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College of Health and Medical Science
College of Health and Medical Science
Course: Pathophysiology
04/20/2024
HYALINE
MEMBRANE
DISEASE(HMD)
Prepared by: Ebisa S.
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Respiratory distress
syndrome (RDS)
Or
Hyaline
membrane disease
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Learning outline
• Definition
• Pathophysiology
• Etiology
• Risk factor
• Clinical manifestation
• Differential diagnosis
• diagnosis
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Objective
At the end of this lesson the students will able to:
• Define what is hyaline membrane disease
• Identify different risk factors of HMD
• Discuss etiology and pathophysiology of HMD or RDS
• Identify clinical manifestation of HMD
• List DDX of HMD
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Respiratory distress syndrome
Definition
Respiratory distress syndrome (RDS), formerly known as
hyaline membrane disease, is a common problem in
preterm infants.
• It is a syndrome in premature infants caused by
developmental insufficiency of pulmonary surfactant
production and structural immaturity in the lungs.
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Etiology and Pathophysiology
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RDS….
• Pulmonary surfactant is a complex system of lipids,proteins
and glycoproteins that is produced in specialized lung cells
called Type II pneumocytes.
• The surfactant is packaged by the cell in structures called
lamellar bodies and extruded into the air space.
• The lamellar bodies then unfold into a complex lining of the
air space.
• This layer reduces the surface tension of the fluid that lines
alveolar air space.
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RDS….
• By reducing surface tension, surfactant prevents the air
spaces from completely collapsing on exhalation.
• In addition, the decreased surface tension allows reopening
of the air space with lower amount of force.
• Therefore, without adequate amount of surfactant , the air
space collapse(atelectasis) and are very difficult to expand
which result in difficult to breath.
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RDS….
The primary cause of RDS is deficiency of pulmonary
surfactant, which is developmentally regulated.
This surfactant prevent the collapse of terminal air
spaces(the future site of alveolar development)
throughout the normal cycle of inhalation and exhalation.
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RDS…
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RDS…..
• Blood oxygen level falls and carbon dioxide rises, resulting in
rising blood acid level and hypoxia.
• Structural immaturity, as manifested by a decreased number
of gas exchange units and thicker walls, also contributes to
the disease process.
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Incidence
• Infant respiratory distress syndrome (IRDS) is the leading cause of
death in premature infants.
• Despite only 1% of all birth complications being attributed to
respiratory distress syndrome, there is a significantly higher
prevalence in prematurely born babes.
• Incidence rate of IRDS in premature infants born at 30 weeks GA are
at 50%, and rise even higher to 93% for infants born prematurely at
28 weeks of GA.
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Risk factors
• Increased risk
• Prematurity
• Maternal diabetes
• Multiple births
• Elective cesarean section without labor
• Perinatal asphyxia
• Decreased risk
• Antenatal steroid prophylaxis
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Clinical manifestation
Symptoms:
Babies with HMD may experience:
• Difficulty breathing at birth that worsens over time.
• Cyanosis (bluish skin coloration).
• Flaring of the nostrils.
• Rapid breathing (tachypnea).
• Grunting sounds during breathing.
• Chest retractions (pulling in at the ribs and sternum).
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Differential diagnosis
Early-onset sepsis
Bacterial Pneumonia
Cyanotic heart disease
Transient tachypnea
Persistent pulmonary hypertension
Non-pulmonary systemic disorders, such as hypothermia,
hypoglycemia, anemia, polycythemia, or metabolic
acidosis
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Diagnosis
HMD or RDS is diagnosed through a combination of
assessments, including:
• Physical appearance, color, and breathing efforts.
• Chest X-rays, which often show a unique "ground glass"
appearance.
• Blood gas tests (measuring oxygen, carbon dioxide, and
acidity in arterial blood).
• Echocardiography (to rule out heart problems)
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Treatment
Continuous positive airway pressure (CPAP)
adequate oxygenation and ventilation,
administration of exogenous surfactant.
General supportive measures
Temprature
Fluid,metabolic and nutrition
Circulation and anemia
Antibiotic when indicated
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Specific interventions are:
Antenatal corticosteroid therapy:
Are indicated in pregnant women 24-34 weeks' gestation at
high risk of preterm delivery within the next 7 days.
Optimal benefit begins 24 hrs after initiation of therapy and
lasts seven days.
Early surfactant therapy:
prophylactic use of surfactant in preterm newborn <27 weeks'
gestation.
Early CPAP administration in the delivery room.
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Complication
Long term complications include
bronchopulmonary dysplasia (BPD)
neurodevelopmental impairment
retinopathy of prematurity (ROP).
Death
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Reference
• 1. Infant Respiratory Distress Syndrome (Hyaline Membrane Disease)
• 2. Infant respiratory distress syndrome - Wikipedia
• 3. Hyaline Membrane Disease (HMD) - Respiratory Distress Syndrome
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THANK YOU
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