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Hot 
Topics 
in 
ICM 
Steve 
Mathieu 
Consultant 
in 
Intensive 
Care 
Medicine 
Queen 
Alexandra 
Hospital, 
Portsmouth 
12th 
September 
2014 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
Hot 
Topics/QuesCon 
spoDng 
• Syllabus 
• Examiners 
report 
• Review 
arCcles 
& 
key 
papers 
– 
JICS 
• Guidelines 
• Review 
FICM 
& 
ICS 
websites 
• CriCcal 
Eye 
• Other 
resources 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
Any 
dodgy 
ones?
Examiners 
Report 
April/May 
2014 
hRp://www.ficm.ac.uk/sites/default/files/document-­‐files/EXM-­‐FFICM-­‐Summary-­‐ChairmanReport-­‐April2014_0.pdf
FFICM 
March 
2013 
April 
2014
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
Original 
Ar4cles 
Reviews 
Case 
reports 
CAT 
reviews 
Others 
July 
2014 
Echo 
in 
PE 
Quality 
(pressure 
ulcers) 
DKA 
Acute 
mesenteric 
ischaemia 
Epidural 
abscess 
JW 
GI 
haemorrhage 
Mixed 
OD 
Acromegaly 
StaCn 
& 
VAP 
SEPSISPAM 
ProtecCve 
venClaCon 
in 
abdominal 
surgery 
Heart 
rate 
control 
in 
sepCc 
shock 
Delirium 
April 
2014 
Tracheostomy 
VAP 
Improving 
Cmeliness 
of 
Cme-­‐criCcal 
transfers 
HIT 
HepaCCs 
B 
& 
C 
SedaCon 
Electrical 
muscle 
sCmulaCon 
in 
ICU 
(CIPN) 
HD 
for 
dabigatran 
associated 
coagulopathy 
Wernickes 
PaCent 
with 
tetanus 
TBI 
Hope 
ICU 
(delirium) 
CSL 
or 
HES 
TTM 
Prone 
venClaCon 
Capnography 
Jan 
2014 
COMET-­‐UK 
(CO 
monitoring) 
Tracheostomy 
Right 
heart 
failure 
StabilisaCon 
and 
transport 
of 
criCcally 
ill 
child 
ECG 
and 
trauma 
Rhabdomyolysis 
PancreaCCs 
MDMA 
toxicity 
Hyperthyroidism 
Pulmonary 
haemorrhage 
and 
AKI 
TracMan 
AKI 
Organ 
donaCon 
Surveillance 
for 
VAP 
PE 
supplement 
October 
2013 
Echo 
NAVA 
venClaCon 
Pain 
Brainstem 
tesCng 
Plasma 
exchange 
in 
HUS 
Intralipid 
in 
felodipine 
toxicity 
Tracheostomy 
Transfusion 
strategies 
for 
upper 
GI 
bleed 
Prone 
TXA 
Survey 
on 
rehab 
aeer 
criCcal 
illness 
Echo 
in 
UK 
Blood 
transfusion 
in 
ICU 
BIS 
monitoring 
Faecal 
inconCnence 
in 
ICU 
July 
2013 
Noise 
level 
in 
ICU 
(delirium) 
Serious 
Hazards 
of 
Transfusion 
(SHOT) 
Medical 
support 
for 
heart 
failure 
PCT 
NO 
OTC 
deficiency 
Hyperkalaemia 
in 
HIV 
paCent 
with 
‘PCP’ 
ICP 
monitoring 
SedaCon 
Gentamycin 
& 
vancomycin 
Ancillary 
tests 
in 
diagnosis 
of 
brainstem 
tesCng 
LCP
Guidelines 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
Standards 
-­‐ 
quality 
• Staffing 
– Consultant 
presence 
• 24/7 
& 
within 
30 
minutes 
– Consultant: 
paCent 
1:8 
– 
1:15; 
ICU 
resident/ 
paCent 
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, 
dieCcians 
• Opera4onal 
– Large 
ICUs 
divided 
into 
pods 
of 
8-­‐15 
paCents 
– 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 
paCent 
• Equipment 
– Training 
• Data 
Collec4on 
– ICNARC 
– Risk 
register 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
NCEPOD 
2014: 
Tracheostomy 
• DocumentaCon 
& 
consent 
– IndicaCons, 
type, 
inner 
tube, 
reasons 
for 
failed 
extubaCon/why 
no 
trial 
of 
extubaCon 
• Different 
types 
of 
tubes 
• Rapidly 
available 
difficult 
airway 
trolley 
• Training 
programmes 
in 
blocked/displaced 
tubes 
• Capnography 
• Discharge 
of 
paCents 
with 
tracheostomy 
• MDT 
– 
physio 
& 
SALT 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
Tracheostomy 
standards 
ICS 
• IndicaCons 
for 
tracheostomy 
• CauCons 
and 
contraindicaCons 
• Consent 
• Equipment 
• Ultrasound 
• Anaesthesia 
• Staffing 
• Types 
of 
tracheostomy 
tubes 
• Inner 
cannulae 
• ComplicaCon 
– Early 
– Late 
– Airway 
emergencies
Guidelines 
• Blood 
transfusion 
– ABLE 
MulCcentre 
UK 
RBC 
transfusion 
(7d 
vs. 
