Böger G I, Hoopmann M, Busse R, Budinger M, Welte T, Böger R H
Arbeitsgruppe Klinische Pharmakologie, Institut für Experimentelle und Klinische Pharmakologie und Toxikologie, Universitätsklinikum Hamburg-Eppendorf, Martinistr. 52, 20246 Hamburg, Germany.
Z Kardiol. 2003 Jun;92(6):466-75. doi: 10.1007/s00392-003-0942-3.
Drug therapy of coronary heart disease (CHD) is a life-long treatment. With every change from in-patient to out-patient care and back, changes in medication may occur. If a drug is chosen which provides no proven long-term benefit in terms of reduced morbidity and mortality, the expected therapeutic benefit may be missed. We investigated in 224 patients admitted to the medical departments of two hospitals (one with a specialized Cardiology Unit, one with a General Internal Medicine Unit) the prescriptions for CHD by the general practitioner before admittance into the hospital, the prescriptions recommended at the time of discharge, and the prescriptions made by the general practitioner three months after discharge. Of the drug classes with proven effects on morbidity and mortality (acetylsalicylic acid, beta-blockers, statins, ACE inhibitors), none had sufficiently high prescription rates. Prescription rates at discharge were 30% for beta-blockers and statins, 70% for acetylsalicylic acid, and 60% for ACE inhibitors. Only in patients with acute myocardial infarction were the prescription rates for these drug classes higher at this time point. The presence of contraindications was not of prime importance for the low prescription rates, as even in patients without contraindications prescription rates were not significantly higher than in the total patient cohort. Out of the patients with hypercholesterolemia, one third of those treated in the Cardiology Department and two thirds of those treated in the General Internal Medicine Department were not given any lipid-lowering medication. Prescription rates for those drug classes that provide symptomatic relief but have little impact on mortality rates (calcium channel blockers, nitrates) were high in both hospitals. The present study shows that evidence-based guidelines for the drug treatment of coronary heart disease are not adequately put into practice.
冠心病(CHD)的药物治疗是一种终身治疗。每次从住院治疗转变为门诊治疗,再变回住院治疗时,用药可能会发生变化。如果选择的药物在降低发病率和死亡率方面未被证明具有长期益处,可能会错过预期的治疗效果。我们调查了两家医院(一家设有专门的心脏病科,一家设有普通内科)内科收治的224例患者,了解他们入院前全科医生开具的冠心病处方、出院时推荐的处方以及出院三个月后全科医生开具的处方。在对发病率和死亡率有已证实疗效的药物类别(乙酰水杨酸、β受体阻滞剂、他汀类药物、ACE抑制剂)中,没有一种药物的处方率足够高。出院时β受体阻滞剂和他汀类药物的处方率为30%,乙酰水杨酸为70%,ACE抑制剂为60%。仅在急性心肌梗死患者中,这些药物类别的处方率在这个时间点更高。禁忌症的存在对于低处方率并非至关重要,因为即使在没有禁忌症的患者中,处方率也没有显著高于整个患者队列。在高胆固醇血症患者中,心脏病科治疗的患者中有三分之一、普通内科治疗的患者中有三分之二未接受任何降脂药物治疗。在两家医院中,那些能缓解症状但对死亡率影响不大的药物类别(钙通道阻滞剂、硝酸盐)的处方率都很高。本研究表明,冠心病药物治疗的循证指南未得到充分实施。