Results 1 to 10 of about 4,482 (205)

A man with hypophosphataemia [PDF]

open access: yesBMJ, 2011
Case report; A section on BMJ, 2011, v.
Kung, AW   +5 more
core   +5 more sources

Understanding and Managing Infusion Reactions and Hypophosphataemia With Intravenous Iron—A Nurses' Consensus Paper [PDF]

open access: yesNursing Open
Aim To provide evidence‐based guidance on practical aspects and potential safety concerns (infusion reactions and hypophosphataemia) related to the use of intravenous iron from a nursing perspective. Design A modified Delphi consensus method.
Aileen Fraser   +5 more
doaj   +2 more sources

Hypophosphataemia risk associated with ferric carboxymaltose in heart failure: A pooled analysis of clinical trials [PDF]

open access: yesESC Heart Failure, 2023
Aims Iron deficiency is a common finding among patients with heart failure (HF) and is associated with adverse outcomes, including decreased quality of life, increased risk of hospitalization, and decreased survival.
Giuseppe MC Rosano   +2 more
doaj   +2 more sources

Treatment-resistant hypophosphataemia after ferric carboxymaltose: expanding the spectrum of 6H syndrome (hypophosphataemia, hyperphosphaturia, hypovitaminosis D, hypocalcaemia, secondary hyperparathyroidism, high fibroblast growth factor-23) [PDF]

open access: yesEuropean Journal of Case Reports in Internal Medicine
Background: Ferric carboxymaltose (FCM) is widely used to treat iron deficiency anaemia (IDA), particularly in patients with gastrointestinal disease who are intolerant of oral iron. While generally well tolerated, FCM is increasingly recognised to cause
Luqmaan Rashid
doaj   +2 more sources

Severe hypercalcaemia and hypophosphataemia with an optimised preterm parenteral nutrition formulation in two epochs of differing phosphate supplementation [PDF]

open access: yesArchives of Disease in Childhood: Fetal and Neonatal Edition, 2017
Objective: To compare in two epochs of differing phosphate provision serum calcium, phosphate, potassium, and sodium concentrations and the frequency of abnormality of these electrolytes and of sepsis in preterm infants who received an optimised higher ...
Susan Stirling, Paul Clarke
exaly   +2 more sources

Benefit of burosumab in adults with X-linked hypophosphataemia (XLH) is maintained with long-term treatment

open access: yesRMD Open, 2023
Objectives To report the impact of continued burosumab treatment on clinical laboratory tests of efficacy, patient-reported outcomes (PROs) and ambulatory function in adults with X-linked hypophosphataemia who continued from a 96-week phase 3 study into ...
Peter Kamenický   +2 more
exaly   +3 more sources

Improvements with burosumab treatment in an early access programme for adults with X-linked hypophosphataemia: A case series of three patients [PDF]

open access: yesBone Reports
X-linked hypophosphataemia (XLH) is a life-long phosphate-wasting disorder that causes skeletal deformities, pain, stiffness, and fatigue and impairs quality of life. Burosumab was approved for use in adults in 2020.
Julia Day   +2 more
doaj   +2 more sources

Hypophosphataemia, fibroblast growth factor 23 and third-generation intravenous iron compounds: a narrative review

open access: yesDrugs in Context, 2021
Third-generation intravenous (i.v.) iron preparations are safe and efficacious and are increasingly used in the treatment of iron-deficiency anaemia.
Xenophon Kassianides, Sunil Bhandari
doaj   +1 more source

Clinical factors associated with severe hypophosphataemia after kidney transplant

open access: yesBMC Nephrology, 2021
Background The mechanism by which hypophosphataemia develops following kidney transplantation remains debated, and limited research is available regarding risk factors. This study aimed to assess the association between recipient and donor variables, and
Maximilian R. Ralston   +3 more
doaj   +1 more source

X-linked hypophosphataemic rickets in children: clinical phenotype, therapeutic strategies, and molecular background

open access: yesEndokrynologia Polska, 2021
INTRODUCTION: X-linked hypophosphataemic rickets (XLHR) is the most common form of hypophosphataemic rickets (HR), which is caused by mutations in the PHEX gene.
Monika Obara-Moszynska   +5 more
doaj   +1 more source

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