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Samir JABER
Department of Critical Care Medicine and Anesthesiology (DAR B)Saint Eloi University Hospital and Montpellier School of Medicine
80 Avenue Augustin Fliche; 34295 Montpellier. FRANCEMail : [email protected] ; Tel : +33 4 67 33 72 71
Ventilation des patients à poumons sains :
Réduire le volume courant ?
Marseille – 17 Avril 2014
Déclaration de liens
Déclare les liens suivants (consultants) :
• Drager France • Maquet France• Fisher Paykel• Hamilton
Background
De-recruitment Overdistension
Low TV No PEEP
High TV High PI P
Atelectotrauma Barotrauma Volutrauma
Release of I nflammatory
cytokines
Release of I nflammatory
cytokines
Biotrauma (IL-1β, IL-6, IL-8, TNF-α)
Ventilator-associated lung injury (VALI)
Adapted from Tusman G et al. Curr Opin Anesthesiol 2012
mor
bidy
risk
VT
High VT > 12 ml/kgVery low VT (without PEEP)
AtelectasisAtelectotrauma
AtelectasisAtelectotrauma
VILI
(Ventilator Induced
Lung Injury)
VILI
(Ventilator Induced
Lung Injury)
Opt
imal
VT
Tidal volume (VT) : how much is too much ?
Evolution of Mortality over Time in Patients Receivi ng Mechanical Ventilation
Andrés Esteban1, Fernando Frutos-Vivar1, Alfonso Muriel2, Niall D. Ferguson3, Oscar Peñuelas1, Victor Abraira2, Konstantinos Raymondos4, Fernando Rios5, Nicolas Nin1, Carlos
Apezteguía5, Damian A. Violi6, Arnaud W. Thille7, Laurent Brochard8, Marco González9, Asisclo J. Villagomez10, Javier Hurtado11, Andrew R. Davies12, Bin Du13, Salvatore M.
Maggiore14, Paolo Pelosi15, Luis Soto16, Vinko Tomicic17, Gabriel D’Empaire18, DimitriosMatamis19, Fekri Abroug20, Rui P. Moreno21, Marco Antonio Soares22, Yaseen Arabi23, Freddy Sandi24, Manuel Jibaja25, Pravin Amin26, Younsuck Koh27, Michael A. Kuiper28, Hans-Henrik
Bülow29, Amine Ali Zeggwagh30, and Antonio Anzueto31
AJRCCM Vol. 188, No. 2 (2013), pp. 220-230
Is there a rationale to use lung protective
ventilation in patients with normal lungs ?
Is there a rationale to use lung protective
ventilation in patients with normal lungs ?
Ventilator-associated lung injury in patients without acute lung injury at the onset of mechanical ventilationOgnjen Gajic, MD; Saqib I. Dara, MD; Jose L. Mendez, MD; Adebola O. Adesanya, MD; Emir Festic, MD; Sean M. Caples, MD; Rimki Rana, MD; Jennifer L. St. Sauver, PhD; James F. Lymp, PhD; Bekele Afessa, MD; Rolf D. Hubmayr, MD
Gajic O. et al Crit Care Med 2004
A retrospective cohort study of 332 patients with « normal lungs » at the onset of mechanical ventilation and who received mechanical ventilation for ≥24h 4 ICUs of a tertiary referral center
Incidence ALI: N=80 patients (24%)
Ventilation with lower tidal volumes as compared to conventional tidal volumes for patients without acute lung injury - A preventive randomized controlled trialRogier M Determann, Annick Royakkers, Esther K Wolthuis, Alexander P Vlaar, Goda Choi, Frederique Paulus, Jorrit-Jan Hofstra, Mart J de Graaff, Johanna C Korevaar and Marcus J Schultz
10 ml/kg PBW
6 ml/kg PBW
13.5% vs. 2.6%
Determann RM et al. Crit care 2010
Lower Tidal Volumes in Patients without
Preexisting Lung Injury
Serpa Neto A et al , JAMA. 2012 Oct 24;308(16):1651-9
Lower Tidal Volumes in Patients without
Preexisting Lung Injury
Serpa Neto A et al , JAMA. 2012 Oct 24;308(16):1651-9
Lower Tidal Volumes in Patients without
