Primary Care Cardiovascular Journal (pccj)最新文献

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Give medical therapy a chance 给药物治疗一个机会
Primary Care Cardiovascular Journal (pccj) Pub Date : 1900-01-01 DOI: 10.3132/PCCJ.2009.007
A. Begg
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引用次数: 0
Implementing the NICE guideline for secondary prevention of MI 实施NICE心肌梗死二级预防指南
Primary Care Cardiovascular Journal (pccj) Pub Date : 1900-01-01 DOI: 10.3132/PCCJ.2008.038
J. Skinner
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引用次数: 0
The European perspective 欧洲人的视角
Primary Care Cardiovascular Journal (pccj) Pub Date : 1900-01-01 DOI: 10.3132/PCCJ.2008.018
R. Hobbs
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引用次数: 0
Prasugrel: the evidence supporting NICE’s recommendation for the treatment of acute coronary syndromes (ACS) 普拉格雷:支持NICE推荐治疗急性冠脉综合征(ACS)的证据
Primary Care Cardiovascular Journal (pccj) Pub Date : 1900-01-01 DOI: 10.3132/PCCJ.2010.024
M. Kirby
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引用次数: 0
Rosiglitazone: how should we be using this oral hypoglycaemic drug after studies indicating increased MI risk have resulted in changes in recommendations? 罗格列酮:在研究表明心肌梗死风险增加导致推荐量改变后,我们应该如何使用这种口服降糖药?
Primary Care Cardiovascular Journal (pccj) Pub Date : 1900-01-01 DOI: 10.3132/PCCJ.2008.004
B. Karet
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引用次数: 1
C-reactive protein as a marker of cardiovascular risk. Chicken, egg or turkey? c反应蛋白作为心血管风险的标志。鸡肉、鸡蛋还是火鸡?
Primary Care Cardiovascular Journal (pccj) Pub Date : 1900-01-01 DOI: 10.3132/PCCJ.2008.036
B. Karet
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引用次数: 0
Prescribing for patients with chronic kidney disease 为慢性肾病患者开处方
Primary Care Cardiovascular Journal (pccj) Pub Date : 1900-01-01 DOI: 10.3132/PCCJ.2009.033
M. Kirby
{"title":"Prescribing for patients with chronic kidney disease","authors":"M. Kirby","doi":"10.3132/PCCJ.2009.033","DOIUrl":"https://doi.org/10.3132/PCCJ.2009.033","url":null,"abstract":"clinical response and plasma drug concentration, where measurement is possible. Other important factors that need to be taken into consideration include dehydration, pre-existing heart failure and concomitant drug therapy.2 On the whole, loading doses do not usually need to be adjusted in patients with chronic kidney disease and dose adjustments can be made by reducing the maintenance dose of the drug, less frequent dosing intervals or both. Information in the BNF1 is based on creatinine clearance, because published information on the effects of renal impairment or drug elimination is usually given in terms of creatinine clearance as a surrogate of GFR. However, serum creatinine concentration is unreliable and the creatinine clearance test is now rarely used, having been replaced by the estimated GFR (eGFR). The two measures of renal function are not interchangeable but, in practice, eGFR can be used to determine dosage adjustments in place of creatinine clearance for most drugs and for most patients of average build and height. However, for potentially toxic drugs with a small safety margin and for patients who are very underor overweight, the absolute GFR should be used. This is calculated by multiplying the eGFR by the individual patient’s body surface area/1.73. P atients with renal impairment, particularly when elderly, tolerate drug side-effects less well and, importantly, some drugs are not effective when renal function is reduced. The British National Formulary (BNF) provides some important principles of dose adjustment in renal impairment.1 The level of renal function below which the dose of a drug must be reduced depends on the proportion of the drug eliminated by renal excretion or its toxicity. Not all drugs are toxic and in this case precision in dosing is less important. However, for more toxic drugs, which may have a small safety margin, dose regimens based on glomerular filtration rate (GFR) should be used. When initiating drug treatment in patients with chronic kidney disease (CKD) stage 3A, caution and careful thought are needed rather than dose adjustment, but greater care is needed in CKD stages 3B, 4 and 5. There are situations where both efficacy and toxicity are closely related to plasma drug concentration. In these situations, careful observation is necessary and subsequent doses should be adjusted according to Chronic kidney disease (CKD) affects renal drug elimination and other important processes involved in drug disposition, including absorption, drug distribution and non-renal clearance. As a result, the reduced renal excretion of a drug or its metabolites can cause toxicity and the sensitivity to some drugs is increased even if elimination is unimpaired. THERAPEUTICS REVIEW","PeriodicalId":308856,"journal":{"name":"Primary Care Cardiovascular Journal (pccj)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"133887942","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cardiovascular risk management series: 3 Identifying high-risk patients 心血管风险管理系列:3识别高危患者
Primary Care Cardiovascular Journal (pccj) Pub Date : 1900-01-01 DOI: 10.3132/PCCJ.2009.011
A. Hoes, E. Washbrook, R. Jackson
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引用次数: 0
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