Final Review Flashcards

1
Q

Composition of Pulmonary Surfactant

A

Mainly composed of depomitoylphosphatidlycholine (Lecithin) and shinogomyelinand

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2
Q

Surfactant Treatment

A

Most surfactant will be reprocessed and recycled in alveolar type 2 cells

This is why babies only need 1-2 treatment

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3
Q

Common Surfactant

A

Bovine Lipid Extract Surfactant (BLES)

Beractant (Survata)

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4
Q

Surfactant Production in the Body

A

Surfactant is produced in type two alveolar cells at 24 weeks gestation

Surfactant is then stored in the lambellar bodies

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5
Q

When is Surfactant Contraindicated

A

Pulmonary Hemorrhage

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6
Q

BLES Dosing

A

5 ml/kg

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7
Q

Neonatal Aspiration Risk

A

The airway is more anterior and superior putting neonates at a higher aspiration risk

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8
Q

Compliance in Neonates

A

Increased compliance

Cartilage is under developed creating high airway reistance and more collapse in the lower airway

Accessory muscle are under developed so they are more susceptible to failure

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9
Q

Neonate Respiratory Anatomy Compared to Adult

Laryngeal Shape

A

Neonate: Funnel Shape

Adult: Rectangular

Laryngeal soft tissue and lymph nodes which meakes them more susceptible to swelling and injury.

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10
Q

Neonate Respiratory Anatomy Compared to Adult

Shape and Location of Epiglottis

A

Neonate: Long/C1

Adult: Flat C4

large and floppy epiglottis (in infants we are using the miller blade to help move the large floppy epiglottis).

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11
Q

Neonate Respiratory Anatomy Compared to Adult

Resting Poistion of Diaphragm

A

Higher in neonates

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12
Q

Carina Position in Neonates

A

Carina is higher (3rdvertebrae), T4/5 by age 10

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13
Q

Infants Neck Flexion

A

Infants have poor neck flexion = higher obstruction risk

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14
Q

Infants Airway

A

Infant airway is more funnel shaped, narrowest point is cricoid

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15
Q

Neonatal Epiglottis

A

Infant epiglottis is OMEGA Ω shaped, less flexible, more horizontal

Neonate: Long/C1

Adult: Flat C4

large and floppy epiglottis (in infants we are using the miller blade to help move the large floppy epiglottis).

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16
Q

Infants Tongue Position

A

Infants have large tongue with posterior placements

Adults have a porportional tongue size

Larger amounts of lymph tissue = higher obstruction risk

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17
Q

Neonate Respiratory Anatomy Compared to Adult

Thoracic Shape

A

Neonate: Bullet shaped

Adult: Conical shaped

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18
Q

Neonate Respiratory Anatomy Compared to Adult

Laryngeal Shape

A

Neonate: Funnel Shape

Adult: Rectangular

Laryngeal soft tissue and lymph nodes which meakes them more susceptible to swelling and injury.

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19
Q

Neonate Respiratory Anatomy Compared to Adult

Anteroposterior transverse diameter ratio

A

Neonate: 1:1

Adult: 1:2

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20
Q

Neonate Respiratory Anatomy Compared to Adult

Body Surface Area/Body Size Ratio

A

Neonate: 9 x adult

Large heart and belly- increase impedance for tidal volume as the heart is taking up more room

Adult: Normal

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21
Q

Identifing the Patient is Hypoxic

A

Low SO2 and PaO2

PvO2 <35 mmHg

O2 Delivery <8 ml/kg/min

High lactate >2.8

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22
Q

Criteria to Consider SBT

A

Resolution of the disease

Adequate oxygenation

HR ≤ 140 bpm, stable blood pressure, stable cardiac rhythm, no ongoing myocardial ischemia, and no uncompensated shock.

No significant uncompensated respiratory acidosis (i.e. pH < 7.30).

Adequate mentation (GCS >= 13) or tracheostomy in place.

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23
Q

Before you Begin a SBT you need to check oxygenation what measure are you looking at

A

PaO2 ≥ 60mmHg

PaO2/ FiO2 > 150-200 or SpO2 >= 90%, with PEEP ≤ 5-8 cmH2O and FiO2 ≤ 0.4 (or as otherwise described in the regional O2 Protocol).

