Literature DB >> 2185966

Long-term treatment with the somatostatin analogue SMS 201-995: alternative to pancreatectomy in persistent hyperinsulinaemic hypoglycaemia of infancy.

B Glaser1, H Landaw.   

Abstract

Nine patients with persistent hyperinsulinaemic hypoglycaemia of infancy (PHHI), aged 3 days to 11 months, received octreotide therapy at a dose of 5-10 micrograms s.c. every 4-8 h according to glucose response. The response to octreotide was variable and unpredictable. Two patients could not be weaned off intravenous glucose and 2 others could be weaned off but required continuous nasogastric feedings. In the remaining 5 patients relatively normal feeding schedules were instituted. Long-term ambulatory treatment is an attractive alternative to surgery in such patients if the family can cope with the injections and dietary regimens. Although octreotide suppresses growth hormone secretion, all patients continue to grow during octreotide treatment.

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Year:  1990        PMID: 2185966     DOI: 10.1159/000200258

Source DB:  PubMed          Journal:  Digestion        ISSN: 0012-2823            Impact factor:   3.216


  8 in total

Review 1.  Management strategies for neonatal hypoglycemia.

Authors:  Courtney B Sweet; Stephanie Grayson; Mark Polak
Journal:  J Pediatr Pharmacol Ther       Date:  2013-07

2.  Different neurologic outcomes in two patients with neonatal hyperinsulinemic hypoglycemia.

Authors:  E Zammarchi; L Filippi; C Fonda; P A Benedetti; D Pistone; M A Donati
Journal:  Childs Nerv Syst       Date:  1996-07       Impact factor: 1.475

Review 3.  Clinical use of the long acting somatostatin analogue octreotide in pediatrics.

Authors:  M T Tauber; A G Harris; P Rochiccioli
Journal:  Eur J Pediatr       Date:  1994-05       Impact factor: 3.183

4.  Surgical treatment of hyperinsulinaemic hypoglycaemia in infancy and childhood.

Authors:  L Spitz; R K Bhargava; D B Grant; J V Leonard
Journal:  Arch Dis Child       Date:  1992-02       Impact factor: 3.791

5.  Conservatively treated Congenital Hyperinsulinism (CHI) due to K-ATP channel gene mutations: reducing severity over time.

Authors:  Maria Salomon-Estebanez; Sarah E Flanagan; Sian Ellard; Lindsey Rigby; Louise Bowden; Zainab Mohamed; Jacqueline Nicholson; Mars Skae; Caroline Hall; Ross Craigie; Raja Padidela; Nuala Murphy; Tabitha Randell; Karen E Cosgrove; Mark J Dunne; Indraneel Banerjee
Journal:  Orphanet J Rare Dis       Date:  2016-12-01       Impact factor: 4.123

6.  Treatment with long-acting lanreotide autogel in early infancy in patients with severe neonatal hyperinsulinism.

Authors:  Heike Corda; Sebastian Kummer; Alena Welters; Norbert Teig; Dirk Klee; Ertan Mayatepek; Thomas Meissner
Journal:  Orphanet J Rare Dis       Date:  2017-06-02       Impact factor: 4.123

Review 7.  Somatostatin analogues for the treatment of hyperinsulinaemic hypoglycaemia.

Authors:  Basma Haris; Saras Saraswathi; Khalid Hussain
Journal:  Ther Adv Endocrinol Metab       Date:  2020-12-02       Impact factor: 3.565

Review 8.  Somatostatin receptors in congenital hyperinsulinism: Biology to bedside.

Authors:  Mirjam E van Albada; Klaus Mohnike; Mark J Dunne; Indi Banerjee; Stephen F Betz
Journal:  Front Endocrinol (Lausanne)       Date:  2022-09-27       Impact factor: 6.055

  8 in total

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