15-­‐25d) 
– Transfusion 
triggers 
– 
TRICC 
& 
Villaneuva 
– Guidelines 
on 
the 
management 
of 
anemia 
and 
RBC 
transfusion 
in 
adult 
criCcally 
ill 
paCents 
h"p://www.bcshguidelines.com/documents/BCSH_Cri;cal_Care_Guidelines_Final_Version_22_10_12.pdf 
– Serious 
Hazards 
of 
Transfusion 
(SHOT) 
– 
JICS 
July 
2013 
• CalculaCon 
of 
Cerebral 
Perfusion 
Pressure 
• AF 
management 
– 
NICE 
& 
JICS 
• Clinical 
Guidelines 
on 
management 
of 
pain, 
agitaCon 
and 
delirium 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth 
• Transfusion 
Triggers 
• Blood 
conservaCon 
• Pre-­‐transfusion 
clinical 
assessment 
• Rate 
of 
transfusion/fluid 
balance 
• InvesCgaCon 
adverse 
events 
• Storage 
duraCon
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth 
CCM 
2013
Some 
guidelines 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
ConsultaCons 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
CriCcal 
Eye 
No 
6: 
Core 
standards 
Examiners 
report 
No 
5: 
FICM 
ConsultaCons: 
IV 
fluids 
(NICE 
– 
IV 
therapy 
in 
adults 
in 
hospital 
Dec 
2013) 
Head 
injury 
& 
specialist 
centres 
Quality 
– 
quality 
indicators? 
No 
4: 
1st 
Examiners 
report 
– 
March 
2013
The 
key 
papers 
in 
CriCcal 
Care 
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 
" unanCcipated 
ICU 
admission 
" ProlongaCon 
ICU 
stay 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
Summary 
of 
NAP 
4 
" 25% 
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
RecommendaCons 
" Capnography 
" Airway 
equipment 
" Back 
up 
planning 
" Staffing 
" PaCent 
transfers 
" EducaCon/training 
" Tracheostomy 
tube 
design 
" Team 
working 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
TracMan 
• 909 
intubated 
paCents 
• Respiratory 
failure 
– < 
4 
days 
– Predicted 
to 
need 
MV 
for 
further 
7 
days 
• Tracheostomy 
Cming 
• Early 
(≤ 
4 
days) 
vs 
late 
(aeer 
10 
days) 
• No 
difference 
in 
– 30/7Mortality; 
ICU 
LOS; 
ComplicaCons 
• Only 
45% 
late 
group 
received 
Academic Department of Critical Care 
trache 
Queen Alexandra Hospital Portsmouth
OSCAR 
• 795 
paCents 
with 
moderate 
-­‐ 
severe 
ARDS 
(<26.7kPa 
/ 
200mmHg) 
• CMV 
vs. 
HFOV 
(MV 
<7 
days) 
• No 
difference 
in 
– 30/7 
mortality 
(41%) 
– DuraCon 
anCmicrobial 
agents 
(2/3 
chest 
sepsis) 
– VasoacCve 
support 
duraCon 
– ICU 
LOS 
– Hospital 
LOS 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
OSCILLATE 
• 548 
paCents 
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 
sedaCon 
– More 
NMBA’s 
– More 
vasopressors 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth 
OSCAR 
OSCILLATE 
29 
ICU’s 
UK 
39 
ICU’s 
5 
countries 
795 
paCents 
548 
paCents 
(planned 
1200) 
PaO2:FiO2 
< 
200mmHg 
Bilateral 
pulmonary 
infiltrates 
MV 
for 
LESS 
than 
7 
consecuCve 
days 
at 
the 
point 
of 
randomisaCon 
PaO2:FiO2 
< 
200mmHg 
FiO2 
> 
0.5 
Bilateral 
pulmonary 
infiltrates 
MV 
for 
LESS 
than 
3 
consecuCve 
days 
at 
the 
point 
of 
randomisaCon 
Encouraged 
to 
use 
PC 
6-­‐8mls/kg 
and 
use 
ARDS 
protocol 
for 
FiO2 
& 
PEEP 
R 
100 
venClator 
PEEP 
11 
CV 
– 
PC 
6mls/kg, 
3100 
B 
venClator 
Recruitment 
maneuvers 
before 
HFOV 
Protocol 
specified 
high 
PEEP 
for 
CV 
(PEEP 
13) 
30d 
mortality 
42% 
vs. 
41% 
(HFOV 
vs. 
CV) 
30d 
mortality 
40% 
vs. 
29% 
Hospital 
mortality 
47% 
vs. 
35% 
(HFOV 
vs. 
CV) 
More 
NMBA’s 
More 
midazolam, 
vasoacCve 
drugs, 
NMBA’s 
in 
HFOV 
Lower 
PEEP 
strategy 
? 
recruitment 
maneuvers 
of 
lung 
before 
HFOV 
injurious 
Mortality 
41% 
in 
control 
group 
Mortality 
35% 
in 
control 
group
PROSEVA 
• 466 
paCents 
with 
severe 
ARDS 
• Prone 
posiCon 
vs 
supine 
posiCon 
• Prone 
posiCon 
was 
associated 
with 
– Improved 
mortality 
• 28 
day: 
16% 
vs 
33% 
• 90 
day: 
24% 
vs 
41% 
– Less 
cardiac 
arrests 
– No 
difference 
in 
complicaCons 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
PROSEVA 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
ARDS 
-­‐ 
lots 
of 
trials 
" HFOV 
" Nitric 
Oxide 
" Surfactant 
" Perflourocarbon 
" 
" Late 
steroids 
(LaSRS)" 
" Prostaglandin 
E1 
" 
" Lysophylline 
(LARMA)" 
" Ketoconazole 
(KARMA) 
" Streptokinase 
" StaCns 
(HARP 
2, 
SAILS) 
" 
" Neutrophil 
elastase 
inhibitor 
" 
" ImmunonutriCon 
(Eden-­‐ 
Omega)" 
" rhAPC 
" 
" Albuterol/salmeterol 
(BALTI 
I 
& 
II, 
ALTA) 
" 
" Lower 
Vt 
! 
" ? 
Furosemide 
(FACTT) 
! 
