Childhood hypophosphatasia: to treat or not to treat.
Eric T RushPublished in: Orphanet journal of rare diseases (2018)
Asfotase alfa (Strensiq™), is a first-in-class bone-targeted recombinant tissue nonspecific alkaline phosphatase which has shown significant improvements in morbidity and mortality in patients with perinatal and infantile hypophosphatasia. Subsequent research has also shown improvements in morbidity for patients with childhood hypophosphatasia as measured by improvement in rickets, growth, strength, mobility, and quality of life. This enzyme replacement therapy has generally been well-tolerated, with most adverse reactions being mild-to-moderate in nature. The author shares their approach to decisions on commencement of ERT based from experience of managing approximately fifteen patients across the age spectrum. This approach focuses on assessing the severity of five key manifestations of childhood HPP: decreased mobility, pain, rickets, deficits of growth, and fractures.
Keyphrases
- replacement therapy
- smoking cessation
- end stage renal disease
- early life
- chronic kidney disease
- ejection fraction
- childhood cancer
- peritoneal dialysis
- traumatic brain injury
- prognostic factors
- bone mineral density
- cancer therapy
- spinal cord injury
- postmenopausal women
- young adults
- body composition
- patient reported
- bone regeneration
- cell free