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接受抑酸药物单独治疗和联合使用双膦酸盐药物的患者的骨折风险。

Fracture risk in patients receiving acid-suppressant medication alone and in combination with bisphosphonates.

机构信息

Utrecht Institute for Pharmaceutical Sciences, Universiteit Utrecht, Utrecht, The Netherlands.

出版信息

Osteoporos Int. 2009 Dec;20(12):1989-98. doi: 10.1007/s00198-009-0891-4. Epub 2009 Mar 31.

DOI:10.1007/s00198-009-0891-4
PMID:19333676
Abstract

SUMMARY

Previous studies have found an association between acid suppressants and fracture risk. We assessed fracture risk in patients taking concomitant acid suppressant and bisphosphonates. Positive associations were observed for any hip and vertebral fracture. The effect size was modest; however, the significance lies in the widespread prescribing of acid suppressants.

INTRODUCTION

Previous studies have found that acid-suppressive medication (ASM) is associated with an increased risk of fracture. Bisphosphonates can cause upper gastrointestinal problems, and patients may be prescribed ASM to minimise these effects.

METHODS

A retrospective cohort study using the GPRD was conducted in patients aged 40 years and older starting proton pump inhibitors (PPI, N = 234,144), H(2) receptor antagonists (H(2)RA, N = 166,798) or bisphosphonates (N = 67,309). Fracture risk in current versus past use of ASM and concomitant use of bisphosphonate plus ASM versus bisphosphonate alone was compared using time-dependent Cox regression.

RESULTS

In the 6 months before initiating bisphosphonate therapy, 20.1% of patients received a PPI and 7.5% an H(2)RA. Current PPI use was associated with an increased risk of any (adjusted relative rate (ARR) 1.15, 95% CI 1.10-1.20), hip (ARR 1.22, 95% CI 1.10-1.37), and vertebral fracture (ARR 1.40, 95% CI 1.11-1.78); and concomitant bisphosphonates and PPIs with an increased risk of any (ARR 1.08, 95% CI 1.01-1.16) and hip fracture (ARR 1.24, 95% CI 1.08-1.42).

CONCLUSIONS

ASM is associated with an increased risk of fracture when taken alone or in combination with bisphosphonates. Given the frequency of coprescription of ASM and bisphosphonates, this issue requires further investigation.

摘要

摘要

先前的研究发现,酸抑制剂与骨折风险之间存在关联。我们评估了同时服用酸抑制剂和双膦酸盐的患者的骨折风险。任何髋部和椎体骨折都与阳性关联有关。虽然作用大小适中,但意义在于酸抑制剂的广泛应用。

引言

先前的研究发现,酸抑制药物(ASM)与骨折风险增加有关。双膦酸盐可能会引起上胃肠道问题,患者可能会被开处方使用 ASM 来最小化这些影响。

方法

使用 GPRD 进行了一项回顾性队列研究,纳入了年龄在 40 岁及以上开始使用质子泵抑制剂(PPI,N=234144)、H2 受体拮抗剂(H2RA,N=166798)或双膦酸盐(N=67309)的患者。使用时间依赖性 Cox 回归比较了当前和过去使用 ASM 以及同时使用双膦酸盐加 ASM 与单独使用双膦酸盐的骨折风险。

结果

在开始双膦酸盐治疗的 6 个月前,20.1%的患者接受了 PPI,7.5%的患者接受了 H2RA。当前 PPI 的使用与任何(调整后的相对风险率(ARR)1.15,95%CI 1.10-1.20)、髋部(ARR 1.22,95%CI 1.10-1.37)和椎体骨折(ARR 1.40,95%CI 1.11-1.78)的风险增加相关;同时使用双膦酸盐和 PPI 与任何(ARR 1.08,95%CI 1.01-1.16)和髋部骨折(ARR 1.24,95%CI 1.08-1.42)的风险增加相关。

结论

当单独使用或与双膦酸盐联合使用时,ASM 与骨折风险增加相关。鉴于 ASM 和双膦酸盐联合使用的频率,这一问题需要进一步调查。

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