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RT134 Disease Processes

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This flashcard explains Respiratory Distress Syndrome (Hyaline Membrane Disease) as a surfactant deficiency leading to alveolar collapse, reduced lung compliance, and hypoxemia, with pathophysiology involving membrane formation, impaired gas exchange, and further lung damage.

What is Respiratory Distress Syndrome or Hyaline Membrane Disease and what is its Pathophysiology?

Def: Surfactant deficiency of the lung causing decreased lung compliance and atelectasis

Patho:
-Collapse of the alveoli after each breath
-Plasma leaks out of the lung tissue
-Forms a hyaline membrane
Lack of surfactant-Alveolar Collapse
Increased Pressures needed-leads to vasoconstriction, acidosis, hypoxemia
Capillary endothelial damage with fluid leaking into alveolar space
Diffusion of O2 and CO2 difficult due to decreased pulmonary blood flow and atelectasis
Over inflation further damages Type II cells
Formation of hyaline membrane

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Key Terms

Term
Definition

What is Respiratory Distress Syndrome or Hyaline Membrane Disease and what is its Pathophysiology?

Def: Surfactant deficiency of the lung causing decreased lung compliance and atelectasis

Who are the infants at risk of RDS?

Premature infants

How can we detect RDS?

L/S ratio 2:1
PG+
Shake Test (Foam Stability Index>48) i

What are the clinical signs of RDS?

10 possible signs

Intercostal retractions

Expiratory Grunting

Nasal Flar...

How can we treat RDS?

Oxygen Therapy

Nasal CPAP

Steroids

How can we manage RDS?

Surfactant Replacement Therapy (Prophylactic or Rescue)

Prophylactic:
.30 FiO2 to ma...

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TermDefinition

What is Respiratory Distress Syndrome or Hyaline Membrane Disease and what is its Pathophysiology?

Def: Surfactant deficiency of the lung causing decreased lung compliance and atelectasis

Patho:
-Collapse of the alveoli after each breath
-Plasma leaks out of the lung tissue
-Forms a hyaline membrane
Lack of surfactant-Alveolar Collapse
Increased Pressures needed-leads to vasoconstriction, acidosis, hypoxemia
Capillary endothelial damage with fluid leaking into alveolar space
Diffusion of O2 and CO2 difficult due to decreased pulmonary blood flow and atelectasis
Over inflation further damages Type II cells
Formation of hyaline membrane

Who are the infants at risk of RDS?

Premature infants

How can we detect RDS?

L/S ratio 2:1
PG+
Shake Test (Foam Stability Index>48) i

What are the clinical signs of RDS?

10 possible signs

Intercostal retractions

Expiratory Grunting

Nasal Flaring

Tachypnea

Apnea

Decreased BS

Cyanosis

Metabolic and/or Respiratory Acidosis

Poor Peripheral Perfusion

Hypotension/shock

How can we treat RDS?

Oxygen Therapy

Nasal CPAP

Steroids

Exogenous Surfactant

Ventilatory Support--HFOV vs Conventional Vent

Pulse Ox/TCM

How can we manage RDS?

Surfactant Replacement Therapy (Prophylactic or Rescue)

Prophylactic:
.30 FiO2 to maintain PaO2>50 or O2 sat>90%
-CXR consistent with RDS

What are the Management Strategies for RDS?

What is the Main objective for these management strategies?

*Lung Protective strategies

Gentle suctioning prn

Minimal handling--cluster care

Fluid and electrolyte balance-keep on the dry side

Maintain blood glucose 45-120 mg%

Amp and Gent antibiotics

To do whatever I can do to avoid the use of Positive pressure ventilation.

What is PPHN?

Failure of shunts to close during transition from fetal circulation due to lack of O2

High PVR causing RightHe to Left shunt

Hypoxemia and acidemia causes further ­PVR and perpetuates the cycle

What are the clinical signs of PPHN?

6 signs

Severe Respiratory Distress

Cyanosis

Hypoxemia on 100% O2 with positive pressure

unexplained by degree of lung disease

CXR shows ¯Vascular Markings and enlarged heart

Breath sounds—rales

What 2 conditions need to Ruled out or diagnosed in the presence of PPHN?

Severe causing RDS
congenital Heart Defect

in general, just becuase you caught PPHN doesnt mean that that is the only thing wrong. could be PNA, diaphragmatic hernia, etc.

What is the true test for R-L shunt in PPHN?

What are some secondary tests? (3)

Contrast echocardiography used to confirm shunting

Ductal blood gas, 02 hyperoxia challenge (100% for 20 mins, hyper ventilation test)

What is the treatment for PPHN?

Prevent hypoxemia, acidosis and hypothermia

Correct hypoxemia by reversing R>L shunting

Drug Therapy [(INO, oxygen, Priscoline (tolazoline)] - drugs to reduce PVR

PPV with 100% Oxygen

What is the Vent strategy for PPHN?

High rate with short I-time. use just enough to move the chest

With a goal to Reduce PaCO2 to a level where PaO2 rises above 100mmHg.

Use enough FiO2 to keep PaO2 > 120mmHg if possible

What 3 drugs are used to treat PPHN?

What is the main objective of these drugs and its goal?

iNO, oxygen, Priscoline (tolazoline)

they are drugs to reduce PVR with the goal of closing the Patent ductus arteriosis

What is the most recognized site of infection in new borns within the first 24 hours of life?

