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酒石酸尼古丁液体灌肠剂治疗对一线治疗无反应的轻度至中度活动性左侧溃疡性结肠炎:一项试点研究。

Nicotine tartrate liquid enemas for mildly to moderately active left-sided ulcerative colitis unresponsive to first-line therapy: a pilot study.

作者信息

Sandborn W J, Tremaine W J, Leighton J A, Lawson G M, Zins B J, Compton R F, Mays D C, Lipsky J J, Batts K P, Offord K P, Hurt R D, Green J

机构信息

Inflammatory Bowel Disease Clinic, Mayo Clinic, Rochester, Minnesota 55905, USA.

出版信息

Aliment Pharmacol Ther. 1997 Aug;11(4):663-71. doi: 10.1046/j.1365-2036.1997.00208.x.

Abstract

BACKGROUND

Ulcerative colitis is predominantly a disease of non-smokers, and transdermal nicotine is therapeutic but often results in side-effects. Administration of nicotine as a liquid rectal enema results in less systemic nicotine absorption.

AIM

To determine the safety and clinical response of nicotine tartrate liquid enemas for active left-side ulcerative colitis in a pilot study.

METHODS

Ten non-smoking patients with mildly to moderately active left-sided ulcerative colitis unresponsive to first-line therapy were treated in an open protocol with nightly nicotine tartrate liquid enemas at a dose of 3 mg nicotine base for 1 week then 6 mg for 3 weeks. Clinical assessments were determined at baseline and 4 weeks by endoscopy, physician assessment and a patient diary of daily symptoms. Peak and trough serum nicotine and trough plasma cotinine were determined by gas chromatography/mass spectrometry and high performance liquid chromatography, respectively.

RESULTS

After 4 weeks of treatment, 5/7 patients (71%) showed clinical and sigmoidoscopic improvement (per protocol analysis). The other three patients discontinued therapy within 7 days because of inability to retain the liquid enemas. No patients showed histologic improvement. Six of the patients who completed the 4-week study had peak and trough serum nicotine concentration determined, only 1 of 6 patients had a detectable peak nicotine concentration (value 2.3 ng/mL), and all six patients had undetectable trough nicotine concentrations. The mean trough plasma cotinine concentration was 13 +/- 10 ng/mL. Transient and mild adverse events occurred in 4/10 patients (nausea, lightheadedness, tremor, sleep disturbance). Given the low or undetectable serum nicotine concentrations, these adverse events are not likely to be related to the nicotine enemas.

CONCLUSIONS

Nicotine tartrate liquid enemas administrated at a dose of 3 mg nicotine base/day for 1 week and then 6 mg/day for 3 weeks are safe and appear to result in clinical improvement in some patients with mildly to moderately active, left-sided ulcerative colitis unresponsive to first-line therapy. Placebo-controlled trials are warranted to confirm these preliminary findings.

摘要

背景

溃疡性结肠炎主要是一种非吸烟者的疾病,经皮尼古丁具有治疗作用,但常导致副作用。以液体直肠灌肠剂形式给予尼古丁可减少全身尼古丁吸收。

目的

在一项初步研究中确定酒石酸尼古丁液体灌肠剂治疗活动性左侧溃疡性结肠炎的安全性和临床反应。

方法

10例对一线治疗无反应的轻度至中度活动性左侧溃疡性结肠炎非吸烟患者,采用开放方案,每晚给予酒石酸尼古丁液体灌肠剂,剂量为尼古丁碱3mg,持续1周,然后6mg,持续3周。在基线和4周时通过内镜检查、医生评估和患者每日症状日记进行临床评估。分别通过气相色谱/质谱法和高效液相色谱法测定血清尼古丁的峰浓度和谷浓度以及血浆可替宁的谷浓度。

结果

治疗4周后,5/7例患者(71%)显示临床和乙状结肠镜检查有改善(按方案分析)。另外3例患者因无法保留液体灌肠剂在7天内停止治疗。没有患者显示组织学改善。完成4周研究的6例患者测定了血清尼古丁的峰浓度和谷浓度,6例患者中只有1例有可检测到的尼古丁峰浓度(值为2.3ng/mL),所有6例患者的谷尼古丁浓度均未检测到。血浆可替宁平均谷浓度为13±10ng/mL。4/10例患者发生短暂和轻度不良事件(恶心、头晕、震颤、睡眠障碍)。鉴于血清尼古丁浓度低或无法检测到,这些不良事件不太可能与尼古丁灌肠剂有关。

结论

以尼古丁碱剂量3mg/天给予酒石酸尼古丁液体灌肠剂1周,然后6mg/天给予3周是安全的,并且似乎可使一些对一线治疗无反应的轻度至中度活动性左侧溃疡性结肠炎患者临床症状改善。有必要进行安慰剂对照试验以证实这些初步发现。

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