Journal of pediatric endocrinology & metabolism : JPEM · 2022
Continuous glucose monitoring in an infant with panhypopituitarism having hypoglycemia on growth hormone therapy.
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Kiuchi Kaho, Sato Takeshi, Nakano Satsuki, Ishii Tomohiro, Hasegawa Tomonobu
Аннотация
OBJECTIVES: The usefulness of continuous glucose monitoring (CGM) in infants with panhypopituitarism (PH) having hypoglycemia is yet to be explored. The potential adverse effects of growth hormone (GH) replacement therapy, such as hyperglycemia, cannot be comprehensively evaluated using the conventional measurement.
CASE PRESENTATION: A 2-month-old infant with PH, including severe GH deficiency, had hypoglycemia despite frequent feeding. Glucose levels were monitored using CGM before and after GH replacement therapy. The proportion of time for hypoglycemia decreased from 4.9 to 0% (p<0.017). Hyperglycemia did not increase. The CGM method did not contribute to any adverse events requiring intervention. Our patient only experienced minor bleeding and no episode of cellulitis.
CONCLUSIONS: CGM is useful in controlling glucose levels in infants with hypoglycemia and PH.
CASE PRESENTATION: A 2-month-old infant with PH, including severe GH deficiency, had hypoglycemia despite frequent feeding. Glucose levels were monitored using CGM before and after GH replacement therapy. The proportion of time for hypoglycemia decreased from 4.9 to 0% (p<0.017). Hyperglycemia did not increase. The CGM method did not contribute to any adverse events requiring intervention. Our patient only experienced minor bleeding and no episode of cellulitis.
CONCLUSIONS: CGM is useful in controlling glucose levels in infants with hypoglycemia and PH.