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24
Q

Initiation of spontaneous breathing trial

A

To perform the SBT, the RRT will place the patient on PSV of 7cmH2O and PEEP of 5 cmH2O.

If Automatic Tube Compensation (ATC) is used, then set PSV to 0.

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25
First 5 min of SBT
Terminate the test is any of the below occurs ## Footnote RR \> 38 Rapid shallow breathing index (Tobin ratio) \> 105 Sweating, anxiety or change in mental status SpO2 \< 90% for \> 5 minutes Signs of distress or paradoxical breathing HR \> 140 bpm or a 20% change Systolic BP \< 90 or \> 180 mmHg New dysrhythmia or myocardial ischemia
26
After first 5 min of SBT
For patients ventilated \< 72 hours, continue for 30 minutes. For patients ventilated \> 72 hours, continue the trial for 60-120 minutes. Monitoring should be done after the first 5 minutes and Q15 there after.
27
Initiating Mechanical Ventilation Goals
FiO2 at 0.60 and then adjust to maintain SpO2 \> 90%. The physician must order a target SpO2 Note: Default values will be SpO2 ≥ 88% and ≤ 92% for patients with obstructive lungs and chronic CO2 retention, and SpO2 ≥ 90% for all other patients.
28
When does the physician need to be notified of changes to FiO2
a. The FiO2 has to be set at \> 0.60. b. The FiO2 has to be increased by \> 0.30. This excludes changes for treatment such as suctioning
29
Arterial Blood Gas Protocol PA Catheter
Mixed Venous samples will be drawn Q12h in a patient having a PA catheter It is not mandatory to draw an arterial sample in conjunction with each mixed venous draw.
30
Weaning Parameters POINTS OF EMPHASIS
Patient should be on PEEP \< 8 cm H2 O and F1O2\< 0.60. Patient’s own minute ventilation should not be greater than 12Lpm. Try to place the pt in sitting position or elevate their head in order to optimize pulmonary mechanics
31
Rapid Shallow Breathing Index (Tobin Ratio)
Rapid Shallow Breathing Index (Tobin Ratio) = f (bpm) / VT (L)). This ratio is determined after the patient had been breathing spontaneously for one minute.
32
Infants = 32 Weeks 1st Week of Life Target blood gas
Blood Gas \>/= 7.20 PCO2 = 45-55 (40-50 in 1st 48 hours of life) SpO2= 88-92% Do not treat metabolic acidosis with hyperventilaion
33
Criteria for Possible HFV
You only need one of these but will probably have more than one RR \> 80 bpm Vt \>5ml/kg PIP \>25 cmH2O MAP \>12 cmH2O AND FiO2 \>0.40
34
Infants = 32 Weeks 1st Week of Life Order of Weaning
Volume (4 ml/kg) or PIP (\<18 cmH2O) depending on mode PEEP and Ti Rate (5-10 increments until you reach 20)
35
VAP
Ventilator associated pneumonia (VAP) is a nosocomial infection occurring in patients receiving mechanical ventilatory support that is not present at the time of intubation and that develops **more than 48 hours after the initiation of that support.** VAP can derive from endogenous bacteria (the baby’s own oropharyngeal flora) or exogenous bacteria (eg: Pseudomonas aeruginosa). VAP is associated with prolonged hospitalization and increased mortality, especially in the very low birth weight infant.
36
T-Piece Resusictator During Resucictation
To deliver inspiration - place finger over the PEEP cap. To deliver expiration - remove finger from PEEP cap. Inspiratory time is operator controlled. A longer expiratory time is optimal, therefore the PEEP cap occlusion should be limited to approximately 0.5 seconds, regardless of the intended respiratory rate. To achieve target respiratory rate of 40-60 breaths/minute repeat
37
Consider Extubation in Neonates When
RR \> 40 with a set RR= 20 bpm AND Vt= 4ml/kg with PIP \<18 cmH2O AND MAP 7-8 cmH2O AND FiO2 \<0.30 AND Patient breathign comfortably, hemodynamically stable, no significant increase in TcPCO2, EtCO2 for 1 hour prior to extubation
38
