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      Necrotising enterocolitis in a newborn infant treated with octreotide for chylous effusion: is octreotide safe?

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      BMJ Case Reports
      BMJ

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          Abstract

          Octreotide is a somatostatin analogue used for treating congenital chylothorax and congenital hyperinsulinism in infants. By increasing splanchnic arteriolar resistance and decreasing gastrointestinal blood flow, octreotide indirectly reduces lymphatic flow in chylous effusions.

          Splanchnic ischaemia following octreotide predisposes infants to necrotising enterocolitis (NEC). Although NEC occurrence in infants treated with octreotide for hyperinsulinaemic hypoglycaemia has been reported widely, its incidence in infants with chylothroax is low. We describe a case of congenital chylothorax in a preterm infant who had poor response to thoracentesis. Although octreotide initiation lead to resolution of chylothorax, he developed NEC. Cessation of octreotide and medical management resulted in rapid resolution of NEC. Since octreotide is generally used as the first-line treatment for chylous effusion, the risk of NEC should be considered, especially when the dosage is increased. Infants on octreotide should be closely observed for early signs and symptoms of NEC to avert surgical emergency.

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          Most cited references21

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              Sirolimus for the treatment of complicated vascular anomalies in children.

              Vascular anomalies comprise a diverse group of diagnoses. While infantile hemangiomas are common, the majority of these conditions are quite rare and have not been widely studied. Some of these lesions, though benign, can impair vital structures, be deforming, or even become life-threatening. Vascular tumors such as kaposiform hemangioendotheliomas (KHE) and complicated vascular malformations have proven particularly difficult to treat.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                BMJ Case Reports
                BMJ Case Rep
                BMJ
                1757-790X
                February 11 2020
                February 2020
                February 11 2020
                February 2020
                : 13
                : 2
                : e232062
                Article
                10.1136/bcr-2019-232062
                bb7c0b1d-9cf1-4e97-b462-6a081d0c9a0c
                © 2020
                History

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