For parents of premature infants, a diagnosis of Bronchopulmonary Dysplasia (BPD) can feel like a significant hurdle in an already challenging journey. Watching a baby struggle to breathe or require prolonged support from machines is emotionally taxing and stressful. BPD involves irritation and underdevelopment of the lungs, making breathing difficult and exhausting for the infant. Treatment is critical not only to ease the immediate work of breathing but also to support the infant’s overall growth, ensuring that their lungs can eventually develop into healthy, functional organs. 

Because BPD typically affects premature babies whose lungs were not fully developed at birth, treatment is highly specialized. The severity of the condition varies greatly; some infants need only mild support for a few weeks, while others require intensive care for months. Consequently, medication and therapy choices are tailored specifically to the baby’s respiratory needs, growth rate, and other medical conditions (National Heart, Lung, and Blood Institute, 2023). 

Overview of treatment options for Bronchopulmonary Dysplasia 

The primary goal of treating BPD is to support the infant’s breathing while allowing the lungs to mature and heal naturally. This approach focuses on minimizing further injury to the delicate lung tissue, improving oxygenation, and ensuring the baby grows, as lung tissue grows and heals best when the infant is gaining weight. 

Treatment is often a combination of respiratory support (such as oxygen therapy or ventilators), high-calorie nutrition, and fluid management. Medications are used to manage symptoms that interfere with breathing, such as fluid buildup in the lungs or tightening of the airways. While respiratory support technologies are central to care, pharmaceutical treatments are essential for managing the inflammation and fluid dynamics that complicate the condition. 

Medications used for Bronchopulmonary Dysplasia 

Doctors use specific classes of medications to handle the physiological challenges of BPD. These drugs help clear fluid, open airways, and reduce inflammation. 

Diuretics: Diuretics, such as furosemide or chlorothiazide, are common medications for infants with BPD. They help the kidneys remove excess fluid, reducing pulmonary edema in the lungs, which makes breathing difficult. Clinical experience suggests that diuretics can temporarily improve lung mechanics, allowing the baby to breathe with less effort. 

Bronchodilators: Bronchodilators, like albuterol, open airways and are given by nebulizer or inhaler. Not all infants with BPD respond, but they help babies with airway constriction or wheezing. They are used as needed or scheduled briefly during flare-ups. 

Corticosteroids: Steroids reduce inflammation. Strong systemic corticosteroids (e.g., dexamethasone) can help wean a baby off a ventilator in severe cases but are used cautiously and briefly due to potential long-term growth and development effects. Inhaled steroids may also manage chronic airway inflammation with fewer systemic side effects. 

Viral Prophylaxis: Because infants with BPD are at high risk for severe respiratory infections, doctors typically prescribe palivizumab. This is a monthly injection of antibodies given during the viral season to protect against Respiratory Syncytial Virus (RSV), which can be life-threatening for these infants. 

How these medications work 

The medications used for BPD target the mechanical and chemical barriers to easy breathing. 

Diuretics signal kidneys to filter more sodium and water, reducing overall body fluid. This lessens fluid in the lung tissue, making lungs lighter and easier for the baby to expand. 

Bronchodilators relax the tightened muscles around airways in BPD, widening them to improve airflow in and out of the lungs. 

Corticosteroids suppress the immune system’s inflammatory response, lowering airway swelling. This opens up space for air and improves oxygen absorption. 

Side effects and safety considerations 

Treating fragile infants requires careful monitoring, as medications can affect their delicate metabolic balance. 

Diuretics can deplete vital electrolytes, such as potassium and calcium, potentially lowering bone density, a concern for premature infants. Doctors monitor blood work and may supplement electrolytes. 

Bronchodilators can cause rapid heart rate or jitteriness. Corticosteroids pose risks to blood sugar, blood pressure, and long-term neurodevelopment, requiring careful weighing of benefits versus risks for improved breathing. 

Due to the immune-suppressing effect of steroids, parents must monitor for infection signs and seek immediate medical care for respiratory distress, like blue skin, rapid breathing, or retractions. Since everyone’s experience with the condition and its treatments can vary, working closely with a qualified healthcare provider helps ensure safe and effective care. 

References 

  1. National Heart, Lung, and Blood Institute. https://www.nhlbi.nih.gov 
  1. MedlinePlus. https://medlineplus.gov 
  1. American Lung Association. https://www.lung.org 
  1. KidsHealth. https://kidshealth.org 

Medications for Bronchopulmonary Dysplasia

These are drugs that have been approved by the US Food and Drug Administration (FDA), meaning they have been determined to be safe and effective for use in Bronchopulmonary Dysplasia.

Found 1 Approved Drug for Bronchopulmonary Dysplasia

Synagis

Generic Name
Palivizumab

Synagis

Generic Name
Palivizumab
Synagis is indicated for the prevention of serious lower respiratory tract disease caused by respiratory syncytial virus (RSV) in pediatric patients: with a history of premature birth (less than or equal to 35 weeks gestational age) and who are 6 months of age or younger at the beginning of RSV season, with bronchopulmonary dysplasia (BPD) that required medical treatment within the previous 6 months and who are 24 months of age or younger at the beginning of RSV season, with hemodynamically significant congenital heart disease (CHD) and who are 24 months of age or younger at the beginning of RSV season. Synagis is a respiratory syncytial virus (RSV) F protein inhibitor monoclonal antibody indicated for the prevention of serious lower respiratory tract disease caused by respiratory syncytial virus (RSV) in pediatric patients: with a history of premature birth (less than or equal to 35 weeks gestational age) and who are 6 months of age or younger at the beginning of RSV season, with bronchopulmonary dysplasia (BPD) that required medical treatment within the previous 6 months and who are 24 months of age or younger at the beginning of RSV season, with hemodynamically significant congenital heart disease (CHD) and who are 24 months of age or younger at the beginning of RSV season. Limitations of Use: The safety and efficacy of Synagis have not been established for treatment of RSV disease. ( 1 ) Limitations of Use: The safety and efficacy of Synagis have not been established for treatment of RSV disease [see Warnings and Precautions.
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