移至主內容

Surgery for curvature of the spine in patients with Duchenne muscular dystrophy

Review question

What is the effectiveness and safety of spinal surgery to treat scoliosis in patients with Duchenne muscular dystrophy (DMD)?

Background

Scoliosis, or curvature of the spine, is common in patients with DMD. It is usually progressive, and surgery is often performed to halt its progression, improve cosmetic appearance, facilitate care, preserve upper limb and respiratory function, and hopefully increase life expectancy. We wished to learn whether spinal surgery was better or worse than the alternatives.

Study characteristics

We found no randomized controlled trials.

Key results and quality of the evidence

We found 49 relevant studies, however they were not clinical trials but prospective or retrospective reviews of case series. The quality of evidence was very low because no clinical trial was available. This is an updated review, and an updated search was undertaken in which no new studies were found.

Conclusion

No randomized controlled clinical trials are available to evaluate the effectiveness of scoliosis surgery in patients with DMD. Randomized controlled clinical trials are needed in this group of patients to evaluate the benefits and risks of different surgical treatments.

The evidence is current to 5 January 2015.

背景

Scoliosis in patients with Duchenne muscular dystrophy (DMD) is usually progressive and is treated with surgery. However, it is unclear whether the existing evidence is sufficiently scientifically rigorous to support a recommendation for spinal surgery for most patients with DMD and scoliosis. This is an updated review, and an updated search was undertaken in which no new studies were found for inclusion.

目的

To determine the effectiveness and safety of spinal surgery in patients with DMD with scoliosis. We intended to test whether spinal surgery is effective in increasing survival and improving respiratory function, quality of life, and overall functioning, and whether spinal surgery is associated with severe adverse effects.

搜尋策略

On 16 June 2015 we searched the Cochrane Neuromuscular Disease Group Specialized Register, the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, EMBASE, and CINAHL Plus. We also searched ProQuest Dissertation and Thesis database (January 1980 to June 2015), the National Institutes of Health Clinical Trials Database (6 January 2015), and the WHO International Clinical Trials Registry Platform (17 June 2015), and checked references. We imposed no language restrictions.

選擇標準

We planned to include controlled clinical trials using random or quasi-random allocation of treatment evaluating all forms of spinal surgery for scoliosis in patients with DMD in the review. The control interventions would have been no treatment, non-operative treatment, or a different form of spinal surgery.

資料收集與分析

We used standard methodological procedures expected by The Cochrane Collaboration. Two review authors independently examined the search results and evaluated the study characteristics against inclusion criteria in order to decide which studies to include in the review.

主要結果

Of the 49 relevant studies we found, none met the inclusion criteria for the review because they were not clinical trials, but prospective or retrospective reviews of case series.

作者結論

Since no randomized controlled clinical trials were available to evaluate the effectiveness of scoliosis surgery in patients with DMD, we can make no good evidence-based conclusion to guide clinical practice. Patients with scoliosis should be informed as to the uncertainty of benefits and potential risks of surgery for scoliosis. Randomized controlled trials are needed to investigate the effectiveness of scoliosis surgery, in terms of quality of life, functional status, respiratory function, and life expectancy.

引用文獻
Cheuk DKL, Wong V, Wraige E, Baxter P, Cole A. Surgery for scoliosis in Duchenne muscular dystrophy. Cochrane Database of Systematic Reviews 2015, Issue 10. Art. No.: CD005375. DOI: 10.1002/14651858.CD005375.pub4.

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