Hunyor S N
Aust N Z J Med. 1975 Dec;5(6):530-6. doi: 10.1111/j.1445-5994.1975.tb03857.x.
In 30 refractory hypertensives a hydrallazine beta blocker combination was added to or substituted for previous antihypertensives. Over a mean period of 12 months a good or satisfactory blood pressure response resulted in 12 patients each, while six others had an unsatisfactory outcome. (Good = diastolic pressure (DP) less than 95 mmHg; Satisfactory = deltaDP greater than 15 mmHg or DP 95-105 mmHg; Unsatisfactory = DP greater than 105 mmHg or deltaDP less than 15mmHg.) Twelve of the patients had significant renal disease with serum creatinine greater than 2 mg/100 ml, but in these there was no evidence that renal hydrallazine retention potentiated an antihypertensive effect. Those with an unsatisfactory response were receiving slightly higher doses hydrallazine and propranol when compared with good responders. The average dose of hydrallazine was 258 mg/day and of propranolol 308 mg/day. Transient headache was not uncommon at the commencement of hydrallazine therapy. Angina and vertebro-basilar insufficiency were each aggravated in one patient, but resolved with dosage adjustment. A lupuslike rash developed in one patient, a slow acetylator on 300 mg hydrallazine/day who had received a total of 92 g over eleven months. The genetically determined acetylator phenotype was assessed in 75 subjects. A little over one third were found to be rapid acetylators. Those with slow acetylator phenotype did not show a more favourable phenotype did not show a more favourable blood-pressure response to equivalent doses of hydrallazine.
在30例顽固性高血压患者中,将肼屈嗪与β受体阻滞剂联合使用或用其替代先前使用的抗高血压药物。在平均12个月的时间里,12例患者血压反应良好或令人满意,另有12例患者血压反应同样令人满意,而其余6例患者的治疗效果不理想。(良好=舒张压(DP)低于95 mmHg;满意=舒张压下降幅度(ΔDP)大于15 mmHg或DP为95 - 105 mmHg;不满意=DP大于105 mmHg或ΔDP小于15 mmHg。)12例患者患有严重肾病,血清肌酐大于2 mg/100 ml,但在这些患者中,没有证据表明肾内肼屈嗪潴留会增强抗高血压作用。与反应良好的患者相比,治疗效果不理想的患者服用的肼屈嗪和普萘洛尔剂量略高。肼屈嗪的平均剂量为258 mg/天,普萘洛尔为308 mg/天。在开始使用肼屈嗪治疗时,短暂性头痛并不少见。1例患者的心绞痛和椎基底动脉供血不足均加重,但通过调整剂量得到缓解。1例患者出现狼疮样皮疹,该患者为慢乙酰化者,每天服用300 mg肼屈嗪,在11个月内共服用了92 g。对75名受试者的乙酰化表型进行了基因测定。发现略超过三分之一的人是快乙酰化者。慢乙酰化表型的患者对同等剂量的肼屈嗪并未表现出更有利的血压反应。