Abstract:A high rate of bleeding control was achieved with octreotide during acute gastrointestinal bleeding in children with portal hypertension. However, controlled studies are needed for more definitive description of its clinical effects. The role of octreotide is less clear in gastrointestinal bleeding unrelated to portal hypertension.
“…Although octreotide is not labeled for use in children, case reports, case series, and cohort studies document the use of octreotide in children for several indications, including pancreatitis, chylothorax, and gastrointestinal bleeding [10–19]. In infants, the most common indication is treatment of congenital chylothorax, chylothorax secondary to thoracic surgery, congenital hyperinsulinism, and gastrointestinal bleeding [12–14].…”
Background
Octreotide is used off-label in infants for treatment of chylothorax, congenital hyperinsulinism, and gastrointestinal bleeding. The safety profile octreotide in hospitalized infants has not been described; we sought to fill this information gap.
Methods
We identified all infants exposed to at least 1 dose of octreotide from a cohort of 887,855 infants discharged from 333 neonatal intensive care units managed by the Pediatrix Medical Group between 1997 and 2012. We collected laboratory and clinical information while infants were exposed to octreotide and described the frequency of baseline diagnoses, laboratory abnormalities, and adverse events (AEs).
Results
A total of 428 infants received 490 courses of octreotide. The diagnoses most commonly associated with octreotide use were chylothorax (50%), pleural effusion (32%), and hypoglycemia (22%). The most common laboratory AEs that occurred during exposure to octreotide were thrombocytopenia (47/1000 infant-days), hyperkalemia (21/1000 infant-days), and leukocytosis (20/1000 infant-days). Hyperglycemia occurred in 1/1000 infant-days and hypoglycemia in 3/1000 infant-days. Hypotension requiring pressors (12%) was the most common clinical AE that occurred during exposure to octreotide. Necrotizing enterocolitis was observed in 9/490 (2%) courses, and death occurred in 11 (3%) infants during octreotide administration.
Conclusion
Relatively few AEs occurred during off-label use of octreotide in this cohort of infants. Additional studies are needed to further evaluate the safety, dosing, and efficacy of this medication in infants.
“…Although octreotide is not labeled for use in children, case reports, case series, and cohort studies document the use of octreotide in children for several indications, including pancreatitis, chylothorax, and gastrointestinal bleeding [10–19]. In infants, the most common indication is treatment of congenital chylothorax, chylothorax secondary to thoracic surgery, congenital hyperinsulinism, and gastrointestinal bleeding [12–14].…”
Background
Octreotide is used off-label in infants for treatment of chylothorax, congenital hyperinsulinism, and gastrointestinal bleeding. The safety profile octreotide in hospitalized infants has not been described; we sought to fill this information gap.
Methods
We identified all infants exposed to at least 1 dose of octreotide from a cohort of 887,855 infants discharged from 333 neonatal intensive care units managed by the Pediatrix Medical Group between 1997 and 2012. We collected laboratory and clinical information while infants were exposed to octreotide and described the frequency of baseline diagnoses, laboratory abnormalities, and adverse events (AEs).
Results
A total of 428 infants received 490 courses of octreotide. The diagnoses most commonly associated with octreotide use were chylothorax (50%), pleural effusion (32%), and hypoglycemia (22%). The most common laboratory AEs that occurred during exposure to octreotide were thrombocytopenia (47/1000 infant-days), hyperkalemia (21/1000 infant-days), and leukocytosis (20/1000 infant-days). Hyperglycemia occurred in 1/1000 infant-days and hypoglycemia in 3/1000 infant-days. Hypotension requiring pressors (12%) was the most common clinical AE that occurred during exposure to octreotide. Necrotizing enterocolitis was observed in 9/490 (2%) courses, and death occurred in 11 (3%) infants during octreotide administration.
Conclusion
Relatively few AEs occurred during off-label use of octreotide in this cohort of infants. Additional studies are needed to further evaluate the safety, dosing, and efficacy of this medication in infants.
“…No larger series but numerous case reports have been published so far 17 18. In paediatric liver disease with portal hypertension leading to acute haemorrhage, however, octreotide treatment was shown to be safe and effective 8 19. In infants, adrenal suppression and growth retardation were described, but followed by catch-up growth 8…”
“…Eroglu and colleagues have reported a response rate of 50% to octreotide in gastrointestinal bleeding in patients without portal hypertension. However, effectiveness was particularly true for patients where the bleeding source was a discrete ulcer or a procedure site [9]. Octreotide has been shown to reduce splanchnic circulation as one of the suggested mechanism to treat GI bleed.…”
Section: Discussionmentioning
confidence: 99%
“…Gastrointestinal bleeding was the leading cause of hemorrhage (46.9%), followed by hemorrhagic cystitis (31.8%) and diffuse alveolar hemorrhage (13.3%).Response in terms of cessation or significant reduction of bleeding was observed in the majority of patients (69/ 113, 61.1%) [8]. Eroglu has reported a response rate of 50% to octreotide in gastrointestinal bleeding in patients without portal hypertension [9]. We present a 10 month-old female child, who had three episodes of life threatening lower GI bleeding post unrelated UCBT controlled successfully each time by use of rFVIIa and octreotide infusion and review of literature.…”
Post hematopoietic stem cell transplantation (HSCT) gastrointestinal (GI) bleeding is a dreaded complication. There are only five other reports (one randomised trial and four case reports) of use of rFVIIa for massive lower GI bleeding post-allogeneic HSCT. In only one publication, two adult patients showed complete response. Eroglu has reported a response rate of 50% to octreotide in gastrointestinal bleeding in patients without portal hypertension. We present a 10 month-old female child, who had three episodes of life threatening lower GI bleeding post unrelated Umbilical Stem Cell Transplant (UCBT) controlled successfully each time by use of rFVIIa and octreotide infusion and review of literature. To our knowledge this is the first and youngest case reported, in which both rFVIIa and octreotide have been used successfully to control life threatening lower GI bleeding post UCBT.
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