Castillo Heidi, Samson-Fang Lisa
Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Dev Med Child Neurol. 2009 Jan;51(1):17-29. doi: 10.1111/j.1469-8749.2008.03222.x.
This systematic review of the effects of bisphosphonate treatment in children with osteogenesis imperfecta was conducted using the American Academy for Cerebral Palsy and Developmental Medicine methodology for developing systematic reviews of treatment interventions (Revision 1.1) 2004. Despite a large body of published literature, there have been only eight studies with a sufficiently high level of internal validity to be truly informative. These studies confirm improvement in bone density. Many, but not all studies, demonstrate reduction in fracture rate and enhanced growth. There has been extremely limited evaluation of broader treatment impacts such as deformity, need for orthopedic surgery, pain, functioning, or quality of life. Short-term side effects were minimal. Which medication and dosing regimen is optimal and how long patients should be treated are unclear. This body of evidence would be strengthened by a larger controlled trial, because many studies lacked adequate power to evaluate stated outcomes. These studies do not address the impacts of bisphosphonates in children with milder forms of osteogenesis imperfecta and severe forms that are not due to mutations in the type I pro-collagen gene (e.g. types VII and VIII). Additional research is needed into treatment of infants. More studies evaluating medication choices, optimal dosing, duration of treatment, post-treatment impacts, and long-term side effects are necessary.
本项关于双膦酸盐治疗成骨不全患儿效果的系统评价,采用了美国脑性瘫痪与发育医学学会制定的治疗干预措施系统评价方法(2004年修订版1.1)。尽管已发表了大量文献,但仅有八项研究具有足够高的内部效度,能够提供真正有价值的信息。这些研究证实骨密度有所改善。许多(但并非所有)研究表明骨折率降低且生长加快。对于诸如畸形、骨科手术需求、疼痛、功能或生活质量等更广泛的治疗影响,评估极为有限。短期副作用极小。哪种药物和给药方案最佳以及患者应接受多长时间的治疗尚不清楚。由于许多研究缺乏足够的效力来评估既定结果,因此开展一项更大规模的对照试验将强化这一证据体系。这些研究未涉及双膦酸盐对症状较轻的成骨不全患儿以及非I型前胶原基因突变所致严重类型(如VII型和VIII型)的影响。需要对婴儿治疗进行更多研究。有必要开展更多研究来评估药物选择、最佳剂量、治疗持续时间、治疗后影响以及长期副作用。