Where does the MAC Catheter Attach
Attaches to the proximal end of ETT using wye connector, same as inline suctioning Does not need the diconnection of teh closed system Surfactant will be dleivered at distal end of ETT reducign the risk for obstruction
39
Closed Suctioning in Neonates
Suction level- 100-120 mmHg Preoxygenate by setting FiO2 5-10% above current FiO2 for ~20 sec Insertion catheter and apply suction for 1-3 sec before withdrawal Pull out the catheter in a straight motion (without twirling) to prevent kinking. Time from insertion to complete withdrawal should not exceed 5 seconds.
40
ARDSnet Algorithm ABG
**Oxygenation:** PaO2 55-90 and SpO2 88-95% **Ventilation:** pH 7.30-7.45
41
SUCTIONING ENDOTRACHEAL TUBES: NEONATAL Open Suction Procedure-What Should You Adjust Suction To
Adjust suction to **80-100mmHg** and test by kinking tube and reading suction gauge
42
Primary CPAP Management in the Delivery Room GA 26-28 Weeks Principals
Maintain optimal lung volume and FRC In L&D and acute phase **avoid CPAP \>6** **in infants 26-28 weeks** Early surfactant does not mean immediate surfactant rather surfactant should be administers in NICU when possible
43
Primary CPAP Management in the Delivery Room GA 26-28 Weeks What are your first steps
Clear airway Initiate CPAP +5, FiO2 0.30 Dry and Stimulate Attach pulse ox
44
Primary CPAP Management in the Delivery Room GA 26-28 Weeks You just assessed that the patient is spontaneously breathing
Assess that heart rate If above 100-Move on to next assessment If below 100-Begin neopuff and NRP
45
Primary CPAP Management in the NICU GA 26-28 Weeks CXR and Blood Gas
Pneumothorax-Discontinued CPAP, intubate, early surfactant, drain pneumothorax as indicated Hypoinflation: Consider increasing CPAP or consider intubation, and early surfactant Hypercarbia (arterial): Consider incresing CPAP
46
Primary CPAP Management in the Delivery Room GA 26-28 Weeks You just assessed that the patient's heart rate, what do you assess next
Assess WOB and SpO2 **Mild WOB and SpO2 within range**- Maintain CPAP at +5 and FiO2 at 0.30 and prepare to move to NICU **Moderate or Severe WOB and/or SpO2 not within range**- Increase CPAP by 1 (Max 6) and increase FiO2 by 0.10-0.20 to achieve targeted SpO2. Then reass WOB and SpO2 if now mild WOB and SpO2 then mainatin level and move to NICU. If after you make your changes and then FiO2 is \>0.60 or there is **severe WOB** then consider intubation
47
Primary CPAP Management in the NICU GA 26-28 Weeks Moderate WOB OR FiO2 \>0.3
Assess interface fit and seal Assess need for suctioning Review with dr consider CXR and blood gas Increase CPAP by 1 with a max CPAP of 6
48
Primary CPAP Management in the NICU GA 26-28 Weeks Mild WOB and FiO2 \<0.30
Leave CPAP at same level until able to maintain target SpO2 with FiO2 \<0.25 SpO2 \>92% for 6.24 hours AND FiO2 \<0.25 (if no review with dr and increase CPAP). If yes then review histogram
49
Reviewing Histogram
SpO2 \>85% for 80% of the time and no significant apneas No-Optimize CPAP for 2-5 days and optimize caffeine Yes-Wean CPAP by 1
50
Normal ICP
5-15 mmHg
51
Rapid Shallow Breathing Index Calculation
Tobin Score RR/Tidal Volume
52
Bradycardia is persisting even after CPR
**Epinphrine** **Atropine** Consider pacing
53
Atropine
Think bratropine used for increase vagal tone and primary AV block
54
Epinephrine Dosing
0.01 mg/kg and 0.01 ml/mg Repeat every 3-5 min
55
Suction Levels for Children
80-100 mmHg for both open and closed
56
What Happends When Secretions Build Up in the Suction Catheter
Increased Resistance Decreased ability to efectivly remove secretions Can be due to the fact that we are using too small of a catheter
57
Suction Level for Neonates
60-80 mmHg for both closed and open suctioning
58
High Suction Levels
