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Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland
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Page 1: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

Non-invasive positive pressure ventilation in the neonate

Peter C. RimensbergerPediatric and Neonatal ICU

University Hospital of GenevaSwitzerland

Page 2: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

In the year 2008: BPD incidence = 35% < 29 wks COIN-trial, NEJM 2008

COIN-trial

610 infants, 25-to-28-weeks’ gestation, randomized toCPAP intubation + ventilation

at 5 minutes after birth

Page 3: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

Elastic work of breathing

Adult

Infant

Infant(Reduced Compliance)

Volume(%VC)

Volume(%VC)

Volume(%VC)

Pressure

ThoraxLungsChest wallWork = P * V

ACB: Move the chest wall from the resting position

AXC: Overcome resistive forces

Page 4: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

Inward distortion of the rib cage on the volume displaced by the diaphragma

Innefficient ventilation and waist of work

Page 5: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

Thoraco-abdominal Asynchrony(the noncoincident motion of the rib cage and abdomen during breathing)

If the rib cage is sucked in or retracted as abdominal excursions occur (e.g., in upper airway obstruction),

or the abdomen is retracted as the rib cage expands (e.g., diaphragmatic paralysis)

Prisk GK Pediatric Pulmonology 2002; 34:462–472

Page 6: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

25 weeks: Abdominal (red) & Chest Wall (green) Movements Synchronized NIPPV: Better ventilation

NCPAP NIPPV

Courtesy of Simon Bignall

Thoracoabdominal Asynchrony Synchrony

Page 7: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

SNIPPV1) To avoid the need for endotracheal intubation in preterm infants with

respiratory failureBarrington KJ Pediatrics 2001; 107: 638–41 (RCT)De Paoli AG Acta Paediatrica 2003; 92: 70–5 (review and meta-analysis)Khalaf MN Pediatrics 2001; 108: 13–7 (RCT)Santin R Perinatol 2004; 24: 487–93 (prospective observational study)Friedlich P Perinat 1999; 19: 413 (RCT)

2) It has been shown to be particularly effective in decreasing reintubation when compared with nasal CPAP as an extubation mode Barrington KJ Pediatrics 2001; 107: 638–41 (RCT)Khalaf MN Pediatrics 2001; 108: 13–7 (RCT)Friedlich P Perinat 1999; 19: 413 (RCT)

3) SNIPPV has been used as an alternative to continued endotracheal mechanical ventilation after surfactant therapy in 28- to 34-week gestation infants with respiratory distress syndrome Santin R Perinatol 2004; 24: 487–93 (prospective observational study)

4) Work of breathing has also been shown to be decreased with the use of SNIPPV compared to nasal CPAP Kiciman NM Pediatr Pulmonol 1998; 25: 175–81

Page 8: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

Reintubation after extubation:

A prospective RCT comparing SNIPPV vs NCPAP

(Khalaf MN, et al. Pediatrics 2001;108:13-17)

Criteria for extubation: 1. MAP = 4-6 cm H2O 2. IMV 25/minute 3. PIP 16 cm H2O 4. PEEP 5 cm H2O 5. FiO2 0.35 6. Aminophylline level 8 mg/L 7. Hematocrit 40%

After extubation: 1. SNIPPV: PIP +4, same IMV-PEEP 2. NCPAP: 4- 6 3. FiO2: O2 saturations 90-96%

Criteria for re-intubation: 1. pH < 7.25 2. PaCO2 > 60 mmHg 3. PaO2 < 50 mmHg despite a FiO2 of 0.7 4. A single episode of apnea requiring bag and mask resuscitation 5. Frequent ( 3/hr) apnea/bradycardia spells 6. Multiple ( 3/hr) desaturation episodes despite a FiO2 of 1.0

Page 9: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

SNIPPV (n =34)

NCPAP (n =30)

p value

Age at study (d) 4 (1 -83) 2.5 (1 -106) 0.95

Wt. at study (gm) 1110 55 1200 75 0.32

Pre -MAP (cm H2O) 4.9 0.2 5.1 0.2 0.38

Pre -FiO2 0.30 0.02 0.30 0.01 0.84

AR (cm/H2O/L/s) 169 16 205 21 0.18

LC (ml/cmH 2O) 0.74 0.02 0.8 0.1 0.57

Post -pH 7.36 + 0.03 7.34 + 0.02 0.14

Post -CO 2 (mmHg) 37 + 1.0 40 + 2.0 0.06

Apnea (n) 2.24 0.8 2.03 0.7 0.84 Success (n, %) 32 (94) 18 (60) < 0.01

+

+

+

+

+

+

+

+

+

+

++

+

Reintubation after extubation:

