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Angiogenesis in the Ischemic Rat Lung
Published on: February 8, 2013
Clinical investigation of systemic-pulmonary collateral arteries
Chang-Hsien Yu1, Ming-Ren Chen
1Division of Pediatric Cardiology, Department of Pediatrics, Mackay Memorial Hospital, 92, Sec 2, Chun-San N. Road, Taipei, 104, Taiwan. sienna60@ms1.mmh.org.tw
Insights
Systemic-pulmonary collateral arteries can be normal in newborns and often resolve. Predisposing factors, however, may cause these vascular connections to persist, potentially augmenting pulmonary blood flow.
Area of Science:
- Cardiovascular Medicine
- Pediatric Cardiology
- Vascular Biology
Background:
- Systemic-pulmonary collateral arteries (SPCA) are abnormal vascular connections.
- They are known to develop in pediatric patients with congenital heart disease, chronic pulmonary infections, and prematurity.
- Current understanding suggests SPCA originate from the vascular plexus that forms pulmonary and bronchial vasculature.
Purpose of the Study:
- To review patients diagnosed with SPCA.
- To evaluate potential risk factors associated with their development.
- To determine the incidence of unsuspected SPCA in healthy infants.
Main Methods:
- Retrospective review of 284 patients with SPCA over a 4-year period.
- Patient categorization into groups: premature, heart disease, pulmonary disease, healthy, and others.
- Analysis of demographic data, echocardiography results, and follow-up conditions.
Main Results:
- The study reviewed 284 patients with SPCA.
- Among 92 healthy children with SPCA, 52 were identified during routine health screening.
- An estimated incidence of 1.57% for unsuspected SPCA in healthy 1-month-old infants was calculated (52/3314).
Conclusions:
- SPCA may be a normal finding in neonates and typically resolve over time.
- Persistence of SPCA can be influenced by predisposing factors.
- Persistent SPCA may serve to augment pulmonary blood flow in certain pediatric conditions.
Abstract:
Systemic-pulmonary collateral arteries are known to develop in children with congenital heart disease, chronic pulmonary infection, and prematurity. At present, these abnormal connections between the systemic and the pulmonary systems are thought to develop from the vascular plexus, which normally gives rise to the pulmonary and bronchial vasculature. The objective of this study was to review our patients with systemic-pulmonary collateral arteries and evaluate possible risk factors. The records of patients with systemic-pulmonary collateral arteries seen at our hospital over a 4-year period were retrospectively reviewed. They were grouped into one of the following five categories: premature, heart disease, pulmonary disease, healthy, and others. Age, gender, weight, and the results of echocardiography were recorded, as was the condition on follow-up. We reviewed the records of 284 patients: 130 premature, 13 heart disease, 30 pulmonary disease, 92 healthy, and 19 others. Over the same period, 3314 healthy 1-month-old infants had undergone echocardiography for health screening. Among the 92 healthy children with systemic-pulmonary collateral arteries, 52 were diagnosed at the health-screening exam. Therefore, we estimate the incidence of unsuspected systemic-pulmonary collateral arteries in healthy 1-month-old infants to be 1.57% (52/3314). We conclude that systemic-pulmonary collateral arteries may be present normally after birth and then gradually disappear. However, if there are certain predisposing factors, they may persist in order to augment pulmonary flow.
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