Zoledronic acid (zoledronate) in children with osteogenesis imperfecta (OI)

被引:0
作者
Maria Sanchez-Sanchez, Luz [1 ]
Uriel Cabrera-Pedroza, Alfredo [1 ]
Palacios-Saucedo, Gerardo [1 ]
机构
[1] Ctr Med Nacl Noreste, Serv Pediat, UMAE 25, Monterrey, NL, Mexico
来源
GACETA MEDICA DE MEXICO | 2015年 / 151卷 / 02期
关键词
Osteogenesis imperfecta; Zoledronic acid; Zoledronate; OLPADRONATE; BISPHOSPHONATES;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Zoledronic acid or zoledronate is a potent bisphosphonate that recently has been used in children with osteoporosis and osteogenesis imperfecta (OI), so it could be an option in the treatment of children with this terrible disease that virtually condemns them to a life of pain and prostration. The aim of this study was to evaluate the clinical and biochemical conditions of pediatric patients with OI before and after treatment with zoledronate. Results: We included 14 patients, median age six years (6 months to 14 years), eight (57.1%) males and six (42.9%) females, weight 19 kg (5.8-45 kg). According to the type of OI, six (42.9%) were type I, six (42.9%) type III, and two (14.2%) type IV. The functional score (Bleck) previous to treatment was 4 (1-9) and 6 (2-9) after treatment (p = 0.001). Pain intensity prior to zoledronate was 2 (1-9) and 0 (0-2) after (p = 0.008). Previous fractures five (1-15) and post-treatment one (0-2) (p = 0.001). There were no significant differences in calcium, phosphorus, alkaline phosphatase, and parathyroid hormone. Conclusions: Zoledronic acid decreases the number of bone fractures and pain in children with osteogenesis imperfecta and improves functional status. The most common side effects were fever and bone pain within five days after the infusion, which disappear with paracetamol. No adverse long-term effects such as hypocalcemia or hypoparathyroidism were reported.
引用
收藏
页码:164 / 168
页数:5
相关论文
共 25 条
  • [1] Biphosphonates
    Allgrove, J
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1997, 76 (01) : 73 - 75
  • [2] Almeida M, 2010, J ORTHOPAED TRAUMATO, V11, P7
  • [3] Osteogenesis imperfecta: Practical treatment guidelines
    Antoniazzi F.
    Mottes M.
    Fraschini P.
    Brunelli P.C.
    Tatò L.
    [J]. Paediatric Drugs, 2000, 2 (6): : 465 - 488
  • [4] BLECK EE, 1981, CLIN ORTHOP RELAT R, P111
  • [5] Brown JJ, 2009, J PEDIATR ENDOCR MET, V22, P55
  • [6] Osteogenesis Imperfecta: Update on presentation and management
    Cheung, Moira S.
    Glorieux, Francis H.
    [J]. REVIEWS IN ENDOCRINE & METABOLIC DISORDERS, 2008, 9 (02) : 153 - 160
  • [7] BONE-MINERAL CONTENT AND DENSITY IN HEALTHY-SUBJECTS AND IN OSTEOGENESIS IMPERFECTA
    DAVIE, MWJ
    HADDAWAY, MJ
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1994, 70 (04) : 331 - 334
  • [8] Osteogenesis imperfecta in childhood: Treatment strategies
    Engelbert, RHH
    Pruijs, HEH
    Beemer, FA
    Helders, PJM
    [J]. ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION, 1998, 79 (12): : 1590 - 1594
  • [9] Surgical treatment of osteogenesis imperfecta: current concepts
    Esposito, Paul
    Plotkin, Horacio
    [J]. CURRENT OPINION IN PEDIATRICS, 2008, 20 (01) : 52 - 57
  • [10] Treatment of osteogenesis imperfecta: Who, why, what?
    Glorieux, Francis H.
    [J]. HORMONE RESEARCH, 2007, 68 : 8 - 11