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Understanding the Pathophysiology, Implications, and Treatment Options of Patent Ductus Arteriosus in the Neonatal
Cristin Conrad1, Desi Newberry
1Department of Graduate Nursing Science, East Carolina University, Greenville, North Carolina.
Insights
Patent ductus arteriosus (PDA) in premature infants is a common condition. Reviewing pathophysiology and treatment options like pharmacologic or surgical management is crucial for improving neonatal outcomes.
Area of Science:
- Neonatal Medicine
- Pediatric Cardiology
- Perinatal Research
Background:
- Patent ductus arteriosus (PDA) is a persistent fetal shunt impacting premature neonates.
- Delayed closure affects up to 80% of infants born at 25-28 weeks gestation.
- PDA leads to pulmonary overcirculation and systemic hypoperfusion.
Purpose of the Study:
- To review the pathophysiology of PDA.
- To explore current treatment options for PDA in neonates.
Main Methods:
- Conducted a literature review from 2013-2018.
- Utilized databases: PubMed, CINAHL, and Google Scholar.
- Searched terms: neonate, PDA, pathophysiology, pharmacotherapy, nursing, ligation, indomethacin, ibuprofen, acetaminophen.
Main Results:
- Optimal PDA treatment remains debated, with options including conservative, pharmacologic (indomethacin, ibuprofen, acetaminophen), and surgical management.
- Treatments can be prophylactic, presymptomatic, or symptomatic.
- Associated morbidities include chronic lung disease, retinopathy of prematurity, and neurodevelopmental delay.
Conclusions:
- Lack of a universal PDA severity scoring system hinders research comparisons and meta-analyses.
- Consistent definitions and scoring are needed for accurate outcome assessment.
- Clinicians and nurses must understand PDA treatments and potential side effects for optimal neonatal care.
Background:
Patent ductus arteriosus (PDA) is the persistence of a fetal shunt between the pulmonary artery and the aorta. This structure normally closes in the first 3 days after birth; however, closure is delayed in up to 80% of infants born at 25 to 28 weeks of gestation. Persistent PDA results in pulmonary overcirculation and systemic hypoperfusion.
Purpose:
The purpose of this article is to review pathophysiology and treatment options for PDA.
Methods:
A literature review was conducted using PubMed, CINAHL, and Google Scholar (2013-2018). Search terms included neonate, PDA, pathophysiology, pharmacotherapy, nursing, ligation, indomethacin, ibuprofen, and acetaminophen (paracetamol).
Results:
Optimal treatment remains contentious. Options include conservative/medical, pharmacologic, and surgical management. Conservative/medical management includes mild fluid restriction, increased airway pressures, and supportive care. Pharmacologic treatment is accomplished using indomethacin, ibuprofen, or acetaminophen. Surgical intervention is by direct closure or by percutaneous ligation. Treatment may be prophylactic, presymptomatic, or symptomatic. Long-term morbidities associated with PDA include chronic lung disease, retinopathy of prematurity, and neurodevelopmental delay.
Implications For Research:
Absence of a universal scoring system for severity of PDA limits accuracy of comparisons among research studies. Lack of a consistent definition also makes it difficult to aggregate data for meta-analyses. Adoption of a consistent scoring system for hemodynamic significance would facilitate comparisons of outcomes among research studies.
Implications For Practice:
Clinicians should be aware of treatment options for PDA and their implications on neonatal outcomes. For nurses, anticipation of possible side effects is important for performance of focused assessments.
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