Preexisting Lung Injury in ICU: A Metaanalysis
Serpa Neto A et al , Curr Opin Crit Care 2014, 20:25–32
Lower Tidal Volumes in Patients without
Preexisting Lung Injury in ICU: A Metaanalysis
Serpa Neto A et al , Curr Opin Crit Care 2014, 20:25–32
Courtesy of Prof. Serpa Neto A,
PROTECTIVE VENTILATION IN ICU
LUNG PROTECTIVE VENTILATION WITH LOWER TIDAL VOLUMES TO PREVENT ACUTE RESPIRATORY DISTRESS SYNDROME IN INTENSIVE CARE UNIT PATIENTS UNDER
MECHANICAL VENTILATION: A systematic review and meta-analysis using individual data of 2,184 patien ts
Ary Serpa Neto MD MSc, Sabrine NT Hemmes MD, Carmen SV Barbas MD PhD, Michelle Biehl MD, Rogier M Determann MD PhD, Jonathan Elmer MD PhD,
Gilberto Friedman MD PhD, Ognjen Gajic MD PhD, Rita Linko MD PhD, Roselaine Pinheiro de Oliveira MD PhD, Esther K Wolthuis MD PhD, Marcelo Gama de Abreu
MD PhD, Paolo Pelosi MD, Marcus J Schultz MD PhD
VENTILAÇÃO PROTETORA NA UTIPROTECTIVE VENTILATION IN ICU
Courtesy of Prof. Serpa Neto A, Prof Pelosi
VENTILAÇÃO PROTETORA NA UTIPROTECTIVE VENTILATION IN ICU
Courtesy of Prof. Serpa Neto A,
VENTILAÇÃO PROTETORA NA UTIPROTECTIVE VENTILATION IN ICU
Courtesy of Prof. Serpa Neto A,
VENTILAÇÃO PROTETORA NA UTIPROTECTIVE VENTILATION IN ICU
Courtesy of Prof. Serpa Neto A,
… and in the operating room,
What is the evidence ?
In ICU patients In the OR
Patients with injured lungs
Patients with healthy lungs
Improved morbidityand morality: YES
Improved morbidity: YES
Recommendations:Limit VT < 10 ml/kg PBW
5 < PEEP < 15 cmH2O
Impact on Postoperative outcome: ?
Patients with healthy lungs
Recommendations:VT ?
PEEP ?
Lung Protective Mechanical Ventilation
Low TV and PEEP
Large TV and zero PEEP Low TV and zero PEEP
1963
� Approximately 30% of patients still ventilated with TV ≥10 ml.kg-1 IBW� Female sex and BMI were independently associated with the use of high TV
2161 patients between January and June 2006 in 97 anaesthesia units from 49 hospitals
10
A multicentre observational study of intraoperative ventilatory management during general anaesthesia: tidal volumes and relation to body weight
Jaber S, Coisel et al. Anaesthesia 2012; 67, 999–1008
1-4 cmH2O0 cmH2O
5-8 cmH2O >9 cmH2O
PEEP is “rarely” used during general anesthesia
� A combination of PEEP ≥5 cmH2O and TV <10 ml/kg IBW was used in less than 5% of patients
A multicentre observational study of intraoperative ventilatory management during general anaesthesia: tidal volumes and relation to body weight
Jaber S, Coisel et al. Anaesthesia 2012; 67, 999–1008
� 80% of patients received zero PEEP, and PEEP ≥5 cmH2O in less than 15%
High Tidal Volumes in Mechanically Ventilated PatientsIncrease Organ Dysfunction after Cardiac SurgeryLellouche F et al. Anesthesiology 2012 116:1072-82
Low VT(<10 ml/kg PBW)
High VT(>12 ml/kg PBW)
Retrospective analysis of prospectively collected data in 3434 patients between 2004 and 2006
Postoperative outcomes
0
2
4
6
8
10
12
14
MOF Need for MV > 48 h Renal failure Mortality
VT < 10 ml/kg PBW
VT > 12 ml/kg PBW
Nu
mb
er
(%)
of
pa
tie
nts
P=0.006
P=0.01
P=0.004
P=0.59
Retrospective analysis of prospectively collected data in 3434 patients between 2004 and 2006
High Tidal Volumes in Mechanically Ventilated PatientsIncrease Organ Dysfunction after Cardiac SurgeryLellouche F et al. Anesthesiology 2012 116:1072-82
RCT studiesin the OR
?