" Cisatricurium 
" Prone 
‘back’ 
in 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
BALTI 
-­‐ 
2012 
• 162 
paCents; 
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
StaCns 
in 
ARDS 
• MulCcentre, 
RCT 
• RosuvastaCn 
vs. 
placebo 
in 
ARDS 
• StaCn 
may 
modulate 
inflammatory 
response 
• 745 
paCents 
(trial 
stopped 
early 
because 
of 
fuClity) 
• Primary 
outcome: 
• 60d 
mortality: 
28.5% 
vs. 
24.9% 
(staCn 
vs. 
placebo) 
• VenClator 
free 
days: 
15.1 
vs. 
15.1 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
StaCn 
& 
VAP 
• 300 
paCents 
with 
suspected 
VAP 
(CPIS 
≥ 
5) 
• SimvastaCn 
60mg 
vs 
placebo 
• No 
difference 
in 
– 28d 
survival 
– ICU 
or 
hospital 
mortality 
– DuraCon 
MV 
– Delta 
SOFA 
• Increased 
mortality 
in 
staCn 
naieve 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
Magnesium 
in 
asthma 
• 1200 
paCents 
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
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth 
• Meta-­‐analysis 
• 16 
trials 
inc 
PEITHO, 
MAPPETT, 
MOPETT, 
TOPCOT 
• Thrombolysis 
+ 
anCcoagulaCon 
vs. 
anCcoagulaCon 
alone 
• All 
cause 
mortality 
less 
in 
thrombolysis 
group 
but 
major 
bleeding 
& 
ICH 
higher
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 
func4on 
at 
180 
days 
33°C 
(54%) 
with 
36°C 
(52%) 
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 
paCents 
• Cooling 
effecCve 
(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 
paCents 
with 
cardiogenic 
shock 
secondary 
to 
AMI 
• IABP 
vs 
no 
IABP 
• All 
received 
early 
revascularisaCon 
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 
reinfarcCon 
rate 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
VSE 
in 
cardiac 
arrest 
• 268 
paCents 
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 
dysfuncCon 
Aca•d eamndic 
Department of Critical Care 
Queen Alexandra Hospital Portsmouth
SEPSIS
Ferrer: 
Empiric 
anCbioCcs 
in 
sepsis 
• RetrospecCve 
observaConal 
cohort 
study 
• 165 
ICUs 
– 
Europe, 
US 
& 
S 
America 
• Jan 
2005-­‐ 
Feb 
2010 
• 18,000 
paCents 
with 
sepCc 
shock 
• Delay 
in 
anCbioCcs 
administraCon 
over 
first 
6 
hours 
aeer 
idenCficaCon 
of 
SS 
or 
sepCc 
shock 
-­‐> 
increased 
mortality 
• < 
1 
hr 
24.6%; 
1-­‐2h 
25.9% 
> 
6h 
33% 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
SEPSISPAM 
• RCT, 
mulCcentre, 
29 
French 
ICUs 
• March 
2010 
– 
Dec 
2011 
• SepCc 
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 
creaCnine 
and 
need 
for 
RRT 
was 
lower 
in 
higher 
MAP 
group 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
OPTIMISE 
• RCT, 
mulCcentre, 
17 
UK 
ICUs 
• 734 
paCents 
• > 
50y 
undergoing 
GI 
surgery 
with 
one 
or 
more 
‘high 
risk’ 
risk 
factors 
• Algorithm-­‐directed 
care 
dictaCng 
colloid 
and 
dopexamine 
administraCon 
using 
vs. 
clinician 
directed 
care 
without 
use 
of 
CO 
monitoring 
• Primary 
outcome: 
composite 
of 
30d 
mortality 
and 
mod/major 
complicaCons 
– IntervenCon: 
36.6% 
– Control 
arm: 
43.4% 
• No 
SS 
difference 
in 
secondary 
outcomes 
– POMS, 
infecCous 
complicaCons, 
criCcal 
care 
free 
days 
at 
30d, 
mortality 
at 
30d 
and 
180d, 
hospital 
LOS 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
PROWESS 
SHOCK 
• Randomised, 
controlled, 
mulCcentre, 
parallel 
group 
study 
• 1,697 
paCents 
with 
sepCc 
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
VANISH 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth 
Vasopressin 
& 
corCcosteroids 
in 
SepCc 
Shock. 
A 
Pilot 
Study 
– 
Gordon 
A, 
2014 
HydrocorCsone 
-­‐ 
vasopressin 
sparing 
-­‐ 
reduced 
duraCon 
vasopressin 
-­‐ 
reduced 
dose 
vasopressin 
-­‐ 
no 
effect 
on 
vasopressin 
levels
B 
blockers 
in 
sepCc 
shock 
• Open 
label, 
single 
unit 
• SepCc 
shock 
+ 
HR 
≥ 
95 
+ 
NADR 
• 77 
paCents 
– 
esmolol 
infusion 
(HR 
80-­‐94) 
vs 
77 
paCents 
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
CirculaCon 
Sepsis 
& 
EGDT 
ProMISe 
– 
UK 
– 
soon… 
ARISE 
– 
Australia 
– 
ESICM 
2014 
ProCESS 
– 
US 
-­‐ 
complete 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
ProCESS 
• RCT 
31 
ICUs 
in 
US 
• 03/2008 
– 
05/2013 
• 1351 
paCents 
with 
sepCc 
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
IVOIRE 
Study 
• Randomised, 
open 
study 
• 18 
ICU’s 
in 
France, 
Belgium 
and 
Netherlands 
2005-­‐2010 
• 140 
pts 
with 
sepCc 
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
Fluids 
• Don’t 
give 
too 
much 
• Don’t 
give 
too 
liRle 
• Make 
sure 
you 
give 
the 
right 
amount 
• Starches 
bad…very 
bad 
AssociaCon 
of 
HES 
administraCon 
with 
mortality 
and 
AKI 
in 
criCcally 
ill 
paCents 
requiring 
volume 
resuscitaCon. 
