Zhou J P, Lin Y Y, Zhu M F, Situ X X, Wang J
Department of Oncology Rehabilitation, Nan'ao People's Hospital, Dapeng New District of Shenzhen, Shenzhen 518000, China.
Clinical Medical College of Acupuncture Moxibustion and Rehabilitation, Guangzhou University of Chinese Medicine, Guangzhou 511400, China.
Zhonghua Shao Shang Yu Chuang Mian Xiu Fu Za Zhi. 2025 Jun 20;41(6):543-551. doi: 10.3760/cma.j.cn501225-20250205-00051.
To explore the clinical effects of extracorporeal shock wave therapy (ESWT) combined with complex decongestive therapy (CDT) in the treatment of lower limb lymphedema after cervical cancer surgery. This study was a prospective randomized controlled trial. From April 2023 to December 2024, 64 patients were admitted to the Department of Oncology Rehabilitation of Nan'ao People's Hospital of Dapeng New District of Shenzhen. All patients were female, aged 33-75 years. The patients were divided into control group treated with CDT alone and combined treatment group treated with ESWT and CDT according to the random number table method, with 32 patients in each group. Four patients withdrew in the research process, and 30 patients were included in each group finally. Before treatment and at the end of 4 weeks of treatment (hereinafter referred to as after treatment), the skin stiffness was measured using a portable MyotonPRO device at the superficial projection position of vastus lateralis, vastus medialis, vastus intermedius, medial gastrocnemius, and lateral gastrocnemius to reflect the degree of skin fibrosis of lower limb, the circumferences were measured at the mid-knee, 10 cm and 20 cm above the superior patellar border, and the mid-ankle, 10 cm and 20 cm below the inferior patellar border to reflect the severity degree of edema of lower limb, the life quality was scored using the simplified Chinese version of the lower limb lymphedema functioning, disability, and health questionnaire (Lymph-ICF-LL), and the pain intensity was scored using the visual analogue scale (VAS). The differences of the above indexes were calculated between before and after treatment. The skin stiffness at the superficial projection position of vastus lateralis, vastus medialis, vastus intermedius, medial gastrocnemius, and lateral gastrocnemius of patients in combined treatment group after treatment was significantly smaller than that in control group (with values of 2.78, 2.04, 3.12, 2.01, and 2.35, respectively, <0.05). The differences in skin stiffness between before and after treatment at the superficial projection position of the above-mentioned muscles of patients in combined treatment group was (65±23), (24±8), (25±8), (65±27), and (69±34) N/m, respectively, which were significantly larger than (49±23), (16±19), (8±9), (45±39), and (43±42) N/m in control group (with values of -2.75 -2.35, -7.47, -2.33, and -2.64, respectively, <0.05), and the mean differences between groups (95% confidence intervals) were 16 (5 to 28), 9 (1 to 17), 17 (12 to 21), 20 (3 to 36), and 26 (4 to 49) N/m, respectively. The circumferences at 10 cm and 20 cm below the inferior patellar border, mid-knee, and 10 cm and 20 cm above the superior patellar border of patients in combined treatment group after treatment were significantly smaller than those in control group (with values of -2.41, -2.49, -2.44, -2.21, and -2.36, respectively, <0.05). The circumference differences between before and after treatment at the above-mentioned locations of patients in combined treatment group were significantly larger than those in control group (with values of 2.21, 3.62, 3.35, 4.14, and 3.89, respectively, <0.05), and the mean differences between groups (95% confidence intervals) were 2.3 (0.1 to 4.6), 2.4 (1.0 to 3.8), 2.1 (0.8 to 3.4), 3.5 (1.6 to 5.4), and 3.4 (1.5 to 5.2) cm, respectively. The VAS scores of lower limb and the total Lymph-ICF-LL scores of patients in combined treatment group after treatment were significantly lower than those in control group (with values of -2.46 and -2.63, respectively, <0.05); the differences of VAS scores of lower limb and the total Lymph-ICF-LL scores between before and after treatment of patients in combined treatment group were significantly higher than those in control group (with values of 2.34 and 3.32, respectively, <0.05), and the mean differences between groups (95% confidence intervals) were 0.5 (0 to 0.9) and 6 (2 to 9), respectively. Combined application of ESWT and CDT shows superior efficacy in alleviating lower limb lymphedema and skin fibrosis after cervical cancer surgery, and can relieve pain and improve patients' quality of life.
探讨体外冲击波疗法(ESWT)联合综合消肿治疗(CDT)对宫颈癌术后下肢淋巴水肿的临床疗效。本研究为前瞻性随机对照试验。2023年4月至2024年12月,深圳市大鹏新区南澳人民医院肿瘤康复科收治64例患者。所有患者均为女性,年龄33 - 75岁。根据随机数字表法将患者分为单纯CDT治疗的对照组和ESWT联合CDT治疗的联合治疗组,每组32例。研究过程中有4例患者退出,最终每组纳入30例患者。在治疗前及治疗4周结束时(以下简称治疗后),使用便携式MyotonPRO设备在股外侧肌、股内侧肌、股中间肌、腓肠内侧肌和腓肠外侧肌的体表投影位置测量皮肤硬度,以反映下肢皮肤纤维化程度;在髌骨上缘中点、髌骨上缘上方10 cm和20 cm、踝关节中点、髌骨下缘下方10 cm和20 cm测量周径,以反映下肢水肿严重程度;使用下肢淋巴水肿功能、残疾和健康问卷(Lymph - ICF - LL)简化中文版对生活质量进行评分,使用视觉模拟评分法(VAS)对疼痛强度进行评分。计算治疗前后上述指标的差异。联合治疗组患者治疗后股外侧肌、股内侧肌、股中间肌、腓肠内侧肌和腓肠外侧肌体表投影位置的皮肤硬度明显小于对照组(分别为2.78、2.04、3.12、2.01和2.35,P<0.05)。联合治疗组患者上述肌肉体表投影位置治疗前后皮肤硬度的差异分别为(65±23)、(24±8)、(25±8)、(65±27)和(69±34)N/m,明显大于对照组的(49±23)、(16±19)、(8±9)、(45±39)和(43±42)N/m(分别为P值 - 2.75、 - 2.35、 - 7.47、 - 2.33和 - 2.64,P<0.05),组间平均差异(95%置信区间)分别为16(5至28)、9(1至17)、17(12至21)、20(3至36)和26(4至49)N/m。联合治疗组患者治疗后髌骨下缘下方10 cm和20 cm、膝关节中点及髌骨上缘上方10 cm和20 cm处的周径明显小于对照组(分别为P值 - 2.41、 - 2.49、 - 2.44、 - 2.21和 - 2.36,P<0.05)。联合治疗组患者上述部位治疗前后周径差异明显大于对照组(分别为P值2.21、3.62、3.35、4.14和3.89,P<0.05),组间平均差异(95%置信区间)分别为2.3(0.1至4.6)、2.4(1.0至3.8)、2.1(0.8至3.4)、3.5(1.6至5.4)和3.4(1.5至5.2)cm。联合治疗组患者治疗后下肢VAS评分及Lymph - ICF - LL总分明显低于对照组(分别为P值 - 2.46和 - 2.63,P<0.05);联合治疗组患者下肢VAS评分及Lymph - ICF - LL总分治疗前后差异明显高于对照组(分别为P值2.34和3.32,P<0.05),组间平均差异(95%置信区间)分别为0.5(0至0.9)和6(2至9)。ESWT与CDT联合应用在减轻宫颈癌术后下肢淋巴水肿和皮肤纤维化方面显示出卓越疗效,且能缓解疼痛并改善患者生活质量。