Suction flow is proportional to suction level when flow is smooth and laminar However flow in suction system will be turbulent and disorderly so if suction increases by 50% then flow may only increase by 20-25%
59
Sputum Induction Procedure
Do in AM and get 3 samples If needed can rinse mouth and pretreat with bronchodilator
60
Incentive Spirometry
Increases transpulmonary pressure gradient by decreasing Pplat Inspiration will cause a drop in Pplat due to expansion of the thorax allowing negtaive Palva and more gas to flow into alveoli and lung expansion
61
Medication Calculation
(What you want/what you have) x quantity is comes in
62
Lung Protective Strategy
Permissive Hypercapnia-PaCO2 of 45-55 mmHg pH ≥ 7.25 VT~ 4 mL/kg Peak pressures should be \< 25 cmH2O
63
Neonatal ABG Goals
pH \>7.25 PaCO2 45-55 PaO2 45-65 HCO3 15-18 SpO2 85-92
64
BPD and Mechanical Ventilation
Permissvie Hypercapnia VT4-6 mL/kg Goal pH ≥ 7.25 Peak pressures \< 25 cmH2O Target lower SpO2 85-94% Volume-targeted modes tend to work best for BPD.
65
Congenital Diaphragmatic Hernia ABG Goals
pH \>7.25 Pre-ductal SpO2 85%, though ideal is 90-95%
66
PPHN Ventilation Goals
Target low to normal PaCO2 (35-40) and pH 7.40-7.45 Hyperoxygenate PaO2 \>100mmHg Nitric Oxide Therapy
67
Cyanotic Defect and Target SpO2
Rule of 40s ## Footnote pH 7.40 PaCO2 40s PaO2 40s SpO2 70-80% žThese mimic in-utero conditions and maintain a PDA
68
Mechanical Ventilation and Harmful Effects on Respiratory Sys.
**V/Q Mismatching** * Increase shunt and deadspace * Decreased pulmonary perfusion **Ventilator Induced Lung Injury** * Barotrauma, volutrauma, shear stress, atelectatrauma, biotrauma **​Oxygen toxicity**
69
PC CMV Absolute Pressure Decreased Ti sec
Ti tot Decreased Te Increase I:E Decrease Pmean Decrease
70
PC CMV Absolute Pressures Decreased in Compliance
Vt Decrease Ve Decrease Ti dyn Decrease
71
PC CMV Absolute Pressure Increased in PEEP
PIP Decrease Pplat Decrease Pmean Increased
72
PC CMV Delta Pressure Decreased Rate
Ve Decreased Te Increases I:E Decrease Pmean Decrease
73
PC CMV Delta Pressure Increased Ti sec
Ti tot Increased Te Decrease I:E Increased Pmean Increased
74
PC CMV Absolute Pressure Increased Rate
Ve Increase Te Decrease I:E Increase Pmean Increase
75
VC-CMV Vt Increased
76
PC CMV Delta Pressures Resistance Decreased
Ti dyn Decreased
77
PC CMV Pressure Control Delta Increased PC
PIP Increased Pplat Increased Vt Increased Ve Increased Pmean Increased
78
Atelectrauma
Caused by the repeated opening and closing of alveoli due to inappropriate PEEP Usually occurs in dependent area
79
PPV and Renal System
* Urinary output (UO) due to changes in CO * Endocrinological Effects * Increased ADH release * Decreased ANP release * Activation of the renin-angiotensin-aldosterone system * Abnormal ABGs PaO2 results in decreased renal function and UO * Function is dramatically decreased when \< 40 mmHg * PaCO2 \> 65 mmHg decreases kidney function
80
PC CMV Delta Pressure Decreased Ti sec
Ti tot Decreased Te Increase I:E Decrease Pmean Decrease
81
PC CMV Delta Pressures Increased in Compliance
Vt Increase Minute Ventilation Increase Ti Dyn Increased
82
PC CMV Absolute Pressure Decreased Rate
Ve Decreased Te Increases I:E Decrease Pmean Decrease
83
PPV-Increase Intrapulmonary Shunt
Perfusion will go to gravity dependent areas and ventilation will go to gravity independent areas The gravity dependent areas will be located on the posterior side when the patient is lying on their back
84
Oxygen Index
OI = (FiO2 \* MAP \*100) / PaO2 ## Footnote If you are using FiO2 as a decimal then times by 100 if you are using it was a whole number then you do not need to multiple by 100 Positively correlated with mortality risk You want a low OI (the lower the better) with \<5 being normal When you are in the 20 you need to begin to look at things such as ECMO because you lungs can no longer properly oxygenate the blood
