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多西环素稳定腹主动脉瘤的随机试验。

Doxycycline for stabilization of abdominal aortic aneurysms: a randomized trial.

出版信息

Ann Intern Med. 2013 Dec 17;159(12):815-23. doi: 10.7326/0003-4819-159-12-201312170-00007.

Abstract

BACKGROUND

Doxycycline inhibits formation and progression of abdominal aortic aneurysms (AAAs) in preclinical models of the disease, but it is unclear whether and how this observation translates to humans.

OBJECTIVE

To test whether doxycycline inhibits AAA progression in humans.

DESIGN

Randomized, placebo-controlled, double-blind trial. (Dutch Trial Registry: NTR 1345) SETTING: 14 Dutch hospitals.

PATIENTS

286 patients with small AAAs between October 2008 and June 2011.

INTERVENTION

Daily dose of 100 mg of doxycycline (n = 144) or placebo (n = 142) for 18 months.

MEASUREMENTS

The primary outcome measure was aneurysm growth at 18 months, as estimated by repeated single-observer ultrasonography. Secondary outcomes included growth at 6 and 12 months and the need for elective surgery.

RESULTS

Mean aneurysm diameter (approximately 43 mm) and other baseline characteristics were similar in both groups. Doxycycline treatment was associated with increased aneurysm growth (4.1 mm in the doxycycline group vs. 3.3 mm in the placebo group at 18 months; difference, 0.8 mm [95% CI, 0.1 to 1.4 mm]; P = 0.016 mm). Twenty-one patients receiving doxycycline and 22 patients receiving placebo had elective surgical repair (Kaplan–Meier estimates were 16.1% for those receiving doxycycline and 16.5% for those receiving placebo; difference, -0.4% [CI, -9.3% to 8.5%]; P = 0.83). Time to repair was similar in the groups (P = 0.92).

LIMITATIONS

This study focuses on patients with small AAAs. As such, whether the data can be extrapolated to larger AAAs (>55 mm) is unclear. The high number of elective repairs (n = 43) was unanticipated. Moreover, the study did not follow patients who withdrew because of an adverse effect.

CONCLUSION

This trial found that 18 months of doxycycline therapy did not reduce aneurysm growth and did not influence the need for AAA repair or time to repair.

PRIMARY FUNDING SOURCE

The Netherlands Organisation for Health Research and Development, and the NutsOhra Fund.

摘要

背景

多西环素可抑制临床前模型中腹主动脉瘤(AAA)的形成和进展,但尚不清楚这一观察结果是否以及如何转化为人类。

目的

测试多西环素是否可抑制人类 AAA 的进展。

设计

随机、安慰剂对照、双盲试验。(荷兰试验注册处:NTR 1345)

地点

14 家荷兰医院。

患者

2008 年 10 月至 2011 年 6 月期间患有小 AAA 的 286 名患者。

干预措施

每日剂量为 100mg 多西环素(n=144)或安慰剂(n=142),治疗 18 个月。

测量

主要结局指标为 18 个月时重复单观察者超声估计的动脉瘤生长。次要结局指标包括 6 个月和 12 个月时的生长情况以及择期手术的需要。

结果

两组的平均动脉瘤直径(约 43mm)和其他基线特征相似。多西环素治疗与动脉瘤生长增加相关(多西环素组 18 个月时为 4.1mm,安慰剂组为 3.3mm;差异为 0.8mm[95%CI,0.1 至 1.4mm];P=0.016mm)。21 名接受多西环素治疗的患者和 22 名接受安慰剂治疗的患者进行了择期手术修复(Kaplan-Meier 估计值分别为接受多西环素治疗的患者为 16.1%,接受安慰剂治疗的患者为 16.5%;差异为-0.4%[CI,-9.3%至 8.5%];P=0.83)。两组的修复时间相似(P=0.92)。

局限性

本研究侧重于小 AAA 患者。因此,数据是否可以外推至更大的 AAA(>55mm)尚不清楚。预计会有大量的择期修复(n=43)。此外,该研究未随访因不良反应而退出的患者。

结论

本试验发现,18 个月的多西环素治疗并未减少动脉瘤生长,也未影响 AAA 修复的需要或修复时间。

主要资金来源

荷兰健康研究与发展组织和 NutsOhra 基金。

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