Lewis R V, McDevitt D G
Med Toxicol. 1986 Sep-Oct;1(5):343-61. doi: 10.1007/BF03259848.
beta-Blocking drugs are widely used throughout the world and serious adverse reactions are relatively uncommon. Most of those which do occur are pharmacologically predictable and may be avoided by ensuring that patients who are to be given beta-blockers do not have a predisposition to the development of bronchospasm, cardiac failure or peripheral ischaemia. In some situations, the use of a beta 1-selective blocking drug may reduce the risk of a severe adverse reaction, but there is little evidence that other ancillary properties such as partial agonist activity are of relevance in this context. Long term experience with many of the beta-blockers in current use suggests that unpredictable major adverse reactions such as the practolol oculomucocutaneous syndrome are unlikely to be repeated, although some of these drugs may be associated with immunological disturbances and some have been implicated in the development of retroperitoneal fibrosis. beta-Blocking drugs appear to be associated with a number of subjective side effects including muscle fatigue, peripheral coldness and some neurological symptoms. These side effects are highly subjective and are therefore difficult to quantify and it is not known whether they are of major importance in terms of their effect upon patients' overall well-being. It cannot be assumed that simply because such side effects can be elicited that they do, in fact, matter. However, because beta-blockers are often prescribed for patients who have no symptoms and for whom the benefits of therapy are generally small, such side effects would be of considerable importance if they had an overall effect upon quality of life. There are theoretical reasons to suppose that the incidence and severity of such side effects may be related to the ancillary properties of the individual drugs, but there is little evidence that parameters such as beta 1-selectivity, or partial agonist activity are clinically important determinants of the severity of these side effects. Lipophilicity, however, may be associated with an increased incidence of neurological symptoms. beta-Blocking drugs may cause a variety of metabolic disturbances including an increase in serum VLDL-cholesterol concentrations. However, long term studies have not shown that such disturbances are associated with an increased risk of cardiovascular disease, indicating that such metabolic changes may not be of major importance in practice. beta-Blocking drugs may be involved in a number of interactions with other drugs, but few of these have been shown to be of clinical significance.(ABSTRACT TRUNCATED AT 400 WORDS)
β受体阻滞剂在世界各地广泛使用,严重不良反应相对少见。确实发生的大多数不良反应在药理学上是可预测的,通过确保接受β受体阻滞剂治疗的患者没有支气管痉挛、心力衰竭或外周缺血的易患倾向,这些不良反应是可以避免的。在某些情况下,使用β1选择性阻断药物可能会降低严重不良反应的风险,但几乎没有证据表明其他辅助特性,如部分激动剂活性,在这种情况下具有相关性。目前使用的许多β受体阻滞剂的长期经验表明,像心得宁眼-粘膜-皮肤综合征这样不可预测的严重不良反应不太可能再次出现,尽管其中一些药物可能与免疫紊乱有关,并且一些药物与腹膜后纤维化的发生有关。β受体阻滞剂似乎与一些主观副作用有关,包括肌肉疲劳、外周发冷和一些神经症状。这些副作用主观性很强,因此难以量化,而且不知道它们对患者整体健康状况的影响是否至关重要。不能仅仅因为能引发这些副作用就认为它们实际上很重要。然而,由于β受体阻滞剂经常被开给没有症状且治疗益处通常较小的患者,如果这些副作用对生活质量有总体影响,那么它们就会相当重要。有理论依据推测这些副作用的发生率和严重程度可能与个别药物的辅助特性有关,但几乎没有证据表明β1选择性或部分激动剂活性等参数是这些副作用严重程度的临床重要决定因素。然而,亲脂性可能与神经症状发生率增加有关。β受体阻滞剂可能会引起多种代谢紊乱,包括血清极低密度脂蛋白胆固醇浓度升高。然而,长期研究并未表明这些紊乱与心血管疾病风险增加有关,这表明这种代谢变化在实际中可能并不重要。β受体阻滞剂可能与其他药物发生多种相互作用,但其中很少有被证明具有临床意义的。(摘要截选至400字)