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Effect of Chest Physiotherapy on Improving Pulmonary Function in Dealing With Congenital Heart Disease and Lung
Manali A Boob1, Moli Jain2, Divya M Badjate1
1Department of Cardio-Respiratory Physiotherapy, Ravi Nair Physiotherapy College, Datta Meghe Institute of Medical Sciences, Wardha, IND.
Insights
This case report details a successful cardiorespiratory physiotherapy intervention for an infant with complex congenital heart defects, including patent ductus arteriosus (PDA) and pulmonary arterial hypertension (PAH). The treatment optimized the infant's cardiorespiratory function and recovery.
Area of Science:
- Pediatric Cardiology
- Neonatal Physiology
- Thoracic Surgery
Background:
- Patent ductus arteriosus (PDA) is a congenital heart defect where the ductus arteriosus fails to close post-birth.
- Complex congenital heart disease in infants can present with significant cardiorespiratory compromise.
Observation:
- A three-month-old infant presented with cough, poor feeding, and respiratory distress.
- Diagnosed with PDA, pulmonary arterial hypertension (PAH), atrial septal defect (ASD), coarctation of the aorta (COA), and pneumonia.
- Underwent left posterolateral thoracotomy for PDA ligation and coarctation repair.
Findings:
- Cardiorespiratory physiotherapy was implemented to address post-surgical recovery.
- Treatment focused on improving oxygen saturation, functional capacity, respiration, and cardiovascular function.
- The infant demonstrated optimal functional recovery, as evidenced by FLACC scale and arterial blood gas analysis.
Implications:
- This case highlights the critical role of targeted cardiorespiratory physiotherapy in managing infants with complex congenital heart disease post-surgery.
- Effective physiotherapy can significantly enhance functional recovery and improve clinical outcomes in this vulnerable population.
- Demonstrates a multidisciplinary approach to optimizing infant cardiorespiratory health.
Abstract:
Patent ductus arteriosus (PDA) is a condition in which the ductus arteriosus fails to close after birth. We present the case of a three-month-old female infant admitted to a tertiary care center with the complaint of cough, poor feeding, and breathing difficulties. Based on the investigatory finding, she was diagnosed with PDA with pulmonary arterial hypertension (PAH), an atrial septal defect (ASD), coarctation of the aorta (COA), and pneumonia. In this patient, a left posterolateral thoracotomy was done to accomplish PDA ligation and coarctation repair. The outcomes of the infants were documented using the face, legs, activity, cry, consolability (FLACC) scale, and arterial blood gas analysis. The therapeutic aim specified an increase in oxygen saturation, enhanced total functional capacity, optimized respiration, cleared chest secretions, and normalized cardiovascular function. The effectiveness of the cardiorespiratory physiotherapy treatment regimen based on the patient's existing state of health is the focus of this case report. The outcome variable indicated that the patient's functional recovery was optimal.
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