Ribichini Flavio, Ferrero Valeria, Feola Mauro, Rognoni Andrea, Brunelleschi Sandra, Vacca Giovanni, Vassanelli Corrado
Division of Cardiology of the University of Verona, Verona, Italy.
J Interv Cardiol. 2007 Jun;20(3):209-13. doi: 10.1111/j.1540-8183.2007.00256.x.
Oral treatment with prednisone has demonstrated efficacy in reducing restenosis after percutaneous coronary interventions (PCI). However, administration of steroids at high dose may raise concerns in terms of applicability and tolerability. Monitoring the occurrence of possible side-effects is therefore mandatory.
Secondary effects of oral prednisone in this setting is analyzed. The "expected" secondary effects of the steroid treatment are described, together with the "unexpected" occurrence of likely drug-induced neutropenia observed in patients prescribed prednisone and thienopyridines simultaneously after PCI.
Two-hundred and twenty patients were monitored for the occurrence of side-effects of the prednisone therapy. Twenty-eight patients (14%) had side-effects likely related to the prednisone treatment: gastric pain (4%), increment of arterial pressure needing upgrading of antihypertensive treatment (4%), edema (1.8%), and concomitant infections (1.4%). In three patients (1.4%), agranulocytosis was detected at the time of the routine blood cell count scheduled 4 weeks after PCI in otherwise asymptomatic patients. Neutropenia subsided completely after withdrawal of prednisone and thienopyridine in all cases and the blood cell formula normalized within 3 weeks.
Side-effects of oral prednisone given after PCI to reduce restenosis occur in less than 15% of patients. Complaints are mild and reversible and can be easily managed with adjunctive diuretic and antacid drugs. The occurrence of agranulocytosis after prednisone had never been reported before, but was observed in 1.4% of our patients receiving simultaneously a thienopyridine. To explain such an unusual event we propose the hypothesis of a possible metabolic interaction between prednisone and thienopyridines.
泼尼松口服治疗已证明在经皮冠状动脉介入治疗(PCI)后减少再狭窄方面有效。然而,高剂量使用类固醇可能在适用性和耐受性方面引发担忧。因此,监测可能的副作用的发生是必要的。
分析了泼尼松在这种情况下的次要影响。描述了类固醇治疗的“预期”次要影响,以及在PCI后同时服用泼尼松和噻吩并吡啶的患者中观察到的可能由药物引起的中性粒细胞减少的“意外”发生情况。
对220例患者进行了泼尼松治疗副作用发生情况的监测。28例患者(14%)出现了可能与泼尼松治疗相关的副作用:胃痛(4%)、血压升高需要升级抗高血压治疗(4%)、水肿(1.8%)和并发感染(1.4%)。在3例患者(1.4%)中,在PCI后4周进行的常规血细胞计数时,在其他方面无症状的患者中检测到粒细胞缺乏症。所有病例在停用泼尼松和噻吩并吡啶后中性粒细胞减少完全消退,血细胞计数在3周内恢复正常。
PCI后给予泼尼松口服以减少再狭窄,副作用发生在不到15%的患者中。症状轻微且可逆,可通过辅助使用利尿剂和抗酸药物轻松处理。泼尼松后发生粒细胞缺乏症此前从未有过报道,但在我们同时接受噻吩并吡啶治疗的1.4%的患者中观察到。为了解释这一不寻常事件,我们提出泼尼松和噻吩并吡啶之间可能存在代谢相互作用的假说。