High TV group(n = 51)
Low TV group(n = 50)
TV, ml/kg PBW 12.0 ± 2.3 6.7 ± 1.1
PEEP, cmH2O 5 5
Recruitment maneuver 0 0
Minute ventilation, l 6.2 ± 1.9 7.8 ± 2.1
Duration of surgery, h 6.1 ± 2.1 6.1 ± 2.7
Protective Mechanical Ventilation during General An esthesia for Open Abdominal Surgery Improves Postoperative Pulmonary Function
Severgnini P. et al. Anesthesiology 2013
56 Patients undergoing elective open abdominal surg ery
STANDARD VENTILATION TV 9 ml/kg PBW
zero PEEP
PROTECTIVE VENTILATIONTV 7 ml/kg PBW
10 cmH2O PEEP + RM VS.
ClinicalTrials.govA service of the U.S. National Institutes of Health
● Protective Ventilation During General Anesthesia for Open Abdominal Surgery (PROVHILO study)
Control group Intervention group
VT 8 ml/kg IBW
PEEP ≤ 2 cmH2O
No Recruitment maneuver
VT 8 ml/kg IBW
PEEP 12 cmH2O
Recruitment maneuvers :
1. After intubation
2. After any disconnection from the ventilator
3. Before detubation
● Intraoperative Protective Ventilation in Abdominal Surgery (IMPROVE Study)
Control group Intervention group
VT 10-12 ml/kg IBW
No PEEP
No Recruitment maneuver
VT 6-8 ml/kg IBW
PEEP 6-8 cmH2O
Recruitment maneuvers :
1. After intubation
2. Repeated every 30-40 min
N = 900
N = 400
Study design
INtraoperative PROtective VEntilation in abdominal surgery
The IMPROVE Trial
Lung-Protective Ventilation
N=200
Non-Protective VentilationN=200
VS.
VT 10 to 12 ml/kg PBWNo PEEPNo Recruitment Maneuver
VT 6 to 8 ml/kg PBWPEEP 6 to 8 cmH2ORecruitment Maneuver
Recruitment maneuver=CPAP 30 cmH2O during 30 sec
After intubation and every 30min thereafter
In both groups:- Plateau pressure <30 cmH2O- Volume-controlled ventilation mode- FiO2 adjusted to maintain SpO2 ≥95% - RR adjusted to maintain ETCO2 between 35 and 40 mmHg
The IMPROVE TrialIntraoperative Protective Ventilation in Abdominal Surgery
A pragmatic multicenter, double-blinded, randomized controlled trial
Inclusion criteria- All adult patients older than 40 years (<90 yrs)- Scheduled for Abdominal laparoscopic or non-laparoscopic surgery- With an expected duration of at least 2 hours- And a preoperative risk index for pulmonary complications ≥2
(Arozullah AM et al. Ann Intern Med 2001)
The IMPROVE TrialIntraoperative Protective Ventilation in Abdominal Surgery
Non inclusion criteria- Mechanical ventilation of >1H within the last 2 weeks before surgery- Body mass index ≥35 kg/m2
- Acute respiratory failure (pneumonia, ALI or ARDS)- Emergency- Sepsis or septic shock- Progressive neuromuscular illness- Intra-thoracic surgery- Pregnancy- Refusal to participate
Inclusion criteria- All adult patients older than 40 years (<90 yrs)- Scheduled for Abdominal laparoscopic or non-laparoscopic surgery- With an expected duration of at least 2 hours- And a preoperative risk index for pulmonary complications ≥2
(Arozullah AM et al. Ann Intern Med 2001)
The IMPROVE TrialIntraoperative Protective Ventilation in Abdominal Surgery