(Khalaf MN, et al. Pediatrics 2001;108:13-17)

Page 10: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

A Prospective Observational Pilot Study: SNIPPV as a Primary Mode of Ventilation In Infants > or = 28 Weeks with RDS

(Santin RS, et al. J Perinatol 2004;24:487-93)

SNIPPV (n=24)

CV (n=35) P value

Birth weight (grams) * 1582 ± 77 1511 ± 103 0.92

Gestational age (weeks) * 31.2 ± 0.5 31.0 ± 0.4 0.89

Gender (male, n, %) 15 (63) 22(62) 0.88

Antenatal steroids (n, %) 18 (75) 24 (68) 0.90

Apgar at 5 minutes (median) 8 8 0.87

Age at surfactant instillation (h)* 3.1 ± 1.4 2.7 ± 0.49 0.49

Mean ± SEM

Page 11: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

A Prospective Observational Pilot Study: SNIPPV as a Primary Mode of Ventilation In Infants > or = 28 Weeks with RDS

(Santin RS, et al. J Perinatol 2004;24:487-93)

SNIPPV (n=24)

CV (n=35)

p value

OI pre-surfactant instillation (cm H2O) 6.0 ± 1.0 5.5 ± 0.6 0.67

Duration of endotracheal intubation (days) 0.3 ± 0.0 2.40 ± 0.4 0.001

Duration of SNIPPV (days) 2.8 ± 0.4 3.1 ± 0.7 0.68

Duration of CPAP (days) 0.3 ± 0.3 0.2 ± 0.1 0.71

Duration of nasal cannula (days) 3.8 ± 1.5 5.1 ± 1.3 0.3

Duration of supplemental O2 (days) 8.2 ± 3.3 15.0 ± 3.2 0.04

Duration of parenteral nutrition (days) 8.4 ± 0.8 12.1 ± 1.6 0.02

Length of stay (days) 29.1 ± 3.3 37.5 ± 3.0 0.04

Mean ± SEMOI: Oxygenation Index

Page 12: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

Kugelmann A J Pediatr 2007;150:521-6

NIMV versus NCPAP for Respiratory Distress Syndrome: A Randomized, Controlled, Prospective Study

Page 13: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

Kugelmann A J Pediatr 2007;150:521-6

Infants treated initially with NIPPV needed less ETT ventilation than infants treated with NCPAP.

Infants treated with NIPPV had a decreased incidence of BPD compared with those treated with NCPAP

Page 14: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

A RANDOMIZED CONTROLLED TRIAL OF SYNCHRONIZED NASAL INTERMITTENT POSITIVE PRESSURE (SNIPPV) VENTILATION IN RDS

(Bhandari V, et al. J Perinatol 2007;27:697-703)

SURF-N-SAVE STUDY: HYPOTHESIS

Primary mode SNIPPV (defined as its use in the acute phase of

RDS, following the administration of the first dose of surfactant)

initiated shortly after birth would decrease the incidence of BPD

and/or death in smaller premature babies when compared to

conventional endotracheal mode of ventilation.

Page 15: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

INCLUSION CRITERIA 1. <32 weeks gestational age.

2. Birth weight 600-1250 grams

3. RDS requiring intubation and surfactant therapy within one hour of birth. The need for intubation /surfactant was based on the following:

a. Fi02 > 0.4 to maintain Sa02 > 90%.

b. Chest radiograph consistent with RDS

EXCLUSION CRITERIA (any one)

1. Nasopharyngeal pathology.a. Choanal atresia.b. Cleft lip or palate.

2. Major congenital anomalies, especially thoracic or cardiac defects.

3. Clinical parameters for exclusion ninety minutes after initial surfactant therapy (approximately 2½ hours after birth).

a. Oxygenation index (OI=[(Fi02)(mean airway pressure)]/Pa02) > 9.

b. No indwelling arterial line.c. More than two isotonic fluid boluses.d. Continuous medication infusion for blood pressure support.e. Fi02 > 0.8.