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 
resuscita;on 
fluid 
for 
pa;ents 
with 
sepsis. 
17 
studies, 
1977 
pa;ents. 
Crit 
Care 
Med 
2011 
Albios 
Study 
– 
GaXnoni 
(video 
ion 
ESICM 
website) 
“lets 
talk 
about 
fluid 
responsiveness” 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
ALBIOS 
• RCT, 
100 
ICUs 
in 
Italy 
• Aug 
2008 
– 
Feb 
2012 
• 1818 
paCents 
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
6S 
Study 
• 804 
ICU 
pts 
with 
severe 
sepsis 
• Compared 
fluid 
resuscitaCon 
– 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 
resuscitaCon 
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 
/ 
HepaCc 
failure 
-­‐ 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
CRISTAL 
Study 
• 2857 
sequenCal 
ICU 
paCents 
2003-­‐2012 
57 
ICU’s 
• Colloids 
vs 
CSL 
for 
all 
fluid 
intervenCons 
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
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
ESICM 
statement 
on 
colloids 
1. 
Recommend 
not 
to 
use 
HES 
with 
mw 
≥ 
200kDa 
in 
paCents 
with 
severe 
sepsis 
or 
risk 
of 
AKI 
2. 
Suggest 
avoid 
6% 
HES 
or 
gelaCn 
in 
these 
groups 
3. 
Recommend 
not 
to 
use 
colloids 
in 
paCents 
with 
head 
injury 
and 
not 
to 
administer 
gelaCns 
and 
HES 
in 
orhan 
donors 
4. 
Suggest 
avoid 
hyperoncoCc 
soluCons 
for 
fluid 
resuscitaCon 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
Passive 
Leg 
Raise
TRAUMA
TXA 
" CRASH 
-­‐ 
2 
Lancet 
2010 
• tranexamic 
acid 
in 
reducing 
transfusion 
requirements 
and 
death 
from 
significant 
haemorrhage 
following 
injury 
• 20,000 
paCents 
• Risk 
of 
haemorrhage 
reduced 
by 
0.8% 
• No 
reducCon 
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 
effecCve 
if 
within 
first 
3 
hours. 
Beyond 
this 
Cme 
mortality 
increases 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
TXA 
" CRASH 
– 
2 
Does 
TXA 
reduce 
the 
risk 
of 
intracranial 
bleeding 
in 
pa4ents 
with 
TBI? 
BMJ 
2011 
• 250 
of 
the 
20,000 
paCents 
eligible. 
• Brain 
haemorrhage 
growth 
5mm 
vs. 
8mm 
(TXA 
vs. 
placebo) 
• Not 
SS 
• No 
menCon 
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. 
CoagulaCon 
monitoring 
and 
measures 
to 
support 
coagulaCon 
should 
be 
implemented 
early 
2. 
Damage 
control 
surgery 
3. 
Physiological 
targets, 
suggested 
use 
& 
dosing 
of 
fluids, 
blood 
products 
and 
TXA 
4. 
PaCents 
on 
anCplatelet 
agents 
and/or 
oral 
anCcoagulants 
require 
special 
aRenCon 
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
Neuro-­‐ICU 
ICP 
Monitoring 
• MulCcentre 
RCT 
of 
324 
paCents 
Bolivia 
and 
Ecuador 
• Intraparenchymal 
ICP 
monitoring 
vs. 
clinical 
& 
imaging 
• No 
difference 
in 
mortality 
or 
neuropsycholoigcal 
status 
at 
6/12 
A 
Trial 
of 
Intracranial-­‐Pressure 
Monitoring 
in 
TraumaCc 
Brain 
Injury 
Randall 
M. 
Chesnut 
et 
al 
N 
Engl 
J 
Med 
2012; 
367:2471-­‐2481 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
Neuro
CATIS 
• 4,071 
paCents 
• Within 
48 
hrs 
ischaemic 
stroke 
• nonthrombolysed 
and 
↑BP 
• Hypertension 
therapy 
vs 
no 
BP 
Rx 
• BP 
control 
effecCve 
• 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 
paCents 
• The 
quesCon: 
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 
DIFFERENCE 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
Delirium 
HOPE 
ICU 
• 142 
paCents 
with 
delirium 
• CAM-­‐ICU 
assessment 
• Double 
blinded 
• Haloperidol 
vs. 
placebo 
• No 
change 
in 
duraCon 
of 
delirium 
in 
criCcally 
ill 
paCents 
• Haloperidol 
should 
be 
reserved 
for 
short 
term 
management 
on 
acute 
agitaCon 
Effect 
of 
intravenous 
haloperidol 
on 
the 
dura4on 
of 
delirium 
and 
coma 
in 
cri4cally 
ill 
pa4ents 
(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
TreaCng 
delerium 
101 
MV 
pa4ents 
RCT 
haloperidol 
vs. 
ziprasidone 
vs 
placebo 
21/7 
study 
period 
No 
difference 
in 
any 
of 
the 
groups!
The 
beginning; 
Kress 
NEJM 
2000 
ReducCon 
in 
LOS 
Girard 
Lancet 
2008 
Decreased 
ICU 
stay, 
Cme 
on 
venClator 
and 
mortality 
Strom 
Lancet 
2010 
ReducCon 
in 
LOS 
and 
venClator 
days 
No 
sedaCon 
group 
-­‐ 
boluses 
of 
morphine, 
well 
established 
in 
insCtuCon, 
more 
agitated 
delerium 
in 
no 
sedaCon 
group 
Ryker 
JAMA 
2009 
ReducCon 
in 
venClator 
days 
and 
delirium 
Jacob 
JAMA 
2012 
PRODEX/MIDEX 
No 
beRer 
than 
midaz 
or 
propofol 
at 
maintaining 
light 
to 
mod 
sedaCon 
and 
more 
adverse 
effects. 
