Songpatanasilp Thawee, Mumtaz Malik, Chhabra Harvinder, Yu Maria, Sorsaburu Sebastian
Phramongkutklao College of Medicine, 315 Ratchavithi Rd, Ratchathavee, Bangkok 10400, Thailand.
Singapore Med J. 2014 Sep;55(9):493-501. doi: 10.11622/smedj.2014120.
We evaluated reduced back pain in a multiethnic population treated with teriparatide and/or antiresorptives in real-life clinical settings over 12 months.
This prospective observational study comprised 562 men and postmenopausal women (mean age 68.8 years) receiving either teriparatide (n = 230), antiresorptives (raloxifene or bisphosphonates; n = 322), or both (n = 10) for severe osteoporosis. The primary endpoint was the relative risk of new/worsening back pain at six months.
At baseline, a higher proportion of teriparatide-treated than antiresorptive-treated patients had severe back pain (30.9% vs. 17.7%), extreme pain/discomfort (25.3% vs. 16.8%), extreme anxiety/depression (16.6% vs. 7.8%) and were confined to bed (10.0% vs. 5.3%). Teriparatide-treated patients had higher visual analog scale (VAS) scores for pain (5.8 ± 2.42 vs. 5.1 ± 2.58) and lower mean European Quality of Life-5 Dimensions (EQ-5D) scores (37.7 ± 29.15 vs. 45.5 ± 31.42) than antiresorptive-treated patients. The incidence of new/worsening back pain at six months for patients on teriparatide and antiresorptives was 9.8% and 10.3% (relative risk 0.99, 95% confidence interval 0.80-1.23), respectively. The incidence of severe back pain at 12 months was 1.3% and 1.6% in the teriparatide and antiresorptive treatment groups, respectively. Teriparatide-treated patients had lower mean VAS (2.71 ± 2.21 vs. 3.30 ± 2.37) and EQ‑5D (46.1 ± 33.18 vs. 55.4 ± 32.65) scores at 12 months. More teriparatide-treated patients felt better (82.7% vs. 71.0%) and were very satisfied with treatment (49.4% vs. 36.8%) compared to antiresorptive-treated patients.
Patients treated with either teriparatide or antiresorptives had similar risk of new/worsening back pain at six months.
我们评估了在现实临床环境中接受特立帕肽和/或抗吸收药物治疗12个月的多民族人群中背痛减轻的情况。
这项前瞻性观察性研究纳入了562名男性和绝经后女性(平均年龄68.8岁),他们因严重骨质疏松症接受特立帕肽治疗(n = 230)、抗吸收药物(雷洛昔芬或双膦酸盐;n = 322)治疗或两者联合治疗(n = 10)。主要终点是6个月时新发/加重背痛的相对风险。
在基线时,接受特立帕肽治疗的患者中,有严重背痛的比例高于接受抗吸收药物治疗的患者(30.9%对17.7%)、极度疼痛/不适(25.3%对16.8%)、极度焦虑/抑郁(16.6%对7.8%),且卧床的比例也更高(10.0%对5.3%)。与接受抗吸收药物治疗的患者相比,接受特立帕肽治疗的患者疼痛的视觉模拟量表(VAS)评分更高(5.8±2.42对5.1±2.58),欧洲生活质量五维度(EQ - 5D)平均得分更低(37.7±29.15对45.5±31.42)。接受特立帕肽和抗吸收药物治疗的患者在6个月时新发/加重背痛的发生率分别为9.8%和10.3%(相对风险0.99,95%置信区间0.80 - 1.23)。在12个月时,特立帕肽和抗吸收药物治疗组中严重背痛的发生率分别为1.3%和1.6%。在12个月时,接受特立帕肽治疗的患者VAS平均得分更低(2.71±2.21对3.30±2.37),EQ - 5D得分也更低(46.1±33.18对55.4±32.65)。与接受抗吸收药物治疗的患者相比,更多接受特立帕肽治疗的患者感觉好转(82.7%对71.0%),并且对治疗非常满意(49.4%对36.8%)。
接受特立帕肽或抗吸收药物治疗的患者在6个月时新发/加重背痛的风险相似。