MLB Medical College Campus Jhansi India.
Pain Physician. 2020 Sep;23(5):E517-E524.
Epidural steroid injection (ESI) is widely used to manage low back pain. ESIs are commonly performed to treat pain accompanying intervertebral disc prolapse, spinal stenosis, facet joint pathologies, and other degenerative spinal pathologies. Corticosteroids for musculoskeletal conditions, regardless of the route of administration, can reduce bone mineral density (BMD) and increase the risk of fracture. With paraspinal administration of steroids, the severity of risk is enhanced as the steroid is being deposited in close proximity to bone. BMD and molecular markers of bone metabolism are the standard methods to assess the effect of any insult on bone strength and bone metabolism. Carboxy terminal crosslinked telopeptides of type 1 collagen (sCTX) and serum Procollagen Type I N-terminal propeptide (P1NP) are the reference markers of bone resorption and formation, respectively.
We conducted this study to determine the effect of ESI on BMD and bone turnover markers.
This was a prospective observational cohort study, involving a cohort of 264 patients between the ages of 40 to 60 years who were advised to undergo ESI at L3-4 or L4-5 by their pain physician.
Research was conducted at a tertiary care teaching hospital pain clinic in collaboration with the department of orthopaedics and radiodiagnosis.
Serum CTX-1, P1NP, and pre-ESI BMD of the spine, femur neck, and dual femur were evaluated at baseline; these same parameters were serially evaluated post ESI on follow-ups at 1, 3, and 6 months. Additional follow-up at 10 days post ESI was called for evaluation of bone turnover markers (BTMs). A paired t test was used to analyze changes in BMD and BTMs vs baseline within the group. Cumulative incidence and relative risk of moderate to markedly low BMD were calculated using standard formulas. Any fractures sustained during follow-ups were also evaluated thoroughly and quantified separately. A P value less than .05 was considered statistically significant.
The proportion of pre-ESI moderately to markedly low BMD was 10.22% in the study population. There was a statistically significant increase in serum CTX 10 days post ESI which persisted at the one-month and 3-month follow-ups. There was no significant change in serum P1NP level post ESI after 7 days and at the one-month follow-up. The mean value of serum P1NP was, however, significantly higher at the 3-month follow-up. Statistical comparison of the mean BMD value at the spine and femur neck revealed statistically significant decline 3 months post ESI. There was no significant impact of ESI on the total femur BMD. The cumulative incidence of moderately low to markedly low BMD over a period of 6 months in the study population was 45 out of 223, i.e., 20.17%.
The study's primary limitations included its high dropout rate, a larger reference range for BTMs, making them a less specific tool for comparison, and the absence of a control group. ESI has a negative impact on the BMD of the hip and spine. Reduced BMD should be considered as a potential side effect of ESI.
硬膜外类固醇注射(ESI)被广泛用于治疗腰痛。ESIs 通常用于治疗椎间盘突出、椎管狭窄、小关节病变和其他退行性脊柱病变引起的疼痛。无论给药途径如何,皮质类固醇治疗肌肉骨骼疾病都会降低骨密度(BMD)并增加骨折风险。由于类固醇被沉积在靠近骨骼的地方,因此在脊柱旁给予类固醇时,风险的严重程度会增强。BMD 和骨代谢的分子标志物是评估任何损伤对骨强度和骨代谢影响的标准方法。I 型胶原羧基末端交联肽(sCTX)和血清 I 型前胶原 N 端前肽(P1NP)分别是骨吸收和形成的参考标志物。
我们进行这项研究是为了确定 ESI 对 BMD 和骨转换标志物的影响。
这是一项前瞻性观察性队列研究,涉及年龄在 40 至 60 岁之间的 264 名患者,他们的疼痛医生建议在 L3-4 或 L4-5 处进行 ESI。
在一家三级护理教学医院的疼痛诊所与骨科和放射诊断科合作进行研究。
在基线时评估血清 CTX-1、P1NP 和脊柱、股骨颈和双股骨的 ESI 前 BMD;在 1、3 和 6 个月的随访中连续评估这些相同的参数。在 ESI 后 10 天进行额外的随访,以评估骨转换标志物(BTMs)。使用配对 t 检验分析组内 BMD 和 BTMs 与基线相比的变化。使用标准公式计算中度至明显低 BMD 的累积发生率和相对风险。还彻底评估和单独量化随访期间发生的任何骨折。P 值小于.05 被认为具有统计学意义。
研究人群中 ESI 前中度至明显低 BMD 的比例为 10.22%。ESI 后 10 天血清 CTX 1 显著增加,并持续至 1 个月和 3 个月随访。ESI 后 7 天和 1 个月随访时血清 P1NP 水平无显著变化。然而,血清 P1NP 的平均值在 3 个月随访时显著升高。对脊柱和股骨颈的平均 BMD 值进行统计学比较显示,3 个月后 ESI 后有统计学意义的下降。ESI 对总股骨 BMD 没有显著影响。在研究人群中,6 个月内中度至明显低 BMD 的累积发生率为 45 例(223 例中的 20.17%)。
该研究的主要局限性包括高脱落率、骨转换标志物的参考范围较大,使其成为比较不太具体的工具,以及缺乏对照组。ESI 对髋部和脊柱的 BMD 有负面影响。应将降低的 BMD 视为 ESI 的潜在副作用。