Primary outcome measure
A composite of major pulmonary and extra-pulmonary complications to postoperative Day 7
� Pulmonary: Postoperative pneumoniaNeed for NIV or tracheal intubation for ARF
� Extra-pulmonary: Sepsis, Severe sepsis and septic shockPostoperative Death
The IMPROVE TrialIntraoperative Protective Ventilation in Abdominal Surgery
Secondary outcomes
� Pulmonary complications:- Incidence of all-causes pulmonary complications, scored using a 4 grades scale- Postoperative atelectasis- Postoperative pneumonia- Need for NIV or tracheal intubation for ARF- Postoperative ALI or ARDS
All causes of pulmonary and extra-pulmonary complications to Day 30 after surgery
� Extra-pulmonary complications: - Sepsis, severe sepsis and septic shock- Surgical complications (re-intervention, anastomotic leak)- Need for unexpected ICU admission- Intraoperative ventilation-related adverse events- Duration of ICU and Hospital stay- All cause mortality to Day 30
The IMPROVE TrialIntraoperative Protective Ventilation in Abdominal Surgery
Results
Characteristics at baseline Non-protective VentilationGroup (n=200)
Lung-protective VentilationGroup (n=200)
Age – yr 63.4±10.0 61.6±11.0
Male sex – no. (%) 121 (60.5) 116 (58.0)
Height – cm 169.5±9.0 169.1±8.8
Actual body weight – kg 71.3±13.9 71.4±14.2
Predicted body weight – kg 63.8±9.9 63.3±9.7
Body mass index – kg/m2 24.7±3.8 24.8±3.8
Preoperative risk index – no. (%)
Class 2 100 (50.0) 101 (50.5)
Class 3 94 (47) 93 (46.5)
Class 4 or more 6 (3.0) 6 (3.0)
Laparoscopic surgery – no. (%) 44 (22.0) 41 (20.5)
Current smoker – no. (%) 50 (25) 51 (25.5)
Alcohol intake – no. (%) 10 (5) 21 (10.5)
COPD – no. (%) 20 (20.0) 20 (20.0)
Weight loss > 10% – no. (%) 44 (22.0) 40 (20)
The IMPROVE TrialIntraoperative Protective Ventilation in Abdominal Surgery
Intraoperative procedures Non-protective VentilationGroup (n=200)
Lung-protective VentilationGroup (n=200) P Value
Tidal volume – ml 719.0±127.8 406.7±75.6 <0.001
Tidal volume – ml per kg PBW 11.1±1.1 6.4±0.8 <0.001
PEEP – cmH2O – median (IQR)
At baseline 0 (0–0) 6 (6–8) <0.001
End of surgery 0 (0–0) 6 (6–8) <0.001
Recruitment maneuver – median (IQR) 0 (0–0) 9 (6–12) <0.001
Peak pressure – cmH2O
At baseline 20.1±4.9 18.9±3.6 0.04
End of surgery 20.6±4.4 20.0±4.0 0.15
Plateau pressure – cmH2O
At baseline 16.1±4.3 15.2±3.0 0.02
End of surgery 16.6±3.5 15.2±2.6 <0.001
FiO2 – % 47.2±7.6 46.4±7.3 0.27
The IMPROVE TrialIntraoperative Protective Ventilation in Abdominal Surgery
Intraoperative procedures Non-protective VentilationGroup (n=200)
Lung-protective VentilationGroup (n=200) P Value
Epidural use – no. (%) 77 (38.5) 83 (41.5) 0.61
Volume of fluids – median (IQR)
Crystalloids 2.0 (1.3–3.5) 1.5 (2.0–3.0) 0.47
Colloids 0.5 (0.25–1.0) 0.5 (0.5–1.0) 0.97
Duration of surgery – no. (%) 0.95
2-4 hours 76 (39.6) 75 (38.5)
4-6 hours 75 (39.1) 76 (38.9)
>6 hours 41 (21.3) 44 (22.6)