Increased 
paCent 
interacCons. 
Less 
vent 
days 
than 
midazolam 
Mehta 
2013 
For 
MV 
paCents 
managed 
with 
protocolised 
sedaCon, 
the 
additon 
of 
daily 
sedaCon 
interrupCon 
did 
not 
reduce 
duraCon 
MV 
or 
ICU 
LOS
The 
beginning; 
Kress 
NEJM 
2000 
ReducCon 
in 
LOS 
Girard 
Lancet 
2008 
Decreased 
ICU 
stay, 
Cme 
on 
venClator 
and 
mortality 
Strom 
Lancet 
2010 
ReducCon 
in 
LOS 
and 
venClator 
days 
No 
sedaCon 
group 
-­‐ 
boluses 
of 
morphine, 
well 
established 
in 
insCtuCon, 
more 
agitated 
delerium 
in 
no 
sedaCon 
group 
Ryker 
JAMA 
2009 
ReducCon 
in 
venClator 
days 
and 
delirium 
Jacob 
JAMA 
2012 
PRODEX/MIDEX 
No 
beRer 
than 
midaz 
or 
propofol 
at 
maintaining 
light 
to 
mod 
sedaCon 
and 
more 
adverse 
effects. 
Increased 
paCent 
interacCons. 
Less 
vent 
days 
than 
midazolam 
Mehta 
2013 
For 
MV 
paCents 
managed 
with 
protocolised 
sedaCon, 
the 
additon 
of 
daily 
sedaCon 
interrupCon 
did 
not 
reduce 
duraCon 
MV 
or 
ICU 
LOS
Don’t 
forget 
the 
simple 
things…. 
• Small 
RCT 
136 
paCents 
• 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
GastrointesCnal
Acute 
UGI 
Bleed 
• Randomised, 
parallel 
group 
study 
• 921 
pts 
with 
severe 
upper 
GI 
bleeding 
• Compared 
restricCve 
(Hb 
<7g/dL) 
vs 
liberal 
transfusion 
strategy 
(Hb<9g/dL) 
• RestricCve 
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
GastrointensCnal
The 
SuDDICU 
study 
SDD 
12 
meta-­‐analyses 
of 
28 
RCT’s. 
10 
show 
reduced 
pneumonia 
rate; 
6 
show 
morality 
benefit 
• Why 
have 
clinicians 
avoided 
implemenCng 
it 
in 
UK? 
• What 
are 
the 
barriers? 
• What 
further 
evidence 
is 
required 
before 
full 
scale 
clinical 
implementaCon 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
SystemaCc 
review: 
CCM 
2010 
• Those 
paCents 
receiving 
enteral 
nutriCon, 
stress 
ulcer 
prophylaxis 
may 
not 
be 
required 
and 
may 
actually 
increase 
VAP
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 
" SystemaCc 
review 
of 
21 
arCcles 
" 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 
(venClaCon, 
vasoacCve 
drugs, 
RRT) 
" Mackle 
-­‐ 
-­‐ if 
MV 
and 
vasoacCve 
drugs 
hospital 
mortality 
86% 
-­‐ If 
MV, 
vasoacCve 
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
Intraabdominal 
pressures
FuncConal 
disability 
5 
years 
aeer 
ARDS 
" 109 
survivors 
from 
’98 
-­‐ 
’01 
" Interview, 
PFT’s, 
6 
min 
walk 
test, 
resCng 
& 
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
Some 
guidelines 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth
Suggested 
resources 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth 
• JICS 
• Sign 
up 
to 
criCcalcarereviews.com 
• Podcasts 
• LITFL 
• FFICM 
& 
ICS
Best 
of 
Luck! 
Academic Department of Critical Care 
Queen Alexandra Hospital Portsmouth 
www.wessexics.com 
@WessexICS 
@WICSBoRomLine 
@stevemathieu75

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Pincer 12th sept2014 1

  • 1. Hot Topics in ICM Steve Mathieu Consultant in Intensive Care Medicine Queen Alexandra Hospital, Portsmouth 12th September 2014 Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 2. Hot Topics/QuesCon spoDng • Syllabus • Examiners report • Review arCcles & key papers – JICS • Guidelines • Review FICM & ICS websites • CriCcal Eye • Other resources Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 4. Examiners Report April/May 2014 hRp://www.ficm.ac.uk/sites/default/files/document-­‐files/EXM-­‐FFICM-­‐Summary-­‐ChairmanReport-­‐April2014_0.pdf
  • 5. FFICM March 2013 April 2014
  • 6. Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 7. Original Ar4cles Reviews Case reports CAT reviews Others July 2014 Echo in PE Quality (pressure ulcers) DKA Acute mesenteric ischaemia Epidural abscess JW GI haemorrhage Mixed OD Acromegaly StaCn & VAP SEPSISPAM ProtecCve venClaCon in abdominal surgery Heart rate control in sepCc shock Delirium April 2014 Tracheostomy VAP Improving Cmeliness of Cme-­‐criCcal transfers HIT HepaCCs B & C SedaCon Electrical muscle sCmulaCon in ICU (CIPN) HD for dabigatran associated coagulopathy Wernickes PaCent with tetanus TBI Hope ICU (delirium) CSL or HES TTM Prone venClaCon Capnography Jan 2014 COMET-­‐UK (CO monitoring) Tracheostomy Right heart failure StabilisaCon and transport of criCcally ill child ECG and trauma Rhabdomyolysis PancreaCCs MDMA toxicity Hyperthyroidism Pulmonary haemorrhage and AKI TracMan AKI Organ donaCon Surveillance for VAP PE supplement October 2013 Echo NAVA venClaCon Pain Brainstem tesCng Plasma exchange in HUS Intralipid in felodipine toxicity Tracheostomy Transfusion strategies for upper GI bleed Prone TXA Survey on rehab aeer criCcal illness Echo in UK Blood transfusion in ICU BIS monitoring Faecal inconCnence in ICU July 2013 Noise level in ICU (delirium) Serious Hazards of Transfusion (SHOT) Medical support for heart failure PCT NO OTC deficiency Hyperkalaemia in HIV paCent with ‘PCP’ ICP monitoring SedaCon Gentamycin & vancomycin Ancillary tests in diagnosis of brainstem tesCng LCP
