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一项双盲、安慰剂对照研究,比较原发性痛经患者中吡罗昔康三种单剂量方案与布洛芬的疗效。

A double-blind, placebo-controlled study comparing three single-dose regimens of piroxicam with ibuprofen in patients with primary dysmenorrhea.

作者信息

Pasquale S A, Rathauser R, Dolese H M

机构信息

Department of Obstetrics and Gynecology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, New Brunswick 08903.

出版信息

Am J Med. 1988 May 20;84(5A):30-4. doi: 10.1016/0002-9343(88)90474-3.

Abstract

Sixty-eight women with primary dysmenorrhea were randomly assigned to one of five four-times-daily treatment groups for a minimum of three days and a maximum of five days. Three of the groups received different initial single-daily doses of piroxicam, which were followed on each treatment day with placebo for the second through fourth doses, namely, piroxicam 20 mg daily for five days (piroxicam 20 mg for five days); piroxicam 40 mg on Day 1, followed by piroxicam 20 mg on Days 2 through 5 (piroxicam 40 mg for one day); and piroxicam 40 mg on Days 1 and 2, followed by piroxicam 20 mg on Days 3 through 5 (piroxicam 40 mg for two days). The fourth group received ibuprofen 400 mg four times per day, and the fifth group received placebo four times per day. Patients determined the severity of overall discomfort and pelvic-abdominal pain at baseline and prior to each dose using a four-point numerical scale. Supplemental ibuprofen, 400 mg four times per day, was provided for those patients requiring additional pain relief. Patients also made a global determination of overall relief at the end of the study. At 24 hours, the results revealed that piroxicam 40 mg for two days, piroxicam 20 mg for five days, and ibuprofen provided significantly more relief of overall discomfort compared with placebo (p = 0.003, p = 0.018, and p = 0.026, respectively). All four active treatment groups also experienced significantly more relief of pelvic-abdominal pain compared with placebo: piroxicam 40 mg for two days followed by three days of 20 mg (p = 0.002), piroxicam 40 mg for one day followed by four days of 20 mg (p = 0.023), piroxicam 20 mg for five days (p = 0.012), and ibuprofen (p = 0.011). A significantly smaller percentage of patients treated with piroxicam 40 mg for two days required supplemental medication as compared with those treated with piroxicam 20 mg for five days (p = 0.035) and patients treated with placebo (p = 0.010). A greater amount of overall relief was obtained by patients treated with piroxicam 40 mg for two days compared with patients treated with piroxicam 40 mg for one day (p = 0.041) and placebo-treated patients (p = 0.001). It was concluded that single daily doses of piroxicam 20 mg and 40 mg were as effective as ibuprofen, 400 mg four times per day, for the relief of primary dysmenorrhea.

摘要

68名原发性痛经女性被随机分配到五个每日服药四次的治疗组中的一组,治疗时间最短三天,最长五天。其中三个组接受不同初始单日剂量的吡罗昔康,随后在每个治疗日的第二至第四剂服用安慰剂,即吡罗昔康20毫克每日服用五天(吡罗昔康20毫克服用五天);第1天服用吡罗昔康40毫克,第2至5天服用吡罗昔康20毫克(吡罗昔康40毫克服用一天);第1和2天服用吡罗昔康40毫克,第3至5天服用吡罗昔康20毫克(吡罗昔康40毫克服用两天)。第四组每天服用四次布洛芬400毫克,第五组每天服用四次安慰剂。患者在基线时以及每次服药前使用四点数字量表确定总体不适和盆腔腹痛的严重程度。为那些需要额外止痛的患者提供补充布洛芬,每日四次,每次400毫克。患者在研究结束时还对总体缓解情况进行了综合判定。在24小时时,结果显示,与安慰剂相比,吡罗昔康40毫克服用两天、吡罗昔康20毫克服用五天以及布洛芬在总体不适缓解方面显著更有效(分别为p = 0.003、p = 0.018和p = 0.026)。与安慰剂相比,所有四个活性治疗组在盆腔腹痛缓解方面也显著更有效:吡罗昔康40毫克服用两天后接着三天服用20毫克(p = 0.002),吡罗昔康40毫克服用一天后接着四天服用20毫克(p = 0.023),吡罗昔康20毫克服用五天(p = 0.012),以及布洛芬(p = 0.011)。与服用吡罗昔康20毫克五天的患者(p = 0.035)和服用安慰剂的患者(p = 0.010)相比,服用吡罗昔康40毫克两天的患者中需要补充药物的比例显著更小。与服用吡罗昔康40毫克一天的患者(p = 0.041)和服用安慰剂的患者(p = 0.001)相比,服用吡罗昔康40毫克两天的患者获得了更大程度的总体缓解。得出的结论是,每日单次剂量的吡罗昔康20毫克和40毫克与每日四次服用400毫克布洛芬在缓解原发性痛经方面效果相当。

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