Blood loss – ml – median (IQR) 300 (125–550) 300 (100–500) 0.29
Blood transfusion – no. (%) 37 (18.5) 34 (17.0) 0.79
Need for vasopressor – no. (%) 42 (21.1) 35 (17.7) 0.45
More than 60% of surgical procedures were ≥4 hours
The IMPROVE TrialIntraoperative Protective Ventilation in Abdominal Surgery
Intraoperative procedures Non-protective VentilationGroup (n=200)
Lung-protective VentilationGroup (n=200) P Value
Epidural use – no. (%) 77 (38.5) 83 (41.5) 0.61
Volume of fluids – median (IQR)
Crystalloids 2.0 (1.3–3.5) 1.5 (2.0–3.0) 0.47
Colloids 0.5 (0.25–1.0) 0.5 (0.5–1.0) 0.97
Duration of surgery – no. (%) 0.95
2-4 hours 76 (39.6) 75 (38.5)
4-6 hours 75 (39.1) 76 (38.9)
>6 hours 41 (21.3) 44 (22.6)
Blood loss – ml – median (IQR) 300 (125–550) 300 (100–500) 0.29
Blood transfusion – no. (%) 37 (18.5) 34 (17.0) 0.79
Need for vasopressor – no. (%) 42 (21.1) 35 (17.7) 0.45
No difference in the intraoperative volume of fluids and blood losses
The IMPROVE TrialIntraoperative Protective Ventilation in Abdominal Surgery
0
5
10
15
20
25
30N
umbe
r of
eve
nts
(%)
Non-protectiveventilation
group (N= 200)
Lung-protectiveventilation
group (N= 200)
27.5 %
10.5 %
The IMPROVE TrialIntraoperative Protective Ventilation in Abdominal Surgery
Primary Outcome Measure
P<0.001
The IMPROVE TrialIntraoperative Protective Ventilation in Abdominal Surgery
1 3 7 15 30
0.00
0.
10
0.20
0.
30
0.50
0.
40
Pro
babi
lity
of e
vent
Days since surgery
Non-protective ventilat ion
Lung-protective ventilat ion
Log-rank test, P<0.001
Major Pulmonary and Extra-pulmonary Complications to Postoperative day 30
The IMPROVE TrialIntraoperative Protective Ventilation in Abdominal Surgery
1 3 7 15 30
0.00
0.
10
0.20
0.
30
0.50
0.
40
Pro
babi
lity
of e
vent
Days since surgery
Non-protective ventilat ion
Lung-protective ventilat ion
Log-rank test, P<0.001
Probability for requiring intubation or non-invasive ventilationfor ARF to Postoperative Day 30
PROVHILO - a worldwide multicenter randomized controlled trial on protective ventilation during
general anesthesia for open abdominal surgery
Hemmes SN et al. LANCET 2014 in press
Vt = 8 ml/kg IBW
PEEP or RM
alone are not
enough !
PEEP 10 cmH2O
RM+PEEPRM+ZEEP
0
10
20
30
40
50
60
70
80
Anesthesia 5 min 20 min 40 min
Com
plia
nce
(ml/c
mH
2O)
0
100
200
300
400
500
600
Awake Anesthesia 5 min 20 min 40 min
PaO
2/F
iO2
(mm
Hg)
Prevention of Atelectasis in Morbidly Obese Patients during General Anesthesia and Paralysis
A Computerized Tomography Study
Henrik Reinius, M.D., Lennart Jonsson, M.D., Sven Gustafsson, M.D., Ph.D., Magnus Sundbom, M.D., Ph.D., Olov Duvernoy, M.D., Ph.D.Paolo Pelosi, M.D., Ph.D., Goran Hedenstierna, M.D., Ph.D., Filip Freden, M.D., Ph.D. Anesthesiology 2009
✱✱
✱
†✱ ✱
✱
✱
✱
✱
RM = CPAP 55 cmH2O for 10 sec AND/OR PEEP=+10 cmH2O
Awake After induction 5 min 20 min
PEEP
RM+PEEP
RM+ZEEP
Quelle est la procédure qui marche le plus et/ou le mieux ?