  • 8. Guidelines Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 9. Standards -­‐ quality • Staffing – Consultant presence • 24/7 & within 30 minutes – Consultant: paCent 1:8 – 1:15; ICU resident/ paCent 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, dieCcians • Opera4onal – Large ICUs divided into pods of 8-­‐15 paCents – 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 paCent • Equipment – Training • Data Collec4on – ICNARC – Risk register Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 10. NCEPOD 2014: Tracheostomy • DocumentaCon & consent – IndicaCons, type, inner tube, reasons for failed extubaCon/why no trial of extubaCon • Different types of tubes • Rapidly available difficult airway trolley • Training programmes in blocked/displaced tubes • Capnography • Discharge of paCents with tracheostomy • MDT – physio & SALT Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 11. Tracheostomy standards ICS • IndicaCons for tracheostomy • CauCons and contraindicaCons • Consent • Equipment • Ultrasound • Anaesthesia • Staffing • Types of tracheostomy tubes • Inner cannulae • ComplicaCon – Early – Late – Airway emergencies
  • 12. Guidelines • Blood transfusion – ABLE MulCcentre UK RBC transfusion (7d vs. 15-­‐25d) – Transfusion triggers – TRICC & Villaneuva – Guidelines on the management of anemia and RBC transfusion in adult criCcally ill paCents h"p://www.bcshguidelines.com/documents/BCSH_Cri;cal_Care_Guidelines_Final_Version_22_10_12.pdf – Serious Hazards of Transfusion (SHOT) – JICS July 2013 • CalculaCon of Cerebral Perfusion Pressure • AF management – NICE & JICS • Clinical Guidelines on management of pain, agitaCon and delirium Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 13. Academic Department of Critical Care Queen Alexandra Hospital Portsmouth • Transfusion Triggers • Blood conservaCon • Pre-­‐transfusion clinical assessment • Rate of transfusion/fluid balance • InvesCgaCon adverse events • Storage duraCon
  • 14. Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 15. Academic Department of Critical Care Queen Alexandra Hospital Portsmouth CCM 2013
  • 16. Some guidelines Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 17. ConsultaCons Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 18. CriCcal Eye No 6: Core standards Examiners report No 5: FICM ConsultaCons: IV fluids (NICE – IV therapy in adults in hospital Dec 2013) Head injury & specialist centres Quality – quality indicators? No 4: 1st Examiners report – March 2013
  • 19. The key papers in CriCcal Care Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 20. 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 " unanCcipated ICU admission " ProlongaCon ICU stay Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 21. Summary of NAP 4 " 25% 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
  • 22. RecommendaCons " Capnography " Airway equipment " Back up planning " Staffing " PaCent transfers " EducaCon/training " Tracheostomy tube design " Team working Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 23. TracMan • 909 intubated paCents • Respiratory failure – < 4 days – Predicted to need MV for further 7 days • Tracheostomy Cming • Early (≤ 4 days) vs late (aeer 10 days) • No difference in – 30/7Mortality; ICU LOS; ComplicaCons • Only 45% late group received Academic Department of Critical Care trache Queen Alexandra Hospital Portsmouth
  • 24. OSCAR • 795 paCents with moderate -­‐ severe ARDS (<26.7kPa / 200mmHg) • CMV vs. HFOV (MV <7 days) • No difference in – 30/7 mortality (41%) – DuraCon anCmicrobial agents (2/3 chest sepsis) – VasoacCve support duraCon – ICU LOS – Hospital LOS Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 25. OSCILLATE • 548 paCents 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 sedaCon – More NMBA’s – More vasopressors Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 26. Academic Department of Critical Care Queen Alexandra Hospital Portsmouth OSCAR OSCILLATE 29 ICU’s UK 39 ICU’s 5 countries 795 paCents 548 paCents (planned 1200) PaO2:FiO2 < 200mmHg Bilateral pulmonary infiltrates MV for LESS than 7 consecuCve days at the point of randomisaCon PaO2:FiO2 < 200mmHg FiO2 > 0.5 Bilateral pulmonary infiltrates MV for LESS than 3 consecuCve days at the point of randomisaCon Encouraged to use PC 6-­‐8mls/kg and use ARDS protocol for FiO2 & PEEP R 100 venClator PEEP 11 CV – PC 6mls/kg, 3100 B venClator Recruitment maneuvers before HFOV Protocol specified high PEEP for CV (PEEP 13) 30d mortality 42% vs. 41% (HFOV vs. CV) 30d mortality 40% vs. 29% Hospital mortality 47% vs. 35% (HFOV vs. CV) More NMBA’s More midazolam, vasoacCve drugs, NMBA’s in HFOV Lower PEEP strategy ? recruitment maneuvers of lung before HFOV injurious Mortality 41% in control group Mortality 35% in control group
  • 27. PROSEVA • 466 paCents with severe ARDS • Prone posiCon vs supine posiCon • Prone posiCon was associated with – Improved mortality • 28 day: 16% vs 33% • 90 day: 24% vs 41% – Less cardiac arrests – No difference in complicaCons Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 28. PROSEVA Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 29. ARDS -­‐ lots of trials " HFOV " Nitric Oxide " Surfactant " Perflourocarbon " " Late steroids (LaSRS)" " Prostaglandin E1 " " Lysophylline (LARMA)" " Ketoconazole (KARMA) " Streptokinase " StaCns (HARP 2, SAILS) " " Neutrophil elastase inhibitor " " ImmunonutriCon (Eden-­‐ Omega)" " rhAPC " " Albuterol/salmeterol (BALTI I & II, ALTA) " " Lower Vt ! " ? Furosemide (FACTT) ! " Cisatricurium " Prone ‘back’ in Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 30. BALTI -­‐ 2012 • 162 paCents; 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
  • 31. StaCns in ARDS • MulCcentre, RCT • RosuvastaCn vs. placebo in ARDS • StaCn may modulate inflammatory response • 745 paCents (trial stopped early because of fuClity) • Primary outcome: • 60d mortality: 28.5% vs. 24.9% (staCn vs. placebo) • VenClator free days: 15.1 vs. 15.1 Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 32. StaCn & VAP • 300 paCents with suspected VAP (CPIS ≥ 5) • SimvastaCn 60mg vs placebo • No difference in – 28d survival – ICU or hospital mortality – DuraCon MV – Delta SOFA • Increased mortality in staCn naieve Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 33. Magnesium in asthma • 1200 paCents 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
