Hauser Ross A, Sprague Ingrid Schaefer
Caring Medical and Rehabilitation Services, SC, Oak Park, IL, USA.
Cleveland, OH, USA.
Clin Med Insights Arthritis Musculoskelet Disord. 2014 Feb 17;7:13-20. doi: 10.4137/CMAMD.S13098. eCollection 2014.
We retrospectively evaluated the effectiveness of prolotherapy in resolving pain, stiffness, and crepitus, and improving physical activity in consecutive chondromalacia patients from February 2008 to September 2009. Sixty-nine knees that received prolotherapy in 61 patients (33 female and 36 male) who were 18-82 years old (average, 47.2 years) were enrolled. Patients received 24 prolotherapy injections (15% dextrose, 0.1% procaine, and 10% sarapin) with a total of 40 cc in the anterior knee. At least 6 weeks after their last prolotherapy session, patients provided self-evaluation of knee pain upon rest, activities of daily living (ADL) and exercise, range of motion (ROM), stiffness, and crepitus. Symptom severity, sustained improvement of symptoms, number of pain pills needed, and patient satisfaction before treatment and improvement after treatment were recorded. Following prolotherapy, patients experienced statistically significant decreases in pain at rest, during ADL, and exercise. Stiffness and crepitus decreased after prolotherapy, and ROM increased. Patients reported improved walking ability and exercise ability after prolotherapy. For daily pain level, ROM, daily stiffness, crepitus, and walking and exercise ability, sustained improvement of over 75% was reported by 85% of patients. Fewer patients required pain medication. No side effects of prolotherapy were noted. The average length of time from last prolotherapy session was 14.7 months (range, 6 months to 8 years). Only 3 of 16 knees were still recommended for surgery after prolotherapy. Prolotherapy ameliorates chondromalacia patella symptoms and improves physical ability. Patients experience long-term improvement without requiring pain medications. Prolotherapy should be considered a first-line, conservative therapy for chondromalacia patella.
我们回顾性评估了2008年2月至2009年9月期间连续就诊的髌骨软化症患者接受注射疗法在缓解疼痛、僵硬和摩擦音以及改善身体活动方面的有效性。纳入了61例年龄在18 - 82岁(平均47.2岁)的患者的69个膝关节,这些膝关节接受了注射疗法(15%葡萄糖、0.1%普鲁卡因和10%沙巴蛇毒),共向前膝注射24次,总量为40 cc。在最后一次注射疗法至少6周后,患者对静息时的膝关节疼痛、日常生活活动(ADL)和运动、活动范围(ROM)、僵硬程度和摩擦音进行自我评估。记录治疗前和治疗后症状的严重程度、症状的持续改善情况、所需止痛片的数量以及患者满意度。注射疗法后,患者在静息、ADL和运动时的疼痛有统计学意义的显著降低。注射疗法后僵硬和摩擦音减轻,ROM增加。患者报告注射疗法后行走能力和运动能力有所改善。对于日常疼痛水平、ROM、日常僵硬程度、摩擦音以及行走和运动能力,85%的患者报告持续改善超过75%。需要止痛药物的患者减少。未观察到注射疗法的副作用。距最后一次注射疗法的平均时间为14.7个月(范围为6个月至8年)。注射疗法后,16个膝关节中只有3个仍被建议进行手术。注射疗法可改善髌骨软化症症状并提高身体能力。患者无需止痛药物即可获得长期改善。注射疗法应被视为髌骨软化症的一线保守治疗方法。