85
Biotrauma
Due to atelectrauma and volutrauma the lung **releases inflammatory mediators** This can result in injury to other organs
86
Volume Support Mode
Spontaneous Mode Pressure Limited Flow Cycled Volume Targeted
87
PAV How to Manipulate Tidal Volume with E Senesitivity
A decrease in E sensitivity will increase tidal volume and Ti Unless the patient is air hungry then they will be trying to breath at a high peak volume and it will cut them off faster= smaller breath
88
What will happen to tidal volume if you decrease the resistance in pressure control
Volume will stay the same and Tidy will get shorter What will happen to tidal volume if you decrease the compliance in pressure control Decrease TC and Ti dyn and volume will go down
89
Porportional Assist Ventilation
Used to **assist spontanesou ventilation** as the breath that will be delivered is similar to pressure support but the **support level if variable and porportional to spontaneous effort** This means that the harder the patient works the more support the vent will deliver - POSITIVE FEEDBACK
90
Porportional Assist Ventilation and E Sensitivity
E Sensitivity set at 27% (27% of inspiratory peak flow) Pressure support patient trigger pressure limited flow cycles (flow cycle=e sensitivity) You will never get equilibrium on a pressure support breath
91
Mandatory Minute Ventilation
There is a set MV and if it is not reached the ventilator will kick and deliver mandory breaths until the set MV has been reached
92
AHS Initiation of SBT
PSV of 7 and PEEP of 5 unless there is automatic tube compensation then you put PSV to 0 In first 5 minute monitor tobin score (\>105), sweating, anxiety, mental status, SpO2 \>90% If any negative changes occur increase PSV and inform physician
93
Tobin Score
Also known as rapid shallow breathing index = (RR)/ (Vt) An RSBI \< 105 breaths/min/L has been widely accepted by healthcare professionals as a criteria for weaning to extubation. Whereas patients with RSBI \> 105 will have a high chance of failure and require re-intubation.
94
Length of SBT
If pt has been ventilated \>72 hours continue SBT 60-120 min If pt has been ventilated \<72 hours continue SBT 30 min Monitoring should be done first 5 min and the Q15 after
95
European Consensus and Delivery Room Oxygenation
Oxygen for resusucitation should be controlled via a blender An initial concentration of 30% oxygen is appriopraite of babies \<28 GA For babies that are 28-10 week use an FiO2 of 21-30
96
European Consensus and Spontaneous Breathing Babies
In spontaneous breathing babies stabilize babies with CPAP at 6 cmH2O via mask or nasal prongs
97
European Consensus Saturation Goals
Saturation goals should be 90-94%
98
In Labor and Delivery and Acut ephase what should you keep CPAP under
\<6
99
CPAP Waveforms
Variable flow is most desireable and is seen in CPAP system (ex. Arabella) Sechrist systems will deliver a constant flow
100
SiPAP Machine
SiPAP is a brand name **Less expiratory resistance and lower flows** due to the flip flop gate which will manage baseline pressure Delivers **stable baseline pressure** Uses the Graesby capsule
101
Arabella System
Most common method of NIV (CPAP) with infants Can use nasal prongs or nasal mask
102
Do you set flow or pressure in CPAP
With CPAP set the flow to get the pressure you need (you don’t set pressure because of the leaks)
103
What will happen to the ABG if the baby is crying
Will be more acidotic
104
BiPhasic Mode Basic Settings
6/9 (FiO2 0.5-0.3) 7/10 (FiO2 \>0.5) Rate: 20 Ti: 1 sec. Separation of 3 cmH2O
105
Indications of CPAP
PaO2 \< 50 mmHg when FiO2 \>0.60 Minute Ventilation is Adequate PaCO2 is \>50 and pH 7.25 Respiratory Distress