QUESTION n°2
« petit volume courant »
(6 ml/kg)
PEPouManœuvre de
recrutementou
Quelle est la procédure qui marche le plus et/ou le mieux ?
Réponse (probable) n°2
« petit volume courant »
(6 ml/kg)PEP
Manœuvre de recrutement
ou ou
+ +x x
Quelle est la procédure qui marche le plus et/ou le mieux ?
Réponse (probable) n°2
« petit volume courant »
(6 ml/kg)PEP Manœuvre de
recrutement+ +oux oux
= Association des 3 procédures ++
Serpa Neto ASerpa Neto A
INTRAOPERATIVE VENTILATOR SETTINGS AND POSTOPERATIV E ACUTE RESPIRATORY DISTRESS SYNDROME: An individual data
meta-analysis of 3,659 patients
Ary Serpa Neto MD MSc, Sabrine NT Hemmes MD, Carmen SV Barbas MD PhD, Martin Beiderlinden MD, Michelle Biehl MD, Ana Fernandez-Bustamante MD PhD, Emmanuel Futier MD PhD, Ognjen Gajic MD PhD, Samir Jaber MD PhD , Alf Kozian MD PhD, Marc Licker MD, Wen-Qian Lin MD, Stavros G Memtsoudis MD PhD, Dinis Reis Miranda MD, Pierre Moine MD, Domenico Paparella MD, Marco Ranieri MD PhD, Federica Scavonetto MD, Thomas Schilling
MD PhD DEAA, Gabriele Selmo MD, Paolo Severgnini MD PhD, Juraj Sprung MD PhD, Sugantha Sundar MD, Daniel Talmor MD PhD, Tanja Treschan MD, Gerardo Tusman MD PhD, Mari Carmen Unzueta MD PhD, Toby N Weingarten MD, Esther K Wolthuis MD PhD, Hermann
Wrigge MD PhD, Marcelo Gama de Abreu MD PhD, Paolo Pelosi MD, Marcus J Schultz MD PhD
Intraoperative Mechanical Ventilation
Courtesy of Prof. Serpa Neto A, et al.
Intraoperative Mechanical Ventilation
Courtesy of Prof. Serpa Neto A, et al.
Intraoperative Mechanical Ventilation
Courtesy of Prof. Serpa Neto A, et al.
Intraoperative Mechanical Ventilation
Courtesy of Prof. Serpa Neto A, et al.
Intraoperative Mechanical Ventilation
Courteesy of Prof. Serpa Neto A, et al.
Conclusion
healthy lungs injured lungs
Objectives in volume-controlled mode (VC)
Initial settings
6 < VT < 7 ml/kg PBW
6 < PEEP < 7 cmH2O
Recruitment maneuvers (repeated every 30-45 min and each derecruitment
procedures (suctioning…) )
12 < RR < 25 breath/min
30% < FiO2 < 50%
Target values and monitoring
Plateau pressure < 25 cmH2O
35 < EtCO2 < 45 mmHg(ABG if presence of EtCO2 > 45 mmHg
SpO2 ≥ 95%
Initial settings
4 < VT ≤ 6 ml/kg PBW
8 < PEEP < 15 cmH2O
Recruitment maneuvers (in selected patients)
15 < RR < 35 breath/min
50% < FiO2 < 80%
Target values and monitoring
Plateau pressure < 30 cmH2O
40 < PaCO2 < 60 mmHg and 7.30 < Ph < 7.40(repeated ABG to optimize)
SpO2 ≥ 92%
A. B.
Many thanks
Montpellier(France)