  • 34. Academic Department of Critical Care Queen Alexandra Hospital Portsmouth • Meta-­‐analysis • 16 trials inc PEITHO, MAPPETT, MOPETT, TOPCOT • Thrombolysis + anCcoagulaCon vs. anCcoagulaCon alone • All cause mortality less in thrombolysis group but major bleeding & ICH higher
  • 35. 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 func4on at 180 days 33°C (54%) with 36°C (52%) Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 36. Pre-­‐hospital hypothermia • Prehospital cooling vs. standard care • 2L of cold normal saline once ROSC • 1,359 OOHCA paCents • Cooling effecCve (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
  • 37. IABP – SHOCK II • 600 paCents with cardiogenic shock secondary to AMI • IABP vs no IABP • All received early revascularisaCon 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 reinfarcCon rate Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 38. VSE in cardiac arrest • 268 paCents 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 dysfuncCon Aca•d eamndic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 40. Ferrer: Empiric anCbioCcs in sepsis • RetrospecCve observaConal cohort study • 165 ICUs – Europe, US & S America • Jan 2005-­‐ Feb 2010 • 18,000 paCents with sepCc shock • Delay in anCbioCcs administraCon over first 6 hours aeer idenCficaCon of SS or sepCc shock -­‐> increased mortality • < 1 hr 24.6%; 1-­‐2h 25.9% > 6h 33% Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 41. SEPSISPAM • RCT, mulCcentre, 29 French ICUs • March 2010 – Dec 2011 • SepCc 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 creaCnine and need for RRT was lower in higher MAP group Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 42. OPTIMISE • RCT, mulCcentre, 17 UK ICUs • 734 paCents • > 50y undergoing GI surgery with one or more ‘high risk’ risk factors • Algorithm-­‐directed care dictaCng colloid and dopexamine administraCon using vs. clinician directed care without use of CO monitoring • Primary outcome: composite of 30d mortality and mod/major complicaCons – IntervenCon: 36.6% – Control arm: 43.4% • No SS difference in secondary outcomes – POMS, infecCous complicaCons, criCcal care free days at 30d, mortality at 30d and 180d, hospital LOS Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 43. PROWESS SHOCK • Randomised, controlled, mulCcentre, parallel group study • 1,697 paCents with sepCc 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
  • 44. VANISH Academic Department of Critical Care Queen Alexandra Hospital Portsmouth Vasopressin & corCcosteroids in SepCc Shock. A Pilot Study – Gordon A, 2014 HydrocorCsone -­‐ vasopressin sparing -­‐ reduced duraCon vasopressin -­‐ reduced dose vasopressin -­‐ no effect on vasopressin levels
  • 45. B blockers in sepCc shock • Open label, single unit • SepCc shock + HR ≥ 95 + NADR • 77 paCents – esmolol infusion (HR 80-­‐94) vs 77 paCents 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
  • 46. CirculaCon Sepsis & EGDT ProMISe – UK – soon… ARISE – Australia – ESICM 2014 ProCESS – US -­‐ complete Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 47. ProCESS • RCT 31 ICUs in US • 03/2008 – 05/2013 • 1351 paCents with sepCc 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
  • 48. IVOIRE Study • Randomised, open study • 18 ICU’s in France, Belgium and Netherlands 2005-­‐2010 • 140 pts with sepCc 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
  • 49. Fluids • Don’t give too much • Don’t give too liRle • Make sure you give the right amount • Starches bad…very bad AssociaCon of HES administraCon with mortality and AKI in criCcally ill paCents requiring volume resuscitaCon. 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 resuscita;on fluid for pa;ents with sepsis. 17 studies, 1977 pa;ents. Crit Care Med 2011 Albios Study – GaXnoni (video ion ESICM website) “lets talk about fluid responsiveness” Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 50. ALBIOS • RCT, 100 ICUs in Italy • Aug 2008 – Feb 2012 • 1818 paCents 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
  • 51. 6S Study • 804 ICU pts with severe sepsis • Compared fluid resuscitaCon – 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
  • 52. CHEST Study • 7000 ICU pts • Fluid resuscitaCon 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 / HepaCc failure -­‐ Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 53. CRISTAL Study • 2857 sequenCal ICU paCents 2003-­‐2012 57 ICU’s • Colloids vs CSL for all fluid intervenCons 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
  • 54. Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 55. ESICM statement on colloids 1. Recommend not to use HES with mw ≥ 200kDa in paCents with severe sepsis or risk of AKI 2. Suggest avoid 6% HES or gelaCn in these groups 3. Recommend not to use colloids in paCents with head injury and not to administer gelaCns and HES in orhan donors 4. Suggest avoid hyperoncoCc soluCons for fluid resuscitaCon Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 58. TXA " CRASH -­‐ 2 Lancet 2010 • tranexamic acid in reducing transfusion requirements and death from significant haemorrhage following injury • 20,000 paCents • Risk of haemorrhage reduced by 0.8% • No reducCon 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 effecCve if within first 3 hours. Beyond this Cme mortality increases Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 59. TXA " CRASH – 2 Does TXA reduce the risk of intracranial bleeding in pa4ents with TBI? BMJ 2011 • 250 of the 20,000 paCents eligible. • Brain haemorrhage growth 5mm vs. 8mm (TXA vs. placebo) • Not SS • No menCon 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
