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接受皮质类固醇治疗的哮喘患者中的骨质疏松症。

Osteoporosis in the corticosteroid-treated patient with asthma.

作者信息

Ledford D, Apter A, Brenner A M, Rubin K, Prestwood K, Frieri M, Lukert B

机构信息

Department of Internal Medicine, University of South Florida, James A. Haley VA Hospital, Tampa 33612, USA.

出版信息

J Allergy Clin Immunol. 1998 Sep;102(3):353-62. doi: 10.1016/s0091-6749(98)70120-4.

Abstract

Osteoporosis affects 40% of white women older than 45 years of age and 15% of white men older than 50 years of age, resulting in approximately 1.5 million annual fractures in the United States. Systemic corticosteroid therapy increases the probability of osteoporosis, even with alternate-day dosing and with dosages sufficiently low so as not to affect the hypothalamic-pituitary-adrenal axis. Inhaled corticosteroid therapy may affect bone density if high-dose therapy is given to select individuals. The potential of increasing osteoporosis with inhaled corticosteroid asthma therapy is a concern because of the availability of more potent inhaled corticosteroid agents and recommendations that inhaled corticosteroid therapy be initiated earlier in the course of asthma. This article provides suggestions, on the basis of the medical literature and consensus of the authors when specific information was not available, for assessing and treating osteoporosis in subjects with asthma. Suggested risk categories are "low risk" (inhaled corticosteroid dosage of < or =800 microg of heclomethasone dipropionate [BDP]/day in adults or < or =400 microg BDP or equivalent in children), "moderate risk" (inhaled BDP >800 microg/day in adults or >400 microg/day in children), and "high risk" (systemic corticosteroid therapy 4 times a year or daily or alternate-day systemic corticosteroid therapy). Dosage of nasal corticosteroid probably should be added to the orally inhaled corticosteroid for total burden of inhaled corticosteroid. Potential treatment strategies based on risk factors and bone density if indicated are offered to assist physicians treating patients with asthma.

摘要

骨质疏松症影响40%的45岁以上白人女性和15%的50岁以上白人男性,在美国每年导致约150万例骨折。全身用皮质类固醇疗法会增加患骨质疏松症的可能性,即使采用隔日给药且剂量足够低以至于不影响下丘脑 - 垂体 - 肾上腺轴。对于某些个体,如果给予高剂量吸入性皮质类固醇疗法,可能会影响骨密度。由于有更强效的吸入性皮质类固醇药物可供使用,且建议在哮喘病程中更早开始吸入性皮质类固醇疗法,因此吸入性皮质类固醇哮喘治疗导致骨质疏松症增加的可能性令人担忧。本文根据医学文献并在缺乏具体信息时基于作者的共识,提供了评估和治疗哮喘患者骨质疏松症的建议。建议的风险类别为“低风险”(成人吸入丙酸倍氯米松[BDP]剂量≤800微克/天或儿童≤400微克BDP或等效剂量)、“中度风险”(成人吸入BDP>800微克/天或儿童>400微克/天)和“高风险”(每年全身用皮质类固醇治疗4次或每日或隔日全身用皮质类固醇治疗)。对于吸入性皮质类固醇的总负担,可能应将鼻用皮质类固醇的剂量加到口服吸入性皮质类固醇中。根据风险因素和骨密度(如适用)提供了潜在的治疗策略,以协助治疗哮喘患者的医生。

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