Jagannath Vanitha A, Thaker Vidhu, Chang Anne B, Price Amy I
Department of Paediatrics, American Mission Hospital, Manama, Manama, Bahrain, PO Box 1.
Cochrane Database Syst Rev. 2017 Aug 22;8(8):CD008482. doi: 10.1002/14651858.CD008482.pub5.
Cystic fibrosis is a genetic disorder which can lead to multiorgan dysfunction. Malabsorption of fat and fat-soluble vitamins (A, D, E, K) may occur and can cause subclinical deficiencies of some of these vitamins. Vitamin K is known to play an important role in both blood coagulation and bone formation. Supplementation with vitamin K appears to be one way of addressing the deficiency, but there is very limited agreement on the appropriate dose and frequency of use of these supplements. This is an updated version of the review.
To assess the effects of vitamin K supplementation in people with cystic fibrosis and to determine the optimal dose and route of administration of vitamin K for both routine and therapeutic use.
We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group's Trials Register comprising references identified from comprehensive electronic database searches and handsearches of relevant journals and abstract books of conference proceedings.Most recent search: 30 January 2017.
Randomised and quasi-randomised controlled trials of all preparations of vitamin K used as a supplement compared to either no supplementation (or placebo) at any dose or route and for any duration, in children or adults diagnosed with cystic fibrosis (by sweat test or genetic testing).
Two authors independently screened papers, extracted trial details and assessed their risk of bias.
Two trials (total of 32 participants) each lasting one month were included in the review and were assessed as having a moderate risk of bias. One was a dose-ranging parallel group trial in children (aged 8 to 18 years); and the other (with an older cohort) had a cross-over design comparing supplements to no treatment, but no separate data were reported for the first intervention period. Neither of the trials addressed any of the primary outcomes (coagulation, bone formation and quality of life). Both trials reported the restoration of serum vitamin K and undercarboxylated osteocalcin levels to the normal range after one month of daily supplementation with 1 mg of vitamin K.
AUTHORS' CONCLUSIONS: Evidence from randomised controlled trials on the benefits of routine vitamin K supplementation for people with CF is currently weak and limited to two small trials of short duration. However, no harm was found and until further evidence is available, the present recommendations should be adhered to.
囊性纤维化是一种可导致多器官功能障碍的遗传性疾病。脂肪及脂溶性维生素(A、D、E、K)的吸收不良可能会发生,并可能导致其中一些维生素的亚临床缺乏。已知维生素K在血液凝固和骨骼形成中均发挥重要作用。补充维生素K似乎是解决这种缺乏的一种方法,但对于这些补充剂的合适剂量和使用频率,人们的共识非常有限。这是该综述的更新版本。
评估补充维生素K对囊性纤维化患者的影响,并确定常规和治疗用途中维生素K的最佳剂量和给药途径。
我们检索了Cochrane囊性纤维化和遗传疾病小组的试验注册库,其中包括通过全面电子数据库检索以及对相关期刊和会议论文摘要集进行手工检索而识别出的参考文献。最近一次检索日期为2017年1月30日。
在经汗液试验或基因检测确诊为囊性纤维化的儿童或成人中,将所有用作补充剂的维生素K制剂与未补充(或安慰剂)任何剂量、任何途径且持续任何时长的情况进行比较的随机和半随机对照试验。
两位作者独立筛选论文,提取试验细节并评估其偏倚风险。
该综述纳入了两项试验(共32名参与者),每项试验持续一个月,评估为具有中度偏倚风险。一项是针对儿童(8至18岁)的剂量范围平行组试验;另一项(参与者年龄较大)采用交叉设计,比较补充剂与不治疗的情况,但未报告第一个干预期的单独数据。两项试验均未涉及任何主要结局(凝血、骨骼形成和生活质量)。两项试验均报告,每日补充1毫克维生素K一个月后,血清维生素K和未羧化骨钙素水平恢复到正常范围。
目前,关于常规补充维生素K对囊性纤维化患者益处的随机对照试验证据薄弱,且仅限于两项短期的小型试验。然而,未发现有害影响,在获得进一步证据之前,应遵循当前建议。