Josse R G
University of Toronto.
CMAJ. 1996 Oct 1;155(7):929-34.
To present recent evidence on the use of ovarian hormone therapy (OHT) for osteoporosis and outline safe and effective regimens.
Estrogen alone, estrogen and progestins, progestins alone; various treatment regimens.
Fracture and loss of bone mineral density in osteoporosis; increased bone mass, prevention of fractures and improved quality of life associated with OHT.
Relevant clinical studies and reports, including the Nurses' Health Study and the Post-menopausal Estrogen/Progestin Interventions (PEPI) Trial, were studied with emphasis on recent prospective, randomized, controlled trials. Current clinical practice was determined by survey.
Reducing fractures, increasing bone mineral density and minimizing side effects of treatment were given a high value.
BENEFITS, HARMS AND COSTS: Proper management of osteoporosis minimizes injury and disability, improves quality of life and reduces the personal and social costs associated with the condition. OHT is the front-line pharmaceutical therapy for prevention and treatment of osteoporosis in post-menopausal women. In those who are able and willing to comply with therapy, OHT prevents bone loss and fractures. Hormone therapy may also decrease risk of coronary artery disease. Cyclic progestin protects against endometrial cancer in patients receiving estrogen. Potential harms include breast cancer and endometrial cancer related to dosage and duration of therapy. Mastalgia and especially resumption of menstrual bleeding affect compliance.
Use of OHT should be considered as early as possible in the perimenopausal period for women at increased risk of osteoporosis. Guidelines are provided for assessment of osteoporosis risk. Physicians and their patients should take into account the absolute and relative contraindications to OHT. Women with a uterus should be given estrogen in combination with a progestin. Ideally, therapy would be continued for a minimum of 10 years beyond menopause for maximum bone protection. Women using OHT should be carefully monitored and evaluated for possible adverse events. This should include regular screening mammography, breast examination and, for some, endometrial surveillance. Specific dosages and treatment regimens are outlined.
介绍卵巢激素疗法(OHT)用于治疗骨质疏松症的最新证据,并概述安全有效的治疗方案。
单独使用雌激素、雌激素与孕激素联合使用、单独使用孕激素;各种治疗方案。
骨质疏松症患者的骨折情况及骨矿物质密度降低情况;OHT相关的骨量增加、骨折预防及生活质量改善。
对相关临床研究和报告进行了研究,包括护士健康研究和绝经后雌激素/孕激素干预(PEPI)试验,重点关注近期的前瞻性、随机、对照试验。通过调查确定当前临床实践。
高度重视减少骨折、增加骨矿物质密度以及将治疗副作用降至最低。
益处、危害和成本:对骨质疏松症进行适当管理可将损伤和残疾降至最低,改善生活质量,并降低与该疾病相关的个人和社会成本。OHT是绝经后女性预防和治疗骨质疏松症的一线药物治疗方法。对于有能力且愿意遵医嘱治疗的患者,OHT可预防骨质流失和骨折。激素疗法还可能降低冠状动脉疾病的风险。周期性孕激素可预防接受雌激素治疗患者的子宫内膜癌。潜在危害包括与治疗剂量和持续时间相关的乳腺癌和子宫内膜癌。乳房疼痛,尤其是月经出血的恢复会影响治疗依从性。
对于骨质疏松症风险增加的女性,应在围绝经期尽早考虑使用OHT。提供了评估骨质疏松症风险的指南。医生及其患者应考虑OHT的绝对和相对禁忌症。有子宫的女性应给予雌激素与孕激素联合使用。理想情况下,治疗应在绝经后至少持续10年,以实现最大程度的骨骼保护。使用OHT的女性应接受仔细监测和评估,以发现可能的不良事件。这应包括定期进行乳房钼靶筛查、乳房检查,对部分患者还应进行子宫内膜监测。概述了具体的剂量和治疗方案。