Effect of allopurinol on mortality and hospitalisations in chronic heart failure: a retrospective cohort study

被引:114
|
作者
Struthers, AD [1 ]
Donnan, PT
Lindsay, P
McNaughton, D
Broomhall, J
MacDonald, TM
机构
[1] Ninewells Hosp, Dept Clin Pharmacol & Therapeut, Dundee DD1 9SY, Scotland
[2] Ninewells Hosp, Med Monitoring Unit, Dundee DD1 9SY, Scotland
关键词
D O I
10.1136/heart.87.3.229
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To examine whether allopurinol is associated with any alteration in mortality and hospitalisations in patients with chronic heart failure (CHF). This hypothesis is based on previous data that a high urate concentration is independently associated with mortality with a risk ratio of 4.23 in CHF. Design: Retrospective cohort study. Setting: Medicines Monitoring Unit, Ninewells Hospital, Dundee, UK. Patients: 1760 CHF patients divided into four groups: those on no allopurinol, those on long term low dose allopurinol, those on short term low dose allopurinol, and those on long term high dose allopurinol. Main outcome measures: Total mortality, cardiovascular mortality, cardiovascular hospitalisations, cardiovascular mortality or hospitalisations. Results: Long term low dose allopurinol was associated with a significant worsening in mortality over those who never received allopurinol (relative risk 2.04, 95% confidence interval (Cl) 1.48 to 2.81). This may be because low dose allopurinol is insufficient to negate the adverse effect of a high orate concentration. However, long term high dose (greater than or equal to 300 mg/day) allopurinol was associated with a significantly better mortality than longstanding low dose allopurinol (relative risk 0.59, 95% Cl 0.37 to 0.95). This may mean that high dose allopurinol can fully negate the adverse effect of urate and return the mortality to normal. Conclusions: Long term high dose allopurinol may be associated with a better mortality than long term low dose allopurinol in patients with CHF because of a dose related beneficial effect of allopurinol against the well described adverse effect of urate. Further work is required to substantiate or refute this finding.
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收藏
页码:229 / 234
页数:6
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