined as BC
or sample from normally sterile site showing yeast/mould cells in a microbiological or histopathological report
• 383 (0.6%) were admitted with or developed IFD
• Conclusion: Incidence of IFD in non-neutropenic,
critically ill patients is low
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
4 steps to keep up with the literature after the exam
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Sign up to criticalcarereviews.com
Check out emlitofnote.com, The Bottom Line & LITFL, ScanCrit & icmcasesummaries
Get a twitter account and follow #FOAMcc & #FOAMed http://www.wessexics.com/Wessex_ICM_Blog/files/5af570b612a8f22d6841f96179a2fc92-16.html
Podcasts – emcrit, RAGE, St.Emlyns, CRIT-IQ, PHARM, JICScast, FOAMcast, Critical Care Practitioner
Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
Best of Luck!
@stevemathieu75
wessexics.com portsmouthicu.com