Alastair Hutchison

Prof. Alastair Hutchison

orcid

Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 June 2003 in Kidney International
Verified
Journal Article
Closed access
PDPatrick C. D'HAese
Patrick C. D'HAese
GSGoce B. Spasovski
Goce B. Spasovski
ASAleksander Sikole
Aleksander Sikole
AHAlastair Hutchison
Alastair Hutchison
TFTony J. Freemont
Tony J. Freemont
MBMarc E. De Broe
Marc E. De Broe

1 November 1993 in Kidney International
Verified
Journal Article
Closed access
AHAlastair Hutchison
Alastair Hutchison
RWRick W. Whitehouse
Rick W. Whitehouse
HBHelen F. Boulton
Helen F. Boulton
JAJudy E. Adams
Judy E. Adams
EME. Barbara Mawer
E. Barbara Mawer
RGRam Gokal
Ram Gokal

1 November 2005 in Kidney International
Verified
Journal Article
Closed access
PDF file
ASAngela M. Summers
Angela M. Summers
MCMarc J. Clancy
Marc J. Clancy
FSFysal Syed
Fysal Syed
NHNicola Harwood
Nicola Harwood
PBPaul E.C. Brenchley
Paul E.C. Brenchley
RGR.A.M. Gokal
R.A.M. Gokal

1 October 2000 in Kidney International
Verified
Journal Article
Closed access
MPMichael L. Picton
Michael L. Picton
PMPhilip R. Moore
Philip R. Moore
EME. Barbara Mawer
E. Barbara Mawer
DHDavid Houghton
David Houghton
AFAnthony J. Freemont
Anthony J. Freemont
JHJudith A. Hoyland
Judith A. Hoyland

4 April 2005 in Nephron Clinical Practice
Verified
Journal Article
Closed access
PDF file
AHAlastair Hutchison
Alastair Hutchison
BMB. Maes
B. Maes
JVJ. Vanwalleghem
J. Vanwalleghem
GAG. Asmus
G. Asmus
EME. Mohamed
E. Mohamed
AVA. Vosskühler
A. Vosskühler
Background/Aims: Hyperphosphatemia is an important clinical consequence of renal failure, and its multiple adverse systemic effects are associated with significantly increased risks of morbidity and mortality in dialysis patients. Existing oral phosphate binders have not permitted control of serum phosphate within currently accepted guidelines. This study compares lanthanum carbonate with calcium carbonate for control of serum phosphate in hemodialysis patients. Methods: In this European multicentre study, 800 patients were randomised to receive either lanthanum or calcium carbonate and the dose titrated over 5 weeks to achieve control of serum phosphate. Serum levels of phosphate, calcium and parathryoid hormone were followed over the following 20 weeks. Results: Around 65% of patients in each group achieved phosphate control, but in the calcium carbonate group this was at the expense of significant hypercalcemia (20.2% of patients vs. 0.4%). Consequently, calcium x phosphate product tended to be better controlled in the lanthanum group. Conclusion: This 6-month study demonstrates that serum phosphate control with lanthanum carbonate (750–3,000 mg/day) is similar to that seen with calcium carbonate (1,500–9,000 mg/day), but with a significantly reduced incidence of hypercalcemia. Lanthanum carbonate is well tolerated and may be more effective in reducing calcium x phosphate product than calcium carbonate.

1 May 1999 in Kidney International
Verified
Journal Article
Closed access
ACAlfonso M. Cueto-Manzano
Alfonso M. Cueto-Manzano
SKShaikh Konel
Shaikh Konel
AHAlastair Hutchison
Alastair Hutchison
VCVivion Crowley
Vivion Crowley
MFMichael W. France
Michael W. France
RGRam Gokal
Ram Gokal