Clinical Study on Ginger Moxibustion Combined with Adalimumab to Improve Anxiety and Life Quality in Patients with Crohn's Disease at Mild and Moderate Active Stages
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摘要:
目的 观察铺姜灸联合阿达木单抗治疗对轻、中度活动期克罗恩病伴焦虑患者情绪及生活质量的影响。 方法 选择符合纳入标准的轻、中度活动期伴焦虑的克罗恩病患者60例, 随机分为治疗组和对照组各30例。对照组予阿达木单抗标准化治疗, 治疗组在对照组基础上联合铺姜灸治疗, 疗程均为12周, 观察2组患者中医证候积分及临床疗效、焦虑缓解应答率、治疗前后克罗恩病活动指数(CDAI)评分、炎症性肠病生存质量(IBDQ)评分及安全性指标的变化情况。 结果 治疗后, 2组患者中医证候积分均明显降低(P < 0.05, P < 0.01), 治疗组优于对照组(P < 0.05, P < 0.01);治疗组临床疗效、焦虑情绪缓解应答率优于对照组(P < 0.05);2组患者IBDQ评分均明显升高(P < 0.05, P < 0.01), 治疗组优于对照组(P < 0.05);2组患者CDAI评分均显著降低(P < 0.05, P < 0.01), 治疗组优于对照组(P < 0.05, P < 0.01)。 结论 铺姜灸联合阿达木单抗治疗可改善轻、中度活动期克罗恩病患者焦虑及生活质量。 Abstract:OBJECTIVE To observe the effect of ginger moxibustion combined with Adalimumab on the mood and life quality of patients with anxiety and Crohn's disease at mild and moderate active stages. METHODS 60 patients with anxiety and Crohn's disease at mild and moderate active stages who met the inclusion criteria were selected and randomly divided into the treatment group and control group with 30 cases each.The control group was given a standardized treatment of Adalimumab, and the treatment group was treated with ginger moxibustion on the basis of the control group.The course of treatment was 12 weeks.Observe the changes in TCM syndrome score and clinical efficacy, anxiety relief response rate, Crohn's disease activity index (CDAI) score, Inflammatory bowel disease quality of life (IBDQ) score, and safety indicators of the two groups of patients before and after treatment. RESULTS After treatment, the TCM syndrome scores of both groups were significantly reduced (P < 0.05, P < 0.01), and the treatment group was superior to the control group (P < 0.05, P < 0.01);the clinical efficacy and anxiety relief response rate of the treatment group were better than those of the control group (P < 0.05);the IBDQ scores of both groups were significantly increased (P < 0.05, P < 0.01), and the treatment group was better than the control group (P < 0.05);the CDAI scores of both groups significantly decreased (P < 0.05, P < 0.01), and the treatment group was better than the control group (P < 0.05, P < 0.01). CONCLUSION Ginger moxibustion combined with Adalimumab can improve the anxiety and life quality of patients with Crohn's disease at mild and moderate active stages. -
Key words:
- ginger moxibustion /
- Adalimumab /
- Crohn's disease /
- anxiety /
- quality of life
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表 1 2组患者基线数据[M(P25, P75), n=30]