Lungs

What are the sources of PNA?

intrapartum

  • Aspiration in utero

  • Aspiration during delivery

What are contributing factors to PNA?

premature rupture of the membrane (can introduce bacteria too soon)

Prolonged labor

Excessive obstrectric manipulation

Maternal GI infection

Infection (GBS, ecoli, herpes, listeria)

What are signs and symptoms of PNA?

5 signs and symptoms

MOM says Baby doesn’t “look” right/“Not acting right”

Rapid Respiratory deterioration

Apnea and/or bradycardia Especially

Temp instability

hypotension/poor perfusion

What does temperature instability appear like for term and preterm babies with PNA?

Term—hyperthermia

Preterm-– hypothermia

What are the treatment options for PNA?

Careful assessment and monitoring

Antibiotic Therapy

Fluid/Electrolyte support

Blood Products/volume replacement

Respiratory Support as needed

What do you watch out for in babies with PNA?

Watch out for septic shock!

What are risk factors for Merconium aspiration?

Prolonged gestation >42 weeks

SGA

IUGR

Placental insufficiency (hypertension, Preeclampsia, Previa, Abruption)

Intrapartum asphyxia (Cord prolapse or Prolonged labor)

What causes Merconium Aspiration?

Fetal asphyxia to intestinal hypoxia then to hyperperiastalsis then anal sphincter relaxation causes merconium to enter the amniotic fluid.

this can happen before or after delivery

How can merconium aspiration happen after delivery?

baby can swallow the merconium during delivery cause a reflux and aspirate it into the lungs

What are some clinical signs of merconium aspiration?

Tachypnea with intercostal retractions

Cyanosis, grunting, flaring

Increased AP thoracic diameter

Coarse bronchial breath sounds

Airway obstruction/Air Trapping

Complete (atelectasis)

Incomplete (ball – valve action blocking airway from exhalation)

Alert, anxious LOOK

What are treatment options for Merconium Aspiration?

Lung protection strategy

MOST IMPT, Do not stimulate to breathe.

When do you follow merconium protocols after the baby is born with suspected merconium aspiration?

If the baby is non-vigorous and flacid use merconium protocols

If the baby is vigorous and crying on their own, just treat the PNA

What do you do in merconium protocols?

| 3 things

intubate at first breath

Direct tracheal suction below cords with DeLee suction which connects directly and uses ET tube for suction.

PPV

HFOV is recommended

If conventional, high pressures with short i-times
Hyperoxygenate with hypocapnea, Alkalosis

What is the Vent strategy for RDS?

.30 FiO2

| maintain PaO2>50 or O2 sat>90%

What does a CXR from RDS look like?

Uniform reticulogranular appearance
AKA ground glass

Low lung volumes

Air Bronchograms

Atelectasis

What does a CXR from PNA in infants look like?

| 2 things

Diffuse Bilateral infiltrates

patchy infiltrate in perihilar area

What is TTHN?

Failure of fetal lung fluid to clear causing respiratory distress

What are signs and symptoms of TTHN?

Minics clinical early RDS

Tachypnea resulting in hyperventilation

Mild respiratory alkalemia

Cyanosis

Barrel – shaped chest

Retracitons/grunting

What does TTHN in CXR look like?

Wet LUNG

Perihilar congestion

There may be small collections of liquid at the costophrenic angles

Progressive clearing within 48-72 hours

What is the treatment for TTHN?

Supplemental Oxygen
100% by Head Hood
High flow nasal oxygen (vapotherm)

NCPAP
4 – 6 cwp
100% O2

What is PIE or air leaks?

Pulmonary Diseases

Stiff non compliant lungs

Aspriation syndromes

Hypoplastic lungs

Congenital lobar or pulmonary interstitial emphysema

Positive pressure ventilation

What are some prevention strategies for PIE?

HFV

Permissive Hypercapnea

Keep airways clear

Pressure gauges

Recognition of infants at risk

what are some signs and symptoms of PIE?

Restless

Irritable

Lethargy

Tachypnea

Increased respiratory effort profound general cyanosis

Bradycardia

Decreased of shifted breath sounds

Chest asymmetry

Severe hypotension and poor peripheral perfusion

Cardiac arrest

What are conformations of PIE/Air leaks?

Transilumination of the Chest

| CXR

What are treatment options for PIE?

Needle aspiration 2nd intercostal space midclavicular line

Oxygen therapy
HFV

What is BPD?

A Chronic lung condition that starts with severe RDS.
has 4 stages

Presents it self in Infants requiring high ventilator settings with high FiO2 after 10 days

What is the treatment for BPD?

Use lowest ventilatory support and FiO2 to permit lung to heal.

Titrate Fi02 keeping sats 88 – 92

HFOV recommended in early stages of RDS to prevent BPD.

Good nutrition to support lung growth

Treat infections

What is Chornal atresia and how do you check for it?

Formation of bone that blocks ventilation through the nasal passage.

Babies are obligate nose breathers. they can only breathe through crying.

conformation with size 6 french catheter's inability to pass through nose.

What is esophageal atresia?

it is a birth defect wherein the esophagus is narrow or absence of connection to stomach.

What is the most common esophageal atresia?

Esophageal atresia with distal transesophegeal Fistula.

What are some clinical signs and symptoms of TEF and EA?

Inability of pass OG tube (This is Very impt Point)

Excessive drooling due to inability to swallow

Aspiration of gastric secretions

Choking/coughing with first feeding

Episodes of cyanosis

In RDS, what would show up on a CXR?

Air bronchograms

Ground glass