Webb E L, Godfrey J C, Rosenbaum R, Zisblatt M, Vukovich R A, Neiss E S
J Int Med Res. 1984;12(3):147-53. doi: 10.1177/030006058401200303.
The efficacy of a once-daily combination of chlorthalidone 50 mg plus triamterene 50 mg or chlorthalidone 100 mg plus triamterene 100 mg was compared to that of chlorthalidone 50 mg or 100 mg. This double-blind study was carried out in eighty-eight patients over a treatment period of 12 weeks. All patients entered the active medication period of 12 weeks after a placebo run-in period of 3 to 7 days, during which pretibial or malleolar pitting oedema averaging 2 to 4 mm developed. All patients started at the lower doses, i.e. forty-one started on chlorthalidone 50 mg plus triamterene 50 mg and forty-seven started on chlorthalidone 50 mg. The protocol provided for doubling the dose (but not for reducing it thereafter) at any time during the 12-week period when control of oedema was deemed inadequate. Eight of the combination therapy patients and sixteen of those on chlorthalidone required the higher doses. By Week 12, 96% of the chlorthalidone plus triamterene patients and 100% of the chlorthalidone patients had shown a reduction of at least 2 mm in depth of pits, and 92% and 72%, respectively, had complete disappearance of oedema. The decreases in pitting oedema were paralleled by mean weight losses of 2.4 kg and 3.1 kg, respectively, for the combination treatment group and the chlorthalidone group. Average serum potassium levels throughout the 12-week treatment period were 3.70 mEq/L for the patients taking the combination compared to 3.41 mEq/L of those taking chlorthalidone.(ABSTRACT TRUNCATED AT 250 WORDS)
将氯噻酮50毫克加氨苯蝶啶50毫克或氯噻酮100毫克加氨苯蝶啶100毫克每日一次联合用药的疗效与氯噻酮50毫克或100毫克的疗效进行了比较。这项双盲研究在88名患者中进行,治疗期为12周。所有患者在经过3至7天的安慰剂导入期后进入12周的活性药物治疗期,在此期间出现平均2至4毫米的胫前或踝部凹陷性水肿。所有患者均从较低剂量开始,即41名患者开始服用氯噻酮50毫克加氨苯蝶啶50毫克,47名患者开始服用氯噻酮50毫克。方案规定,在12周期间,当认为水肿控制不充分时,可在任何时间将剂量加倍(但此后不得降低)。联合治疗组中有8名患者和服用氯噻酮的患者中有16名需要更高剂量。到第12周时,氯噻酮加氨苯蝶啶组96%的患者和氯噻酮组100%的患者凹陷深度至少减少了2毫米,水肿完全消失的患者分别为92%和72%。联合治疗组和氯噻酮组的凹陷性水肿减轻的同时,平均体重分别减轻了2.4千克和3.1千克。在整个12周治疗期间,服用联合用药的患者平均血清钾水平为3.70毫当量/升,而服用氯噻酮的患者为3.41毫当量/升。(摘要截短至250字)