  • 60. Trauma Haemorrhage 1. CoagulaCon monitoring and measures to support coagulaCon should be implemented early 2. Damage control surgery 3. Physiological targets, suggested use & dosing of fluids, blood products and TXA 4. PaCents on anCplatelet agents and/or oral anCcoagulants require special aRenCon 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
  • 61. Neuro-­‐ICU ICP Monitoring • MulCcentre RCT of 324 paCents Bolivia and Ecuador • Intraparenchymal ICP monitoring vs. clinical & imaging • No difference in mortality or neuropsycholoigcal status at 6/12 A Trial of Intracranial-­‐Pressure Monitoring in TraumaCc Brain Injury Randall M. Chesnut et al N Engl J Med 2012; 367:2471-­‐2481 Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 62. Neuro
  • 63. CATIS • 4,071 paCents • Within 48 hrs ischaemic stroke • nonthrombolysed and ↑BP • Hypertension therapy vs no BP Rx • BP control effecCve • No difference – death and major disability • 14 days / hospital discharge • 3 months Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 64. 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
  • 65. 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 paCents • The quesCon: 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 DIFFERENCE Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 66. Delirium HOPE ICU • 142 paCents with delirium • CAM-­‐ICU assessment • Double blinded • Haloperidol vs. placebo • No change in duraCon of delirium in criCcally ill paCents • Haloperidol should be reserved for short term management on acute agitaCon Effect of intravenous haloperidol on the dura4on of delirium and coma in cri4cally ill pa4ents (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
  • 67. TreaCng delerium 101 MV pa4ents RCT haloperidol vs. ziprasidone vs placebo 21/7 study period No difference in any of the groups!
  • 68. The beginning; Kress NEJM 2000 ReducCon in LOS Girard Lancet 2008 Decreased ICU stay, Cme on venClator and mortality Strom Lancet 2010 ReducCon in LOS and venClator days No sedaCon group -­‐ boluses of morphine, well established in insCtuCon, more agitated delerium in no sedaCon group Ryker JAMA 2009 ReducCon in venClator days and delirium Jacob JAMA 2012 PRODEX/MIDEX No beRer than midaz or propofol at maintaining light to mod sedaCon and more adverse effects. Increased paCent interacCons. Less vent days than midazolam Mehta 2013 For MV paCents managed with protocolised sedaCon, the additon of daily sedaCon interrupCon did not reduce duraCon MV or ICU LOS
  • 69. The beginning; Kress NEJM 2000 ReducCon in LOS Girard Lancet 2008 Decreased ICU stay, Cme on venClator and mortality Strom Lancet 2010 ReducCon in LOS and venClator days No sedaCon group -­‐ boluses of morphine, well established in insCtuCon, more agitated delerium in no sedaCon group Ryker JAMA 2009 ReducCon in venClator days and delirium Jacob JAMA 2012 PRODEX/MIDEX No beRer than midaz or propofol at maintaining light to mod sedaCon and more adverse effects. Increased paCent interacCons. Less vent days than midazolam Mehta 2013 For MV paCents managed with protocolised sedaCon, the additon of daily sedaCon interrupCon did not reduce duraCon MV or ICU LOS
  • 70. Don’t forget the simple things…. • Small RCT 136 paCents • Used NEECHAM score • Delirium (20%) similar but less mild confusion with ear plugs and good night sleep <50% vs. 25%
  • 71. Guidelines for managing delirium Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 73. Acute UGI Bleed • Randomised, parallel group study • 921 pts with severe upper GI bleeding • Compared restricCve (Hb <7g/dL) vs liberal transfusion strategy (Hb<9g/dL) • RestricCve 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
  • 75. The SuDDICU study SDD 12 meta-­‐analyses of 28 RCT’s. 10 show reduced pneumonia rate; 6 show morality benefit • Why have clinicians avoided implemenCng it in UK? • What are the barriers? • What further evidence is required before full scale clinical implementaCon Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 76. SystemaCc review: CCM 2010 • Those paCents receiving enteral nutriCon, stress ulcer prophylaxis may not be required and may actually increase VAP
  • 77. 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
  • 78. Hepatology • ALD " Alcohol related illness costs NHS £1.7 billion/year " SystemaCc review of 21 arCcles " 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 (venClaCon, vasoacCve drugs, RRT) " Mackle -­‐ -­‐ if MV and vasoacCve drugs hospital mortality 86% -­‐ If MV, vasoacCve 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
  • 80. FuncConal disability 5 years aeer ARDS " 109 survivors from ’98 -­‐ ’01 " Interview, PFT’s, 6 min walk test, resCng & 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
  • 81. Some guidelines Academic Department of Critical Care Queen Alexandra Hospital Portsmouth
  • 82. Suggested resources Academic Department of Critical Care Queen Alexandra Hospital Portsmouth • JICS • Sign up to criCcalcarereviews.com • Podcasts • LITFL • FFICM & ICS
  • 83. Best of Luck! Academic Department of Critical Care Queen Alexandra Hospital Portsmouth www.wessexics.com @WessexICS @WICSBoRomLine @stevemathieu75