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    <title>OAR@UM Collection:</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/3627</link>
    <description />
    <pubDate>Wed, 15 Apr 2026 14:26:50 GMT</pubDate>
    <dc:date>2026-04-15T14:26:50Z</dc:date>
    <item>
      <title>Transcatheter closure of symptomatic aortopulmonary window in an infant</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/4126</link>
      <description>Title: Transcatheter closure of symptomatic aortopulmonary window in an infant
Authors: Pillekamp, Frank; Hannes, Tobias; Koch, Daniel; Brockmeier, Konrad; Sreeram, Narayanswami
Abstract: An aortopulmonary window is a rare congenital cardiac defect. In the majority&#xD;
of symptomatic neonates and infants, primary surgical repair is the treatment&#xD;
of choice. In selected infants, catheter closure of the defect with a device may&#xD;
be feasible. This article reports on the successful closure of an AP window in a 12&#xD;
month old infant, using a 6mm Amplatzer septal occluder. The procedure and&#xD;
follow-up were uneventful.</description>
      <pubDate>Tue, 01 Jan 2008 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://www.um.edu.mt/library/oar/handle/123456789/4126</guid>
      <dc:date>2008-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Change of size and type of patent ductus arteriosus in a one year old infant during routine echocardiographic study</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/4125</link>
      <description>Title: Change of size and type of patent ductus arteriosus in a one year old infant during routine echocardiographic study
Authors: Galal, Mohammed Omar; Turkistani, H.; Sultan, A.
Abstract: There are only very few publications which document reactivity of patent&#xD;
ductus arteriosus. This report documentes the reactivity of a patent arterial&#xD;
duct in a one year old infant, 6.5 kg weight during a routine echocardiographic&#xD;
color Doppler study. Echocardiographic images were obtained during&#xD;
conscious sedation.</description>
      <pubDate>Tue, 01 Jan 2008 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://www.um.edu.mt/library/oar/handle/123456789/4125</guid>
      <dc:date>2008-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Unusual echocardiographic finding leading to diagnosis of pulmonary sequestration</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/4124</link>
      <description>Title: Unusual echocardiographic finding leading to diagnosis of pulmonary sequestration
Authors: Baloria, A.; Vinayak, S.; Arora, R.; Mishra, Smita
Abstract: Pulmonary sequestration is an embryonic mass of non- functioning lung tissue that&#xD;
does not communicate with the tracheobronchial tree and has a reported incidence of&#xD;
0.15%-6.4% of all the pulmonary malformations.  This anomaly is classified as either&#xD;
intralobar or extralobar with the later variety lying outside the normal investment of&#xD;
visceral pleura. The arterial supply is predominantly by an anomalous artery usually&#xD;
arising from either abdominal or thoracic aorta, while the venous drainage occurs&#xD;
commonly via systemic rather than pulmonary veins. Identification of the anomalous arterial supply has therapeutic implication because the majority of infants clinically present large shunt lesions attributed to these&#xD;
channels in early infancy.&#xD;
 The diagnosis in such cases is usually established by computed tomography (CT), angiography, magnetic resonance angiography and conventional angiography. This article reports a 28 day old neonate who presented with features of large shunt lesion, in which echocardiography was instrumental in the diagnosis of a large collateral supplying the sequestrated lung.</description>
      <pubDate>Tue, 01 Jan 2008 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://www.um.edu.mt/library/oar/handle/123456789/4124</guid>
      <dc:date>2008-01-01T00:00:00Z</dc:date>
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