Table 1. Comparison of baseline information between the two groups of patients [M(P25, P75), n=30]
组别 男 女 活动期 年龄/岁 病程/月 学历 HAMA评分 轻 中 专科及以下 专科以上 治疗组 26 4 12 18 22.00(17.75, 31.25) 1.00(1.00, 28.50) 16 14 14.00(11.50, 16.00) 对照组 25 5 14 16 24.00(17.00, 30.00) 4.00(0.00, 36.00) 21 9 14.50(12.00, 18.00) 表 2 中医证候积分评分标准
Table 2. Evaluation standard of TCM syndrome score
症状 0 1 2 3 主症 腹痛 无 轻微,隐痛 隐痛或胀痛 剧痛或绞痛 腹泻 无 每日<4次 每日≥4次,<6次 每日≥6次 便质 成形 不能成形 稀溏 如水样 脓血便 无 偶有 脓血便为主 全部为脓血便 腹胀 无 腹胀或食后腹胀 较重,每日≥6 h 腹胀如鼓 次症 情绪抑郁或急躁易怒 无 偶有 易发 急躁易怒难以控制 食少纳呆 无 饮食稍有减少 饮食减少 饮食明显减少 疲乏 无 偶感疲乏 疲乏较重 四肢无力 善太息 无 偶有 精神刺激后发作 频作 表 3 2组患者治疗前后中医证候积分比较[M(P25, P75), n=30]
Table 3. Comparison of TCM syndrome scores before and after treatment between the two groups of patients [M(P25, P75), n=30]
组别 时间 腹痛 腹泻 便质 脓血便 腹胀 治疗组 治疗前 1.00(0, 1.00) 1.00(1.00, 1.25) 1.00(0, 1.25) 0(0, 1.00) 0(0, 0) 治疗后 0(0, 0)**## 0(0, 0)**## 0(0, 1.00)**# 0(0, 0)**# 0(0, 0) 对照组 治疗前 0.50(0, 1.00) 1.00(1.00, 1.00) 1.00(1.00, 1.00) 0(0, 1.00) 0(0, 1.00) 治疗后 0(0, 1.00) 1.00(0, 1.00)** 1.00(0, 1.00)** 0(0, 0)* 0(0, 1.00) 组别 时间 情绪抑郁或急躁易怒 食少纳呆 疲乏 善太息 总积分 观察组 治疗前 1.00(1.00, 2.00) 1.00(1.00, 2.00) 1.00(0, 1.00) 1.00(1.00, 2.00) 7.00(5.75, 9.00) 治疗后 0(0, 0)**## 0(0, 0)**## 0(0, 0)** 0(0, 0)**## 1.00(0, 3.00)**## 对照组 治疗前 1.00(1.00, 1.00) 1.00(1.00, 2) 0(0, 0) 1.00(1.00, 1.00) 7.00(6.00, 9.00) 治疗后 0(0, 1.00)** 1.00(0, 1.00)** 0(0, 1.00)** 0(0, 1.00)** 3.00(1.75, 4.00)** 注: 组内比较, *P < 0.05, * *P < 0.01;组间比较, #P < 0.05, ##P < 0.01。 表 4 2组患者中医临床疗效比较(n=30)
Table 4. Comparison of TCM clinical curative effect between the two groups(n=30)
组别 例数 有效 无效 有效率/% 治疗组 30 26 4 86.70# 对照组 30 18 12 60.00 注: 组间比较, χ2=5.455, #P < 0.05。 表 5 2组患者治疗后焦虑缓解应答率比较(n=30)
Table 5. Comparison of anxiety relief response rate after treatment between the two groups(n=30)
组别 治疗后焦虑缓解 应答率/% 有效 无效 治疗组 25 5 83.30# 对照组 18 12 60.00 注: 组间比较, χ2=4.022, #P < 0.05。 表 6 2组患者治疗前后CDAI评分比较(x±s, n=30)
Table 6. Comparison of CDAI scores before and after treatment between the two groups(x±s, n=30)
组别 治疗前 治疗后 治疗组 222.81±39.95 111.77±31.93**# 对照组 221.52±37.94 132.60±41.50** 注: 组内比较, * *P < 0.01;组间比较, #P < 0.05。 表 7 2组患者治疗前后IBDQ评分比较(x±s, n=30)
Table 7. Comparison of IBDQ scores before and after treatment between the two groups(x ±s, n=30)
组别 时间 肠道症状(B) 全身症状(S) 情感功能(E) 社会功能(SF) 总分 治疗组 治疗前 49.67±9.33 22.10±4.60 51.80±9.21 18.94±5.92 142.77±25.54 治疗后 64.00±3.82**## 28.93±4.35**## 67.17±5.40**## 28.63±4.34**# 188.73±15.59**## 对照组 治疗前 52.53±10.21 20.90±6.12 55.70±10.79 22.17±7.31 150.33±29.30 治疗后 56.93±9.46* 24.87±4.29** 60.30±9.89* 26.20±4.36** 168.30±24.98** 注: 组内比较, *P < 0.05, * *P < 0.01;组间比较, #P < 0.05, ##P < 0.01。 -
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