A RANDOMIZED CONTROLLED TRIAL OF SYNCHRONIZED NASAL INTERMITTENT POSITIVE PRESSURE (SNIPPV) VENTILATION IN RDS

(Bhandari V, et al. J Perinatol 2007;27:697-703)

Page 16: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

A RANDOMIZED CONTROLLED TRIAL OF SYNCHRONIZED NASAL INTERMITTENT POSITIVE PRESSURE (SNIPPV) VENTILATION IN RDS

(Bhandari V, et al. J Perinatol 2007;27:697-703)

Longterm Outcome: Mental or Psychomotor Developmental Intex

There were no statistically significant differences in the MDI (mean SD; CV (n=8) versus SNIPPV (n=7); 88.13 10.32 versus 81.43 17.54) or PDI (88.38 11.87 versus 84.29 19.47) scores in the infants, assessed at a median (25th –75th centile) corrected GA of 22 (20.5-24) months.

PrimaryOutcome:

Birth weight (grams)* 858 ± 27 915 ± 41 0.24

Gestational age (weeks)* 27.0 ± 0.4 26.9 ± 0.3 0.93

CV (n=21)

SNIPPV (n=20)

P value

BPD or Deaths (n, %) 11 (52) 4 (20) 0.03

BPD (n, %) 7 (33) 2 (10) 0.04

Deaths (n, %) 4 (19) 2 (10) 0.66

Air leaks (n, %) 1 (5) 1 (5) 1.0

PDA (n, %) 3 (14) 4 (20) 0.70 IVH (n, %) 6 (29) 6 (30) 1.0

PVL (n, %) 1 (5) 2 ( 10) 0.61

Page 17: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

In the year 2008: BPD incidence = 35% < 29 wks COIN-trial, NEJM 2008

COIN-trial

610 infants, 25-to-28-weeks’ gestation, randomized toCPAP intubation + ventilation

at 5 minutes after birth

Page 18: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

- As extubation mode

- To control apnea, avoiding extubation

- Primary mode (with or without surfactant use): more data needed

Strategizing SNIPPV

Page 19: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

IMV

SIMV

Assist/Control

FSVPSV

Synchronization Principles

Page 20: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

Graseby CapsuleInfant Flow Advanced

Viasys “ SIPAP”

Flow sensorGinevri “ Giulia”

SLE 5000

Babylog 8000

NAVA-system sensing of diaphragmatic electrical activity

Maquet “Servo-I”

SNIPPV: Trigger systems for synchronization

Page 21: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

How to set Ti in a spontaneous breathing patient on a pressure support mode ?

Flow

Pressure

Tinsp.PIP

Pressure Control Pressure Support

Peak Flow

25%

“Flow termination criteria”

0 flow

Ti Te

PEEP

PS above PEEP

0 flow

?

Page 22: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

Termination Sensitivity = Cycle-off Criteria

Flow

Peak Flow (100%)

TS 5%

Tinsp. (eff.)

Leak

Time

Set maximal Tinsp.

TS 30%

Page 23: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

200 a.u.

10 seconds

Feeding, baby moving28 weeks, 1486g

Sleeping, 30 weeks, 1158 g

Sleeping, 30 weeks, 1205 g

Sleeping, 30 weeks, 1158 g

Baby awake, 28 weeks, 1486g

Sleeping, 30 weeks, 1205 g

Beck et al, PAS 2006

Neural breathing pattern in the preterm (room air, no vent)

1

2

3

Page 24: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

Non-invasive neurally adjusted ventilatory assist (NAVA)

in rabbits with acute lung injury

Beck J et al. Intensive Care Med (2008) 34:316–323

Page 25: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

Non-invasive neurally adjusted ventilatory assist (NAVA)

in rabbits with acute lung injury

Beck J et al. Intensive Care Med 2008; 34:316–323

Page 26: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

baby 440 grams

Page 27: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

baby 440 grams

1st experience

Page 28: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

baby 440 grams

Page 29: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

baby 440 grams

Page 30: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

J.Beck ICM 2008

“NAVA can deliver assist in synchrony and proportionally to EAdi after extubation, with a leaky non-invasive interface”

Page 31: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

Conclusions

Meta-Analysis: “NIPPV is a useful method of

augmenting the beneficial effects of NCPAP in

preterm infants…..reassuring absence of the

gastrointestinal side-effects that were reported in

previous case series.” (Cochrane Collaboration)

Issues to be solved

Patient selection

Indications

Synchronization during NIPPV

Page 32: Non-invasive positive pressure ventilation in the neonate Peter C. Rimensberger Pediatric and Neonatal ICU University Hospital of Geneva Switzerland.

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