106
Neonatal Respiratory Failure
PaCO2 \> 60 mmHg pH \< 7.25
107
Pediatric Positive Pressure Devices Pressure Targeted
BiLevel/BiPAP (Pressure Support) When there is a high WOB we will use pressure support rather than CPAP
108
Pediatric Positive Pressure Devices Pressure Targeted Advantages
Leak compensation Spontaneous and time modes
109
Pediatric Positive Pressure Devices Volume Targeted
Portable home ventilators Most devices do not have a pressure support feature Do not trigger well or support spontaneous breathing Set up so Vt is greater than physiologic Vt
110
Factors Unique to Pediatric Patients that Promote Complications of NPPV
**Aspiration**-Immaturity of airway protective reflexes **Reflux**-Impaired gastroesophageal sphincter function during infancy **Upper Airway Obstruction**-Anatomical factors, difficulty clearing secretions, large oral leak, mouth breathing **Agitation**-Anxiety, incomplete understanding, developmental disorders
111
PRVC Compliance Decreases
**Vt will remain the same** so there will be an **increase in Pplat an PIP (overall increase in Pmean)** **MV will not change** because RR and Vt is set **Tidyn decreases and Tistatic will increase, but Titotal does not change** **Flow will increase**
112
PRVC Resistance Decreases
Pressure will remain the same but flow will change due to the changing airway diameter **Tidyn decreases and Tistatic increases (Titotal does not change)** **Peak flow will be directly proportional to resistance but overall flow will not change** (and we can not measure)
113
PRESSURE CONTROL VOLUME REGULATED AS TI DECREASES
**Titotal will decrease** and may decrease to the point where we are no longer meetign equilibrium before exhalation starts Because Ti total is shorter it means that Te is longer, so **I:E will decrease** As Ti decreases **PIP will increase** in order to deliver set Vt Because the time that we are dleivering the pressure has decrease there will be a **overall decreased in Pmean**
114
Pressure Control Compliance Increases
**Vt will increase** because we can increase the volume delivered at certain pressures, because Vt is changing **MV will increase** **Tidyn will increase and Tistatic will decrease**, but **Titotal will not change** so I:E will not change The change in Tidyn will **increase flow** and **decrease Pmean**
115
Pressure Control Resistance Increases
The only thing that will change is that your **Ti dyn will get longer** Remember as resistance increase your flow will decrease making a longer Ti dyn and a short Ti static
116
Mechanical Ventilation and BPD with a PDA
When there is a left to right shunt it can lead to chronic pulmonary edema (BPD) making the baby oxygen dependant So when the baby cries it will create pressure in their lungs creating a right to left shunt which will decrease saturation, but as soon as the baby relaxes their saturations will improve
117
BPD AND OXYGENATION
Supplemental oxygen is the main therapy for infants with BPD but the appropriate target remains controversial Oxygen saturations are accepted at 85-90% after preterm birth Keep in mind though that patients with severe BPD usually are \<36 weeks which is past the time when ROP is a major concern For BPD, growth failure, respiratory exacerbations and PPHN however we accept saturations of 92-95%
118
Severe Refractory Hypoxemia in Neonates
PaO2 \< 50mmHg despite CPAP and FiO2\> 0.60
119
Silverman Index
The higher the silverman score the high the distress Score 10=Severe respirtory distress Score \>/=7 Impending respirtroy failure Score 0 No respirtory distress
120
Long Acting B2 Agonists (LABA)
Oxeze® (Formoterol) Serevent® (Salmeterol) Onbrez® (Indacaterol) Streverdi® (Oladaterol)\*Not on the market yet
121
LAMA/LABA
Ultibro® (Glycopyronnium/Indacaterol) Anoro® (Umeclidinium/Vilanterol)