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Lookup NU author(s): Arpit Gupta, Dr Katherine Eastham, Dr David Spencer
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Background: Hypomagnesaemia in patients with cystic fibrosis (CF) is underrecognized although the true incidence is unknown. Many patients are asymptomatic, although severe deficiency may be associated with muscle weakness, cramps and tetany. Hypomagnesaemia may be a risk factor for post-transplant complications including convulsions, which may be exacerbated by the use of calcineurin inhibitors. The aims of the present study were to describe serum magnesium levels and to investigate the relationship between magnesium levels and age, and renal function measurements in patients with CF referred to a transplant centre for lung transplant assessment. Methods: We reviewed the data of all 106 CF patients referred for transplant assessment from January 1995 to December 2003. Demographic and biochemical data were recorded and the explanatory variables were subjected to univariate analysis and linear regression analysis. Results: Mean serum magnesium level was 0.75 mmol/L (range 0.46-1.03, normal range 0.74-1.1). 57% of patients had hypomagnesaemia. Serum magnesium levels were not associated with age, serum creatinine or GFR. Conclusions: Hypomagnesaemia is a common finding in patients with CF referred for lung transplant assessment. Serum magnesium levels should be monitored in all CF patients being referred for lung transplant irrespective of the results of other renal function tests. Published by Elsevier B.V.
Author(s): Gupta A, Eastham KM, Wrightson N, Spencer DA
Publication type: Conference Proceedings (inc. Abstract)
Publication status: Published
Conference Name: 18th Annual North American Cystic Fibrosis Conference
Year of Conference: 2007
Pages: 360-362
ISSN: 1569-1993
Publisher: Journal of Cystic Fibrosis, Elsevier BV
URL: http://dx.doi.org/10.1016/j.jcf.2007.01.004
DOI: 10.1016/j.jcf.2007.01.004
Library holdings: Search Newcastle University Library for this item
ISBN: 18735010
